Literature DB >> 11080514

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

C Leelayuwat1, A Romphruk, A Lulitanond, S Trakulsomboon, V Thamlikitkul.   

Abstract

Burkholderia 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<0.0000001). 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.

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Year:  2000        PMID: 11080514     DOI: 10.1016/s0001-706x(00)00137-6

Source DB:  PubMed          Journal:  Acta Trop        ISSN: 0001-706X            Impact factor:   3.112


  7 in total

1.  PCR analyses of tRNA intergenic spacer, 16S-23S internal transcribed spacer, and randomly amplified polymorphic DNA reveal inter- and intraspecific relationships of Enterobacter cloacae strains.

Authors:  M M Clementino; I de Filippis; C R Nascimento; R Branquinho; C L Rocha; O B Martins
Journal:  J Clin Microbiol       Date:  2001-11       Impact factor: 5.948

2.  Use of a variable amplicon typing scheme reveals considerable variation in the accessory genomes of isolates of Burkholderia pseudomallei.

Authors:  Kwanjit Duangsonk; Daniel Gal; Mark Mayo; C Anthony Hart; Bart J Currie; Craig Winstanley
Journal:  J Clin Microbiol       Date:  2006-04       Impact factor: 5.948

Review 3.  An objective approach for Burkholderia pseudomallei strain selection as challenge material for medical countermeasures efficacy testing.

Authors:  Kristopher E Van Zandt; Apichai Tuanyok; Paul S Keim; Richard L Warren; H Carl Gelhaus
Journal:  Front Cell Infect Microbiol       Date:  2012-09-26       Impact factor: 5.293

4.  Multilocus sequence types of clinical Burkholderia pseudomallei isolates from peninsular Malaysia and their associations with disease outcomes.

Authors:  Abdel Rahman Zueter; Zaidah Abdul Rahman; Mahmoud Abumarzouq; Azian Harun
Journal:  BMC Infect Dis       Date:  2018-01-02       Impact factor: 3.090

5.  Identification of melioidosis outbreak by multilocus variable number tandem repeat analysis.

Authors:  Bart J Currie; Asha Haslem; Talima Pearson; Heidie Hornstra; Benjamin Leadem; Mark Mayo; Daniel Gal; Linda Ward; Daniel Godoy; Brian G Spratt; Paul Keim
Journal:  Emerg Infect Dis       Date:  2009-02       Impact factor: 6.883

6.  Using BOX-PCR to exclude a clonal outbreak of melioidosis.

Authors:  Bart J Currie; Daniel Gal; Mark Mayo; Linda Ward; Daniel Godoy; Brian G Spratt; John J LiPuma
Journal:  BMC Infect Dis       Date:  2007-06-30       Impact factor: 3.090

7.  Source-identifying biomarker ions between environmental and clinical Burkholderia pseudomallei using whole-cell matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS).

Authors:  Suthamat Niyompanich; Janthima Jaresitthikunchai; Kitima Srisanga; Sittiruk Roytrakul; Sumalee Tungpradabkul
Journal:  PLoS One       Date:  2014-06-10       Impact factor: 3.240

  7 in total

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