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A direct capture method for purification and detection of viral nucleic acid enables epidemiological surveillance of SARS-CoV-2
Studies have demonstrated that SARS-CoV-2 RNA can be detected in the feces of infected individuals. This finding spurred investigation into using wastewater-based epidemiology (WBE) to monitor SARS-CoV-2 RNA and track the appearance and spread of COVID-19 in communities. SARS-CoV-2 is present at low...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Promega Corporation. Published by Elsevier B.V.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8262391/ https://www.ncbi.nlm.nih.gov/pubmed/34252764 http://dx.doi.org/10.1016/j.scitotenv.2021.148834 |
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author | Mondal, Subhanjan Feirer, Nathan Brockman, Michael Preston, Melanie A. Teter, Sarah J. Ma, Dongping Goueli, Said A. Moorji, Sameer Saul, Brigitta Cali, James J. |
author_facet | Mondal, Subhanjan Feirer, Nathan Brockman, Michael Preston, Melanie A. Teter, Sarah J. Ma, Dongping Goueli, Said A. Moorji, Sameer Saul, Brigitta Cali, James J. |
author_sort | Mondal, Subhanjan |
collection | PubMed |
description | Studies have demonstrated that SARS-CoV-2 RNA can be detected in the feces of infected individuals. This finding spurred investigation into using wastewater-based epidemiology (WBE) to monitor SARS-CoV-2 RNA and track the appearance and spread of COVID-19 in communities. SARS-CoV-2 is present at low levels in wastewater, making sample concentration a prerequisite for sensitive detection and utility in WBE. Whereas common methods for isolating viral genetic material are biased toward intact virus isolation, it is likely that a relatively low percentage of the total SARS-CoV-2 RNA genome in wastewater is contained within intact virions. Therefore, we hypothesized that a direct unbiased total nucleic acid(TNA) extraction method could overcome the cumbersome protocols, variability and low recovery rates associated with the former methods. This led to development of a simple, rapid, and modular alternative to existing purification methods. In an initial concentration step, chaotropic agents are added to raw sewage allowing binding of nucleic acid from free nucleoprotein complexes, partially intact, and intact virions to a silica matrix. The eluted nucleic acid is then purified using manual or semi-automated methods. RT-qPCR enzyme mixes were formulated that demonstrate substantial inhibitor resistance. In addition, multiplexed probe-based RT-qPCR assays detecting the N1, N2 (nucleocapsid) and E (envelope) gene fragments of SARS-CoV-2 were developed. The RT-qPCR assays also contain primers and probes to detect Pepper Mild Mottle Virus (PMMoV), a fecal indicator RNA virus present in wastewater, and an exogenous control RNA to measure effects of RT-qPCR inhibitors. Using this workflow, we monitored wastewater samples from three wastewater treatment plants (WWTP) in Dane County, Wisconsin. We also successfully sequenced a subset of samples to ensure compatibility with a SARS-CoV-2 amplicon panel and demonstrated the potential for SARS-CoV-2 variant detection. Data obtained here underscore the potential for wastewater surveillance of SARS-CoV-2 and other infectious agents in communities. |
format | Online Article Text |
id | pubmed-8262391 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Promega Corporation. Published by Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82623912021-07-07 A direct capture method for purification and detection of viral nucleic acid enables epidemiological surveillance of SARS-CoV-2 Mondal, Subhanjan Feirer, Nathan Brockman, Michael Preston, Melanie A. Teter, Sarah J. Ma, Dongping Goueli, Said A. Moorji, Sameer Saul, Brigitta Cali, James J. Sci Total Environ Article Studies have demonstrated that SARS-CoV-2 RNA can be detected in the feces of infected individuals. This finding spurred investigation into using wastewater-based epidemiology (WBE) to monitor SARS-CoV-2 RNA and track the appearance and spread of COVID-19 in communities. SARS-CoV-2 is present at low levels in wastewater, making sample concentration a prerequisite for sensitive detection and utility in WBE. Whereas common methods for isolating viral genetic material are biased toward intact virus isolation, it is likely that a relatively low percentage of the total SARS-CoV-2 RNA genome in wastewater is contained within intact virions. Therefore, we hypothesized that a direct unbiased total nucleic acid(TNA) extraction method could overcome the cumbersome protocols, variability and low recovery rates associated with the former methods. This led to development of a simple, rapid, and modular alternative to existing purification methods. In an initial concentration step, chaotropic agents are added to raw sewage allowing binding of nucleic acid from free nucleoprotein complexes, partially intact, and intact virions to a silica matrix. The eluted nucleic acid is then purified using manual or semi-automated methods. RT-qPCR enzyme mixes were formulated that demonstrate substantial inhibitor resistance. In addition, multiplexed probe-based RT-qPCR assays detecting the N1, N2 (nucleocapsid) and E (envelope) gene fragments of SARS-CoV-2 were developed. The RT-qPCR assays also contain primers and probes to detect Pepper Mild Mottle Virus (PMMoV), a fecal indicator RNA virus present in wastewater, and an exogenous control RNA to measure effects of RT-qPCR inhibitors. Using this workflow, we monitored wastewater samples from three wastewater treatment plants (WWTP) in Dane County, Wisconsin. We also successfully sequenced a subset of samples to ensure compatibility with a SARS-CoV-2 amplicon panel and demonstrated the potential for SARS-CoV-2 variant detection. Data obtained here underscore the potential for wastewater surveillance of SARS-CoV-2 and other infectious agents in communities. Promega Corporation. Published by Elsevier B.V. 2021-11-15 2021-07-07 /pmc/articles/PMC8262391/ /pubmed/34252764 http://dx.doi.org/10.1016/j.scitotenv.2021.148834 Text en © 2021 Promega Corporation Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Mondal, Subhanjan Feirer, Nathan Brockman, Michael Preston, Melanie A. Teter, Sarah J. Ma, Dongping Goueli, Said A. Moorji, Sameer Saul, Brigitta Cali, James J. A direct capture method for purification and detection of viral nucleic acid enables epidemiological surveillance of SARS-CoV-2 |
title | A direct capture method for purification and detection of viral nucleic acid enables epidemiological surveillance of SARS-CoV-2 |
title_full | A direct capture method for purification and detection of viral nucleic acid enables epidemiological surveillance of SARS-CoV-2 |
title_fullStr | A direct capture method for purification and detection of viral nucleic acid enables epidemiological surveillance of SARS-CoV-2 |
title_full_unstemmed | A direct capture method for purification and detection of viral nucleic acid enables epidemiological surveillance of SARS-CoV-2 |
title_short | A direct capture method for purification and detection of viral nucleic acid enables epidemiological surveillance of SARS-CoV-2 |
title_sort | direct capture method for purification and detection of viral nucleic acid enables epidemiological surveillance of sars-cov-2 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8262391/ https://www.ncbi.nlm.nih.gov/pubmed/34252764 http://dx.doi.org/10.1016/j.scitotenv.2021.148834 |
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