FlhE functions as a chaperone to prevent formation of periplasmic flagella in Gram-negative bacteria.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
14 Jul 2024
Historique:
received: 25 03 2024
accepted: 04 07 2024
medline: 15 7 2024
pubmed: 15 7 2024
entrez: 14 7 2024
Statut: epublish

Résumé

The bacterial flagellum, which facilitates motility, is composed of ~20 structural proteins organized into a long extracellular filament connected to a cytoplasmic rotor-stator complex via a periplasmic rod. Flagellum assembly is regulated by multiple checkpoints that ensure an ordered gene expression pattern coupled to the assembly of the various building blocks. Here, we use epifluorescence, super-resolution, and transmission electron microscopy to show that the absence of a periplasmic protein (FlhE) prevents proper flagellar morphogenesis and results in the formation of periplasmic flagella in Salmonella enterica. The periplasmic flagella disrupt cell wall synthesis, leading to a loss of normal cell morphology resulting in cell lysis. We propose that FlhE functions as a periplasmic chaperone to control assembly of the periplasmic rod, thus preventing formation of periplasmic flagella.

Identifiants

pubmed: 39004688
doi: 10.1038/s41467-024-50278-0
pii: 10.1038/s41467-024-50278-0
doi:

Substances chimiques

Molecular Chaperones 0
Bacterial Proteins 0
Periplasmic Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

5921

Subventions

Organisme : EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council)
ID : agreement no. 864971

Informations de copyright

© 2024. The Author(s).

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Auteurs

Manuel Halte (M)

Institute of Biology, Humboldt-Universität zu Berlin, Philippstr. 13, 10115, Berlin, Germany. manuel.halte@hu-berlin.de.

Ekaterina P Andrianova (EP)

Department of Microbiology, The Ohio State University, Columbus, OH, 43210, USA.

Christian Goosmann (C)

Max Planck Institute for Infection Biology, Charitéplatz 1, 10117, Berlin, Germany.

Fabienne F V Chevance (FFV)

School of Biological Sciences, University of Utah, Salt Lake City, UT, USA.

Kelly T Hughes (KT)

School of Biological Sciences, University of Utah, Salt Lake City, UT, USA.

Igor B Zhulin (IB)

Department of Microbiology, The Ohio State University, Columbus, OH, 43210, USA.

Marc Erhardt (M)

Institute of Biology, Humboldt-Universität zu Berlin, Philippstr. 13, 10115, Berlin, Germany. marc.erhardt@hu-berlin.de.
Max Planck Unit for the Science of Pathogens, Charitéplatz 1, 10117, Berlin, Germany. marc.erhardt@hu-berlin.de.

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