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Mechanisms of viral mutation

The remarkable capacity of some viruses to adapt to new hosts and environments is highly dependent on their ability to generate de novo diversity in a short period of time. Rates of spontaneous mutation vary amply among viruses. RNA viruses mutate faster than DNA viruses, single-stranded viruses mut...

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Detalles Bibliográficos
Autores principales: Sanjuán, Rafael, Domingo-Calap, Pilar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5075021/
https://www.ncbi.nlm.nih.gov/pubmed/27392606
http://dx.doi.org/10.1007/s00018-016-2299-6
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author Sanjuán, Rafael
Domingo-Calap, Pilar
author_facet Sanjuán, Rafael
Domingo-Calap, Pilar
author_sort Sanjuán, Rafael
collection PubMed
description The remarkable capacity of some viruses to adapt to new hosts and environments is highly dependent on their ability to generate de novo diversity in a short period of time. Rates of spontaneous mutation vary amply among viruses. RNA viruses mutate faster than DNA viruses, single-stranded viruses mutate faster than double-strand virus, and genome size appears to correlate negatively with mutation rate. Viral mutation rates are modulated at different levels, including polymerase fidelity, sequence context, template secondary structure, cellular microenvironment, replication mechanisms, proofreading, and access to post-replicative repair. Additionally, massive numbers of mutations can be introduced by some virus-encoded diversity-generating elements, as well as by host-encoded cytidine/adenine deaminases. Our current knowledge of viral mutation rates indicates that viral genetic diversity is determined by multiple virus- and host-dependent processes, and that viral mutation rates can evolve in response to specific selective pressures.
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spelling pubmed-50750212016-11-04 Mechanisms of viral mutation Sanjuán, Rafael Domingo-Calap, Pilar Cell Mol Life Sci Review The remarkable capacity of some viruses to adapt to new hosts and environments is highly dependent on their ability to generate de novo diversity in a short period of time. Rates of spontaneous mutation vary amply among viruses. RNA viruses mutate faster than DNA viruses, single-stranded viruses mutate faster than double-strand virus, and genome size appears to correlate negatively with mutation rate. Viral mutation rates are modulated at different levels, including polymerase fidelity, sequence context, template secondary structure, cellular microenvironment, replication mechanisms, proofreading, and access to post-replicative repair. Additionally, massive numbers of mutations can be introduced by some virus-encoded diversity-generating elements, as well as by host-encoded cytidine/adenine deaminases. Our current knowledge of viral mutation rates indicates that viral genetic diversity is determined by multiple virus- and host-dependent processes, and that viral mutation rates can evolve in response to specific selective pressures. Springer International Publishing 2016-07-08 2016 /pmc/articles/PMC5075021/ /pubmed/27392606 http://dx.doi.org/10.1007/s00018-016-2299-6 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.
spellingShingle Review
Sanjuán, Rafael
Domingo-Calap, Pilar
Mechanisms of viral mutation
title Mechanisms of viral mutation
title_full Mechanisms of viral mutation
title_fullStr Mechanisms of viral mutation
title_full_unstemmed Mechanisms of viral mutation
title_short Mechanisms of viral mutation
title_sort mechanisms of viral mutation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5075021/
https://www.ncbi.nlm.nih.gov/pubmed/27392606
http://dx.doi.org/10.1007/s00018-016-2299-6
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