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Constrained evolution drives limited influenza diversity

H3N2 influenza A viruses have been widely circulating in human populations since the pandemic of 1968. A striking feature of the evolutionary development of this strain has been its 'canalized' nature, with narrow evolutionary trees dominated by long trunks with few branching, or bifurcati...

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Detalles Bibliográficos
Autores principales: Thomas, Paul G, Hertz, Tomer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3357320/
https://www.ncbi.nlm.nih.gov/pubmed/22613866
http://dx.doi.org/10.1186/1741-7007-10-43
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author Thomas, Paul G
Hertz, Tomer
author_facet Thomas, Paul G
Hertz, Tomer
author_sort Thomas, Paul G
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description H3N2 influenza A viruses have been widely circulating in human populations since the pandemic of 1968. A striking feature of the evolutionary development of this strain has been its 'canalized' nature, with narrow evolutionary trees dominated by long trunks with few branching, or bifurcation events and a consequent lack of standing diversity at any single point. This is puzzling, as one might expect that the strong human immune response against the virus would create an environment encouraging more diversity, not less. Previous models have used various assumptions in order to account for this finding. A new analysis published in BMC Biology suggests that this processive evolution down a single path can be recapitulated by a relatively simple model incorporating only two primary parameters - the mutation rate of the virus, and the immunological distance created by each mutation - so long as these parameters are within a particular narrow but biologically plausible range. See research article: http://www.biomedcentral.com/1741-7007/10/38
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spelling pubmed-33573202012-05-22 Constrained evolution drives limited influenza diversity Thomas, Paul G Hertz, Tomer BMC Biol Commentary H3N2 influenza A viruses have been widely circulating in human populations since the pandemic of 1968. A striking feature of the evolutionary development of this strain has been its 'canalized' nature, with narrow evolutionary trees dominated by long trunks with few branching, or bifurcation events and a consequent lack of standing diversity at any single point. This is puzzling, as one might expect that the strong human immune response against the virus would create an environment encouraging more diversity, not less. Previous models have used various assumptions in order to account for this finding. A new analysis published in BMC Biology suggests that this processive evolution down a single path can be recapitulated by a relatively simple model incorporating only two primary parameters - the mutation rate of the virus, and the immunological distance created by each mutation - so long as these parameters are within a particular narrow but biologically plausible range. See research article: http://www.biomedcentral.com/1741-7007/10/38 BioMed Central 2012-05-21 /pmc/articles/PMC3357320/ /pubmed/22613866 http://dx.doi.org/10.1186/1741-7007-10-43 Text en Copyright ©2012 Thomas and Hertz; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Commentary
Thomas, Paul G
Hertz, Tomer
Constrained evolution drives limited influenza diversity
title Constrained evolution drives limited influenza diversity
title_full Constrained evolution drives limited influenza diversity
title_fullStr Constrained evolution drives limited influenza diversity
title_full_unstemmed Constrained evolution drives limited influenza diversity
title_short Constrained evolution drives limited influenza diversity
title_sort constrained evolution drives limited influenza diversity
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3357320/
https://www.ncbi.nlm.nih.gov/pubmed/22613866
http://dx.doi.org/10.1186/1741-7007-10-43
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