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SARS-CoV-2 variants, spike mutations and immune escape
Although most mutations in the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) genome are expected to be either deleterious and swiftly purged or relatively neutral, a small proportion will affect functional properties and may alter infectivity, disease severity or interactions with hos...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8167834/ https://www.ncbi.nlm.nih.gov/pubmed/34075212 http://dx.doi.org/10.1038/s41579-021-00573-0 |
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author | Harvey, William T. Carabelli, Alessandro M. Jackson, Ben Gupta, Ravindra K. Thomson, Emma C. Harrison, Ewan M. Ludden, Catherine Reeve, Richard Rambaut, Andrew Peacock, Sharon J. Robertson, David L. |
author_facet | Harvey, William T. Carabelli, Alessandro M. Jackson, Ben Gupta, Ravindra K. Thomson, Emma C. Harrison, Ewan M. Ludden, Catherine Reeve, Richard Rambaut, Andrew Peacock, Sharon J. Robertson, David L. |
author_sort | Harvey, William T. |
collection | PubMed |
description | Although most mutations in the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) genome are expected to be either deleterious and swiftly purged or relatively neutral, a small proportion will affect functional properties and may alter infectivity, disease severity or interactions with host immunity. The emergence of SARS-CoV-2 in late 2019 was followed by a period of relative evolutionary stasis lasting about 11 months. Since late 2020, however, SARS-CoV-2 evolution has been characterized by the emergence of sets of mutations, in the context of ‘variants of concern’, that impact virus characteristics, including transmissibility and antigenicity, probably in response to the changing immune profile of the human population. There is emerging evidence of reduced neutralization of some SARS-CoV-2 variants by postvaccination serum; however, a greater understanding of correlates of protection is required to evaluate how this may impact vaccine effectiveness. Nonetheless, manufacturers are preparing platforms for a possible update of vaccine sequences, and it is crucial that surveillance of genetic and antigenic changes in the global virus population is done alongside experiments to elucidate the phenotypic impacts of mutations. In this Review, we summarize the literature on mutations of the SARS-CoV-2 spike protein, the primary antigen, focusing on their impacts on antigenicity and contextualizing them in the protein structure, and discuss them in the context of observed mutation frequencies in global sequence datasets. |
format | Online Article Text |
id | pubmed-8167834 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81678342021-06-01 SARS-CoV-2 variants, spike mutations and immune escape Harvey, William T. Carabelli, Alessandro M. Jackson, Ben Gupta, Ravindra K. Thomson, Emma C. Harrison, Ewan M. Ludden, Catherine Reeve, Richard Rambaut, Andrew Peacock, Sharon J. Robertson, David L. Nat Rev Microbiol Review Article Although most mutations in the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) genome are expected to be either deleterious and swiftly purged or relatively neutral, a small proportion will affect functional properties and may alter infectivity, disease severity or interactions with host immunity. The emergence of SARS-CoV-2 in late 2019 was followed by a period of relative evolutionary stasis lasting about 11 months. Since late 2020, however, SARS-CoV-2 evolution has been characterized by the emergence of sets of mutations, in the context of ‘variants of concern’, that impact virus characteristics, including transmissibility and antigenicity, probably in response to the changing immune profile of the human population. There is emerging evidence of reduced neutralization of some SARS-CoV-2 variants by postvaccination serum; however, a greater understanding of correlates of protection is required to evaluate how this may impact vaccine effectiveness. Nonetheless, manufacturers are preparing platforms for a possible update of vaccine sequences, and it is crucial that surveillance of genetic and antigenic changes in the global virus population is done alongside experiments to elucidate the phenotypic impacts of mutations. In this Review, we summarize the literature on mutations of the SARS-CoV-2 spike protein, the primary antigen, focusing on their impacts on antigenicity and contextualizing them in the protein structure, and discuss them in the context of observed mutation frequencies in global sequence datasets. Nature Publishing Group UK 2021-06-01 2021 /pmc/articles/PMC8167834/ /pubmed/34075212 http://dx.doi.org/10.1038/s41579-021-00573-0 Text en © Springer Nature Limited 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Review Article Harvey, William T. Carabelli, Alessandro M. Jackson, Ben Gupta, Ravindra K. Thomson, Emma C. Harrison, Ewan M. Ludden, Catherine Reeve, Richard Rambaut, Andrew Peacock, Sharon J. Robertson, David L. SARS-CoV-2 variants, spike mutations and immune escape |
title | SARS-CoV-2 variants, spike mutations and immune escape |
title_full | SARS-CoV-2 variants, spike mutations and immune escape |
title_fullStr | SARS-CoV-2 variants, spike mutations and immune escape |
title_full_unstemmed | SARS-CoV-2 variants, spike mutations and immune escape |
title_short | SARS-CoV-2 variants, spike mutations and immune escape |
title_sort | sars-cov-2 variants, spike mutations and immune escape |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8167834/ https://www.ncbi.nlm.nih.gov/pubmed/34075212 http://dx.doi.org/10.1038/s41579-021-00573-0 |
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