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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Authors. Published by Elsevier Inc. 2022
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.
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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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