Membrane depolarization kills dormant Bacillus subtilis cells by generating a lethal dose of ROS

verfasst von

Declan A. Gray, Biwen Wang, Margareth Sidarta, Fabián A. Cornejo, Jurian Wijnheijmer, Rupa Rani, Pamela Gamba, Kürşad Turgay, Michaela Wenzel, Henrik Strahl, Leendert W. Hamoen

Abstract

The bactericidal activity of several antibiotics partially relies on the production of reactive oxygen species (ROS), which is generally linked to enhanced respiration and requires the Fenton reaction. Bacterial persister cells, an important cause of recurring infections, are tolerant to these antibiotics because they are in a dormant state. Here, we use Bacillus subtilis cells in stationary phase, as a model system of dormant cells, to show that pharmacological induction of membrane depolarization enhances the antibiotics’ bactericidal activity and also leads to ROS production. However, in contrast to previous studies, this results primarily in production of superoxide radicals and does not require the Fenton reaction. Genetic analyzes indicate that Rieske factor QcrA, the iron-sulfur subunit of respiratory complex III, seems to be a primary source of superoxide radicals. Interestingly, the membrane distribution of QcrA changes upon membrane depolarization, suggesting a dissociation of complex III. Thus, our data reveal an alternative mechanism by which antibiotics can cause lethal ROS levels, and may partially explain why membrane-targeting antibiotics are effective in eliminating persisters.

Organisationseinheit(en)

Institut für Mikrobiologie

Externe Organisation(en)

Newcastle University
Centre for Antibiotic Resistance Research in Gothenburg (CARe)
Universiteit van Amsterdam (UvA)
Chalmers University of Technology
Max-Planck-Forschungsstelle für die Wissenschaft der Pathogene (MPUSP)

Typ

Artikel

Journal

Nature Communications

Band

15

Anzahl der Seiten

13

ISSN

2041-1723

Publikationsdatum

11.08.2024

Publikationsstatus

Elektronisch veröffentlicht (E-Pub)

Peer-reviewed

Ja

ASJC Scopus Sachgebiete

Chemie (insg.), Biochemie, Genetik und Molekularbiologie (insg.), Physik und Astronomie (insg.)

Elektronische Version(en)

https://doi.org/10.1038/s41467-024-51347-0 (Zugang: Offen)