TB Research

Efficacy of novel regimens targeting oxidative phosphorylation in.

Dongshuo Li, Liang Li, Ye Zhang, Kai Cheng, Wenwen Liang, Eric Nuermberger, Xianglong Qi, Lei Fu, et al. (13 authors)

Antimicrobial agents and chemotherapy · 2025-06

Abstract

in both replicating and non-replicating states relies on oxidative phosphorylation (OxPhos) to generate ATP for its growth and survival. Our research delved into the efficacy of novel regimens targeting the OxPhos pathway in murine models. The combination of bedaquiline, clofazimine, pyrazinamide, alongside telacebec, and SQ109 was investigated against both wild-typeH37Rv and anmutant with cross-resistance between bedaquiline and clofazimine. The results demonstrated that the combination regimens, particularly bedaquiline + clofazimine + pyrazinamide (BCZ) along with telacebec (BCZT) and SQ109 (BCZS), exhibit significantly enhanced bactericidal activity compared to bedaquiline alone and sterilizing potential against. Notably, the BCZT regimen showed superior activity compared to other treatment regimens inmutant-infected BALB/c mice. The addition of T to BCZ prevented the amplification of bedaquiline-resistant mutants and reduced the number of mice relapsing. Our finding underscores the potential of targeting the OxPhos pathway to combat, paving the way for innovative approaches in tuberculosis therapy.

MeSH terms

  • Mycobacterium tuberculosis
  • Oxidative Phosphorylation
  • Animals
  • Antitubercular Agents
  • Diarylquinolines
  • Clofazimine
  • Mice
  • Pyrazinamide
  • Mice, Inbred BALB C
  • Microbial Sensitivity Tests
  • Female
  • Drug Therapy, Combination
  • Imidazoles
  • Adamantane
  • Piperidines
  • Ethylenediamines
  • Pyridines