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Steinert RE, Rehman A, Sadabad MS, Milanese A, Wittwer-Schegg J, Burton JP, Spooren A. Microbial micronutrient sharing, gut redox balance and keystone taxa as a basis for a new perspective to solutions targeting health from the gut. Gut Microbes 2025; 17:2477816. [PMID: 40090884 PMCID: PMC11913388 DOI: 10.1080/19490976.2025.2477816] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 09/13/2024] [Revised: 02/05/2025] [Accepted: 03/05/2025] [Indexed: 03/18/2025] Open
Abstract
In health, the gut microbiome functions as a stable ecosystem maintaining overall balance and ensuring its own survival against environmental stressors through complex microbial interaction. This balance and protection from stressors is maintained through interactions both within the bacterial ecosystem as well as with its host. As a consequence, the gut microbiome plays a critical role in various physiological processes including maintaining the structure and function of the gut barrier, educating the gut immune system, and modulating the gut motor, digestive/absorptive, as well as neuroendocrine system all of which are crucial for human health and disease pathogenesis. Pre- and probiotics, widely available and clinically established, offer various health benefits primarily by beneficially modulating the gut microbiome. However, their clinical outcomes can vary significantly due to differences in host physiology, diets, individual microbiome compositions, and other environmental factors. This perspective paper highlights emerging scientific insights into the importance of microbial micronutrient sharing, gut redox balance, keystone species, and the gut barrier in maintaining a diverse and functional microbial ecosystem, and their relevance to human health. We propose a novel approach that targets microbial ecosystems and keystone taxa performance by supplying microbial micronutrients in the form of colon-delivered vitamins, and precision prebiotics [e.g. human milk oligosaccharides (HMOs) or synthetic glycans] as components of precisely tailored ingredient combinations to optimize human health. Such a strategy may effectively support and stabilize microbial ecosystems, providing a more robust and consistent approach across various individuals and environmental conditions, thus, overcoming the limitations of current single biotic solutions.
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Affiliation(s)
- Robert E. Steinert
- Health, Nutrition & Care (HNC), Dsm-Firmenich, Kaiseraugst, Switzerland
- Department of Surgery and Transplantation, University Hospital Zurich (USZ) and University of Zurich (UZH), Zürich, Switzerland
| | - Ateequr Rehman
- Health, Nutrition & Care (HNC), Dsm-Firmenich, Kaiseraugst, Switzerland
| | | | - Alessio Milanese
- Data Science, Science & Research, Dsm-Firmenich, Delft, Netherlands
| | | | - Jeremy P. Burton
- Department of Microbiology and Immunology, The University of Western Ontario, London, Canada
| | - Anneleen Spooren
- Health, Nutrition & Care (HNC), Dsm-Firmenich, Kaiseraugst, Switzerland
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2
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Jiang Y, Luo J, Guo X, Qiao Y, Li Y, Zhang Y, Zhou R, Vaculík M, Li T. Phyllosphere microbiome assists the hyperaccumulating plant in resisting heavy metal stress. J Environ Sci (China) 2025; 154:563-574. [PMID: 40049897 DOI: 10.1016/j.jes.2024.05.032] [Citation(s) in RCA: 2] [Impact Index Per Article: 2.0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 12/18/2023] [Revised: 05/17/2024] [Accepted: 05/20/2024] [Indexed: 05/13/2025]
Abstract
Phyllosphere microbiome plays an irreplaceable role in maintaining plant health under stress, but its structure and functions in heavy metal-hyperaccumulating plants remain elusive. Here, the phyllosphere microbiome, inhabiting hyperaccumulating (HE) and non-hyperaccumulating ecotype (NHE) of Sedum alfredii grown in soils with varying heavy metal concentration, was characterized. Compared with NHE, the microbial community α-diversity was greater in HE. Core phyllosphere taxa with high relative abundance (>10 %), including Streptomyces and Nocardia (bacteria), Cladosporium and Acremonium (fungi), were significantly related to cadmium (Cd) and zinc (Zn) concentration and biomass of host plants. Moreover, microbial co-occurrence networks in HE exhibited greater complexity than those in NHE. Additionally, proportions of positive associations in HE bacterial networks increased with the rising heavy metal concentration, indicating a higher resistance of HE phyllosphere microbiome to heavy metal stress. Furthermore, in contrast to NHE, microbial community functions, primarily involved in heavy metal stress resistance, were more abundant in HE, in which microbiome assisted hosts to resist heavy metal stress better. Collectively, this study indicated that phyllosphere microbiome of the hyperaccumulator played an indispensable role in assisting hosts to resist heavy metal stress, and provided new insights into phyllosphere microbial application potential in phytoremediation.
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Affiliation(s)
- Yue Jiang
- Ministry of Education Key Laboratory of Environmental Remediation and Ecological Health, College of Environmental and Resource Sciences, Zhejiang University, Hangzhou 310058, China
| | - Jipeng Luo
- Ministry of Education Key Laboratory of Environmental Remediation and Ecological Health, College of Environmental and Resource Sciences, Zhejiang University, Hangzhou 310058, China
| | - Xinyu Guo
- Ministry of Education Key Laboratory of Environmental Remediation and Ecological Health, College of Environmental and Resource Sciences, Zhejiang University, Hangzhou 310058, China
| | - Yabei Qiao
- Ministry of Education Key Laboratory of Environmental Remediation and Ecological Health, College of Environmental and Resource Sciences, Zhejiang University, Hangzhou 310058, China
| | - Yuhang Li
- Ministry of Education Key Laboratory of Environmental Remediation and Ecological Health, College of Environmental and Resource Sciences, Zhejiang University, Hangzhou 310058, China
| | - Yu Zhang
- Ministry of Education Key Laboratory of Environmental Remediation and Ecological Health, College of Environmental and Resource Sciences, Zhejiang University, Hangzhou 310058, China
| | - Runhui Zhou
- Ministry of Education Key Laboratory of Environmental Remediation and Ecological Health, College of Environmental and Resource Sciences, Zhejiang University, Hangzhou 310058, China
| | - Marek Vaculík
- Department of Plant Physiology, Faculty of Natural Sciences, Comenius University in Bratislava, Bratislava 84215, Slovakia
| | - Tingqiang Li
- Ministry of Education Key Laboratory of Environmental Remediation and Ecological Health, College of Environmental and Resource Sciences, Zhejiang University, Hangzhou 310058, China; Zhejiang Provincial Key Laboratory of Agricultural Resources and Environment, Hangzhou 310058, China.
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3
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Darriaut R, Roose-Amsaleg C, Vanhove M, Monard C. Microbiome engineering to palliate microbial dysbiosis occurring in agroecosystems. Microbiol Res 2025; 297:128178. [PMID: 40220558 DOI: 10.1016/j.micres.2025.128178] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/17/2025] [Revised: 03/28/2025] [Accepted: 04/07/2025] [Indexed: 04/14/2025]
Abstract
Plant health and productivity are closely tied to the fluctuations of soil microbiomes, which regulate biogeochemical processes and plant-soil interactions. However, environmental and anthropogenic stressors, including climate change, intensive agricultural practices, and industrial activities, disrupt these microbial communities. This microbial imbalance reduces soil fertility, plant health, and biodiversity, threatening agroecosystem sustainability. This review explores the mechanisms driving microbial dysbiosis in soil and plant environments. Plants under stress release chemical signals through root exudates, dynamically recruiting beneficial microbes to counteract microbial imbalances. Moreover, this review evaluates traditional methods to alleviate these stress-induced microbial alterations, such as microbial inoculants and organic soil amendments, alongside innovative strategies like phage therapy, CRISPR, and small RNA-based technologies. Despite these advancements, the practical implementation of microbiome interventions faces significant challenges. These include regulatory hurdles, economic constraints, and the need for long-term field studies to validate efficacy and ensure environmental safety.
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Affiliation(s)
- Romain Darriaut
- Univ Rennes, CNRS, ECOBIO (Ecosystèmes, biodiversité, évolution) - UMR 6553, Rennes F-35000, France.
| | - Céline Roose-Amsaleg
- Univ Rennes, CNRS, ECOBIO (Ecosystèmes, biodiversité, évolution) - UMR 6553, Rennes F-35000, France
| | - Mathieu Vanhove
- Univ Rennes, CNRS, ECOBIO (Ecosystèmes, biodiversité, évolution) - UMR 6553, Rennes F-35000, France
| | - Cécile Monard
- Univ Rennes, CNRS, ECOBIO (Ecosystèmes, biodiversité, évolution) - UMR 6553, Rennes F-35000, France
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4
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Chen H, Zhong S, Liu Z, Hu Z, Wang C, Zhou Y, Xu N, Zhao F, Li D, Hu Y. Microbiome-metabolomic insights into the systemic regulation in Fangxian Huangjiu fermentation. Food Chem 2025; 481:143980. [PMID: 40154057 DOI: 10.1016/j.foodchem.2025.143980] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/04/2025] [Revised: 03/04/2025] [Accepted: 03/19/2025] [Indexed: 04/01/2025]
Abstract
Metabolic forces drive microecological succession in Huangjiu fermentation. This study investigates the dynamic metabolic-microbial interplay during Fangxian Huangjiu fermentation. Temporal changes of metabolome and microbiome revealed a syntropic relationship that purified the microbial community with convergent metabolic patterns. With species turnover driving microbial community structure, early-stage microbiomes exhibited great functional diversity. Functions related to energy and molecular building blocks were enriched at the end of early stage, and contributed greatly to microbial adaptation, highlighting the importance of metabolic forces in shaping community structure. Proteobacteria were identified as key facilitators of diverse metabolic activities, and Enterobacter emerged as a fundamental microbial community particularly for materials transformation. Correlation analysis enriched amino acid metabolism pathways. Further, Pantoea ananatis and Wickerhamomyces anomalus were isolated to enhance sphingosine-1-phosphate, γ-aminobutyric acid, and creatine levels without altering physicochemical properties. The study offers insights into the regulation of Huangjiu fermentation, and suggested potential micobiome manipulation to optimize characteristics.
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Affiliation(s)
- Haiyin Chen
- Key Laboratory of Fermentation Engineering (Ministry of Education), Hubei Key Laboratory of Industrial Microbiology, National "111" Center for Cellular Regulation and Molecular Pharmaceutics, Hubei Research Center of Food Fermentation Engineering and Technology, Cooperative Innovation Center of Industrial Fermentation (Ministry of Education & Hubei Province), Hubei University of Technology, Wuhan, 430068, Hubei, China
| | - Sicheng Zhong
- Key Laboratory of Fermentation Engineering (Ministry of Education), Hubei Key Laboratory of Industrial Microbiology, National "111" Center for Cellular Regulation and Molecular Pharmaceutics, Hubei Research Center of Food Fermentation Engineering and Technology, Cooperative Innovation Center of Industrial Fermentation (Ministry of Education & Hubei Province), Hubei University of Technology, Wuhan, 430068, Hubei, China
| | - Zhijie Liu
- Key Laboratory of Fermentation Engineering (Ministry of Education), Hubei Key Laboratory of Industrial Microbiology, National "111" Center for Cellular Regulation and Molecular Pharmaceutics, Hubei Research Center of Food Fermentation Engineering and Technology, Cooperative Innovation Center of Industrial Fermentation (Ministry of Education & Hubei Province), Hubei University of Technology, Wuhan, 430068, Hubei, China
| | - Zhao Hu
- Hubei Lulingwang Liquor Industry Co., Ltd, Fangxian 442399, Hubei, China
| | - Chao Wang
- Key Laboratory of Fermentation Engineering (Ministry of Education), Hubei Key Laboratory of Industrial Microbiology, National "111" Center for Cellular Regulation and Molecular Pharmaceutics, Hubei Research Center of Food Fermentation Engineering and Technology, Cooperative Innovation Center of Industrial Fermentation (Ministry of Education & Hubei Province), Hubei University of Technology, Wuhan, 430068, Hubei, China
| | - Yuke Zhou
- Key Laboratory of Fermentation Engineering (Ministry of Education), Hubei Key Laboratory of Industrial Microbiology, National "111" Center for Cellular Regulation and Molecular Pharmaceutics, Hubei Research Center of Food Fermentation Engineering and Technology, Cooperative Innovation Center of Industrial Fermentation (Ministry of Education & Hubei Province), Hubei University of Technology, Wuhan, 430068, Hubei, China
| | - Ning Xu
- Key Laboratory of Fermentation Engineering (Ministry of Education), Hubei Key Laboratory of Industrial Microbiology, National "111" Center for Cellular Regulation and Molecular Pharmaceutics, Hubei Research Center of Food Fermentation Engineering and Technology, Cooperative Innovation Center of Industrial Fermentation (Ministry of Education & Hubei Province), Hubei University of Technology, Wuhan, 430068, Hubei, China
| | - Fuquan Zhao
- Hubei Lulingwang Liquor Industry Co., Ltd, Fangxian 442399, Hubei, China
| | - Dongsheng Li
- Key Laboratory of Fermentation Engineering (Ministry of Education), Hubei Key Laboratory of Industrial Microbiology, National "111" Center for Cellular Regulation and Molecular Pharmaceutics, Hubei Research Center of Food Fermentation Engineering and Technology, Cooperative Innovation Center of Industrial Fermentation (Ministry of Education & Hubei Province), Hubei University of Technology, Wuhan, 430068, Hubei, China
| | - Yong Hu
- Key Laboratory of Fermentation Engineering (Ministry of Education), Hubei Key Laboratory of Industrial Microbiology, National "111" Center for Cellular Regulation and Molecular Pharmaceutics, Hubei Research Center of Food Fermentation Engineering and Technology, Cooperative Innovation Center of Industrial Fermentation (Ministry of Education & Hubei Province), Hubei University of Technology, Wuhan, 430068, Hubei, China; Hubei Xizhiyuan Bioengineering Co., Ltd, 445099, Hubei, China.
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5
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Xie E, Chen Z, Zhang X, Zhang X, Zheng L, Wang X, Zhang D. Stable isotope probing and oligotyping reveal the impact of organophosphorus pesticides on the carbon fixation related bacterioplankton lineage. JOURNAL OF HAZARDOUS MATERIALS 2025; 492:138159. [PMID: 40187249 DOI: 10.1016/j.jhazmat.2025.138159] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 12/10/2024] [Revised: 03/31/2025] [Accepted: 04/01/2025] [Indexed: 04/07/2025]
Abstract
Freshwater bacterioplankton communities play a pivotal role in global carbon fixation and energy exchange. However, establishing direct linkages between environmental stressors like organophosphorus pesticides (OPPs) and the ecological functions, such as carbon-fixing related microorganisms (CFMs), remains challenging. This study investigated the effects of four OPPs - two phosphates (dichlorvos, monocrotophos) and two phosphorothioates (omethoate, parathion) - on bacterioplankton communities using stable isotope probing, high-throughput sequencing and oligotyping analysis. Seven CFMs were identified. All OPPs significantly reduced total biomass (from 7.87 ×104 to 2.30-4.11 ×104 cells/mL) but stimulated CFMs proliferation. Notably, phosphorothioates induced a greater increase in CFMs abundance (36.84 %-57.18 %, up from 21.1 %) compared to phosphates (23.85 %-37.10 %; p < 0.05). Principal coordinate analysis (PCoA) revealed that phosphorothioates exerted stronger effects on microbial community and CFMs oligotypes structure compared to phosphates (p < 0.05). Variance partitioning analysis (VPA) identified pesticide type as the dominant driver of community structure. PICRUSt2 prediction demonstrated that OPPs suppressed oxidoreductase pathways linked to energy metabolism while activating transferase pathways associated with microbial stress resistance. Phosphorothioates depleted 64 pathways and enhanced 208 pathways, far exceeding phosphate impacts (2 depleted, 22 enhanced), indicating the phosphorothioates played a more important role on bacterioplankton communities than phosphate. Additionally, OPPs exposure reduced functional redundancy and destabilized community stability in bacterioplankton, potentially granting CFMs a long-term competitive advantage and elevating algal bloom risks. These findings provide insights into active CFMs in aquatic systems and their responses to diverse OPPs, offering new perspectives for managing organophosphorus pesticide contamination.
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Affiliation(s)
- En Xie
- College of Water Resources and Civil Engineering, China Agricultural University, Beijing 100083, PR China; Engineering Research Center for Agricultural Water-Saving and Water Resources, Ministry of Education, Beijing 100083, PR China.
| | - Ziwei Chen
- College of Water Resources and Civil Engineering, China Agricultural University, Beijing 100083, PR China
| | - Xu Zhang
- Chongqing Nanan District ecology and environment Bureau, Chongqing 401336, PR China
| | - Xinyuan Zhang
- College of Water Resources and Civil Engineering, China Agricultural University, Beijing 100083, PR China
| | - Lei Zheng
- College of Water Sciences, Beijing Normal University, Beijing 100875, PR China
| | - Xue Wang
- College of Water Sciences, Beijing Normal University, Beijing 100875, PR China
| | - Dayi Zhang
- College of New Energy and Environment, Jilin University, Changchun 130021, PR China.
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6
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Cheng Y, Zheng X, Jiang Y, Xiao Q, Luo Q, Ding Y. Key genes and microbial ecological clusters involved in organophosphate ester degradation in agricultural fields of a typical watershed in southwest China. JOURNAL OF HAZARDOUS MATERIALS 2025; 492:138076. [PMID: 40209409 DOI: 10.1016/j.jhazmat.2025.138076] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 11/23/2024] [Revised: 03/06/2025] [Accepted: 03/24/2025] [Indexed: 04/12/2025]
Abstract
Organophosphate esters (OPEs) are widely used as flame retardants and plasticizers, and they have raised global concern due to their persistence, bioaccumulation, and potential toxicity. However, OPE contamination characteristics and microbial degradation mechanisms in agricultural soils remain poorly understood. This study investigated agricultural soils from the riparian zone of the Anning River Basin in southwest China. The concentrations of 12 OPEs were determined using gas chromatography-tandem mass spectrometry. The results revealed that the total OPE concentration was moderate, with triethyl phosphate being the most abundant compound. Metagenomic techniques and Bayesian linear regression analysis were employed in combination with the Kyoto Encyclopedia of Genes and Genomes database to identify potential degradation pathways for triethyl phosphate and tris (2-chloroethyl) phosphate. The phoA, phoB, phoD, and glpQ genes, which encode phosphatases, catalyze ester bond cleavage, thereby facilitating the degradation of OPEs. Further microbial interaction network analysis identified core OPE-degrading microorganisms, including Pimelobacter simplex, Nocardioides sp. JS614, Nocardioides daphniae, and Methylocystis heyeri. Additionally, neutral community models indicated that environmental selection drives microbial community structure. In conclusion, this study provides an in-depth understanding of OPE contamination and its microbial degradation mechanisms in agricultural soils, offering theoretical insights for pollution management and remediation strategies.
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Affiliation(s)
- Yu Cheng
- College of Geography, China West Normal University, Nanchong 637009, PR China; Sichuan Provincial Engineering Laboratory of Monitoring and Control for Soil Erosion on Dry Valleys, China West Normal University, Nanchong 637009, PR China
| | - Xuehao Zheng
- College of Geography, China West Normal University, Nanchong 637009, PR China; Sichuan Provincial Engineering Laboratory of Monitoring and Control for Soil Erosion on Dry Valleys, China West Normal University, Nanchong 637009, PR China; Agro-Environmental Protection Institute, Ministry of Agriculture and Rural Affairs, Tianjin 300191, PR China.
| | - Yukun Jiang
- Key Laboratory of Ecological Restoration of Regional Contaminated Environment, Ministry of Education, College of Environment, Shenyang University, Shenyang 110044, China
| | - Qiang Xiao
- Sichuan Provincial Engineering Laboratory of Monitoring and Control for Soil Erosion on Dry Valleys, China West Normal University, Nanchong 637009, PR China
| | - Qing Luo
- Key Laboratory of Ecological Restoration of Regional Contaminated Environment, Ministry of Education, College of Environment, Shenyang University, Shenyang 110044, China.
| | - Yongzhen Ding
- Agro-Environmental Protection Institute, Ministry of Agriculture and Rural Affairs, Tianjin 300191, PR China.
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7
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Liu J, Chen Y, Sun B, Xu D, Wang J, Sun Z, Liu P, Jing F, Song Y, Xia B. Toxicological effects of micro/nanoplastics and benzo[a]pyrene on cellular and molecular responses of Apostichopus japonicus (Selenka, 1867) during intestinal regeneration. JOURNAL OF HAZARDOUS MATERIALS 2025; 491:138003. [PMID: 40120257 DOI: 10.1016/j.jhazmat.2025.138003] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 10/15/2024] [Revised: 03/14/2025] [Accepted: 03/18/2025] [Indexed: 03/25/2025]
Abstract
Micro(nano)plastics (M/NPs) are pervasive in marine environments. Benzo[a]pyrene (B[a]P), a typical polycyclic aromatic hydrocarbon (PAH), possesses teratogenic, mutagenic, and carcinogenic properties. B[a]P can accumulate on M/NPs, altering their toxicity. This study investigated individual and combined effects of M/NPs and B[a]P on the intestinal regeneration of the benthic invertebrate Apostichopus japonicus. Eviscerated sea cucumbers were exposed to 0.1 mg L-1 M/NPs (80 nm [NP80] or 20 μm [MP20]) and/or 0.03 μg L-1 B[a]P for 28 days. Cell proliferation, antioxidant and immunoenzyme activity, gene expression, and microbial community in the regenerated intestine were assessed. It demonstrated that combined exposure prolonged regeneration process, leading to increased oxidative stress and intestinal damage. Differential gene expression analysis revealed that co-exposure and single NP80 exposure both significantly changed translation-related processes, while single MP20 exposure primarily affected lipid metabolism. All treatments significantly altered the intestinal microbiota. Under the MP20+B[a]P treatment, Ralstonia abundance significantly increased, while Cobetia and Paracoccus abundances decreased. In general, co-exposure exerted more detrimental effects on intestinal regeneration than any single exposure, with MP20+B[a]P demonstrating more severe impacts. This study provides novel insights into the biotoxicity of M/NPs and B[a]P, contributing to better understanding of the detriments of microplastics and PAHs on marine benthic invertebrates.
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Affiliation(s)
- Ji Liu
- School of Marine Science and Engineering, Qingdao Agricultural University, Qingdao, Shandong Province 266109, China
| | - Yanru Chen
- School of Marine Science and Engineering, Qingdao Agricultural University, Qingdao, Shandong Province 266109, China
| | - Baiqin Sun
- School of Marine Science and Engineering, Qingdao Agricultural University, Qingdao, Shandong Province 266109, China
| | - Dongxue Xu
- School of Marine Science and Engineering, Qingdao Agricultural University, Qingdao, Shandong Province 266109, China
| | - Jinye Wang
- School of Marine Science and Engineering, Qingdao Agricultural University, Qingdao, Shandong Province 266109, China
| | - Zhenlong Sun
- Jiangsu Zhongyang Group Co., Ltd., Nantong, Jiangsu Province 226600, China.
| | - Peng Liu
- Shandong Fisheries Development and Resources Conservation Center, Jinan, Shandong Province 250013, China
| | - Futao Jing
- Shandong Fisheries Development and Resources Conservation Center, Jinan, Shandong Province 250013, China
| | - Yize Song
- School of Marine Science and Engineering, Qingdao Agricultural University, Qingdao, Shandong Province 266109, China
| | - Bin Xia
- School of Marine Science and Engineering, Qingdao Agricultural University, Qingdao, Shandong Province 266109, China.
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Wang K, Flury M, Kuzyakov Y, Zhang H, Zhu W, Jiang R. Aluminum and microplastic release from reflective agricultural films disrupt microbial communities and functions in soil. JOURNAL OF HAZARDOUS MATERIALS 2025; 491:137891. [PMID: 40081051 DOI: 10.1016/j.jhazmat.2025.137891] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 12/03/2024] [Revised: 02/14/2025] [Accepted: 03/07/2025] [Indexed: 03/15/2025]
Abstract
Reflective agricultural films are widely used in vegetable production and orchards to repel pests, accelerate fruit ripening, and boost yields. These films, composed of a plastic base metallized with aluminum (Al), degrade over time in soil, releasing Al and microplastics. This study investigated the aging and weathering of Al-coated reflective films (polyethylene terephthalate, PET-based) under UV radiation, simulated rainfall, and soil burial for up to 120 days, assessing the effects of released Al and microplastics on soil chemistry and microbial communities. Weathering was confirmed by the formation of C-O/CO functional groups, an increasing carbonyl index, and the oxidation of Al to Al₂O₃, as shown by Fourier-transform infrared (FTIR) and X-ray photoelectron spectroscopy (XPS). Faster Al-coated shedding and PET oxidation were observed in the soil environment. Microplastics (0.5 % w/w) from the films reduced soil micronutrient availability (Fe, Mn, Cu), suppressed functional genes involved in carbon, nitrogen, and phosphorus cycling, and shifted microbial communities towards oligotrophic bacteria enrichment (e.g., RB41, Candidatus_Udaeobacter, Gemmatimonadetes, and Chloroflexi) while reducing copiotrophic bacteria (e.g., Sphingomonas, Ellin6067, Dongia, Puia, and Flavisolibacter). Therefore, these findings highlight that reflective film weathering strongly alters soil nutrient content and microbial community composition, with potential implications for soil health and agricultural sustainability.
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Affiliation(s)
- Kai Wang
- Research Center for Cultural Landscape Protection and Ecological Restoration, China-Portugal Joint Laboratory of Cultural Heritage Conservation Science Supported by the Belt and Road Initiative, Gold Mantis School of Architecture, Soochow University, Suzhou 215006, China; College of Natural Resources and Environment, Northwest A&F University, Yangling 712100, China
| | - Markus Flury
- Department of Crop and Soil Sciences, Washington State University, Pullman 99164 and Puyallup, WA 98371, United States
| | - Yakov Kuzyakov
- Department of Agricultural Soil Science, Georg-August, University of Göttingen, Göttingen 37077, Germany; Bioeconomy Research Institute, Vytautas Magnus University, Agriculture Academy, Studentu 11, LT-53361 Akademija, Kaunas Reg., Lithuania
| | - Hao Zhang
- Research Center for Cultural Landscape Protection and Ecological Restoration, China-Portugal Joint Laboratory of Cultural Heritage Conservation Science Supported by the Belt and Road Initiative, Gold Mantis School of Architecture, Soochow University, Suzhou 215006, China; College of Natural Resources and Environment, Northwest A&F University, Yangling 712100, China
| | - Wei Zhu
- College of Civil and Architecture Engineering, Chuzhou University, Chuzhou 239000, China
| | - Rui Jiang
- Research Center for Cultural Landscape Protection and Ecological Restoration, China-Portugal Joint Laboratory of Cultural Heritage Conservation Science Supported by the Belt and Road Initiative, Gold Mantis School of Architecture, Soochow University, Suzhou 215006, China.
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9
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Zhao X, Chen A, Gong X, Zhang P, Cui K, Li S, Zhang W, Zhu C, Gang H, Huo J, Xie F, Qin D. Metabolite-mediated responses of phyllosphere microbiota to powdery mildew infection in resistant and susceptible black currant cultivars. HORTICULTURE RESEARCH 2025; 12:uhaf092. [PMID: 40371437 PMCID: PMC12077297 DOI: 10.1093/hr/uhaf092] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Track Full Text] [Download PDF] [Figures] [Subscribe] [Scholar Register] [Received: 12/05/2024] [Accepted: 03/18/2025] [Indexed: 05/16/2025]
Abstract
Plant-metabolite-microbe interactions play essential roles in disease suppression. Most studies focus on the root exudates and rhizosphere microbiota to fight soil-borne pathogens, but it is poorly understood whether the changes in phyllosphere metabolites can actively recruit beneficial microbes to enhance disease resistance. In this study, the differences of phyllosphere microbial communities and key leaf metabolites were systematically explored in resistant and susceptible black currant cultivars related to powdery mildew (PM) by integrating microbiome and metabolomic analyses. The results showed that the diversity and composition of microbiome changed, as highlighted by a reduction in microbial alpha-diversity and beta-diversity of susceptible cultivars. An increasing fungal network complexity and a decreasing bacterial network complexity occurred in resistant cultivar. Bacillus, Burkholderia (bacteria), and Penicillium (fungi) were identified as keystone microorganisms and resistance effectors in resistant cultivar. Metabolites such as salicylic acid, trans-zeatin, and griseofulvin were more abundant in resistant cultivar, which had a positive regulatory effect on the abundance of bacterial and fungal keystones. These findings unravel that resistant cultivar can enrich beneficial microorganisms by adjusting leaf metabolites, thus showing the external disease-resistant response. Moreover, the reduced stomatal number and increased tissue thickness were observed in resistant cultivar, suggesting inherent physical structure also provides a basic defense against PM pathogens. Therefore, resistant black currant cultivar displayed multilevel defense responses of physical structures, metabolites, and microorganisms to PM pathogens. Collectively, our study highlights the potential for utilizing phyllosphere microbiome dynamics and metabolomic adjustments in agricultural practices, plant breeding, and microbiome engineering to develop disease-resistant crops.
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Affiliation(s)
- Xueying Zhao
- College of Horticulture & Landscape Architecture, Northeast Agricultural University, No 600, Changjiang Road, Xiangfang District, Harbin City, Heilongjiang Province, China
- National-Local Joint Engineering Research Center for Development and Utilization of Small Fruits in Cold Regions, Northeast Agricultural University, No 600, Changjiang Road, Xiangfang District, Harbin City, Heilongjiang Province, China
| | - Along Chen
- College of Horticulture & Landscape Architecture, Northeast Agricultural University, No 600, Changjiang Road, Xiangfang District, Harbin City, Heilongjiang Province, China
| | - Xiaonan Gong
- Shandong Provincial Forestry Protection and Development Service Center, No.5948, Second Ring East Road, LixiaDistrict, Jinan City, Shandong Province, China
| | - Peng Zhang
- College of Horticulture & Landscape Architecture, Northeast Agricultural University, No 600, Changjiang Road, Xiangfang District, Harbin City, Heilongjiang Province, China
- National-Local Joint Engineering Research Center for Development and Utilization of Small Fruits in Cold Regions, Northeast Agricultural University, No 600, Changjiang Road, Xiangfang District, Harbin City, Heilongjiang Province, China
| | - Kaojia Cui
- College of Horticulture & Landscape Architecture, Northeast Agricultural University, No 600, Changjiang Road, Xiangfang District, Harbin City, Heilongjiang Province, China
- National-Local Joint Engineering Research Center for Development and Utilization of Small Fruits in Cold Regions, Northeast Agricultural University, No 600, Changjiang Road, Xiangfang District, Harbin City, Heilongjiang Province, China
| | - Shuxian Li
- College of Horticulture & Landscape Architecture, Northeast Agricultural University, No 600, Changjiang Road, Xiangfang District, Harbin City, Heilongjiang Province, China
- National-Local Joint Engineering Research Center for Development and Utilization of Small Fruits in Cold Regions, Northeast Agricultural University, No 600, Changjiang Road, Xiangfang District, Harbin City, Heilongjiang Province, China
| | - Weixia Zhang
- College of Horticulture & Landscape Architecture, Northeast Agricultural University, No 600, Changjiang Road, Xiangfang District, Harbin City, Heilongjiang Province, China
- National-Local Joint Engineering Research Center for Development and Utilization of Small Fruits in Cold Regions, Northeast Agricultural University, No 600, Changjiang Road, Xiangfang District, Harbin City, Heilongjiang Province, China
| | - Chenqiao Zhu
- College of Horticulture & Landscape Architecture, Northeast Agricultural University, No 600, Changjiang Road, Xiangfang District, Harbin City, Heilongjiang Province, China
- National-Local Joint Engineering Research Center for Development and Utilization of Small Fruits in Cold Regions, Northeast Agricultural University, No 600, Changjiang Road, Xiangfang District, Harbin City, Heilongjiang Province, China
| | - Huixin Gang
- College of Horticulture & Landscape Architecture, Northeast Agricultural University, No 600, Changjiang Road, Xiangfang District, Harbin City, Heilongjiang Province, China
- National-Local Joint Engineering Research Center for Development and Utilization of Small Fruits in Cold Regions, Northeast Agricultural University, No 600, Changjiang Road, Xiangfang District, Harbin City, Heilongjiang Province, China
| | - Junwei Huo
- College of Horticulture & Landscape Architecture, Northeast Agricultural University, No 600, Changjiang Road, Xiangfang District, Harbin City, Heilongjiang Province, China
- National-Local Joint Engineering Research Center for Development and Utilization of Small Fruits in Cold Regions, Northeast Agricultural University, No 600, Changjiang Road, Xiangfang District, Harbin City, Heilongjiang Province, China
| | - Fuchun Xie
- College of Animal Science and Technology, Northeast Agricultural University, No 600, Changjiang Road, Xiangfang District, Harbin City, Heilongjiang Province, China
| | - Dong Qin
- College of Horticulture & Landscape Architecture, Northeast Agricultural University, No 600, Changjiang Road, Xiangfang District, Harbin City, Heilongjiang Province, China
- National-Local Joint Engineering Research Center for Development and Utilization of Small Fruits in Cold Regions, Northeast Agricultural University, No 600, Changjiang Road, Xiangfang District, Harbin City, Heilongjiang Province, China
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10
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Qiao Y, Shen M, Kong L, Sun Y, Wang S, Gao Y, Xue J, Jiang Q, Cheng D, Liu Y. Better ecosystem resistibility but with severer risk deriving from potential pathogens and antibiotic resistances in marine sediments adjacent to Yellow River estuary under oil contamination. ENVIRONMENTAL RESEARCH 2025; 276:121486. [PMID: 40147517 DOI: 10.1016/j.envres.2025.121486] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 12/22/2024] [Revised: 03/24/2025] [Accepted: 03/25/2025] [Indexed: 03/29/2025]
Abstract
Estuaries, a vital coastal system, exhibit extensive anthropogenic impacts on their ecological integrity. However, little is known about microbial responses and associated risks in marine sediments around Yellow River estuary (YRE) at an outbreak of oil pollution. Herein, via molecular sequencing and physicochemical experiments, the characteristics of microbiota, potential pathogens and antibiotic resistance were comprehensively investigated in sediments collected from three areas with varying distances to YRE at diesel-polluted microcosms. Specifically, higher stability, stronger stochasticity-dominated assembly processes and more abundant petroleum metabolic pathways were observed in bacterial community nearest to the estuary (YE). Furthermore, an enrichment of potential pathogens and antibiotics resistance genes (ARGs), those mainly related to multidrug-resistance efflux pumps, as well as the accelerated dissemination of ARGs, all were found across all regions along the pollution time, especially those in YE. Several core pathogens (e.g., Pseudomonas) were simultaneously related with multidrug resistances and their transmissions, and a more robust relationship among them was found in YE. Culturable experiments demonstrated numerous potential pathogens were capable of efficiently degrading oil contaminants. A global investigation revealed the sediment pathogens with oil degradation potential were widely distributed in shallow- and deep-sea water bodies, with higher abundance in coastal zones, suggesting extensive pathogenic risks from these bacteria also in oil-polluted aquatic environments. Altogether, the findings unmask the sound resistibility but with serious hazard of potential pathogens and antibiotic resistance in oil-contaminated sediment ecosystem nearest to YRE, and offer novel insights and potential targets for estuarine risk assessment and control.
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Affiliation(s)
- Yanlu Qiao
- College of Safety and Environmental Engineering, Shandong University of Science and Technology, Qingdao, Shandong 266590, China
| | - Mingan Shen
- College of Safety and Environmental Engineering, Shandong University of Science and Technology, Qingdao, Shandong 266590, China
| | - Lingbing Kong
- College of Safety and Environmental Engineering, Shandong University of Science and Technology, Qingdao, Shandong 266590, China
| | - Yudi Sun
- College of Safety and Environmental Engineering, Shandong University of Science and Technology, Qingdao, Shandong 266590, China
| | - Shuo Wang
- College of Safety and Environmental Engineering, Shandong University of Science and Technology, Qingdao, Shandong 266590, China
| | - Yu Gao
- College of Safety and Environmental Engineering, Shandong University of Science and Technology, Qingdao, Shandong 266590, China
| | - Jianliang Xue
- College of Safety and Environmental Engineering, Shandong University of Science and Technology, Qingdao, Shandong 266590, China
| | - Qing Jiang
- College of Safety and Environmental Engineering, Shandong University of Science and Technology, Qingdao, Shandong 266590, China
| | - Dongle Cheng
- College of Safety and Environmental Engineering, Shandong University of Science and Technology, Qingdao, Shandong 266590, China; Institute of Yellow River Delta Earth Surface Processes and Ecological Integrity, Shandong University of Science and Technology, Qingdao, Shandong 266590, China
| | - Yuyang Liu
- College of Safety and Environmental Engineering, Shandong University of Science and Technology, Qingdao, Shandong 266590, China; Institute of Yellow River Delta Earth Surface Processes and Ecological Integrity, Shandong University of Science and Technology, Qingdao, Shandong 266590, China.
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11
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Huang Y, Feng J, Wang X, Zhang Y, Zhang S. Microplastic type and concentration affect prokaryotic community structure and species coexistence in deep-sea cold seep sediments. JOURNAL OF HAZARDOUS MATERIALS 2025; 489:137727. [PMID: 40010225 DOI: 10.1016/j.jhazmat.2025.137727] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 11/06/2024] [Revised: 02/20/2025] [Accepted: 02/22/2025] [Indexed: 02/28/2025]
Abstract
As important methane hydrate storage sites, cold seep areas are threatened by microplastics (MPs) contamination. To assess the environmental impact of MPs on microbial communities in cold seep sediments, an incubation experiment was conducted using cold seep sediment amended with different concentration of polyamide (PA), polyethylene (PE), polyethylene terephthalate (PET), and polypropylene (PP) microplastics. The results showed that the different type and concentration of MPs significantly altered the prokaryotic community structures. The PE and PET addition highly changed the relative abundance of bacterial taxa in the bacterial community, while the proportion of archaeal species in the archaeal community was significantly altered in 0.5 % MPs treatments. All of the MPs reduced the network complexity of the bacterial and archaeal communities, such as the lower average degree and greater average path length. Furthermore, the MPs treatments also significantly decreased the network stability of prokaryotic communities. The lower network complexity led to lower network stability was observed in the archaeal community. The formation of oxidative functional groups on PE and PET MP surface based on FTIR analysis suggested that biodegradation could occur in cold seep sediment. Together, these results provide new evidence that MPs could change the structures and species coexistence of prokaryotic communities in cold seep sediments.
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Affiliation(s)
- Yongji Huang
- South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou 510301, China; Guangdong Basic Research Center of Excellence for Ecological Security and Green Development, Guangdong University of Technology, Guangzhou 510006, China; University of Chinese Academy of Sciences, Beijing 100049, China
| | - Jingchun Feng
- Guangdong Basic Research Center of Excellence for Ecological Security and Green Development, Guangdong University of Technology, Guangzhou 510006, China; Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou), Guangzhou 511458, China.
| | - Xinyuan Wang
- Guangdong Basic Research Center of Excellence for Ecological Security and Green Development, Guangdong University of Technology, Guangzhou 510006, China; Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou), Guangzhou 511458, China
| | - Yue Zhang
- Guangdong Basic Research Center of Excellence for Ecological Security and Green Development, Guangdong University of Technology, Guangzhou 510006, China
| | - Si Zhang
- South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou 510301, China; Guangdong Basic Research Center of Excellence for Ecological Security and Green Development, Guangdong University of Technology, Guangzhou 510006, China; Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou), Guangzhou 511458, China.
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12
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Delgado-Baquerizo M, Singh BK, Liu YR, Sáez-Sandino T, Coleine C, Muñoz-Rojas M, Bastida F, Trivedi P. Integrating ecological and evolutionary frameworks for SynCom success. THE NEW PHYTOLOGIST 2025; 246:1922-1933. [PMID: 40177999 DOI: 10.1111/nph.70112] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 10/25/2024] [Accepted: 03/11/2025] [Indexed: 04/05/2025]
Abstract
Use of synthetic microbial communities (SynComs) is a promising approach that harnesses nature-based solutions to support soil fertility and food security, mitigate climate change impacts, and restore terrestrial ecosystems. Several microbial products are in the market, and many others are at different stages of development and commercialization. Yet, we are still far from being able to fully harness the potential and successful applications of such biotechnological tools. The limited field efficiency and efficacy of SynComs have significantly constrained commercial opportunities, resulting in market growth falling below expectations. To overcome these challenges and manage expectations, it is critical to address current limitations, failures, and potential environmental consequences of SynComs. In this Viewpoint, we explore how using multiple eco-evolutionary theories can inform SynCom design and success. We further discuss the current status of SynComs and identify the next steps needed to develop and deploy the next generation of tools to boost their ability to support multiple ecosystem services, including food security and environmental sustainability.
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Affiliation(s)
- Manuel Delgado-Baquerizo
- Laboratorio de Biodiversidad y Funcionamiento Ecosistémico, Instituto de Recursos Naturales y Agrobiología de Sevilla (IRNAS), Consejo Superior de Investigaciones Científicas (CSIC), Av. Reina Mercedes 10, E-41012, Sevilla, Spain
| | - Brajesh K Singh
- Hawkesbury Institute for the Environment, Western Sydney University, Penrith, 2751, NSW, Australia
| | - Yu-Rong Liu
- State Key Laboratory of Agricultural Microbiology and College of Resources and Environment, Huazhong Agricultural University, Wuhan, 430070, China
| | - Tadeo Sáez-Sandino
- Hawkesbury Institute for the Environment, Western Sydney University, Penrith, 2751, NSW, Australia
| | - Claudia Coleine
- Department of Ecological and Biological Sciences, University of Tuscia, 01100, Viterbo, Italy
| | - Miriam Muñoz-Rojas
- Laboratorio de Biodiversidad y Funcionamiento Ecosistémico, Instituto de Recursos Naturales y Agrobiología de Sevilla (IRNAS), Consejo Superior de Investigaciones Científicas (CSIC), Av. Reina Mercedes 10, E-41012, Sevilla, Spain
| | - Felipe Bastida
- CEBAS-CSIC, Campus Universitario de Espinardo, E-30100, Murcia, Spain
| | - Pankaj Trivedi
- Microbiome Network and Department of Agricultural Biology, Colorado State University, Fort Collins, 80523, CO, USA
- Department of Plant and Soil Science, Institute of Genomics for Crop Abiotic Stress Tolerance (IGCAST), Texas Tech University, Lubbock, TX, 79409, USA
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13
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Hu J, Chen T, Lian CA, Wang L, Zhuang W, Yu K. Deciphering factors influencing planktonic and sedimentary microbial assembly processes in Midwest salinity lakes. Appl Microbiol Biotechnol 2025; 109:124. [PMID: 40410607 PMCID: PMC12102102 DOI: 10.1007/s00253-025-13498-y] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 12/23/2024] [Revised: 04/22/2025] [Accepted: 04/23/2025] [Indexed: 05/25/2025]
Abstract
The salt lake ecosystem, characterized by extreme environmental gradients, harbors microbes that uniquely adapt to high salt stress through natural selection. However, how abiotic and biotic factors shape the microbial community assembly in Yuncheng Salt Lakes remains unclear. Here, we investigated the assembly processes and meta co-occurrence patterns of microbiota in both water and sediment sampled from 14 distinct wide range of salinity lakes in the Shanxi Yuncheng area, Midwest of China, using 16S rRNA and 18S rRNA gene sequencing technology combined with multivariate ecological and statistical methods. Habitat differentiation led to the differences in microbial diversity, co-occurrence patterns, and community assembly between sedimentary and planktonic communities. Sedimentary prokaryotes were more shaped by deterministic processes than planktonic bacterial communities. Salinity was a major abiotic factor influencing the balance between stochastic and deterministic processes in both sediment and water. Enhanced microbial interactions within sediments exhibited a more prominent impact in shaping community assembly, as indicated by the stronger association between network-inferred species and prokaryotic βNTI. Moreover, we revealed significant differences in how core species concerning βNTI responded to biotic and abiotic factors. Our findings elucidated the ecological process underlying microbial communities in Yuncheng Salt Lakes and shed light on the mechanism of microorganisms to maintain community complexity and diversity in the extreme environment. KEY POINTS: • Sedimentary prokaryotes were more shaped by deterministic processes than planktonic prokaryotic communities. • Salinity was a major factor influencing the balance between stochastic and deterministic process. • Inter-domain and intra-domain symbiotic interactions within sedimentary communities represent key biotic factors influencing their community assembly.
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Affiliation(s)
- Jincheng Hu
- School of Environment and Energy, Peking University Shenzhen Graduate School, Shenzhen, 518055, China
| | - Tianyi Chen
- School of Environment and Energy, Peking University Shenzhen Graduate School, Shenzhen, 518055, China
- Environmental Microbiome and Innovative Genomics Laboratory, College of Environmental Sciences and Engineering, Peking University, Beijing, 100871, China
| | - Chun-Ang Lian
- School of Environment and Energy, Peking University Shenzhen Graduate School, Shenzhen, 518055, China
| | - Li Wang
- State Key Laboratory for Managing Biotic and Chemical Threats to the Quality and Safety of Agro-Products, Institute of Plant Virology, Ningbo University, Ningbo, 315211, China
| | - Weiqin Zhuang
- Department of Civil and Environmental Engineering, The University of Auckland, Auckland, New Zealand
| | - Ke Yu
- School of Environment and Energy, Peking University Shenzhen Graduate School, Shenzhen, 518055, China.
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14
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Heyer R, Wolf M, Benndorf D, Uzzau S, Seifert J, Grenga L, Pabst M, Schmitt H, Mesuere B, Van Den Bossche T, Haange SB, Jehmlich N, Di Luca M, Ferrer M, Serrano-Villar S, Armengaud J, Bode HB, Hellwig P, Masselot CR, Léonard R, Wilmes P. Metaproteomics in the One Health framework for unraveling microbial effectors in microbiomes. MICROBIOME 2025; 13:134. [PMID: 40410872 PMCID: PMC12100821 DOI: 10.1186/s40168-025-02119-5] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Download PDF] [Figures] [Subscribe] [Scholar Register] [Received: 01/09/2025] [Accepted: 04/21/2025] [Indexed: 05/25/2025]
Abstract
One Health seeks to integrate and balance the health of humans, animals, and environmental systems, which are intricately linked through microbiomes. These microbial communities exchange microbes and genes, influencing not only human and animal health but also key environmental, agricultural, and biotechnological processes. Preventing the emergence of pathogens as well as monitoring and controlling the composition of microbiomes through microbial effectors including virulence factors, toxins, antibiotics, non-ribosomal peptides, and viruses holds transformative potential. However, the mechanisms by which these microbial effectors shape microbiomes and their broader functional consequences for host and ecosystem health remain poorly understood. Metaproteomics offers a novel methodological framework as it provides insights into microbial dynamics by quantifying microbial biomass composition, metabolic functions, and detecting effectors like viruses, antimicrobial resistance proteins, and non-ribosomal peptides. Here, we highlight the potential of metaproteomics in elucidating microbial effectors and their impact on microbiomes and discuss their potential for modulating microbiomes to foster desired functions.
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Affiliation(s)
- Robert Heyer
- Multidimensional Omics Analyses Group, Leibniz-Institut für Analytische Wissenschaften - ISAS - e.V., Bunsen-Kirchhoff-Straße 11, 44139, Dortmund, Germany.
- Multidimensional Omics Analyses Group, Faculty of Technology, Bielefeld University, Universitätsstraße 25, 33615, Bielefeld, Germany.
| | - Maximilian Wolf
- Multidimensional Omics Analyses Group, Faculty of Technology, Bielefeld University, Universitätsstraße 25, 33615, Bielefeld, Germany
| | - Dirk Benndorf
- Bioprocess Engineering, Otto-Von-Guericke University Magdeburg, Universitätsplatz 2, 39106, Magdeburg, Germany
- Bioprocess Engineering, Max Planck Institute for Dynamics of Complex Technical Systems Magdeburg, Sandtorstraße 1, 39106, Magdeburg, Germany
- Applied Biosciences and Process Engineering, Anhalt University of Applied Sciences, Köthen, Germany
| | - Sergio Uzzau
- Department of Biomedical Sciences, University of Sassari, 07100, Sassari, Italy
| | - Jana Seifert
- Institute of Animal Science, University of Hohenheim, Emil-Wolff-Str, Stuttgart, Germany
- HoLMiR - Hohenheim Center for Livestock Microbiome Research, University of Hohenheim, Leonore-Blosser-Reisen Weg, Stuttgart, Germany
| | - Lucia Grenga
- Département Médicaments Et Technologies Pour La Santé (DMTS), Université Paris-Saclay, CEA, INRAE, SPI, Bagnols-Sur-Cèze, France
| | - Martin Pabst
- Department of Biotechnology, Delft University of Technology, Delft, The Netherlands
| | - Heike Schmitt
- Department of Biotechnology, Delft University of Technology, Delft, The Netherlands
- Institute for Infectious Disease Control, National Institute for Public Health and the Environment (RIVM), Bilthoven, The Netherlands
| | - Bart Mesuere
- Department of Applied Mathematics, Computer Science and Statistics, Ghent University, 9000, Ghent, Belgium
| | - Tim Van Den Bossche
- VIB - UGent Center for Medical Biotechnology, VIB, 9052, Ghent, Belgium
- Department of Biomolecular Medicine, Faculty of Medicine and Health Sciences, Ghent University, 9052, Ghent, Belgium
| | - Sven-Bastiaan Haange
- Department of Molecular Toxicology, Helmholtz-Centre for Environmental Research - UFZ GmbH, Permoserstrasse 15, 04318, Leipzig, Germany
| | - Nico Jehmlich
- Department of Molecular Toxicology, Helmholtz-Centre for Environmental Research - UFZ GmbH, Permoserstrasse 15, 04318, Leipzig, Germany
| | | | - Manuel Ferrer
- Instituto de Catalisis y Petroleoquimica (ICP), CSIC, 28049, Madrid, Spain
| | - Sergio Serrano-Villar
- Department of Infectious Diseases, Hospital Universitario Ramon y Cajal, Instituto de Investigación Sanitaria Ramón y Cajal (IRYCIS), CIBER de Enfermedades Infecciosas, Madrid, Spain
| | - Jean Armengaud
- Département Médicaments Et Technologies Pour La Santé (DMTS), Université Paris-Saclay, CEA, INRAE, SPI, Bagnols-Sur-Cèze, France
| | - Helge B Bode
- Department of Natural Products in Organismic Interactions, Max-Planck-Institut for Terrestrial Microbiology, Karl-Von-Frisch-Str. 10, 35043, Marburg, Germany
- Center for Synthetic Microbiology (SYNMIKRO), Phillips University Marburg, 35043, Marburg, Germany
- Department of Chemistry, Phillips University Marburg, 35043, Marburg, Germany
| | - Patrick Hellwig
- Bioprocess Engineering, Otto-Von-Guericke University Magdeburg, Universitätsplatz 2, 39106, Magdeburg, Germany
- Bioprocess Engineering, Max Planck Institute for Dynamics of Complex Technical Systems, Sandtorstraße 1, 39106, Magdeburg, Germany
| | | | - Renaud Léonard
- Université de Lille, CNRS, UMR, 8576 - UGSF, Lille, France
| | - Paul Wilmes
- Luxembourg Centre for Systems Biomedicine, University of Luxembourg, L-4362, Esch-Sur-Alzette, Luxembourg
- Department of Life Sciences and Medicine, University of Luxembourg, L-4362, Esch-Sur-Alzette, Luxembourg
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15
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Pantigoso HA, Ossowicki A, Stringlis IA, Carrión VJ. Hub metabolites at the root-microbiome interface: unlocking plant drought resilience. TRENDS IN PLANT SCIENCE 2025:S1360-1385(25)00106-2. [PMID: 40393817 DOI: 10.1016/j.tplants.2025.04.007] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Subscribe] [Scholar Register] [Received: 12/18/2024] [Revised: 03/26/2025] [Accepted: 04/09/2025] [Indexed: 05/22/2025]
Abstract
Drought is one of the most devastating environmental challenges, severely affecting agriculture, ecosystems, and global food security. Effective strategies to predict and mitigate drought are limited. The root-soil-microbiome interface is pivotal in mediating plant resilience to drought. Recent studies highlight dynamics between plant root exudates and microbial communities, influencing stress tolerance through chemical signaling under drought. By integrating plant molecular biology, root chemistry, and microbiome research, we discuss insights into how these mechanisms can be harnessed to enhance crop resilience. Here, we focus on the interplay between plants and their microbiomes with metabolites as a central point of interactions. We synthesize recent developments, identify critical knowledge gaps, and propose future directions to leverage plant-microbe interactions to improve plant drought tolerance.
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Affiliation(s)
- Hugo A Pantigoso
- Institute of Biology, Leiden University, Sylviusweg 72, 2333 BE Leiden, The Netherlands
| | - Adam Ossowicki
- Departamento de Microbiología, Facultad de Ciencias, Campus Universitario de Teatinos s/n, Universidad de Málaga, 29010 Málaga, Spain; Departamento de Protección de Cultivos, Instituto de Hortofruticultura Subtropical y Mediterránea 'La Mayora', Campus Universitario de Teatinos, Universidad de Málaga-Consejo Superior de Investigaciones Científicas (IHSM-UMA-CSIC), 29010 Málaga, Spain
| | - Ioannis A Stringlis
- Laboratory of Plant Pathology, Agricultural University of Athens, 75 Iera Odos str., 11855 Athens, Greece
| | - Víctor J Carrión
- Institute of Biology, Leiden University, Sylviusweg 72, 2333 BE Leiden, The Netherlands; Departamento de Microbiología, Facultad de Ciencias, Campus Universitario de Teatinos s/n, Universidad de Málaga, 29010 Málaga, Spain; Departamento de Protección de Cultivos, Instituto de Hortofruticultura Subtropical y Mediterránea 'La Mayora', Campus Universitario de Teatinos, Universidad de Málaga-Consejo Superior de Investigaciones Científicas (IHSM-UMA-CSIC), 29010 Málaga, Spain; Department of Microbial Ecology, Netherlands Institute of Ecology (NIOO-KNAW), Droevendaalsesteeg 10, 6708 PB Wageningen, The Netherlands.
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16
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Sun T, Liu H, Wang N, Huang M, Banerjee S, Jousset A, Xu Y, Shen Q, Wang S, Wang X, Wei Z. Interactions with native microbial keystone taxa enhance the biocontrol efficiency of Streptomyces. MICROBIOME 2025; 13:126. [PMID: 40390122 PMCID: PMC12087250 DOI: 10.1186/s40168-025-02120-y] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Download PDF] [Figures] [Subscribe] [Scholar Register] [Received: 11/16/2024] [Accepted: 04/21/2025] [Indexed: 05/21/2025]
Abstract
BACKGROUND Streptomyces spp. are known for producing bioactive compounds that suppress phytopathogens. However, previous studies have largely focused on their direct interactions with pathogens and plants, often neglecting their interactions with the broader soil microbiome. In this study, we hypothesized that these interactions are critical for effective pathogen control. We investigated a diverse collection of Streptomyces strains to select those with strong protective capabilities against tomato wilt disease caused by Ralstonia solanacearum. Leveraging a synthetic community (SynCom) established in our lab, alongside multiple in planta and in vitro co-cultivation experiments, as well as transcriptomic and metabolomic analyses, we explored the synergistic inhibitory mechanisms underlying bacterial wilt resistance facilitated by both Streptomyces and the soil microbiome. RESULTS Our findings indicate that direct antagonism by Streptomyces is not sufficient for their biocontrol efficacy. Instead, the efficacy was associated with shifts in the rhizosphere microbiome, particularly the promotion of two native keystone taxa, CSC98 (Stenotrophomonas maltophilia) and CSC13 (Paenibacillus cellulositrophicus). In vitro co-cultivation experiments revealed that CSC98 and CSC13 did not directly inhibit the pathogen. Instead, the metabolite of CSC13 significantly enhanced the inhibition efficiency of Streptomyces R02, a highly effective biocontrol strain in natural soil. Transcriptomic and metabolomic analyses revealed that CSC13's metabolites induced the production of Erythromycin E in Streptomyces R02, a key compound that directly suppressed R. solanacearum, as demonstrated by our antagonism tests. CONCLUSIONS Collectively, our study reveals how beneficial microbes engage with the native soil microbiome to combat pathogens, suggesting the potential of leveraging microbial interactions to enhance biocontrol efficiency. These findings highlight the significance of intricate microbial interactions within the microbiome in regulating plant diseases and provide a theoretical foundation for devising efficacious biocontrol strategies in sustainable agriculture. Video Abstract.
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Affiliation(s)
- Tianyu Sun
- Jiangsu Provincial Key Lab for Solid Organic Waste Utilization, Key Lab of Organic-Based Fertilizers of China, Jiangsu Collaborative Innovation Center for Solid Organic Wastes, Educational Ministry Engineering Center of Resource-saving fertilizers, Nanjing Agricultural University, Nanjing, 210095, China
| | - Hongwei Liu
- College of Agro-Grassland Science, Nanjing Agricultural University, Nanjing, Jiangsu, 210095, People's Republic of China
- Hawkesbury Institute for the Environment, Western Sydney University, Penrith, NSW, 2753, Australia
| | - Ningqi Wang
- Jiangsu Provincial Key Lab for Solid Organic Waste Utilization, Key Lab of Organic-Based Fertilizers of China, Jiangsu Collaborative Innovation Center for Solid Organic Wastes, Educational Ministry Engineering Center of Resource-saving fertilizers, Nanjing Agricultural University, Nanjing, 210095, China
| | - Mingcong Huang
- Jiangsu Provincial Key Lab for Solid Organic Waste Utilization, Key Lab of Organic-Based Fertilizers of China, Jiangsu Collaborative Innovation Center for Solid Organic Wastes, Educational Ministry Engineering Center of Resource-saving fertilizers, Nanjing Agricultural University, Nanjing, 210095, China
| | - Samiran Banerjee
- Department of Microbiological Sciences, North Dakota State University, Fargo, ND, USA
| | - Alexandre Jousset
- Jiangsu Provincial Key Lab for Solid Organic Waste Utilization, Key Lab of Organic-Based Fertilizers of China, Jiangsu Collaborative Innovation Center for Solid Organic Wastes, Educational Ministry Engineering Center of Resource-saving fertilizers, Nanjing Agricultural University, Nanjing, 210095, China
| | - Yangchun Xu
- Jiangsu Provincial Key Lab for Solid Organic Waste Utilization, Key Lab of Organic-Based Fertilizers of China, Jiangsu Collaborative Innovation Center for Solid Organic Wastes, Educational Ministry Engineering Center of Resource-saving fertilizers, Nanjing Agricultural University, Nanjing, 210095, China
| | - Qirong Shen
- Jiangsu Provincial Key Lab for Solid Organic Waste Utilization, Key Lab of Organic-Based Fertilizers of China, Jiangsu Collaborative Innovation Center for Solid Organic Wastes, Educational Ministry Engineering Center of Resource-saving fertilizers, Nanjing Agricultural University, Nanjing, 210095, China
| | - Shimei Wang
- Jiangsu Provincial Key Lab for Solid Organic Waste Utilization, Key Lab of Organic-Based Fertilizers of China, Jiangsu Collaborative Innovation Center for Solid Organic Wastes, Educational Ministry Engineering Center of Resource-saving fertilizers, Nanjing Agricultural University, Nanjing, 210095, China.
| | - Xiaofang Wang
- Jiangsu Provincial Key Lab for Solid Organic Waste Utilization, Key Lab of Organic-Based Fertilizers of China, Jiangsu Collaborative Innovation Center for Solid Organic Wastes, Educational Ministry Engineering Center of Resource-saving fertilizers, Nanjing Agricultural University, Nanjing, 210095, China.
| | - Zhong Wei
- Jiangsu Provincial Key Lab for Solid Organic Waste Utilization, Key Lab of Organic-Based Fertilizers of China, Jiangsu Collaborative Innovation Center for Solid Organic Wastes, Educational Ministry Engineering Center of Resource-saving fertilizers, Nanjing Agricultural University, Nanjing, 210095, China.
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17
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Jourdain L, Gu W. Designing synthetic microbial communities for enhanced anaerobic waste treatment. Appl Environ Microbiol 2025:e0040425. [PMID: 40377302 DOI: 10.1128/aem.00404-25] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 05/18/2025] Open
Abstract
Synthetic microbial communities (SynComs) are powerful tools for investigating microbial interactions and community assembly by focusing on minimal yet functionally representative members. Here, we will highlight key principles for designing SynComs, specifically emphasizing the anaerobic digestion (AD) microbiome for waste treatment and upcycling. The AD process has traditionally been used to reduce organic waste volume while producing biogas as a renewable energy source. Its microbiome features well-defined trophic layers and metabolic groups. There has been growing interest in repurposing the AD process to produce value-added products and chemical precursors, contributing to sustainable waste management and the goals of a circular economy. Optimizing the AD process requires a better understanding of microbial interactions and the influence of both biotic and abiotic parameters, where SynComs offer great promise. Focusing on AD microbiomes, we review the principles of SynComs' design, including keystone taxa and function, cross-feeding interactions, and metabolic redundancy, as well as how modeling approaches could guide SynComs design. Furthermore, we address practical considerations for working with AD SynComs and examine constructed SynComs designed for anaerobic waste digestion. Finally, we discuss the challenges associated with designing and applying SynComs to enhance our understanding of the AD process. This review aims to explore the use of synthetic communities in studying anaerobic digestion and highlights their potential for developing innovative biotechnological processes.
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Affiliation(s)
- Lisa Jourdain
- MICROBE laboratory, Institute of Environmental Engineering, School of Architecture, Civil and Environmental Engineering, Swiss Federal Institute of Technology, Lausanne, Switzerland
| | - Wenyu Gu
- MICROBE laboratory, Institute of Environmental Engineering, School of Architecture, Civil and Environmental Engineering, Swiss Federal Institute of Technology, Lausanne, Switzerland
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18
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Dörr AK, Imangaliyev S, Karadeniz U, Schmidt T, Meyer F, Kraiselburd I. Distinguishing critical microbial community shifts from normal temporal variability in human and environmental ecosystems. Sci Rep 2025; 15:16934. [PMID: 40374711 DOI: 10.1038/s41598-025-01781-x] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/07/2025] [Accepted: 05/08/2025] [Indexed: 05/17/2025] Open
Abstract
Differentiating significant microbial community changes from normal fluctuations is vital for understanding microbial dynamics in human and environmental ecosystems. This knowledge could enable early warning systems to monitor critical changes affecting human or environmental health. We applied 16S rRNA gene sequencing and time-series analysis to model bacterial abundance trajectories in human gut and wastewater microbiomes. We evaluated various model architectures using datasets from two human studies and five wastewater settings. Long short-term memory (LSTM) models consistently outperformed other models in predicting bacterial abundances and detecting outliers, as measured by multiple metrics. Prediction intervals for each genus allowed us to identify significant changes and signaling shifts in community states. This study proposes a machine learning model capable of monitoring microbial communities and providing insights into their responses to internal and external factors in medical and environmental settings.
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Affiliation(s)
- Ann-Kathrin Dörr
- Department of Medicine, Institute for Artificial Intelligence in Medicine, University Hospital Essen, University of Duisburg-Essen, Essen, Germany
- Department of Computer Science, University of Duisburg-Essen, Essen, Germany
| | - Sultan Imangaliyev
- Department of Medicine, Institute for Artificial Intelligence in Medicine, University Hospital Essen, University of Duisburg-Essen, Essen, Germany
| | - Utku Karadeniz
- Department of Computer Science, University of Duisburg-Essen, Essen, Germany
| | - Tina Schmidt
- Emschergenossenschaft/Lippeverband, Kronprinzenstraße 24, 45128, Essen, Germany
| | - Folker Meyer
- Department of Medicine, Institute for Artificial Intelligence in Medicine, University Hospital Essen, University of Duisburg-Essen, Essen, Germany
- Department of Computer Science, University of Duisburg-Essen, Essen, Germany
| | - Ivana Kraiselburd
- Department of Medicine, Institute for Artificial Intelligence in Medicine, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
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19
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Zhu H, Li Q, El-Sappah AH, Sun Y, Liu Y, Pan S, Zhu K, Sun X, Xiong T, Luo H, Wu T, Li L, Ma Y, Wang N. Influence of two sorghum varieties on metabolic factors, microbial community, and flavor component precursors of strong-flavor Baijiu Zaopei. Food Chem 2025; 474:143079. [PMID: 39921974 DOI: 10.1016/j.foodchem.2025.143079] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 11/04/2024] [Revised: 01/14/2025] [Accepted: 01/23/2025] [Indexed: 02/10/2025]
Abstract
As the primary raw material for Baijiu brewing, sorghum variety exerts an intricate influence on the taste profile of strong-flavor Baijiu. However, how sorghum variety comprehensively affects Baijiu flavor formation through fermentation by microorganisms and metabolites remains largely unknown. Using 16S&ITS rRNA gene sequencing and non-targeted metabolomics, in this study we comprehensively analyzed the changes in microbial communities and metabolites during fermentation of a glutinous and non-glutinous sorghum variety. The results showed that these varieties significantly affected microbial diversity and community structure, and their interactions, among which, there were particularly complex interactions among bacterial communities, while the effects of "functional differentiation" and "community aggregation" of fungal communities were prominent. Furthermore, three bacterial and nine fungal genera were identified as core microorganisms related to changes in glycerophospholipids during fermentation, that led to a change in ester content, ultimately improving Baijiu quality. These findings provide reference for the selection of brewing materials.
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Affiliation(s)
- Hui Zhu
- School of Bioengineering, Sichuan University of Science and Engineering, Yibin 644000, China; Sichuan Province Engineering Technology Research Center of Liquor-Making Grains, Yibin 644000, China; Liquor Making Biotechnology and Intelligent Manufacturing of Key Laboratory of China National Light Industry, Yibin 644000, China
| | - Qiang Li
- School of Bioengineering, Sichuan University of Science and Engineering, Yibin 644000, China; Sichuan Province Engineering Technology Research Center of Liquor-Making Grains, Yibin 644000, China; Liquor Making Biotechnology and Intelligent Manufacturing of Key Laboratory of China National Light Industry, Yibin 644000, China
| | - Ahmed H El-Sappah
- College of Agriculture, Forestry, and Food Engineering, Yibin University, Yibin 644000, China; Genetics Department, Faculty of Agriculture, Zagazig University, Zagazig, Egypt
| | - Yong Sun
- State Key Laboratory of Food Science and Technology, Nanchang University, Nanchang 330047, China
| | - Ying Liu
- Sichuan Yibin Hengshengfu Liquor Industry Group Co., Ltd., Yibin 644007, China
| | - Shijiang Pan
- Yibin City Agricultural and Rural Bureau, Yibin 644000, China
| | - Ke Zhu
- Cuiping District Agricultural and Rural Bureau, Yibin 644000, China
| | - Xiaoke Sun
- Sichuan Yibin Hengshengfu Liquor Industry Group Co., Ltd., Yibin 644007, China
| | - Tao Xiong
- Cuiping District Agricultural and Rural Bureau, Yibin 644000, China
| | - Huibo Luo
- School of Bioengineering, Sichuan University of Science and Engineering, Yibin 644000, China; Sichuan Province Engineering Technology Research Center of Liquor-Making Grains, Yibin 644000, China; Liquor Making Biotechnology and Intelligent Manufacturing of Key Laboratory of China National Light Industry, Yibin 644000, China
| | - Tao Wu
- School of Food and Biotechnology, Xihua University, Chengdu 610039, China
| | - Linjuan Li
- School of Bioengineering, Sichuan University of Science and Engineering, Yibin 644000, China; Sichuan Province Engineering Technology Research Center of Liquor-Making Grains, Yibin 644000, China; Liquor Making Biotechnology and Intelligent Manufacturing of Key Laboratory of China National Light Industry, Yibin 644000, China
| | - Yi Ma
- School of Bioengineering, Sichuan University of Science and Engineering, Yibin 644000, China; Sichuan Province Engineering Technology Research Center of Liquor-Making Grains, Yibin 644000, China; Liquor Making Biotechnology and Intelligent Manufacturing of Key Laboratory of China National Light Industry, Yibin 644000, China.
| | - Ning Wang
- School of Bioengineering, Sichuan University of Science and Engineering, Yibin 644000, China; Sichuan Province Engineering Technology Research Center of Liquor-Making Grains, Yibin 644000, China; Liquor Making Biotechnology and Intelligent Manufacturing of Key Laboratory of China National Light Industry, Yibin 644000, China.
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20
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Praeg N, Steinwandter M, Urbach D, Snethlage MA, Alves RP, Apple ME, Bilovitz P, Britton AJ, Bruni EP, Chen TW, Dumack K, Fernandez-Mendoza F, Freppaz M, Frey B, Fromin N, Geisen S, Grube M, Guariento E, Guisan A, Ji QQ, Jiménez JJ, Maier S, Malard LA, Minor MA, Mc Lean CC, Mitchell EAD, Peham T, Pizzolotto R, Taylor AFS, Vernon P, van Tol JJ, Wu D, Wu Y, Xie Z, Weber B, Illmer P, Seeber J. Biodiversity in mountain soils above the treeline. Biol Rev Camb Philos Soc 2025. [PMID: 40369817 DOI: 10.1111/brv.70028] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/26/2024] [Revised: 04/04/2025] [Accepted: 04/17/2025] [Indexed: 05/16/2025]
Abstract
Biological diversity in mountain ecosystems has been increasingly studied over the last decade. This is also the case for mountain soils, but no study to date has provided an overall synthesis of the current state of knowledge. Here we fill this gap with a first global analysis of published research on cryptogams, microorganisms, and fauna in mountain soils above the treeline, and a structured synthesis of current knowledge. Based on a corpus of almost 1400 publications and the expertise of 37 mountain soil scientists worldwide, we summarise what is known about the diversity and distribution patterns of each of these organismal groups, specifically along elevation, and provide an overview of available knowledge on the drivers explaining these patterns and their changes. In particular, we document an elevation-dependent decrease in faunal diversity above the treeline, while for cryptogams there is an initial increase above the treeline, followed by a decrease towards the nival belt. Thus, our data confirm the key role that elevation plays in shaping the biodiversity and distribution of these organisms in mountain soils. The response of prokaryote diversity to elevation, in turn, was more diverse, whereas fungal diversity appeared to be substantially influenced by plants. As far as available, we describe key characteristics, adaptations, and functions of mountain soil species, and despite a lack of ecological information about the uncultivated majority of prokaryotes, fungi, and protists, we illustrate the remarkable and unique diversity of life forms and life histories encountered in alpine mountain soils. By applying rule- as well as pattern-based literature-mining approaches and semi-quantitative analyses, we identified hotspots of mountain soil research in the European Alps and Central Asia and revealed significant gaps in taxonomic coverage, particularly among biocrusts, soil protists, and soil fauna. We further report thematic priorities for research on mountain soil biodiversity above the treeline and identify unanswered research questions. Building upon the outcomes of this synthesis, we conclude with a set of research opportunities for mountain soil biodiversity research worldwide. Soils in mountain ecosystems above the treeline fulfil critical functions and make essential contributions to life on land. Accordingly, seizing these opportunities and closing knowledge gaps appears crucial to enable science-based decision making in mountain regions and formulating laws and guidelines in support of mountain soil biodiversity conservation targets.
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Affiliation(s)
- Nadine Praeg
- Department of Microbiology, Universität Innsbruck, Technikerstrasse 25d, Innsbruck, 6020, Austria
| | - Michael Steinwandter
- Institute for Alpine Environment, Eurac Research, Viale Druso 1, Bozen/Bolzano, 39100, Italy
| | - Davnah Urbach
- Global Mountain Biodiversity Assessment (GMBA), University of Bern, Altenbergrain 21, Bern, 3013, Switzerland
- Institute of Plant Sciences, University of Bern, Altenbergrain 21, Bern, 3013, Switzerland
- Centre Interdisciplinaire de Recherche sur la Montagne, University of Lausanne, Ch. de l'Institut 18, Bramois/Sion, 1967, Switzerland
| | - Mark A Snethlage
- Global Mountain Biodiversity Assessment (GMBA), University of Bern, Altenbergrain 21, Bern, 3013, Switzerland
- Institute of Plant Sciences, University of Bern, Altenbergrain 21, Bern, 3013, Switzerland
- Centre Interdisciplinaire de Recherche sur la Montagne, University of Lausanne, Ch. de l'Institut 18, Bramois/Sion, 1967, Switzerland
| | - Rodrigo P Alves
- Institute of Biology, Division of Plant Sciences, University of Graz, Holteigasse 6, Graz, 8010, Austria
| | - Martha E Apple
- Department of Biological Sciences, Montana Technological University, Butte, 59701, MT, USA
| | - Peter Bilovitz
- Institute of Biology, Division of Plant Sciences, University of Graz, Holteigasse 6, Graz, 8010, Austria
| | - Andrea J Britton
- Ecological Sciences, The James Hutton Institute, Craigiebuckler, Aberdeen, AB15 8QH, Scotland, UK
| | - Estelle P Bruni
- Laboratory of Soil Biodiversity, University of Neuchâtel, Rue Emile-Argand 11, Neuchâtel, 2000, Switzerland
| | - Ting-Wen Chen
- Biology Centre of the Czech Academy of Sciences, Institute of Soil Biology and Biogeochemistry, Na Sádkách 702/7, České Budějovice, 37005, Czech Republic
- J.F. Blumenbach Institute of Zoology and Anthropology, University of Göttingen, Untere Karspüle 2, Göttingen, 37073, Germany
| | - Kenneth Dumack
- Terrestrial Ecology, Cologne Biocenter, University of Cologne, Zülpicher Strasse 47b, Cologne, 50674, Germany
| | - Fernando Fernandez-Mendoza
- Institute of Biology, Division of Plant Sciences, University of Graz, Holteigasse 6, Graz, 8010, Austria
| | - Michele Freppaz
- Department of Agricultural, Forest and Food Sciences, University of Turin, Largo Paolo Braccini 2, Grugliasco, 10095, Italy
- Research Center on Natural Risks in Mountain and Hilly Environments, University of Turin, Largo Paolo Braccini 2, Grugliasco, 10095, Italy
| | - Beat Frey
- Forest Soils and Biogeochemistry, Swiss Federal Research Institute WSL, Birmensdorf, 8903, Switzerland
| | - Nathalie Fromin
- CEFE, Univ Montpellier, CNRS, EPHE, IRD, Univ Paul Valéry Montpellier 3, Route de Mende 34199, Montpellier Cedex 5, France
| | - Stefan Geisen
- Laboratory of Nematology, Wageningen University and Research, Droevendaalsesteeg 1, Wageningen 6708PB, The Netherlands
| | - Martin Grube
- Institute of Biology, Division of Plant Sciences, University of Graz, Holteigasse 6, Graz, 8010, Austria
| | - Elia Guariento
- Institute for Alpine Environment, Eurac Research, Viale Druso 1, Bozen/Bolzano, 39100, Italy
| | - Antoine Guisan
- Department of Ecology and Evolution (DEE), University of Lausanne, Biophore, Lausanne, 1015, Switzerland
- Institute of Earth Surface Dynamics (IDYST), University of Lausanne, Géopolis, Lausanne, 1015, Switzerland
| | - Qiao-Qiao Ji
- Northeast Institute of Geography and Agroecology, Chinese Academy of Sciences, 4888 Shengbei Street, Changchun, 130102, China
| | - Juan J Jiménez
- Instituto Pirenaico de Ecología (IPE), Consejo Superior de Investigaciones Cientificas (CSIC), Avda. Ntra. Sra. de la Victoria 16, Jaca, 22700, Huesca, Spain
| | - Stefanie Maier
- Institute of Biology, Division of Plant Sciences, University of Graz, Holteigasse 6, Graz, 8010, Austria
| | - Lucie A Malard
- Department of Ecology and Evolution (DEE), University of Lausanne, Biophore, Lausanne, 1015, Switzerland
| | - Maria A Minor
- School of Food Technology and Natural Sciences, Massey University, Riddett Road, Palmerston North, 4410, New Zealand
| | - Cowan C Mc Lean
- Department of Soil, Crop and Climate Sciences, University of the Free State, 205 Nelson Mandela Drive, Bloemfontein, 9300, South Africa
| | - Edward A D Mitchell
- Laboratory of Soil Biodiversity, University of Neuchâtel, Rue Emile-Argand 11, Neuchâtel, 2000, Switzerland
| | - Thomas Peham
- Department of Ecology, Universität Innsbruck, Technikerstrasse 25, Innsbruck, 6020, Austria
| | - Roberto Pizzolotto
- Dipartimento di Biologia, Ecologia e Scienze della Terra, University of Calabria, Ponte Pietro Bucci 4b, Rende, 87036, Italy
| | - Andy F S Taylor
- Ecological Sciences, The James Hutton Institute, Craigiebuckler, Aberdeen, AB15 8QH, Scotland, UK
| | - Philippe Vernon
- UMR 6553 EcoBio CNRS, University of Rennes, Biological Station, Paimpont, 35380, France
| | - Johan J van Tol
- Department of Soil, Crop and Climate Sciences, University of the Free State, 205 Nelson Mandela Drive, Bloemfontein, 9300, South Africa
| | - Donghui Wu
- Northeast Institute of Geography and Agroecology, Chinese Academy of Sciences, 4888 Shengbei Street, Changchun, 130102, China
- Key Laboratory of Vegetation Ecology, Ministry of Education, Northeast Normal University, 2555 Jingyue Street, Changchun, 130117, China
| | - Yunga Wu
- Key Laboratory of Vegetation Ecology, Ministry of Education, Northeast Normal University, 2555 Jingyue Street, Changchun, 130117, China
| | - Zhijing Xie
- Key Laboratory of Vegetation Ecology, Ministry of Education, Northeast Normal University, 2555 Jingyue Street, Changchun, 130117, China
| | - Bettina Weber
- Institute of Biology, Division of Plant Sciences, University of Graz, Holteigasse 6, Graz, 8010, Austria
| | - Paul Illmer
- Department of Microbiology, Universität Innsbruck, Technikerstrasse 25d, Innsbruck, 6020, Austria
| | - Julia Seeber
- Institute for Alpine Environment, Eurac Research, Viale Druso 1, Bozen/Bolzano, 39100, Italy
- Department of Ecology, Universität Innsbruck, Technikerstrasse 25, Innsbruck, 6020, Austria
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21
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Tanaka E, Umeki D, Kido S, Makishima R, Tamaki Y, Murakami T, Fujiwara M, Saijo Y. Biocontrol of Bacterial Wilt Disease Using Plant-Associated Bacterial Communities in Tomato. MOLECULAR PLANT-MICROBE INTERACTIONS : MPMI 2025:MPMI09240114R. [PMID: 40354312 DOI: 10.1094/mpmi-09-24-0114-r] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Subscribe] [Scholar Register] [Indexed: 05/14/2025]
Abstract
Host-protective or disease-suppressive microorganisms are emerging as sustainable solutions for controlling crop diseases, such as bacterial wilt. However, the efficacy of biocontrol strategies is often constrained by limited resilience under varying environmental conditions and interactions with native microbial communities in the field. One major challenge is that introduced biocontrol microbes often face suppression by indigenous microbes due to competitive interactions. Synthetic communities (SynComs) offer a promising alternative strategy. However, conventional approaches to assembling SynComs by combining different microbial isolates often result in antagonism and competition among strains, leading to ineffective and inconsistent outcomes. In this study, we assembled a bacterial wilt-suppressive SynCom for tomato, composed of bacterial isolates derived from co-cultured microbial complexes associated with healthy plants. This SynCom demonstrates significant disease-suppressive effects against Ralstonia pseudosolanacearum in tomato seedlings under both axenic and soil conditions. Additionally, our findings suggest the presence of an optimal SynCom colonization level in plants, which is crucial for effective disease suppression. The SynCom also exhibits direct antibiotic activity and modulates the plant-associated microbiome. Our results provide an effective approach to constructing SynComs with consistent and effective disease-suppressive properties within microbial community contexts. [Formula: see text] Copyright © 2025 The Author(s). This is an open access article distributed under the CC BY-NC-ND 4.0 International license.
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Affiliation(s)
- Eriko Tanaka
- Yanmar Holdings Co., Ltd., 1-32 Chayamachi Kita-ku, Osaka, Japan
| | - Daisuke Umeki
- Yanmar Holdings Co., Ltd., 1-32 Chayamachi Kita-ku, Osaka, Japan
| | - Shota Kido
- Nara Institute of Science and Technology, Graduate School of Biological Sciences, 8916-5 Takayama-cho, Ikoma, Nara, Japan
| | - Rikako Makishima
- Yanmar Holdings Co., Ltd., 1-32 Chayamachi Kita-ku, Osaka, Japan
| | - Yuko Tamaki
- Nara Institute of Science and Technology, Graduate School of Biological Sciences, 8916-5 Takayama-cho, Ikoma, Nara, Japan
| | - Takumi Murakami
- School of Life Science and Technology, Tokyo Institute of Technology, 2-12-1 Ookayama, Meguro-ku, Tokyo, Japan
- Advanced Genomics Center, National Institute of Genetics, 1111 Yata, Mishima, Shizuoka, Japan
| | | | - Yusuke Saijo
- Nara Institute of Science and Technology, Graduate School of Biological Sciences, 8916-5 Takayama-cho, Ikoma, Nara, Japan
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22
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Tong A, Liu W, Liu X, Zhu J, Zhou Y, Li J. Comparative analysis of actinorhizal nodule and associated soil microorganism diversity and structure in three Alnus species. FRONTIERS IN PLANT SCIENCE 2025; 16:1572494. [PMID: 40406724 PMCID: PMC12095336 DOI: 10.3389/fpls.2025.1572494] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Download PDF] [Figures] [Subscribe] [Scholar Register] [Received: 02/10/2025] [Accepted: 04/15/2025] [Indexed: 05/26/2025]
Abstract
Background Due to the importance of biological nitrogen fixation in terrestrial ecosystems, actinorhizal symbiosis has attracted more and more attention. Alders (Alnus) are important actinorhizal plants, but little is known about the diversity of symbiotic microbiota in the actinorhizal nodules. In addition, it remains unclear about the influence of the host species and habitats on the microbial community of alder root nodules and rhizospheric soils. Methods In this study we sequenced the hyper-variable regions of the 16S rRNA from the root nodules and their rhizosphere soils of three alder species (Alnus mandshurica, A. sibirica, A. japonica) in northeastern China to explore the diversity, composition, network association, and nitrogen cycling pathway of the microbial communities in the actinorhizal nodules and associated soils. Results The results showed that the microbial community α-diversity decreased significantly from the associated soil to the root nodule, and the microbial diversity in the root nodule of A. sibirica was not affected by the habitats. The dominant microbe genus in alder nodules was Frankia, whose abundance was significantly higher than that in associated soil samples. Furthermore, the abundance of Frankia was affected by alder tree species, but not by the habitats. The most significant taxon in the nodules of all the three alders was Frankia genus, which was negatively correlated with other six genera of microbes. The main function of microorganisms in alder nodules is nitrogen fixation, which is not affected by tree species and their habitats. Conclusion These findings suggest that the host determines the microbial community composition in the root nodule of three alders. This study provides valuable insights into the effects of alder species and habitats on the microbial communities of alder nodules and associated soils.
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Affiliation(s)
- Aizi Tong
- Key Laboratory of Evaluation and Application of Changbai Mountain Biological Germplasm Resources of Jilin Province, College of Life Science, Tonghua Normal University, Tonghua, China
| | - Wei Liu
- Key Laboratory of Evaluation and Application of Changbai Mountain Biological Germplasm Resources of Jilin Province, College of Life Science, Tonghua Normal University, Tonghua, China
| | - Xiaoliang Liu
- Key Laboratory of Evaluation and Application of Changbai Mountain Biological Germplasm Resources of Jilin Province, College of Life Science, Tonghua Normal University, Tonghua, China
| | - Junyi Zhu
- Key Laboratory of Evaluation and Application of Changbai Mountain Biological Germplasm Resources of Jilin Province, College of Life Science, Tonghua Normal University, Tonghua, China
| | - You Zhou
- Key Laboratory of Evaluation and Application of Changbai Mountain Biological Germplasm Resources of Jilin Province, College of Life Science, Tonghua Normal University, Tonghua, China
| | - Jianhua Li
- Biology Department, Hope College, Holland, MI, United States
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23
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Zhang M, Hu Y, Ma Y, Hou T, Wang J, Che Q, Chen B, Wang Q, Feng G. Soil Bacterial Diversity and Community Structure of Cotton Rhizosphere under Mulched Drip-Irrigation in Arid and Semi-arid Regions of Northwest China. MICROBIAL ECOLOGY 2025; 88:39. [PMID: 40327084 PMCID: PMC12055924 DOI: 10.1007/s00248-025-02540-1] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 02/05/2025] [Accepted: 04/24/2025] [Indexed: 05/07/2025]
Abstract
Xinjiang is situated in an arid and semi-arid region, where abundant heat and sunlight create highly favorable conditions for cotton cultivation. Xinjiang's cotton output accounts for nearly one-quarter of global production. Moreover, the implementation of advanced planting techniques, such as 'dwarfing, high-density, early-maturing' strategies combined with mulched drip irrigation, ensures stable and high yields in this region. Despite these advancements, limited research has focused on the microbial mechanisms in cotton fields employing these advanced planting methods. In this study, high-throughput sequencing technology was utilized to investigate the diversity and composition of bacterial and phoD (Alkaline phosphatases encoding gene) communities in the rhizosphere of cotton grown under different yield levels in Xinjiang Province, China. The Mantel test, redundancy analysis (RDA) and partial least squares path modeling (PLS-PM) were employed to explore the interactions between soil bacterial and phoD communities, their network structures, and environmental factors. The bacterial and phoD communities in the cotton rhizosphere were predominantly composed of nine bacterial phyla (i.e., Proteobacteria, Actinobacteria, Acidobacteria, Gemmatimonadetes, Chloroflexi, Bacteroidetes, Rokubacteria, Firmicutes, and Nitrospirae) and five phoD phyla (i.e., Proteobacteria, Actinobacteria, Planctomycetes, Acidobacteria, and Firmicutes), respectively. Alpha diversity analysis indicated that the medium yield cotton field (MYF) exhibited higher bacterial richness and diversity indices compared to low yield (LYF) and high yield (HYF) fields. The symbiotic network analysis of LYF revealed greater values of average degree, number of edges, and modularity, suggesting a more complex network structure in both bacterial and phoD communities. The Mantel test, RDA, and PLS-PM model identified soil pH, electrical conductivity (EC), organic phosphorus (OP), available phosphorus (AP), total nitrogen (TN), microbial biomass carbon (MBC), and clay content as the main driving factors influencing changes in the rhizosphere bacterial community diversity and network structure. These findings provide a theoretical basis for future research aimed at improving soil quality and cotton yield.
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Affiliation(s)
- Man Zhang
- College of Resources and Environment, Xinjiang Agricultural University, Urumqi, 830052, Xinjiang, China
| | - Yang Hu
- College of Resources and Environment, Xinjiang Agricultural University, Urumqi, 830052, Xinjiang, China
| | - Yue Ma
- College of Resources and Environment, Xinjiang Agricultural University, Urumqi, 830052, Xinjiang, China
| | - Tianyu Hou
- College of Resources and Environment, Xinjiang Agricultural University, Urumqi, 830052, Xinjiang, China
| | - Juanhong Wang
- College of Resources and Environment, Xinjiang Agricultural University, Urumqi, 830052, Xinjiang, China
| | - Qingxuan Che
- College of Resources and Environment, Xinjiang Agricultural University, Urumqi, 830052, Xinjiang, China
| | - Bolang Chen
- College of Resources and Environment, Xinjiang Agricultural University, Urumqi, 830052, Xinjiang, China.
| | - Qinghui Wang
- Agricultural Mechanisation Institute, Xinjiang Academy of Agricultural Sciences, Urumqi, 830091, Xinjiang, China.
| | - Gu Feng
- College of Resources and Environmental Sciences, China Agricultural University, Beijing, 100083, China
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24
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Dijoux J, Gigante S, Lecellier G, Guentas L, Burtet-Sarramegna V. Plant nickel-exclusion versus hyperaccumulation: a microbial perspective. MICROBIOME 2025; 13:110. [PMID: 40320560 PMCID: PMC12051281 DOI: 10.1186/s40168-025-02098-7] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Download PDF] [Figures] [Subscribe] [Scholar Register] [Received: 11/05/2024] [Accepted: 03/24/2025] [Indexed: 05/08/2025]
Abstract
BACKGROUND In New Caledonia, nearly 2000 plant species grow on ultramafic substrates, which contain prominent levels of heavy metals and are deficient in essential plant nutrients. To colonize these habitats, such plants, known as metallophytes, have developed various adaptive behaviors towards metals (exclusion, tolerance, or hyperaccumulation). Ultramafic substrates also host many unique microorganisms, which are adapted to metallic environments and capable of boosting plant growth while assisting plants in acquiring essential micronutrients. Hence, plant-microbiota interactions play a key role in adapting to environmental stress. Here, we hypothesised that microbial associations in the different aboveground and underground compartments of metallophytes could be associated to their metal hyperaccumulation or exclusion phenotypes. This hypothesis was tested using a systematic comparative metabarcoding approach on the different compartments of two New Caledonian metallophytes belonging to the same genus and living in sympatry on ultramafic substrates: Psychotria gabriellae, a nickel-hyperaccumulator (Ni-HA), and Psychotria semperflorens, the related non-accumulator (nA) species. RESULTS The study of the diversity and specificity of fungal amplicon sequence variants (ASVs) reveals a structuring of fungal communities at both the plant phenotype and compartment levels. In contrast, the structure of bacterial communities was primarily shaped by the belowground compartments. Additionally, we observed a lower diversity in the bacterial communities of the aboveground compartments of each species. For each plant species, we highlighted a distinct global microbial signature (biomarkers), as well as compartment-specific microbial associations. CONCLUSION To our knowledge, this study is the first to systematically compare the microbiomes associated with different compartments of New Caledonian metallophyte species growing on the same substrate and under identical environmental conditions but exhibiting different adaptive phenotypes. Our results reveal distinct microbial biomarkers between the Ni-hyperaccumulator and non-accumulator Psychotria species. Most of the highlighted biomarkers are abundant in various plants under metal stress and may contribute to improving the phytoextraction or phytostabilization processes. They are also known to tolerate heavy metals and enhance metal stress tolerance in plants. The present findings highlight that the microbial perspective is essential for better understanding the mechanisms of hyperaccumulation and exclusion at the whole-plant level. Video Abstract.
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Affiliation(s)
- Julie Dijoux
- Institute of Exact and Applied Sciences, University of New Caledonia, 145 Avenue James Cook, Noumea, New Caledonia, BP R4, 98851.
| | - Sarah Gigante
- Institute of Exact and Applied Sciences, University of New Caledonia, 145 Avenue James Cook, Noumea, New Caledonia, BP R4, 98851
| | - Gael Lecellier
- Institute of Exact and Applied Sciences, University of New Caledonia, 145 Avenue James Cook, Noumea, New Caledonia, BP R4, 98851
| | - Linda Guentas
- Institute of Exact and Applied Sciences, University of New Caledonia, 145 Avenue James Cook, Noumea, New Caledonia, BP R4, 98851
| | - Valérie Burtet-Sarramegna
- Institute of Exact and Applied Sciences, University of New Caledonia, 145 Avenue James Cook, Noumea, New Caledonia, BP R4, 98851.
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Jian J, Feng S, Xu Y, Jia M, Huang H, Zheng X, Liu H, Xu H. Bacterial community assembly processes mediate soil functioning under cadmium stress in the agroecosystem. JOURNAL OF HAZARDOUS MATERIALS 2025; 494:138496. [PMID: 40339367 DOI: 10.1016/j.jhazmat.2025.138496] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Subscribe] [Scholar Register] [Received: 02/27/2025] [Revised: 04/19/2025] [Accepted: 05/03/2025] [Indexed: 05/10/2025]
Abstract
Elucidating the effects of community assembly processes on soil functioning represents a crucial challenge in theoretical ecology, particularly under cadmium (Cd) stress, where our understanding remains limited. In this study, we therefore used amplicon sequencing and a quantitative-PCR-based chip to analyze the changes in bacterial community characteristics, soil functioning and their interrelationships in agroecosystems under different levels of Cd stress. The results indicated that Cd stress led to a decline in community diversity (Z-score), network complexity and stability, an increase in species turnover, and a regulation of community structure. Cd stress significantly increased the relative importance of dispersal limitation and homogeneous selection, reducing community drift and rendering the community more deterministic. Finally, Cd stress significantly reduced soil functional potential (Z-score) and soil functional stability (Z-score), impairing soil carbon, nitrogen, phosphorus, and sulfur cycling. It is noteworthy that correlation and random forest analyses revealed significant effects of specific community assembly processes, including dispersal limitation, homogeneous selection, drift (and others), on changes in soil functional potential (Z-score). The results emphasize the pivotal role of community assembly processes in dictating soil functioning under Cd stress, thereby offering novel insights into the comprehension of microbial-driven mechanisms governing soil functioning.
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Affiliation(s)
- Jiannan Jian
- Key Laboratory of Bio-resource and Eco-Environment of Ministry of Education, College of Life Sciences, Sichuan University, Chengdu, Sichuan 610065, PR China
| | - Shuang Feng
- Key Laboratory of Bio-resource and Eco-Environment of Ministry of Education, College of Life Sciences, Sichuan University, Chengdu, Sichuan 610065, PR China
| | - Yi Xu
- Mianzhu Municipal Bureau of Agriculture and Rural Affairs, Mianzhu, Sichuan 618200, PR China
| | - Maohang Jia
- Key Laboratory of Bio-resource and Eco-Environment of Ministry of Education, College of Life Sciences, Sichuan University, Chengdu, Sichuan 610065, PR China
| | - Huayan Huang
- Key Laboratory of Bio-resource and Eco-Environment of Ministry of Education, College of Life Sciences, Sichuan University, Chengdu, Sichuan 610065, PR China
| | - Xin Zheng
- Key Laboratory of Bio-resource and Eco-Environment of Ministry of Education, College of Life Sciences, Sichuan University, Chengdu, Sichuan 610065, PR China
| | - Huakang Liu
- Key Laboratory of Bio-resource and Eco-Environment of Ministry of Education, College of Life Sciences, Sichuan University, Chengdu, Sichuan 610065, PR China; Key Laboratory of Environment Protection, Soil ecological protection and pollution control, Sichuan University & Department of Ecology and Environment of Sichuan, Chengdu, Sichuan 610065, PR China.
| | - Heng Xu
- Key Laboratory of Bio-resource and Eco-Environment of Ministry of Education, College of Life Sciences, Sichuan University, Chengdu, Sichuan 610065, PR China; Key Laboratory of Environment Protection, Soil ecological protection and pollution control, Sichuan University & Department of Ecology and Environment of Sichuan, Chengdu, Sichuan 610065, PR China.
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Wang M, Pan X, Yue Z, Deng R, Li Z, Wang J. Seasonal variation drives species coexistence and community succession in microbial communities of stratified acidic pit lakes. JOURNAL OF ENVIRONMENTAL MANAGEMENT 2025; 381:125177. [PMID: 40199217 DOI: 10.1016/j.jenvman.2025.125177] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 01/08/2025] [Revised: 03/20/2025] [Accepted: 03/28/2025] [Indexed: 04/10/2025]
Abstract
Acidic pit lakes (APLs) are a special type of ecosystem and represent a significant environmental issue worldwide. While previous studies have explored the structure and function of microbial communities in APLs stratification, natural attenuation, and remediation processes, little is known about the succession patterns of microbial association networks and the underlying assembly mechanisms during seasonal succession. In this study, the distribution characteristics and succession patterns of prokaryotic and eukaryotic microorganisms in APLs across different seasons were investigated using 16S rRNA and 18S rRNA high-throughput sequencing technologies, combined with ecological and multivariate statistical methods. The diversity, composition and structure of prokaryotic and eukaryotic microbial communities showed obvious seasonal differences, and the surface waters were more susceptible to seasonal disturbances. Temperature is the most critical factor influencing the seasonal succession of microbial communities. During the year-round succession, variable selection (40.86 %) dominated in the prokaryotic community and homogeneous selection (69.64 %) dominated in the eukaryotic community. Moreover, the proportion of deterministic processes increased with increasing water temperature differences. Co-occurrence networks were more complex and inter-kingdom exchanges were more frequent during the warm seasons (summer and autumn), and microbial communities were more stable during the cool seasons (spring and winter). Meanwhile, the inter-kingdom interactions between eukaryotes and prokaryotes are predominantly positive in all seasons except autumn, which may serve as a strategy to resist environmental stress. These findings indicate that there is a significant seasonal heterogeneity between eukaryotes and prokaryotes in APLs, providing valuable insights into the ecological processes of microbial community succession in extreme environments.
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Affiliation(s)
- Meichen Wang
- School of Resources and Environmental Engineering, Hefei University of Technology, Hefei, Anhui, 230009, China; Anhui Engineering Research Center of Industrial Wastewater Treatment and Resource Recovery, Hefei University of Technology, Hefei, Anhui, 230009, China; Key Laboratory of Nanominerals and Pollution Control of Anhui Higher Education Institutes, Hefei University of Technology, Hefei, Anhui, 230009, China
| | - Xin Pan
- School of Resources and Environmental Engineering, Hefei University of Technology, Hefei, Anhui, 230009, China; Anhui Engineering Research Center of Industrial Wastewater Treatment and Resource Recovery, Hefei University of Technology, Hefei, Anhui, 230009, China; Key Laboratory of Nanominerals and Pollution Control of Anhui Higher Education Institutes, Hefei University of Technology, Hefei, Anhui, 230009, China; Anhui Engineering Consulting Institute, Hefei, Anhui, 230051, China
| | - Zhengbo Yue
- School of Resources and Environmental Engineering, Hefei University of Technology, Hefei, Anhui, 230009, China; Anhui Engineering Research Center of Industrial Wastewater Treatment and Resource Recovery, Hefei University of Technology, Hefei, Anhui, 230009, China; Key Laboratory of Nanominerals and Pollution Control of Anhui Higher Education Institutes, Hefei University of Technology, Hefei, Anhui, 230009, China
| | - Rui Deng
- School of Resources and Environmental Engineering, Hefei University of Technology, Hefei, Anhui, 230009, China; Anhui Engineering Research Center of Industrial Wastewater Treatment and Resource Recovery, Hefei University of Technology, Hefei, Anhui, 230009, China; Key Laboratory of Nanominerals and Pollution Control of Anhui Higher Education Institutes, Hefei University of Technology, Hefei, Anhui, 230009, China
| | - Ziyi Li
- School of Resources and Environmental Engineering, Hefei University of Technology, Hefei, Anhui, 230009, China; Anhui Engineering Research Center of Industrial Wastewater Treatment and Resource Recovery, Hefei University of Technology, Hefei, Anhui, 230009, China; Key Laboratory of Nanominerals and Pollution Control of Anhui Higher Education Institutes, Hefei University of Technology, Hefei, Anhui, 230009, China
| | - Jin Wang
- School of Resources and Environmental Engineering, Hefei University of Technology, Hefei, Anhui, 230009, China; Anhui Engineering Research Center of Industrial Wastewater Treatment and Resource Recovery, Hefei University of Technology, Hefei, Anhui, 230009, China; Key Laboratory of Nanominerals and Pollution Control of Anhui Higher Education Institutes, Hefei University of Technology, Hefei, Anhui, 230009, China.
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Ding S, Zhong J, Du S, Liu X, Yao A, Xu X, Wu D. Exploring the function of key species in different composting stages for effective waste biotransformation. JOURNAL OF ENVIRONMENTAL MANAGEMENT 2025; 381:125234. [PMID: 40186974 DOI: 10.1016/j.jenvman.2025.125234] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 01/07/2025] [Revised: 03/24/2025] [Accepted: 04/01/2025] [Indexed: 04/07/2025]
Abstract
Composting is a microbial-driven process that plays a vital role in recycling waste and promoting sustainable production. To develop more effective bioaugmentation strategies, this study examined three successive stages in an aerobic composting system, focusing on microbial community adaptation to high-temperature stress (mode_2) and nutrient-poor conditions (mode_3). The results revealed a shift from an r-strategy (rapid growth) to a K-strategy (thriving under resource-limited conditions). Community succession was predominantly driven by deterministic processes (>90 %) and exhibited strong cooperative interactions. Using multiple statistical approaches, key species were identified for each condition. These species enhanced microbial network connectivity under environmental stresses, increasing network edges by 29 %-35 %. Under high-temperature stress, Bacillus and Ureibacillus maintained core functions, while Chelativorans and Aeribacillus contributed to key metabolic pathways, including amino acid metabolism. In nutrient-poor conditions, Saccharomonospora and Pseudoxanthomonas enhanced overall system functionality, and Novibacillus played a key role in carbon and nitrogen cycling, particularly nitrogen fixation. Predictive models for microbial community stability (R2 = 0.68-0.97) were developed based on these key species to enable rapid assessment of system stability. Overall, this study identifies essential microbes involved in composting across different environmental conditions and clarifies their functional roles, providing valuable insights for optimizing aerobic composting efficiency and advancing waste resource management.
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Affiliation(s)
- Shang Ding
- College of Environmental and Resource Sciences, Zhejiang University, Hangzhou, 310058, People's Republic of China.
| | - Jialin Zhong
- College of Environmental and Resource Sciences, Zhejiang University, Hangzhou, 310058, People's Republic of China.
| | - Shuwen Du
- College of Environmental and Resource Sciences, Zhejiang University, Hangzhou, 310058, People's Republic of China.
| | - Xiaofan Liu
- College of Environmental and Resource Sciences, Zhejiang University, Hangzhou, 310058, People's Republic of China.
| | - Aiping Yao
- Jinhua Academy of Agricultural Sciences, Jinhua, 321000, People's Republic of China.
| | - Xinhua Xu
- College of Environmental and Resource Sciences, Zhejiang University, Hangzhou, 310058, People's Republic of China.
| | - Donglei Wu
- College of Environmental and Resource Sciences, Zhejiang University, Hangzhou, 310058, People's Republic of China; Zhejiang Ecological Civilization Academy, Anji, 313300, People's Republic of China.
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Huang X, Li R, Xu J, Kang J, Chen X, Han B, Xue Y. Integrated multi-omics uncover viruses, active fermenting microbes and their metabolic profiles in the Daqu microbiome. Food Res Int 2025; 208:116061. [PMID: 40263874 DOI: 10.1016/j.foodres.2025.116061] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 07/12/2024] [Revised: 01/08/2025] [Accepted: 02/22/2025] [Indexed: 04/24/2025]
Abstract
The coexistence and coevolution of viruses and fermenting microbes have a significant impact on the structure and function of microbial communities. Although the presence of viruses in Daqu, the fermentation starter for Chinese Baijiu, has been documented, their specific effects on the community composition and metabolic functions of low, medium, and high-temperature Daqu remain unclear. In this study, we employed multi-omics technology to explore the distribution of viruses and active bacteria and fungi in various Daqu and their potential metabolic roles. Viral metagenomic sequencing showed a predominance of Parvoviridae in High-Temperature Daqu (HTQ), while Genomoviridae were dominant in Medium-Temperature Daqu (MTQ) and Low- Temperature Daqu (LTQ). Phages belonging to the Siphoviridae, Podoviridae, Herelleviridae, and Myoviridae families showed significantly different abundances across three Daqu groups. Metatranscriptomic analysis showed that fungal communities were most active in LTQ, whereas bacterial communities were dominant in MTQ and HTQ. By employing the CRISPR-Cas spacer, a higher predicted number of phage-host linkages was identified in LTQ, particularly with hosts including Lactobacillus, Staphylococcus, Acinetobacter, Enterobacter, and Bacillus. Correlation analysis showed that bacteria like Acinetobacter, Lactobacillus, and Streptococcus exhibited the strongest associations with metabolites, particularly amino acids and organic acids. The potential phage-induced metabolic differences in the three Daqu groups were mainly linked to pathways involved in the metabolism of amino acids, sugars, and organic acids. Overall, our study elucidates the impact of viruses on shaping microbial composition and influencing metabolic functions in Daqu. These results improve our comprehension of viruses and microbes in Daqu microbial communities and provide valuable insights for enhancing quality control in Daqu production.
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Affiliation(s)
- Xiaoning Huang
- Beijing Laboratory for Food Quality and Safety, College of Food Science and Nutritional Engineering, China Agricultural University, Beijing 10083, China; Department of Bioengineering, University of Illinois Urbana-Champaign, Urbana, IL 61801, USA
| | - Rengshu Li
- Beijing Laboratory for Food Quality and Safety, College of Food Science and Nutritional Engineering, China Agricultural University, Beijing 10083, China
| | - Jinguo Xu
- College of Food Science and Engineering, Yangzhou University, Yangzhou 225127, China
| | - Jiamu Kang
- School of Food Science and Engineering, Hainan University, Haikou 570228, China
| | - Xiaoxue Chen
- Beijing Laboratory for Food Quality and Safety, College of Food Science and Nutritional Engineering, China Agricultural University, Beijing 10083, China
| | - Beizhong Han
- Beijing Laboratory for Food Quality and Safety, College of Food Science and Nutritional Engineering, China Agricultural University, Beijing 10083, China
| | - Yansong Xue
- Beijing Laboratory for Food Quality and Safety, College of Food Science and Nutritional Engineering, China Agricultural University, Beijing 10083, China.
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Davis RA, Mafune KK, Winkler MKH. Biodegradable hydrogels and microbial consortia as a treatment for soil dysbiosis. Front Microbiol 2025; 16:1565940. [PMID: 40376461 PMCID: PMC12078290 DOI: 10.3389/fmicb.2025.1565940] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/24/2025] [Accepted: 04/11/2025] [Indexed: 05/18/2025] Open
Abstract
Terrestrial microbial communities drive many soil processes and can be pushed into a state of dysbiosis upon disturbance. This dysregulation negatively impacts soil biogeochemical cycles, which threatens plant and soil health. Effective treatment of soil dysbiosis requires simultaneous restoration of multiple system components, addressing both the physical structure of soil and its microbial communities. Hydrogels with microbial consortia simultaneously remedy soil hydrodynamics while promoting microbial reestablishment. The purpose of this review is to shed light on soil management practices through the lens of soil dysbiosis. This is important to address not only for soil health and crop productivity, but also to mitigate climate change through improved soil carbon sequestration and reduced greenhouse gas emissions. This review positions hydrogels and microbes as tools for the treatment of soil dysbiosis, contributing to agricultural and climate resilience.
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Lim TW, Huang S, Burrow MF, McGrath C. A randomised crossover clinical trial of the efficacy of an ultrasonic cleaner combined with a denture cleanser on the microbiome on removable dentures among community-dwelling older adults. J Dent 2025; 156:105709. [PMID: 40127751 DOI: 10.1016/j.jdent.2025.105709] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/27/2025] [Revised: 03/18/2025] [Accepted: 03/21/2025] [Indexed: 03/26/2025] Open
Abstract
OBJECTIVE To evaluate and characterise the microbial compositional changes of removable dentures after interventions by comparing the efficacy of the test arm (a portable self-operated ultrasonic cleaner combined with an enzymatic peroxide-based denture cleanser solution) to the control arm (immersion of the denture in the same cleanser solution followed by conventional brushing). MATERIALS AND METHODS A prospective, single-blind, block-randomised, two-period crossover, controlled clinical trial was conducted, involving 56 community-dwelling older adults wearing removable acrylic dentures. They were block-randomized into the test/control or control/test denture cleaning sequence. Type IIB Restriction-site Associated DNA for Microbiome metagenomic sequencing was adopted to characterize the species-resolved microbial composition for denture biofilm. RESULTS For the intervention effect, the overall microbial richness in both arms was not significantly different based on the Chao 1 index (P = 0.343). However, Beta diversity analysis (Jaccard qualitative distance matrix) demonstrated significant differences in the microbial community structures between the Test and Control arms after interventions, confirmed by the Permanova test (R2 = 0.01118, P = 0.034). Among the opportunistic pathogenic bacteria, Pseudomonas aeruginosa was detected as one of the top 30 species by relative abundance at the end of the clinical trial, and Enterobacter kobei was significantly enriched in the control arm, as determined by LEfSe analysis. CONCLUSIONS The microbial community of denture biofilm samples after both interventions were significantly 'shifted' and had limited numbers of opportunistic pathogens, suggesting the interventions equally effective in mitigating the overall number of pathogenic bacteria. CLINICAL SIGNIFICANCE Denture cleaning intervention using ultrasonic cleaner combined with immersion in denture cleanser solution appears to be effective in shifting the denture microbiome with reduced pathogenic bacteria among community-dwelling denture wearers.
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Affiliation(s)
- Tong Wah Lim
- Division of Restorative Dental Sciences, Faculty of Dentistry, The University of Hong Kong, Sai Ying Pun, Hong Kong SAR
| | - Shi Huang
- Division of Applied Oral Sciences and Community Dental Care, Faculty of Dentistry, The University of Hong Kong, Hong Kong SAR
| | - Michael Francis Burrow
- Division of Restorative Dental Sciences, Faculty of Dentistry, The University of Hong Kong, Sai Ying Pun, Hong Kong SAR
| | - Colman McGrath
- Division of Applied Oral Sciences and Community Dental Care, Faculty of Dentistry, The University of Hong Kong, Hong Kong SAR.
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Jia Y, Huang D, Lan X, Sun X, Lin W, Sun W, Wang Y. Community structure and metabolic potentials of keystone taxa and their associated bacteriophages within rice root endophytic microbiome in response to metal(loid)s contamination. ENVIRONMENTAL POLLUTION (BARKING, ESSEX : 1987) 2025; 372:126028. [PMID: 40064231 DOI: 10.1016/j.envpol.2025.126028] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 11/14/2024] [Revised: 03/03/2025] [Accepted: 03/07/2025] [Indexed: 03/17/2025]
Abstract
Heavy metal (HM) contamination of agricultural products is of global environmental concern as it directly threatened the food safety. Plant-associated microbiome, particularly endophytic microbiome, hold the potential for mitigating HM stress as well as promoting plant growth. The metabolic potentials of the endophytes, especially those under the HM stresses, have not been well addressed. Rice, a major staple food worldwide, is more vulnerable to HM contamination compared to other crops and therefore requires special attentions. Therefore, this study selected rice as the target plants. Geochemical analysis and amplicon sequencing were combined to characterize the rice root endophytic bacterial communities and identify keystone taxa in two HM-contaminated rice fields. Metagenomic analysis was employed to investigate the metabolic potentials of these keystone taxa. Burkholderiales and Rhizobiales were identified as predominant keystone taxa. The metagenome-assembled genome (MAG)s associated with these keystone populations suggested that they possessed diverse genetic potentials related to metal resistance and transformation (e.g., As resistance and cycling, V reduction, Cr efflux and reduction), and plant growth promotion (nitrogen fixation, phosphate solubilization, oxidative stress resistance, indole-3-acetic acid, and siderophore production). Moreover, bacteriophages encoding auxiliary metabolism genes (AMGs) associated with the HM resistance as well as nitrogen and phosphate acquisition were identified, suggesting that these phages may contribute to these crucial biogeochemical processes within rice roots. The current findings revealed the beneficial roles of rice endophytic keystone taxa and their associated bacteriophages within HM-contaminated rice root endophytic microbiome, which may provide valuable insights on future applications of employing root microbiome for safety management of agriculture productions.
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Affiliation(s)
- Yanlong Jia
- School of Chemistry and Environmental Engineering, Hanshan Normal University, Chaozhou, 521041, China; School of Resources and Environmental Engineering, Guizhou Institute of Technology, Guiyang, 550002, China
| | - Duanyi Huang
- National-Regional Joint Engineering Research Center for Soil Pollution Control and Remediation in South China, Guangdong Key Laboratory of Integrated Agro-Environmental Pollution Control and Management, Institute of Eco-Environmental and Soil Sciences, Guangdong Academy of Sciences, Guangzhou, 510650, China; College of Environmental Science and Engineering, Hunan University, Changsha, 410082, China
| | - Xiaolong Lan
- School of Chemistry and Environmental Engineering, Hanshan Normal University, Chaozhou, 521041, China.
| | - Xiaoxu Sun
- National-Regional Joint Engineering Research Center for Soil Pollution Control and Remediation in South China, Guangdong Key Laboratory of Integrated Agro-Environmental Pollution Control and Management, Institute of Eco-Environmental and Soil Sciences, Guangdong Academy of Sciences, Guangzhou, 510650, China
| | - Wenjie Lin
- School of Chemistry and Environmental Engineering, Hanshan Normal University, Chaozhou, 521041, China
| | - Weimin Sun
- National-Regional Joint Engineering Research Center for Soil Pollution Control and Remediation in South China, Guangdong Key Laboratory of Integrated Agro-Environmental Pollution Control and Management, Institute of Eco-Environmental and Soil Sciences, Guangdong Academy of Sciences, Guangzhou, 510650, China; College of Environmental Science and Engineering, Hunan University, Changsha, 410082, China
| | - Yize Wang
- National-Regional Joint Engineering Research Center for Soil Pollution Control and Remediation in South China, Guangdong Key Laboratory of Integrated Agro-Environmental Pollution Control and Management, Institute of Eco-Environmental and Soil Sciences, Guangdong Academy of Sciences, Guangzhou, 510650, China.
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Zheng H, Liu D, Li Y, Chen Z, Li J, Dong Y, Yang C, Miao Y, Yuan J, Ding W. Wetland restoration suppresses microbial carbon metabolism by altering keystone species interactions. Front Microbiol 2025; 16:1570703. [PMID: 40371112 PMCID: PMC12075313 DOI: 10.3389/fmicb.2025.1570703] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/04/2025] [Accepted: 04/17/2025] [Indexed: 05/16/2025] Open
Abstract
Soil bacteria play a pivotal role in regulating multifaceted functions of terrestrial ecosystems. Unraveling the succession of bacterial communities and the feedback mechanism on soil organic carbon (SOC) dynamics help embed the ecology of microbiome into C cycling model. However, how wetland restoration drives soil bacterial community assembly and species association to regulate microbial C metabolism remains unclear. Here, we investigated soil bacterial diversity, community structure and co-occurrence network, enzyme activities and SOC decomposition in restored wetlands for one, three, and four years from paddy fields in Northeast China. Wetland restoration for three and four years increased taxonomic (richness) and phylogenetic diversities by 2.39-3.96% and 2.13-3.02%, respectively, and increased the relative contribution of nestedness to community dissimilarity, indicating increased richness changed soil bacterial community structure. However, wetland restoration for three and four years decreased the richness index of aerobic Firmicutes by 5.04-5.74% due to stronger anaerobic condition characterized by increased soil Fe2+/Fe3+ from 0.20 to 0.64. Besides, wetland restoration for four years decreased network complexity (characterized by decreased node number by 2.51%, edge number by 9.62%, positive/negative edge number by 6.37%, average degree by 5.74% and degree centralization by 6.34%). Robustness index decreased with the increase of restoration duration, while vulnerability index increased with the increase of restoration duration, indicating that wetland restoration decreased network stability of soil bacterial communities. These results might be because stronger anaerobic condition induced the decrease of aerobic Bacilli richness index in keystone module, thereby reducing positive association within keystone module. Decreased positive species association within keystone module in turn weakened microbial C metabolism by decreasing hydrolase activities from 7.49 to 5.37 mmol kg SOC-1 h-1 and oxidase activities from 627 to 411 mmol kg SOC-1 h-1, leading to the decrease of SOC decomposition rate from 1.39 to 1.08 g C kg SOC-1 during wetland restoration. Overall, our results suggested that although wetland restoration after agricultural abandonment increased soil bacterial diversity, it decreased positive association within Bacilli-dominated keystone module under stronger anaerobic condition, which weakened microbial C metabolism and SOC decomposition.
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Affiliation(s)
- Huijie Zheng
- State Key Laboratory of Soil and Sustainable Agriculture, Institute of Soil Science, Chinese Academy of Sciences, Nanjing, China
- University of Chinese Academy of Sciences, Beijing, China
| | - Deyan Liu
- Co-Innovation Center for Sustainable Forestry in Southern China, Nanjing Forestry University, Nanjing, China
| | - Ye Li
- State Key Laboratory of Soil and Sustainable Agriculture, Institute of Soil Science, Chinese Academy of Sciences, Nanjing, China
| | - Zengming Chen
- State Key Laboratory of Soil and Sustainable Agriculture, Institute of Soil Science, Chinese Academy of Sciences, Nanjing, China
| | - Junjie Li
- State Key Laboratory of Soil and Sustainable Agriculture, Institute of Soil Science, Chinese Academy of Sciences, Nanjing, China
- University of Chinese Academy of Sciences, Beijing, China
| | - Yanhong Dong
- State Key Laboratory of Soil and Sustainable Agriculture, Institute of Soil Science, Chinese Academy of Sciences, Nanjing, China
- University of Chinese Academy of Sciences, Beijing, China
| | - Cong Yang
- State Key Laboratory of Soil and Sustainable Agriculture, Institute of Soil Science, Chinese Academy of Sciences, Nanjing, China
- University of Chinese Academy of Sciences, Beijing, China
| | - Yuncai Miao
- State Key Laboratory of Soil and Sustainable Agriculture, Institute of Soil Science, Chinese Academy of Sciences, Nanjing, China
| | - Junji Yuan
- State Key Laboratory of Soil and Sustainable Agriculture, Institute of Soil Science, Chinese Academy of Sciences, Nanjing, China
| | - Weixin Ding
- State Key Laboratory of Soil and Sustainable Agriculture, Institute of Soil Science, Chinese Academy of Sciences, Nanjing, China
- University of Chinese Academy of Sciences, Nanjing, China
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Ji D, Zhang J, Li F, Li W, Bi L, Li W, Fu Y, Wang Y. Divergent Driving Mechanisms Shape the Temporal Dynamics of Benthic Prokaryotic and Eukaryotic Microbial Communities in Coastal Subtidal Zones. Microorganisms 2025; 13:1050. [PMID: 40431222 PMCID: PMC12114215 DOI: 10.3390/microorganisms13051050] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Grants] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 03/29/2025] [Revised: 04/27/2025] [Accepted: 04/28/2025] [Indexed: 05/29/2025] Open
Abstract
Benthic microbial communities are a vital component of coastal subtidal zones, playing an essential role in nutrient cycling and energy flow, and are fundamental to maintaining the stability and functioning of marine ecosystems. However, the response of benthic prokaryotic and eukaryotic microbial communities to environmental changes remains poorly understood. Herein, we conducted a nearly semimonthly annual sampling survey to investigate the temporal patterns and underlying mechanisms of benthic prokaryotic and eukaryotic microbial communities in the subtidal sediments of Sanshan Island, situated in the eastern Laizhou Bay of the Bohai Sea, China. The results showed that the temporal variations in benthic microbial communities followed a distinct seasonal pattern, with turnover playing a more dominant role in community succession. Nonetheless, contrasting temporal variations were observed in the alpha diversity of benthic prokaryotic and eukaryotic microbial communities, as well as in the dominant taxa across different microbial communities. Water temperature, dissolved oxygen, electrical conductivity, salinity, total nitrogen (TN), NH4+, and PO43- were identified as the predominant environmental drivers. The assembly of benthic microbial communities was driven by different ecological processes, in which stochastic processes mainly shaped the benthic prokaryotic communities, while deterministic processes dominated the assembly of benthic eukaryotic microbial communities. Interactions within benthic microbial communities were primarily characterized by mutualistic or cooperative relationships, but the ability of prokaryotic and eukaryotic microbial communities to maintain stability under environmental disturbances showed notable differences. These results shed light on the temporal dynamics and potential driving mechanisms of benthic prokaryotic and eukaryotic microbial communities under environmental disturbances, highlighting the distinct roles of prokaryotic and eukaryotic communities in coastal subtidal zones and providing valuable insights for the management and conservation of coastal subtidal marine ecosystems.
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Affiliation(s)
- Daode Ji
- School of Ocean, Yantai University, Yantai 264005, China; (D.J.); (J.Z.)
| | - Jianfeng Zhang
- School of Ocean, Yantai University, Yantai 264005, China; (D.J.); (J.Z.)
| | - Fan Li
- Shandong Provincial Key Laboratory of Restoration for Marine Ecology, Shandong Marine Resource and Environment Research Institute, Observation and Research Station of Laizhou Bay Marine Ecosystem, MNR, Yantai 264006, China;
| | - Wensheng Li
- Laizhou Mingbo Aquatic Co., Ltd., Sanshan Island Street, Yantai 261418, China;
| | - Luping Bi
- Fujian Province Key Laboratory for Coastal Ecology and Environmental Studies, College of the Environment and Ecology, Xiamen University, Xiamen 361102, China;
- Key Laboratory of the Ministry of Education for Coastal and Wetland Ecosystem, College of the Environment and Ecology, Xiamen University, Xiamen 361102, China
| | - Wenlu Li
- State Key Laboratory of Marine Environmental Science, College of Ocean and Earth Sciences, Institute of Marine Microbes and Ecospheres, Xiamen University, Xiamen 361102, China; (W.L.); (Y.F.)
- Fujian Key Laboratory of Marine Carbon Sequestration, Xiamen University, Xiamen 361102, China
| | - Yingjun Fu
- State Key Laboratory of Marine Environmental Science, College of Ocean and Earth Sciences, Institute of Marine Microbes and Ecospheres, Xiamen University, Xiamen 361102, China; (W.L.); (Y.F.)
- Fujian Key Laboratory of Marine Carbon Sequestration, Xiamen University, Xiamen 361102, China
| | - Yunfeng Wang
- School of Ocean, Yantai University, Yantai 264005, China; (D.J.); (J.Z.)
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Weitzman CL, Day K, Brown GP, Gibb K, Christian K. Differential Temporal Shifts in Skin Bacteria on Wild and Captive Toads. MICROBIAL ECOLOGY 2025; 88:35. [PMID: 40301143 PMCID: PMC12040999 DOI: 10.1007/s00248-025-02537-w] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Subscribe] [Scholar Register] [Received: 01/21/2025] [Accepted: 04/17/2025] [Indexed: 05/01/2025]
Abstract
Skin bacteria on amphibian hosts play an important role in host health, but those communities are also constantly shifting based on environmental and host-related feedback. On some hosts, stability of skin communities depends on relatively abundant taxa, with less abundant taxa more readily entering and exiting the system. Cane toads (Rhinella marina) have invaded widespread, diverse tropical ecosystems, with varying ecology, physiology, and behaviour in different environments. In this study, we described temporal patterns of skin bacterial communities on cane toads at a site in northern Australia through the wet and dry seasons over two years. Toads in the wild population were paired with a captive-held population, housed in a semi-natural environment, to detect effects of time and season on wild toads, explore bacterial transience and volatility in skin taxa, and determine the extent to which skin communities on captive toads represent those on the wild population. We found community differences by captivity status, sampling timepoint, and season, with increased richness in the wet season on wild toads. Bacterial communities also became more similar among individuals (lower dispersion) in the wet season. Captive toads harboured more stable communities over time, likely owing to the reduced bacterial reservoirs experienced while in captivity. We propose that cane toads, with varied movement patterns among their diverse invaded habitats, provide an interesting direction for future work understanding the influences of habitat and movement on skin microbes, and the flexibility of microbial symbiotic interactions in invasive hosts.
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Affiliation(s)
- Chava L Weitzman
- Research Institute for the Environment and Livelihoods, Charles Darwin University, Casuarina, NT, Australia.
| | - Kimberley Day
- Research Institute for the Environment and Livelihoods, Charles Darwin University, Casuarina, NT, Australia
| | - Gregory P Brown
- School of Natural Sciences, Macquarie University, Sydney, NSW, Australia
| | - Karen Gibb
- Research Institute for the Environment and Livelihoods, Charles Darwin University, Casuarina, NT, Australia
| | - Keith Christian
- Research Institute for the Environment and Livelihoods, Charles Darwin University, Casuarina, NT, Australia
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Peng SX, Gao SM, Lin ZL, Luo ZH, Zhang SY, Shu WS, Meng F, Huang LN. Biogeography and ecological functions of underestimated CPR and DPANN in acid mine drainage sediments. mBio 2025:e0070525. [PMID: 40298441 DOI: 10.1128/mbio.00705-25] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/27/2025] [Accepted: 04/08/2025] [Indexed: 04/30/2025] Open
Abstract
Recent genomic surveys have uncovered candidate phyla radiation (CPR) bacteria and DPANN archaea as major microbial dark matter lineages in various anoxic habitats. Despite their extraordinary diversity, the biogeographic patterns and ecological implications of these ultra-small and putatively symbiotic microorganisms have remained elusive. Here, we performed metagenomic sequencing on 90 geochemically diverse acid mine drainage sediments sampled across southeast China and recovered 282 CPR and 189 DPANN nonredundant metagenome-assembled genomes, which collectively account for up to 28.6% and 31.2% of the indigenous prokaryotic communities, respectively. We found that, remarkably, geographic distance represents the primary factor driving the large-scale ecological distribution of both CPR and DPANN organisms, followed by pH and Fe. Although both groups might be capable of iron reduction through a flavin-based extracellular electron transfer mechanism, significant differences are found in their metabolic capabilities (with complex carbon degradation and chitin degradation being more prevalent in CPR whereas fermentation and acetate production being enriched in DPANN), indicating potential niche differentiation. Predicted hosts are mainly Acidobacteriota, Bacteroidota, and Proteobacteria for CPR and Thermoplasmatota for DPANN, and extensive, unbalanced metabolic exchanges between these symbionts and putative hosts are displayed. Together, our results provide initial insights into the complex interplays between the two lineages and their physicochemical environments and host populations at a large geographic scale.IMPORTANCECandidate phyla radiation (CPR) bacteria and DPANN archaea constitute a significant fraction of Earth's prokaryotic diversity. Despite their ubiquity and abundance, especially in anoxic habitats, we know little about the community patterns and ecological drivers of these ultra-small, putatively episymbiotic microorganisms across geographic ranges. This study is facilitated by a large collection of CPR and DPANN metagenome-assembled genomes recovered from the metagenomes of 90 sediments sampled from geochemically diverse acid mine drainage (AMD) environments across southeast China. Our comprehensive analyses have allowed first insights into the biogeographic patterns and functional differentiation of these major enigmatic prokaryotic groups in the AMD model system.
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Affiliation(s)
- Sheng-Xuan Peng
- School of Life Sciences, Sun Yat-Sen University, Guangzhou, China
| | - Shao-Ming Gao
- School of Life Sciences, Sun Yat-Sen University, Guangzhou, China
| | - Zhi-Liang Lin
- School of Life Sciences, Sun Yat-Sen University, Guangzhou, China
| | - Zhen-Hao Luo
- School of Life Sciences, Sun Yat-Sen University, Guangzhou, China
| | - Si-Yu Zhang
- School of Life Sciences, Sun Yat-Sen University, Guangzhou, China
| | - Wen-Sheng Shu
- School of Life Sciences, South China Normal University, Guangzhou, Guangdong, China
| | - Fangang Meng
- School of Environmental Science and Engineering, Sun Yat-Sen University, Guangzhou, Guangdong, China
| | - Li-Nan Huang
- School of Life Sciences, Sun Yat-Sen University, Guangzhou, China
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Zhang H, Li Z, Li X, Peng X, Zhang X, Zhang S, Ge F, Zhang L, Wu Z, Liu B. Host selection and nutrient status jointly drive algal and bacterial interactions in epiphytic biofilms of submerged macrophytes: Structural and functional insights. ENVIRONMENTAL RESEARCH 2025; 279:121743. [PMID: 40311900 DOI: 10.1016/j.envres.2025.121743] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Subscribe] [Scholar Register] [Received: 03/09/2025] [Revised: 04/28/2025] [Accepted: 04/29/2025] [Indexed: 05/03/2025]
Abstract
Epiphytic biofilms play a crucial role in aquatic biogeochemical cycles but are simultaneously influenced by host selection and eutrophication. However, the compositional structure and interaction mechanisms of these factors on algal and bacterial communities remain poorly understood. In this study, we employed Confocal Laser Scanning Microscopy (CLSM), Scanning Electron Microscopy (SEM), and high-throughput sequencing to investigate the physicochemical properties, algal and bacterial diversity, and community structure of epiphytic biofilms on two submerged macrophytes - Vallisneria natans (VN) and Hydrilla verticillata (HV) - across three urban shallow lakes with varying trophic levels in the Yangtze River Basin. Our results revealed distinct algal and bacterial communities influenced by both host plants and lake nutrient conditions, with unique core species identified in VN, HV, and the surrounding water. Host-environment effects index (HEEI = 1.79) indicated that bacterial communities were predominantly shaped by host selection, exhibiting lower diversity in HV (1.66 ± 0.92) and VN (2.31 ± 1.12) biofilms compared to surrounding waters (3.80 ± 0.47). In contrast, algal communities were primarily regulated by environmental factors (HEEI = 0.43), with higher diversity in less eutrophic lakes. Algal-bacterial co-occurrence network analysis revealed greater network complexity in VN biofilms than that in HV, with predominantly synergistic interactions facilitating carbon and nitrogen cycling. Eutrophication increased biofilm thickness, nutrient content, and extracellular polymeric substance (EPS) production but reduced microbial diversity and altered community interaction patterns. This study advances our understanding of epiphytic biofilms and offers insights into optimizing host-microbe interactions for improving lake restoration strategies.
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Affiliation(s)
- Haokun Zhang
- Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, 430072, China; University of Chinese Academy of Sciences, Beijing, 100049, China
| | - Zhuxi Li
- Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, 430072, China; School of Environmental Studies, China University of Geosciences, Wuhan, 430074, China
| | - Xia Li
- Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, 430072, China; School of Environmental Studies, China University of Geosciences, Wuhan, 430074, China
| | - Xue Peng
- Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, 430072, China
| | - Xiaowen Zhang
- Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, 430072, China; University of Chinese Academy of Sciences, Beijing, 100049, China
| | - Shuxian Zhang
- Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, 430072, China; University of Chinese Academy of Sciences, Beijing, 100049, China
| | - Fangjie Ge
- Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, 430072, China
| | - Lu Zhang
- Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, 430072, China
| | - Zhenbin Wu
- Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, 430072, China; School of Environmental Studies, China University of Geosciences, Wuhan, 430074, China
| | - Biyun Liu
- Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, 430072, China.
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Wasimuddin, Chiaia-Hernandez A, Terrettaz C, Thoenen L, Caggìa V, Mateo P, Coll-Crespi M, Notter M, Mukherjee M, Chavez-Capilla T, Ronchi F, Ganal-Vonarburg SC, Grosjean M, Bigalke M, Spielvogel S, Macpherson A, Mestrot A, Hapfelmeier S, Erb M, Schlaeppi K, Ramette A. Component specific responses of the microbiomes to common chemical stressors in the human food chain. ENVIRONMENTAL MICROBIOME 2025; 20:43. [PMID: 40296074 PMCID: PMC12039292 DOI: 10.1186/s40793-025-00700-x] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Grants] [Track Full Text] [Subscribe] [Scholar Register] [Received: 12/20/2024] [Accepted: 04/03/2025] [Indexed: 04/30/2025]
Abstract
Along a food chain, microbiomes occur in each component and often contribute to the functioning or the health of their host or environment. 'One Health' emphasizes the connectivity of each component's health. Chemical stress typically causes dysbiotic microbiomes, but it remains unclear whether chemical stressors consistently affect the microbiomes of food chain components. Here, we challenged food chain components, including water, sediments, soil, plants, and animals, with three chemical stresses consisting of arsenic (toxic trace element), benzoxazinoids (bioactive plant metabolites), and terbuthylazine (herbicide). We analysed 1064 microbiomes to assess their commonalities and differences in their stress responses. We found that chemical stressors overall decreased microbiome diversity in soil, but not in the other microbiomes. In response to stress, all food chain communities strongly shifted in their composition, generally becoming compositionally more similar to each other. In addition, we observed stochastic effects in host-associated communities (plant, animal). Dysbiotic microbiomes were characterized by different sets of bacteria, which responded specifically to the three chemical stressors. Microbial co-occurrence patterns significantly shifted with either decreased (water, sediment, plant, animal) or increased (soil) network sparsity and numbers of keystone taxa following stress treatments. These results suggest major re-distribution of specific taxa in the overall stress- and component-specific responses of microbiomes with the community stability of plant and animal microbiomes being the most affected by chemical stresses.
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Affiliation(s)
- Wasimuddin
- Institute for Infectious Diseases, University of Bern, Bern, Switzerland
- Food Safety and Animal Health Research, Norwegian Veterinary Institute, Ås, Norway
| | - Aurea Chiaia-Hernandez
- Institute of Geography, University of Bern, Bern, Switzerland
- Oeschger Center for Climate Change Research, University of Bern, Bern, Switzerland
| | - Céline Terrettaz
- Institute of Plant Sciences, University of Bern, Bern, Switzerland
| | - Lisa Thoenen
- Institute of Plant Sciences, University of Bern, Bern, Switzerland
| | - Veronica Caggìa
- Institute of Plant Sciences, University of Bern, Bern, Switzerland
| | - Pierre Mateo
- Institute of Plant Sciences, University of Bern, Bern, Switzerland
| | | | - Matheus Notter
- Institute for Infectious Diseases, University of Bern, Bern, Switzerland
| | - Mohana Mukherjee
- Institute for Infectious Diseases, University of Bern, Bern, Switzerland
| | | | - Francesca Ronchi
- Department of Visceral Surgery and Medicine, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland
- Department for BioMedical Research, University of Bern, Bern, Switzerland
| | - Stephanie C Ganal-Vonarburg
- Department of Visceral Surgery and Medicine, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland
- Department for BioMedical Research, University of Bern, Bern, Switzerland
| | - Martin Grosjean
- Institute of Geography, University of Bern, Bern, Switzerland
- Oeschger Center for Climate Change Research, University of Bern, Bern, Switzerland
| | - Moritz Bigalke
- Institute of Geography, University of Bern, Bern, Switzerland
- Institute of Applied Geoscience, Technical University Darmstadt, Darmstadt, Germany
| | - Sandra Spielvogel
- Institute for Plant Nutrition and Soil Science, Christian Albrechts University Kiel, Kiel, Germany
| | - Andrew Macpherson
- Department of Visceral Surgery and Medicine, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland
- Department for BioMedical Research, University of Bern, Bern, Switzerland
| | - Adrien Mestrot
- Institute of Geography, University of Bern, Bern, Switzerland
| | | | - Matthias Erb
- Institute of Plant Sciences, University of Bern, Bern, Switzerland
| | - Klaus Schlaeppi
- Institute of Plant Sciences, University of Bern, Bern, Switzerland.
- Department of Environmental Sciences, University of Basel, Basel, Switzerland.
| | - Alban Ramette
- Institute for Infectious Diseases, University of Bern, Bern, Switzerland.
- Multidisciplinary Center for Infectious Diseases (MCID), University of Bern, Bern, Switzerland.
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38
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Ren H, Hong H, Zha B, Lamlom SF, Qiu H, Cao Y, Sun R, Wang H, Ma J, Zhang H, Sun L, Yang Q, Zhou C, Liu X, Wang X, Zhang C, Zhang F, Zhao K, Yuan R, Abdelghany AM, Zhang B, Zheng Y, Wang J, Lu W. Soybean productivity can be enhanced by understanding rhizosphere microbiota: evidence from metagenomics analysis from diverse agroecosystems. MICROBIOME 2025; 13:105. [PMID: 40287775 PMCID: PMC12034204 DOI: 10.1186/s40168-025-02104-y] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 09/10/2024] [Accepted: 04/02/2025] [Indexed: 04/29/2025]
Abstract
BACKGROUND Microbial communities associated with roots play a crucial role in the growth and health of plants and are constantly influenced by plant development and alterations in the soil environment. Despite extensive rhizosphere microbiome research, studies examining multi-kingdom microbial variation across large-scale agricultural gradients remain limited. RESULTS This study investigates the rhizosphere microbial communities associated with soybean across 13 diverse geographical locations in China. Using high-throughput shotgun metagenomic sequencing on the BGISEQ T7 platform with 10 GB per sample, we identified a total of 43,337 microbial species encompassing bacteria, archaea, fungi, and viruses. Our analysis revealed significant site-specific variations in microbial diversity and community composition, underscoring the influence of local environmental factors on microbial ecology. Principal coordinate analysis (PCoA) indicated distinct clustering patterns of microbial communities, reflecting the unique environmental conditions and agricultural practices of each location. Network analysis identified 556 hub microbial taxa significantly correlated with soybean yield traits, with bacteria showing the strongest associations. These key microorganisms were found to be involved in critical nutrient cycling pathways, particularly in carbon oxidation, nitrogen fixation, phosphorus solubilization, and sulfur metabolism. Our findings demonstrate the pivotal roles of specific microbial taxa in enhancing nutrient cycling, promoting plant health, and improving soybean yield, with significant positive correlations (r = 0.5, p = 0.039) between microbial diversity and seed yield. CONCLUSION This study provides a comprehensive understanding of the diversity and functional potential of rhizosphere microbiota in enhancing soybean productivity. The findings underscore the importance of integrating microbial community dynamics into crop management strategies to optimize nutrient cycling, plant health, and yield. While this study identifies key microbial taxa with potential functional roles, future research should focus on isolating and validating these microorganisms for their bioremediation and biofertilization activities under field conditions. This will provide actionable insights for developing microbial-based agricultural interventions to improve crop resilience and sustainability. Video Abstract.
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Affiliation(s)
- Honglei Ren
- Soybean Research Institute of Heilongjiang Academy of Agriculture Sciences, Harbin, 150086, China.
| | - Huilong Hong
- National Key Facility for Crop Gene Resources and Genetic Improvement, Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing, 100081, China
| | - Bire Zha
- Soybean Research Institute of Heilongjiang Academy of Agriculture Sciences, Harbin, 150086, China
- College of Modern Agriculture and Ecological Environmentofaq , Heilongjiang University, Harbin, 150006, China
| | - Sobhi F Lamlom
- Plant Production Department, Faculty of Agriculture Saba Basha, Alexandria University, Alexandria, 21531, Egypt
| | - Hongmei Qiu
- Jilin Academy of Agriculture Sciences (Northeast Agricultural Research Center of China), Changchun, 130033, China
| | - Yongqiang Cao
- Crop Research Institute of Liaoning Academy of Agriculture Sciences, Shenyang, 110161, China
| | - Rujian Sun
- Hulunbuir Institute of Agriculture and Animal Husbandry, Hulunbuir, 021000, China
| | - Haorang Wang
- Jiangsu Xuhuai Regional Institute of Agricultural Sciences, Xuzhou, 221131, China
| | - Junkui Ma
- Shanxi Agricultural University/ Shanxi Academy of Agricultural Sciences, the Industrial Crop Institute, Taiyuan, 030031, China
| | - Hengbin Zhang
- Xinjiang Academy of Agricultural and Reclamation Science, Shihezi, 832000, China
| | - Liping Sun
- Jiangxi Academy of Agricultural Sciences, Nanchang, 330200, China
| | - Qing Yang
- Institute of Cereal and Oil Crops, Hebei Academy of Agricultural and Forestry Sciences, Shijiazhuang, 050035, China
| | - Changjun Zhou
- Daqing Branch of Heilongjiang Academy of Agricultural Sciences, Daqing, 163316, China
| | - Xiulin Liu
- Soybean Research Institute of Heilongjiang Academy of Agriculture Sciences, Harbin, 150086, China
| | - Xueyang Wang
- Soybean Research Institute of Heilongjiang Academy of Agriculture Sciences, Harbin, 150086, China
| | - Chunlei Zhang
- Soybean Research Institute of Heilongjiang Academy of Agriculture Sciences, Harbin, 150086, China
| | - Fengyi Zhang
- Soybean Research Institute of Heilongjiang Academy of Agriculture Sciences, Harbin, 150086, China
| | - Kezhen Zhao
- Soybean Research Institute of Heilongjiang Academy of Agriculture Sciences, Harbin, 150086, China
| | - Rongqiang Yuan
- Soybean Research Institute of Heilongjiang Academy of Agriculture Sciences, Harbin, 150086, China
| | - Ahmed M Abdelghany
- Crop Science Department, Faculty of Agriculture, Damanhour University, Damanhur, 22516, Egypt
| | - Bixian Zhang
- Institute of Biotechnology of Heilongjiang Academy of Agricultural Sciences, Harbin, 150086, China.
| | - Yuhong Zheng
- Jilin Academy of Agriculture Sciences (Northeast Agricultural Research Center of China), Changchun, 130033, China.
| | - Jiajun Wang
- Soybean Research Institute of Heilongjiang Academy of Agriculture Sciences, Harbin, 150086, China.
| | - Wencheng Lu
- Heihe Branch Institute of Heilongjiang Academy of Agricultural Sciences, Heihe, 164300, China.
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Pan S, Zhang W, Yan F, Ding Y, Hellweger FL, Shang J, Yan Y, Yu F, Li Y. Keystone microbial taxa identified by deep learning reveal mechanisms of phosphorus stoichiometric homeostasis in submerged macrophytes under different hydrodynamic states. WATER RESEARCH 2025; 282:123721. [PMID: 40311292 DOI: 10.1016/j.watres.2025.123721] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Subscribe] [Scholar Register] [Received: 09/30/2024] [Revised: 03/26/2025] [Accepted: 04/24/2025] [Indexed: 05/03/2025]
Abstract
Phosphorus (P) pollution in aquatic ecosystems triggers eutrophication, disrupting ecological processes. Although phytoremediation using submerged macrophytes is promising, its efficacy depends on plant-microbe interactions and stoichiometric homeostasis. A significant knowledge gap exists regarding the assembly and impact of key microbial communities on stoichiometric homeostasis under fluctuating environmental conditions, hindering the optimization of phytoremediation strategies. Given that hydrodynamic fluctuations are a primary source of environmental variability in aquatic systems, this study explored the intricate relationships among stoichiometric homeostasis, microbial community structure, and ecosystem stability, with a specific focus on their impact on rhizosphere P metabolism in Vallisneria natans and Myriophyllum spicatum under different hydrodynamic states. A Deep Learning-based Keystoneness Taxa Identification (DLKTI) framework was developed to identify key microbial taxa. Microbial community stability analysis preceded key taxa determination to enhance result reliability and ecological relevance based on the premise that distinct states provide a more dependable baseline for attributing observed changes to specific perturbations rather than to inherent fluctuations. These findings indicate that the key taxa identified by the DLKTI framework adequately characterized the overall ecological features of the microbial community (average ρ = 0.39, p<0.05). Moreover, including microbial pools and diversity indices of the screened key microbial taxa improved the explanatory power for submerged macrophyte traits (5% and 6%, respectively) and rhizosphere oxidative stress responses (25% and 4%, respectively). Partial least squares path modeling demonstrated the crucial role of stoichiometric homeostasis for P in ecosystem functioning (path coefficient of inhibition of phytoplankton growth = 0.58, p<0.001). The findings elucidating plant-microbe interaction patterns under different hydrodynamic states allow for the development of targeted interventions to enhance rhizosphere P metabolism, thereby increasing the efficiency of phytoremediation for eutrophication management and aquatic ecosystem restoration.
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Affiliation(s)
- Shenyang Pan
- State Key Laboratory of Water Cycle and Water Security in River Basin, College of Environment, Hohai University, Nanjing 210098, China
| | - Wenlong Zhang
- State Key Laboratory of Water Cycle and Water Security in River Basin, College of Environment, Hohai University, Nanjing 210098, China.
| | - Feng Yan
- Faculty of Engineering, University of Auckland, Auckland 1142, New Zealand
| | - Yanan Ding
- Nanjing Institute of Environmental Sciences, Ministry of Ecology and Environment, Nanjing 210042, China
| | - Ferdi L Hellweger
- Water Quality Engineering, Technical University of Berlin, Berlin 10623, Germany
| | - Jiahui Shang
- State Key Laboratory of Water Cycle and Water Security in River Basin, College of Environment, Hohai University, Nanjing 210098, China
| | - Yuting Yan
- State Key Laboratory of Water Cycle and Water Security in River Basin, College of Environment, Hohai University, Nanjing 210098, China
| | - Feng Yu
- State Key Laboratory of Water Cycle and Water Security in River Basin, College of Environment, Hohai University, Nanjing 210098, China
| | - Yi Li
- State Key Laboratory of Water Cycle and Water Security in River Basin, College of Environment, Hohai University, Nanjing 210098, China.
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Tang Y, Nian L, Zhao X, Li J, Wang Z, Dong L. Bio-Organic Fertilizer Application Enhances Silage Maize Yield by Regulating Soil Physicochemical and Microbial Properties. Microorganisms 2025; 13:959. [PMID: 40431133 PMCID: PMC12114197 DOI: 10.3390/microorganisms13050959] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Grants] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 03/17/2025] [Revised: 04/09/2025] [Accepted: 04/15/2025] [Indexed: 05/29/2025] Open
Abstract
Silage maize is vital to livestock development in northern China, but intensive chemical fertilization has led to soil degradation and reduced productivity. Bio-organic fertilizers offer a sustainable alternative, though their effects on soil multifunctionality remain underexplored. This study evaluated the impact of combining decomposed cow manure, Bacillus amyloliquefaciens, and mineral potassium fulvic acid with chemical fertilizers (NPK) on silage maize yield, soil microbial diversity, and ecosystem multifunctionality (EMF). Field experiments showed that bio-organic fertilization increased silage maize yield by 10.23% compared to chemical fertilizers alone, primarily by boosting labile organic carbon and soil enzyme activity. It also enhanced bacterial richness and diversity, with little effect on fungal communities. Microbial network analysis revealed more complex and stable bacterial networks under bio-organic treatments, indicating strengthened microbial interactions. Random forest and structural equation modeling (SEM) identified soil carbon storage and bacterial diversity as key drivers of EMF, which integrates soil functions such as nutrient cycling, decomposition, enzyme activity, and microbial diversity. These findings suggest that soil bacterial diversity and its interactions with soil properties are critical to both crop productivity and soil health. The optimal fertilization strategy for silage maize in this region involves the combined use of cattle manure, Bacillus amyloliquefaciens, mineral potassium fulvic acid, and NPK fertilizers. This approach improves yield, microbial diversity, and soil multifunctionality. Future studies should consider environmental variables and crop varieties across diverse regions to support broader application.
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Affiliation(s)
- Ying Tang
- Institute of Soil, Fertilizer and Water-Saving Agriculture, Gansu Academy of Agricultural Sciences, Lanzhou 730070, China; (L.N.); (X.Z.); (J.L.); (Z.W.); (L.D.)
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Yan J, Li X, Pan Z, Lin X, Zuo Q, Zhou J, Zhou S, Sui F, Zhang L, Fischel MHH. Red mud causes dynamic changes in the soil microbial community and cadmium fractions in a slightly cadmium-contaminated paddy soil. JOURNAL OF HAZARDOUS MATERIALS 2025; 493:138349. [PMID: 40267706 DOI: 10.1016/j.jhazmat.2025.138349] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Subscribe] [Scholar Register] [Received: 01/23/2025] [Revised: 04/09/2025] [Accepted: 04/18/2025] [Indexed: 04/25/2025]
Abstract
Red mud is a highly alkaline industrial by-product rich in iron oxides with great potential for soil cadmium remediation. Although the stabilization of Cd by red mud is well reported in rice potted and field experiments, the influence of red mud on microbial communities in paddy soil and the contribution of soil microbial communities subjected to red mud in Cd stabilization remain unknown. This study used high-throughput sequencing and bioinformatics, combined with a sequential extraction procedure, to determine the microbiological mechanisms of rice Cd reduction by red mud and information on the corresponding soil Cd fraction. The results showed that red mud significantly increased the soil pH and iron and manganese oxide-bound Cd fractions. Red mud application influenced the microbial beta diversity rather than the alpha diversity, especially for bacteria. Unique taxa associated with iron reduction (e.g., phylum Firmicutes and genus Anaeromyxobacter) were enriched at the rice-filling stage, which may contribute to the stabilization of Cd. Red mud application caused little difference in the fungal communities. A 2 % red mud amendment successfully decreased the grain Cd content in a high Cd-accumulating rice cultivar by 72 %. Red mud effectively reduces Cd accumulation in the short-term and demonstrates potential for remedial applications. This study provides microbiological evidence for stabilizing Cd in red mud, but its long-term environmental impact and field applicability require further research.
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Affiliation(s)
- Jiali Yan
- School of Civil Engineering and Architecture, Chuzhou University, Chuzhou 239000, China
| | - Xuwei Li
- Nanjing Institute of Environmental Science, Ministry of Ecology and Environment of the People's Republic of China, Nanjing 210042, China
| | - Zhengguo Pan
- School of Civil Engineering and Architecture, Chuzhou University, Chuzhou 239000, China
| | - Xiaochen Lin
- Nanjing Institute of Environmental Science, Ministry of Ecology and Environment of the People's Republic of China, Nanjing 210042, China
| | - Qinglin Zuo
- School of Resources and Environmental Engineering, Anhui University, Hefei 230601, China
| | - Jiankang Zhou
- Key Laboratory of Soil Pollution Control and Remediation of Henan Province, College of Resources and Environment, Henan Agricultural University, Zhengzhou, China
| | - Shiqi Zhou
- School of Civil Engineering and Architecture, Chuzhou University, Chuzhou 239000, China
| | - Fuqing Sui
- Key Laboratory of Soil Pollution Control and Remediation of Henan Province, College of Resources and Environment, Henan Agricultural University, Zhengzhou, China.
| | - Lei Zhang
- School of Civil Engineering and Architecture, Chuzhou University, Chuzhou 239000, China.
| | - Matthew H H Fischel
- Sustainable Agricultural Systems Laboratory, USDA-Agricultural Research Service, Beltsville, MD 20705, USA
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Wei Y, Zhu Y, Nian L, Yang L, Yue M, Mao Z, Li L. Response of rhizosphere microbial community characteristics and ecosystem multifunctionality to the addition of crude oil in Achnatherum splendens and Pennisetum alopecuroides. Front Microbiol 2025; 16:1553070. [PMID: 40303472 PMCID: PMC12037595 DOI: 10.3389/fmicb.2025.1553070] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 12/30/2024] [Accepted: 03/28/2025] [Indexed: 05/02/2025] Open
Abstract
This study aimed to reveal the effects of crude oil addition on the characteristics of soil microbial communities and ecosystem multifunctionality in Achnatherum splendens and Pennisetum alopecuroides. Specifically, it explored how crude oil addition influences the relationship between soil nutrient regulation, microbial community characteristics, and ecosystem multifunctionality. The results indicated that as crude oil addition increased, the Shannon index and Chao1 index for soil bacteria and fungi in both Achnatherum splendens and Pennisetum alopecuroides increased. Conversely, while the Shannon index for soil archaea in both species increased, the Chao1 index decreased. The ecological network analysis indicated that a strong collaborative relationship existed between species in the soil bacterial communities of Achnatherum splendens and Pennisetum alopecuroides exposed to 10 g/kg crude oil, as well as between species in the soil fungal and archaeal communities of Achnatherum splendens exposed to 40 g/kg crude oil. A strong collaborative relationship was also observed between species in the soil fungal and archaeal communities of Pennisetum alopecuroides exposed to 10 g/kg crude oil. The bacterial and fungal communities exerted a significant direct negative regulatory effect on the soil ecosystem multifunctionality of Achnatherum splendens and Pennisetum alopecuroides, while the archaeal communities had a significant direct positive regulatory effect. Additionally, the multifunctionality index of the soil ecosystem in Achnatherum splendens and Pennisetum showed a significant decline with increasing crude oil addition. This is likely due to the higher toxicity of high-concentration crude oil, which negatively impacts the soil biological community, leading to reduced biodiversity and disruptions in nutrient cycles. This study explores the characteristics of bacterial, fungal, and archaeal communities and ecosystem multifunctionality under different levels of crude oil, which can provide theoretical support for evaluating the restoration of Achnatherum splendens and Pennisetum alopecuroides from crude oil pollution.
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Affiliation(s)
- Ying Wei
- Xi'an Botanical Garden of Shaanxi Province/Institute of Botany of Shaanxi Province, Xi'an, China
- Shaanxi Engineering Research Centre for Conservation and Utilization of Botanical Resources, Xi’an, China
| | - Yukun Zhu
- Shaanxi Provincial Dongzhuang Water Conservancy Engineering Co., Ltd., Xi'an, China
| | - Lili Nian
- Institute of Soil, Fertilizer and Water-Saving Agriculture, Gansu Academy of Agricultural Sciences, Lanzhou, China
| | - Liqun Yang
- Shaanxi Provincial Water Resources Information Education and Promotion Center, Xi'an, China
| | - Ming Yue
- Xi'an Botanical Garden of Shaanxi Province/Institute of Botany of Shaanxi Province, Xi'an, China
- Shaanxi Engineering Research Centre for Conservation and Utilization of Botanical Resources, Xi’an, China
| | - Zhuxin Mao
- Xi'an Botanical Garden of Shaanxi Province/Institute of Botany of Shaanxi Province, Xi'an, China
- Shaanxi Engineering Research Centre for Conservation and Utilization of Botanical Resources, Xi’an, China
| | - Lijuan Li
- Xi'an Botanical Garden of Shaanxi Province/Institute of Botany of Shaanxi Province, Xi'an, China
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Liu H, Guo A, Sun H, Hu C, Liu C. Deteriorated abatement of micropollutants in biological activated carbon filters with aged media: Key role of permeability. WATER RESEARCH 2025; 274:123059. [PMID: 39778309 DOI: 10.1016/j.watres.2024.123059] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 10/21/2024] [Revised: 12/02/2024] [Accepted: 12/26/2024] [Indexed: 01/11/2025]
Abstract
Biological activated carbon (BAC) filtration is vital for the abatement of micropollutants in drinking water. However, limited information is available on contaminant removal in BAC filters with aged media (e.g., >6 year) which are commonly operated at water treatment plants, and mechanistic insights into linkages among media age, microbial community, and contaminant removal still lack. In this study, the effects of media age on the abatement of eight micropollutants with various functional groups were investigated. The abatement of micropollutants decreased with increasing media age. Pseudo-first-order rate constants for contaminant removal in 6- and 15-year BAC were (0.3-3.1) × 10-3 and (0.2-2.6) × 10-3 s-1, compared to (0.9-4.3) × 10-3 s-1 in 3.5-year BAC filter. Biosorption- and biodegradation-dominated contaminant removal depended on protein and adenosine triphosphate concentrations in biofilm, respectively. Micro-computed tomography revealed the formation of biofilm-dominated clogging with rare voids and channels in 15-year BAC, resulting in low permeability. The decreased permeability led to deficient dissolved O2 and nutrient supply and thus changed microbial community assembly process, reducing community diversity and function. Core members including families of Saprospiraceae, Chitinophagaceae, Rhodocyclaceae, Comamonadaceae, and Nitrospiraceae in 3.5-year BAC were affiliated with active aerobic metabolism and contaminant biodegradation capacity. Abundances of these functional microbes and genes decreased with increasing media age. Simultaneously, protein in biofilm decreased, thereby decreasing biosorption. The findings of this study reveal the pivotal role of permeability in shaping microbial community and function and the corresponding micropollutant removal in BAC filters with aged media.
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Affiliation(s)
- Hang Liu
- Key Laboratory of Drinking Water Science and Technology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China
| | - Anning Guo
- Key Laboratory of Drinking Water Science and Technology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China; Institute of Resources and Environmental Engineering, Shanxi University, Taiyuan, 030006, China
| | - Huifang Sun
- Institute of Resources and Environmental Engineering, Shanxi University, Taiyuan, 030006, China
| | - Chengzhi Hu
- Key Laboratory of Drinking Water Science and Technology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China; University of Chinese Academy of Sciences, Beijing 100049, China
| | - Chao Liu
- Key Laboratory of Drinking Water Science and Technology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China; University of Chinese Academy of Sciences, Beijing 100049, China.
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Wang X, Gao L, Wang S, Zhang X, Feng R, Jia S. Metagenomic insights into the assembly, function, and key taxa of bacterial community in full-scale pesticide wastewater treatment processes. ENVIRONMENTAL RESEARCH 2025; 271:121037. [PMID: 39920962 DOI: 10.1016/j.envres.2025.121037] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 12/17/2024] [Revised: 01/28/2025] [Accepted: 02/02/2025] [Indexed: 02/10/2025]
Abstract
Pesticide wastewater emerges as a typical refractory wastewater, characterized by complex composition and high toxicity, posing significant treatment challenges. Bacterial communities are responsible for biological treatment of refractory wastewater in full-scale pesticide wastewater treatment plants (PWWTPs), providing important implications for optimizing system performance and improving management strategies. However, the knowledge of their composition, diversity, function, assembly patterns, and biological interactions remains limited. Therefore, this study applied high-throughput sequencing, machine learning models, and statistical analysis to investigate key features of bacterial communities in eight PWWTPs. We found that Proteobacteria and Bacteroidota were the most abundant phyla, with Pseudomonas, Hyphomicrobium, Comamonas, and Thauera being dominant genera. Bacterial community distribution and diversity varied significantly among influents, sludges, and effluents, with sludges and effluents exhibiting higher diversity, richness, and evenness compared to influents. Deterministic processes primarily shaped the bacterial communities, accounting for 77.12%, 61.44%, and 64.05% of variation in influents, sludges, and effluents, respectively. Homogeneous selection explained 47.71%, 31.37%, and 31.37% of variation across these communities. Key modules (Module 1 in influents, Modules 3 and 4 in sludges, and Module 1 in effluents) were significantly associated with various metabolic and degradative functions (p < 0.05). Core taxa identified by Random Forest analysis were strongly linked to key metabolic and degradation functions, such as the metabolism of cofactors and vitamins, carbohydrates, and amino acids as well as the degradation of benzoate, aminobenzoate, nitrotoluene, chloroalkane, and chloroalkene. This study deepens our understanding of bacterial community dynamics and key features in pesticide wastewater treatment systems, offering scientific guidance for process optimization, efficiency improvement, and system stability assessment.
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Affiliation(s)
- Xiaoxiao Wang
- College of Resources and Environmental Sciences, Nanjing Agricultural University, Nanjing, 210095, China
| | - Linjun Gao
- College of Resources and Environmental Sciences, Nanjing Agricultural University, Nanjing, 210095, China
| | - Shuya Wang
- College of Resources and Environmental Sciences, Nanjing Agricultural University, Nanjing, 210095, China
| | - Xian Zhang
- College of Resources and Environmental Sciences, Nanjing Agricultural University, Nanjing, 210095, China
| | - Ruonan Feng
- College of Resources and Environmental Sciences, Nanjing Agricultural University, Nanjing, 210095, China
| | - Shuyu Jia
- College of Resources and Environmental Sciences, Nanjing Agricultural University, Nanjing, 210095, China.
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45
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Shi H, Sun B, Sun B, Wang X, Li B, Wu F, Tian T. Bacillus velezensis TB918 mitigates garlic dry rot disease by forming consortia with Pseudomonas in the rhizosphere and bulb. Front Microbiol 2025; 16:1567108. [PMID: 40303477 PMCID: PMC12037484 DOI: 10.3389/fmicb.2025.1567108] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/26/2025] [Accepted: 04/01/2025] [Indexed: 05/02/2025] Open
Abstract
Garlic dry rot (GDR), primarily caused by Fusarium proliferatum, is a significant postharvest disease that leads to substantial economic losses. Our previous research demonstrated that supplementing Bacillus-based biocontrol formulations with sucrose could boost its efficiency in protecting plants by building a hostile rhizomicrobiome for destructive soil-borne pathogens. B. velezensis TB918, previously isolated from pepper rhizosphere soil, exhibited a strong in vitro antifungal effect on Fusarium. In this study, we conducted a field experiment to investigate the efficacy of B. velezensis TB918 in controlling GDR, and explored the changes in microbial communities in garlic plants and rhizosphere soil following the application of TB918 with or without sucrose supplementation. Using 16S rRNA and ITS amplicon sequencing, we found that the introduction of TB918 significantly increased the abundance of Pseudomonas in garlic rhizosphere, especially when combined with sucrose. Three Pseudomonas strains were isolated from garlic tissues and rhizosphere soil treated with TB918 and sucrose, among which the GP2 strain exhibited antagonistic effects against pathogen ad planta. Co-culture and colonization assays showed that TB918 facilitated the biofilm formation of Pseudomonas strain by forming consortia. Interestingly, the abundance of potentially non-pathogenic Fusarium concentricum also increased, suggesting a potential niche exclusion effect. Our results demonstrated that TB918 in combination with sucrose effectively reduced the incidence of GDR during storage. This study provides valuable insights into the use of biocontrol agents and sucrose to modulate the garlic microbial community and suppress soil-borne pathogens.
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Affiliation(s)
- Haowen Shi
- Institute of Plant Protection, Tianjin Academy of Agricultural Sciences, Tianjin, China
| | - Bingbing Sun
- Institute of Plant Protection, Tianjin Academy of Agricultural Sciences, Tianjin, China
| | - Beiying Sun
- Department of Geography, University College London, London, United Kingdom
| | - Xiuli Wang
- Lanzhou Productivity Promoting Center, Gansu, China
| | - Bing Li
- Tianjin Agricultural Development Service Center, Tianjin, China
| | - Feng Wu
- Institute of Vegetables, Tianjin Academy of Agricultural Sciences, Tianjin, China
| | - Tao Tian
- Institute of Plant Protection, Tianjin Academy of Agricultural Sciences, Tianjin, China
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46
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Zhou H, Tang L, Fenton KA, Song X. Exploring and evaluating microbiome resilience in the gut. FEMS Microbiol Ecol 2025; 101:fiaf046. [PMID: 40302016 PMCID: PMC12065411 DOI: 10.1093/femsec/fiaf046] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 08/16/2024] [Revised: 03/30/2025] [Accepted: 04/28/2025] [Indexed: 05/01/2025] Open
Abstract
The gut ecosystem is closely related to human gastrointestinal health and overall wellness. Microbiome resilience refers to the capability of a microbial community to resist or recover from perturbations to its original state of balance. So far, there is no consensus on the criteria for assessing microbiome resilience. This article provides new insights into the metrics and techniques for resilience assessment. We discussed several potential parameters, such as microbiome structure, keystone species, biomarkers, persistence degree, recovery rate, and various research techniques in microbiology, metagenomics, biochemistry, and dynamic modeling. The article further explores the factors that influence the gut microbiome resilience. The microbiome structure (i.e. abundance and diversity), keystone species, and microbe-microbe interplays determine microbiome resilience. Microorganisms employ a variety of mechanisms to achieve the microbiome resilience, including flexible metabolism, quorum sensing, functional redundancy, microbial cooperation, and competition. Host-microbe interactions play a crucial role in maintaining microbiome stability and functionality. Unlike other articles, we focus on the regulation of host immune system on microbiome resilience. The immune system facilitates bacterial preservation and colonization, community construction, probiotic protection, and pathogen elimination through the mechanisms of immunological tolerance, immune-driven microbial compartmentalization, and immune inclusion and exclusion. Microbial immunomodulation indirectly modulates microbiome resilience.
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Affiliation(s)
- Huimin Zhou
- Department of Microbiology, College of Basic Medical Sciences, Dalian Medical University, Dalian, 116044, China
| | - Li Tang
- Department of Microecology, College of Basic Medical Sciences, Dalian Medical University, Dalian, 116044, China
| | - Kristin A Fenton
- Department of Medical Biology, Faculty of Health Sciences, UiT The Arctic University of Norway, Tromsø, 9037, Norway
| | - Xiaobo Song
- Department of Medical Biology, Faculty of Health Sciences, UiT The Arctic University of Norway, Tromsø, 9037, Norway
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Zheng L, Yan Y, Li Q, Du J, Lu X, Xu L, Xie Q, Chen Y, Zhang A, Zhao B. Microbial Diversity, Co-Occurrence Patterns, and Functional Genes of Bacteria in Aged Coking Contaminated Soils by Polycyclic Aromatic Hydrocarbons: Implications to Soil Health and Bioremediation. Microorganisms 2025; 13:869. [PMID: 40284704 PMCID: PMC12029627 DOI: 10.3390/microorganisms13040869] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Grants] [Track Full Text] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/18/2025] [Revised: 03/23/2025] [Accepted: 04/02/2025] [Indexed: 04/29/2025] Open
Abstract
PAH contamination from coking plants have received widespread attention. However, the microbial diversity, co-occurrence patterns, and functional genes of bacteria in aged coking contaminated soils by PAHs are still not clear. In our study, we used a macro-genetic approach to detect PAH-contaminated soils from both a coking production area (CA group) and an office zone (OA group) in an abandoned coking plant, and analyzed the characteristic bacteria and function genes, microbial network interaction patterns, and soil P-cycling in long-term PAH-contaminated soils. The results revealed that Proteobacteria were significantly positively correlated with PAHs and Betaprobacteria bacterium rifcsplowo2 12 full 6514, candidatus Muproteobacteria bacterium RBG16609, and Sulfurifustis variabilis, which belong to Proteobacteria, were characteristic bacteria in PAH-contaminated soils. The phn, which is the PAH degradation gene, was abundantly expressed in the PAH-contaminated soil. The phn gene cluster genes (phnE, phnC, and phnD) were significantly expressed in the CA group of PAH-contaminated soils (p < 0.05). By integrating microbial diversity, network structure, and functional genes, it offers a comprehensive understanding of soil ecosystem response indicators to prolonged PAH stress. The results of this study will provide new ideas for constructing an assessment index system for soil health and screening biomarkers for PAH-contaminated soils.
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Affiliation(s)
- Liping Zheng
- State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China; (L.Z.); (L.X.); (Q.X.)
- University of Chinese Academy of Sciences, Beijing 100049, China
- Nanjing Institute of Environmental Sciences, Ministry of Ecology and Environment, Nanjing 210042, China; (Y.Y.); (Q.L.); (J.D.); (X.L.)
| | - Yifan Yan
- Nanjing Institute of Environmental Sciences, Ministry of Ecology and Environment, Nanjing 210042, China; (Y.Y.); (Q.L.); (J.D.); (X.L.)
| | - Qun Li
- Nanjing Institute of Environmental Sciences, Ministry of Ecology and Environment, Nanjing 210042, China; (Y.Y.); (Q.L.); (J.D.); (X.L.)
| | - Junyang Du
- Nanjing Institute of Environmental Sciences, Ministry of Ecology and Environment, Nanjing 210042, China; (Y.Y.); (Q.L.); (J.D.); (X.L.)
| | - Xiaosong Lu
- Nanjing Institute of Environmental Sciences, Ministry of Ecology and Environment, Nanjing 210042, China; (Y.Y.); (Q.L.); (J.D.); (X.L.)
| | - Li Xu
- State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China; (L.Z.); (L.X.); (Q.X.)
- University of Chinese Academy of Sciences, Beijing 100049, China
- School of Environment, Hangzhou Institute for Advanced Study, UCAS, Hangzhou 310024, China;
| | - Qunhui Xie
- State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China; (L.Z.); (L.X.); (Q.X.)
- University of Chinese Academy of Sciences, Beijing 100049, China
- School of Environment, Hangzhou Institute for Advanced Study, UCAS, Hangzhou 310024, China;
| | - Yangsheng Chen
- School of Environment, Hangzhou Institute for Advanced Study, UCAS, Hangzhou 310024, China;
| | - Aiguo Zhang
- Nanjing Institute of Environmental Sciences, Ministry of Ecology and Environment, Nanjing 210042, China; (Y.Y.); (Q.L.); (J.D.); (X.L.)
| | - Bin Zhao
- School of Environment, Hangzhou Institute for Advanced Study, UCAS, Hangzhou 310024, China;
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Hernández-García JA, Bernal JS, Antony-Babu S, Villa-Tanaca L, Hernández-Rodríguez C, De-la-Vega-Camarillo E. Teosinte-derived SynCom and precision biofertilization modulate the maize microbiome, enhancing growth, yield, and soil functionality in a Mexican field. Front Microbiol 2025; 16:1534327. [PMID: 40270813 PMCID: PMC12015678 DOI: 10.3389/fmicb.2025.1534327] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 11/25/2024] [Accepted: 03/24/2025] [Indexed: 04/25/2025] Open
Abstract
Modern agriculture faces the challenge of optimizing fertilization practices while maintaining soil resilience and microbial diversity, both critical for sustainable crop production. We evaluated the effects of multiple fertilization strategies on soil microbial communities and plant performance, comparing conventional methods (urea-based and phosphorus fertilizers applied manually or via drone-assisted precision delivery) with biofertilization using a synthetic microbial consortium (SynCom) derived from teosinte-associated microbes. This SynCom consisted of seven bacterial strains: Serratia nematodiphila EDR2, Klebsiella variicola EChLG19, Bacillus thuringiensis EML22, Pantoea agglomerans EMH25, Bacillus thuringiensis EBG39, Serratia marcescens EPLG52, and Bacillus tropicus EPP72. High-throughput sequencing revealed significant shifts in bacterial and fungal communities across treatments. Untreated soils showed limited diversity, dominated by Enterobacteriaceae (>70%). Conventional fertilization gradually reduced Enterobacteriaceae while increasing Pseudomonas and Lysinibacillus populations. Drone-assisted conventional fertilization notably enhanced Acinetobacter and Rhizobiales growth. Biofertilization treatments produced the most pronounced shifts, reducing Enterobacteriaceae below 50% while significantly increasing beneficial taxa like Bacillus, Pantoea, and Serratia. Network analysis demonstrated that microbial interaction complexity increased across treatments, with Bacillus emerging as a keystone species. Drone-assisted biofertilization fostered particularly intricate microbial networks, enhancing synergistic relationships involved in nutrient cycling and biocontrol, though maintaining the stability of these complex interactions requires careful monitoring. Our findings provide key insights into how precision biofertilization with teosinte-derived microbial consortia can sustainably reshape the maize microbiome, improving crop performance and soil resilience.
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Affiliation(s)
- Juan Alfredo Hernández-García
- Laboratorio de Biología Molecular de Bacterias y Levaduras, Departamento de Microbiología, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Ciudad de México, México
| | - Julio S. Bernal
- Department of Entomology, Texas A&M University, College Station, TX, United States
| | - Sanjay Antony-Babu
- Department of Plant Pathology and Microbiology, Texas A&M University, College Station, TX, United States
| | - Lourdes Villa-Tanaca
- Laboratorio de Biología Molecular de Bacterias y Levaduras, Departamento de Microbiología, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Ciudad de México, México
| | - César Hernández-Rodríguez
- Laboratorio de Biología Molecular de Bacterias y Levaduras, Departamento de Microbiología, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Ciudad de México, México
| | - Esaú De-la-Vega-Camarillo
- Laboratorio de Biología Molecular de Bacterias y Levaduras, Departamento de Microbiología, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Ciudad de México, México
- Department of Entomology, Texas A&M University, College Station, TX, United States
- Department of Plant Pathology and Microbiology, Texas A&M University, College Station, TX, United States
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49
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Marian M, Antonielli L, Pertot I, Perazzolli M. Amplicon sequencing and culture-dependent approaches reveal core bacterial endophytes aiding freezing stress tolerance in alpine Rosaceae plants. mBio 2025; 16:e0141824. [PMID: 39998219 PMCID: PMC11980557 DOI: 10.1128/mbio.01418-24] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 05/08/2024] [Accepted: 01/21/2025] [Indexed: 02/26/2025] Open
Abstract
Wild plants growing in alpine regions are associated with endophytic microbial communities that may support plant growth and survival under cold conditions. The structure and function of endophytic bacterial communities were characterized in flowers, leaves, and roots of three alpine Rosaceae plants in Alpine areas using a combined amplicon sequencing and culture-dependent approaches to determine the role of core taxa on plant freezing stress tolerance. Amplicon sequencing analysis revealed that plant tissue, collection site, and host plant are the main factors affecting the richness, diversity, and taxonomic structure of endophytic bacterial communities in alpine Rosaceae plants. Core endophytic bacterial taxa were identified as 31 amplicon sequence variants highly prevalent across all plant tissues. Psychrotolerant bacterial endophytes belonging to the core taxa of Duganella, Erwinia, Pseudomonas, and Rhizobium genera mitigated freezing stress in strawberry plants, demonstrating the beneficial role of endophytic bacterial communities and their potential use for cold stress mitigation in agriculture.IMPORTANCEFreezing stress is one of the major abiotic stresses affecting fruit production in Rosaceae crops. Current strategies to reduce freezing damage include physical and chemical methods, which have several limitations in terms of costs, efficacy, feasibility, and environmental impacts. The use or manipulation of plant-associated microbial communities was proposed as a promising sustainable approach to alleviate cold stress in crops, but no information is available on the possible mitigation of freezing stress in Rosaceae plants. A combination of amplicon sequencing, culture-dependent, and plant bioassay approaches revealed the beneficial role of the endophytic bacterial communities in alpine Rosaceae plants. In particular, we showed that culturable psychrotolerant bacterial endophytes belonging to the core taxa of Duganella, Erwinia, Pseudomonas, and Rhizobium genera can mitigate freezing stress on strawberry seedlings. Overall, this study demonstrates the potential use of psychrotolerant bacterial endophytes for the development of biostimulants for cold stress mitigation in agriculture.
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Affiliation(s)
- Malek Marian
- Center Agriculture Food Environment (C3A), University of Trento, San Michele all'Adige, Italy
| | - Livio Antonielli
- Center for Health & Bioresources, Bioresources Unit, AIT Austrian Institute of Technology, Tulln, Austria
| | - Ilaria Pertot
- Center Agriculture Food Environment (C3A), University of Trento, San Michele all'Adige, Italy
- Research and Innovation Centre, Fondazione Edmund Mach, San Michele all'Adige, Italy
| | - Michele Perazzolli
- Center Agriculture Food Environment (C3A), University of Trento, San Michele all'Adige, Italy
- Research and Innovation Centre, Fondazione Edmund Mach, San Michele all'Adige, Italy
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50
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He Q, Wang S, Feng K, Hou W, Zhang W, Li F, Zhang Y, Hai W, Sun Y, Deng Y. The Same Source of Microbes has a Divergent Assembly Trajectory Along a Hot Spring Flowing Path. Mol Ecol 2025; 34:e17727. [PMID: 40087983 DOI: 10.1111/mec.17727] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 07/01/2024] [Revised: 02/24/2025] [Accepted: 03/03/2025] [Indexed: 03/17/2025]
Abstract
Hot spring microbial mats represent intricate biofilms that establish self-sustaining ecosystems, hosting diverse microbial communities which facilitate a range of biochemical processes and contribute to the structural and functional complexity of these systems. While community structuring across mat depth has received substantial attention, mechanisms shaping horizontal spatial composition and functional structure of these communities remain understudied. Here, we explored the contributions of species source, local environment and species interaction to microbial community assembly processes in six microbial mat regions following a flow direction with a temperature decreasing from 73.3°C to 52.8°C. Surprisingly, we found that despite divergent community structures and potential functions across different microbial mats, large proportions of the community members (45.50%-80.29%) in the recipient mat communities originated from the same source community at the upper limit of temperature for photosynthetic life. This finding indicated that the source species were dispersed with water and subsequently filtered and shaped by local environmental factors. Furthermore, critical species with specific functional attributes played a pivotal role in community assembly by influencing potential interactions with other microorganisms. Therefore, species dispersal via water flow, environmental variables, and local species interaction jointly governed microbial assembly, elucidating assembly processes in the horizontal dimension of hot spring microbial mats and providing insights into microbial community assembly within extreme biospheres.
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Affiliation(s)
- Qing He
- CAS Key Laboratory for Environmental Biotechnology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences (CAS), Beijing, China
| | - Shang Wang
- CAS Key Laboratory for Environmental Biotechnology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences (CAS), Beijing, China
| | - Kai Feng
- CAS Key Laboratory for Environmental Biotechnology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences (CAS), Beijing, China
| | - Weiguo Hou
- State Key Laboratory of Biogeology and Environmental Geology, China University of Geosciences, Beijing, China
| | - Wenhui Zhang
- State Key Laboratory of Biogeology and Environmental Geology, China University of Geosciences, Beijing, China
| | - Fangru Li
- State Key Laboratory of Biogeology and Environmental Geology, China University of Geosciences, Beijing, China
| | - Yidi Zhang
- State Key Laboratory of Biogeology and Environmental Geology, China University of Geosciences, Beijing, China
| | - Wanming Hai
- State Key Laboratory of Biogeology and Environmental Geology, China University of Geosciences, Beijing, China
| | - Yuxuan Sun
- State Key Laboratory of Biogeology and Environmental Geology, China University of Geosciences, Beijing, China
| | - Ye Deng
- CAS Key Laboratory for Environmental Biotechnology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences (CAS), Beijing, China
- College of Resources and Environment, University of Chinese Academy of Sciences, Beijing, China
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