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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>
Background:
The facultative, intracellular bacterium Burkholderia pseudomallei is the causative agent of melioidosis, a serious infectious disease of humans and animals. We identified and categorized tandem repeat arrays and their distribution throughout the genome of B. pseudomallei strain K96243 in order to develop a genetic typing method for B. pseudomallei. We then screened 104 of the potentially polymorphic loci across a diverse panel of 31 isolates including B. pseudomallei, B. mallei and B. thailandensis in order to identify loci with varying degrees of polymorphism. A subset of these tandem repeat arrays were subsequently developed into a multiple-locus VNTR analysis to examine 66 B. pseudomallei and 21 B. mallei isolates from around the world, as well as 95 lineages from a serial transfer experiment encompassing ~18,000 generations.
Results:
B. pseudomallei contains a preponderance of tandem repeat loci throughout its genome, many of which are duplicated elsewhere in the genome. The majority of these loci are composed of repeat motif lengths of 6 to 9 bp with 4 to 10 repeat units and are predominately located in intergenic regions of the genome. Across geographically diverse B. pseudomallei and B.mallei isolates, the 32 VNTR loci displayed between 7 and 28 alleles, with Nei's diversity values ranging from 0.47 and 0.94. Mutation rates for these loci are comparable (>10-5 per locus per generation) to that of the most diverse tandemly repeated regions found in other less diverse bacteria.
Conclusion:
The frequency, location and duplicate nature of tandemly repeated regions within the B. pseudomallei genome indicate that these tandem repeat regions may play a role in generating and maintaining adaptive genomic variation. Multiple-locus VNTR analysis revealed extensive diversity within the global isolate set containing B. pseudomallei and B. mallei, and it detected genotypic differences within clonal lineages of both species that were identical using previous typing methods. Given the health threat to humans and livestock and the potential for B. pseudomallei to be released intentionally, MLVA could prove to be an important tool for fine-scale epidemiological or forensic tracking of this increasingly important environmental pathogen.
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.
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