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Article: Quantifying influenza virus diversity and transmission in humans

TitleQuantifying influenza virus diversity and transmission in humans
Authors
Issue Date2016
Citation
Nature Genetics, 2016, v. 48 n. 2, p. 195-200 How to Cite?
AbstractInfluenza A virus is characterized by high genetic diversity. However, most of what is known about influenza evolution has come from consensus sequences sampled at the epidemiological scale that only represent the dominant virus lineage within each infected host. Less is known about the extent of within-host virus diversity and what proportion of this diversity is transmitted between individuals. To characterize virus variants that achieve sustainable transmission in new hosts, we examined within-host virus genetic diversity in household donor-recipient pairs from the first wave of the 2009 H1N1 pandemic when seasonal H3N2 was co-circulating. Although the same variants were found in multiple members of the community, the relative frequencies of variants fluctuated, with patterns of genetic variation more similar within than between households. We estimated the effective population size of influenza A virus across donor-recipient pairs to be approximately 100-200 contributing members, which enabled the transmission of multiple lineages, including antigenic variants.
Persistent Identifierhttp://hdl.handle.net/10722/223374
ISSN
2021 Impact Factor: 41.307
2020 SCImago Journal Rankings: 18.861
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorPoon, LLM-
dc.contributor.authorSong, T-
dc.contributor.authorRosenfeld, R-
dc.contributor.authorLin, X-
dc.contributor.authorRogers, MB-
dc.contributor.authorZhou, B-
dc.contributor.authorSebra, R-
dc.contributor.authorHalpin, RA-
dc.contributor.authorGuan, Y-
dc.contributor.authorTwaddle, A-
dc.contributor.authorDePasse, JV-
dc.contributor.authorStockwell, TB-
dc.contributor.authorWentworth, DE-
dc.contributor.authorHolmes, EC-
dc.contributor.authorGreenbaum, B-
dc.contributor.authorPeiris, JSM-
dc.contributor.authorCowling, BJ-
dc.contributor.authorGhedin, E-
dc.date.accessioned2016-02-23T01:57:34Z-
dc.date.available2016-02-23T01:57:34Z-
dc.date.issued2016-
dc.identifier.citationNature Genetics, 2016, v. 48 n. 2, p. 195-200-
dc.identifier.issn1061-4036-
dc.identifier.urihttp://hdl.handle.net/10722/223374-
dc.description.abstractInfluenza A virus is characterized by high genetic diversity. However, most of what is known about influenza evolution has come from consensus sequences sampled at the epidemiological scale that only represent the dominant virus lineage within each infected host. Less is known about the extent of within-host virus diversity and what proportion of this diversity is transmitted between individuals. To characterize virus variants that achieve sustainable transmission in new hosts, we examined within-host virus genetic diversity in household donor-recipient pairs from the first wave of the 2009 H1N1 pandemic when seasonal H3N2 was co-circulating. Although the same variants were found in multiple members of the community, the relative frequencies of variants fluctuated, with patterns of genetic variation more similar within than between households. We estimated the effective population size of influenza A virus across donor-recipient pairs to be approximately 100-200 contributing members, which enabled the transmission of multiple lineages, including antigenic variants.-
dc.languageeng-
dc.relation.ispartofNature Genetics-
dc.titleQuantifying influenza virus diversity and transmission in humans-
dc.typeArticle-
dc.identifier.emailPoon, LLM: llmpoon@hkucc.hku.hk-
dc.identifier.emailGuan, Y: yguan@hkucc.hku.hk-
dc.identifier.emailPeiris, JSM: malik@hkucc.hku.hk-
dc.identifier.emailCowling, BJ: bcowling@hku.hk-
dc.identifier.authorityPoon, LLM=rp00484-
dc.identifier.authorityGuan, Y=rp00397-
dc.identifier.authorityPeiris, JSM=rp00410-
dc.identifier.authorityCowling, BJ=rp01326-
dc.identifier.doi10.1038/ng.3479-
dc.identifier.pmcidPMC4731279-
dc.identifier.scopuseid_2-s2.0-84956621342-
dc.identifier.hkuros256982-
dc.identifier.volume48-
dc.identifier.issue2-
dc.identifier.spage195-
dc.identifier.epage200-
dc.identifier.eissn1546-1718-
dc.identifier.isiWOS:000369043900018-
dc.identifier.issnl1061-4036-

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