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Deep mutational scanning identifies SARS-CoV-2 Nucleocapsid escape mutations of currently available rapid antigen tests
The effects of mutations in continuously emerging variants of SARS-CoV-2 are a major concern for the performance of rapid antigen tests. To evaluate the impact of mutations on 17 antibodies used in 11 commercially available antigen tests with emergency use authorization, we measured antibody binding...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Authors. Published by Elsevier Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9420710/ https://www.ncbi.nlm.nih.gov/pubmed/36084631 http://dx.doi.org/10.1016/j.cell.2022.08.010 |
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author | Frank, Filipp Keen, Meredith M. Rao, Anuradha Bassit, Leda Liu, Xu Bowers, Heather B. Patel, Anamika B. Cato, Michael L. Sullivan, Julie A. Greenleaf, Morgan Piantadosi, Anne Lam, Wilbur A. Hudson, William H. Ortlund, Eric A. |
author_facet | Frank, Filipp Keen, Meredith M. Rao, Anuradha Bassit, Leda Liu, Xu Bowers, Heather B. Patel, Anamika B. Cato, Michael L. Sullivan, Julie A. Greenleaf, Morgan Piantadosi, Anne Lam, Wilbur A. Hudson, William H. Ortlund, Eric A. |
author_sort | Frank, Filipp |
collection | PubMed |
description | The effects of mutations in continuously emerging variants of SARS-CoV-2 are a major concern for the performance of rapid antigen tests. To evaluate the impact of mutations on 17 antibodies used in 11 commercially available antigen tests with emergency use authorization, we measured antibody binding for all possible Nucleocapsid point mutations using a mammalian surface-display platform and deep mutational scanning. The results provide a complete map of the antibodies’ epitopes and their susceptibility to mutational escape. Our data predict no vulnerabilities for detection of mutations found in variants of concern. We confirm this using the commercial tests and sequence-confirmed COVID-19 patient samples. The antibody escape mutational profiles generated here serve as a valuable resource for predicting the performance of rapid antigen tests against past, current, as well as any possible future variants of SARS-CoV-2, establishing the direct clinical and public health utility of our system. |
format | Online Article Text |
id | pubmed-9420710 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Authors. Published by Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94207102022-08-30 Deep mutational scanning identifies SARS-CoV-2 Nucleocapsid escape mutations of currently available rapid antigen tests Frank, Filipp Keen, Meredith M. Rao, Anuradha Bassit, Leda Liu, Xu Bowers, Heather B. Patel, Anamika B. Cato, Michael L. Sullivan, Julie A. Greenleaf, Morgan Piantadosi, Anne Lam, Wilbur A. Hudson, William H. Ortlund, Eric A. Cell Article The effects of mutations in continuously emerging variants of SARS-CoV-2 are a major concern for the performance of rapid antigen tests. To evaluate the impact of mutations on 17 antibodies used in 11 commercially available antigen tests with emergency use authorization, we measured antibody binding for all possible Nucleocapsid point mutations using a mammalian surface-display platform and deep mutational scanning. The results provide a complete map of the antibodies’ epitopes and their susceptibility to mutational escape. Our data predict no vulnerabilities for detection of mutations found in variants of concern. We confirm this using the commercial tests and sequence-confirmed COVID-19 patient samples. The antibody escape mutational profiles generated here serve as a valuable resource for predicting the performance of rapid antigen tests against past, current, as well as any possible future variants of SARS-CoV-2, establishing the direct clinical and public health utility of our system. The Authors. Published by Elsevier Inc. 2022-09-15 2022-08-29 /pmc/articles/PMC9420710/ /pubmed/36084631 http://dx.doi.org/10.1016/j.cell.2022.08.010 Text en © 2022 The Authors 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 Frank, Filipp Keen, Meredith M. Rao, Anuradha Bassit, Leda Liu, Xu Bowers, Heather B. Patel, Anamika B. Cato, Michael L. Sullivan, Julie A. Greenleaf, Morgan Piantadosi, Anne Lam, Wilbur A. Hudson, William H. Ortlund, Eric A. Deep mutational scanning identifies SARS-CoV-2 Nucleocapsid escape mutations of currently available rapid antigen tests |
title | Deep mutational scanning identifies SARS-CoV-2 Nucleocapsid escape mutations of currently available rapid antigen tests |
title_full | Deep mutational scanning identifies SARS-CoV-2 Nucleocapsid escape mutations of currently available rapid antigen tests |
title_fullStr | Deep mutational scanning identifies SARS-CoV-2 Nucleocapsid escape mutations of currently available rapid antigen tests |
title_full_unstemmed | Deep mutational scanning identifies SARS-CoV-2 Nucleocapsid escape mutations of currently available rapid antigen tests |
title_short | Deep mutational scanning identifies SARS-CoV-2 Nucleocapsid escape mutations of currently available rapid antigen tests |
title_sort | deep mutational scanning identifies sars-cov-2 nucleocapsid escape mutations of currently available rapid antigen tests |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9420710/ https://www.ncbi.nlm.nih.gov/pubmed/36084631 http://dx.doi.org/10.1016/j.cell.2022.08.010 |
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