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Connecting within-host dynamics to the rate of viral molecular evolution

Viruses evolve rapidly, providing a unique system for understanding the processes that influence rates of molecular evolution. Neutral theory posits that the evolutionary rate increases linearly with the mutation rate. The occurrence of deleterious mutations causes this relationship to break down at...

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Autores principales: Peck, Kayla M., Chan, Carmen H. S., Tanaka, Mark M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5014490/
https://www.ncbi.nlm.nih.gov/pubmed/27774285
http://dx.doi.org/10.1093/ve/vev013
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author Peck, Kayla M.
Chan, Carmen H. S.
Tanaka, Mark M.
author_facet Peck, Kayla M.
Chan, Carmen H. S.
Tanaka, Mark M.
author_sort Peck, Kayla M.
collection PubMed
description Viruses evolve rapidly, providing a unique system for understanding the processes that influence rates of molecular evolution. Neutral theory posits that the evolutionary rate increases linearly with the mutation rate. The occurrence of deleterious mutations causes this relationship to break down at high mutation rates. Previous studies have identified this as an important phenomenon, particularly for RNA viruses which can mutate at rates near the extinction threshold. We propose that in addition to mutation dynamics, viral within-host dynamics can also affect the between-host evolutionary rate. We present an analytical model that predicts the neutral evolution rate for viruses as a function of both within-host parameters and deleterious mutations. To examine the effect of more detailed aspects of the virus life cycle, we also present a computational model that simulates acute virus evolution using target cell-limited dynamics. Using influenza A virus as a case study, we find that our simulation model can predict empirical rates of evolution better than a model lacking within-host details. The analytical model does not perform as well as the simulation model but shows how the within-host basic reproductive number influences evolutionary rates. These findings lend support to the idea that the mutation rate alone is not sufficient to predict the evolutionary rate in viruses, instead calling for improved models that account for viral within-host dynamics.
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spelling pubmed-50144902016-10-21 Connecting within-host dynamics to the rate of viral molecular evolution Peck, Kayla M. Chan, Carmen H. S. Tanaka, Mark M. Virus Evol Research Article Viruses evolve rapidly, providing a unique system for understanding the processes that influence rates of molecular evolution. Neutral theory posits that the evolutionary rate increases linearly with the mutation rate. The occurrence of deleterious mutations causes this relationship to break down at high mutation rates. Previous studies have identified this as an important phenomenon, particularly for RNA viruses which can mutate at rates near the extinction threshold. We propose that in addition to mutation dynamics, viral within-host dynamics can also affect the between-host evolutionary rate. We present an analytical model that predicts the neutral evolution rate for viruses as a function of both within-host parameters and deleterious mutations. To examine the effect of more detailed aspects of the virus life cycle, we also present a computational model that simulates acute virus evolution using target cell-limited dynamics. Using influenza A virus as a case study, we find that our simulation model can predict empirical rates of evolution better than a model lacking within-host details. The analytical model does not perform as well as the simulation model but shows how the within-host basic reproductive number influences evolutionary rates. These findings lend support to the idea that the mutation rate alone is not sufficient to predict the evolutionary rate in viruses, instead calling for improved models that account for viral within-host dynamics. Oxford University Press 2015-10-02 /pmc/articles/PMC5014490/ /pubmed/27774285 http://dx.doi.org/10.1093/ve/vev013 Text en © The Author 2015. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Peck, Kayla M.
Chan, Carmen H. S.
Tanaka, Mark M.
Connecting within-host dynamics to the rate of viral molecular evolution
title Connecting within-host dynamics to the rate of viral molecular evolution
title_full Connecting within-host dynamics to the rate of viral molecular evolution
title_fullStr Connecting within-host dynamics to the rate of viral molecular evolution
title_full_unstemmed Connecting within-host dynamics to the rate of viral molecular evolution
title_short Connecting within-host dynamics to the rate of viral molecular evolution
title_sort connecting within-host dynamics to the rate of viral molecular evolution
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5014490/
https://www.ncbi.nlm.nih.gov/pubmed/27774285
http://dx.doi.org/10.1093/ve/vev013
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