1
|
Keer A, Oza Y, Mongad D, Ramakrishnan D, Dhotre D, Ahmed A, Zumla A, Shouche Y, Sharma A. Assessment of seasonal variations in antibiotic resistance genes and microbial communities in sewage treatment plants for public health monitoring. ENVIRONMENTAL POLLUTION (BARKING, ESSEX : 1987) 2025; 375:126367. [PMID: 40320120 DOI: 10.1016/j.envpol.2025.126367] [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: 12/20/2024] [Revised: 04/28/2025] [Accepted: 05/01/2025] [Indexed: 05/09/2025]
Abstract
The spread of antimicrobial resistance (AMR) around the globe, especially in the urban cities with high population, is a major concern. Therefore, the current study aims at identifying antibiotic resistant bacteria, microbial community compositions and the quantification of antimicrobial resistant genes from six sewage treatment plants (STPs) across Pune city in Maharashtra, India. A total of 106 isolates obtained were tested against six antibiotics in which the highest resistance was observed against trimethoprim (24.53 %). The qPCR assays of seven antibiotic resistance genes revealed abundance of blaimp-1 and mecA genes in the summer and monsoon seasons followed by blaNDM-1 gene in the summer and winter seasons. The alpha diversity indices depicted highest microbial diversity of inlet samples during winter, followed by inlet samples during the summer and monsoon seasons. Comparative analysis revealed Bifidobacterium (51 %), Pseudomonas (28.7 %) and Zoogloea (17.6 %) as the most abundant genera in the inlet samples during the summer, monsoon and winter seasons respectively while Acinetobacter (31 %) and Flavobacterium (23 % in winter and 18.2 % in summer) dominated the outlet samples. The co-network analysis revealed positive and negative interactions in the winter and monsoon but only positive interactions in the summer season. Venn diagrams showed higher abundance of ASVs in the outlet samples than the inlet. The top genera correlated exactly opposite with the pH compared to BOD and COD. PICRUSt2-based functional prediction revealed a higher abundance of methicillin resistance, β-lactamase resistance and multidrug resistance genes in inlet samples while chloramphenicol resistance was found higher in outlet samples. Further, we observed that potential pathogens causing infectious disease such as pertussis, shigellosis and tuberculosis were present in all three seasons.
Collapse
Affiliation(s)
- Abhishek Keer
- BRIC- National Centre for Cell Science, Pune, 411007, India
| | - Yukti Oza
- BRIC- National Centre for Cell Science, Pune, 411007, India
| | | | - Dinesh Ramakrishnan
- Leibniz Institute for Agricultural Engineering and Bioeconomy, Max-Eyth-Allee 100, 14469, Potsdam, Germany
| | - Dhiraj Dhotre
- BRIC- National Centre for Cell Science, Pune, 411007, India
| | - Abdelfattah Ahmed
- Leibniz Institute for Agricultural Engineering and Bioeconomy, Max-Eyth-Allee 100, 14469, Potsdam, Germany
| | - Alimuddin Zumla
- Department of Infection, Division of Infection and Immunity, Centre for Clinical Microbiology, University College London, Gower Street, London, WC1E 6BT, UK
| | - Yogesh Shouche
- BRIC- National Centre for Cell Science, Pune, 411007, India
| | - Avinash Sharma
- BRIC- National Centre for Cell Science, Pune, 411007, India.
| |
Collapse
|
2
|
Phan T, Brozak S, Pell B, Ciupe SM, Ke R, Ribeiro RM, Gitter A, Mena KD, Perelson AS, Kuang Y, Wu F. Post-recovery viral shedding shapes wastewater-based epidemiological inferences. COMMUNICATIONS MEDICINE 2025; 5:193. [PMID: 40405003 DOI: 10.1038/s43856-025-00908-5] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 08/28/2024] [Accepted: 05/12/2025] [Indexed: 05/24/2025] Open
Abstract
BACKGROUND The prolonged viral shedding from the gastrointestinal tract is well documented for numerous pathogens, including SARS-CoV-2. However, the impact of prolonged viral shedding on epidemiological inferences using wastewater data is not yet fully understood. METHODS To gain a better understanding of this phenomenon at the population level, we extended a wastewater-based modeling framework that integrates viral shedding dynamics, viral load data in wastewater, case report data, and an epidemic model. RESULTS Our results indicate that as an outbreak progresses, the viral load from recovered individuals gradually becomes predominant, surpassing that from the infectious population. This phenomenon leads to a dynamic relationship between model-inferred and reported daily incidence over the course of an outbreak. Sensitivity analyses on the duration and rate of viral shedding for recovered individuals reveal that accounting for this phenomenon can considerably advance prediction of transmission peak timing. Furthermore, extensive viral shedding from the recovered population toward the conclusion of an epidemic wave may overshadow viral signals from newly infected cases carrying emerging variants, which can delay the rapid recognition of emerging variants based on viral load. CONCLUSIONS These findings highlight the necessity of integrating post-recovery viral shedding to enhance the accuracy and utility of wastewater-based epidemiological analysis.
Collapse
Affiliation(s)
- Tin Phan
- Theoretical Biology and Biophysics, Los Alamos National Laboratory, Los Alamos, NM, USA
| | - Samantha Brozak
- School of Mathematical and Statistical Sciences, Arizona State University, Tempe, AZ, USA
| | - Bruce Pell
- Department of Mathematics and Computer Science, Lawrence Technological University, Southfield, MI, USA
| | - Stanca M Ciupe
- Department of Mathematics, Virginia Tech, Blacksburg, VA, USA
- Virginia Tech Center for the Mathematics of Biosystems, Blacksburg, VA, USA
| | - Ruian Ke
- Theoretical Biology and Biophysics, Los Alamos National Laboratory, Los Alamos, NM, USA
| | - Ruy M Ribeiro
- Theoretical Biology and Biophysics, Los Alamos National Laboratory, Los Alamos, NM, USA
| | - Anna Gitter
- Department of Environmental and Occupational Health Sciences, School of Public Health, The University of Texas Health Science Center at Houston, Houston, TX, USA
| | - Kristina D Mena
- Department of Environmental and Occupational Health Sciences, School of Public Health, The University of Texas Health Science Center at Houston, Houston, TX, USA
| | - Alan S Perelson
- Theoretical Biology and Biophysics, Los Alamos National Laboratory, Los Alamos, NM, USA
- Santa Fe Institute, Santa Fe, NM, USA
| | - Yang Kuang
- School of Mathematical and Statistical Sciences, Arizona State University, Tempe, AZ, USA
| | - Fuqing Wu
- Department of Environmental and Occupational Health Sciences, School of Public Health, The University of Texas Health Science Center at Houston, Houston, TX, USA.
| |
Collapse
|
3
|
Länsivaara A, Palmroth M, Kaarela O, Hyöty H, Oikarinen S, Lehto KM. Virus detection in influent, activated sludge, and effluent from municipal wastewater treatment plants using composite and grab samples in Finland. ENVIRONMENTAL RESEARCH 2025; 279:121776. [PMID: 40324624 DOI: 10.1016/j.envres.2025.121776] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Subscribe] [Scholar Register] [Received: 09/25/2024] [Revised: 04/15/2025] [Accepted: 05/03/2025] [Indexed: 05/07/2025]
Abstract
Wastewater-based surveillance has been commonly used as a monitoring tool for public health. Also, viruses present in wastewater can pose a health risk. In this study, we screened enterovirus, rhinovirus, norovirus GI and GII, pan-adenovirus, and gastroenteritis-causing adenovirus F40/41 in different wastewater sample types using reverse transcription quantitative polymerase chain reaction and quantitative polymerase chain reaction. We analyzed composite influent samples (N = 22), grab influent samples (N = 20), composite effluent samples (N = 78), grab effluent samples (N = 21), and activated sludge samples (N = 34) collected from six municipal wastewater treatment plants in the Pirkanmaa region of Finland. We detected the viruses in the influent to discover if they had the potential to be monitored using wastewater-based surveillance. In addition, we studied viruses in effluent and activated sludge to detect viruses that persisted in treatment processes. Furthermore, all sample types were compared to discover differences in the viral contents of different wastewater sample types. We detected all the studied viruses in influent, while in activated sludge, we detected enterovirus, pan-adenovirus, and adenovirus F40/41, and in effluent enterovirus, norovirus GI and GII, pan-adenovirus, and adenovirus F40/41 were identified. In addition, the relative amount of all the viruses was the highest in the influent. Our study also showed that composite sampling was a more representative and sensitive method for virus monitoring in wastewater than grab sampling, as the relative amount of the viruses present in composite samples was higher than in grab samples. Since we found abundant viruses in effluent, further studies are required to assess their infectivity and potential health risks as environmental pollutants.
Collapse
Affiliation(s)
- Annika Länsivaara
- Faculty of Medicine and Health Technology, Tampere University, P.O. Box 541, FI-33014, Tampere, Finland
| | - Marja Palmroth
- Faculty of Engineering and Natural Sciences, Tampere University, P.O. Box 541, FI-33014, Tampere, Finland
| | - Outi Kaarela
- Faculty of Engineering and Natural Sciences, Tampere University, P.O. Box 541, FI-33014, Tampere, Finland
| | - Heikki Hyöty
- Faculty of Medicine and Health Technology, Tampere University, P.O. Box 541, FI-33014, Tampere, Finland
| | - Sami Oikarinen
- Faculty of Medicine and Health Technology, Tampere University, P.O. Box 541, FI-33014, Tampere, Finland.
| | - Kirsi-Maarit Lehto
- Faculty of Medicine and Health Technology, Tampere University, P.O. Box 541, FI-33014, Tampere, Finland; Faculty of Veterinary Medicine, University of Helsinki, Helsingin Yliopisto, P.O. Box 66, FI-00014, Helsinki, Finland
| |
Collapse
|
4
|
Ibañez JM, Zambrana R, Carreras P, Obregón V, Irazoqui JM, Vera PA, Lattar TE, Blanco Fernández MD, Puebla AF, Amadio AF, Torres C, López Lambertini PM. Phylodynamic of Tomato Brown Rugose Fruit Virus and Tomato Chlorosis Virus, Two Emergent Viruses in Mixed Infections in Argentina. Viruses 2025; 17:533. [PMID: 40284976 PMCID: PMC12031183 DOI: 10.3390/v17040533] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/21/2025] [Revised: 03/20/2025] [Accepted: 03/31/2025] [Indexed: 04/29/2025] Open
Abstract
Tobamovirus fructirugosum (ToBRFV) and Crinivirus tomatichlorosis (ToCV) are emerging viral threats to tomato production worldwide, with expanding global distribution. Both viruses exhibit distinct biological characteristics and transmission mechanisms that influence their spread. This study aimed to reconstruct the complete genomes of ToBRFV and ToCV from infected tomato plants and wastewater samples in Argentina to explore their global evolutionary dynamics. Additionally, it compared the genetic diversity of ToBRFV in plant tissue and sewage samples. Using metagenomic analysis, the complete genome sequences of two ToBRFV isolates and two ToCV isolates from co-infected tomatoes, along with four ToBRFV isolates from sewage, were obtained. The analysis showed that ToBRFV exhibited higher genetic diversity in environmental samples than in plant samples. Phylodynamic analysis indicated that both viruses had a recent, single introduction in Argentina but predicted different times for ancestral diversification. The evolutionary analysis estimated that ToBRFV began its global diversification in June 2013 in Israel, with rapid diversification and exponential growth until 2020, after which the effective population size declined. Moreover, ToCV's global expansion was characterized by exponential growth from 1979 to 2010, with Turkey identified as the most probable location with the current data available. This study highlights how sequencing and monitoring plant viruses can enhance our understanding of their global spread and impact on agriculture.
Collapse
Affiliation(s)
- Julia M. Ibañez
- Estación Experimental Agropecuaria Bella Vista, Instituto Nacional de Tecnología Agropecuaria (INTA), Ruta 27-Km 38,3, Bella Vista, Corrientes 3432, Argentina; (J.M.I.); (V.O.); (T.E.L.)
| | - Romina Zambrana
- Instituto de Investigaciones en Bacteriología y Virología Molecular (IBaViM), Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Junin 956, 4th floor, Ciudad Autónoma de Buenos Aires 1113, Argentina; (R.Z.); (M.D.B.F.); (C.T.)
| | - Pamela Carreras
- Instituto de Patología Vegetal, Centro de Investigaciones Agropecuarias, Instituto Nacional de Tecnología Agropecuaria (IPAVE-CIAP-INTA), Av. 11 de Septiembre, X5014MGO, Córdoba 4755, Argentina;
- Unidad de Fitopatología y Modelización Agrícola (UFYMA) INTA-Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Av. 11 de Septiembre, X5014MGO, Córdoba 4755, Argentina
| | - Verónica Obregón
- Estación Experimental Agropecuaria Bella Vista, Instituto Nacional de Tecnología Agropecuaria (INTA), Ruta 27-Km 38,3, Bella Vista, Corrientes 3432, Argentina; (J.M.I.); (V.O.); (T.E.L.)
| | - José M. Irazoqui
- Instituto de Investigaciones de la Cadena Láctea (IDICAL) INTA-CONICET, Ruta 34 km 227, Rafaela, Santa Fe 2300, Argentina; (J.M.I.); (A.F.A.)
| | - Pablo A. Vera
- Unidad de Genómica y Bioinformática (UGB), Instituto de Agrobiotecnología y Biología Molecular (IABiMo), INTA-CONICET, De los Reseros y N. Repetto, Hurlingham, Ciudad Autónoma de Buenos Aires 1686, Argentina; (P.A.V.); (A.F.P.)
| | - Tatiana E. Lattar
- Estación Experimental Agropecuaria Bella Vista, Instituto Nacional de Tecnología Agropecuaria (INTA), Ruta 27-Km 38,3, Bella Vista, Corrientes 3432, Argentina; (J.M.I.); (V.O.); (T.E.L.)
| | - María D. Blanco Fernández
- Instituto de Investigaciones en Bacteriología y Virología Molecular (IBaViM), Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Junin 956, 4th floor, Ciudad Autónoma de Buenos Aires 1113, Argentina; (R.Z.); (M.D.B.F.); (C.T.)
| | - Andrea F. Puebla
- Unidad de Genómica y Bioinformática (UGB), Instituto de Agrobiotecnología y Biología Molecular (IABiMo), INTA-CONICET, De los Reseros y N. Repetto, Hurlingham, Ciudad Autónoma de Buenos Aires 1686, Argentina; (P.A.V.); (A.F.P.)
| | - Ariel F. Amadio
- Instituto de Investigaciones de la Cadena Láctea (IDICAL) INTA-CONICET, Ruta 34 km 227, Rafaela, Santa Fe 2300, Argentina; (J.M.I.); (A.F.A.)
| | - Carolina Torres
- Instituto de Investigaciones en Bacteriología y Virología Molecular (IBaViM), Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Junin 956, 4th floor, Ciudad Autónoma de Buenos Aires 1113, Argentina; (R.Z.); (M.D.B.F.); (C.T.)
| | - Paola M. López Lambertini
- Instituto de Patología Vegetal, Centro de Investigaciones Agropecuarias, Instituto Nacional de Tecnología Agropecuaria (IPAVE-CIAP-INTA), Av. 11 de Septiembre, X5014MGO, Córdoba 4755, Argentina;
- Unidad de Fitopatología y Modelización Agrícola (UFYMA) INTA-Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Av. 11 de Septiembre, X5014MGO, Córdoba 4755, Argentina
| |
Collapse
|
5
|
Nguyen Thanh L, Hachad M, McQuaid N, Krylova K, Thanh LNH, Visentin F, Burnet JB, Quete FS, Maere T, Tsitouras A, Vanrolleghem P, Frigon D, Loeb S, Dorner S, Goitom E. Hydrological and physicochemical parameters associated with SARS-CoV-2 and pepper mild mottle virus wastewater concentrations for a large-combined sewer system. JOURNAL OF WATER AND HEALTH 2025; 23:413-427. [PMID: 40156218 DOI: 10.2166/wh.2025.352] [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: 10/04/2024] [Accepted: 01/13/2025] [Indexed: 04/01/2025]
Abstract
During COVID-19, surveillance of SARS-CoV-2 in wastewater has been a promising tool for tracking viral infection at the community level. However, in addition to the shedding rates within the community, SARS-CoV-2 concentrations in raw wastewater are influenced by several environmental factors. This study investigated the effects of wastewater characteristics on the viral quantification of SARS-CoV-2 and pepper mild mottle virus (PMMoV) for a large wastewater system with combined sewers. Principal component analysis illustrated that water temperature negatively correlates with SARS-CoV-2 and PMMoV in wastewater, but flow rate and EC are highly correlated with SARS-CoV-2 in spring and winter. The normalization using EC enhanced the correlation with clinical data compared to normalization using pH, flow rate, and raw SARS-CoV-2. The normalization using PMMoV reduced the correlation with clinical data. Multiple linear and random forest (RF) applied to predict the concentrations of SARS-CoV-2 in wastewater, given the confirmed cases and physicochemical parameters. RF regression was the best model to predict SARS-CoV-2 in wastewater (R2=0.8), with the most important variables being the confirmed cases followed by water temperature. RF model is a potent predictor of the presence of SARS-CoV-2 in wastewater. This enhances the degree of reliability between community outbreaks and SARS-CoV-2 monitoring.
Collapse
Affiliation(s)
- Luan Nguyen Thanh
- Département des génies civil, géologique et des mines, Polytechnique Montréal, Montréal, Canada E-mail:
| | - Mounia Hachad
- Département des génies civil, géologique et des mines, Polytechnique Montréal, Montréal, Canada
| | - Natasha McQuaid
- Département des génies civil, géologique et des mines, Polytechnique Montréal, Montréal, Canada
| | - Kateryna Krylova
- Département des génies civil, géologique et des mines, Polytechnique Montréal, Montréal, Canada
| | - Loan Nguyen Ha Thanh
- Département des génies civil, géologique et des mines, Polytechnique Montréal, Montréal, Canada
| | - Flavia Visentin
- Département des génies civil, géologique et des mines, Polytechnique Montréal, Montréal, Canada
| | - Jean-Baptiste Burnet
- Département des génies civil, géologique et des mines, Polytechnique Montréal, Montréal, Canada
| | | | - Thomas Maere
- Department of Civil and Water Engineering, Université Laval, Quebec City, QC, Canada
| | | | - Peter Vanrolleghem
- Department of Civil and Water Engineering, Université Laval, Quebec City, QC, Canada
| | - Dominic Frigon
- Department of Civil Engineering, McGill University, Montreal, QC, Canada
| | - Stephanie Loeb
- Department of Civil Engineering, McGill University, Montreal, QC, Canada
| | - Sarah Dorner
- Département des génies civil, géologique et des mines, Polytechnique Montréal, Montréal, Canada
| | - Eyerusalem Goitom
- Département des génies civil, géologique et des mines, Polytechnique Montréal, Montréal, Canada
| |
Collapse
|
6
|
Wagner JPS, Rech MF, Prandi BA, Franco AC, Rigotto C, Horn F. Epidemiological monitoring of sewage sludge and wastewater from an upflow anaerobic sludge blanket reactor using SARS-CoV-2 as a model. WATER SCIENCE AND TECHNOLOGY : A JOURNAL OF THE INTERNATIONAL ASSOCIATION ON WATER POLLUTION RESEARCH 2025; 91:333-343. [PMID: 40018894 DOI: 10.2166/wst.2025.014] [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: 03/11/2024] [Accepted: 01/15/2025] [Indexed: 03/01/2025]
Abstract
This study explores the potential of sludge-based monitoring from an upflow anaerobic sludge blanket reactor for epidemiological surveillance, using SARS-CoV-2 as a model. We monitored SARS-CoV-2 copy numbers and mutations, and compared concentrations in sludge to concentrations in wastewater samples taken on the same days. From January to August 2021, 32 sludge samples were analyzed; 30 (93%) were positive for SARS-CoV-2, and copy numbers varied from 0.147 to 2.314 copies ×106/L. In wastewater samples collected on the same days, 31 (96%) were positive for SARS-CoV-2, and copy numbers ranged from 0.058 to 3.014 copies ×106/L. The concentration of SARS-CoV-2 in the sludge rose along with confirmed hospitalization cases in March, while wastewater SARS-CoV-2 concentrations rose 2 weeks earlier along with numbers of new confirmed cases. Mutations of variants of concern, Gamma and Delta, were identified in sludge samples in the same months that they became dominant in the corresponding regions. Our results indicate that, although monitoring of sewage sludge was not effective in anticipating infection numbers, it is a promising way to gain insight into the epidemiological situation in a city or region.
Collapse
Affiliation(s)
- João Pedro Stepan Wagner
- Departamento de Biofísica, Universidade Federal do Rio Grande do Sul, Porto Alegre 90650-001, Brasil
| | - Maria Fernanda Rech
- Departamento de Biofísica, Universidade Federal do Rio Grande do Sul, Porto Alegre 90650-001, Brasil
| | - Bruno Aschidamini Prandi
- Departamento de Microbiologia, Imunologia e Parasitologia, Universidade Federal do Rio Grande do Sul, Porto Alegre 90035-003, Brasil
| | - Ana Cláudia Franco
- Departamento de Microbiologia, Imunologia e Parasitologia, Universidade Federal do Rio Grande do Sul, Porto Alegre 90035-003, Brasil
| | - Caroline Rigotto
- Departamento de Virologia, Instituto de Ciências da Saúde, Laboratório de Microbiologia Molecular Universidade Feevale, Novo Hamburgo 93525-075, Brasil E-mail:
| | - Fabiana Horn
- Departamento de Biofísica, Universidade Federal do Rio Grande do Sul, Porto Alegre 90650-001, Brasil
| |
Collapse
|
7
|
Mannarà G, Martinelli M, Giubbi C, Rizza M, Giordano E, Perdoni F, Bruno E, Morella A, Azzellino A, Turolla A, Pedrini R, Malpei F, La Rosa G, Suffredini E, Cereda D, Ammoni E, Villa S, Pregnolato F, Lavitrano M, Franzetti A, Musumeci R, Cocuzza CE. Wastewater Surveillance for SARS-CoV-2 in Northern Italy: An Evaluation of Three Different Gene Targets. Microorganisms 2025; 13:236. [PMID: 40005602 PMCID: PMC11857900 DOI: 10.3390/microorganisms13020236] [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: 12/31/2024] [Revised: 01/15/2025] [Accepted: 01/16/2025] [Indexed: 02/27/2025] Open
Abstract
Wastewater-based epidemiology has emerged as a complementary tool for the monitoring of COVID-19 pandemic waves and for the circulation of viral variants. The selection, standardization, and dynamics of different SARS-CoV-2 RNA targets in wastewater requires further investigation. In the present study, 106 wastewater samples were collected over a 24-month period from the wastewater treatment plant of Sondrio, north Italy, and were analyzed for the presence of SARS-CoV-2 RNA through the quantification of ORF1b, N1, and N3 gene targets via one-step real-time qPCR. In general, the three RNA targets demonstrated different performances and dynamics over the studied time period, underlying the usefulness of multiple viral targets in the surveillance of SARS-CoV-2 in wastewater. During the first 12 months, the quantification of the selected SARS-CoV-2 viral targets also correlated with the reported clinical cases in the same geographical area; however, from the overall data analysis this did not appear to significantly anticipate the epidemic waves. In conclusion, this study further supports the use of wastewater surveillance as a real time indicator of the human circulation of SARS-CoV-2. Moreover, the use of multiple viral gene targets has been shown to improve the reliability of SARS-CoV-2 surveillance in wastewater over time.
Collapse
Affiliation(s)
- Giulio Mannarà
- School of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy; (G.M.); (M.M.); (C.G.); (M.R.); (E.G.); (F.P.); (M.L.)
| | - Marianna Martinelli
- School of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy; (G.M.); (M.M.); (C.G.); (M.R.); (E.G.); (F.P.); (M.L.)
| | - Chiara Giubbi
- School of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy; (G.M.); (M.M.); (C.G.); (M.R.); (E.G.); (F.P.); (M.L.)
| | - Michelle Rizza
- School of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy; (G.M.); (M.M.); (C.G.); (M.R.); (E.G.); (F.P.); (M.L.)
| | - Eleonora Giordano
- School of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy; (G.M.); (M.M.); (C.G.); (M.R.); (E.G.); (F.P.); (M.L.)
| | - Federica Perdoni
- School of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy; (G.M.); (M.M.); (C.G.); (M.R.); (E.G.); (F.P.); (M.L.)
| | - Erika Bruno
- Department of Earth and Environmental, Sciences—DISAT, University of Milano-Bicocca, 20126 Milan, Italy; (E.B.); (A.F.)
| | - Annalisa Morella
- Società per l’Ecologia e l’Ambiente (SECAM) S.P.A., 23100 Sondrio, Italy;
| | - Arianna Azzellino
- Department of Civil and Environmental Engineering, Politecnico di Milano, 20133 Milan, Italy; (A.A.); (A.T.); (R.P.); (F.M.)
| | - Andrea Turolla
- Department of Civil and Environmental Engineering, Politecnico di Milano, 20133 Milan, Italy; (A.A.); (A.T.); (R.P.); (F.M.)
| | - Ramon Pedrini
- Department of Civil and Environmental Engineering, Politecnico di Milano, 20133 Milan, Italy; (A.A.); (A.T.); (R.P.); (F.M.)
| | - Francesca Malpei
- Department of Civil and Environmental Engineering, Politecnico di Milano, 20133 Milan, Italy; (A.A.); (A.T.); (R.P.); (F.M.)
| | - Giuseppina La Rosa
- National Center for Water Safety (CeNSia), Istituto Superiore di Sanità, 00161 Rome, Italy;
| | - Elisabetta Suffredini
- Department of Food Safety, Nutrition and Veterinary Public Health, Istituto Superiore di Sanità, 00161 Rome, Italy;
| | - Danilo Cereda
- UO Prevenzione, DG Welfare, Regione Lombardia, 20124 Milan, Italy; (D.C.); (E.A.); (F.P.)
| | - Emanuela Ammoni
- UO Prevenzione, DG Welfare, Regione Lombardia, 20124 Milan, Italy; (D.C.); (E.A.); (F.P.)
| | - Simone Villa
- Department of Computer Science, University of Milan, 20133 Milan, Italy;
| | - Francesca Pregnolato
- UO Prevenzione, DG Welfare, Regione Lombardia, 20124 Milan, Italy; (D.C.); (E.A.); (F.P.)
| | - Marialuisa Lavitrano
- School of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy; (G.M.); (M.M.); (C.G.); (M.R.); (E.G.); (F.P.); (M.L.)
| | - Andrea Franzetti
- Department of Earth and Environmental, Sciences—DISAT, University of Milano-Bicocca, 20126 Milan, Italy; (E.B.); (A.F.)
| | - Rosario Musumeci
- School of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy; (G.M.); (M.M.); (C.G.); (M.R.); (E.G.); (F.P.); (M.L.)
| | - Clementina E. Cocuzza
- School of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy; (G.M.); (M.M.); (C.G.); (M.R.); (E.G.); (F.P.); (M.L.)
| |
Collapse
|
8
|
Rosengart AL, Bidwell AL, Wolfe MK, Boehm AB, Townes FW. Spatiotemporal Variability of the Pepper Mild Mottle Virus Biomarker in Wastewater. ACS ES&T WATER 2025; 5:341-350. [PMID: 39816978 PMCID: PMC11731321 DOI: 10.1021/acsestwater.4c00866] [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: 09/10/2024] [Revised: 12/03/2024] [Accepted: 12/04/2024] [Indexed: 01/18/2025]
Abstract
Since the start of the coronavirus-19 pandemic, the use of wastewater-based epidemiology (WBE) for disease surveillance has increased throughout the world. Because wastewater measurements are affected by external factors, processing WBE data typically includes a normalization step in order to adjust wastewater measurements (e.g., viral ribonucleic acid (RNA) concentrations) to account for variation due to dynamic population changes, sewer travel effects, or laboratory methods. Pepper mild mottle virus (PMMoV), a plant RNA virus abundant in human feces and wastewater, has been used as a fecal contamination indicator and has been used to normalize wastewater measurements extensively. However, there has been little work to characterize the spatiotemporal variability of PMMoV in wastewater, which may influence the effectiveness of PMMoV for adjusting or normalizing WBE measurements. Here, we investigate its variability across space and time using data collected over a two-year period from sewage treatment plants across the United States. We find that most variation in PMMoV measurements can be attributed to longitude and latitude followed by site-specific variables. Further research into cross-geographical and -temporal comparability of PMMoV-normalized pathogen concentrations would strengthen the utility of PMMoV in WBE.
Collapse
Affiliation(s)
- AnnaElaine L. Rosengart
- Department
of Statistics & Data Science, Dietrich College of Humanities and
Social Sciences, Carnegie Mellon University, Pittsburgh, Pennsylvania 15213, United States
| | - Amanda L. Bidwell
- Department
of Civil & Environmental Engineering, School of Engineering and
Doerr School of Sustainability, Stanford
University, Stanford, California 94305, United States
| | - Marlene K. Wolfe
- Gangarosa
Department of Environmental Health, Rollins School of Public Health, Emory University, Atlanta, Georgia 30322, United States
| | - Alexandria B. Boehm
- Department
of Civil & Environmental Engineering, School of Engineering and
Doerr School of Sustainability, Stanford
University, Stanford, California 94305, United States
| | - F. William Townes
- Department
of Statistics & Data Science, Dietrich College of Humanities and
Social Sciences, Carnegie Mellon University, Pittsburgh, Pennsylvania 15213, United States
| |
Collapse
|
9
|
Thompson C, Leal CV, da Silva Faustino R, Leomil L, Jagadeeshwari U, Sharma R, de Oliveira M, Tschoeke D, Felix T, Macedo L, Khouri R, Koolen H, Landuci F, de Rezende C, Strobel Í, de Moraes L, P Ramos PI, de Souza H, Motta F, Barral-Netto M, Aguiar-Oliveira MDL, de Siqueira M, Sasikala C, Thompson F. Co-occurrence of SARS-CoV-2 variants in rivers and sewage in India and Brazil. THE SCIENCE OF THE TOTAL ENVIRONMENT 2025; 958:178089. [PMID: 39705959 DOI: 10.1016/j.scitotenv.2024.178089] [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] [Revised: 12/10/2024] [Accepted: 12/10/2024] [Indexed: 12/23/2024]
Abstract
The genomic monitoring of SARS-CoV-2 variants of concern (VOCs) in riverine and sewage water has been widely used as an epidemiological tool worldwide. But its utility for epidemiological assessments still needs to be evaluated in some areas. Our study encompassed thirteen Brazilian rivers spanning a vast urban expanse across the states of Rio de Janeiro, São Paulo, and Paraná. The sampled rivers in Rio de Janeiro are heavily contaminated with sewage. Meanwhile, the Indian samples were all wastewater before joining the water bodies from urban regions (Andhra Pradesh and Telangana). The viral copies were quantified using quantitative polymerase chain reaction (qPCR) in all examined samples (N = 91). The abundance of viral particles varied from 567 to 85,700,000 copies/ml. Subsequently, Illumina CovidSeq was applied to identify the major variants. In Brazil, while a single SARS-CoV-2 VOC was identified for just a few samples (6/50, 12 %), most samples harbored multiple VOCs (44/50, 88 %). In India only one probed sample had a single variant identified. Gamma (2021) and Omicron (2021 and 2022) were the most abundant variants. Delta and Omicron genetic material were detected in Rio de Janeiro city rivers before Brazil's first cases of these variants. Several negative samples in the Real-Time RT-PCR (qPCR) turned out to have SARS-CoV-2 sequences suggesting CovidSeq was more sensitive than RT-PCR for virus detection in environmental samples. Sewage surveillance holds promise for early detection of emerging variants driving pandemic waves, exemplified by the Delta and Omicron variants, potentially offering a preemptive advantage over clinical sample reports.
Collapse
Affiliation(s)
- Cristiane Thompson
- Laboratory of Microbiology, Instituto de Biologia, Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro, Brazil.
| | - Camille V Leal
- Laboratory of Microbiology, Instituto de Biologia, Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro, Brazil
| | | | - Luciana Leomil
- Laboratory of Microbiology, Instituto de Biologia, Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro, Brazil
| | - Uppada Jagadeeshwari
- Bacterial Discovery Laboratory, Centre for Environment, JNTUH University College Of Engineering, Science & Technology Hyderabad (UCESTH), India
| | - Richa Sharma
- Bacterial Discovery Laboratory, Centre for Environment, JNTUH University College Of Engineering, Science & Technology Hyderabad (UCESTH), India
| | - Marcelo de Oliveira
- Laboratory of Microbiology, Instituto de Biologia, Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro, Brazil
| | - Diogo Tschoeke
- Laboratory of Microbiology, Instituto de Biologia, Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro, Brazil
| | - Thais Felix
- Laboratory of Microbiology, Instituto de Biologia, Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro, Brazil
| | - Larissa Macedo
- Laboratory of Microbiology, Instituto de Biologia, Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro, Brazil
| | - Ricardo Khouri
- Medicine and Precision Health Laboratory (MeSP2), Instituto Gonçalo Moniz, FIOCRUZ, Bahia, Brazil
| | | | - Felipe Landuci
- Laboratory of Microbiology, Instituto de Biologia, Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro, Brazil
| | - Carlos de Rezende
- Laboratory of Environmental Sciences (LCA), Center of Biosciences and Biotechnology (CBB), State University of Northern of Rio de Janeiro Darcy Ribeiro (UENF), Campos dos Goytacazes, Brazil
| | - Ícaro Strobel
- Medicine and Precision Health Laboratory (MeSP2), Instituto Gonçalo Moniz, FIOCRUZ, Bahia, Brazil
| | - Laíse de Moraes
- Medicine and Precision Health Laboratory (MeSP2), Instituto Gonçalo Moniz, FIOCRUZ, Bahia, Brazil
| | - Pablo Ivan P Ramos
- Center for Data and Knowledge Integration for Health (CIDACS), Instituto Gonçalo Moniz, FIOCRUZ, Bahia, Brazil
| | - Heitor de Souza
- Department of Clinical Medicine, Hospital Universitário Clementino Fraga Filho (HUCFF), Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro, Brazil
| | - Fernando Motta
- Laboratory of Respiratory Viruses, Instituto Oswaldo Cruz -FIOCRUZ, Rio de Janeiro, Brazil
| | - Manoel Barral-Netto
- Medicine and Precision Health Laboratory (MeSP2), Instituto Gonçalo Moniz, FIOCRUZ, Bahia, Brazil
| | | | - Marilda de Siqueira
- Laboratory of Respiratory Viruses, Instituto Oswaldo Cruz -FIOCRUZ, Rio de Janeiro, Brazil
| | - Chintalapati Sasikala
- Bacterial Discovery Laboratory, Centre for Environment, JNTUH University College Of Engineering, Science & Technology Hyderabad (UCESTH), India; Smart Microbiological Services, 5-3-357, Rashtrapathi Road, Secunderabad 500003, India.
| | - Fabiano Thompson
- Laboratory of Microbiology, Instituto de Biologia, Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro, Brazil.
| |
Collapse
|
10
|
Meadows T, Coats ER, Narum S, Top EM, Ridenhour BJ, Stalder T. Epidemiological model can forecast COVID-19 outbreaks from wastewater-based surveillance in rural communities. WATER RESEARCH 2025; 268:122671. [PMID: 39488168 PMCID: PMC11614685 DOI: 10.1016/j.watres.2024.122671] [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: 03/05/2024] [Revised: 08/28/2024] [Accepted: 10/19/2024] [Indexed: 11/04/2024]
Abstract
Wastewater has emerged as a crucial tool for infectious disease surveillance, offering a valuable means to bridge the equity gap between underserved communities and larger urban municipalities. However, using wastewater surveillance in a predictive manner remains a challenge. In this study, we tested if detecting SARS-CoV-2 in wastewater can forecast outbreaks in rural communities. Under the CDC National Wastewater Surveillance program, we monitored the SARS-CoV-2 in the wastewater of five rural communities and a small city in Idaho (USA). We then used a particle filter method coupled with a stochastic susceptible-exposed-infectious-recovered (SEIR) model to infer active case numbers using quantities of SARS-CoV-2 in wastewater. Our findings revealed that while high daily variations in wastewater viral load made real-time interpretation difficult, the SEIR model successfully factored out this noise, enabling accurate forecasts of the Omicron outbreak in five of the six towns shortly after initial increases in SARS-CoV-2 concentrations were detected in wastewater. The model predicted outbreaks with a lead time of 0 to 11 days (average of 6 days +/- 4) before the surge in reported clinical cases. This study not only underscores the viability of wastewater-based epidemiology (WBE) in rural communities-a demographic often overlooked in WBE research-but also demonstrates the potential of advanced epidemiological modeling to enhance the predictive power of wastewater data. Our work paves the way for more reliable and timely public health guidance, addressing a critical gap in the surveillance of infectious diseases in rural populations.
Collapse
Affiliation(s)
- Tyler Meadows
- Department of Mathematics and Statistics, Queen's University, Kingston, Ontario, Canada; Institute for Modeling Collaboration and Innovation (IMCI), University of Idaho, Moscow, ID, USA
| | - Erik R Coats
- Department of Civil and Environmental Engineering, University of Idaho, Moscow, ID, USA; Institute for Modeling Collaboration and Innovation (IMCI), University of Idaho, Moscow, ID, USA; Bioinformatics and Computational Biology Graduate Program (BCB), Moscow, ID, USA
| | - Solana Narum
- Department of Civil and Environmental Engineering, University of Idaho, Moscow, ID, USA; Bioinformatics and Computational Biology Graduate Program (BCB), Moscow, ID, USA
| | - Eva M Top
- Institute for Modeling Collaboration and Innovation (IMCI), University of Idaho, Moscow, ID, USA; Bioinformatics and Computational Biology Graduate Program (BCB), Moscow, ID, USA; Department of Biological Sciences, University of Idaho, Moscow, ID, USA; Institute for Interdisciplinary Data Sciences (IIDS), University of Idaho, Moscow, ID, USA
| | - Benjamin J Ridenhour
- Institute for Modeling Collaboration and Innovation (IMCI), University of Idaho, Moscow, ID, USA; Bioinformatics and Computational Biology Graduate Program (BCB), Moscow, ID, USA; Institute for Interdisciplinary Data Sciences (IIDS), University of Idaho, Moscow, ID, USA; Department of Mathematics and Statistical Science, University of Idaho, Moscow, ID, USA
| | - Thibault Stalder
- Institute for Modeling Collaboration and Innovation (IMCI), University of Idaho, Moscow, ID, USA; Department of Biological Sciences, University of Idaho, Moscow, ID, USA; Institute for Interdisciplinary Data Sciences (IIDS), University of Idaho, Moscow, ID, USA; INSERM, CHU Limoges, RESINFIT, U1092, Univ. Limoges, F-87000, Limoges, France.
| |
Collapse
|
11
|
Mancini P, Brandtner D, Veneri C, Bonanno Ferraro G, Iaconelli M, Puzelli S, Facchini M, Di Mario G, Stefanelli P, Lucentini L, Muratore A, Suffredini E, La Rosa G. Evaluation of Trends in Influenza A and B Viruses in Wastewater and Human Surveillance Data: Insights from the 2022-2023 Season in Italy. FOOD AND ENVIRONMENTAL VIROLOGY 2024; 17:6. [PMID: 39644457 PMCID: PMC11625071 DOI: 10.1007/s12560-024-09622-2] [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: 08/06/2024] [Accepted: 11/21/2024] [Indexed: 12/09/2024]
Abstract
Wastewater-based epidemiology (WBE) is a recognized, dynamic approach to monitoring the transmission of pathogens in communities through urban wastewater. This study aimed to detect and quantify influenza A and B viruses in Italian wastewater during the 2022-2023 season (October 2022 to April 2023). A total of 298 wastewater samples were collected from 67 wastewater treatment plants (WTPs) across the country. These samples were analyzed for influenza A and B viruses (IAV, IBV) using primers originally developed by the Centers for Disease Control and Prevention (CDC) for real-time PCR and adapted for digital PCR. The overall detection rates of IAV and IBV across the entire study period were 19.1% and 16.8%, respectively. The prevalence of IAV in wastewater showed a gradual increase from October to December 2022, peaking at 61% in December. In contrast, IBV peaked at 36% in February 2023. This temporal discrepancy in peak concentrations suggests different seasonal patterns for the two influenza types. These trends mirrored human surveillance data, which showed influenza A cases peaking at 46% in late December and declining to around 2% by April 2023, and influenza B cases starting to increase significantly in January 2023 and peaking at about 14% in March. IAV concentrations ranged from 9.80 × 102 to 1.94 × 105 g.c./L, while IBV concentrations ranged from 1.07 × 103 to 1.43 × 104 g.c./L. Overall, the environmental data were consistent with the human surveillance trends observed during the study period in the country. These results demonstrate the value of WBE in tracking epidemiological patterns and highlight its potential as a complementary tool to infectious diseases surveillance systems.
Collapse
Affiliation(s)
- P Mancini
- National Center for Water Safety (CeNSiA), Istituto Superiore di Sanità, Viale Regina Elena 299, 00161, Rome, Italy
| | - D Brandtner
- Departments of Infectious Disease, Istituto Superiore di Sanità, Rome, Italy
| | - C Veneri
- National Center for Water Safety (CeNSiA), Istituto Superiore di Sanità, Viale Regina Elena 299, 00161, Rome, Italy
| | - G Bonanno Ferraro
- National Center for Water Safety (CeNSiA), Istituto Superiore di Sanità, Viale Regina Elena 299, 00161, Rome, Italy
| | - M Iaconelli
- National Center for Water Safety (CeNSiA), Istituto Superiore di Sanità, Viale Regina Elena 299, 00161, Rome, Italy
| | - S Puzelli
- Departments of Infectious Disease, Istituto Superiore di Sanità, Rome, Italy
| | - M Facchini
- Departments of Infectious Disease, Istituto Superiore di Sanità, Rome, Italy
| | - G Di Mario
- Departments of Infectious Disease, Istituto Superiore di Sanità, Rome, Italy
| | - P Stefanelli
- Departments of Infectious Disease, Istituto Superiore di Sanità, Rome, Italy
| | - L Lucentini
- National Center for Water Safety (CeNSiA), Istituto Superiore di Sanità, Viale Regina Elena 299, 00161, Rome, Italy
| | - A Muratore
- National Center for Water Safety (CeNSiA), Istituto Superiore di Sanità, Viale Regina Elena 299, 00161, Rome, Italy
| | - E Suffredini
- Department of Food Safety, Nutrition and Veterinary Public Health, Istituto Superiore di Sanità, Rome, Italy
| | - G La Rosa
- National Center for Water Safety (CeNSiA), Istituto Superiore di Sanità, Viale Regina Elena 299, 00161, Rome, Italy.
| |
Collapse
|
12
|
Veneri C, Brandtner D, Mancini P, Bonanno Ferraro G, Iaconelli M, Suffredini E, Petrillo M, Leoni G, Paracchini V, Gawlik BM, Marchini A, La Rosa G. Tracking the Spread of the BA.2.86 Lineage in Italy Through Wastewater Analysis. FOOD AND ENVIRONMENTAL VIROLOGY 2024; 16:449-457. [PMID: 38918335 PMCID: PMC11525314 DOI: 10.1007/s12560-024-09607-1] [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: 04/17/2024] [Accepted: 05/29/2024] [Indexed: 06/27/2024]
Abstract
The emergence of new SARS-CoV-2 variants poses challenges to global surveillance efforts, necessitating swift actions in their detection, evaluation, and management. Among the most recent variants, Omicron BA.2.86 and its sub-lineages have gained attention due to their potential immune evasion properties. This study describes the development of a digital PCR assay for the rapid detection of BA.2.86 and its descendant lineages, in wastewater samples. By using this assay, we analyzed wastewater samples collected in Italy from September 2023 to January 2024. Our analysis revealed the presence of BA.2.86 lineages already in October 2023 with a minimal detection rate of 2% which then rapidly increased, becoming dominant by January 2024, accounting for a prevalence of 62%. The findings emphasize the significance of wastewater-based surveillance in tracking emerging variants and underscore the efficacy of targeted digital PCR assays for environmental monitoring.
Collapse
Affiliation(s)
- C Veneri
- National Center for Water Safety (CeNSiA), Istituto Superiore di Sanità, Viale Regina Elena 299, 00161, Rome, Italy
| | - D Brandtner
- Department of Infectious Diseases, Istituto Superiore di Sanità, Rome, Italy
| | - P Mancini
- National Center for Water Safety (CeNSiA), Istituto Superiore di Sanità, Viale Regina Elena 299, 00161, Rome, Italy
| | - G Bonanno Ferraro
- National Center for Water Safety (CeNSiA), Istituto Superiore di Sanità, Viale Regina Elena 299, 00161, Rome, Italy
| | - M Iaconelli
- National Center for Water Safety (CeNSiA), Istituto Superiore di Sanità, Viale Regina Elena 299, 00161, Rome, Italy
| | - E Suffredini
- Department of Food Safety, Nutrition and Veterinary Public Health, Istituto Superiore di Sanità, Rome, Italy
| | - M Petrillo
- Seidor Italy S.r.l., 20129, Milan, Italy
| | - G Leoni
- European Commission, Joint Research Centre (JRC), Ispra, Italy
| | - V Paracchini
- European Commission, Joint Research Centre (JRC), Ispra, Italy
| | - B M Gawlik
- European Commission, Joint Research Centre (JRC), Ispra, Italy
| | - A Marchini
- European Commission, Joint Research Centre (JRC), Geel, Belgium
| | - G La Rosa
- National Center for Water Safety (CeNSiA), Istituto Superiore di Sanità, Viale Regina Elena 299, 00161, Rome, Italy.
| |
Collapse
|
13
|
Adeola AO, Paramo L, Fuoco G, Naccache R. Emerging hazardous chemicals and biological pollutants in Canadian aquatic systems and remediation approaches: A comprehensive status report. THE SCIENCE OF THE TOTAL ENVIRONMENT 2024; 954:176267. [PMID: 39278485 DOI: 10.1016/j.scitotenv.2024.176267] [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: 04/04/2024] [Revised: 09/04/2024] [Accepted: 09/12/2024] [Indexed: 09/18/2024]
Abstract
Emerging contaminants can be natural or synthetic materials, as well as materials of a chemical, or biological origin; these materials are typically not controlled or monitored in the environment. Canada is home to nearly 7 % of the world's renewable water supply and a wide range of different kinds of water systems, including the Great Lake, rivers, canals, gulfs, and estuaries. Although the majority of these pollutants are present in trace amounts (μg/L - ng/L concentrations), several studies have reported their detrimental impact on both human health and the biota. In Canadian aquatic environments, concentrations of pharmaceuticals (as high as 115 μg/L), pesticides (as high as 1.95 μg/L), bioavailable heavy metals like dissolved mercury (as high as 135 ng/L), and hydrocarbon/crude oil spills (as high as 4.5 million liters) have been documented. Biological threats such as genetic materials of the contagious SARS-CoV-2 virus have been reported in the provinces of Québec, Ontario, Saskatchewan and Manitoba provinces, as well as in the Nunavut territory, with a need for more holistic research. These toxins and emerging pollutants are associated with nefarious short and long-term health effects, with the potential for bioaccumulation in the environment. Hence, this Canadian-focused report provides the footprints for water and environmental sustainability, in light of this emerging threat to the environment and society. Several remediation pathways/tools that have been explored by Canadian researchers, existing challenges and prospects are also discussed. The review concludes with preventive measures and strategies for managing the inventory of emerging contaminants in the environment.
Collapse
Affiliation(s)
- Adedapo O Adeola
- Department of Chemistry and Biochemistry and the Centre for NanoScience Research, Concordia University, Montreal, QC H4B 1R6, Canada; Quebec Centre for Advanced Materials, Department of Chemistry and Biochemistry, Concordia University, Montreal, QC H4B 1R6, Canada.
| | - Luis Paramo
- Department of Chemistry and Biochemistry and the Centre for NanoScience Research, Concordia University, Montreal, QC H4B 1R6, Canada; Quebec Centre for Advanced Materials, Department of Chemistry and Biochemistry, Concordia University, Montreal, QC H4B 1R6, Canada
| | - Gianluca Fuoco
- Department of Chemistry and Biochemistry and the Centre for NanoScience Research, Concordia University, Montreal, QC H4B 1R6, Canada; Quebec Centre for Advanced Materials, Department of Chemistry and Biochemistry, Concordia University, Montreal, QC H4B 1R6, Canada
| | - Rafik Naccache
- Department of Chemistry and Biochemistry and the Centre for NanoScience Research, Concordia University, Montreal, QC H4B 1R6, Canada; Quebec Centre for Advanced Materials, Department of Chemistry and Biochemistry, Concordia University, Montreal, QC H4B 1R6, Canada.
| |
Collapse
|
14
|
Kadam PP, Mestry T, Mistry N, Nilgiriwala KS. Wastewater-based genomic surveillance of SARS-CoV-2 in vulnerable communities in Mumbai. Indian J Med Res 2024; 160:570-577. [PMID: 39913514 PMCID: PMC11801778 DOI: 10.25259/ijmr_299_24] [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: 02/16/2024] [Accepted: 08/30/2024] [Indexed: 02/11/2025] Open
Abstract
Background & objectives The global impact of COVID-19, with over 45 million cases and 533,300 deaths in India alone, necessitates effective surveillance methods. Traditional approaches face challenges in detecting pre-symptomatic and asymptomatic cases, prompting the exploration of wastewater-based epidemiology (WBE). This study focuses on Mumbai's vulnerable slums, aiming to assess the potential of WBE as an alternative surveillance method. Methods Genomic surveillance of SARS-CoV-2 was conducted in Mumbai's vulnerable settings (slums) for 11 months (August 2022 to June 2023). Wastewater samples from open drains and sewage treatment plants were correlated with reported COVID-19 cases in the city. Early detection of emerging viral variants and seasonal variations in viral load were explored. Results Correlations were identified between wastewater samples and reported COVID-19 cases in Mumbai's vulnerable slums, with early detection occurring three weeks before clinical diagnoses, underscoring the potential utility of WBE. Genomic sequencing provided insights into the viral variants, identifying shifts in predominant variants. Seasonal variations showed higher viral concentrations in summer and monsoon, potentially associated with accelerated droplet evaporation in early summer and droplet-based transmission during mid-summer and monsoon. Interpretation & conclusions Wastewater-based epidemiology emerges as a cost-effective and rapid early warning system, providing crucial insights into virus behaviour and evolution. Particularly significant for countries like India, WBE aids in outbreak monitoring and targeted interventions. The global integration of wastewater surveillance emphasizes its importance in comprehensive pandemic monitoring, establishing it as an integral component of public health strategies worldwide.
Collapse
Affiliation(s)
| | - Tejal Mestry
- Department of Tuberculosis, The Foundation for Medical Research, Mumbai, India
| | - Nerges Mistry
- Department of Tuberculosis, The Foundation for Medical Research, Mumbai, India
| | | |
Collapse
|
15
|
Yang S, Jiao Y, Dong Q, Li S, Xu C, Liu Y, Sun L, Huang X. Evaluating approach uncertainties of quantitative detection of SARS-CoV-2 in wastewater: Concentration, extraction and amplification. THE SCIENCE OF THE TOTAL ENVIRONMENT 2024; 951:175285. [PMID: 39102960 DOI: 10.1016/j.scitotenv.2024.175285] [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: 01/17/2024] [Revised: 06/10/2024] [Accepted: 08/02/2024] [Indexed: 08/07/2024]
Abstract
Substantial uncertainties pose challenges to the accuracy of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) quantification in wastewater. We conducted a comprehensive evaluation of two concentration methods, three nucleic acid extraction methods, and the amplification performance of eight primer-probe sets. Our results showed that the two concentration methods exhibited similar recovery rates. Specifically, using a 30 kDa cut-off ultrafilter and a centrifugal force of 2500 g achieved the highest virus recovery rates (27.32 ± 8.06 % and 26.37 ± 7.77 %, respectively), with lower corresponding quantification uncertainties of 29.51 % and 29.47 % in ultrafiltration methods. Similarly, a 15 % PEG concentration with 1.5 M NaCl markedly improved virus recovery (26.76 ± 5.92 % and 28.47 ± 6.74 %, respectively), and reducing variation to 22.16 % and 23.66 % in the PEG precipitation method. Additionally, employing a vigorous bead-beating approach at 6 m/s during viral RNA extraction significantly increased RNA yield, with an efficiency reaching up to 82.18 %. Among the evaluated eight primer-probe sets, the E_Sarbeco primer-probe set provided the most stable and consistent quantitative results across various sample matrices. These findings are crucial for establishing robust viral quantification protocols and enhancing methodological precision for effective wastewater surveillance, enabling sensitive and precise detection of SARS-CoV-2.
Collapse
Affiliation(s)
- Shaolin Yang
- State Key Joint Laboratory of Environment Simulation and Pollution Control, School of Environment, Tsinghua University, Beijing 10084, China
| | - Yang Jiao
- Beijing Chaoyang Center for Disease Control and Prevention, Beijing 100021, China
| | - Qian Dong
- State Key Joint Laboratory of Environment Simulation and Pollution Control, School of Environment, Tsinghua University, Beijing 10084, China
| | - Siqi Li
- State Key Joint Laboratory of Environment Simulation and Pollution Control, School of Environment, Tsinghua University, Beijing 10084, China
| | - Chenyang Xu
- State Key Joint Laboratory of Environment Simulation and Pollution Control, School of Environment, Tsinghua University, Beijing 10084, China
| | - Yanchen Liu
- State Key Joint Laboratory of Environment Simulation and Pollution Control, School of Environment, Tsinghua University, Beijing 10084, China.
| | - Lingli Sun
- Beijing Chaoyang Center for Disease Control and Prevention, Beijing 100021, China.
| | - Xia Huang
- State Key Joint Laboratory of Environment Simulation and Pollution Control, School of Environment, Tsinghua University, Beijing 10084, China.
| |
Collapse
|
16
|
Bastardo-Méndez M, Rangel HR, Pujol FH, Grillet ME, Jaspe RC, Malaver N, Rodríguez M, Zamora-Figueroa A. Detection of SARS-CoV-2 in wastewater as an earlier predictor of COVID-19 epidemic peaks in Venezuela. Sci Rep 2024; 14:27294. [PMID: 39516586 PMCID: PMC11549330 DOI: 10.1038/s41598-024-78982-3] [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: 06/03/2024] [Accepted: 11/05/2024] [Indexed: 11/16/2024] Open
Abstract
Wastewater-based epidemiological surveillance has proven to be a useful and cost-effective tool for detecting COVID-19 outbreaks. Here, our objective was to evaluate its potential as an early warning system in Venezuela by detecting SARS-CoV-2 RNA in wastewater and its correlation with reported cases of COVID-19. Viral RNA was concentrated from wastewater collected at various sites in Caracas (northern Venezuela), from September 2021 to July 2023, using the polyethylene glycol (PEG) precipitation method. Viral quantification was performed by RT-qPCR targeting the N1 and ORF1ab genes. A significant association (p < 0.05) was found between viral load in wastewater and reported cases of COVID-19 up to six days after sampling. During the whole study, two populated areas of the city were persistent hotspots of viral infection. The L452R mutation, suggestive of the presence of the Delta variant, was identified in the only sample where a complete genomic sequence could be obtained. Significant differences (p < 0.05) between the physicochemical conditions of the wastewater samples positive and negative for the virus were found. Our results support proof of concept that wastewater surveillance can serve as an early warning system for SARS-CoV-2 outbreaks, complementing public health surveillance in those regions where COVID-19 is currently underreported.
Collapse
Affiliation(s)
- Marjorie Bastardo-Méndez
- Laboratorio de Ecología de Microorganismos, Centro de Ecología Aplicada, Instituto de Zoología y Ecología Tropical, Facultad de Ciencias, Universidad Central de Venezuela (UCV), Caracas, Venezuela
| | - Héctor R Rangel
- Laboratorio de Virología Molecular, Centro de Microbiología y Biología Celular, Instituto Venezolano de Investigaciones Científicas (IVIC), Altos de Pipe, Miranda, Venezuela
| | - Flor H Pujol
- Laboratorio de Virología Molecular, Centro de Microbiología y Biología Celular, Instituto Venezolano de Investigaciones Científicas (IVIC), Altos de Pipe, Miranda, Venezuela
| | - María-Eugenia Grillet
- Centro de Ecología y Evolución, Instituto de Zoología y Ecología Tropical, Facultad de Ciencias, Universidad Central de Venezuela (UCV), Caracas, Venezuela
| | - Rossana C Jaspe
- Laboratorio de Virología Molecular, Centro de Microbiología y Biología Celular, Instituto Venezolano de Investigaciones Científicas (IVIC), Altos de Pipe, Miranda, Venezuela
| | - Nora Malaver
- Laboratorio de Ecología de Microorganismos, Centro de Ecología Aplicada, Instituto de Zoología y Ecología Tropical, Facultad de Ciencias, Universidad Central de Venezuela (UCV), Caracas, Venezuela
| | - María Rodríguez
- Laboratorio de Ecología de Microorganismos, Centro de Ecología Aplicada, Instituto de Zoología y Ecología Tropical, Facultad de Ciencias, Universidad Central de Venezuela (UCV), Caracas, Venezuela
| | - Alejandra Zamora-Figueroa
- Laboratorio de Ecología de Microorganismos, Centro de Ecología Aplicada, Instituto de Zoología y Ecología Tropical, Facultad de Ciencias, Universidad Central de Venezuela (UCV), Caracas, Venezuela.
- Laboratorio de Virología Molecular, Centro de Microbiología y Biología Celular, Instituto Venezolano de Investigaciones Científicas (IVIC), Altos de Pipe, Miranda, Venezuela.
| |
Collapse
|
17
|
Mercier E, D'Aoust PM, Renouf E, Tomalty E, Addo FG, Nguyen TB, Wong CH, Ramsay NT, Tian X, Hegazy N, Kabir MP, Jia JJ, Wan S, Pisharody L, Szulc P, MacKenzie AE, Delatolla R. Effective method to mitigate impact of rain or snowmelt sewer flushing events on wastewater-based surveillance measurements. THE SCIENCE OF THE TOTAL ENVIRONMENT 2024; 956:177351. [PMID: 39489448 DOI: 10.1016/j.scitotenv.2024.177351] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Subscribe] [Scholar Register] [Received: 07/12/2024] [Revised: 10/03/2024] [Accepted: 10/31/2024] [Indexed: 11/05/2024]
Abstract
Wastewater-based surveillance (WBS) is increasingly used for monitoring disease targets in wastewaters around the world. This study, performed in Ottawa, Canada, identifies a decrease in SARS-CoV-2 wastewater measurements during snowmelt-induced sewer flushing events. Observations first revealed a correlation between suppressed viral measurements and periods of increased sewage flowrates, air temperatures above 0 °C during winter months, and solids mass flux increases. These correlations suggest that high sewage flowrates from snowmelt events or intense precipitation events lead to the scouring of previously settled solids in sewers and the subsequent entrainment of these solids into the transported wastewaters. Collection of WBS samples during flushing events hence contains a heterogeneous mixture of solids, including resuspended solids with varying degrees of decay. Therefore flushing events can present a challenge for accurately measuring disease target viral signals when using solids-based analytical methods. This study demonstrates that resuspended solids entrained in the wastewaters during flushing events retain PMMoV signal while the SARS-CoV-2 signal is significantly reduced due to the slower decay rate of pepper mild mottle virus (PMMoV) compared to SARS-CoV-2 within wastewaters. Hence current normalization methods using PMMoV are shown to be ineffective in correcting for flushing events and the associated resuspension of settled solids, as the PMMoV signal of settled solids within sewers does not account for the differential decay rates experiences by SARS-CoV-2 signal in settled solids. Instead, this study identifies RNA to PMMoV correction factor as an effective approach to correct for flushing events and to realign SARS-CoV-2 signal with COVID-19 hospital admission rates within communities. As such, the study highlights the key physicochemical parameters necessary to identify flushing events that affect SARS-CoV-2 WBS measurements and introduces a novel RNA to PMMoV correction factor approach for solids-based analysis of SARS-CoV-2 during flushing events, enhancing the accuracy of WBS data for public health decision-making.
Collapse
Affiliation(s)
- Elisabeth Mercier
- Department of Civil Engineering, University of Ottawa, Ottawa K1N 6N5, Canada
| | - Patrick M D'Aoust
- Department of Civil Engineering, University of Ottawa, Ottawa K1N 6N5, Canada
| | - Elizabeth Renouf
- Department of Civil Engineering, University of Ottawa, Ottawa K1N 6N5, Canada
| | - Emma Tomalty
- Department of Civil Engineering, University of Ottawa, Ottawa K1N 6N5, Canada
| | - Felix G Addo
- Department of Civil Engineering, University of Ottawa, Ottawa K1N 6N5, Canada
| | - Tram Bich Nguyen
- Department of Civil Engineering, University of Ottawa, Ottawa K1N 6N5, Canada
| | - Chandler H Wong
- Department of Civil Engineering, University of Ottawa, Ottawa K1N 6N5, Canada
| | - Nathan T Ramsay
- Department of Civil Engineering, University of Ottawa, Ottawa K1N 6N5, Canada
| | - Xin Tian
- Department of Civil Engineering, University of Ottawa, Ottawa K1N 6N5, Canada
| | - Nada Hegazy
- Department of Civil Engineering, University of Ottawa, Ottawa K1N 6N5, Canada
| | - Md Pervez Kabir
- Department of Civil Engineering, University of Ottawa, Ottawa K1N 6N5, Canada
| | - Jian-Jun Jia
- Department of Civil Engineering, University of Ottawa, Ottawa K1N 6N5, Canada
| | - Shen Wan
- Department of Civil Engineering, University of Ottawa, Ottawa K1N 6N5, Canada
| | - Lakshmi Pisharody
- Department of Civil Engineering, University of Ottawa, Ottawa K1N 6N5, Canada
| | - Pawel Szulc
- City of Ottawa (Engineering Services), Ottawa K1J 1K6, Canada
| | - Alex E MacKenzie
- Children's Hospital of Eastern Ontario Research Institute, Ottawa K1H 8L1, Canada
| | - Robert Delatolla
- Department of Civil Engineering, University of Ottawa, Ottawa K1N 6N5, Canada.
| |
Collapse
|
18
|
Yang Y, Tan J, Wang F, Sun W, Shi H, Cheng Z, Xie Y, Zhou X. Preconcentration and detection of SARS-CoV-2 in wastewater: A comprehensive review. Biosens Bioelectron 2024; 263:116617. [PMID: 39094290 DOI: 10.1016/j.bios.2024.116617] [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: 05/22/2024] [Revised: 07/17/2024] [Accepted: 07/29/2024] [Indexed: 08/04/2024]
Abstract
Severe acute respiratory syndrome coronaviruses 2 (SARS-CoV-2) causing coronavirus disease 2019 (COVID-19) affected the health of human beings and the global economy. The patients with SARS-CoV-2 infection had viral RNA or live infectious viruses in feces. Thus, the possible transmission of SARS-CoV-2 through wastewater received great attentions. Moreover, SARS-CoV-2 in wastewater can serve as an early indicator of the infection within communities. We summarized the preconcentration and detection technology of SARS-CoV-2 in wastewater aiming at the complex matrices of wastewater and low virus concentration and compared their performance characteristics. We described the emerging tests that would be possible to realize the rapid detection of SARS-CoV-2 in fields and encourage academics to advance their technologies beyond conception. We concluded with a brief discussion on the outlook for integrating preconcentration and the detection of SARS-CoV-2 with emerging technologies.
Collapse
Affiliation(s)
- Yihan Yang
- School of Environment, Tsinghua University, Beijing, 100084, China
| | - Jisui Tan
- School of Environment, Tsinghua University, Beijing, 100084, China
| | - Fan Wang
- School of Environment, Tsinghua University, Beijing, 100084, China
| | - Weiming Sun
- School of Environment, Tsinghua University, Beijing, 100084, China
| | - Hanchang Shi
- School of Environment, Tsinghua University, Beijing, 100084, China
| | - Zhao Cheng
- School of Environment, Tsinghua University, Beijing, 100084, China
| | - Yangcun Xie
- Chinese Academy of Environmental Planning, Beijing, 100043, China.
| | - Xiaohong Zhou
- School of Environment, Tsinghua University, Beijing, 100084, China.
| |
Collapse
|
19
|
Chen X, Balliew J, Bauer CX, Deegan J, Gitter A, Hanson BM, Maresso AW, Tisza MJ, Troisi CL, Rios J, Mena KD, Boerwinkle E, Wu F. Revealing patterns of SARS-CoV-2 variant emergence and evolution using RBD amplicon sequencing of wastewater. J Infect 2024; 89:106284. [PMID: 39341403 DOI: 10.1016/j.jinf.2024.106284] [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: 07/18/2024] [Revised: 09/06/2024] [Accepted: 09/20/2024] [Indexed: 10/01/2024]
Abstract
OBJECTIVES Rapid evolution of SARS-CoV-2 has resulted in the emergence of numerous variants, posing significant challenges to public health surveillance. Clinical genome sequencing, while valuable, has limitations in capturing the full epidemiological dynamics of circulating variants in the general population. This study aimed to monitor the SARS-CoV-2 variant community dynamics and evolution using receptor-binding domain (RBD) amplicon sequencing of wastewater samples. METHODS We sequenced wastewater from El Paso, Texas, over 17 months, compared the sequencing data with clinical genome data, and performed biodiversity analysis to reveal SARS-CoV-2 variant dynamics and evolution. RESULTS We identified 91 variants and observed waves of dominant variants transitioning from BA.2 to BA.2.12.1, BA.4&5, BQ.1, and XBB.1.5. Comparison with clinical genome sequencing data revealed earlier detection of variants and identification of unreported outbreaks. Our results also showed strong consistency with clinical data for dominant variants at the local, state, and national levels. Alpha diversity analyses revealed significant seasonal variations, with the highest diversity observed in winter. By segmenting the outbreak into lag, growth, stationary, and decline phases, we found higher variant diversity during the lag phase, likely due to lower inter-variant competition preceding outbreak growth. CONCLUSIONS Our findings underscore the importance of low transmission periods in facilitating rapid mutation and variant evolution. Our approach, integrating RBD amplicon sequencing with wastewater surveillance, demonstrates effectiveness in tracking viral evolution and understanding variant emergence, thus enhancing public health preparedness.
Collapse
Affiliation(s)
- Xingwen Chen
- School of Public Health, University of Texas Health Science Center at Houston, TX, USA; Texas Epidemic Public Health Institute (TEPHI), UTHealth Houston, Houston, TX, USA
| | | | - Cici X Bauer
- School of Public Health, University of Texas Health Science Center at Houston, TX, USA; Texas Epidemic Public Health Institute (TEPHI), UTHealth Houston, Houston, TX, USA
| | - Jennifer Deegan
- School of Public Health, University of Texas Health Science Center at Houston, TX, USA; Texas Epidemic Public Health Institute (TEPHI), UTHealth Houston, Houston, TX, USA
| | - Anna Gitter
- School of Public Health, University of Texas Health Science Center at Houston, TX, USA; Texas Epidemic Public Health Institute (TEPHI), UTHealth Houston, Houston, TX, USA
| | - Blake M Hanson
- School of Public Health, University of Texas Health Science Center at Houston, TX, USA; Texas Epidemic Public Health Institute (TEPHI), UTHealth Houston, Houston, TX, USA
| | - Anthony W Maresso
- TAILOR Labs, Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, TX, USA
| | - Michael J Tisza
- The Alkek Center for Metagenomics and Microbiome Research, Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, TX, USA
| | - Catherine L Troisi
- School of Public Health, University of Texas Health Science Center at Houston, TX, USA; Texas Epidemic Public Health Institute (TEPHI), UTHealth Houston, Houston, TX, USA
| | - Janelle Rios
- School of Public Health, University of Texas Health Science Center at Houston, TX, USA; Texas Epidemic Public Health Institute (TEPHI), UTHealth Houston, Houston, TX, USA
| | - Kristina D Mena
- School of Public Health, University of Texas Health Science Center at Houston, TX, USA; Texas Epidemic Public Health Institute (TEPHI), UTHealth Houston, Houston, TX, USA
| | - Eric Boerwinkle
- School of Public Health, University of Texas Health Science Center at Houston, TX, USA; Texas Epidemic Public Health Institute (TEPHI), UTHealth Houston, Houston, TX, USA
| | - Fuqing Wu
- School of Public Health, University of Texas Health Science Center at Houston, TX, USA; Texas Epidemic Public Health Institute (TEPHI), UTHealth Houston, Houston, TX, USA.
| |
Collapse
|
20
|
Shanmugam BK, Alqaydi M, Abdisalam D, Shukla M, Santos H, Samour R, Petalidis L, Oliver CM, Brudecki G, Salem SB, Elamin W. A Narrative Review of High Throughput Wastewater Sample Processing for Infectious Disease Surveillance: Challenges, Progress, and Future Opportunities. INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH 2024; 21:1432. [PMID: 39595699 PMCID: PMC11593539 DOI: 10.3390/ijerph21111432] [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: 09/05/2024] [Revised: 10/09/2024] [Accepted: 10/15/2024] [Indexed: 11/28/2024]
Abstract
During the recent COVID-19 pandemic, wastewater-based epidemiological (WBE) surveillance played a crucial role in evaluating infection rates, analyzing variants, and identifying hot spots in a community. This expanded the possibilities for using wastewater to monitor the prevalence of infectious diseases. The full potential of WBE remains hindered by several factors, such as a lack of information on the survival of pathogens in sewage, heterogenicity of wastewater matrices, inconsistent sampling practices, lack of standard test methods, and variable sensitivity of analytical techniques. In this study, we review the aforementioned challenges, cost implications, process automation, and prospects of WBE for full-fledged wastewater-based community health screening. A comprehensive literature survey was conducted using relevant keywords, and peer reviewed articles pertinent to our research focus were selected for this review with the aim of serving as a reference for research related to wastewater monitoring for early epidemic detection.
Collapse
Affiliation(s)
| | - Maryam Alqaydi
- RASID Laboratory, M42 Healthcare, Abu Dhabi P.O. Box 4200, United Arab Emirates
| | - Degan Abdisalam
- RASID Laboratory, M42 Healthcare, Abu Dhabi P.O. Box 4200, United Arab Emirates
| | - Monika Shukla
- RASID Laboratory, M42 Healthcare, Abu Dhabi P.O. Box 4200, United Arab Emirates
| | - Helio Santos
- RASID Laboratory, M42 Healthcare, Abu Dhabi P.O. Box 4200, United Arab Emirates
| | - Ranya Samour
- RASID Laboratory, M42 Healthcare, Abu Dhabi P.O. Box 4200, United Arab Emirates
| | - Lawrence Petalidis
- RASID Laboratory, M42 Healthcare, Abu Dhabi P.O. Box 4200, United Arab Emirates
| | | | - Grzegorz Brudecki
- RASID Laboratory, M42 Healthcare, Abu Dhabi P.O. Box 4200, United Arab Emirates
| | - Samara Bin Salem
- Abu Dhabi Quality and Conformity Council (ADQCC), Abu Dhabi P.O. Box 2282, United Arab Emirates
| | - Wael Elamin
- RASID Laboratory, M42 Healthcare, Abu Dhabi P.O. Box 4200, United Arab Emirates
| |
Collapse
|
21
|
Freitas JF, Oliveira TT, Agnez-Lima LF. Metaviromic reveals the dynamics and diversity of the virosphere in wastewater samples from Natal, Brazil. ENVIRONMENTAL POLLUTION (BARKING, ESSEX : 1987) 2024; 359:124752. [PMID: 39154883 DOI: 10.1016/j.envpol.2024.124752] [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: 05/09/2024] [Revised: 07/03/2024] [Accepted: 07/28/2024] [Indexed: 08/20/2024]
Abstract
The COVID-19 pandemic underscored the significance of omics technology and Wastewater-Based Epidemiology for epidemic preparedness. This study investigates the virosphere in wastewater samples from Natal (Brazil), aiming to understand its structure, relationships, and potential. Metaviromic analysis was used on DNA and RNA from weekly samples collected over a year (June/2021 to May/2022) from three wastewater treatment plants. The virosphere showed stability, particularly in viruses infecting microorganisms and plants. However, an alternation of representatives of viruses that infect animals has been observed. Among the most abundant viruses infecting microorganisms are genera associated with the bacterial genera Escherichia, Pseudomonas, and Caulobacte. Regarding the viruses infecting plants, Sobemovirus and Tobamovirus are the most abundant genera. Odontoglossum ringspot virus was identified as a possible RNA virus biomarker. Among DNA viruses infecting animals, genera Bocaparvovirus and Mastadenovirus are the most prevalent. Intriguingly, some Poxviridae family members were observed in the samples. Co-occurrence network analysis identified potential biomarkers like Volepox virus, Anatid herpesvirus 1, and Caviid herpesvirus 2. Among RNA viruses affecting animals, Mamastrovirus, Rotavirus, and Norovirus genera were the most abundant pathogens. Furthermore, members of the Coronaviridae family exhibited a high degree of centrality values in the co-occurrence network, even connecting with unclassified viruses. The study emphasizes the importance of research in understanding the roles of unclassified viruses. In addition, we observed an association between Coronaviridae reads, rainfall, and the number of reported COVID-19 cases. Our study highlights the diversity and complexity of the viral community in wastewater and the need for research to understand better the ecological roles unclassified viruses play. Such advances will significantly contribute to our preparedness and response to future viral threats. Furthermore, our study contributes to knowledge of virosphere dynamics, offering insights that can contribute to the direction of future public health policies and interventions.
Collapse
Affiliation(s)
- Júlia Firme Freitas
- Laboratório de Biologia Molecular e Genômica, Centro de Biociências, Departamento de Genética, Universidade Federal do Rio Grande do Norte, Natal, Brazil
| | - Thais Teixeira Oliveira
- Laboratório de Biologia Molecular e Genômica, Centro de Biociências, Departamento de Genética, Universidade Federal do Rio Grande do Norte, Natal, Brazil
| | - Lucymara Fassarella Agnez-Lima
- Laboratório de Biologia Molecular e Genômica, Centro de Biociências, Departamento de Genética, Universidade Federal do Rio Grande do Norte, Natal, Brazil.
| |
Collapse
|
22
|
Shelton K, Deshpande GN, Sanchez GJ, Vogel JR, Miller AC, Florea G, Jeffries ER, De Leόn KB, Stevenson B, Kuhn KG. Real-Time Monitoring of SARS-CoV-2 Variants in Oklahoma Wastewater through Allele-Specific RT-qPCR. Microorganisms 2024; 12:2001. [PMID: 39458310 PMCID: PMC11509313 DOI: 10.3390/microorganisms12102001] [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: 09/04/2024] [Revised: 09/27/2024] [Accepted: 09/30/2024] [Indexed: 10/28/2024] Open
Abstract
During the COVID-19 pandemic, wastewater surveillance was used to monitor community transmission of SARS-CoV-2. As new genetic variants emerged, the need for timely identification of these variants in wastewater became an important focus. In response to increased reports of Omicron transmission across the United States, the Oklahoma Wastewater Surveillance team utilized allele-specific RT-qPCR assays to detect and differentiate variants, such as Omicron, from other variants found in wastewater in Oklahoma. The PCR assays showed presence of the Omicron variant in Oklahoma on average two weeks before official reports, which was confirmed through genomic sequencing of selected wastewater samples. Through continued surveillance from November 2021 to January 2022, we also demonstrated the transition from prevalence of the Delta variant to prevalence of the Omicron variant in local communities. We further assessed how this transition correlated with certain demographic factors characterizing each community. Our results highlight RT-qPCR assays as a rapid, simple, and cost-effective method for monitoring the community spread of SARS-CoV-2 genetic variants in wastewater. Additionally, they demonstrate that specific demographic factors such as ethnic composition and household income can correlate with the timing of SARS-CoV-2 variant introduction and spread.
Collapse
Affiliation(s)
- Kristen Shelton
- School of Civil Engineering and Environmental Science, University of Oklahoma, Norman, OK 73071, USA; (K.S.); (G.J.S.); (J.R.V.); (A.C.M.)
| | - Gargi N. Deshpande
- Department of Biostatistics and Epidemiology, Hudson College of Public Health, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA;
| | - Gilson J. Sanchez
- School of Civil Engineering and Environmental Science, University of Oklahoma, Norman, OK 73071, USA; (K.S.); (G.J.S.); (J.R.V.); (A.C.M.)
| | - Jason R. Vogel
- School of Civil Engineering and Environmental Science, University of Oklahoma, Norman, OK 73071, USA; (K.S.); (G.J.S.); (J.R.V.); (A.C.M.)
| | - A. Caitlin Miller
- School of Civil Engineering and Environmental Science, University of Oklahoma, Norman, OK 73071, USA; (K.S.); (G.J.S.); (J.R.V.); (A.C.M.)
| | - Gabriel Florea
- Oklahoma Medical Research Foundation, Oklahoma City, OK 73104, USA;
| | - Erin R. Jeffries
- School of Biological Sciences, University of Oklahoma, Norman, OK 73019, USA; (E.R.J.); (K.B.D.L.); (B.S.)
| | - Kara B. De Leόn
- School of Biological Sciences, University of Oklahoma, Norman, OK 73019, USA; (E.R.J.); (K.B.D.L.); (B.S.)
| | - Bradley Stevenson
- School of Biological Sciences, University of Oklahoma, Norman, OK 73019, USA; (E.R.J.); (K.B.D.L.); (B.S.)
- Earth and Planetary Science, Northwestern University, Evanston, IL 60208, USA
| | - Katrin Gaardbo Kuhn
- Department of Biostatistics and Epidemiology, Hudson College of Public Health, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA;
| |
Collapse
|
23
|
Diamanti C, Nousis L, Bozidis P, Koureas M, Kyritsi M, Markozannes G, Simantiris N, Panteli E, Koutsolioutsou A, Tsilidis K, Hadjichristodoulou C, Koutsotoli A, Christaki E, Alivertis D, Bartzokas A, Gartzonika K, Dovas C, Ntzani E. Wastewater Surveillance of SARS-CoV-2: A Comparison of Two Concentration Methods. Viruses 2024; 16:1398. [PMID: 39339875 PMCID: PMC11436116 DOI: 10.3390/v16091398] [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: 08/05/2024] [Revised: 08/27/2024] [Accepted: 08/28/2024] [Indexed: 09/30/2024] Open
Abstract
Wastewater surveillance is crucial for the epidemiological monitoring of SARS-CoV-2. Various concentration techniques, such as skimmed milk flocculation (SMF) and polyethylene glycol (PEG) precipitation, are employed to isolate the virus effectively. This study aims to compare these two methods and determine the one with the superior recovery rates. From February to December 2021, 24-h wastewater samples were collected from the Ioannina Wastewater Treatment Plant's inlet and processed using both techniques. Subsequent viral genome isolation and a real-time RT-qPCR detection of SARS-CoV-2 were performed. The quantitative analysis demonstrated a higher detection sensitivity with a PEG-based concentration than SMF. Moreover, when the samples were positive by both methods, PEG consistently yielded higher viral loads. These findings underscore the need for further research into concentration methodologies and the development of precise protocols to enhance epidemiological surveillance through wastewater analysis.
Collapse
Affiliation(s)
- Christina Diamanti
- Department of Hygiene and Epidemiology, Faculty of Medicine, University of Ioannina, 45100 Ioannina, Greece; (C.D.); (L.N.); (G.M.); (N.S.); (E.P.); (K.T.); (A.K.)
| | - Lambros Nousis
- Department of Hygiene and Epidemiology, Faculty of Medicine, University of Ioannina, 45100 Ioannina, Greece; (C.D.); (L.N.); (G.M.); (N.S.); (E.P.); (K.T.); (A.K.)
| | - Petros Bozidis
- Department of Microbiology, Faculty of Medicine, School of Health Sciences, University of Ioannina, 45110 Ioannina, Greece; (P.B.); (K.G.)
| | - Michalis Koureas
- Laboratory of Hygiene and Epidemiology, Faculty of Medicine, University of Thessaly, 22 Papakyriazi Str., 41222 Larissa, Greece; (M.K.); (M.K.); (C.H.)
| | - Maria Kyritsi
- Laboratory of Hygiene and Epidemiology, Faculty of Medicine, University of Thessaly, 22 Papakyriazi Str., 41222 Larissa, Greece; (M.K.); (M.K.); (C.H.)
| | - George Markozannes
- Department of Hygiene and Epidemiology, Faculty of Medicine, University of Ioannina, 45100 Ioannina, Greece; (C.D.); (L.N.); (G.M.); (N.S.); (E.P.); (K.T.); (A.K.)
| | - Nikolaos Simantiris
- Department of Hygiene and Epidemiology, Faculty of Medicine, University of Ioannina, 45100 Ioannina, Greece; (C.D.); (L.N.); (G.M.); (N.S.); (E.P.); (K.T.); (A.K.)
| | - Eirini Panteli
- Department of Hygiene and Epidemiology, Faculty of Medicine, University of Ioannina, 45100 Ioannina, Greece; (C.D.); (L.N.); (G.M.); (N.S.); (E.P.); (K.T.); (A.K.)
| | | | - Konstantinos Tsilidis
- Department of Hygiene and Epidemiology, Faculty of Medicine, University of Ioannina, 45100 Ioannina, Greece; (C.D.); (L.N.); (G.M.); (N.S.); (E.P.); (K.T.); (A.K.)
| | - Christos Hadjichristodoulou
- Laboratory of Hygiene and Epidemiology, Faculty of Medicine, University of Thessaly, 22 Papakyriazi Str., 41222 Larissa, Greece; (M.K.); (M.K.); (C.H.)
- National Public Health Organization, 15123 Athens, Greece;
| | - Alexandra Koutsotoli
- Department of Hygiene and Epidemiology, Faculty of Medicine, University of Ioannina, 45100 Ioannina, Greece; (C.D.); (L.N.); (G.M.); (N.S.); (E.P.); (K.T.); (A.K.)
| | - Eirini Christaki
- 1st Division of Internal Medicine & Infectious Diseases Unit, University Hospital of Ioannina, Faculty of Medicine, University of Ioannina, 45500 Ioannina, Greece;
| | - Dimitrios Alivertis
- Department of Biological Applications and Technology, University of Ioannina, Ioannina 45110, Greece;
| | - Aristides Bartzokas
- Laboratory of Meteorology, Department of Physics, University of Ioannina, Ioannina, Greece;
| | - Konstantina Gartzonika
- Department of Microbiology, Faculty of Medicine, School of Health Sciences, University of Ioannina, 45110 Ioannina, Greece; (P.B.); (K.G.)
| | - Chrysostomos Dovas
- Diagnostic Laboratory, School of Veterinary Medicine, Faculty of Health Sciences, Aristotle University of Thessaloniki, 54627 Thessaloniki, Greece;
| | - Evangelia Ntzani
- Department of Hygiene and Epidemiology, Faculty of Medicine, University of Ioannina, 45100 Ioannina, Greece; (C.D.); (L.N.); (G.M.); (N.S.); (E.P.); (K.T.); (A.K.)
- Center for Evidence Synthesis in Health, Department of Health Services, Policy and Practice, School of Public Health, Brown University, Providence, RI 02912, USA
- Biomedical Research Institute, Foundation for Research and Technology, 45110 Ioannina, Greece
| |
Collapse
|
24
|
D'Souza N, Porter AM, Rose JB, Dreelin E, Peters SE, Nowlin PJ, Carbonell S, Cissell K, Wang Y, Flood MT, Rachmadi AT, Xi C, Song P, Briggs S. Public health use and lessons learned from a statewide SARS-CoV-2 wastewater monitoring program (MiNET). Heliyon 2024; 10:e35790. [PMID: 39220928 PMCID: PMC11363850 DOI: 10.1016/j.heliyon.2024.e35790] [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: 04/28/2023] [Revised: 05/27/2024] [Accepted: 08/02/2024] [Indexed: 09/04/2024] Open
Abstract
The global SARS-CoV-2 monitoring effort has been extensive, resulting in many states and countries establishing wastewater-based epidemiology programs to address the spread of the virus during the pandemic. Challenges for programs include concurrently optimizing methods, training new laboratories, and implementing successful surveillance programs that can rapidly translate results for public health, and policy making. Surveillance in Michigan early in the pandemic in 2020 highlights the importance of quality-controlled data and explores correlations with wastewater and clinical case data aggregated at the state level. The lessons learned and potential measures to improve public utilization of results are discussed. The Michigan Network for Environmental Health and Technology (MiNET) established a network of laboratories that partnered with local health departments, universities, wastewater treatment plants (WWTPs) and other stakeholders to monitor SARS-CoV-2 in wastewater at 214 sites in Michigan. MiNET consisted of nineteen laboratories, twenty-nine local health departments, 6 Native American tribes, and 60 WWTPs monitoring sites representing 45 % of Michigan's population from April 6 and December 29, 2020. Three result datasets were created based on quality control criteria. Wastewater results that met all quality assurance criteria (Dataset Mp) produced strongest correlations with reported clinical cases at 16 days lag (rho = 0.866, p < 0.05). The project demonstrated the ability to successfully track SARS-CoV-2 on a large, state-wide scale, particularly data that met the outlined quality criteria and provided an early warning of increasing COVID-19 cases. MiNET is currently poised to leverage its competency to complement public health surveillance networks through environmental monitoring for new and emerging pathogens of concern and provides a valuable resource to state and federal agencies to support future responses.
Collapse
Affiliation(s)
- Nishita D'Souza
- Department of Fisheries and Wildlife, Michigan State University, East Lansing, MI, USA
| | - Alexis M. Porter
- Annis Water Resources Insititute, Grand Valley State University, Muskegon, MI, USA
| | - Joan B. Rose
- Department of Fisheries and Wildlife, Michigan State University, East Lansing, MI, USA
| | - Erin Dreelin
- Department of Fisheries and Wildlife, Michigan State University, East Lansing, MI, USA
| | - Susan E. Peters
- Michigan Department of Health and Human Services, Lansing, MI, USA
| | | | - Samantha Carbonell
- Department of Microbiology and Molecular Genetics, Michigan State University, East Lansing, MI, USA
| | | | - Yili Wang
- University of Michigan, Ann Arbor, Michigan, USA
| | - Matthew T. Flood
- Department of Fisheries and Wildlife, Michigan State University, East Lansing, MI, USA
| | | | - Chuanwu Xi
- University of Michigan, Ann Arbor, Michigan, USA
| | - Peter Song
- University of Michigan, Ann Arbor, Michigan, USA
| | - Shannon Briggs
- Michigan Department of Environment, Great Lakes, and Energy, Lansing, MI, USA
| | - the Michigan Network for Environmental Health and Technology (MiNET) consortium
- Department of Fisheries and Wildlife, Michigan State University, East Lansing, MI, USA
- Annis Water Resources Insititute, Grand Valley State University, Muskegon, MI, USA
- Michigan Department of Health and Human Services, Lansing, MI, USA
- Northern Michigan Regional Laboratory, Gaylord, MI, USA
- Department of Microbiology and Molecular Genetics, Michigan State University, East Lansing, MI, USA
- Saginaw Valley State University, Michigan, USA
- University of Michigan, Ann Arbor, Michigan, USA
- Institute of Environmental Science and Research (ESR), New Zealand
- Michigan Department of Environment, Great Lakes, and Energy, Lansing, MI, USA
| |
Collapse
|
25
|
Merrett JE, Nolan M, Hartman L, John N, Flynn B, Baker L, Schang C, McCarthy D, Lister D, Cheng NN, Crosbie N, Poon R, Jex A. Highly sensitive wastewater surveillance of SARS-CoV-2 variants by targeted next-generation amplicon sequencing provides early warning of incursion in Victoria, Australia. Appl Environ Microbiol 2024; 90:e0149723. [PMID: 39012098 PMCID: PMC11337797 DOI: 10.1128/aem.01497-23] [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: 08/29/2023] [Accepted: 06/06/2024] [Indexed: 07/17/2024] Open
Abstract
The future of the COVID pandemic and its public health and societal impact will be determined by the profile and spread of emerging variants and the timely identification and response to them. Wastewater surveillance of SARS-CoV-2 has been widely adopted in many countries across the globe and has played an important role in tracking infection levels and providing useful epidemiological information that cannot be adequately captured by clinical testing alone. However, novel variants can emerge rapidly, spread globally, and markedly alter the trajectory of the pandemic, as exemplified by the Delta and Omicron variants. Most mutations linked to the emergence of new SARS-CoV-2 variants are found within variable regions of the SARS-CoV-2 Spike protein. We have developed a duplex hemi-nested PCR method that, coupled with short amplicon sequencing, allows simultaneous typing of two of the most highly variable and informative regions of the Spike gene: the N-terminal domain and the receptor binding motif. Using this method in an operationalized public health program, we identified the first known incursion of Omicron BA.1 into Victoria, Australia and demonstrated how sensitive amplicon sequencing methods can be combined with wastewater surveillance as a relatively low-cost solution for early warning of variant incursion and spread.IMPORTANCEThis study offers a rapid, cost-effective, and sensitive approach for monitoring SARS-CoV-2 variants in wastewater. The method's flexibility permits timely modifications, enabling the integration of emerging variants and adaptations to evolving SARS-CoV-2 genetics. Of particular significance for low- and middle-income regions with limited surveillance capabilities, this technique can potentially be utilized to study a range of pathogens or viruses that possess diverse genetic sequences, similar to influenza.
Collapse
Affiliation(s)
- James E. Merrett
- Population Health and Immunity Division, Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia
| | - Monica Nolan
- Victorian Department of Health, Melbourne, Victoria, Australia
| | - Leon Hartman
- Population Health and Immunity Division, Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia
| | - Nijoy John
- Population Health and Immunity Division, Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia
- Faculty of Science, The University of Melbourne, Parkville, Victoria, Australia
| | - Brianna Flynn
- Population Health and Immunity Division, Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia
| | - Louise Baker
- Population Health and Immunity Division, Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia
| | - Christelle Schang
- Environmental and Public Health Microbiology Lab, Monash University, Clayton, Victoria, Australia
| | - David McCarthy
- Environmental and Public Health Microbiology Lab, Monash University, Clayton, Victoria, Australia
- School of Civil and Environmental Engineering, Queensland University of Technology, Brisbane, Queensland, Australia
| | - David Lister
- Victorian Department of Health, Melbourne, Victoria, Australia
| | - Ngai Ning Cheng
- Victorian Department of Health, Melbourne, Victoria, Australia
- South Australian Water Corporation, Adelaide, South Australia, Australia
| | - Nick Crosbie
- Melbourne Water Corporation, Docklands, Victoria, Australia
| | - Rachael Poon
- Victorian Department of Health, Melbourne, Victoria, Australia
| | - Aaron Jex
- Population Health and Immunity Division, Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia
- Faculty of Science, The University of Melbourne, Parkville, Victoria, Australia
| |
Collapse
|
26
|
Länsivaara A, Lehto KM, Hyder R, Janhonen ES, Lipponen A, Heikinheimo A, Pitkänen T, Oikarinen S. Comparison of Different Reverse Transcriptase-Polymerase Chain Reaction-Based Methods for Wastewater Surveillance of SARS-CoV-2: Exploratory Study. JMIR Public Health Surveill 2024; 10:e53175. [PMID: 39158943 PMCID: PMC11369532 DOI: 10.2196/53175] [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: 09/28/2023] [Revised: 04/09/2024] [Accepted: 05/30/2024] [Indexed: 08/20/2024] Open
Abstract
BACKGROUND Many countries have applied the wastewater surveillance of the COVID-19 pandemic to their national public health monitoring measures. The most used methods for detecting SARS-CoV-2 in wastewater are quantitative reverse transcriptase-polymerase chain reaction (RT-qPCR) and reverse transcriptase-droplet digital polymerase chain reaction (RT-ddPCR). Previous comparison studies have produced conflicting results, thus more research on the subject is required. OBJECTIVE This study aims to compare RT-qPCR and RT-ddPCR for detecting SARS-CoV-2 in wastewater. It also aimed to investigate the effect of changes in the analytical pipeline, including the RNA extraction kit, RT-PCR kit, and target gene assay, on the results. Another aim was to find a detection method for low-resource settings. METHODS We compared 2 RT-qPCR kits, TaqMan RT-qPCR and QuantiTect RT-qPCR, and RT-ddPCR based on sensitivity, positivity rates, variability, and correlation of SARS-CoV-2 gene copy numbers in wastewater to the incidence of COVID-19. Furthermore, we compared 2 RNA extraction methods, column- and magnetic-bead-based. In addition, we assessed 2 target gene assays for RT-qPCR, N1 and N2, and 2 target gene assays for ddPCR N1 and E. Reverse transcription strand invasion-based amplification (RT-SIBA) was used to detect SARS-CoV-2 from wastewater qualitatively. RESULTS Our results indicated that the most sensitive method to detect SARS-CoV-2 in wastewater was RT-ddPCR. It had the highest positivity rate (26/30), and its limit of detection was the lowest (0.06 gene copies/µL). However, we obtained the best correlation between COVID-19 incidence and SARS-CoV-2 gene copy number in wastewater using TaqMan RT-qPCR (correlation coefficient [CC]=0.697, P<.001). We found a significant difference in sensitivity between the TaqMan RT-qPCR kit and the QuantiTect RT-qPCR kit, the first having a significantly lower limit of detection and a higher positivity rate than the latter. Furthermore, the N1 target gene assay was the most sensitive for both RT-qPCR kits, while no significant difference was found between the gene targets using RT-ddPCR. In addition, the use of different RNA extraction kits affected the result when the TaqMan RT-qPCR kit was used. RT-SIBA was able to detect SARS-CoV-2 RNA in wastewater. CONCLUSIONS As our study, as well as most of the previous studies, has shown RT-ddPCR to be more sensitive than RT-qPCR, its use in the wastewater surveillance of SARS-CoV-2 should be considered, especially if the amount of SARS-CoV-2 circulating in the population was low. All the analysis steps must be optimized for wastewater surveillance as our study showed that all the analysis steps including the compatibility of the RNA extraction, the RT-PCR kit, and the target gene assay influence the results. In addition, our study showed that RT-SIBA could be used to detect SARS-CoV-2 in wastewater if a qualitative result is sufficient.
Collapse
Affiliation(s)
- Annika Länsivaara
- Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland
| | - Kirsi-Maarit Lehto
- Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland
| | - Rafiqul Hyder
- Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland
| | | | - Anssi Lipponen
- Expert Microbiology Unit, Finnish Institute for Health and Welfare, Kuopio, Finland
| | - Annamari Heikinheimo
- Department of Food Hygiene and Environmental Health, Faculty of Veterinary Medicine, University of Helsinki, Helsinki, Finland
- Finnish Food Authority - Ruokavirasto, Seinäjoki, Finland
| | - Tarja Pitkänen
- Expert Microbiology Unit, Finnish Institute for Health and Welfare, Kuopio, Finland
| | - Sami Oikarinen
- Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland
| |
Collapse
|
27
|
Gong Z, Song T, Hu M, Che Q, Guo J, Zhang H, Li H, Wang Y, Liu B, Shi N. Natural and socio-environmental factors in the transmission of COVID-19: a comprehensive analysis of epidemiology and mechanisms. BMC Public Health 2024; 24:2196. [PMID: 39138466 PMCID: PMC11321203 DOI: 10.1186/s12889-024-19749-3] [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: 01/22/2024] [Accepted: 08/09/2024] [Indexed: 08/15/2024] Open
Abstract
PURPOSE OF REVIEW There are significant differences in the transmission rate and mortality rate of COVID-19 under environmental conditions such as seasons and climates. However, the impact of environmental factors on the role of the COVID-19 pandemic and the transmission mechanism of the SARS-CoV-2 is unclear. Therefore, a comprehensive understanding of the impact of environmental factors on COVID-19 can provide innovative insights for global epidemic prevention and control policies and COVID-19 related research. This review summarizes the evidence of the impact of different natural and social environmental factors on the transmission of COVID-19 through a comprehensive analysis of epidemiology and mechanism research. This will provide innovative inspiration for global epidemic prevention and control policies and provide reference for similar infectious diseases that may emerge in the future. RECENT FINDINGS Evidence reveals mechanisms by which natural environmental factors influence the transmission of COVID-19, including (i) virus survival and transport, (ii) immune system damage, (iii) inflammation, oxidative stress, and cell death, and (iiii) increasing risk of complications. All of these measures appear to be effective in controlling the spread or mortality of COVID-19: (1) reducing air pollution levels, (2) rational use of ozone disinfection and medical ozone therapy, (3) rational exposure to sunlight, (4) scientific ventilation and maintenance of indoor temperature and humidity, (5) control of population density, and (6) control of population movement. Our review indicates that with the continuous mutation of SARS-CoV-2, high temperature, high humidity, low air pollution levels, and low population density more likely to slow down the spread of the virus.
Collapse
Affiliation(s)
- Zhaoyuan Gong
- Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, Beijing, 100700, China
| | - Tian Song
- Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, Beijing, 100700, China
| | - Mingzhi Hu
- Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, Beijing, 100700, China
| | - Qianzi Che
- Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, Beijing, 100700, China
| | - Jing Guo
- Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, Beijing, 100700, China
| | - Haili Zhang
- Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, Beijing, 100700, China
| | - Huizhen Li
- Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, Beijing, 100700, China
| | - Yanping Wang
- Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, Beijing, 100700, China.
| | - Bin Liu
- Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, Beijing, 100700, China.
| | - Nannan Shi
- Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, Beijing, 100700, China.
| |
Collapse
|
28
|
Zambre S, Katarmal P, Pawar S, Dawkhar S, Iyer P, Rajput V, Kadam P, Bhalerao U, Tupekar M, Shah P, Karmodiya K, Dharne M, Roy B, Koraktar S. Wastewater surveillance of severe acute respiratory syndrome coronavirus-2 in open drains of two Indian megacities captures evolutionary lineage transitions: a zonation approach. ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH INTERNATIONAL 2024; 31:49670-49681. [PMID: 39078552 DOI: 10.1007/s11356-024-34448-7] [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: 04/08/2024] [Accepted: 07/18/2024] [Indexed: 07/31/2024]
Abstract
Wastewater-based environmental surveillance (WBES) has been proven as proxy tool for monitoring nucleic acids of pathogens shed by infected population before clinical outcomes. The poor sewershed network of low to middle-income countries (LMICs) leads to most of the wastewater flow through open drains. We studied the effectiveness of WBES using open drain samples to monitor the emergence of the SARS-CoV-2 variants in 2 megacities of India having dense population through zonation approach. Samples from 28 locations spanned into 5 zones of Pune region, Maharashtra, India, were collected on a weekly basis during October 2021 to July 2022. Out of 1115 total processed samples, 303 (~ 27%) tested positive for SARS-CoV-2. The periodical rise and fall in the percentage positivity of the samples was found to be in sync with the abundance of SARS-CoV-2 RNA and the reported COVID-19 active cases for Pune city. Sequencing of the RNA obtained from wastewater samples confirmed the presence of SARS-CoV-2. Of 337 sequences, lineage identification for 242 samples revealed 265 distinct SARS-CoV-2 variants including 10 highly transmissible ones. Importantly, transition from Delta to Omicron variant could be detected in wastewater samples 2 weeks prior to any clinically reported Omicron cases in India. Thus, this study demonstrates the usefulness of open drain samples for real-time monitoring of a viral pathogen's evolutionary dynamics and could be implemented in LMICs.
Collapse
Affiliation(s)
- Saee Zambre
- Symbiosis School of Biological Sciences, Symbiosis International (Deemed University), Lavale, Maharashtra, India
| | - Poonam Katarmal
- Symbiosis School of Biological Sciences, Symbiosis International (Deemed University), Lavale, Maharashtra, India
| | - Shubhankar Pawar
- Symbiosis School of Biological Sciences, Symbiosis International (Deemed University), Lavale, Maharashtra, India
| | - Snehal Dawkhar
- Symbiosis School of Biological Sciences, Symbiosis International (Deemed University), Lavale, Maharashtra, India
| | - Parvati Iyer
- Symbiosis School of Biological Sciences, Symbiosis International (Deemed University), Lavale, Maharashtra, India
| | - Vinay Rajput
- National Collection of Industrial Microorganisms (NCIM), Biochemical Sciences Division, CSIR-National Chemical Laboratory (NCL), Pune, Maharashtra, 411008, India
| | - Pradnya Kadam
- Department of Biology, Indian Institute of Science Education and Research (IISER), Pune, Maharashtra, 41108, India
| | - Unnati Bhalerao
- Department of Biology, Indian Institute of Science Education and Research (IISER), Pune, Maharashtra, 41108, India
| | - Manisha Tupekar
- Department of Biology, Indian Institute of Science Education and Research (IISER), Pune, Maharashtra, 41108, India
| | - Priyanki Shah
- Pune Knowledge Cluster (PKC), Savitribai Phule Pune University (SPPU), Pune, Maharashtra, India
| | - Krishanpal Karmodiya
- Department of Biology, Indian Institute of Science Education and Research (IISER), Pune, Maharashtra, 41108, India
| | - Mahesh Dharne
- National Collection of Industrial Microorganisms (NCIM), Biochemical Sciences Division, CSIR-National Chemical Laboratory (NCL), Pune, Maharashtra, 411008, India
| | - Bishnudeo Roy
- Symbiosis School of Biological Sciences, Symbiosis International (Deemed University), Lavale, Maharashtra, India
| | - Santosh Koraktar
- Symbiosis School of Biological Sciences, Symbiosis International (Deemed University), Lavale, Maharashtra, India.
| |
Collapse
|
29
|
Panneerselvam S, Manayan Parambil A, Jayaram A, Varamballi P, Mukhopadhyay C, Jagadesh A. Surveillance of influenza A and B viruses from community and hospital wastewater treatment plants. ENVIRONMENTAL MICROBIOLOGY REPORTS 2024; 16:e13317. [PMID: 39171887 PMCID: PMC11339856 DOI: 10.1111/1758-2229.13317] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [MESH Headings] [Grants] [Track Full Text] [Subscribe] [Scholar Register] [Received: 04/02/2024] [Accepted: 07/12/2024] [Indexed: 08/23/2024]
Abstract
Influenza virus is a well-known pathogen that can cause epidemics and pandemics. Several surveillance methods are being followed to monitor the transmission patterns and spread of influenza in the community. Wastewater-based Epidemiology (WBE) can serve as an additional tool to detect the presence of influenza viruses. The current study primarily focuses on surveillance of Influenza A and Influenza B in wastewater treatment plant (WWTP) samples. A total of 100 wastewater samples were collected in July (n = 50) and August (n = 50) 2023 from four different WWTPs in Manipal and Udupi, district of Karnataka, India. The WWTP samples were processed and tested by Real-Time reverse transcriptase PCR (RT-PCR). The data generated was analysed in comparison with the clinical Influenza cases. Of the 100 samples, 18 (18%) tested positive for Influenza A virus and 2 (2%) tested positive for Influenza B virus, with a viral load ranging 1.4 x 102-2.2 x 103 gc/L for influenza A virus and 5.2 x 103-7.7 x 103gc/L for influenza B virus. On correlating the WWTP positivity with clinical case, it was found that influenza clinical cases and virus positivity in wastewater increased simultaneously, emphasizing WBE as a concurrent method for monitoring influenza virus activity.
Collapse
Affiliation(s)
- Sneka Panneerselvam
- Manipal Institute of VirologyManipal Academy of Higher EducationManipalIndia
| | | | - Anup Jayaram
- Manipal Institute of VirologyManipal Academy of Higher EducationManipalIndia
| | - Prasad Varamballi
- Manipal Institute of VirologyManipal Academy of Higher EducationManipalIndia
| | | | - Anitha Jagadesh
- Manipal Institute of VirologyManipal Academy of Higher EducationManipalIndia
| |
Collapse
|
30
|
Boogaerts T, Van Wichelen N, Quireyns M, Burgard D, Bijlsma L, Delputte P, Gys C, Covaci A, van Nuijs ALN. Current state and future perspectives on de facto population markers for normalization in wastewater-based epidemiology: A systematic literature review. THE SCIENCE OF THE TOTAL ENVIRONMENT 2024; 935:173223. [PMID: 38761943 PMCID: PMC11270913 DOI: 10.1016/j.scitotenv.2024.173223] [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: 03/28/2024] [Revised: 05/10/2024] [Accepted: 05/11/2024] [Indexed: 05/20/2024]
Abstract
Wastewater-based epidemiology (WBE) and wastewater surveillance have become a valuable complementary data source to collect information on community-wide exposure through the measurement of human biomarkers in influent wastewater (IWW). In WBE, normalization of data with the de facto population that corresponds to a wastewater sample is crucial for a correct interpretation of spatio-temporal trends in exposure and consumption patterns. However, knowledge gaps remain in identifying and validating suitable de facto population biomarkers (PBs) for refinement of WBE back-estimations. WBE studies that apply de facto PBs (including hydrochemical parameters, utility consumption data sources, endo- and exogenous chemicals, biological biomarkers and signalling records) for relative trend analysis and absolute population size estimation were systematically reviewed from three databases (PubMed, Web of Science, SCOPUS) according to the PRISMA guidelines. We included in this review 81 publications that accounted for daily variations in population sizes by applying de facto population normalization. To date, a wide range of PBs have been proposed for de facto population normalization, complicating the comparability of normalized measurements across WBE studies. Additionally, the validation of potential PBs is complicated by the absence of an ideal external validator, magnifying the overall uncertainty for population normalization in WBE. Therefore, this review proposes a conceptual tier-based cross-validation approach for identifying and validating de facto PBs to guide their integration for i) relative trend analysis, and ii) absolute population size estimation. Furthermore, this review also provides a detailed evaluation of the uncertainty observed when comparing different de jure and de facto population estimation approaches. This study shows that their percentual differences can range up to ±200 %, with some exceptions showing even larger variations. This review underscores the need for collaboration among WBE researchers to further streamline the application of de facto population normalization and to evaluate the robustness of different PBs in different socio-demographic communities.
Collapse
Affiliation(s)
- Tim Boogaerts
- Toxicological Centre, University of Antwerp, Universiteitsplein 1, 2610 Antwerp, Belgium; Exposome Center of Excellence, University of Antwerp, Universiteitsplein 1, 2610 Antwerp, Belgium
| | - Natan Van Wichelen
- Toxicological Centre, University of Antwerp, Universiteitsplein 1, 2610 Antwerp, Belgium; Exposome Center of Excellence, University of Antwerp, Universiteitsplein 1, 2610 Antwerp, Belgium
| | - Maarten Quireyns
- Toxicological Centre, University of Antwerp, Universiteitsplein 1, 2610 Antwerp, Belgium; Exposome Center of Excellence, University of Antwerp, Universiteitsplein 1, 2610 Antwerp, Belgium
| | - Dan Burgard
- Department of Chemistry and Biochemistry, University of Puget Sound, Tacoma, WA, USA
| | - Lubertus Bijlsma
- Environmental and Public Health Analytical Chemistry, Research Institute for Pesticides and Water, University Jaume I, Castellón, Spain
| | - Peter Delputte
- Laboratory for Microbiology, Parasitology and Hygiene, University of Antwerp, Universiteitsplein 1, 2610 Antwerp, Belgium; Infla-Med Center of Excellence, University of Antwerp, Universiteitsplein 1, 2610 Antwerp, Belgium
| | - Celine Gys
- Toxicological Centre, University of Antwerp, Universiteitsplein 1, 2610 Antwerp, Belgium; Exposome Center of Excellence, University of Antwerp, Universiteitsplein 1, 2610 Antwerp, Belgium
| | - Adrian Covaci
- Toxicological Centre, University of Antwerp, Universiteitsplein 1, 2610 Antwerp, Belgium; Exposome Center of Excellence, University of Antwerp, Universiteitsplein 1, 2610 Antwerp, Belgium
| | - Alexander L N van Nuijs
- Toxicological Centre, University of Antwerp, Universiteitsplein 1, 2610 Antwerp, Belgium; Exposome Center of Excellence, University of Antwerp, Universiteitsplein 1, 2610 Antwerp, Belgium
| |
Collapse
|
31
|
Zhang Z, He F, Yi L, Deng Z, Wang R, Shen L, Fu S. Wastewater surveillance together with metaviromic data revealed the unusual resurgence of infectious diseases after the first wave of the COVID-19 outbreak. JOURNAL OF HAZARDOUS MATERIALS 2024; 473:134635. [PMID: 38772110 DOI: 10.1016/j.jhazmat.2024.134635] [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: 12/31/2023] [Revised: 04/01/2024] [Accepted: 05/15/2024] [Indexed: 05/23/2024]
Abstract
How to address public health priorities after COVID-19 is becoming a critical task. To this end, we conducted wastewater surveillance for six leading pathogens, namely, SARS-CoV-2, norovirus, rotavirus, influenza A virus (IAV), enteroviruses and respiratory syncytial virus (RSV), in Nanchang city from January to April 2023. Metaviromic sequencing was conducted at the 1st, 4th, 7th, 9th, 12th and 14th weeks to reveal the dynamics of viral pathogens that were not covered by qPCR. Amplicon sequencing of the conserved region of norovirus GI and GII and the rotavirus and region encoding nonstructural protein of RSV was also conducted weekly. The results showed that after a rapid decrease in SARS-CoV-2 sewage concentrations occurred in January 2023, surges of norovirus, rotavirus, IAV and RSV started at the 6th, 7th, 8th and 11th weeks, respectively. The dynamics of the sewage concentrations of norovirus, rotavirus, IAV and RSV were consistent with the off-season resurgence of the above infectious diseases. Notably, peak sewage concentrations of norovirus GI, GII, rotavirus, IAV and RSV were found at the 6th, 3rd, 7th, 7th and 8th weeks, respectively. Astroviruses also resurge after the 7th week, as revealed by metaviromic data, suggesting that wastewater surveillance together with metaviromic data provides an essential early warning tool for revealing patterns of infectious disease resurgence.
Collapse
Affiliation(s)
- Ziqiang Zhang
- Key Laboratory of Resource Biology and Biotechnology in Western China, Ministry of Education, School of Medicine, Northwest University, Xi'an 710069, China
| | - Fenglan He
- The Collaboration Unit for State Key Laboratory of Infectious Disease Prevention and Control, Jiangxi Provincial Health Commission Key Laboratory of Pathogenic Diagnosis and Genomics of Emerging Infectious Diseases, Nanchang Center for Disease Control and Prevention, Nanchang 330038, Jiangxi, China
| | - Liu Yi
- The Collaboration Unit for State Key Laboratory of Infectious Disease Prevention and Control, Jiangxi Provincial Health Commission Key Laboratory of Pathogenic Diagnosis and Genomics of Emerging Infectious Diseases, Nanchang Center for Disease Control and Prevention, Nanchang 330038, Jiangxi, China
| | - Zhiqiang Deng
- The Collaboration Unit for State Key Laboratory of Infectious Disease Prevention and Control, Jiangxi Provincial Health Commission Key Laboratory of Pathogenic Diagnosis and Genomics of Emerging Infectious Diseases, Nanchang Center for Disease Control and Prevention, Nanchang 330038, Jiangxi, China
| | - Rui Wang
- Key Laboratory of Environment Controlled Aquaculture (KLECA), Ministry of Education, Dalian Ocean University, Dalian 116023, China
| | - Lixin Shen
- Key Laboratory of Resource Biology and Biotechnology in Western China, Ministry of Education, School of Medicine, Northwest University, Xi'an 710069, China.
| | - Songzhe Fu
- Key Laboratory of Resource Biology and Biotechnology in Western China, Ministry of Education, School of Medicine, Northwest University, Xi'an 710069, China.
| |
Collapse
|
32
|
Chen X, Balliew J, Bauer CX, Deegan J, Gitter A, Hanson BM, Maresso AW, Tisza MJ, Troisi CL, Rios J, Mena KD, Boerwinkle E, Wu F. RBD amplicon sequencing of wastewater reveals patterns of variant emergence and evolution. MEDRXIV : THE PREPRINT SERVER FOR HEALTH SCIENCES 2024:2024.07.12.24310301. [PMID: 39040200 PMCID: PMC11261926 DOI: 10.1101/2024.07.12.24310301] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Grants] [Track Full Text] [Download PDF] [Subscribe] [Scholar Register] [Indexed: 07/24/2024]
Abstract
Rapid evolution of SARS-CoV-2 has resulted in the emergence of numerous variants, posing significant challenges to public health surveillance. Clinical genome sequencing, while valuable, has limitations in capturing the full epidemiological dynamics of circulating variants in the general population. This study utilized receptor-binding domain (RBD) amplicon sequencing of wastewater samples to monitor the SARS-CoV-2 community dynamics and evolution in El Paso, TX. Over 17 months, we identified 91 variants and observed waves of dominant variants transitioning from BA.2 to BA.2.12.1, BA.4&5, BQ.1, and XBB.1.5. Our findings demonstrated early detection of variants and identification of unreported outbreaks, while showing strong consistency with clinical genome sequencing data at the local, state, and national levels. Alpha diversity analyses revealed significant periodical variations, with the highest diversity observed in winter and the outbreak lag phases, likely due to lower competition among variants before the outbreak growth phase. The data underscores the importance of low transmission periods for rapid mutation and variant evolution. This study highlights the effectiveness of integrating RBD amplicon sequencing with wastewater surveillance in tracking viral evolution, understanding variant emergence, and enhancing public health preparedness.
Collapse
Affiliation(s)
- Xingwen Chen
- School of Public Health, University of Texas Health Science Center at Houston, TX, USA
- Texas Epidemic Public Health Institute (TEPHI), UTHealth Houston, Houston, TX, USA
| | - John Balliew
- El Paso Water Utility, El Paso, TX, United States
| | - Cici X Bauer
- School of Public Health, University of Texas Health Science Center at Houston, TX, USA
- Texas Epidemic Public Health Institute (TEPHI), UTHealth Houston, Houston, TX, USA
| | - Jennifer Deegan
- School of Public Health, University of Texas Health Science Center at Houston, TX, USA
- Texas Epidemic Public Health Institute (TEPHI), UTHealth Houston, Houston, TX, USA
| | - Anna Gitter
- School of Public Health, University of Texas Health Science Center at Houston, TX, USA
- Texas Epidemic Public Health Institute (TEPHI), UTHealth Houston, Houston, TX, USA
| | - Blake M Hanson
- School of Public Health, University of Texas Health Science Center at Houston, TX, USA
- Texas Epidemic Public Health Institute (TEPHI), UTHealth Houston, Houston, TX, USA
| | - Anthony W Maresso
- TAILOR Labs, Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, TX, USA
| | - Michael J Tisza
- The Alkek Center for Metagenomics and Microbiome Research, Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, TX, USA
| | - Catherine L Troisi
- School of Public Health, University of Texas Health Science Center at Houston, TX, USA
- Texas Epidemic Public Health Institute (TEPHI), UTHealth Houston, Houston, TX, USA
| | - Janelle Rios
- School of Public Health, University of Texas Health Science Center at Houston, TX, USA
- Texas Epidemic Public Health Institute (TEPHI), UTHealth Houston, Houston, TX, USA
| | - Kristina D Mena
- School of Public Health, University of Texas Health Science Center at Houston, TX, USA
- Texas Epidemic Public Health Institute (TEPHI), UTHealth Houston, Houston, TX, USA
| | - Eric Boerwinkle
- School of Public Health, University of Texas Health Science Center at Houston, TX, USA
- Texas Epidemic Public Health Institute (TEPHI), UTHealth Houston, Houston, TX, USA
| | - Fuqing Wu
- School of Public Health, University of Texas Health Science Center at Houston, TX, USA
- Texas Epidemic Public Health Institute (TEPHI), UTHealth Houston, Houston, TX, USA
| |
Collapse
|
33
|
Nainani D, Ng WJ, Wuertz S, Thompson JR. Balancing public health and group privacy: Ethics, rights, and obligations for wastewater surveillance systems. WATER RESEARCH 2024; 258:121756. [PMID: 38781624 DOI: 10.1016/j.watres.2024.121756] [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: 12/27/2023] [Revised: 05/06/2024] [Accepted: 05/07/2024] [Indexed: 05/25/2024]
Abstract
As the threat of COVID-19 recedes, wastewater surveillance - unlike other pandemic-era public health surveillance methods - seems here to stay. Concerns have been raised, however, about the potential risks that wastewater surveillance might pose towards group privacy. Existing scholarship has focused upon using ethics- or human rights-based frameworks as a means of balancing the public health objectives of wastewater surveillance and the potential risks it might pose to group privacy. However, such frameworks greatly lack enforceability. In order to further the strong foundation laid by such frameworks - while addressing their lack of enforceability - this paper proposes the idea of the 'obligation' as an alternative way to regulate wastewater surveillance systems. The legal codification of said obligations provides a method of ensuring that wastewater surveillance systems can be deployed effectively and equitably. Our paper proposes that legal obligations for wastewater surveillance can be created and enforced through transparent and purposeful legislation (which would include limits on power and grant institutions substantial oversight) as well as paying heed to non-legislative legal means of enforcement, such as through courts or contracts. Introducing legal obligations for wastewater surveillance could therefore be highly useful to researchers, policymakers, corporate technologists, and government agencies working in this field.
Collapse
Affiliation(s)
- Dhiraj Nainani
- Singapore Centre for Environmental Life Sciences Engineering (SCELSE), Nanyang Technological University, Singapore
| | - Wei Jie Ng
- Singapore Centre for Environmental Life Sciences Engineering (SCELSE), Nanyang Technological University, Singapore
| | - Stefan Wuertz
- Singapore Centre for Environmental Life Sciences Engineering (SCELSE), Nanyang Technological University, Singapore; School of Civil and Environmental Engineering, Nanyang Technological University, Singapore
| | - Janelle R Thompson
- Singapore Centre for Environmental Life Sciences Engineering (SCELSE), Nanyang Technological University, Singapore; Asian School of the Environment, Nanyang Technological University, Singapore.
| |
Collapse
|
34
|
Goitom E, Ariano S, Gilbride K, Yang MI, Edwards EA, Peng H, Dannah N, Farahbakhsh F, Hataley E, Sarvi H, Sun J, Waseem H, Oswald C. Identification of environmental and methodological factors driving variability of Pepper Mild Mottle Virus (PMMoV) across three wastewater treatment plants in the City of Toronto. THE SCIENCE OF THE TOTAL ENVIRONMENT 2024; 932:172917. [PMID: 38701931 DOI: 10.1016/j.scitotenv.2024.172917] [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: 02/22/2024] [Revised: 04/24/2024] [Accepted: 04/29/2024] [Indexed: 05/06/2024]
Abstract
PMMoV has been widely used to normalize the concentration of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) RNA, influenza, and respiratory syncytial virus (RSV) to account for variations in the fecal content of wastewater. PMMoV is also used as an internal RNA recovery control for wastewater-based epidemiology (WBE) tests. While potentially useful for the interpretation of WBE data, previous studies have suggested that PMMoV concentration can be affected by various physico-chemical characteristics of wastewater. There is also the possibility that laboratory methods, particularly the variability in centrifugation steps to remove supernatant from pellets can cause PMMoV variability. The goal of this study is to improve our understanding of the main drivers of PMMoV variability by assessing the relationship between PMMoV concentration, the physico-chemical characteristics of wastewater, and the methodological approach for concentrating wastewater samples. We analyzed 24-hour composite wastewater samples collected from the influent stream of three wastewater treatment plants (WWTPs) located in the City of Toronto, Ontario, Canada. Samples were collected 3 to 5 times per week starting from the beginning of March 2021 to mid-July 2023. The influent flow rate was used to partition the data into wet and dry weather conditions. Physico-chemical characteristics (e.g., total suspended solids (TSS), biological oxygen demand (BOD), alkalinity, electrical conductivity (EC), and ammonia (NH3)) of the raw wastewater were measured, and PMMoV was quantified. Spatial and temporal variability of PMMoV was observed throughout the study period. PMMoV concentration was significantly higher during dry weather conditions. Multiple linear regression analysis demonstrates that the number and type of physico-chemical parameters that drive PMMoV variability are site-specific, but overall BOD and alkalinity were the most important predictors. Differences in PMMoV concentration for a single WWTP between two different laboratory methods, along with a weak correlation between pellet mass and TSS using one method may indicate that differences in sample concentration and subjective subsampling bias could alter viral recovery and introduce variability to the data.
Collapse
Affiliation(s)
- Eyerusalem Goitom
- Department of Geography & Environmental Studies, Toronto Metropolitan University, Canada
| | - Sarah Ariano
- Department of Geography & Environmental Studies, Toronto Metropolitan University, Canada; Department of Earth and Planetary Sciences, McGill University, Canada
| | - Kim Gilbride
- Department of Chemistry & Biology, Toronto Metropolitan University, Canada
| | - Minqing Ivy Yang
- Department of Chemical Engineering and Applied Chemistry, University of Toronto, Canada
| | - Elizabeth A Edwards
- Department of Chemical Engineering and Applied Chemistry, University of Toronto, Canada
| | - Hui Peng
- Department of Chemistry, University of Toronto, Canada; School of the Environment, University of Toronto, Canada
| | - Nora Dannah
- Department of Chemistry & Biology, Toronto Metropolitan University, Canada
| | - Farnaz Farahbakhsh
- Department of Chemistry & Biology, Toronto Metropolitan University, Canada
| | - Eden Hataley
- Department of Geography & Environmental Studies, Toronto Metropolitan University, Canada
| | - Hooman Sarvi
- Department of Chemistry & Biology, Toronto Metropolitan University, Canada
| | - Jianxian Sun
- Department of Chemistry, University of Toronto, Canada
| | - Hassan Waseem
- Department of Chemistry & Biology, Toronto Metropolitan University, Canada
| | - Claire Oswald
- Department of Geography & Environmental Studies, Toronto Metropolitan University, Canada.
| |
Collapse
|
35
|
Corrêa-Moreira D, da Costa GL, de Lima Neto RG, Pinto T, Salomão B, Fumian TM, Mannarino CF, Prado T, Miagostovich MP, de Souza Ramos L, Souza Dos Santos AL, Oliveira MME. Screening of Candida spp. in wastewater in Brazil during COVID-19 pandemic: workflow for monitoring fungal pathogens. BMC Biotechnol 2024; 24:43. [PMID: 38909197 PMCID: PMC11193224 DOI: 10.1186/s12896-024-00868-z] [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: 01/29/2024] [Accepted: 06/07/2024] [Indexed: 06/24/2024] Open
Abstract
Fungal diseases are often linked to poverty, which is associated with poor hygiene and sanitation conditions that have been severely worsened by the COVID-19 pandemic. Moreover, COVID-19 patients are treated with Dexamethasone, a corticosteroid that promotes an immunosuppressive profile, making patients more susceptible to opportunistic fungal infections, such as those caused by Candida species. In this study, we analyzed the prevalence of Candida yeasts in wastewater samples collected to track viral genetic material during the COVID-19 pandemic and identified the yeasts using polyphasic taxonomy. Furthermore, we investigated the production of biofilm and hydrolytic enzymes, which are known virulence factors. Our findings revealed that all Candida species could form biofilms and exhibited moderate hydrolytic enzyme activity. We also proposed a workflow for monitoring wastewater using Colony PCR instead of conventional PCR, as this technique is fast, cost-effective, and reliable. This approach enhances the accurate taxonomic identification of yeasts in environmental samples, contributing to environmental monitoring as part of the One Health approach, which preconizes the monitoring of possible emergent pathogenic microorganisms, including fungi.
Collapse
Affiliation(s)
- Danielly Corrêa-Moreira
- Laboratory of Taxonomy, Biochemistry and Bioprospecting of Fungi, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, 21040-360, Brazil.
| | - Gisela Lara da Costa
- Laboratory of Taxonomy, Biochemistry and Bioprospecting of Fungi, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, 21040-360, Brazil
| | | | - Tatiana Pinto
- Medical Microbiology Department, Paulo de Goés Institute of Microbiology, Federal University of Rio de Janeiro, Rio de Janeiro, 21941-909, Brazil
| | - Bruna Salomão
- Laboratory of Microbiology, Federal Hospital of Andaraí, Rio de Janeiro, 20541-173, Brazil
| | - Tulio Machado Fumian
- Laboratory of Comparative and Environmental Virology, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, 21040-360, Brazil
| | - Camille Ferreira Mannarino
- Laboratory of Comparative and Environmental Virology, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, 21040-360, Brazil
| | - Tatiana Prado
- Laboratory of Respiratory, Exanthematic, Enteric viruses and Viral Emergencies, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, 21040-360, Brazil
| | - Marize Pereira Miagostovich
- Laboratory of Comparative and Environmental Virology, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, 21040-360, Brazil
| | - Lívia de Souza Ramos
- Laboratory for Advanced Studies of Emerging and Resistant Microorganisms, General Microbiology Department, Institute of Microbiology Paulo de Góes, Federal University of Rio de Janeiro, Rio de Janeiro, 21941-909, Brazil
| | - André Luis Souza Dos Santos
- Laboratory for Advanced Studies of Emerging and Resistant Microorganisms, General Microbiology Department, Institute of Microbiology Paulo de Góes, Federal University of Rio de Janeiro, Rio de Janeiro, 21941-909, Brazil
| | - Manoel Marques Evangelista Oliveira
- Laboratory of Taxonomy, Biochemistry and Bioprospecting of Fungi, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, 21040-360, Brazil.
| |
Collapse
|
36
|
Jimenez BS, Sterling T, Brown A, Modica B, Gibson K, Collins H, Koch C, Schwarz T, Dye KN. Protocol to longitudinally quantify SARS-CoV-2 RNA in wastewater using RT-qPCR and pepper mild mottle virus normalization. STAR Protoc 2024; 5:103001. [PMID: 38598332 PMCID: PMC11011218 DOI: 10.1016/j.xpro.2024.103001] [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: 01/10/2024] [Revised: 02/06/2024] [Accepted: 03/21/2024] [Indexed: 04/12/2024] Open
Abstract
Wastewater surveillance allows severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection levels to be tracked in a community. Here, we present a protocol to longitudinally quantify SARS-CoV-2 RNA in wastewater using quantitative reverse-transcription PCR (RT-qPCR) and pepper mild mottle virus (PMMoV) normalization. We describe steps for the pasteurization of wastewater samples, solids separation, supernatant filtration, viral precipitation and concentration, and RNA extraction. We then detail procedures for RT-qPCR, viral concentration extrapolation, PMMoV normalization, and longitudinal analysis. This protocol has the potential to be used for surveillance of other microorganisms. For complete details on the use and execution of this protocol, please refer to Sanchez Jimenez et al.1.
Collapse
Affiliation(s)
- Bryan Sanchez Jimenez
- Department of Health Sciences, Stetson University, 421 N Woodland Boulevard, DeLand, FL 32723, USA; Department of Microbiology and Immunology, New York Medical College, 40 Sunshine Cottage Road, Valhalla, NY 10595, USA.
| | - Trinity Sterling
- Department of Health Sciences, Stetson University, 421 N Woodland Boulevard, DeLand, FL 32723, USA
| | - Austin Brown
- Department of Health Sciences, Stetson University, 421 N Woodland Boulevard, DeLand, FL 32723, USA
| | - Brian Modica
- Department of Health Sciences, Stetson University, 421 N Woodland Boulevard, DeLand, FL 32723, USA
| | - Kaylee Gibson
- Department of Health Sciences, Stetson University, 421 N Woodland Boulevard, DeLand, FL 32723, USA
| | - Hannah Collins
- Department of Health Sciences, Stetson University, 421 N Woodland Boulevard, DeLand, FL 32723, USA
| | - Carolyn Koch
- Department of Health Sciences, Stetson University, 421 N Woodland Boulevard, DeLand, FL 32723, USA
| | - Tyler Schwarz
- Department of Health Sciences, Stetson University, 421 N Woodland Boulevard, DeLand, FL 32723, USA
| | - Kristine N Dye
- Department of Health Sciences, Stetson University, 421 N Woodland Boulevard, DeLand, FL 32723, USA; Department of Biology, Stetson University, 421 N Woodland Boulevard, DeLand, FL 32723, USA.
| |
Collapse
|
37
|
D'Aoust PM, Hegazy N, Ramsay NT, Yang MI, Dhiyebi HA, Edwards E, Servos MR, Ybazeta G, Habash M, Goodridge L, Poon A, Arts E, Brown RS, Payne SJ, Kirkwood A, Simmons D, Desaulniers JP, Ormeci B, Kyle C, Bulir D, Charles T, McKay RM, Gilbride K, Oswald C, Peng H, Pileggi V, Wang ML, Tong A, Orellano D, DeGroot CT, Delatolla R. SARS-CoV-2 viral titer measurements in Ontario, Canada wastewaters throughout the COVID-19 pandemic. Sci Data 2024; 11:656. [PMID: 38906875 PMCID: PMC11192951 DOI: 10.1038/s41597-024-03414-w] [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: 03/14/2024] [Accepted: 05/23/2024] [Indexed: 06/23/2024] Open
Abstract
During the COVID-19 pandemic, the Province of Ontario, Canada, launched a wastewater surveillance program to monitor SARS-CoV-2, inspired by the early work and successful forecasts of COVID-19 waves in the city of Ottawa, Ontario. This manuscript presents a dataset from January 1, 2021, to March 31, 2023, with RT-qPCR results for SARS-CoV-2 genes and PMMoV from 107 sites across all 34 public health units in Ontario, covering 72% of the province's and 26.2% of Canada's population. Sampling occurred 2-7 times weekly, including geographical coordinates, serviced populations, physico-chemical water characteristics, and flowrates. In doing so, this manuscript ensures data availability and metadata preservation to support future research and epidemic preparedness through detailed analyses and modeling. The dataset has been crucial for public health in tracking disease locally, especially with the rise of the Omicron variant and the decline in clinical testing, highlighting wastewater-based surveillance's role in estimating disease incidence in Ontario.
Collapse
Affiliation(s)
| | | | | | | | | | | | | | - Gustavo Ybazeta
- Health Sciences North Research Institute, Sudbury, ON, Canada
| | | | | | - Art Poon
- Western University, London, ON, Canada
| | - Eric Arts
- Western University, London, ON, Canada
| | | | | | | | | | | | | | | | | | | | | | | | - Claire Oswald
- Toronto Metropolitan University, Toronto, ON, Canada
| | - Hui Peng
- University of Toronto, Toronto, ON, Canada
| | - Vince Pileggi
- Ontario Ministry of the Environment, Conservation and Parks, Toronto, ON, Canada
| | - Menglu L Wang
- Toronto Metropolitan University, Toronto, ON, Canada
| | - Arthur Tong
- Toronto Metropolitan University, Toronto, ON, Canada
| | | | | | | |
Collapse
|
38
|
Fondriest M, Vaccari L, Aldrovandi F, De Lellis L, Ferretti F, Fiorentino C, Mari E, Mascolo MG, Minelli L, Perlangeli V, Bortone G, Pandolfi P, Colacci A, Ranzi A. Wastewater-Based Epidemiology for SARS-CoV-2 in Northern Italy: A Spatiotemporal Model. INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH 2024; 21:741. [PMID: 38928987 PMCID: PMC11203876 DOI: 10.3390/ijerph21060741] [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: 04/04/2024] [Revised: 05/23/2024] [Accepted: 05/31/2024] [Indexed: 06/28/2024]
Abstract
The study investigated the application of Wastewater-Based Epidemiology (WBE) as a tool for monitoring the SARS-CoV-2 prevalence in a city in northern Italy from October 2021 to May 2023. Based on a previously used deterministic model, this study proposed a variation to account for the population characteristics and virus biodegradation in the sewer network. The model calculated virus loads and corresponding COVID-19 cases over time in different areas of the city and was validated using healthcare data while considering viral mutations, vaccinations, and testing variability. The correlation between the predicted and reported cases was high across the three waves that occurred during the period considered, demonstrating the ability of the model to predict the relevant fluctuations in the number of cases. The population characteristics did not substantially influence the predicted and reported infection rates. Conversely, biodegradation significantly reduced the virus load reaching the wastewater treatment plant, resulting in a 30% reduction in the total virus load produced in the study area. This approach can be applied to compare the virus load values across cities with different population demographics and sewer network structures, improving the comparability of the WBE data for effective surveillance and intervention strategies.
Collapse
Affiliation(s)
- Matilde Fondriest
- Regional Agency for Prevention, Environment and Energy of Emilia-Romagna, 40139 Bologna, Italy; (L.V.); (E.M.); (M.G.M.); (G.B.); (A.C.); (A.R.)
| | - Lorenzo Vaccari
- Regional Agency for Prevention, Environment and Energy of Emilia-Romagna, 40139 Bologna, Italy; (L.V.); (E.M.); (M.G.M.); (G.B.); (A.C.); (A.R.)
| | - Federico Aldrovandi
- Alma Mater Institute on Healthy Planet, Department of Biological, Geological and Environmental Sciences, University of Bologna, 40138 Bologna, Italy;
| | | | - Filippo Ferretti
- Local Health Authority of Bologna, Department of Public Health, 40124 Bologna, Italy; (F.F.); (C.F.); (V.P.); (P.P.)
| | - Carmine Fiorentino
- Local Health Authority of Bologna, Department of Public Health, 40124 Bologna, Italy; (F.F.); (C.F.); (V.P.); (P.P.)
| | - Erica Mari
- Regional Agency for Prevention, Environment and Energy of Emilia-Romagna, 40139 Bologna, Italy; (L.V.); (E.M.); (M.G.M.); (G.B.); (A.C.); (A.R.)
- Local Health Authority of Bologna, Department of Public Health, 40124 Bologna, Italy; (F.F.); (C.F.); (V.P.); (P.P.)
| | - Maria Grazia Mascolo
- Regional Agency for Prevention, Environment and Energy of Emilia-Romagna, 40139 Bologna, Italy; (L.V.); (E.M.); (M.G.M.); (G.B.); (A.C.); (A.R.)
| | | | - Vincenza Perlangeli
- Local Health Authority of Bologna, Department of Public Health, 40124 Bologna, Italy; (F.F.); (C.F.); (V.P.); (P.P.)
| | - Giuseppe Bortone
- Regional Agency for Prevention, Environment and Energy of Emilia-Romagna, 40139 Bologna, Italy; (L.V.); (E.M.); (M.G.M.); (G.B.); (A.C.); (A.R.)
| | - Paolo Pandolfi
- Local Health Authority of Bologna, Department of Public Health, 40124 Bologna, Italy; (F.F.); (C.F.); (V.P.); (P.P.)
| | - Annamaria Colacci
- Regional Agency for Prevention, Environment and Energy of Emilia-Romagna, 40139 Bologna, Italy; (L.V.); (E.M.); (M.G.M.); (G.B.); (A.C.); (A.R.)
| | - Andrea Ranzi
- Regional Agency for Prevention, Environment and Energy of Emilia-Romagna, 40139 Bologna, Italy; (L.V.); (E.M.); (M.G.M.); (G.B.); (A.C.); (A.R.)
| |
Collapse
|
39
|
Zhang T, Feng L, Lai S, Peng Z, Lan Y, Yang W. Epidemic intelligence trinity: Detection, risk assessment, and early warning. Chin Med J (Engl) 2024; 137:1313-1315. [PMID: 37758650 PMCID: PMC11190998 DOI: 10.1097/cm9.0000000000002856] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/10/2023] [Indexed: 09/29/2023] Open
Affiliation(s)
- Ting Zhang
- Department of Infectious Diseases, School of Population Medicine and Public Health, Chinese Academy of Medical Science & Peking Union Medical College, Beijing 100730, China
| | - Luzhao Feng
- Department of Infectious Diseases, School of Population Medicine and Public Health, Chinese Academy of Medical Science & Peking Union Medical College, Beijing 100730, China
| | - Shengjie Lai
- WorldPop, School of Geography and Environmental Science, University of Southampton, Southampton, SO17 1BJ, UK
| | - Zhihang Peng
- Department of Epidemiology and Health Statistics, School of Public Health, Nanjing Medical University, Nanjing, Jiangsu 211166, China
| | - Yajia Lan
- Department of Occupational Health and Environmental Health, West China School of Public Health, Sichuan University, Chengdu, Sichuan 610041, China
| | - Weizhong Yang
- Department of Infectious Diseases, School of Population Medicine and Public Health, Chinese Academy of Medical Science & Peking Union Medical College, Beijing 100730, China
| |
Collapse
|
40
|
Pasha ABT, Kotlarz N, Holcomb D, Reckling S, Kays J, Bailey E, Guidry V, Christensen A, Berkowitz S, Engel LS, de Los Reyes F, Harris A. Monitoring SARS-CoV-2 RNA in wastewater from a shared septic system and sub-sewershed sites to expand COVID-19 disease surveillance. JOURNAL OF WATER AND HEALTH 2024; 22:978-992. [PMID: 38935450 DOI: 10.2166/wh.2024.303] [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: 10/10/2023] [Accepted: 02/21/2024] [Indexed: 06/29/2024]
Abstract
Wastewater-based epidemiology has expanded as a tool for collecting COVID-19 surveillance data, but there is limited information on the feasibility of this form of surveillance within decentralized wastewater systems (e.g., septic systems). This study assessed SARS-CoV-2 RNA concentrations in wastewater samples from a septic system servicing a mobile home park (66 households) and from two pumping stations serving a similarly sized (71 households) and a larger (1,000 households) neighborhood within a nearby sewershed over 35 weeks in 2020. Also, raw wastewater from a hospital in the same sewershed was sampled. The mobile home park samples had the highest detection frequency (39/39 days) and mean concentration of SARS-CoV-2 RNA (2.7 × 107 gene copies/person/day for the N1) among the four sampling sites. N1 gene and N2 gene copies were highly correlated across mobile home park samples (Pearson's r = 0.93, p < 0.0001). In the larger neighborhood, new COVID-19 cases were reported every week during the sampling period; however, we detected SARS-CoV-2 RNA in 12% of the corresponding wastewater samples. The results of this study suggest that sampling from decentralized wastewater infrastructure can be used for continuous monitoring of SARS-CoV-2 infections.
Collapse
Affiliation(s)
- A B Tanvir Pasha
- Department of Civil, Construction and Environmental Engineering, North Carolina State University (NC State), 915 Partners Way, Raleigh, NC 27606, USA
| | - Nadine Kotlarz
- Center for Human Health and the Environment, NC State, Raleigh, NC, USA
| | - David Holcomb
- Department of Epidemiology, University of North Carolina, Chapel Hill, NC, USA
| | - Stacie Reckling
- Division of Public Health, North Carolina Department of Health and Human Services, Raleigh, NC, USA
| | - Judith Kays
- Department of Civil, Construction and Environmental Engineering, North Carolina State University (NC State), 915 Partners Way, Raleigh, NC 27606, USA
| | | | - Virginia Guidry
- Division of Public Health, North Carolina Department of Health and Human Services, Raleigh, NC, USA
| | - Ariel Christensen
- Division of Public Health, North Carolina Department of Health and Human Services, Raleigh, NC, USA
| | - Steven Berkowitz
- Division of Public Health, North Carolina Department of Health and Human Services, Raleigh, NC, USA
| | - Lawrence S Engel
- Department of Epidemiology, University of North Carolina, Chapel Hill, NC, USA
| | - Francis de Los Reyes
- Department of Civil, Construction and Environmental Engineering, North Carolina State University (NC State), 915 Partners Way, Raleigh, NC 27606, USA
| | - Angela Harris
- Department of Civil, Construction and Environmental Engineering, North Carolina State University (NC State), 915 Partners Way, Raleigh, NC 27606, USA E-mail:
| |
Collapse
|
41
|
Ngqwala B, Msolo L, Ebomah KE, Nontongana N, Okoh AI. Distribution of SARS-CoV-2 Genomes in Wastewaters and the Associated Potential Infection Risk for Plant Workers in Typical Urban and Peri-Urban Communities of the Buffalo City Region, South Africa. Viruses 2024; 16:871. [PMID: 38932163 PMCID: PMC11209190 DOI: 10.3390/v16060871] [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: 04/22/2024] [Revised: 05/24/2024] [Accepted: 05/24/2024] [Indexed: 06/28/2024] Open
Abstract
The presence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in wastewater has been reported in several studies and similar research can be used as a proxy for an early warning of potential Coronavirus disease 2019 (COVID-19) outbreaks. This study focused on profiling the incidence of SARS-CoV-2 genomes in wastewater samples obtained from facilities located in the Buffalo City Municipality. Raw samples were collected weekly using the grab technique for a period of 48 weeks. Ribonucleic acids were extracted from the samples, using the QIAGEN Powersoil Total RNA Extraction kit, and extracted RNA samples were further profiled for the presence of SARS-CoV-2 genomes using Quantitative Real-Time Polymerase Chain Reaction (qRT-PCR) technique. Furthermore, various environmental matrices were utilized to estimate the potential health risk to plant operators associated with exposure to SARS-CoV-2 viral particles using the quantitative microbiological risk assessment (QMRA) model. Our findings revealed the prevalence of SARS-CoV-2 genomes with concentrations that ranged from 0.22 × 103 to 17.60 × 103 genome copies per milliliter (GC/mL). Different exposure scenarios were employed for the QMRA model, and the findings indicate a probability of infection (P(i)) ranging from 0.93% to 37.81% across the study sites. Similarly, the P(i) was highly significant (p < 0.001) for the 20 mL volumetric intake as compared to other volumetric intake scenarios, and high P(i) was also observed in spring, autumn, and winter for all WWTPs. The P(i) was significantly different (p < 0.05) with respect to the different seasons and with respect to different volume scenarios.
Collapse
Affiliation(s)
- Balisa Ngqwala
- SAMRC Microbial Water Quality Monitoring Centre, University of Fort Hare, Alice 5700, South Africa; (L.M.); (K.E.E.); (N.N.); (A.I.O.)
- Applied and Environmental Microbiology Research Group (AEMREG), Department of Biochemistry and Microbiology, University of Fort Hare, Alice 5700, South Africa
| | - Luyanda Msolo
- SAMRC Microbial Water Quality Monitoring Centre, University of Fort Hare, Alice 5700, South Africa; (L.M.); (K.E.E.); (N.N.); (A.I.O.)
- Applied and Environmental Microbiology Research Group (AEMREG), Department of Biochemistry and Microbiology, University of Fort Hare, Alice 5700, South Africa
| | - Kingsley Ehi Ebomah
- SAMRC Microbial Water Quality Monitoring Centre, University of Fort Hare, Alice 5700, South Africa; (L.M.); (K.E.E.); (N.N.); (A.I.O.)
- Applied and Environmental Microbiology Research Group (AEMREG), Department of Biochemistry and Microbiology, University of Fort Hare, Alice 5700, South Africa
| | - Nolonwabo Nontongana
- SAMRC Microbial Water Quality Monitoring Centre, University of Fort Hare, Alice 5700, South Africa; (L.M.); (K.E.E.); (N.N.); (A.I.O.)
- Applied and Environmental Microbiology Research Group (AEMREG), Department of Biochemistry and Microbiology, University of Fort Hare, Alice 5700, South Africa
| | - Anthony Ifeanyi Okoh
- SAMRC Microbial Water Quality Monitoring Centre, University of Fort Hare, Alice 5700, South Africa; (L.M.); (K.E.E.); (N.N.); (A.I.O.)
- Applied and Environmental Microbiology Research Group (AEMREG), Department of Biochemistry and Microbiology, University of Fort Hare, Alice 5700, South Africa
| |
Collapse
|
42
|
Liu Y, Sapoval N, Gallego-García P, Tomás L, Posada D, Treangen TJ, Stadler LB. Crykey: Rapid identification of SARS-CoV-2 cryptic mutations in wastewater. Nat Commun 2024; 15:4545. [PMID: 38806450 PMCID: PMC11133379 DOI: 10.1038/s41467-024-48334-w] [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: 11/15/2023] [Accepted: 04/29/2024] [Indexed: 05/30/2024] Open
Abstract
Wastewater surveillance for SARS-CoV-2 provides early warnings of emerging variants of concerns and can be used to screen for novel cryptic linked-read mutations, which are co-occurring single nucleotide mutations that are rare, or entirely missing, in existing SARS-CoV-2 databases. While previous approaches have focused on specific regions of the SARS-CoV-2 genome, there is a need for computational tools capable of efficiently tracking cryptic mutations across the entire genome and investigating their potential origin. We present Crykey, a tool for rapidly identifying rare linked-read mutations across the genome of SARS-CoV-2. We evaluated the utility of Crykey on over 3,000 wastewater and over 22,000 clinical samples; our findings are three-fold: i) we identify hundreds of cryptic mutations that cover the entire SARS-CoV-2 genome, ii) we track the presence of these cryptic mutations across multiple wastewater treatment plants and over three years of sampling in Houston, and iii) we find a handful of cryptic mutations in wastewater mirror cryptic mutations in clinical samples and investigate their potential to represent real cryptic lineages. In summary, Crykey enables large-scale detection of cryptic mutations in wastewater that represent potential circulating cryptic lineages, serving as a new computational tool for wastewater surveillance of SARS-CoV-2.
Collapse
Affiliation(s)
- Yunxi Liu
- Department of Computer Science, Rice University, Houston, TX, 77005, USA
| | - Nicolae Sapoval
- Department of Computer Science, Rice University, Houston, TX, 77005, USA
| | - Pilar Gallego-García
- CINBIO, Universidade de Vigo, 36310, Vigo, Spain
- Galicia Sur Health Research Institute (IIS Galicia Sur), SERGAS-UVIGO, Vigo, Spain
| | - Laura Tomás
- CINBIO, Universidade de Vigo, 36310, Vigo, Spain
- Galicia Sur Health Research Institute (IIS Galicia Sur), SERGAS-UVIGO, Vigo, Spain
| | - David Posada
- CINBIO, Universidade de Vigo, 36310, Vigo, Spain
- Galicia Sur Health Research Institute (IIS Galicia Sur), SERGAS-UVIGO, Vigo, Spain
- Department of Biochemistry, Genetics, and Immunology, Universidade de Vigo, 36310, Vigo, Spain
| | - Todd J Treangen
- Department of Computer Science, Rice University, Houston, TX, 77005, USA.
| | - Lauren B Stadler
- Department of Civil and Environmental Engineering, Rice University, Houston, TX, 77005, USA.
| |
Collapse
|
43
|
Starke JC, Bell NS, Martinez CM, Friberg IK, Lawley C, Sriskantharajah V, Hirschberg DL. Measuring SARS-CoV-2 RNA concentrations in neighborhood wastewater. THE SCIENCE OF THE TOTAL ENVIRONMENT 2024; 926:172021. [PMID: 38552966 DOI: 10.1016/j.scitotenv.2024.172021] [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: 09/27/2023] [Revised: 03/22/2024] [Accepted: 03/25/2024] [Indexed: 04/05/2024]
Abstract
Longitudinal wastewater sampling during the COVID-19 pandemic was an important aspect of disease surveillance, adding to a more complete understanding of infection dynamics and providing important data for community public health monitoring and intervention planning. This was largely accomplished by testing SARS-CoV-2 RNA concentrations in samples from municipal wastewater treatment plants (WWTPs). We evaluated the utility of testing for virus levels upstream from WWTP within the residential neighborhoods that feed into the WWTP. We propose that monitoring virus dynamics across residential neighborhoods could reveal important public health-relevant information about community sub-group heterogeneity in virus concentrations. PRINCIPAL RESULTS: Virus concentration patterns display heterogeneity within neighborhoods and between neighborhoods over time. Sewage SARS-CoV-2 RNA concentrations as measured by RT-qPCR also corresponded closely to verified COVID-19 infection counts within individual neighborhoods. More importantly, our data suggest the loss of disease-relevant public health information when sampling occurs only at the level of WWTP instead of upstream in neighborhoods. Spikes in SARS-CoV-2 RNA concentrations in neighborhoods are often masked by dilution from other neighborhoods in the WWTP samples. MAJOR CONCLUSIONS: Wastewater-based epidemiology (WBE) employed at WWTP reliably detects SARS-CoV-2 in a city-sized population but provides less actionable public health information about neighborhoods experiencing greater viral infection and disease. Neighborhood sewershed sampling reveals important population-based information about local virus dynamics and improves opportunities for public health intervention. Longitudinally employed, neighborhood sewershed surveillance may provide a 3-6 day early warning of SARS-CoV-2 infection spikes and, importantly, highly specific information on subpopulations in a community particularly at higher risk at different points in time. Sampling in neighborhoods may thus provide timely and cost-saving information for targeted interventions within communities.
Collapse
Affiliation(s)
| | - Nicole S Bell
- RAIN Incubator, Tacoma, WA, USA; Squally Creek, LLC, Tacoma, WA, USA
| | - Chloe Mae Martinez
- RAIN Incubator, Tacoma, WA, USA; University of Washington-Tacoma, Tacoma, WA, USA
| | | | | | | | - David L Hirschberg
- RAIN Incubator, Tacoma, WA, USA; School of Engineering and Technology, University of Washington-Tacoma, Tacoma, WA, USA
| |
Collapse
|
44
|
Islam G, Gedge A, Ibrahim R, de Melo T, Lara-Jacobo L, Dlugosz T, Kirkwood AE, Simmons D, Desaulniers JP. The role of catchment population size, data normalization, and chronology of public health interventions on wastewater-based COVID-19 viral trends. THE SCIENCE OF THE TOTAL ENVIRONMENT 2024; 937:173272. [PMID: 38763190 DOI: 10.1016/j.scitotenv.2024.173272] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Subscribe] [Scholar Register] [Received: 02/16/2024] [Revised: 04/28/2024] [Accepted: 05/13/2024] [Indexed: 05/21/2024]
Abstract
The severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) pandemic presented the most challenging global crisis in recent times. A pandemic caused by a novel pathogen such as SARS-CoV-2 necessitated the development of innovative techniques for the monitoring and surveillance of COVID-19 infections within communities. Wastewater surveillance (WWS) is recognized as a non-invasive, cost-effective, and valuable epidemiological tool to monitor the prevalence of COVID-19 infections in communities. Seven municipal wastewater sampling sites representing distinct sewershed communities were selected for the surveillance of the SARS-CoV-2 virus in Durham Region, Ontario, Canada over 8 months from March 2021 to October 2021. Viral RNA fragments of SARS-CoV-2 and the normalization target pepper mild mottle virus (PMMoV) were concentrated from wastewater influent using the PEG/NaCl superspeed centrifugation method and quantified using RT-qPCR. Strong significant correlations (Spearman's rs = 0.749 to 0.862, P < 0.001) were observed between SARS-CoV-2 gene copies/mL of wastewater and clinical cases reported in each delineated sewershed by onset date. Although raw wastewater offered higher correlation coefficients with clinical cases by onset date compared to PMMoV normalized data, only one site had a statistically significantly higher Spearman's correlation coefficient value for raw data than normalized data. Implementation of community stay-at-home orders and vaccinations over the course of the study period in 2021 were found to strongly correspond to decreasing SARS-CoV-2 wastewater trends in the wastewater treatment plants and upstream pumping stations.
Collapse
Affiliation(s)
- Golam Islam
- Faculty of Science, Ontario Tech University, 2000 Simcoe St N, Oshawa, ON L1G 0C5, Canada.
| | - Ashley Gedge
- Faculty of Science, Ontario Tech University, 2000 Simcoe St N, Oshawa, ON L1G 0C5, Canada
| | - Reeta Ibrahim
- Faculty of Science, Ontario Tech University, 2000 Simcoe St N, Oshawa, ON L1G 0C5, Canada
| | - Tomas de Melo
- Faculty of Science, Ontario Tech University, 2000 Simcoe St N, Oshawa, ON L1G 0C5, Canada
| | - Linda Lara-Jacobo
- Faculty of Science, Ontario Tech University, 2000 Simcoe St N, Oshawa, ON L1G 0C5, Canada
| | - Thomas Dlugosz
- Faculty of Science, Ontario Tech University, 2000 Simcoe St N, Oshawa, ON L1G 0C5, Canada
| | - Andrea E Kirkwood
- Faculty of Science, Ontario Tech University, 2000 Simcoe St N, Oshawa, ON L1G 0C5, Canada
| | - Denina Simmons
- Faculty of Science, Ontario Tech University, 2000 Simcoe St N, Oshawa, ON L1G 0C5, Canada
| | - Jean-Paul Desaulniers
- Faculty of Science, Ontario Tech University, 2000 Simcoe St N, Oshawa, ON L1G 0C5, Canada
| |
Collapse
|
45
|
Sadare OO, Oke D, Olawuni OA, Olayiwola IA, Moothi K. Modelling and optimization of membrane process for removal of biologics (pathogens) from water and wastewater: Current perspectives and challenges. Heliyon 2024; 10:e29864. [PMID: 38698993 PMCID: PMC11064141 DOI: 10.1016/j.heliyon.2024.e29864] [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: 01/23/2024] [Revised: 03/30/2024] [Accepted: 04/16/2024] [Indexed: 05/05/2024] Open
Abstract
As one of the 17 sustainable development goals, the United Nations (UN) has prioritized "clean water and sanitation" (Goal 6) to reduce the discharge of emerging pollutants and disease-causing agents into the environment. Contamination of water by pathogenic microorganisms and their existence in treated water is a global public health concern. Under natural conditions, water is frequently prone to contamination by invasive microorganisms, such as bacteria, viruses, and protozoa. This circumstance has therefore highlighted the critical need for research techniques to prevent, treat, and get rid of pathogens in wastewater. Membrane systems have emerged as one of the effective ways of removing contaminants from water and wastewater However, few research studies have examined the synergistic or conflicting effects of operating conditions on newly developing contaminants found in wastewater. Therefore, the efficient, dependable, and expeditious examination of the pathogens in the intricate wastewater matrix remains a significant obstacle. As far as it can be ascertained, much attention has not recently been given to optimizing membrane processes to develop optimal operation design as related to pathogen removal from water and wastewater. Therefore, this state-of-the-art review aims to discuss the current trends in removing pathogens from wastewater by membrane techniques. In addition, conventional techniques of treating pathogenic-containing water and wastewater and their shortcomings were briefly discussed. Furthermore, derived mathematical models suitable for modelling, simulation, and control of membrane technologies for pathogens removal are highlighted. In conclusion, the challenges facing membrane technologies for removing pathogens were extensively discussed, and future outlooks/perspectives on optimizing and modelling membrane processes are recommended.
Collapse
Affiliation(s)
- Olawumi O. Sadare
- School of Chemical and Minerals Engineering, Faculty of Engineering, North-West University, Potchefstroom, 2520, South Africa
| | - Doris Oke
- Northwestern-Argonne Institute of Science and Engineering, Northwestern University, Evanston, IL, USA
| | - Oluwagbenga A. Olawuni
- Department of Chemical Engineering, Faculty of Engineering and the Built Environment, Doornfontein Campus, University of Johannesburg, P.O. Box 17011, Johannesburg, 2028, South Africa
| | - Idris A. Olayiwola
- UNESCO-UNISA Africa Chair in Nanoscience and Nanotechnology College of Graduates Studies, University of South Africa, Pretoria 392, South Africa
| | - Kapil Moothi
- School of Chemical and Minerals Engineering, Faculty of Engineering, North-West University, Potchefstroom, 2520, South Africa
| |
Collapse
|
46
|
Girón-Guzmán I, Cuevas-Ferrando E, Barranquero R, Díaz-Reolid A, Puchades-Colera P, Falcó I, Pérez-Cataluña A, Sánchez G. Urban wastewater-based epidemiology for multi-viral pathogen surveillance in the Valencian region, Spain. WATER RESEARCH 2024; 255:121463. [PMID: 38537489 DOI: 10.1016/j.watres.2024.121463] [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: 09/19/2023] [Revised: 02/28/2024] [Accepted: 03/12/2024] [Indexed: 04/24/2024]
Abstract
Wastewater-based epidemiology (WBE) has lately arised as a promising tool for monitoring and tracking viral pathogens in communities. In this study, we analysed WBE's role as a multi-pathogen surveillance strategy to detect the presence of several viral illness causative agents. Thus, an epidemiological study was conducted from October 2021 to February 2023 to estimate the weekly levels of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), Respiratory Syncytial virus (RSV), and Influenza A virus (IAV) in influent wastewater samples (n = 69). In parallel, a one-year study (October 2021 to October 2022) was performed to assess the presence of pathogenic human enteric viruses. Besides, monitoring of proposed viral fecal contamination indicators crAssphage and Pepper mild mottle virus (PMMoV) was also assessed, along with plaque counting of somatic coliphages. Genetic material of rotavirus (RV), human astrovirus (HAStV), and norovirus genogroup I (GI) and GII was found in almost all samples, while hepatitis A and E viruses (HAV and HEV) only tested positive in 3.77 % and 22.64 % of the samples, respectively. No seasonal patterns were overall found for enteric viruses, although RVs had a peak prevalence in the winter months. All samples tested positive for SARS-CoV-2 RNA, with a mean concentration of 5.43 log genome copies per liter (log GC/L). The tracking of the circulating SARS-CoV-2 variants of concern (VOCs) was performed by both duplex RT-qPCR and next generation sequencing (NGS). Both techniques reliably showed how the dominant VOC transitioned from Delta to Omicron during two weeks in Spain in December 2021. RSV and IAV viruses peaked in winter months with mean concentrations 6.40 and 4.10 log GC/L, respectively. Moreover, the three selected respiratory viruses strongly correlated with reported clinical data when normalised by wastewater physico-chemical parameters and presented weaker correlations when normalising sewage concentration levels with crAssphage or somatic coliphages titers. Finally, predictive models were generated for each respiratory virus, confirming high reliability on WBE data as an early-warning system and communities illness monitoring system. Overall, this study presents WBE as an optimal tool for multi-pathogen tracking reflecting viral circulation and diseases trends within a selected area, its value as a multi-pathogen early-warning tool stands out due to its public health interest.
Collapse
Affiliation(s)
- Inés Girón-Guzmán
- Institute of Agrochemistry and Food Technology, IATA-CSIC, Av. Agustín Escardino 7, Paterna, Valencia 46980, Spain
| | - Enric Cuevas-Ferrando
- Institute of Agrochemistry and Food Technology, IATA-CSIC, Av. Agustín Escardino 7, Paterna, Valencia 46980, Spain.
| | - Regino Barranquero
- Institute of Agrochemistry and Food Technology, IATA-CSIC, Av. Agustín Escardino 7, Paterna, Valencia 46980, Spain
| | - Azahara Díaz-Reolid
- Institute of Agrochemistry and Food Technology, IATA-CSIC, Av. Agustín Escardino 7, Paterna, Valencia 46980, Spain
| | - Pablo Puchades-Colera
- Institute of Agrochemistry and Food Technology, IATA-CSIC, Av. Agustín Escardino 7, Paterna, Valencia 46980, Spain
| | - Irene Falcó
- Institute of Agrochemistry and Food Technology, IATA-CSIC, Av. Agustín Escardino 7, Paterna, Valencia 46980, Spain; Department of Microbiology and Ecology, University of Valencia, Valencia, Spain
| | - Alba Pérez-Cataluña
- Institute of Agrochemistry and Food Technology, IATA-CSIC, Av. Agustín Escardino 7, Paterna, Valencia 46980, Spain
| | - Gloria Sánchez
- Institute of Agrochemistry and Food Technology, IATA-CSIC, Av. Agustín Escardino 7, Paterna, Valencia 46980, Spain.
| |
Collapse
|
47
|
Zhang M, Roldan-Hernandez L, Boehm A. Persistence of human respiratory viral RNA in wastewater-settled solids. Appl Environ Microbiol 2024; 90:e0227223. [PMID: 38501669 PMCID: PMC11022535 DOI: 10.1128/aem.02272-23] [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: 12/16/2023] [Accepted: 03/01/2024] [Indexed: 03/20/2024] Open
Abstract
Wastewater-based epidemiology has emerged as a valuable tool for monitoring respiratory viral diseases within communities by analyzing concentrations of viral nucleic-acids in wastewater. However, little is known about the fate of respiratory virus nucleic-acids in wastewater. Two important fate processes that may modulate their concentrations in wastewater as they move from household drains to the point of collection include sorption or partitioning to wastewater solids and degradation. This study investigated the decay kinetics of genomic nucleic-acids of seven human respiratory viruses, including severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), respiratory syncytial virus (RSV), human coronavirus (HCoV)-OC43, HCoV-229E, HCoV-NL63, human rhinovirus (HRV), and influenza A virus (IAV), as well as pepper mild mottle virus (PMMoV) in wastewater solids. Viruses (except for PMMoV) were spiked into wastewater solids and their concentrations were followed for 50 days at three different temperatures (4°C, 22°C, and 37°C). Viral genomic RNA decayed following first-order kinetics with decay rate constants k from 0 to 0.219 per day. Decay rate constants k were not different from 0 for all targets in solids incubated at 4°C; k values were largest at 37°C and at this temperature, k values were similar across nucleic-acid targets. Regardless of temperature, there was limited viral RNA decay, with an estimated 0% to 20% reduction, over the typical residence times of sewage in the piped systems between input and collection point (<1 day). The k values reported herein can be used directly in fate and transport models to inform the interpretation of measurements made during wastewater surveillance.IMPORTANCEUnderstanding whether or not the RNA targets quantified for wastewater-based epidemiology (WBE) efforts decay during transport between drains and the point of sample collection is critical for data interpretation. Here we show limited decay of viral RNA targets typically measured for respiratory disease WBE.
Collapse
Affiliation(s)
- Mengyang Zhang
- Department of Civil and Environmental Engineering, School of Engineering and Doerr School of Sustainability, Stanford University, Stanford, California, USA
| | - Laura Roldan-Hernandez
- Department of Civil and Environmental Engineering, School of Engineering and Doerr School of Sustainability, Stanford University, Stanford, California, USA
| | - Alexandria Boehm
- Department of Civil and Environmental Engineering, School of Engineering and Doerr School of Sustainability, Stanford University, Stanford, California, USA
| |
Collapse
|
48
|
Boehm AB, Shelden B, Duong D, Banaei N, White BJ, Wolfe MK. A retrospective longitudinal study of adenovirus group F, norovirus GI and GII, rotavirus, and enterovirus nucleic acids in wastewater solids at two wastewater treatment plants: solid-liquid partitioning and relation to clinical testing data. mSphere 2024; 9:e0073623. [PMID: 38411118 PMCID: PMC10964402 DOI: 10.1128/msphere.00736-23] [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: 11/28/2023] [Accepted: 02/13/2024] [Indexed: 02/28/2024] Open
Abstract
Enteric infections are important causes of morbidity and mortality, yet clinical surveillance is limited. Wastewater-based epidemiology (WBE) has been used to study community circulation of individual enteric viruses and panels of respiratory diseases, but there is limited work studying the concurrent circulation of a suite of important enteric viruses. A retrospective WBE study was carried out at two wastewater treatment plants located in California, United States. Using digital droplet polymerase chain reaction (PCR), we measured concentrations of human adenovirus group F, enteroviruses, norovirus genogroups I and II, and rotavirus nucleic acids in wastewater solids two times per week for 26 months (n = 459 samples) between February 2021 and mid-April 2023. A novel probe-based PCR assay was developed and validated for adenovirus. We compared viral nucleic acid concentrations to positivity rates for viral infections from clinical specimens submitted to a local clinical laboratory to assess concordance between the data sets. We detected all viral targets in wastewater solids. At both wastewater treatment plants, human adenovirus group F and norovirus GII nucleic acids were detected at the highest concentrations (median concentrations greater than 105 copies/g), while rotavirus RNA was detected at the lowest concentrations (median on the order of 103 copies/g). Rotavirus, adenovirus group F, and norovirus nucleic acid concentrations were positively associated with clinical specimen positivity rates. Concentrations of tested viral nucleic acids exhibited complex associations with SARS-CoV-2 and other respiratory viral nucleic acids in wastewater, suggesting divergent transmission patterns.IMPORTANCEThis study provides evidence for the use of wastewater solids for the sensitive detection of enteric virus targets in wastewater-based epidemiology programs aimed to better understand the spread of enteric disease at a localized, community level without limitations associated with testing many individuals. Wastewater data can inform clinical, public health, and individual decision-making aimed to reduce the transmission of enteric disease.
Collapse
Affiliation(s)
- Alexandria B. Boehm
- Department of Civil and Environmental Engineering, School of Engineering and Doerr School of Sustainability, Stanford University, Stanford, California, USA
| | | | - Dorothea Duong
- Verily Life Sciences LLC, South San Francisco, California, USA
| | - Niaz Banaei
- Department of Pathology, School of Medicine, Stanford University, Palo Alto, California, USA
| | | | - Marlene K. Wolfe
- Gangarosa Department of Environmental Health, Rollins School of Public Health, Emory University, Atlanta, Georgia, USA
| |
Collapse
|
49
|
Leisman KP, Owen C, Warns MM, Tiwari A, Bian GZ, Owens SM, Catlett C, Shrestha A, Poretsky R, Packman AI, Mangan NM. A modeling pipeline to relate municipal wastewater surveillance and regional public health data. WATER RESEARCH 2024; 252:121178. [PMID: 38309063 DOI: 10.1016/j.watres.2024.121178] [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: 09/05/2023] [Revised: 12/18/2023] [Accepted: 01/22/2024] [Indexed: 02/05/2024]
Abstract
As COVID-19 becomes endemic, public health departments benefit from improved passive indicators, which are independent of voluntary testing data, to estimate the prevalence of COVID-19 in local communities. Quantification of SARS-CoV-2 RNA from wastewater has the potential to be a powerful passive indicator. However, connecting measured SARS-CoV-2 RNA to community prevalence is challenging due to the high noise typical of environmental samples. We have developed a generalized pipeline using in- and out-of-sample model selection to test the ability of different correction models to reduce the variance in wastewater measurements and applied it to data collected from treatment plants in the Chicago area. We built and compared a set of multi-linear regression models, which incorporate pepper mild mottle virus (PMMoV) as a population biomarker, Bovine coronavirus (BCoV) as a recovery control, and wastewater system flow rate into a corrected estimate for SARS-CoV-2 RNA concentration. For our data, models with BCoV performed better than those with PMMoV, but the pipeline should be used to reevaluate any new data set as the sources of variance may change across locations, lab methods, and disease states. Using our best-fit model, we investigated the utility of RNA measurements in wastewater as a leading indicator of COVID-19 trends. We did this in a rolling manner for corrected wastewater data and for other prevalence indicators and statistically compared the temporal relationship between new increases in the wastewater data and those in other prevalence indicators. We found that wastewater trends often lead other COVID-19 indicators in predicting new surges.
Collapse
Affiliation(s)
- Katelyn Plaisier Leisman
- Department of Engineering Sciences and Applied Mathematics, Northwestern University, Evanston, IL, USA
| | - Christopher Owen
- Department of Biological Sciences, University of Illinois Chicago, Chicago, IL, USA
| | - Maria M Warns
- Department of Engineering Sciences and Applied Mathematics, Northwestern University, Evanston, IL, USA
| | - Anuj Tiwari
- Discovery Partners Institute, University of Illinois Chicago, Chicago, IL, USA
| | - George Zhixin Bian
- Department of Computer Science, Northwestern University, Evanston, IL, USA
| | - Sarah M Owens
- Biosciences, Argonne National Laboratory, Lemont, IL, USA
| | - Charlie Catlett
- Discovery Partners Institute, University of Illinois Chicago, Chicago, IL, USA; Computing, Environment, and Life Sciences, Argonne National Laboratory, Lemont, IL, USA
| | - Abhilasha Shrestha
- Division of Environmental and Occupational Health Sciences, School of Public Health, University of Illinois Chicago, Chicago, IL, USA
| | - Rachel Poretsky
- Department of Biological Sciences, University of Illinois Chicago, Chicago, IL, USA
| | - Aaron I Packman
- Center for Water Research, Northwestern University, Evanston, IL, USA; Department of Civil and Environmental Engineering, Northwestern University, Evanston, IL, USA
| | - Niall M Mangan
- Department of Engineering Sciences and Applied Mathematics, Northwestern University, Evanston, IL, USA; Center for Water Research, Northwestern University, Evanston, IL, USA.
| |
Collapse
|
50
|
Parkins MD, Lee BE, Acosta N, Bautista M, Hubert CRJ, Hrudey SE, Frankowski K, Pang XL. Wastewater-based surveillance as a tool for public health action: SARS-CoV-2 and beyond. Clin Microbiol Rev 2024; 37:e0010322. [PMID: 38095438 PMCID: PMC10938902 DOI: 10.1128/cmr.00103-22] [Citation(s) in RCA: 1] [Impact Index Per Article: 1.0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 03/16/2024] Open
Abstract
Wastewater-based surveillance (WBS) has undergone dramatic advancement in the context of the coronavirus disease 2019 (COVID-19) pandemic. The power and potential of this platform technology were rapidly realized when it became evident that not only did WBS-measured SARS-CoV-2 RNA correlate strongly with COVID-19 clinical disease within monitored populations but also, in fact, it functioned as a leading indicator. Teams from across the globe rapidly innovated novel approaches by which wastewater could be collected from diverse sewersheds ranging from wastewater treatment plants (enabling community-level surveillance) to more granular locations including individual neighborhoods and high-risk buildings such as long-term care facilities (LTCF). Efficient processes enabled SARS-CoV-2 RNA extraction and concentration from the highly dilute wastewater matrix. Molecular and genomic tools to identify, quantify, and characterize SARS-CoV-2 and its various variants were adapted from clinical programs and applied to these mixed environmental systems. Novel data-sharing tools allowed this information to be mobilized and made immediately available to public health and government decision-makers and even the public, enabling evidence-informed decision-making based on local disease dynamics. WBS has since been recognized as a tool of transformative potential, providing near-real-time cost-effective, objective, comprehensive, and inclusive data on the changing prevalence of measured analytes across space and time in populations. However, as a consequence of rapid innovation from hundreds of teams simultaneously, tremendous heterogeneity currently exists in the SARS-CoV-2 WBS literature. This manuscript provides a state-of-the-art review of WBS as established with SARS-CoV-2 and details the current work underway expanding its scope to other infectious disease targets.
Collapse
Affiliation(s)
- Michael D. Parkins
- Department of Microbiology, Immunology and Infectious Diseases, University of Calgary, Calgary, Alberta, Canada
- Department of Medicine, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada
- O’Brien Institute of Public Health, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada
| | - Bonita E. Lee
- Department of Pediatrics, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada
| | - Nicole Acosta
- Department of Medicine, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada
| | - Maria Bautista
- Department of Biological Sciences, Faculty of Science, University of Calgary, Calgary, Alberta, Canada
| | - Casey R. J. Hubert
- Department of Biological Sciences, Faculty of Science, University of Calgary, Calgary, Alberta, Canada
| | - Steve E. Hrudey
- Department of Laboratory Medicine and Pathology, University of Alberta, Edmonton, Alberta, Canada
| | - Kevin Frankowski
- Advancing Canadian Water Assets, University of Calgary, Calgary, Alberta, Canada
| | - Xiao-Li Pang
- Department of Laboratory Medicine and Pathology, University of Alberta, Edmonton, Alberta, Canada
- Provincial Health Laboratory, Alberta Health Services, Calgary, Alberta, Canada
| |
Collapse
|