| Literature DB >> 35905736 |
Kelley R Hurst-Hess1, Aavrati Saxena2, Paulami Rudra1, Yong Yang1, Pallavi Ghosh3.
Abstract
Rifampicin (RIF), the frontline drug against M. tuberculosis, is completely ineffective against M. abscessus, partially due to the presence of an ADP-ribosyltransferase (Arr) that inactivates RIF. Using RNA-seq, we show that exposure of M. abscessus to sublethal doses of RIF and Rifabutin (RBT), a close analog of RIF, results in an ∼25-fold upregulation of Mab_helR in laboratory and clinical isolates. An isogenic deletion in Mab_helR results in RIF/RBT hypersensitivity, and overexpression of Mab_helR confers RIF tolerance in M. tuberculosis. We demonstrate an increased HelR-RNAP association in RIF-exposed bacteria and a MabHelR-mediated dissociation of RNAP from stalled initiation complexes in vitro. Finally, we show that the tip of the PCh-loop of Mab_helR, present in proximity to RIF, is critical for conferring RIF resistance but dispensable for dissociation of stalled RNAP complexes, suggesting that HelR-mediated RIF resistance requires a step in addition to displacement of RIF-stalled RNAP.Entities:
Keywords: HelD; HelR; Mycobacterium abscessus; RNA polymerase protection; intrinsic resistance; rifabutin; rifampicin
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Year: 2022 PMID: 35905736 PMCID: PMC9444957 DOI: 10.1016/j.molcel.2022.06.034
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 19.328