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dc.contributor.authorAntoine Chaillonen_US
dc.contributor.authorTanawan Samleeraten_US
dc.contributor.authorFaustine Zovedaen_US
dc.contributor.authorSébastien Ballesterosen_US
dc.contributor.authorAlain Moreauen_US
dc.contributor.authorNicole Ngo-Giang-Huongen_US
dc.contributor.authorGonzague Jourdainen_US
dc.contributor.authorSara Gianellaen_US
dc.contributor.authorMarc Lallemanten_US
dc.contributor.authorFrantz Depaulisen_US
dc.contributor.authorFrancis Barinen_US
dc.date.accessioned2018-09-04T09:43:20Z-
dc.date.available2018-09-04T09:43:20Z-
dc.date.issued2014-04-09en_US
dc.identifier.issn19326203en_US
dc.identifier.other2-s2.0-84899580589en_US
dc.identifier.other10.1371/journal.pone.0090421en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84899580589&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/53063-
dc.description.abstractBackground: Mother-to-child transmission (MTCT) is responsible for most pediatric HIV-1 infections worldwide. It can occur during pregnancy, labor, or breastfeeding. Numerous studies have used coalescent and molecular clock methods to understand the epidemic history of HIV-1, but the timing of vertical transmission has not been studied using these methods. Taking advantage of the constant accumulation of HIV genetic variation over time and using longitudinally sampled viral sequences, we used a coalescent approach to investigate the timing of MTCT. Materials and Methods: Six-hundred and twenty-two clonal env sequences from the RNA and DNA viral population were longitudinally sampled from nine HIV-1 infected mother-and-child pairs [range: 277-1034 days]. For each transmission pair, timing of MTCT was determined using a coalescent-based model within a Bayesian statistical framework. Results were compared with available estimates of MTCT timing obtained with the classic biomedical approach based on serial HIV DNA detection by PCR assays. Results: Four children were infected during pregnancy, whereas the remaining five children were infected at time of delivery. For eight out of nine pairs, results were consistent with the transmission periods assessed by standard PCR-based assay. The discordance in the remaining case was likely confused by co-infection, with simultaneous introduction of multiple maternal viral variants at the time of delivery. Conclusions: The study provided the opportunity to validate the Bayesian coalescent approach that determines the timing of MTCT of HIV-1. It illustrates the power of population genetics approaches to reliably estimate the timing of transmission events and deepens our knowledge about the dynamics of viral evolution in HIV-infected children, accounting for the complexity of multiple transmission events. © 2014 Chaillon et al.en_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMedicineen_US
dc.titleEstimating the timing of mother-to-child transmission of the human immunodeficiency virus type 1 using a viral molecular evolution modelen_US
dc.typeJournalen_US
article.title.sourcetitlePLoS ONEen_US
article.volume9en_US
article.stream.affiliationsUniversite Francois-Rabelais Toursen_US
article.stream.affiliationsUniversity of California, San Diegoen_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsCNRS Centre National de la Recherche Scientifiqueen_US
article.stream.affiliationsInstitute of research for development, Thailanden_US
article.stream.affiliationsHarvard School of Public Healthen_US
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