Physiological stress drives the emergence of a Salmonella subpopulation through ribosomal RNA regulation.


Journal

Current biology : CB
ISSN: 1879-0445
Titre abrégé: Curr Biol
Pays: England
ID NLM: 9107782

Informations de publication

Date de publication:
20 Nov 2023
Historique:
received: 08 06 2023
revised: 24 08 2023
accepted: 26 09 2023
medline: 27 11 2023
pubmed: 26 10 2023
entrez: 25 10 2023
Statut: ppublish

Résumé

Bacteria undergo cycles of growth and starvation to which they must adapt swiftly. One important strategy for adjusting growth rates relies on ribosomal levels. Although high ribosomal levels are required for fast growth, their dynamics during starvation remain unclear. Here, we analyzed ribosomal RNA (rRNA) content of individual Salmonella cells by using fluorescence in situ hybridization (rRNA-FISH) and measured a dramatic decrease in rRNA numbers only in a subpopulation during nutrient limitation, resulting in a bimodal distribution of cells with high and low rRNA content. During nutritional upshifts, the two subpopulations were associated with distinct phenotypes. Using a transposon screen coupled with rRNA-FISH, we identified two mutants, DksA and RNase I, acting on rRNA transcription shutdown and degradation, which abolished the formation of the subpopulation with low rRNA content. Our work identifies a bacterial mechanism for regulation of ribosomal bimodality that may be beneficial for population survival during starvation.

Identifiants

pubmed: 37879333
pii: S0960-9822(23)01313-1
doi: 10.1016/j.cub.2023.09.064
pii:
doi:

Substances chimiques

RNA, Ribosomal 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

4880-4892.e14

Subventions

Organisme : NIGMS NIH HHS
ID : R35 GM140709
Pays : United States

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests The authors declare no competing interests.

Auteurs

Camilla Ciolli Mattioli (C)

Department of Immunology and Regenerative Biology, Weizmann Institute of Science, Rehovot 7610001, Israel.

Kfir Eisner (K)

Department of Physics of Complex Systems, Weizmann Institute of Science, Rehovot 7610001, Israel.

Aviel Rosenbaum (A)

Department of Immunology and Regenerative Biology, Weizmann Institute of Science, Rehovot 7610001, Israel.

Mengyu Wang (M)

Department of Physics, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.

Andre' Rivalta (A)

Department of Chemical and Structural Biology, Weizmann Institute of Science, Rehovot 7610001, Israel.

Ariel Amir (A)

Department of Physics of Complex Systems, Weizmann Institute of Science, Rehovot 7610001, Israel.

Ido Golding (I)

Department of Physics, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.

Roi Avraham (R)

Department of Immunology and Regenerative Biology, Weizmann Institute of Science, Rehovot 7610001, Israel. Electronic address: roi.avraham@weizmann.ac.il.

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Classifications MeSH