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dc.contributor.authorC. Ulett, Glenen_US
dc.contributor.authorG. Hirst, Roberten_US
dc.contributor.authorGal, Danielen_US
dc.contributor.authorJ. Currie, Barten_US
dc.contributor.authorKetheesan, Natkunamen_US
dc.contributor.authorL. Barnes, Jodieen_US
dc.contributor.authorLabrooy, Justinen_US
dc.contributor.authorMayo, Marken_US
dc.contributor.authorNorton, Roberten_US
dc.contributor.authorSmith, Christopher Ashhursten_US
dc.contributor.authorW. Clair, Timothyen_US
dc.contributor.authorWarner, Jeffreyen_US
dc.date.accessioned2017-04-04T21:46:44Z
dc.date.available2017-04-04T21:46:44Z
dc.date.issued2001en_US
dc.date.modified2009-09-29T23:14:40Z
dc.identifier.issn12864579en_US
dc.identifier.doi10.1016/S1286-4579(01)01417-4en_AU
dc.identifier.urihttp://hdl.handle.net/10072/25844
dc.description.abstractClinical presentations of melioidosis, caused by Burkholderia pseudomallei are protean, but the mechanisms underlying development of the different forms of disease remain poorly understood. In murine melioidosis, the level of virulence of B. pseudomallei is important in disease pathogenesis and progression. In this study, we used B. pseudomallei-susceptible BALB/c mice to determine the virulence of a library of clinical and environmental B. pseudomallei isolates from Australia and Papua New Guinea. Among 42 non-arabinose-assimilating (ara-) isolates, LD50 ranged from 10 to > 10^6 CFU. There were numerous correlations between virulence and disease presentation in patients; however, this was not a consistent observation. Virulence did not correlate with isolate origin (i.e. clinical vs environmental), since numerous ara- environmental isolates were highly virulent. The least virulent isolate was a soil isolate from Papua New Guinea, which was arabinose assimilating (ara+). Stability of B. pseudomallei virulence was investigated by in vivo passage of isolates through mice and repetitive in vitro subculture. Virulence increased following in vivo exposure in only one of eight isolates tested. In vitro subculture on ferric citrate-containing medium caused attenuation of virulence, and this correlated with changes in colony morphology. Pulsed-field gel electrophoresis and randomly amplified polymorphic DNA typing demonstrated that selected epidemiologically related isolates that had variable clinical outcomes and different in vivo virulence were clonal strains. No molecular changes were observed in isolates after in vivo or in vitro exposure despite changes in virulence. These results indicate that virulence of selected B. pseudomallei isolates is variable, being dependent on factors such as iron bioavailability. They also support the importance of other variables such as inoculum size and host risk factors in determining the clinical severity of melioidosis.en_US
dc.description.peerreviewedYesen_US
dc.description.publicationstatusYesen_AU
dc.languageEnglishen_US
dc.language.isoen_AU
dc.publisherElsevieren_US
dc.publisher.placeFranceen_US
dc.publisher.urihttp://www.sciencedirect.com/science/journal/12864579en_AU
dc.relation.ispartofpagefrom621en_US
dc.relation.ispartofpageto631en_US
dc.relation.ispartofissue8en_AU
dc.relation.ispartofjournalMicrobes and Infectionen_US
dc.relation.ispartofvolume3en_US
dc.subject.fieldofresearchMedical Bacteriologyen_US
dc.subject.fieldofresearchcode110801en_US
dc.titleBurkholderia pseudomallei Virulence: Definition, Stability and Association with Clonalityen_US
dc.typeJournal articleen_US
dc.type.descriptionC1 - Peer Reviewed (HERDC)en_US
dc.type.codeC - Journal Articlesen_US
gro.date.issued2001
gro.hasfulltextNo Full Text


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