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Development and validation of viral load assays to quantitate SARS-CoV-2
SARS-CoV-2 has infected more than 30 million persons throughout the world. A subset of patients suffer serious consequences that require hospitalization and ventilator support. Current tests for SARS-CoV-2 generate qualitative results and are vital to make a diagnosis of the infection. However, they...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Author(s). Published by Elsevier B.V.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7883709/ https://www.ncbi.nlm.nih.gov/pubmed/33600849 http://dx.doi.org/10.1016/j.jviromet.2021.114100 |
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author | Bland, Joshua Kavanaugh, Ashley Hong, Lenny K. Kadkol, Shrihari S. |
author_facet | Bland, Joshua Kavanaugh, Ashley Hong, Lenny K. Kadkol, Shrihari S. |
author_sort | Bland, Joshua |
collection | PubMed |
description | SARS-CoV-2 has infected more than 30 million persons throughout the world. A subset of patients suffer serious consequences that require hospitalization and ventilator support. Current tests for SARS-CoV-2 generate qualitative results and are vital to make a diagnosis of the infection. However, they are not helpful to follow changes in viral loads after diagnosis. The ability to quantitatively assess viral levels is necessary to determine the effectiveness of therapy with anti-viral or immune agents. Viral load analysis is also necessary to determine the replicative potential of strains with different mutations, emergence of resistance to anti-viral agents and the stability of viral nucleic acid and degree of RT-PCR inhibition in different types of collection media. Quantitative viral load analysis in body fluids, plasma and tissue may be helpful to determine the effects of the infection in various organ systems. To address these needs, we developed two assays to quantitate SARS-CoV-2. The assays target either the S or E genes in the virus, produce comparable viral load results, are highly sensitive and specific and have a wide range of quantitation. We believe that these assays will be helpful to manage the clinical course of infected patients and may also help to better understand the biology of infection with SARS-CoV-2. |
format | Online Article Text |
id | pubmed-7883709 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Author(s). Published by Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78837092021-02-16 Development and validation of viral load assays to quantitate SARS-CoV-2 Bland, Joshua Kavanaugh, Ashley Hong, Lenny K. Kadkol, Shrihari S. J Virol Methods Article SARS-CoV-2 has infected more than 30 million persons throughout the world. A subset of patients suffer serious consequences that require hospitalization and ventilator support. Current tests for SARS-CoV-2 generate qualitative results and are vital to make a diagnosis of the infection. However, they are not helpful to follow changes in viral loads after diagnosis. The ability to quantitatively assess viral levels is necessary to determine the effectiveness of therapy with anti-viral or immune agents. Viral load analysis is also necessary to determine the replicative potential of strains with different mutations, emergence of resistance to anti-viral agents and the stability of viral nucleic acid and degree of RT-PCR inhibition in different types of collection media. Quantitative viral load analysis in body fluids, plasma and tissue may be helpful to determine the effects of the infection in various organ systems. To address these needs, we developed two assays to quantitate SARS-CoV-2. The assays target either the S or E genes in the virus, produce comparable viral load results, are highly sensitive and specific and have a wide range of quantitation. We believe that these assays will be helpful to manage the clinical course of infected patients and may also help to better understand the biology of infection with SARS-CoV-2. The Author(s). Published by Elsevier B.V. 2021-05 2021-02-15 /pmc/articles/PMC7883709/ /pubmed/33600849 http://dx.doi.org/10.1016/j.jviromet.2021.114100 Text en © 2021 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 Bland, Joshua Kavanaugh, Ashley Hong, Lenny K. Kadkol, Shrihari S. Development and validation of viral load assays to quantitate SARS-CoV-2 |
title | Development and validation of viral load assays to quantitate SARS-CoV-2 |
title_full | Development and validation of viral load assays to quantitate SARS-CoV-2 |
title_fullStr | Development and validation of viral load assays to quantitate SARS-CoV-2 |
title_full_unstemmed | Development and validation of viral load assays to quantitate SARS-CoV-2 |
title_short | Development and validation of viral load assays to quantitate SARS-CoV-2 |
title_sort | development and validation of viral load assays to quantitate sars-cov-2 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7883709/ https://www.ncbi.nlm.nih.gov/pubmed/33600849 http://dx.doi.org/10.1016/j.jviromet.2021.114100 |
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