Proceedings of the National Academy of Sciences · 2004 · 396 citations · 25 references
Life SciencesGeneticsMicrobiologyComparative GenomicsGenomicsMicrobial PathogenesisBacterial Virulence FactorsMicrobial Virulence FactorsPathogen EvolutionPathogen Virulence FactorsVirulence EvolutionVirulence GenomicsBacterial Virulence GenesEvolution Of Virulence FactorsExpression ProfilingGenetic Determinants Of PathogenicityPathogenicity EvolutionSimple Sequence Repeat AnalysisSimple Sequence RepeatsVirulence Gene Identification
The complete genome sequence of *Burkholderia mallei* ATCC 23344 reveals insights into its pathogenicity and evolutionary history, and the bacterium has attracted renewed study due to concerns about its potential use as a bioweapon. Genome analysis identified putative virulence factors supported by comparative hybridization and expression profiling, and variation in simple sequence repeats in key genes offers a mechanism for antigenic variation. The genome contains numerous insertion sequence elements that have caused extensive deletions and rearrangements compared to *Burkholderia pseudomallei*, as well as over 12,000 simple sequence repeats, whose variation in key genes may drive antigenic variation.
The complete genome sequence of Burkholderia mallei ATCC 23344 provides insight into this highly infectious bacterium's pathogenicity and evolutionary history. B. mallei , the etiologic agent of glanders, has come under renewed scientific investigation as a result of recent concerns about its past and potential future use as a biological weapon. Genome analysis identified a number of putative virulence factors whose function was supported by comparative genome hybridization and expression profiling of the bacterium in hamster liver in vivo . The genome contains numerous insertion sequence elements that have mediated extensive deletions and rearrangements of the genome relative to Burkholderia pseudomallei . The genome also contains a vast number (>12,000) of simple sequence repeats. Variation in simple sequence repeats in key genes can provide a mechanism for generating antigenic variation that may account for the mammalian host's inability to mount a durable adaptive immune response to a B. mallei infection.
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