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dc.contributor.authorTamuri, AUen_US
dc.contributor.authorDos Reis, Men_US
dc.contributor.authorHay, AJen_US
dc.contributor.authorGoldstein, RAen_US
dc.date.accessioned2016-08-10T11:42:40Z
dc.date.available2009-10-15en_US
dc.date.issued2009-11en_US
dc.date.submitted2016-07-22T19:19:09.040Z
dc.identifier.other10.1371/journal.pcbi.1000564
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/14070
dc.descriptionThis is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.en_US
dc.description.abstractThe natural reservoir of Influenza A is waterfowl. Normally, waterfowl viruses are not adapted to infect and spread in the human population. Sometimes, through reassortment or through whole host shift events, genetic material from waterfowl viruses is introduced into the human population causing worldwide pandemics. Identifying which mutations allow viruses from avian origin to spread successfully in the human population is of great importance in predicting and controlling influenza pandemics. Here we describe a novel approach to identify such mutations. We use a sitewise non-homogeneous phylogenetic model that explicitly takes into account differences in the equilibrium frequencies of amino acids in different hosts and locations. We identify 172 amino acid sites with strong support and 518 sites with moderate support of different selection constraints in human and avian viruses. The sites that we identify provide an invaluable resource to experimental virologists studying adaptation of avian flu viruses to the human host. Identification of the sequence changes necessary for host shifts would help us predict the pandemic potential of various strains. The method is of broad applicability to investigating changes in selective constraints when the timing of the changes is known.en_US
dc.description.sponsorshipFunding was provided by the NIMR (MRC), the Wellcome Trust, and the European FP6 FLUPOL contract (SPSB-CT-2007-044263). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.en_US
dc.format.extente1000564 - ?en_US
dc.languageengen_US
dc.language.isoenen_US
dc.relation.ispartofPLoS Comput Biolen_US
dc.subjectAnimalsen_US
dc.subjectAnseriformesen_US
dc.subjectComputational Biologyen_US
dc.subjectGenetic Driften_US
dc.subjectHost-Pathogen Interactionsen_US
dc.subjectHumansen_US
dc.subjectInfluenza A virusen_US
dc.subjectModels, Geneticen_US
dc.subjectPhylogenyen_US
dc.subjectSelection, Geneticen_US
dc.subjectSequence Analysis, Proteinen_US
dc.titleIdentifying changes in selective constraints: host shifts in influenza.en_US
dc.typeArticle
dc.rights.holder© 2009 Tamuri et al.
dc.identifier.doi10.1371/journal.pcbi.1000564en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/19911053en_US
pubs.issue11en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume5en_US
dcterms.dateAccepted2009-10-15en_US


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