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Neutral Theory and Rapidly Evolving Viral Pathogens

The evolution of viral pathogens is shaped by strong selective forces that are exerted during jumps to new hosts, confrontations with host immune responses and antiviral drugs, and numerous other processes. However, while undeniably strong and frequent, adaptive evolution is largely confined to smal...

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Autores principales: Frost, Simon D W, Magalis, Brittany Rife, Kosakovsky Pond, Sergei L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6279309/
https://www.ncbi.nlm.nih.gov/pubmed/29688481
http://dx.doi.org/10.1093/molbev/msy088
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author Frost, Simon D W
Magalis, Brittany Rife
Kosakovsky Pond, Sergei L
author_facet Frost, Simon D W
Magalis, Brittany Rife
Kosakovsky Pond, Sergei L
author_sort Frost, Simon D W
collection PubMed
description The evolution of viral pathogens is shaped by strong selective forces that are exerted during jumps to new hosts, confrontations with host immune responses and antiviral drugs, and numerous other processes. However, while undeniably strong and frequent, adaptive evolution is largely confined to small parts of information-packed viral genomes, and the majority of observed variation is effectively neutral. The predictions and implications of the neutral theory have proven immensely useful in this context, with applications spanning understanding within-host population structure, tracing the origins and spread of viral pathogens, predicting evolutionary dynamics, and modeling the emergence of drug resistance. We highlight the multiple ways in which the neutral theory has had an impact, which has been accelerated in the age of high-throughput, high-resolution genomics.
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spelling pubmed-62793092019-06-01 Neutral Theory and Rapidly Evolving Viral Pathogens Frost, Simon D W Magalis, Brittany Rife Kosakovsky Pond, Sergei L Mol Biol Evol Perspective The evolution of viral pathogens is shaped by strong selective forces that are exerted during jumps to new hosts, confrontations with host immune responses and antiviral drugs, and numerous other processes. However, while undeniably strong and frequent, adaptive evolution is largely confined to small parts of information-packed viral genomes, and the majority of observed variation is effectively neutral. The predictions and implications of the neutral theory have proven immensely useful in this context, with applications spanning understanding within-host population structure, tracing the origins and spread of viral pathogens, predicting evolutionary dynamics, and modeling the emergence of drug resistance. We highlight the multiple ways in which the neutral theory has had an impact, which has been accelerated in the age of high-throughput, high-resolution genomics. Oxford University Press 2018-06 2018-04-24 /pmc/articles/PMC6279309/ /pubmed/29688481 http://dx.doi.org/10.1093/molbev/msy088 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com http://academic.oup.com/journals/pages/about_us/legal/notices This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/about_us/legal/notices)
spellingShingle Perspective
Frost, Simon D W
Magalis, Brittany Rife
Kosakovsky Pond, Sergei L
Neutral Theory and Rapidly Evolving Viral Pathogens
title Neutral Theory and Rapidly Evolving Viral Pathogens
title_full Neutral Theory and Rapidly Evolving Viral Pathogens
title_fullStr Neutral Theory and Rapidly Evolving Viral Pathogens
title_full_unstemmed Neutral Theory and Rapidly Evolving Viral Pathogens
title_short Neutral Theory and Rapidly Evolving Viral Pathogens
title_sort neutral theory and rapidly evolving viral pathogens
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6279309/
https://www.ncbi.nlm.nih.gov/pubmed/29688481
http://dx.doi.org/10.1093/molbev/msy088
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