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Parallel evolution in the emergence of highly pathogenic avian influenza A viruses

Parallel molecular evolution and adaptation are important phenomena commonly observed in viruses. Here, we exploit parallel molecular evolution to understand virulence evolution in avian influenza viruses (AIV). Highly-pathogenic AIVs evolve independently from low-pathogenic ancestors via acquisitio...

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Autores principales: Escalera-Zamudio, Marina, Golden, Michael, Gutiérrez, Bernardo, Thézé, Julien, Keown, Jeremy Russell, Carrique, Loic, Bowden, Thomas A., Pybus, Oliver G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7608645/
https://www.ncbi.nlm.nih.gov/pubmed/33139731
http://dx.doi.org/10.1038/s41467-020-19364-x
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author Escalera-Zamudio, Marina
Golden, Michael
Gutiérrez, Bernardo
Thézé, Julien
Keown, Jeremy Russell
Carrique, Loic
Bowden, Thomas A.
Pybus, Oliver G.
author_facet Escalera-Zamudio, Marina
Golden, Michael
Gutiérrez, Bernardo
Thézé, Julien
Keown, Jeremy Russell
Carrique, Loic
Bowden, Thomas A.
Pybus, Oliver G.
author_sort Escalera-Zamudio, Marina
collection PubMed
description Parallel molecular evolution and adaptation are important phenomena commonly observed in viruses. Here, we exploit parallel molecular evolution to understand virulence evolution in avian influenza viruses (AIV). Highly-pathogenic AIVs evolve independently from low-pathogenic ancestors via acquisition of polybasic cleavage sites. Why some AIV lineages but not others evolve in this way is unknown. We hypothesise that the parallel emergence of highly-pathogenic AIV may be facilitated by permissive or compensatory mutations occurring across the viral genome. We combine phylogenetic, statistical and structural approaches to discover parallel mutations in AIV genomes associated with the highly-pathogenic phenotype. Parallel mutations were screened using a statistical test of mutation-phenotype association and further evaluated in the contexts of positive selection and protein structure. Our resulting mutational panel may help to reveal new links between virulence evolution and other traits, and raises the possibility of predicting aspects of AIV evolution.
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spelling pubmed-76086452020-11-10 Parallel evolution in the emergence of highly pathogenic avian influenza A viruses Escalera-Zamudio, Marina Golden, Michael Gutiérrez, Bernardo Thézé, Julien Keown, Jeremy Russell Carrique, Loic Bowden, Thomas A. Pybus, Oliver G. Nat Commun Article Parallel molecular evolution and adaptation are important phenomena commonly observed in viruses. Here, we exploit parallel molecular evolution to understand virulence evolution in avian influenza viruses (AIV). Highly-pathogenic AIVs evolve independently from low-pathogenic ancestors via acquisition of polybasic cleavage sites. Why some AIV lineages but not others evolve in this way is unknown. We hypothesise that the parallel emergence of highly-pathogenic AIV may be facilitated by permissive or compensatory mutations occurring across the viral genome. We combine phylogenetic, statistical and structural approaches to discover parallel mutations in AIV genomes associated with the highly-pathogenic phenotype. Parallel mutations were screened using a statistical test of mutation-phenotype association and further evaluated in the contexts of positive selection and protein structure. Our resulting mutational panel may help to reveal new links between virulence evolution and other traits, and raises the possibility of predicting aspects of AIV evolution. Nature Publishing Group UK 2020-11-02 /pmc/articles/PMC7608645/ /pubmed/33139731 http://dx.doi.org/10.1038/s41467-020-19364-x Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Escalera-Zamudio, Marina
Golden, Michael
Gutiérrez, Bernardo
Thézé, Julien
Keown, Jeremy Russell
Carrique, Loic
Bowden, Thomas A.
Pybus, Oliver G.
Parallel evolution in the emergence of highly pathogenic avian influenza A viruses
title Parallel evolution in the emergence of highly pathogenic avian influenza A viruses
title_full Parallel evolution in the emergence of highly pathogenic avian influenza A viruses
title_fullStr Parallel evolution in the emergence of highly pathogenic avian influenza A viruses
title_full_unstemmed Parallel evolution in the emergence of highly pathogenic avian influenza A viruses
title_short Parallel evolution in the emergence of highly pathogenic avian influenza A viruses
title_sort parallel evolution in the emergence of highly pathogenic avian influenza a viruses
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7608645/
https://www.ncbi.nlm.nih.gov/pubmed/33139731
http://dx.doi.org/10.1038/s41467-020-19364-x
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