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Are RNA Viruses Adapting or Merely Changing?

RNA viruses and retroviruses fix substitutions approximately 1 million-fold faster than their hosts. This diversification could represent an inevitable drift under purifying selection, the majority of substitutions being phenotypically neutral. The alternative is to suppose that most fixed mutations...

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Detalles Bibliográficos
Autores principales: Sala, Monica, Wain-Hobson, Simon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7081970/
https://www.ncbi.nlm.nih.gov/pubmed/10903368
http://dx.doi.org/10.1007/s002390010062
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author Sala, Monica
Wain-Hobson, Simon
author_facet Sala, Monica
Wain-Hobson, Simon
author_sort Sala, Monica
collection PubMed
description RNA viruses and retroviruses fix substitutions approximately 1 million-fold faster than their hosts. This diversification could represent an inevitable drift under purifying selection, the majority of substitutions being phenotypically neutral. The alternative is to suppose that most fixed mutations are beneficial to the virus, allowing it to keep ahead of the host and/or host population. Here, relative sequence diversification of different proteins encoded by viral genomes is found to be linear. The examples encompass a wide variety of retroviruses and RNA viruses. The smoothness of relative divergence spans quasispeciation following clonal infection, to variation among different isolates of the same virus, to viruses from different species or those associated with different diseases, indicating that the majority of fixed mutations likely reflects drift. This held for both mammalian and plant viruses, indicating that adaptive immunity doesn't necessarily shape the relative accumulation of amino acid substitutions. When compared to their hosts RNA viruses evolution appears conservative.
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spelling pubmed-70819702020-03-23 Are RNA Viruses Adapting or Merely Changing? Sala, Monica Wain-Hobson, Simon J Mol Evol Article RNA viruses and retroviruses fix substitutions approximately 1 million-fold faster than their hosts. This diversification could represent an inevitable drift under purifying selection, the majority of substitutions being phenotypically neutral. The alternative is to suppose that most fixed mutations are beneficial to the virus, allowing it to keep ahead of the host and/or host population. Here, relative sequence diversification of different proteins encoded by viral genomes is found to be linear. The examples encompass a wide variety of retroviruses and RNA viruses. The smoothness of relative divergence spans quasispeciation following clonal infection, to variation among different isolates of the same virus, to viruses from different species or those associated with different diseases, indicating that the majority of fixed mutations likely reflects drift. This held for both mammalian and plant viruses, indicating that adaptive immunity doesn't necessarily shape the relative accumulation of amino acid substitutions. When compared to their hosts RNA viruses evolution appears conservative. Springer-Verlag 2000 /pmc/articles/PMC7081970/ /pubmed/10903368 http://dx.doi.org/10.1007/s002390010062 Text en © Springer-Verlag New York Inc. 2000 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
Sala, Monica
Wain-Hobson, Simon
Are RNA Viruses Adapting or Merely Changing?
title Are RNA Viruses Adapting or Merely Changing?
title_full Are RNA Viruses Adapting or Merely Changing?
title_fullStr Are RNA Viruses Adapting or Merely Changing?
title_full_unstemmed Are RNA Viruses Adapting or Merely Changing?
title_short Are RNA Viruses Adapting or Merely Changing?
title_sort are rna viruses adapting or merely changing?
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7081970/
https://www.ncbi.nlm.nih.gov/pubmed/10903368
http://dx.doi.org/10.1007/s002390010062
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