Protective mechanism of action of the antifungal drug naftifine against Mycobacterium abscessus infection

Antimicrob Agents Chemother. 2026 Feb 4;70(2):e0110525. doi: 10.1128/aac.01105-25. Epub 2026 Jan 14.

Abstract

Mycobacterium abscessus, a rapidly growing nontuberculous mycobacterium, causes chronic pulmonary infections that are difficult to treat due to extensive intrinsic drug resistance. Through high-content screening of 786 FDA-approved drugs against intracellular M. abscessus in human THP-1 macrophages, we identified naftifine, an antifungal allylamine, as a novel antimycobacterial agent with dual-acting therapeutic mechanisms. Naftifine demonstrated potent activity against reference strains and multidrug-resistant clinical isolates. It showed enhanced efficacy in intracellular environments compared to axenic culture, indicating significant host-directed effects. Mechanistic investigations revealed that naftifine operates through a unique dual mechanism. It directly targets bacteria by inhibiting MmpL3 (MAB_4508), the essential mycolic acid transporter, and modulates host immunity through autophagy activation via the mTOR pathway suppression. Whole-genome sequencing of spontaneous naftifine-resistant mutants identified point mutations (S302T and V299G) in MmpL3. Complementation studies confirmed MmpL3 as the primary molecular target. Cross-resistance analysis with other MmpL3 inhibitors (BM212 and AU1235) validated this target identification. Notably, naftifine represents the first MmpL3 inhibitor demonstrated to induce autophagy, distinguishing it from other MmpL3-targeting compounds. Naftifine-induced autophagy enhanced macrophage-mediated bacterial clearance and reduced infection-associated necrosis, improving host cell survival. In vivo studies demonstrated a significant reduction of pulmonary and splenic bacterial burden with reduced lung inflammation. Furthermore, naftifine exhibited synergistic activity with β-lactam antibiotics without antagonizing other clinically used antibiotics. This is the first report demonstrating the unique combination of MmpL3 inhibition and autophagy induction by a single compound against M. abscessus, establishing naftifine as a promising dual-action therapeutic candidate for treating multidrug-resistant infections.

Keywords: FDA-approved drugs; MmpL3; Mycobacterium abscessus; naftifine.

MeSH terms

  • Allylamine* / analogs & derivatives
  • Allylamine* / pharmacology
  • Allylamine* / therapeutic use
  • Animals
  • Anti-Bacterial Agents* / pharmacology
  • Antifungal Agents* / pharmacology
  • Autophagy / drug effects
  • Bacterial Proteins / antagonists & inhibitors
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Humans
  • Macrophages / drug effects
  • Macrophages / microbiology
  • Mice
  • Microbial Sensitivity Tests
  • Mycobacterium Infections, Nontuberculous* / drug therapy
  • Mycobacterium Infections, Nontuberculous* / microbiology
  • Mycobacterium abscessus* / drug effects
  • Mycobacterium abscessus* / genetics
  • THP-1 Cells

Substances

  • Allylamine
  • naftifine
  • Antifungal Agents
  • Anti-Bacterial Agents
  • Bacterial Proteins