Publication:
Within-host evolution of Burkholderia pseudomallei in four cases of acute melioidosis

dc.contributor.authorErin P. Priceen_US
dc.contributor.authorHeidie M. Hornstraen_US
dc.contributor.authorDirek Limmathurotsakulen_US
dc.contributor.authorTamara L. Maxen_US
dc.contributor.authorDerek S. Sarovichen_US
dc.contributor.authorAmy J. Vogleren_US
dc.contributor.authorJulia L. Daleen_US
dc.contributor.authorJennifer L. Gintheren_US
dc.contributor.authorBenjamin Leademen_US
dc.contributor.authorRebecca E. Colmanen_US
dc.contributor.authorJeffrey T. Fosteren_US
dc.contributor.authorApichai Tuanyoken_US
dc.contributor.authorDavid M. Wagneren_US
dc.contributor.authorSharon J. Peacocken_US
dc.contributor.authorTalima Pearsonen_US
dc.contributor.authorPaul Keimen_US
dc.contributor.otherNorthern Arizona Universityen_US
dc.contributor.otherTranslational Genomics Research Instituteen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherUniversity of Cambridgeen_US
dc.date.accessioned2018-09-24T08:49:25Z
dc.date.available2018-09-24T08:49:25Z
dc.date.issued2010-01-01en_US
dc.description.abstractLittle is currently known about bacterial pathogen evolution and adaptation within the host during acute infection. Previous studies of Burkholderia pseudomallei, the etiologic agent of melioidosis, have shown that this opportunistic pathogen mutates rapidly both in vitro and in vivo at tandemly repeated loci, making this organism a relevant model for studying short-term evolution. In the current study, B. pseudomallei isolates cultured from multiple body sites from four Thai patients with disseminated melioidosis were subjected to fine-scale genotyping using multilocus variable-number tandem repeat analysis (MLVA). In order to understand and model the in vivo variable-number tandem repeat (VNTR) mutational process, we characterized the patterns and rates of mutations in vitro through parallel serial passage experiments of B. pseudomallei. Despite the short period of infection, substantial divergence from the putative founder genotype was observed in all four melioidosis cases. This study presents a paradigm for examining bacterial evolution over the short timescale of an acute infection. Further studies are required to determine whether the mutational process leads to phenotypic alterations that impact upon bacterial fitness in vivo. Our findings have important implications for future sampling strategies, since colonies in a single clinical sample may be genetically heterogeneous, and organisms in a culture taken late in the infective process may have undergone considerable genetic change compared with the founder inoculum. © 2010 Price et al.en_US
dc.identifier.citationPLoS Pathogens. Vol.6, No.1 (2010)en_US
dc.identifier.doi10.1371/journal.ppat.1000725en_US
dc.identifier.issn15537374en_US
dc.identifier.issn15537366en_US
dc.identifier.other2-s2.0-77649227884en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/28830
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=77649227884&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectImmunology and Microbiologyen_US
dc.titleWithin-host evolution of Burkholderia pseudomallei in four cases of acute melioidosisen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=77649227884&origin=inwarden_US

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