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A novel diagnostic test to screen SARS-CoV-2 variants containing E484K and N501Y mutations
Spike protein mutations E484K and N501Y carried by SARS-CoV-2 variants have been associated with concerning changes of the virus, including resistance to neutralizing antibodies and increased transmissibility. While the concerning variants are fast spreading in various geographical areas, identifica...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8168736/ https://www.ncbi.nlm.nih.gov/pubmed/33977858 http://dx.doi.org/10.1080/22221751.2021.1929504 |
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author | Zhao, Yanan Lee, Annie Composto, Kaelea Cunningham, Marcus H. Mediavilla, Jose R. Fennessey, Samantha Corvelo, André Chow, Kar Fai Zody, Michael Chen, Liang Kreiswirth, Barry N. Perlin, David S. |
author_facet | Zhao, Yanan Lee, Annie Composto, Kaelea Cunningham, Marcus H. Mediavilla, Jose R. Fennessey, Samantha Corvelo, André Chow, Kar Fai Zody, Michael Chen, Liang Kreiswirth, Barry N. Perlin, David S. |
author_sort | Zhao, Yanan |
collection | PubMed |
description | Spike protein mutations E484K and N501Y carried by SARS-CoV-2 variants have been associated with concerning changes of the virus, including resistance to neutralizing antibodies and increased transmissibility. While the concerning variants are fast spreading in various geographical areas, identification and monitoring of these variants are lagging far behind, due in large part to the slow speed and insufficient capacity of viral sequencing. In response to the unmet need for a fast and efficient screening tool, we developed a single-tube duplex molecular assay for rapid and simultaneous identification of E484K and N501Y mutations from nasopharyngeal swab (NS) samples within 2.5 h from sample preparation to report. Using this tool, we screened a total of 1135 clinical NS samples collected from COVID patients at 8 hospitals within the Hackensack Meridian Health network in New Jersey between late December 2020 and March 2021. Our data revealed dramatic increases in the frequencies of both E484K and N501Y over time, underscoring the need for continuous epidemiological monitoring. |
format | Online Article Text |
id | pubmed-8168736 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-81687362021-06-07 A novel diagnostic test to screen SARS-CoV-2 variants containing E484K and N501Y mutations Zhao, Yanan Lee, Annie Composto, Kaelea Cunningham, Marcus H. Mediavilla, Jose R. Fennessey, Samantha Corvelo, André Chow, Kar Fai Zody, Michael Chen, Liang Kreiswirth, Barry N. Perlin, David S. Emerg Microbes Infect Letter Spike protein mutations E484K and N501Y carried by SARS-CoV-2 variants have been associated with concerning changes of the virus, including resistance to neutralizing antibodies and increased transmissibility. While the concerning variants are fast spreading in various geographical areas, identification and monitoring of these variants are lagging far behind, due in large part to the slow speed and insufficient capacity of viral sequencing. In response to the unmet need for a fast and efficient screening tool, we developed a single-tube duplex molecular assay for rapid and simultaneous identification of E484K and N501Y mutations from nasopharyngeal swab (NS) samples within 2.5 h from sample preparation to report. Using this tool, we screened a total of 1135 clinical NS samples collected from COVID patients at 8 hospitals within the Hackensack Meridian Health network in New Jersey between late December 2020 and March 2021. Our data revealed dramatic increases in the frequencies of both E484K and N501Y over time, underscoring the need for continuous epidemiological monitoring. Taylor & Francis 2021-05-28 /pmc/articles/PMC8168736/ /pubmed/33977858 http://dx.doi.org/10.1080/22221751.2021.1929504 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group, on behalf of Shanghai Shangyixun Cultural Communication Co., Ltd https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Letter Zhao, Yanan Lee, Annie Composto, Kaelea Cunningham, Marcus H. Mediavilla, Jose R. Fennessey, Samantha Corvelo, André Chow, Kar Fai Zody, Michael Chen, Liang Kreiswirth, Barry N. Perlin, David S. A novel diagnostic test to screen SARS-CoV-2 variants containing E484K and N501Y mutations |
title | A novel diagnostic test to screen SARS-CoV-2 variants containing E484K and N501Y mutations |
title_full | A novel diagnostic test to screen SARS-CoV-2 variants containing E484K and N501Y mutations |
title_fullStr | A novel diagnostic test to screen SARS-CoV-2 variants containing E484K and N501Y mutations |
title_full_unstemmed | A novel diagnostic test to screen SARS-CoV-2 variants containing E484K and N501Y mutations |
title_short | A novel diagnostic test to screen SARS-CoV-2 variants containing E484K and N501Y mutations |
title_sort | novel diagnostic test to screen sars-cov-2 variants containing e484k and n501y mutations |
topic | Letter |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8168736/ https://www.ncbi.nlm.nih.gov/pubmed/33977858 http://dx.doi.org/10.1080/22221751.2021.1929504 |
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