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- Publisher Website: 10.1073/pnas.1109314108
- Scopus: eid_2-s2.0-82755190600
- PMID: 22084096
- WOS: WOS:000297463100054
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Article: Temporally structured metapopulation dynamics and persistence of influenza A H3N2 virus in humans
Title | Temporally structured metapopulation dynamics and persistence of influenza A H3N2 virus in humans | ||||||||||||||||
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Authors | |||||||||||||||||
Keywords | Evolution Molecular epidemiology Phylogeography Source-sink | ||||||||||||||||
Issue Date | 2011 | ||||||||||||||||
Publisher | National Academy of Sciences. The Journal's web site is located at http://www.pnas.org | ||||||||||||||||
Citation | Proceedings of the National Academy of Sciences of the United States of America, 2011, v. 108 n. 48, p. 19359-19364 How to Cite? | ||||||||||||||||
Abstract | Populations of seasonal influenza virus experience strong annual bottlenecks that pose a considerable extinction risk. It has been suggested that an influenza source population located in tropical Southeast or East Asia seeds annual temperate epidemics. Here we investigate the seasonal dynamics and migration patterns of influenza A H3N2 virus by analysis of virus samples obtained from 2003 to 2006 from Australia, Europe, Japan, New York, New Zealand, Southeast Asia, and newly sequenced viruses from Hong Kong. In contrast to annual temperate epidemics, relatively low levels of relative genetic diversity and no seasonal fluctuations characterized virus populations in tropical Southeast Asia and Hong Kong. Bayesian phylogeographic analysis using discrete temporal and spatial characters reveal high rates of viral migration between urban centers tested. Although the virus population that migrated between Southeast Asia and Hong Kong persisted through time, this was dependent on virus input from temperate regions and these tropical regions did not maintain a source for annual H3N2 influenza epidemics. We further show that multiple lineages may seed annual influenza epidemics, and that each region may function as a potential source population. We therefore propose that the global persistence of H3N2 influenza A virus is the result of a migrating metapopulation in which multiple different localities may seed seasonal epidemics in temperate regions in a given year. Such complex global migration dynamics may confound control efforts and contribute to the emergence and spread of antigenic variants and drug-resistant viruses. | ||||||||||||||||
Persistent Identifier | http://hdl.handle.net/10722/151762 | ||||||||||||||||
ISSN | 2023 Impact Factor: 9.4 2023 SCImago Journal Rankings: 3.737 | ||||||||||||||||
PubMed Central ID | |||||||||||||||||
ISI Accession Number ID |
Funding Information: This study was supported by Contracts HHSN266200700005C and HHSN272200900007 for the Influenza Genome Sequencing Project of the National Institute of Allergy and Infectious Disease, National Institutes of Health, Department of Health and Human Services; the Area of Excellence Scheme of the University Grants Committee (Grant AoE/M-12/06) of the Hong Kong Special Administrative Region Government; the RAPIDD program of the Science and Technology Directorate, US Department of Homeland Security and the Fogarty International Center, National Institutes of Health (S. R.), a career development award under National Institute of Allergy and Infectious Diseases Contract HHSN266200700005C (to G.J.D.S.); and the Duke-National University of Singapore Signature Research Program funded by the Agency for Science, Technology and Research, Singapore, and the Ministry of Health, Singapore (J.B., D.V., and G.J.D.S.). | ||||||||||||||||
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Bahl, J | en_HK |
dc.contributor.author | Nelson, MI | en_HK |
dc.contributor.author | Chan, KH | en_HK |
dc.contributor.author | Chen, R | en_HK |
dc.contributor.author | Vijaykrishna, D | en_HK |
dc.contributor.author | Halpin, RA | en_HK |
dc.contributor.author | Stockwell, TB | en_HK |
dc.contributor.author | Lin, X | en_HK |
dc.contributor.author | Wentworth, DE | en_HK |
dc.contributor.author | Ghedin, E | en_HK |
dc.contributor.author | Guan, Y | en_HK |
dc.contributor.author | Peiris, JSM | en_HK |
dc.contributor.author | Riley, S | en_HK |
dc.contributor.author | Rambaut, A | en_HK |
dc.contributor.author | Holmes, EC | en_HK |
dc.contributor.author | Smith, GJD | en_HK |
dc.date.accessioned | 2012-06-26T06:28:01Z | - |
dc.date.available | 2012-06-26T06:28:01Z | - |
dc.date.issued | 2011 | en_HK |
dc.identifier.citation | Proceedings of the National Academy of Sciences of the United States of America, 2011, v. 108 n. 48, p. 19359-19364 | en_HK |
dc.identifier.issn | 0027-8424 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/151762 | - |
dc.description.abstract | Populations of seasonal influenza virus experience strong annual bottlenecks that pose a considerable extinction risk. It has been suggested that an influenza source population located in tropical Southeast or East Asia seeds annual temperate epidemics. Here we investigate the seasonal dynamics and migration patterns of influenza A H3N2 virus by analysis of virus samples obtained from 2003 to 2006 from Australia, Europe, Japan, New York, New Zealand, Southeast Asia, and newly sequenced viruses from Hong Kong. In contrast to annual temperate epidemics, relatively low levels of relative genetic diversity and no seasonal fluctuations characterized virus populations in tropical Southeast Asia and Hong Kong. Bayesian phylogeographic analysis using discrete temporal and spatial characters reveal high rates of viral migration between urban centers tested. Although the virus population that migrated between Southeast Asia and Hong Kong persisted through time, this was dependent on virus input from temperate regions and these tropical regions did not maintain a source for annual H3N2 influenza epidemics. We further show that multiple lineages may seed annual influenza epidemics, and that each region may function as a potential source population. We therefore propose that the global persistence of H3N2 influenza A virus is the result of a migrating metapopulation in which multiple different localities may seed seasonal epidemics in temperate regions in a given year. Such complex global migration dynamics may confound control efforts and contribute to the emergence and spread of antigenic variants and drug-resistant viruses. | en_HK |
dc.language | eng | en_US |
dc.publisher | National Academy of Sciences. The Journal's web site is located at http://www.pnas.org | en_HK |
dc.relation.ispartof | Proceedings of the National Academy of Sciences of the United States of America | en_HK |
dc.subject | Evolution | en_HK |
dc.subject | Molecular epidemiology | en_HK |
dc.subject | Phylogeography | en_HK |
dc.subject | Source-sink | en_HK |
dc.subject.mesh | Asia - Epidemiology | en_US |
dc.subject.mesh | Australasia - Epidemiology | en_US |
dc.subject.mesh | Base Sequence | en_US |
dc.subject.mesh | Bayes Theorem | en_US |
dc.subject.mesh | Demography | en_US |
dc.subject.mesh | Disease Outbreaks | en_US |
dc.subject.mesh | Europe - Epidemiology | en_US |
dc.subject.mesh | Evolution, Molecular | en_US |
dc.subject.mesh | Genetic Variation | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Influenza A Virus, H3n2 Subtype - Genetics - Physiology | en_US |
dc.subject.mesh | Influenza, Human - Epidemiology | en_US |
dc.subject.mesh | Models, Biological | en_US |
dc.subject.mesh | Models, Genetic | en_US |
dc.subject.mesh | Molecular Sequence Data | en_US |
dc.subject.mesh | New York - Epidemiology | en_US |
dc.subject.mesh | Phylogeography | en_US |
dc.subject.mesh | Population Dynamics | en_US |
dc.subject.mesh | Reverse Transcriptase Polymerase Chain Reaction | en_US |
dc.subject.mesh | Seasons | en_US |
dc.subject.mesh | Sequence Analysis, Dna | en_US |
dc.title | Temporally structured metapopulation dynamics and persistence of influenza A H3N2 virus in humans | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Guan, Y: yguan@hkucc.hku.hk | en_HK |
dc.identifier.email | Peiris, JSM: malik@hkucc.hku.hk | en_HK |
dc.identifier.email | Riley, S: steven.riley@hku.hk | en_HK |
dc.identifier.email | Smith, GJD: gjsmith@hkucc1.hku.hk | en_HK |
dc.identifier.authority | Guan, Y=rp00397 | en_HK |
dc.identifier.authority | Peiris, JSM=rp00410 | en_HK |
dc.identifier.authority | Riley, S=rp00511 | en_HK |
dc.identifier.authority | Smith, GJD=rp00444 | en_HK |
dc.description.nature | link_to_OA_fulltext | en_US |
dc.identifier.doi | 10.1073/pnas.1109314108 | en_HK |
dc.identifier.pmid | 22084096 | - |
dc.identifier.pmcid | PMC3228450 | - |
dc.identifier.scopus | eid_2-s2.0-82755190600 | en_HK |
dc.identifier.hkuros | 211240 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-82755190600&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 108 | en_HK |
dc.identifier.issue | 48 | en_HK |
dc.identifier.spage | 19359 | en_HK |
dc.identifier.epage | 19364 | en_HK |
dc.identifier.isi | WOS:000297463100054 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Bahl, J=35308668200 | en_HK |
dc.identifier.scopusauthorid | Nelson, MI=15758216500 | en_HK |
dc.identifier.scopusauthorid | Chan, KH=7406034307 | en_HK |
dc.identifier.scopusauthorid | Chen, R=15060989600 | en_HK |
dc.identifier.scopusauthorid | Vijaykrishna, D=12752817700 | en_HK |
dc.identifier.scopusauthorid | Halpin, RA=15822104200 | en_HK |
dc.identifier.scopusauthorid | Stockwell, TB=16242581000 | en_HK |
dc.identifier.scopusauthorid | Lin, X=36164400700 | en_HK |
dc.identifier.scopusauthorid | Wentworth, DE=7004800841 | en_HK |
dc.identifier.scopusauthorid | Ghedin, E=6602723755 | en_HK |
dc.identifier.scopusauthorid | Guan, Y=7202924055 | en_HK |
dc.identifier.scopusauthorid | Peiris, JSM=7005486823 | en_HK |
dc.identifier.scopusauthorid | Riley, S=7102619416 | en_HK |
dc.identifier.scopusauthorid | Rambaut, A=7004230842 | en_HK |
dc.identifier.scopusauthorid | Holmes, EC=35433598300 | en_HK |
dc.identifier.scopusauthorid | Smith, GJD=8344015800 | en_HK |
dc.identifier.citeulike | 10310004 | - |
dc.identifier.issnl | 0027-8424 | - |