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Ultra-rapid detection of SARS-CoV-2 in public workspace environments
Managing the pandemic caused by SARS-CoV-2 requires new capabilities in testing, including the possibility of identifying, in minutes, infected individuals as they enter spaces where they must congregate in a functioning society, including workspaces, schools, points of entry, and commercial busines...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7904170/ https://www.ncbi.nlm.nih.gov/pubmed/33626039 http://dx.doi.org/10.1371/journal.pone.0240524 |
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author | Yaren, Ozlem McCarter, Jacquelyn Phadke, Nikhil Bradley, Kevin M. Overton, Benjamin Yang, Zunyi Ranade, Shatakshi Patil, Kunal Bangale, Rishikesh Benner, Steven A. |
author_facet | Yaren, Ozlem McCarter, Jacquelyn Phadke, Nikhil Bradley, Kevin M. Overton, Benjamin Yang, Zunyi Ranade, Shatakshi Patil, Kunal Bangale, Rishikesh Benner, Steven A. |
author_sort | Yaren, Ozlem |
collection | PubMed |
description | Managing the pandemic caused by SARS-CoV-2 requires new capabilities in testing, including the possibility of identifying, in minutes, infected individuals as they enter spaces where they must congregate in a functioning society, including workspaces, schools, points of entry, and commercial business establishments. Here, the only useful tests (a) require no sample transport, (b) require minimal sample manipulation, (c) can be performed by unlicensed individuals, (d) return results on the spot in much less than one hour, and (e) cost no more than a few dollars. The sensitivity need not be as high as normally required by the FDA for screening asymptomatic carriers (as few as 10 virions per sample), as these viral loads are almost certainly not high enough for an individual to present a risk for forward infection. This allows tests specifically useful for this pandemic to trade-off unneeded sensitivity for necessary speed, simplicity, and frugality. In some studies, it was shown that viral load that creates forward-infection risk may exceed 10(5) virions per milliliter, easily within the sensitivity of an RNA amplification architecture, but unattainable by antibody-based architectures that simply target viral antigens. Here, we describe such a test based on a displaceable probe loop amplification architecture. |
format | Online Article Text |
id | pubmed-7904170 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-79041702021-03-02 Ultra-rapid detection of SARS-CoV-2 in public workspace environments Yaren, Ozlem McCarter, Jacquelyn Phadke, Nikhil Bradley, Kevin M. Overton, Benjamin Yang, Zunyi Ranade, Shatakshi Patil, Kunal Bangale, Rishikesh Benner, Steven A. PLoS One Research Article Managing the pandemic caused by SARS-CoV-2 requires new capabilities in testing, including the possibility of identifying, in minutes, infected individuals as they enter spaces where they must congregate in a functioning society, including workspaces, schools, points of entry, and commercial business establishments. Here, the only useful tests (a) require no sample transport, (b) require minimal sample manipulation, (c) can be performed by unlicensed individuals, (d) return results on the spot in much less than one hour, and (e) cost no more than a few dollars. The sensitivity need not be as high as normally required by the FDA for screening asymptomatic carriers (as few as 10 virions per sample), as these viral loads are almost certainly not high enough for an individual to present a risk for forward infection. This allows tests specifically useful for this pandemic to trade-off unneeded sensitivity for necessary speed, simplicity, and frugality. In some studies, it was shown that viral load that creates forward-infection risk may exceed 10(5) virions per milliliter, easily within the sensitivity of an RNA amplification architecture, but unattainable by antibody-based architectures that simply target viral antigens. Here, we describe such a test based on a displaceable probe loop amplification architecture. Public Library of Science 2021-02-24 /pmc/articles/PMC7904170/ /pubmed/33626039 http://dx.doi.org/10.1371/journal.pone.0240524 Text en © 2021 Yaren et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Yaren, Ozlem McCarter, Jacquelyn Phadke, Nikhil Bradley, Kevin M. Overton, Benjamin Yang, Zunyi Ranade, Shatakshi Patil, Kunal Bangale, Rishikesh Benner, Steven A. Ultra-rapid detection of SARS-CoV-2 in public workspace environments |
title | Ultra-rapid detection of SARS-CoV-2 in public workspace environments |
title_full | Ultra-rapid detection of SARS-CoV-2 in public workspace environments |
title_fullStr | Ultra-rapid detection of SARS-CoV-2 in public workspace environments |
title_full_unstemmed | Ultra-rapid detection of SARS-CoV-2 in public workspace environments |
title_short | Ultra-rapid detection of SARS-CoV-2 in public workspace environments |
title_sort | ultra-rapid detection of sars-cov-2 in public workspace environments |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7904170/ https://www.ncbi.nlm.nih.gov/pubmed/33626039 http://dx.doi.org/10.1371/journal.pone.0240524 |
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