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Population genetics of IFITM3 in Portugal and Central Africa reveals a potential modifier of influenza severity

dc.contributor.authorDavid, S
dc.contributor.authorCorreia, V
dc.contributor.authorAntunes, L
dc.contributor.authorFaria, R
dc.contributor.authorFerrão, J
dc.contributor.authorFaustino, P
dc.contributor.authorNunes, B
dc.contributor.authorMaltez, F
dc.contributor.authorLavinha, J
dc.contributor.authorRebelo de Andrade, H
dc.date.accessioned2017-11-10T12:16:37Z
dc.date.available2018-08-26T00:30:13Z
dc.date.issued2017-08-25
dc.description.abstractInfluenza epidemics are a serious global public health and economic problem. The IFITM3 allele (rs12252-C) was suggested as a strong population-based genetic risk factor for severe influenza virus infection by A(H1N1)pdm09. We analyzed the population genetics of IFITM3 variants in Portuguese general population (n=200) and Central Africans (largely Angolan) (n=148) as well as its association to influenza severity in Portuguese patients (n=41). Seven SNPs, within the 352bp IFITM3 amplicon around rs12252, were identified. SNP distributions in the Portuguese appeared at an intermediate level between the Africans and other Europeans. According to HapMap rs34481144 belongs to the same linkage disequilibrium (LD) block as rs12252, and is in strong LD with rs6421983. A negative association with severe relative to mild disease was observed for allele rs34481144-A, indicating a protective effect under the dominant model. Moreover, haplotype Hap4 with rs34481144-A, not including rs12252-C, was significantly associated to mild influenza. Conversely, although with borderline significance, haplotype Hap1 with rs34481144-G, not including rs12252-C, was associated to severe disease. Moreover, in comparison to the general Portuguese population, statistical significant differences in the frequencies of the protective allele rs34481144-A in the severe disease group, the deleterious Hap1 in the mild disease group and the protective Hap4 in the severe disease group, were observed. The population attributable risk (PAR) for the targeted rs34481144 allele or genotype was of 55.91% and 64.44% in the general population and the mildly infected individuals, respectively. Implication of these variants in disease phenotype needs further validation, namely through functional analysis as is discussed.pt_PT
dc.description.sponsorshipThis study was carried out with financial support from FCT/MEC through national funds and co-financed by FEDER, under the Partnership Agreement PT2020, in the project with reference UID/MULTI/00211/2013pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationImmunogenetics. 2018;70:169-17. doi: 10.1007/s00251-017-1026-2. Epub 2017 Aug 25pt_PT
dc.identifier.doi10.1007/s00251-017-1026-2pt_PT
dc.identifier.issn0093-7711
dc.identifier.other1432-1211
dc.identifier.urihttp://hdl.handle.net/10400.18/4825
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherSpringer Verlag (Germany)pt_PT
dc.relation.publisherversionhttps://link.springer.com/content/pdf/10.1007%2Fs00251-017-1026-2.pdfpt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectIFITM3 genept_PT
dc.subjectinfluenza Viruspt_PT
dc.subjectPopulation Geneticspt_PT
dc.subjectPortugalpt_PT
dc.subjectCentral Africapt_PT
dc.subjectAgentes Microbianos e Ambientept_PT
dc.subjectInfecções Respiratóriaspt_PT
dc.subjectDeterminantes da Saúde e da Doençapt_PT
dc.titlePopulation genetics of IFITM3 in Portugal and Central Africa reveals a potential modifier of influenza severitypt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/5876/UID%2FMulti%2F00211%2F2013/PT
oaire.citation.endPage9pt_PT
oaire.citation.startPage1pt_PT
oaire.citation.titleImmunogeneticspt_PT
oaire.fundingStream5876
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT
relation.isProjectOfPublication4641127c-7dd5-44f4-a3d1-d3c4d744ba51
relation.isProjectOfPublication.latestForDiscovery4641127c-7dd5-44f4-a3d1-d3c4d744ba51

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