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dc.contributor.authorRifat, Dalin
dc.contributor.authorCampodnico, Victoria L.
dc.contributor.authorTao, Jing
dc.contributor.authorMiller, James A.
dc.contributor.authorAlp, Alpaslan
dc.contributor.authorYao, Yufeng
dc.contributor.authorKarakousis, Petros C.
dc.date.accessioned2019-12-12T06:24:58Z
dc.date.available2019-12-12T06:24:58Z
dc.date.issued2017
dc.identifier.issn1746-0913
dc.identifier.urihttps://doi.org/10.2217/fmb-2017-0022
dc.identifier.urihttp://hdl.handle.net/11655/16227
dc.description.abstractAim: There is controversy regarding the potential fitness costs of rifampicin (RIF) resistance-conferring mutations in the Mycobacterium tuberculosis (Mtb) rpoB gene. We characterized the pathogenicity of an Mtb RpoB H526D mutant. Materials & methods: A mutant containing the RpoB H526D mutation was isolated from wild-type Mtb grown on RIF-containing plates and complemented for determination of in vitro and in vivo fitness costs. Results: The RpoB H526D mutant showed reduced survival relative to control strains during progressive hypoxia and delayed growth following resuscitation from nutrient starvation (p < 0.05), which was associated with reduced expression of the resuscitation-promoting factor genes rpfB, rpfC and rpfE. Relative to the isogenic wild-type strain, the mutant showed significantly attenuated growth and long-term survival as well as reduced inflammation in mouse lungs. Conclusion & future perspective: Our data suggest that RpoB H526D mutation confers a fitness cost during growth-limiting conditions in vitro and in mouse lungs.
dc.language.isoen
dc.publisherFuture Medicine Ltd
dc.relation.isversionof10.2217/fmb-2017-0022
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectMicrobiology
dc.titleIn Vitro And In Vivo Fitness Costs Associated With Mycobacterium Tuberculosis Rpob Mutation H526D
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalFuture Microbiology
dc.contributor.departmentTıbbi Mikrobiyoloji
dc.identifier.volume12
dc.identifier.issue9
dc.identifier.startpage753
dc.identifier.endpage765
dc.description.indexWoS


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