Please use this identifier to cite or link to this item: https://hdl.handle.net/10137/7501
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dc.contributor.authorWebb JRen
dc.contributor.authorSarovich DSen
dc.contributor.authorPrice EPen
dc.contributor.authorWard LMen
dc.contributor.authorMayo MJen
dc.contributor.authorCurrie BJen
dc.date2019en
dc.date.accessioned2019-04-08T23:41:01Zen
dc.date.available2019-04-08T23:41:01Zen
dc.date.issued2019-04en
dc.identifier.citationOpen forum infectious diseases 2019-04; 6(4): ofz091en
dc.identifier.issn2328-8957en
dc.identifier.urihttps://hdl.handle.net/10137/7501en
dc.description.abstractThe causative agent of melioidosis is the Gram-negative bacterium Burkholderia pseudomallei. Clinical presentations of melioidosis are notably diverse, with host risk factors considered central to progression from infection to disease and clinical outcome. Ubiquitous and variably present virulence determinants have been described for B pseudomallei, with several variably present minority genotypes associated with specific disease presentations. The lipopolysaccharide (LPS) O-antigen of B pseudomallei is highly diverse with 3 types described. In vitro data suggest differential virulence between LPS types, but it remains unclear whether this LPS O-antigen diversity influences clinical presentation, severity, and outcomes in patients with melioidosis. Whole-genome sequencing was performed to assign an LPS type to 1005 consecutive B pseudomallei strains, each corresponding to a melioidosis patient enrolled in the 28-year Darwin Prospective Melioidosis study. Correlations of LPS genotype with clinical parameters was then undertaken. Bivariate analysis demonstrated that mortality and the rates of bacteremia and septic shock were the same for patients with the 2 predominant B pseudomallei LPS genotypes A (87% of cases) and B (12% of all cases). Mortality was 12% and 12%, bacteremia was 57% and 53%, and septic shock was 22% and 18% for LPS A and LPS B, respectively. Lipopolysaccharide genotype was not associated with melioidosis severity or outcome. These findings suggest that in vitro differential virulence between B pseudomallei LPS genotypes does not translate to clinical significance, and this supports the primary role of host risk factors in determining disease severity and outcomes in melioidosis.en
dc.language.isoengen
dc.subjectLPS O-antigen diversityen
dc.subjectmelioidosisen
dc.subjectvirulenceen
dc.titleBurkholderia pseudomallei Lipopolysaccharide Genotype Does Not Correlate With Severity or Outcome in Melioidosis: Host Risk Factors Remain the Critical Determinant.en
dc.typeJournal Articleen
dc.identifier.journaltitleOpen forum infectious diseasesen
dc.identifier.doi10.1093/ofid/ofz091en
dc.identifier.pubmedidhttps://www.ezpdhcs.nt.gov.au/login?url=https://www.ncbi.nlm.nih.gov/pubmed//30949536en
dc.identifier.affiliationGlobal and Tropical Health Division, Menzies School of Health Research, Darwin, Northern Territory, Australia..en
dc.identifier.affiliationGlobal and Tropical Health Division, Menzies School of Health Research, Darwin, Northern Territory, Australia.. GeneCology Research Centre, University of the Sunshine Coast, Sippy Downs, Queensland, Australia..en
dc.identifier.affiliationGlobal and Tropical Health Division, Menzies School of Health Research, Darwin, Northern Territory, Australia.. GeneCology Research Centre, University of the Sunshine Coast, Sippy Downs, Queensland, Australia..en
dc.identifier.affiliationGlobal and Tropical Health Division, Menzies School of Health Research, Darwin, Northern Territory, Australia..en
dc.identifier.affiliationGlobal and Tropical Health Division, Menzies School of Health Research, Darwin, Northern Territory, Australia..en
dc.identifier.affiliationGlobal and Tropical Health Division, Menzies School of Health Research, Darwin, Northern Territory, Australia.. Department of Infectious Diseases and Northern Territory Medical Program, Royal Darwin Hospital, Northern Territory, Australia..en
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