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Host heterogeneity and epistasis explain punctuated evolution of SARS-CoV-2
Identifying drivers of viral diversity is key to understanding the evolutionary as well as epidemiological dynamics of the COVID-19 pandemic. Using rich viral genomic data sets, we show that periods of steadily rising diversity have been punctuated by sudden, enormous increases followed by similarly...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9974118/ https://www.ncbi.nlm.nih.gov/pubmed/36791146 http://dx.doi.org/10.1371/journal.pcbi.1010896 |
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author | Nielsen, Bjarke Frost Saad-Roy, Chadi M. Li, Yimei Sneppen, Kim Simonsen, Lone Viboud, Cécile Levin, Simon A. Grenfell, Bryan T. |
author_facet | Nielsen, Bjarke Frost Saad-Roy, Chadi M. Li, Yimei Sneppen, Kim Simonsen, Lone Viboud, Cécile Levin, Simon A. Grenfell, Bryan T. |
author_sort | Nielsen, Bjarke Frost |
collection | PubMed |
description | Identifying drivers of viral diversity is key to understanding the evolutionary as well as epidemiological dynamics of the COVID-19 pandemic. Using rich viral genomic data sets, we show that periods of steadily rising diversity have been punctuated by sudden, enormous increases followed by similarly abrupt collapses of diversity. We introduce a mechanistic model of saltational evolution with epistasis and demonstrate that these features parsimoniously account for the observed temporal dynamics of inter-genomic diversity. Our results provide support for recent proposals that saltational evolution may be a signature feature of SARS-CoV-2, allowing the pathogen to more readily evolve highly transmissible variants. These findings lend theoretical support to a heightened awareness of biological contexts where increased diversification may occur. They also underline the power of pathogen genomics and other surveillance streams in clarifying the phylodynamics of emerging and endemic infections. In public health terms, our results further underline the importance of equitable distribution of up-to-date vaccines. |
format | Online Article Text |
id | pubmed-9974118 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-99741182023-03-01 Host heterogeneity and epistasis explain punctuated evolution of SARS-CoV-2 Nielsen, Bjarke Frost Saad-Roy, Chadi M. Li, Yimei Sneppen, Kim Simonsen, Lone Viboud, Cécile Levin, Simon A. Grenfell, Bryan T. PLoS Comput Biol Research Article Identifying drivers of viral diversity is key to understanding the evolutionary as well as epidemiological dynamics of the COVID-19 pandemic. Using rich viral genomic data sets, we show that periods of steadily rising diversity have been punctuated by sudden, enormous increases followed by similarly abrupt collapses of diversity. We introduce a mechanistic model of saltational evolution with epistasis and demonstrate that these features parsimoniously account for the observed temporal dynamics of inter-genomic diversity. Our results provide support for recent proposals that saltational evolution may be a signature feature of SARS-CoV-2, allowing the pathogen to more readily evolve highly transmissible variants. These findings lend theoretical support to a heightened awareness of biological contexts where increased diversification may occur. They also underline the power of pathogen genomics and other surveillance streams in clarifying the phylodynamics of emerging and endemic infections. In public health terms, our results further underline the importance of equitable distribution of up-to-date vaccines. Public Library of Science 2023-02-15 /pmc/articles/PMC9974118/ /pubmed/36791146 http://dx.doi.org/10.1371/journal.pcbi.1010896 Text en https://creativecommons.org/publicdomain/zero/1.0/This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication. |
spellingShingle | Research Article Nielsen, Bjarke Frost Saad-Roy, Chadi M. Li, Yimei Sneppen, Kim Simonsen, Lone Viboud, Cécile Levin, Simon A. Grenfell, Bryan T. Host heterogeneity and epistasis explain punctuated evolution of SARS-CoV-2 |
title | Host heterogeneity and epistasis explain punctuated evolution of SARS-CoV-2 |
title_full | Host heterogeneity and epistasis explain punctuated evolution of SARS-CoV-2 |
title_fullStr | Host heterogeneity and epistasis explain punctuated evolution of SARS-CoV-2 |
title_full_unstemmed | Host heterogeneity and epistasis explain punctuated evolution of SARS-CoV-2 |
title_short | Host heterogeneity and epistasis explain punctuated evolution of SARS-CoV-2 |
title_sort | host heterogeneity and epistasis explain punctuated evolution of sars-cov-2 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9974118/ https://www.ncbi.nlm.nih.gov/pubmed/36791146 http://dx.doi.org/10.1371/journal.pcbi.1010896 |
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