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Kumari S, Kaur P, Mahajan M, Nayak SR, Khanna RR, Rehman MT, AlAjmi MF, Khan MIR. γ-aminobutyric acid (GABA) supplementation modulates phosphorus retention, production of carbon metabolites and defense metabolism under arsenic toxicity in wheat. PLANT SCIENCE : AN INTERNATIONAL JOURNAL OF EXPERIMENTAL PLANT BIOLOGY 2025; 356:112504. [PMID: 40222391 DOI: 10.1016/j.plantsci.2025.112504] [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: 09/09/2024] [Revised: 04/03/2025] [Accepted: 04/07/2025] [Indexed: 04/15/2025]
Abstract
Arsenic (As) stress has been incessantly degrading crop productivity, and thereafter leading to the increasing grave conditions pertaining to the unsustainable food production. In plants, As stress has been considered as one of the serious phytotoxins persisting in the environment, endangering crop shelf life through competing with phosphorus availability. The withholding of As in the staple crop, wheat (Triticum aestivum), is the major concern. It has been advocated the significance of plant signaling molecules, γ-aminobutyric acid (GABA), in mediating plant health response to environmental stresses, but their impacts on As contamination in wheat plants from the perspective of growth and physiological tolerance still remain ambiguous at present. The present study investigated the significance of GABA supplementation in wheat plants on phosphorus and carbon metabolisms, adenosine triphosphatase (ATPase) activity, As accumulation, defense systems, and growth responses under As stress. In this study, GABA supplementation aided in the retention of phosphorus and carbon metabolites, sustained photosynthetic traits, and considerably modulated both chloroplastic and mitochondrial ATPase activity under As stress. Further, As-induced oxidative stress injuries were recovered through the activation of defense metabolites, and suppressed oxidative stress markers and As accumulation, which was found concomitant with the improved As tolerance index. Thus, this investigation offers insightful information that might be useful in future investigations to develop wheat tolerance to withstand under As-contaminated environments.
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Affiliation(s)
- Sarika Kumari
- Department of Botany, Jamia Hamdard, New Delhi, India
| | - Pravneet Kaur
- Department of Botany, Jamia Hamdard, New Delhi, India
| | - Moksh Mahajan
- Department of Botany, Jamia Hamdard, New Delhi, India
| | | | | | - Md Tabish Rehman
- Department of Pharmacognosy, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia
| | - Mohamed F AlAjmi
- Department of Pharmacognosy, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia
| | - M Iqbal R Khan
- Department of Botany, Jamia Hamdard, New Delhi, India; Department of Plant Biotechnology, Korea University, Seoul, South Korea.
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2
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Cheng Z, Wei J, Zhu B, Gu L, Zeng T, Wang H, Du X. Mutation of TaNRAMP5 impacts cadmium transport in wheat. PLANT PHYSIOLOGY AND BIOCHEMISTRY : PPB 2025; 223:109879. [PMID: 40188530 DOI: 10.1016/j.plaphy.2025.109879] [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: 02/24/2025] [Revised: 03/20/2025] [Accepted: 04/01/2025] [Indexed: 04/08/2025]
Abstract
Cadmium (Cd) pollution significantly impacts the normal growth, development, and food safety of wheat. Employing modern molecular biology techniques represents an effective strategy for cultivating low-Cd wheat. Natural resistance-associated macrophage protein 5 (NRAMP5) is a critical heavy metal transporter, however, its function in wheat, particularly in response to Cd stress, remains largely unexplored. Here, we employed the CRISPR/Cas9 gene-editing technology to generate TaNRAMP5 knockout lines (KO). Cd content in wheat was detected by inductively coupled plasma mass spectrometry (ICP-MS). And RNA sequencing was used to explore the key factors of Cd stress response in wheat. The results indicated that under Cd stress, the KO lines exhibited significantly reduced Cd accumulation in the roots compared to the wild type (WT) plants, while the shoots showed an opposite trend. Notably, the knockout of TaNRAMP5 resulted in a 33.46 % reduction in Cd concentration in the grains. Furthermore, the knockout of TaNRAMP5 led to a decrease in wheat grain yield; however, the application increased amounts of compound fertilizers can mitigate the yield loss associated with the TaNRAMP5 mutant. Additionally, transcriptome sequencing revealed significant differences in gene expression profiles between KO and WT plants under Cd stress, particularly in the root samples. Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis indicated that the differently expressed genes (DEGs) induced by Cd stress were primarily involved in processes of "plant hormone signal transduction", "starch and sucrose metabolism", and "phenylpropanoid biosynthesis". Overall, our results suggested that the knockout of TaNRAMP5 can effectively reduce Cd accumulation in wheat. These findings may provide a potential genetic basis for the improving of wheat varieties to reduce Cd contamination in grains and ensure food safety.
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Affiliation(s)
- Zai Cheng
- School of Life Sciences, Guizhou Normal University, Guiyang, 550000, Guizhou Province, China
| | - Jialian Wei
- School of Life Sciences, Guizhou Normal University, Guiyang, 550000, Guizhou Province, China
| | - Bin Zhu
- School of Life Sciences, Guizhou Normal University, Guiyang, 550000, Guizhou Province, China
| | - Lei Gu
- School of Life Sciences, Guizhou Normal University, Guiyang, 550000, Guizhou Province, China
| | - Tuo Zeng
- School of Life Sciences, Guizhou Normal University, Guiyang, 550000, Guizhou Province, China
| | - Hongcheng Wang
- School of Life Sciences, Guizhou Normal University, Guiyang, 550000, Guizhou Province, China
| | - Xuye Du
- School of Life Sciences, Guizhou Normal University, Guiyang, 550000, Guizhou Province, China.
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3
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Manzoor M, Guan DX, Ma LQ. Plant-microbiome interactions for enhanced crop production under cadmium stress: A review. THE SCIENCE OF THE TOTAL ENVIRONMENT 2025; 965:178538. [PMID: 39879949 DOI: 10.1016/j.scitotenv.2025.178538] [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: 10/04/2024] [Revised: 12/20/2024] [Accepted: 01/13/2025] [Indexed: 01/31/2025]
Abstract
Cadmium (Cd) is a toxic heavy metal that has detrimental effects on agriculture crops and human health. Both natural and anthropogenic processes release Cd into the environment, elevating its contents in soils. Under Cd stress, strong plant-microbiome interactions are important in improving crop production, but a systematic review is still missing. This review demonstrates the importance of microbiomes and their interactions with plants in mitigating Cd toxicity and promoting crop growth. Endogenous and exogenous microbiomes play a role to enhance plant's ability to respond to Cd stress. Specifically, the rhizosphere microbiome, which includes plant growth-promoting rhizobacteria and arbuscular mycorrhizal fungi, endosphere microbiome, and phyllosphere microbiome, are involved in Cd accumulation, immobilization, and translocation, and Cd-induced stress management. The mechanisms underlying these plant-microbiome interactions vary depending on the species and varieties of crops, composition and diversity of the microbiome, and level of Cd stress. Among the microbiome-mediated approaches, biosorption, bioprecipitation, and bioaccumulation are promising for Cd remediation in soil. Additionally, the endosphere microbiome, particularly Cd resistant endophytes, reduces Cd toxicity, increases the expression of Cd efflux genes, and enhances crop growth through regulating crops' antioxidant machinery and endogenous hormones. Furthermore, improved agricultural practices modulate the soil and plant microbiomes, thereby reducing Cd stress and increasing crop productivity.
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Affiliation(s)
- Maria Manzoor
- Zhejiang Provincial Key Laboratory of Agricultural Resources and Environment, Institute of Soil and Water Resources and Environmental Science, College of Environmental and Resource Sciences, Zhejiang University, Hangzhou, China
| | - Dong-Xing Guan
- Zhejiang Provincial Key Laboratory of Agricultural Resources and Environment, Institute of Soil and Water Resources and Environmental Science, College of Environmental and Resource Sciences, Zhejiang University, Hangzhou, China.
| | - Lena Q Ma
- Zhejiang Provincial Key Laboratory of Agricultural Resources and Environment, Institute of Soil and Water Resources and Environmental Science, College of Environmental and Resource Sciences, Zhejiang University, Hangzhou, China.
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4
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Davidova S, Milushev V, Satchanska G. The Mechanisms of Cadmium Toxicity in Living Organisms. TOXICS 2024; 12:875. [PMID: 39771090 PMCID: PMC11679562 DOI: 10.3390/toxics12120875] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Grants] [Track Full Text] [Figures] [Subscribe] [Scholar Register] [Received: 08/27/2024] [Revised: 10/29/2024] [Accepted: 11/05/2024] [Indexed: 01/11/2025]
Abstract
Cadmium (Cd) is a toxic metal primarily found as a by-product of zinc production. Cd was a proven carcinogen, and exposure to this metal has been linked to various adverse health effects, which were first reported in the mid-19th century and thoroughly investigated by the 20th century. The toxicokinetics and dynamics of Cd reveal its propensity for long biological retention and predominant storage in soft tissues. Until the 1950s, Cd pollution was caused by industrial activities, whereas nowadays, the main source is phosphate fertilizers, which strongly contaminate soil and water and affect human health and ecosystems. Cd enters the human body mainly through ingestion and inhalation, with food and tobacco smoke being the primary sources. It accumulates in various organs, particularly the kidney and liver, and is known to cause severe health problems, including renal dysfunction, bone diseases, cardiovascular problems, and many others. On a cellular level, Cd disrupts numerous biological processes, inducing oxidative stress generation and DNA damage. This comprehensive review explores Cd pollution, accumulation, distribution, and biological impacts on bacteria, fungi, edible mushrooms, plants, animals, and humans on a molecular level. Molecular aspects of carcinogenesis, apoptosis, autophagy, specific gene expression, stress protein synthesis, and ROS formation caused by Cd were discussed as well. This paper also summarizes how Cd is removed from contaminated environments and the human body.
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Affiliation(s)
- Slavena Davidova
- UPIZ Educational and Research Laboratory of Biology-MF-NBU, New Bulgarian University, 1618 Sofia, Bulgaria; (S.D.); (V.M.)
- Department of Natural Sciences, New Bulgarian University, Montevideo Blvd., 1618 Sofia, Bulgaria
| | - Viktor Milushev
- UPIZ Educational and Research Laboratory of Biology-MF-NBU, New Bulgarian University, 1618 Sofia, Bulgaria; (S.D.); (V.M.)
- Department of Natural Sciences, New Bulgarian University, Montevideo Blvd., 1618 Sofia, Bulgaria
| | - Galina Satchanska
- UPIZ Educational and Research Laboratory of Biology-MF-NBU, New Bulgarian University, 1618 Sofia, Bulgaria; (S.D.); (V.M.)
- Department of Natural Sciences, New Bulgarian University, Montevideo Blvd., 1618 Sofia, Bulgaria
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Jiao Q, Li G, Li L, Lin D, Xu Z, Fan L, Zhang J, Shen F, Liu S, Seth CS, Liu H. Hormetic responses to cadmium exposure in wheat seedlings: insights into morphological, physiological, and biochemical adaptations. ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH INTERNATIONAL 2024; 31:57701-57719. [PMID: 39292310 DOI: 10.1007/s11356-024-34915-1] [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: 02/20/2024] [Accepted: 08/31/2024] [Indexed: 09/19/2024]
Abstract
Cadmium is commonly recognized as toxic to plant growth, low-level Cd has promoting effects on growth performance, which is so-called hormesis. Although Cd toxicity in wheat has been widely investigated, knowledge of growth response to a broad range of Cd concentrations, especially extremely low concentrations, is still unknown. In this study, the morphological, physiological, and biochemical performance of wheat seedlings to a wide range of Cd concentrations (0-100 µΜ) were explored. Low Cd treatment (0.1-0.5 µM) improved wheat biomass and root development by enhancing the photosynthetic system and antioxidant system ability. Photosynthetic rate (Pn) was improved by 5.72% under lower Cd treatment (1 µΜ), but inhibited by 6.05-49.85% from 5 to 100 µΜ. Excessive Cd accumulation induced oxidative injury manifesting higher MDA content, resulting in lower photosynthetic efficiency, stunted growth, and reduction of biomass. Further, the contents of ascorbate, glutathione, non-protein thiols, and phytochelatins were improved under 5-100 µΜ Cd treatment. The ascorbate peroxidase activity in the leaf showed a hormetic dose-response characteristic. Correlation analysis and partial least squares (PLS) results indicated that antioxidant enzymes and metabolites were closely correlated with Cd tolerance and accumulation. The results of the element network, correlation analysis, and PLS showed a crucial role for exogenous Cd levels in K, Fe, Cu, and Mn uptake and accumulation. These results provided a deeper understanding of the hormetic effect of Cd in wheat, which would be beneficial for improving the quality of hazard and risk assessments.
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Affiliation(s)
- Qiujuan Jiao
- College of Resources and Environment, Henan Agricultural University, Zhengzhou, 450046, PR China
| | - Gezi Li
- National Engineering Research Center for Wheat, Henan Agricultural University, Zhengzhou, 450046, PR China
| | - Lantao Li
- College of Resources and Environment, Henan Agricultural University, Zhengzhou, 450046, PR China
| | - Di Lin
- College of Forestry, Henan Agricultural University, Zhengzhou, 450046, PR China
| | - Zhengyang Xu
- College of Resources and Environment, Henan Agricultural University, Zhengzhou, 450046, PR China
| | - Lina Fan
- College of Resources and Environment, Henan Agricultural University, Zhengzhou, 450046, PR China
| | - Jingjing Zhang
- College of Resources and Environment, Henan Agricultural University, Zhengzhou, 450046, PR China
| | - Fengmin Shen
- College of Resources and Environment, Henan Agricultural University, Zhengzhou, 450046, PR China
| | - Shiliang Liu
- College of Resources and Environment, Henan Agricultural University, Zhengzhou, 450046, PR China
| | | | - Haitao Liu
- College of Resources and Environment, Henan Agricultural University, Zhengzhou, 450046, PR China.
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Kim MJ, Heo M, Kim SJ, Song HE, Lee H, Kim NE, Shin H, Do AR, Kim J, Cho YM, Hong YS, Kim WJ, Won S, Yoo HJ. Associations between plasma metabolites and heavy metal exposure in residents of environmentally polluted areas. ENVIRONMENT INTERNATIONAL 2024; 187:108709. [PMID: 38723457 DOI: 10.1016/j.envint.2024.108709] [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: 12/14/2023] [Revised: 04/08/2024] [Accepted: 04/26/2024] [Indexed: 05/19/2024]
Abstract
Heavy metals are commonly released into the environment through industrial processes such as mining and refining. The rapid industrialization that occurred in South Korea during the 1960s and 1970s contributed significantly to the economy of the country; however, the associated mining and refining led to considerable environmental pollution, and although mining is now in decline in South Korea, the detrimental effects on residents inhabiting the surrounding areas remain. The bioaccumulation of toxic heavy metals leads to metabolic alterations in human homeostasis, with disruptions in this balance leading to various health issues. This study used metabolomics to explore metabolomic alterations in the plasma samples of residents living in mining and refining areas. The results showed significant increases in metabolites involved in glycolysis and the surrounding metabolic pathways, such as glucose-6-phosphate, phosphoenolpyruvate, lactate, and inosine monophosphate, in those inhabiting polluted areas. An investigation of the associations between metabolites and blood clinical parameters through meet-in-the-middle analysis indicated that female residents were more affected by heavy metal exposure, resulting in more metabolomic alterations. For women, inhabiting the abandoned mine area, metabolites in the glycolysis and pentose phosphate pathways, such as ribose-5-phosphate and 3-phosphoglycerate, have shown a negative correlation with albumin and calcium. Finally, Mendelian randomization(MR) was used to determine the causal effects of these heavy metal exposure-related metabolites on heavy metal exposure-related clinical parameters. Metabolite biomarkers could provide insights into altered metabolic pathways related to exposure to toxic heavy metals and improve our understanding of the molecular mechanisms underlying the health effects of toxic heavy metal exposure.
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Affiliation(s)
- Mi Jeong Kim
- Biomedical Research Center, Asan Institute for Life Sciences, Asan Medical Center, Seoul, South Korea
| | - Min Heo
- Interdisciplinary Program of Bioinformatics, College of Natural Sciences, Seoul National University, Seoul, South Korea
| | - Su Jung Kim
- Biomedical Research Center, Asan Institute for Life Sciences, Asan Medical Center, Seoul, South Korea
| | - Ha Eun Song
- Biomedical Research Center, Asan Institute for Life Sciences, Asan Medical Center, Seoul, South Korea
| | - Hyoyeong Lee
- Biomedical Research Center, Asan Institute for Life Sciences, Asan Medical Center, Seoul, South Korea
| | - Nam-Eun Kim
- Department of Public Health Sciences, Seoul National University, Seoul, South Korea
| | - Hyeongyu Shin
- Interdisciplinary Program of Bioinformatics, College of Natural Sciences, Seoul National University, Seoul, South Korea
| | - Ah Ra Do
- Interdisciplinary Program of Bioinformatics, College of Natural Sciences, Seoul National University, Seoul, South Korea; RexSoft Corp, Seoul, South Korea
| | - Jeeyoung Kim
- Department of Internal Medicine and Environmental Health Center, Kangwon National University Hospital, Kangwon National University School of Medicine, Chuncheon, South Korea
| | - Yong Min Cho
- Department of Nano Chemical and Biological Engineering, Seokyeong University, Seoul, Republic of Korea
| | - Young-Seoub Hong
- Department of Preventive Medicine, College of Medicine, Dong-A University, 32, Daesin Gongwon-ro, Seo-gu, Busan 49201, Korea
| | - Woo Jin Kim
- Department of Internal Medicine and Environmental Health Center, Kangwon National University Hospital, Kangwon National University School of Medicine, Chuncheon, South Korea
| | - Sungho Won
- Interdisciplinary Program of Bioinformatics, College of Natural Sciences, Seoul National University, Seoul, South Korea; Department of Public Health Sciences, Seoul National University, Seoul, South Korea; Institute of Health and Environment, Seoul National University, Seoul, South Korea; RexSoft Corp, Seoul, South Korea.
| | - Hyun Ju Yoo
- Biomedical Research Center, Asan Institute for Life Sciences, Asan Medical Center, Seoul, South Korea; Department of Convergence Medicine, Asan Institute for Life Sciences, Asan Medical Center, Seoul, South Korea; Department of Digital Medicine, University of Ulsan College of Medicine, Seoul, South Korea.
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7
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Maslennikova D, Koryakov I, Yuldashev R, Avtushenko I, Yakupova A, Lastochkina O. Endophytic Plant Growth-Promoting Bacterium Bacillus subtilis Reduces the Toxic Effect of Cadmium on Wheat Plants. Microorganisms 2023; 11:1653. [PMID: 37512826 PMCID: PMC10386265 DOI: 10.3390/microorganisms11071653] [Citation(s) in RCA: 2] [Impact Index Per Article: 1.0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 06/02/2023] [Revised: 06/19/2023] [Accepted: 06/23/2023] [Indexed: 07/30/2023] Open
Abstract
Heavy metal ions, in particular cadmium (Cd), have a negative impact on the growth and productivity of major crops, including wheat. The use of environmentally friendly approaches, in particular, bacteria that have a growth-stimulating and protective effect, can increase the resistance of plants. The effects of the pre-sowing seed treatment with the plant growth-promoting endophyte Bacillus subtilis 10-4 (BS) on cadmium acetate (Cd)-stressed Triticum aestivum L. (wheat) growth, photosynthetic pigments, oxidative stress parameters, roots' lignin content, and Cd ions accumulation in plants were analyzed. The results showed that the tested Cd-tolerant BS improved the ability of wheat seeds to germinate in the presence of different Cd concentrations (0, 0.1, 0.5, and 1 mM). In addition, the bacterial treatment significantly decreased the damaging effects of Cd stress (1 mM) on seedlings' linear dimensions (lengths of roots and shoots), biomass, as well as on the integrity and permeability of the cell walls (i.e., lipid peroxidation and electrolyte leakage) and resulted in reduced H2O2 generation. The pretreatment with BS prevented the Cd-induced degradation of the leaf photosynthetic pigments chlorophyll (Chl) a, Chl b, and carotenoids. Moreover, the bacterial treatment intensified the lignin deposition in the roots under normal and, especially, Cd stress conditions, thereby enhancing the barrier properties of the cell wall. This manifested in a reduced Cd ions accumulation in the roots and in the restriction of its translocation to the aboveground parts (shoots) of the bacterized plants under Cd stress in comparison with non-bacterized controls. Thus, the pre-sowing seed treatment with the endophyte BS may serve as an eco-friendly approach to improve wheat production in Cd-contaminated areas.
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Affiliation(s)
| | - Igor Koryakov
- Institute of Biochemistry and Genetics UFRC RAS, Ufa 450054, Russia
| | - Ruslan Yuldashev
- Institute of Biochemistry and Genetics UFRC RAS, Ufa 450054, Russia
| | - Irina Avtushenko
- Institute of Biochemistry and Genetics UFRC RAS, Ufa 450054, Russia
- Department of Biology, Ufa University of Sciences and Technology, 32 Zaki Validi, Ufa 450076, Russia
| | - Albina Yakupova
- Institute of Biochemistry and Genetics UFRC RAS, Ufa 450054, Russia
- Department of Biology, Ufa University of Sciences and Technology, 32 Zaki Validi, Ufa 450076, Russia
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Yi Q, Wang Y, Yi C, Li L, Chen Y, Zhou H, Tong F, Liu L, Gao Y, Shi G. Agronomic and ionomics indicators of high-yield, mineral-dense, and low-Cd grains of wheat (Triticum aestivum L.) cultivars. ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY 2023; 261:115120. [PMID: 37302237 DOI: 10.1016/j.ecoenv.2023.115120] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Subscribe] [Scholar Register] [Received: 02/07/2023] [Revised: 06/05/2023] [Accepted: 06/06/2023] [Indexed: 06/13/2023]
Abstract
The accumulation of toxic and essential nutrient elements in wheat grain influences wheat yield, grain nutritional quality, and human health. Here, we assessed the potential for breeding wheat cultivars to combine high yield with low cadmium and high iron and/or zinc concentrations in grains, and we screened appropriate cultivars. A pot experiment was conducted to explore differences in grain cadmium, iron, and zinc concentrations among 68 wheat cultivars, as well as their relationships with other nutrient elements and agronomic characters. The results showed 2.04-, 1.71-, and 1.64-fold differences in grain cadmium, iron, and zinc concentrations, respectively, among the 68 cultivars. Grain cadmium concentration was positively correlated with grain zinc, iron, magnesium, phosphorus, and manganese concentrations. Grain copper concentration was positively correlated with grain zinc and iron concentrations, but not with grain cadmium concentration. Therefore, copper has a potential role in regulating grain iron and zinc accumulation without influencing cadmium concentration in wheat grain. There were no significant relationships between grain cadmium concentration and four important wheat agronomic characters (i.e., grain yield, straw yield, thousand kernel weight, and plant height), indicating that the breeding of low-cadmium-accumulating cultivars with dwarfism and high yield characteristics is possible. On cluster analysis, four cultivars (Ningmai11, Xumai35, Baomai6, and Aikang58) exhibited low-cadmium and high-yield characteristics. Among them, Aikang58 contained moderate iron and zinc concentrations, while Ningmai11 had relatively high iron but low zinc concentrations in the grain. These results imply that it is feasible to breed high-yield dwarf wheat with low cadmium and moderate iron and zinc concentrations in the grain.
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Affiliation(s)
- Qingsong Yi
- State Key Laboratory of Crop Gene Exploration and Utilization in Southwest China/Triticeae Research Institute, Sichuan Agricultural University, Wenjiang 611130, China; Key Laboratory of Agro-Environment in Downstream of Yangtze River Plain, Ministry of Agriculture and Rural Affairs of the People's Republic of China, Institute of Agricultural Resources and Environment, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, China
| | - Yi Wang
- State Key Laboratory of Crop Gene Exploration and Utilization in Southwest China/Triticeae Research Institute, Sichuan Agricultural University, Wenjiang 611130, China
| | - Chao Yi
- Key Laboratory of Agro-Environment in Downstream of Yangtze River Plain, Ministry of Agriculture and Rural Affairs of the People's Republic of China, Institute of Agricultural Resources and Environment, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, China; National Agricultural Experimental Station for Agricultural Environment, Luhe, Minstry of Agriculture and Rural Affairs, China; School of the Environment and Safety Engineering, Jiangsu University, Zhenjiang 212013, China
| | - Linxin Li
- College of Resources and Environmental Sciences, Nanjing Agricultural University, Nanjing 210095, China
| | - Yinglong Chen
- The UWA Institute of Agriculture, and UWA School of Agriculture and Environment, The University of Western Australia, Perth, WA 6009, Australia
| | - Huimin Zhou
- Key Laboratory of Agro-Environment in Downstream of Yangtze River Plain, Ministry of Agriculture and Rural Affairs of the People's Republic of China, Institute of Agricultural Resources and Environment, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, China
| | - Fei Tong
- Key Laboratory of Agro-Environment in Downstream of Yangtze River Plain, Ministry of Agriculture and Rural Affairs of the People's Republic of China, Institute of Agricultural Resources and Environment, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, China; National Agricultural Experimental Station for Agricultural Environment, Luhe, Minstry of Agriculture and Rural Affairs, China
| | - Lizhu Liu
- Key Laboratory of Agro-Environment in Downstream of Yangtze River Plain, Ministry of Agriculture and Rural Affairs of the People's Republic of China, Institute of Agricultural Resources and Environment, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, China; National Agricultural Experimental Station for Agricultural Environment, Luhe, Minstry of Agriculture and Rural Affairs, China
| | - Yan Gao
- Key Laboratory of Agro-Environment in Downstream of Yangtze River Plain, Ministry of Agriculture and Rural Affairs of the People's Republic of China, Institute of Agricultural Resources and Environment, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, China; National Agricultural Experimental Station for Agricultural Environment, Luhe, Minstry of Agriculture and Rural Affairs, China; School of the Environment and Safety Engineering, Jiangsu University, Zhenjiang 212013, China; College of Resources and Environmental Sciences, Nanjing Agricultural University, Nanjing 210095, China.
| | - Gaoling Shi
- Key Laboratory of Agro-Environment in Downstream of Yangtze River Plain, Ministry of Agriculture and Rural Affairs of the People's Republic of China, Institute of Agricultural Resources and Environment, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, China; National Agricultural Experimental Station for Agricultural Environment, Luhe, Minstry of Agriculture and Rural Affairs, China; School of the Environment and Safety Engineering, Jiangsu University, Zhenjiang 212013, China; College of Resources and Environmental Sciences, Nanjing Agricultural University, Nanjing 210095, China.
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9
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Zhang Y, Zhang Y, Wu A. Remediation effects and mechanisms of typical minerals combined with inorganic amendment on cadmium-contaminated soil: a field study in wheat. ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH INTERNATIONAL 2023; 30:38605-38615. [PMID: 36585588 DOI: 10.1007/s11356-022-24976-5] [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: 07/20/2022] [Accepted: 12/21/2022] [Indexed: 06/17/2023]
Abstract
The remediation of cadmium (Cd)-contaminated soil has gained much attention recently because Cd in soil threatens human health through the food chain. Although tremendous progress has been made in the remediation of Cd-contaminated soil in rice acid soil system, the mechanism and effects of Cd-contaminated soil remediation under these amendments in wheat weak alkaline soil are still limited. In this study, the remediation effect and related mechanism of Cd in weakly alkaline soil were carried out using zeolite, diatomite, and sodium bentonite as the main remediation components, supplemented by calcium dihydrogen phosphate and fulvic acid. The results of field experiments showed that the concentration of Cd reduced by 27.3 ~ 31.2% in rhizosphere soil and 34.3 ~ 54.2% in non-rhizosphere soil, and the maximum reduction rate of Cd concentration in wheat grain was 25.5%. The main factors affecting the concentration of Cd in wheat grains include the change in exchangeable Cd, the absorption capacity of wheat root, and the inhibitory effect on Cd transport from stem to grain in this paper. In general, this work provides a new potential management feasible pathway to alleviate the Cd toxicity of weakly alkaline soil and wheat grain.
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Affiliation(s)
- Yuenan Zhang
- (CAS) Key Laboratory of Magnetic Materials and Devices & Zhejiang Engineering Research Center for Biomedical Materials, Cixi Institute of Biomedical Engineering, Chinese Academy of Sciences, Ningbo Institute of Materials Technology and Engineering, 315201, Ningbo, China
| | - Yujie Zhang
- (CAS) Key Laboratory of Magnetic Materials and Devices & Zhejiang Engineering Research Center for Biomedical Materials, Cixi Institute of Biomedical Engineering, Chinese Academy of Sciences, Ningbo Institute of Materials Technology and Engineering, 315201, Ningbo, China.
- University of Chinese Academy of Sciences, Beijing, 100049, China.
| | - Aiguo Wu
- (CAS) Key Laboratory of Magnetic Materials and Devices & Zhejiang Engineering Research Center for Biomedical Materials, Cixi Institute of Biomedical Engineering, Chinese Academy of Sciences, Ningbo Institute of Materials Technology and Engineering, 315201, Ningbo, China
- University of Chinese Academy of Sciences, Beijing, 100049, China
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Luo F, Zhu D, Sun H, Zou R, Duan W, Liu J, Yan Y. Wheat Selenium-binding protein TaSBP-A enhances cadmium tolerance by decreasing free Cd 2+ and alleviating the oxidative damage and photosynthesis impairment. FRONTIERS IN PLANT SCIENCE 2023; 14:1103241. [PMID: 36824198 PMCID: PMC9941557 DOI: 10.3389/fpls.2023.1103241] [Citation(s) in RCA: 5] [Impact Index Per Article: 2.5] [Reference Citation Analysis] [Abstract] [Key Words] [Grants] [Track Full Text] [Figures] [Subscribe] [Scholar Register] [Received: 11/20/2022] [Accepted: 01/20/2023] [Indexed: 06/18/2023]
Abstract
Cadmium, one of the toxic heavy metals, robustly impact crop growth and development and food safety. In this study, the mechanisms of wheat (Triticum aestivum L.) selenium-binding protein-A (TaSBP-A) involved in response to Cd stress was fully investigated by overexpression in Arabidopsis and wheat. As a cytoplasm protein, TaSBP-A showed a high expression in plant roots and its expression levels were highly induced by Cd treatment. The overexpression of TaSBP-A enhanced Cd-toleration in yeast, Arabidopsis and wheat. Meanwhile, transgenic Arabidopsis under Cd stress showed a lower H2O2 and malondialdehyde content and a higher photochemical efficiency in the leaf and a reduction of free Cd2+ in the root. Transgenic wheat seedlings of TaSBP exhibited an increment of Cd content in the root, and a reduction Cd content in the leaf under Cd2+ stress. Cd2+ binding assay combined with a thermodynamics survey and secondary structure analysis indicated that the unique CXXC motif in TaSBP was a major Cd-binding site participating in the Cd detoxification. These results suggested that TaSBP-A can enhance the sequestration of free Cd2+ in root and inhibit the Cd transfer from root to leaf, ultimately conferring plant Cd-tolerance via alleviating the oxidative stress and photosynthesis impairment triggered by Cd stress.
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Affiliation(s)
| | | | | | | | | | | | - Yueming Yan
- Beijing Key Laboratory of Plant Gene Resources and Biotechnology for Carbon Reduction and Environmental Improvement, College of Life Science, Capital Normal University, Beijing, China
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11
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Xu T, Xi J, Ke J, Wang Y, Chen X, Zhang Z, Lin Y. Deciphering soil amendments and actinomycetes for remediation of cadmium (Cd) contaminated farmland. ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY 2023; 249:114388. [PMID: 36508810 DOI: 10.1016/j.ecoenv.2022.114388] [Citation(s) in RCA: 12] [Impact Index Per Article: 6.0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 07/08/2022] [Revised: 09/28/2022] [Accepted: 12/01/2022] [Indexed: 06/17/2023]
Abstract
Soil heavy metal pollution is one of the most serious environmental problems in China, especially cadmium (Cd), which has the most extensive contaminated soil coverage. Therefore, more economical and efficient remediation methods and measures are needed to control soil Cd contamination. In this study, different amendments (biochar (B), organic fertilizer (F), lime (L)) and actinomycetes (A) inoculants were applied to Cd contaminated farmland to explore their effects on wheat growth. Compared with Control, all treatments except A treatment were able to significantly increase the underground parts dry mass of wheat, with the highest increase of 57.19 %. The results showed that the B treatment significantly increased the plant height of wheat by 3.45 %. All treatments increased wheat SOD activity and chlorophyll content and reduced the MDA, which contributes to wheat stress resistance under Cd contamination. F, L and AF treatments can significantly reduce the Cd content in wheat above- and underground parts by up to 56.39 %. Soil amendments can modify the physical and chemical properties of the soil, which in turn affects the absorption of Cd by wheat. Moreover, the addition of soil amendments significantly affects the composition and structure of the rhizospheric soil bacterial community at the wheat jointing stage. The application of organic fertilizer increases the richness and diversity of the bacterial community, while lime makes it significantly decreases it. T-test and microbiome co-occurrence networks show that actinomycetes could not only effectively colonize in local soil, but also effectively enhance the complexity and stability of the rhizosphere microbial community. Considering the practical impact of different treatments on wheat, soil microorganisms, economic benefits and restoration of soil Cd contamination, the application of organic fertilizer and actinomycetes in Cd contaminated soil is a more ideal remediation strategy. This conclusion can be further verified by studying larger repair regions and longer consecutive repair cycles to gain insight into the repair mechanism.
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Affiliation(s)
- Tengqi Xu
- College of Life Sciences, Northwest A&F University, Yangling, Shaanxi 712100, PR China.
| | - Jiao Xi
- College of Life Sciences, Northwest A&F University, Yangling, Shaanxi 712100, PR China.
| | - Jihong Ke
- College of Life Sciences, Northwest A&F University, Yangling, Shaanxi 712100, PR China.
| | - Yufan Wang
- College of Life Sciences, Northwest A&F University, Yangling, Shaanxi 712100, PR China.
| | - Xiaotian Chen
- College of Life Sciences, Northwest A&F University, Yangling, Shaanxi 712100, PR China.
| | - Zengqiang Zhang
- College of Natural Resources and Environment, Northwest A&F University, Yangling, Shaanxi 712100, PR China.
| | - Yanbing Lin
- College of Life Sciences, Northwest A&F University, Yangling, Shaanxi 712100, PR China.
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12
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Zhou M, Zheng S. Multi-Omics Uncover the Mechanism of Wheat under Heavy Metal Stress. Int J Mol Sci 2022; 23:ijms232415968. [PMID: 36555610 PMCID: PMC9785819 DOI: 10.3390/ijms232415968] [Citation(s) in RCA: 3] [Impact Index Per Article: 1.0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 10/28/2022] [Revised: 12/08/2022] [Accepted: 12/13/2022] [Indexed: 12/23/2022] Open
Abstract
Environmental pollution of heavy metals has received growing attention in recent years. Heavy metals such as cadmium, lead and mercury can cause physiological and morphological disturbances which adversely affect the growth and quality of crops. Wheat (Triticum aestivum L.) can accumulate high contents of heavy metals in its edible parts. Understanding wheat response to heavy metal stress and its management in decreasing heavy metal uptake and accumulation may help to improve its growth and grain quality. Very recently, emerging advances in heavy metal toxicity and phytoremediation methods to reduce heavy metal pollution have been made in wheat. Especially, the molecular mechanisms of wheat under heavy metal stress are increasingly being recognized. In this review, we focus on the recently described epigenomics, transcriptomics, proteomics, metabolomics, ionomics and multi-omics combination, as well as functional genes uncovering heavy metal stress in wheat. The findings in this review provide some insights into challenges and future recommendations for wheat under heavy metal stress.
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Affiliation(s)
- Min Zhou
- School of Life Sciences, Chongqing University, Chongqing 401331, China
- Center of Plant Functional Genomics, Institute of Advanced Interdisciplinary Studies, Chongqing University, Chongqing 401331, China
| | - Shigang Zheng
- Chengdu Institute of Biology, Chinese Academy of Sciences, Chengdu 610041, China
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13
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Maslennikova D, Nasyrova K, Chubukova O, Akimova E, Baymiev A, Blagova D, Ibragimov A, Lastochkina O. Effects of Rhizobium leguminosarum Thy2 on the Growth and Tolerance to Cadmium Stress of Wheat Plants. Life (Basel) 2022; 12:1675. [PMID: 36295110 PMCID: PMC9605373 DOI: 10.3390/life12101675] [Citation(s) in RCA: 2] [Impact Index Per Article: 0.7] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 10/07/2022] [Revised: 10/18/2022] [Accepted: 10/18/2022] [Indexed: 06/16/2023] Open
Abstract
Cadmium (Cd) stress is an obstacle for crop production, quality crops, and sustainable agriculture. An important role is played by the application of eco-friendly approaches to improve plant growth and stress tolerance. In the current study, a pre-sowing seed treatment with Rhizobium leguminosarum strains, isolated from the leguminous plants Phaseolus vulgaris (strain Pvu5), Vicia sylvatica (strain VSy12), Trifolium hybridium (strain Thy2), and T. pratense (strain TPr4), demonstrated different effects on wheat (Triticum aestivum L.) plant growth under normal conditions. Among all tested strains, Thy2 significantly increased seed germination, seedling length, fresh and dry biomass, and leaf chlorophyll (Chl) content. Further analysis showed that Thy2 was capable of producing indole-3-acetic acid and siderophores and fixing nitrogen. Under Cd stress, Thy2 reduced the negative effect of Cd on wheat growth and photosynthesis and had a protective effect on the antioxidant system. This was expressed in the additional accumulation of glutathione and proline and the activation of glutathione reductase. In addition, Thy2 led to a significant reduction in oxidative stress, which was evidenced by the data on the stabilization of the ascorbate content and the activity of ascorbate peroxidase. In addition, Thy2 markedly reduced Cd-induced membrane lipid peroxidation and electrolyte leakage in the plants. Thus, the findings demonstrated the ability of the R. leguminosarum strain Thy2, isolated from T. hybridium nodules, to exert a growth-promoting and anti-stress effect on wheat plants. These results suggest that the Thy2 strain may enhance wheat plant growth by mitigating Cd stress, particularly through improving photosynthesis and antioxidant capacity and reducing the severity of oxidative damage. This may provide a basic and biological approach to use the Thy2 strain as a promising, eco-friendly candidate to combat Cd stress in wheat production.
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Affiliation(s)
- Dilara Maslennikova
- Ufa Federal Research Center, Institute of Biochemistry and Genetics, Russian Academy of Sciences, 450054 Ufa, Russia
- Department of Molecular Technologis, Ufa State Petroleum Technical University, 450000 Ufa, Russia
| | - Karina Nasyrova
- Department of Molecular Technologis, Ufa State Petroleum Technical University, 450000 Ufa, Russia
| | - Olga Chubukova
- Ufa Federal Research Center, Institute of Biochemistry and Genetics, Russian Academy of Sciences, 450054 Ufa, Russia
- Department of Molecular Technologis, Ufa State Petroleum Technical University, 450000 Ufa, Russia
| | - Ekaterina Akimova
- Ufa Federal Research Center, Institute of Biochemistry and Genetics, Russian Academy of Sciences, 450054 Ufa, Russia
| | - Andrey Baymiev
- Ufa Federal Research Center, Institute of Biochemistry and Genetics, Russian Academy of Sciences, 450054 Ufa, Russia
| | - Darya Blagova
- Ufa Federal Research Center, Institute of Biochemistry and Genetics, Russian Academy of Sciences, 450054 Ufa, Russia
| | - Almaz Ibragimov
- Ufa Federal Research Center, Institute of Biochemistry and Genetics, Russian Academy of Sciences, 450054 Ufa, Russia
| | - Oksana Lastochkina
- Ufa Federal Research Center, Institute of Biochemistry and Genetics, Russian Academy of Sciences, 450054 Ufa, Russia
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