Isoniazid Bactericidal Activity Involves Electron Transport Chain Perturbation

Author:

Zeng Sheng1,Soetaert Karine2,Ravon Faustine1,Vandeput Marie3,Bald Dirk4,Kauffmann Jean-Michel3,Mathys Vanessa2,Wattiez Ruddy5,Fontaine Véronique1ORCID

Affiliation:

1. Microbiology, Bioorganic and Macromolecular Chemistry Research Unit, Faculté de Pharmacie, Université Libre de Bruxelles, Brussels, Belgium

2. Sciensano, Tuberculosis and Mycobacteria Unit, Brussels, Belgium

3. Pharmacognosy, Bioanalysis and Drug Discovery Research Unit, Faculté de Pharmacie, Université Libre de Bruxelles, Brussels, Belgium

4. Department of Molecular Cell Biology, Amsterdam Institute for Molecules, Medicines and Systems, Faculty of Earth and Life Sciences, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands

5. Department of Proteomics and Microbiology, University of Mons, Mons, Belgium

Abstract

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.

Funder

Les Amis des Instituts Pasteur à Bruxelles

China Scholarship Council

Fonds De La Recherche Scientifique - FNRS

EC | European Regional Development Fund

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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