MmpL3 Is the Cellular Target of the Antitubercular Pyrrole Derivative BM212
Author
Rosa, Valentina La
Poce, Giovanna
Canseco, Julio Ortiz
Buroni, Silvia
Pasca, Maria Rosalia
Biava, Mariangela
Raju, Ravikiran M.
Porretta, Giulio Cesare
Alfonso, Salvatore
Battilocchio, Claudio
Javid, Babak
Sorrentino, Flavia
Ioerger, Thomas R.
Sacchettini, James C.
Manetti, Fabrizio
Botta, Maurizio
Logu, Alessandro De
Rubin, Eric J.
Rossi, Edda De
Published Version
https://doi.org/10.1128/AAC.05270-11Metadata
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La Rosa, Valentina, Giovanna Poce, Julio Ortiz Canseco, Silvia Buroni, Maria Rosalia Pasca, Mariangela Biava, Ravikiran M. Raju, et al. 2011. “MmpL3 Is the Cellular Target of the Antitubercular Pyrrole Derivative BM212.” Antimicrobial Agents and Chemotherapy 56 (1): 324–31. https://doi.org/10.1128/aac.05270-11.Abstract
The 1,5-diarylpyrrole derivative BM212 was previously shown to be active against multidrug-resistant clinical isolates and Mycobacterium tuberculosis residing within macrophages as well as against Mycobacterium avium and other atypical mycobacteria. To determine its mechanism of action, we identified the cellular target. Spontaneous Mycobacterium smegmatis, Mycobacterium bovis BCG, and M. tuberculosis H37Rv mutants that were resistant to BM212 were isolated. By the screening of genomic libraries and by whole-genome sequencing, we found that all the characterized mutants showed mutations in the mmpL3 gene, allowing us to conclude that resistance to BM212 maps to the MmpL3 protein, a member of the MmpL (mycobacterialmembrane protein, large) family. Susceptibility was unaffected by the efflux pump inhibitors reserpine, carbonylcyanide m-chlorophenylhydrazone, and verapamil. Uptake/efflux experiments with [C-14]BM212 demonstrated that resistance is not driven by the efflux of BM212. Together, these data strongly suggest that the MmpL3 protein is the cellular target of BM212.Terms of Use
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