Patterns of large-scale genomic variation in virulent and avirulent Burkholderia species

  1. Catherine Ong1,3,
  2. Chia Huey Ooi2,3,
  3. Dongling Wang1,
  4. Hweeling Chong2,
  5. Kim Chong Ng2,
  6. Fiona Rodrigues2,
  7. May Ann Lee1,4, and
  8. Patrick Tan1,2,4
  1. 1 Defense Medical and Environmental Research Institute, Singapore 169610, Republic of Singapore
  2. 2 National Cancer Centre, Singapore 169610, Republic of Singapore

Abstract

The human diseases melioidosis and glanders are caused by the bacteria Burkholderia pseudomallei and B. mallei respectively, and both species are regarded as potential biowarfare agents. We used B. pseudomallei DNA microarrays to compare the genomes of several clinical and environmental isolates of B. pseudomallei, B. mallei, and B. thailandensis, a closely related but avirulent species. Open reading frames (ORFs) deleted between the three species were associated with diverse cellular functions, including nitrogen and iron metabolism, quorum sensing, and polysaccharide production. Deleted ORFs in B. mallei exhibited significant genomic clustering, whereas deletions in B. thailandensis were more uniformly dispersed, suggesting that B. mallei and B. thailandensis may have diverged from B. pseudomallei and each other via distinct mechanisms. The genomes of independent B. pseudomallei isolates were highly conserved with a large-scale variance of less than 3% between isolates, and at least three distinct molecular subtypes could be defined. An analysis of subtype-specific genomic regions suggests that DNA loss has played an important role in the evolutionary radiation of B. pseudomallei in the natural environment. Our results raise several hypotheses concerning the possible mechanisms underlying the diverse biological properties exhibited by members of the Burkholderia family.

Footnotes

  • [Supplemental material is available online at www.genome.org and Microarray data sets are available at http://www.omniarray.com/bioinformatics/BPM_SupData/.]

  • Article and publication are at http://www.genome.org/cgi/doi/10.1101/gr.1608904.

  • 3 These authors contributed equally to this report.

  • 4 Corresponding authors. E-mail cmrtan{at}nccs.com.sg; fax 65-6-226-5694. E-mail mayann{at}dsta.gov.sg; fax 65 6485 7226.

    • Accepted November 18, 2003.
    • Received June 2, 2003.
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