American Society for Microbiology, Antimicrobial Agents and Chemotherapy, 11(58), p. 6962-6965, 2014
DOI: 10.1128/aac.03486-14
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ABSTRACT We report here a series of five chemically diverse scaffolds that have in vitro activities on replicating and hypoxic nonreplicating bacilli by targeting the respiratory bc 1 complex in Mycobacterium tuberculosis in a strain-dependent manner. Deletion of the cytochrome bd oxidase generated a hypersusceptible mutant in which resistance was acquired by a mutation in qcrB . These results highlight the promiscuity of the bc 1 complex and the risk of targeting energy metabolism with new drugs.