Show simple item record

dc.contributor.authorSmith, Laura J.en
dc.contributor.authorBochkareva, Aleksandraen
dc.contributor.authorRolfe, Matthew D.en
dc.contributor.authorHunt, Debbie M.en
dc.contributor.authorKahramanoglou, Christinaen
dc.contributor.authorBraun, Yvonneen
dc.contributor.authorRodgers, Angelaen
dc.contributor.authorBlockley, Alixen
dc.contributor.authorCoade, Stephenen
dc.contributor.authorLougheed, Kathryn E. A.en
dc.contributor.authorHafneh, Nor Azianen
dc.contributor.authorGlenn, Sarah M.en
dc.contributor.authorCrack, Jason C.en
dc.contributor.authorLe Brun, Nick E.en
dc.contributor.authorSaldanha, José W.en
dc.contributor.authorMakarov, Vadimen
dc.contributor.authorNobeli, Ireneen
dc.contributor.authorArnvig, Kristineen
dc.contributor.authorMukamolova, Galina V.en
dc.contributor.authorBuxton, Roger S.en
dc.contributor.authorGreen, Jeffreyen
dc.date.accessioned2017-07-04T13:29:53Z
dc.date.available2017-07-04T13:29:53Z
dc.date.issued2017-05-08
dc.identifier.citationSmith, L.J. et al. (2017) Cmr is a redox-responsive regulator of DosR that contributes to M. tuberculosis virulence. Nucleic Acids Research, 45 (11), pp. 6600-6612en
dc.identifier.urihttp://hdl.handle.net/2086/14283
dc.descriptionRCUK funded OAen
dc.description.abstractMycobacterium tuberculosis (MTb) is the causative agent of pulmonary tuberculosis (TB). MTb colonizes the human lung, often entering a non-replicating state before progressing to life-threatening active infections. Transcriptional reprogramming is essential for TB pathogenesis. In vitro, Cmr (a member of the CRP/FNR super-family of transcription regulators) bound at a single DNA site to act as a dual regulator of cmr transcription and an activator of the divergent rv1676 gene. Transcriptional profiling and DNA-binding assays suggested that Cmr directly represses dosR expression. The DosR regulon is thought to be involved in establishing latent tuberculosis infections in response to hypoxia and nitric oxide. Accordingly, DNA-binding by Cmr was severely impaired by nitrosation. A cmr mutant was better able to survive a nitrosative stress challenge but was attenuated in a mouse aerosol infection model. The complemented mutant exhibited a ∼2-fold increase in cmr expression, which led to increased sensitivity to nitrosative stress. This, and the inability to restore wild-type behaviour in the infection model, suggests that precise regulation of the cmr locus, which is associated with Region of Difference 150 in hypervirulent Beijing strains of Mtb, is important for TB pathogenesis.en
dc.language.isoenen
dc.publisherOxford University Pressen
dc.titleCmr is a redox-responsive regulator of DosR that contributes to M. tuberculosis virulence.en
dc.typeArticleen
dc.identifier.doihttps://doi.org/10.1093/nar/gkx406
dc.peerreviewedYesen
dc.funderBiotechnology and Biological Sciences Research Council UKen
dc.projectidBB/K000071/1en
dc.cclicenceCC BYen
dc.date.acceptance2017-04-28en
dc.exception.reasonThe output was published as gold open accessen
dc.researchinstituteLeicester Institute for Pharmaceutical Innovation - From Molecules to Practice (LIPI)en


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record