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    Putting the Pieces Together: Solving the Burkholderia Puzzle

    Burkholderia Map

    Courtesy Photo | Global distribution of Burkholderia pseudomallei.... read more read more

    FORT BELVOIR, VIRGINIA, UNITED STATES

    06.22.2017

    Courtesy Story

    Defense Threat Reduction Agency's Chemical and Biological Technologies Department

    Diagnosing any disease is similar to solving a puzzle. Doctors and patients piece together symptoms and run diagnostic tests until the entire picture develops. But, without a reliable diagnostic test, medical personnel are missing vital pieces, relying only on parts of the information. Currently no definitive diagnostic test exists for Burkholderia, a category B agent caused by Burkholderia pseudomallei bacterium, which poses a threat to deployed warfighters.

    The Defense Threat Reduction Agency’s Chemical and Biological Technologies Department is researching whole genome sequencing to improve the specificity of B. pseudomallei assays for enhanced detection and diagnostic devices, filling a critical capability gap for the Department of Defense. Researchers David Wagner, Ph.D., and Paul Keim, Ph.D., of Northern Arizona University (NAU) are working to identify unique B. pseudomallei DNA sequences by analyzing the chromosomes of more than one thousand Burkholderia strains.

    Melioidosis, caused by Burkholderia pseudomallei bacteria, is a potentially fatal disease, a public health threat and potential bioterrorism agent endemic to Southeast Asia and Northern Australia. Contracted through open wounds, ingestion or inhalation, melioidosis can cause respiratory distress, bloodstream infections, liver and splenic abscesses, seizures and death. B. pseudomallei infections are difficult to diagnose due to the variety of symptoms and a lack of diagnostic testing. Current diagnostic practices rely on blood culture and a small collection of serologic tests. The former assay is often non-specific, time consuming and subject to misinterpretation. However, molecular diagnostic approaches, based upon polymerase chain reaction, have focused on available genomic sequences and proven variable with regard to performance.

    Due to the tendency of B. pseudomallei to rearrange its chromosomes and exchange genes, improvements in assay sensitivity and specificity are hampered. Gene exchange has homogenized the overall genetic composition of Burkholderia while allowing the retention of species identity.

    During their course of study, the NAU research team added nearly 1,000 new genome sequences to GenBank, the public genome database housed by the National Center for Biotechnology Information. In addition, NAU isolated one confirmed and three presumptive new Burkholderia species and developed three sets of 50 assays. Each assay set used the same target sequence, but different technological bases. These efforts will help improve new diagnostic techniques for Burkholderia, improving warfighter and public safety.

    Three DTRA-developed sequencing assays, the TaqMan, MagPix and Amplicon, displayed promising results for diagnostic testing and were transitioned to the Joint Program Executive Office for Chemical and Biological Defense for further development.

    The final phase of the NAU effort is focused on the function of the unique sequences; the first step in understanding why this genetic information is conserved in this pathogenic species.

    DTRA CB’s investment in Burkholderia diagnostic assay development has benefitted the DoD while demonstrating the necessity of examining the genomes of infective species, including related, or near-neighbor, species. Improved diagnostic assays will allow for earlier medical intervention for warfighters with Burkholderia, 'solving the puzzle’ for accurate testing and diagnosis.

    NEWS INFO

    Date Taken: 06.22.2017
    Date Posted: 06.22.2017 10:35
    Story ID: 238781
    Location: FORT BELVOIR, VIRGINIA, US

    Web Views: 432
    Downloads: 0

    PUBLIC DOMAIN