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Growth, detection, quantification, and inactivation of SARS-CoV-2
Severe acute respiratory syndrome coronavirus (SARS-CoV)-2 is the agent responsible for the coronavirus disease 2019 (COVID-19) global pandemic. SARS-CoV-2 is closely related to SARS-CoV, which caused the 2003 SARS outbreak. Although numerous reagents were developed to study SARS-CoV infections, few...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Author(s). Published by Elsevier Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7293183/ https://www.ncbi.nlm.nih.gov/pubmed/32838945 http://dx.doi.org/10.1016/j.virol.2020.05.015 |
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author | Case, James Brett Bailey, Adam L. Kim, Arthur S. Chen, Rita E. Diamond, Michael S. |
author_facet | Case, James Brett Bailey, Adam L. Kim, Arthur S. Chen, Rita E. Diamond, Michael S. |
author_sort | Case, James Brett |
collection | PubMed |
description | Severe acute respiratory syndrome coronavirus (SARS-CoV)-2 is the agent responsible for the coronavirus disease 2019 (COVID-19) global pandemic. SARS-CoV-2 is closely related to SARS-CoV, which caused the 2003 SARS outbreak. Although numerous reagents were developed to study SARS-CoV infections, few have been applicable to evaluating SARS-CoV-2 infection and immunity. Current limitations in studying SARS-CoV-2 include few validated assays with fully replication-competent wild-type virus. We have developed protocols to propagate, quantify, and work with infectious SARS-CoV-2. Here, we describe: (1) virus stock generation, (2) RT-qPCR quantification of SARS-CoV-2 RNA; (3) detection of SARS-CoV-2 antigen by flow cytometry, (4) quantification of infectious SARS-CoV-2 by focus-forming and plaque assays; and (5) validated protocols for virus inactivation. Collectively, these methods can be adapted to a variety of experimental designs, which should accelerate our understanding of SARS-CoV-2 biology and the development of effective countermeasures against COVID-19. |
format | Online Article Text |
id | pubmed-7293183 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Author(s). Published by Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72931832020-06-14 Growth, detection, quantification, and inactivation of SARS-CoV-2 Case, James Brett Bailey, Adam L. Kim, Arthur S. Chen, Rita E. Diamond, Michael S. Virology Article Severe acute respiratory syndrome coronavirus (SARS-CoV)-2 is the agent responsible for the coronavirus disease 2019 (COVID-19) global pandemic. SARS-CoV-2 is closely related to SARS-CoV, which caused the 2003 SARS outbreak. Although numerous reagents were developed to study SARS-CoV infections, few have been applicable to evaluating SARS-CoV-2 infection and immunity. Current limitations in studying SARS-CoV-2 include few validated assays with fully replication-competent wild-type virus. We have developed protocols to propagate, quantify, and work with infectious SARS-CoV-2. Here, we describe: (1) virus stock generation, (2) RT-qPCR quantification of SARS-CoV-2 RNA; (3) detection of SARS-CoV-2 antigen by flow cytometry, (4) quantification of infectious SARS-CoV-2 by focus-forming and plaque assays; and (5) validated protocols for virus inactivation. Collectively, these methods can be adapted to a variety of experimental designs, which should accelerate our understanding of SARS-CoV-2 biology and the development of effective countermeasures against COVID-19. The Author(s). Published by Elsevier Inc. 2020-09 2020-06-13 /pmc/articles/PMC7293183/ /pubmed/32838945 http://dx.doi.org/10.1016/j.virol.2020.05.015 Text en © 2020 The Author(s) 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 Case, James Brett Bailey, Adam L. Kim, Arthur S. Chen, Rita E. Diamond, Michael S. Growth, detection, quantification, and inactivation of SARS-CoV-2 |
title | Growth, detection, quantification, and inactivation of SARS-CoV-2 |
title_full | Growth, detection, quantification, and inactivation of SARS-CoV-2 |
title_fullStr | Growth, detection, quantification, and inactivation of SARS-CoV-2 |
title_full_unstemmed | Growth, detection, quantification, and inactivation of SARS-CoV-2 |
title_short | Growth, detection, quantification, and inactivation of SARS-CoV-2 |
title_sort | growth, detection, quantification, and inactivation of sars-cov-2 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7293183/ https://www.ncbi.nlm.nih.gov/pubmed/32838945 http://dx.doi.org/10.1016/j.virol.2020.05.015 |
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