Publication:
Genotype analysis of Burkholderia pseudomallei using randomly amplified polymorphic DNA (RAPD): Indicative of genetic differences amongst environmental and clinical isolates

dc.contributor.authorChanvit Leelayuwaten_US
dc.contributor.authorArunrat Romphruken_US
dc.contributor.authorAroonlug Lulitanonden_US
dc.contributor.authorSuwanna Trakulsomboonen_US
dc.contributor.authorVisanu Thamlikitkulen_US
dc.contributor.otherKhon Kaen Universityen_US
dc.contributor.otherUniversity of Western Australiaen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-09-07T09:11:16Z
dc.date.available2018-09-07T09:11:16Z
dc.date.issued2000-11-02en_US
dc.description.abstractBurkholderia pseudomallei is the causative agent of melioidosis, an infectious disease common in the tropics. Melioidosis is most prevalent in the northeastern part of Thailand. The diseases has diverse clinical manifestations ranging from mild localized to fatal septicemic forms. The bacterial genetic factors contributing to the severity of melioidosis have not been completely identified. We have developed a genotyping method based upon randomly amplified polymorphic DNA (RAPD) analysis. Eighteen deca-oligo nucleotide primers with 70% GC content, eight previously published 60% GC RAPD primers, and four random deca oligomers were tested on nine strains of B. pseudomallei isolated from five patients with localized and four with septicemic melioidosis. The RAPD patterns were analyzed by polyacrylamide gel electrophoresis using a laser based automated fragment analyzer, GS2000. Based upon the pattern complexity, seven pairs consisting of eight primers were chosen for further analysis. Six hundred and thirty-two samples, including duplicates/triplicates, of B. pseudomallei isolated from melioidosis patients and the environment were analyzed. Two controls were included in each run of the test samples. All the samples were tested and patterns analyzed by blinded technical staff. Apparently, the method is reproducible. This is indicated by the RAPD patterns of the two controls of between run assay. Interestingly, some RAPD patterns were more prevalent in the clinical isolates than the environmental specimens and vice versa. For example, Q162KKU4-0 and Q162KKU1-0 were found 3.5 and 3.3 times more often in the clinical specimens (P < 0.025). Likewise, Q162KKU1-1 and Q162KKU4-1 were found 18 and 37 times more often in the environment (P < 0.770001). In addition, there was a bias in the distribution of arabinose positive strains and particular RAPD patterns; RAPD patterns of B. pseudomallei that were found frequently in septicemic patients were less likely to be arabinose positive. The data suggest the existence of bacterial genetic differences between the clinical and environmental isolates of B. pseudomallei. Further analysis of the RAPD patterns searching for common polymorphic DNA fragments and systemic comparative genomic analysis of B. pseudomallei in accordance with the clinical data should reveal genetic factors involved in severity and bacterial pathogenesis of B. pseudomallei in melioidosis. (C) 2000 Published by Elsevier Science B.V.en_US
dc.identifier.citationActa Tropica. Vol.77, No.2 (2000), 229-237en_US
dc.identifier.doi10.1016/S0001-706X(00)00137-6en_US
dc.identifier.issn0001706Xen_US
dc.identifier.other2-s2.0-0034597553en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/25965
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0034597553&origin=inwarden_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titleGenotype analysis of Burkholderia pseudomallei using randomly amplified polymorphic DNA (RAPD): Indicative of genetic differences amongst environmental and clinical isolatesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0034597553&origin=inwarden_US

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