QcrB inhibitor Q203 (Telacebec) can synergize with clofazimine and clarithromycin to control a Mycobacterium avium infection

The targeting of the mycobacterial electron transport chain for drug development has recently garnered significant clinical success. The cytochrome bcc complex within the electron transport chain has emerged as a viable drug target, with the antibiotic Q203 (Telacebec) showing excellent activity against M. tuberculosis in vitro and in vivo. To determine if Q203 can function as an antibiotic against the non-tuberculosis mycobacteria M. avium and M. intracellulare (MAC), MIC and bactericidal studies were performed, both against various laboratory and clinical strains of MAC as well as in vivo infection studies. These studies found that Q203 provides synergistic activity against all tested MAC isolates when combined with clarithromycin and provided significant added benefit in a acute M. avium mouse infection model when combined with clarithromycin and clofazimine.

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Publication Details

Journal
PLoS ONE
Published
2026-04-21
DOI
https://doi.org/10.1371/journal.pone.0344608
Primary Topic
Tuberculosis Research and Epidemiology
Type
article
Field-Weighted Citation Impact
0.00
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article

QcrB inhibitor Q203 (Telacebec) can synergize with clofazimine and clarithromycin to control a Mycobacterium avium infection

Xuejuan Tan, Satoshi Miyagawa, Jeffrey S. Schorey, Garrett C. Moraski et al.
PLoS ONE
Tuberculosis Research and Epidemiology
article

QcrB inhibitor Q203 (Telacebec) can synergize with clofazimine and clarithromycin to control a Mycobacterium avium infection

Xuejuan Tan, Satoshi Miyagawa, Jeffrey S. Schorey, Garrett C. Moraski, Carrie Frey, Katie Mulvey, Yong Cheng, Marvin J. Miller, Toru Mizutare
article en

Abstract

The targeting of the mycobacterial electron transport chain for drug development has recently garnered significant clinical success. The cytochrome bcc complex within the electron transport chain has emerged as a viable drug target, with the antibiotic Q203 (Telacebec) showing excellent activity against M. tuberculosis in vitro and in vivo. To determine if Q203 can function as an antibiotic against the non-tuberculosis mycobacteria M. avium and M. intracellulare (MAC), MIC and bactericidal studies were performed, both against various laboratory and clinical strains of MAC as well as in vivo infection studies. These studies found that Q203 provides synergistic activity against all tested MAC isolates when combined with clarithromycin and provided significant added benefit in a acute M. avium mouse infection model when combined with clarithromycin and clofazimine.

PLoS ONEVol. 21(4)
University of Notre Dame (US), Oklahoma State University (US), Montana State University (US), Shionogi (Japan) (JP), Ark Therapeutic (United States) (US), Futaba (Japan) (JP)
Good health and well-being
Openalex Percentile: Top 15%
Tuberculosis Research and Epidemiology
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