TY - JOUR T1 - Isoniazid Bactericidal Activity Involves Electron Transport Chain Perturbation. JF - Antimicrob Agents Chemother Y1 - 2019 A1 - Zeng, Sheng A1 - Karine Soetaert A1 - Faustine Ravon A1 - Marie Vandeput A1 - Dirk Bald A1 - Kauffmann, Jean-Michel A1 - Vanessa Mathys A1 - Wattiez, Ruddy A1 - VĂ©ronique Fontaine AB -

Accumulating evidence suggests that the bactericidal activity of some antibiotics may not be directly initiated by target inhibition. The activity of isoniazid (INH), a key first-line bactericidal antituberculosis drug currently known to inhibit mycolic acid synthesis, becomes extremely poor under stress conditions, such as hypoxia and starvation. This suggests that the target inhibition may not fully explain the bactericidal activity of the drug. Here, we report that INH rapidly increased BCG cellular ATP levels and enhanced oxygen consumption. The INH-triggered ATP increase and bactericidal activity were strongly compromised by Q203 and bedaquiline, which inhibit mycobacterial cytochrome and FF ATP synthase, respectively. Moreover, the antioxidant -acetylcysteine (NAC) but not 4-hydroxy-2,2,6,6-tetramethylpiperidin-1-oxyl (TEMPOL) abrogated the INH-triggered ATP increase and killing. These results reveal a link between the energetic (ATP) perturbation and INH's killing. Furthermore, the INH-induced energetic perturbation and killing were also abrogated by chemical inhibition of NADH dehydrogenases (NDHs) and succinate dehydrogenases (SDHs), linking INH's bactericidal activity further to the electron transport chain (ETC) perturbation. This notion was also supported by the observation that INH dissipated mycobacterial membrane potential. Importantly, inhibition of cytochrome oxidase significantly reduced cell recovery during INH challenge in a culture settling model, suggesting that the respiratory reprogramming to the cytochrome oxidase contributes to the escape of INH killing. This study implicates mycobacterial ETC perturbation through NDHs, SDHs, cytochrome , and FF ATP synthase in INH's bactericidal activity and pinpoints the participation of the cytochrome oxidase in protection against this drug under stress conditions.

VL - 63 CP - 3 M3 - 10.1128/AAC.01841-18 ER -