Tandem repeat regions within the Burkholderia pseudomallei genome and their application for high resolution

Jana M U'Ren1, James M Schupp, Talima Pearson

  • 1Northern Arizona University, Center for Microbial Genetics and Genomics, Flagstaff, Arizona 86011, USA. juren@email.arizona.edu <juren@email.arizona.edu>

BMC Microbiology
|April 3, 2007
PubMed
Abstract

Insights

This study developed a novel genetic typing method for Burkholderia pseudomallei using multiple-locus VNTR analysis (MLVA). MLVA effectively distinguished between global isolates and clonal lineages, offering a valuable tool for tracking this important pathogen.

Area of Science:

  • Microbiology
  • Genomics
  • Epidemiology

Background:

  • Burkholderia pseudomallei causes melioidosis, a significant infectious disease in humans and animals.
  • Developing a robust genetic typing method is crucial for understanding and controlling B. pseudomallei.
  • Tandem repeat arrays were investigated for their potential as polymorphic markers.

Purpose of the Study:

  • To identify and categorize tandem repeat arrays in the B. pseudomallei genome.
  • To develop a genetic typing method for B. pseudomallei using these arrays.
  • To assess the utility of the developed method for epidemiological and forensic tracking.

Main Methods:

  • Genome-wide identification and categorization of tandem repeat arrays in B. pseudomallei K96243.
  • Screening of 104 polymorphic loci across 31 bacterial isolates (B. pseudomallei, B. mallei, B. thailandensis).
  • Development and application of a multiple-locus VNTR analysis (MLVA) on 66 B. pseudomallei and 21 B. mallei isolates, plus a serial transfer experiment.

Main Results:

  • B. pseudomallei genomes possess numerous tandem repeat loci, predominantly in intergenic regions with 6-9 bp repeat motifs.
  • The 32 developed VNTR loci showed significant polymorphism, with 7-28 alleles and high diversity values (0.47-0.94) across isolates.
  • Mutation rates at these VNTR loci are comparable to highly diverse regions in other bacteria.

Conclusions:

  • Tandem repeat regions in B. pseudomallei likely contribute to adaptive genomic variation.
  • MLVA demonstrated high discriminatory power for global B. pseudomallei and B. mallei isolates, surpassing previous methods.
  • MLVA is a promising tool for fine-scale epidemiological and forensic tracking of B. pseudomallei due to its ability to detect genotypic differences.