Sleeping ribosomes: Bacterial signaling triggers RaiA mediated persistence to aminoglycosides
Manon Lang,
Evelyne Krin,
Chloé Korlowski,
Odile Sismeiro,
Hugo Varet,
Jean-Yves Coppée,
Didier Mazel,
Zeynep Baharoglu
Affiliations
Manon Lang
Département Génomes et Génétique, Institut Pasteur, UMR3525, CNRS, Unité Plasticité du Génome Bactérien, 75015 Paris, France; Sorbonne Université, Collège Doctoral, 75005 Paris, France
Evelyne Krin
Département Génomes et Génétique, Institut Pasteur, UMR3525, CNRS, Unité Plasticité du Génome Bactérien, 75015 Paris, France
Chloé Korlowski
Département Génomes et Génétique, Institut Pasteur, UMR3525, CNRS, Unité Plasticité du Génome Bactérien, 75015 Paris, France
Odile Sismeiro
Biomics Technological Platform, Center for Technological Resources and Research, Institut Pasteur, 75015 Paris, France
Hugo Varet
Biomics Technological Platform, Center for Technological Resources and Research, Institut Pasteur, 75015 Paris, France; Bioinformatics and Biostatistics Hub, Department of Computational Biology, USR 3756 CNRS, Institut Pasteur, 75015 Paris, France
Jean-Yves Coppée
Biomics Technological Platform, Center for Technological Resources and Research, Institut Pasteur, 75015 Paris, France
Didier Mazel
Département Génomes et Génétique, Institut Pasteur, UMR3525, CNRS, Unité Plasticité du Génome Bactérien, 75015 Paris, France; Corresponding author
Zeynep Baharoglu
Département Génomes et Génétique, Institut Pasteur, UMR3525, CNRS, Unité Plasticité du Génome Bactérien, 75015 Paris, France; Corresponding author
Summary: Indole is a molecule proposed to be involved in bacterial signaling. We find that indole secretion is induced by sublethal tobramycin concentrations and increases persistence to aminoglycosides in V. cholerae. Indole transcriptomics showed increased expression of raiA, a ribosome associated factor. Deletion of raiA abolishes the appearance of indole dependent persisters to aminoglycosides, although its overexpression leads to 100-fold increase of persisters, and a reduction in lag phase, evocative of increased active 70S ribosome content, confirmed by sucrose gradient analysis. We propose that, under stress conditions, RaiA-bound inactive 70S ribosomes are stored as “sleeping ribosomes”, and are rapidly reactivated upon stress relief. Our results point to an active process of persister formation through ribosome protection during translational stress (e.g., aminoglycoside treatment) and reactivation upon antibiotic removal. Translation is a universal process, and these results could help elucidate a mechanism of persistence formation in a controlled, thus inducible way.