Diversity of 16S-23S rDNA Internal Transcribed Spacer (ITS) reveals phylogenetic relationships in Burkholderia pseudomallei and its near-neighbors

Andrew Ligouri, Stephanie Warrington, Jennifer Ginther, Talima Pearson, Jolene Bowers, Mindy Glass, Mark Mayo, Vanaporn Wuthiekanun, David Engelthaler, Sharon Peacock, Bart Currie, David Wagner, Paul Keim, Apichai Tuanyok

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    Abstract

    Length polymorphisms within the 16S-23S ribosomal DNA internal transcribed spacer (ITS) have been described as stable genetic markers for studying bacterial phylogenetics. In this study, we used these genetic markers to investigate phylogenetic relationships in Burkholderia pseudomallei and its near-relative species. B. pseudomallei is known as one of the most genetically recombined bacterial species. In silico analysis of multiple B. pseudomallei genomes revealed approximately four homologous rRNA operons and ITS length polymorphisms therein. We characterized ITS distribution using PCR and analyzed via a high-throughput capillary electrophoresis in 1,191 B. pseudomallei strains. Three major ITS types were identified, two of which were commonly found in most B. pseudomallei strains from the endemic areas, whereas the third one was significantly correlated with worldwide sporadic strains. Interestingly, mixtures of the two common ITS types were observed within the same strains, and at a greater incidence in Thailand than Australia suggesting that genetic recombination causes the ITS variation within species, with greater recombination frequency in Thailand. In addition, the B. mallei ITS type was common to B. pseudomallei, providing further support that B. mallei is a clone of B. pseudomallei. Other B. pseudomallei near-neighbors possessed unique and monomorphic ITS types. Our data shed light on evolutionary patterns of B. pseudomallei and its near relative species.

    Original languageEnglish
    Article numbere29323
    Pages (from-to)e29323
    Number of pages8
    JournalPLoS One
    Volume6
    Issue number12
    DOIs
    Publication statusPublished - 14 Dec 2011

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