Dynamic relocalization of cytosolic type III secretion system components prevents premature protein secretion at low external pH.


Journal

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

Informations de publication

Date de publication:
12 03 2021
Historique:
received: 27 03 2020
accepted: 12 02 2021
entrez: 13 3 2021
pubmed: 14 3 2021
medline: 2 4 2021
Statut: epublish

Résumé

Many bacterial pathogens use a type III secretion system (T3SS) to manipulate host cells. Protein secretion by the T3SS injectisome is activated upon contact to any host cell, and it has been unclear how premature secretion is prevented during infection. Here we report that in the gastrointestinal pathogens Yersinia enterocolitica and Shigella flexneri, cytosolic injectisome components are temporarily released from the proximal interface of the injectisome at low external pH, preventing protein secretion in acidic environments, such as the stomach. We show that in Yersinia enterocolitica, low external pH is detected in the periplasm and leads to a partial dissociation of the inner membrane injectisome component SctD, which in turn causes the dissociation of the cytosolic T3SS components. This effect is reversed upon restoration of neutral pH, allowing a fast activation of the T3SS at the native target regions within the host. These findings indicate that the cytosolic components form an adaptive regulatory interface, which regulates T3SS activity in response to environmental conditions.

Identifiants

pubmed: 33712575
doi: 10.1038/s41467-021-21863-4
pii: 10.1038/s41467-021-21863-4
pmc: PMC7954860
doi:

Substances chimiques

Bacterial Proteins 0
Type III Secretion Systems 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1625

Commentaires et corrections

Type : ErratumIn

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Auteurs

Stephan Wimmi (S)

Department of Ecophysiology, Max Planck Institute for Terrestrial Microbiology, Marburg, Germany.

Alexander Balinovic (A)

Max Planck Institute for Terrestrial Microbiology, Marburg, Germany.
Department of Physics, Mellon College of Science, Carnegie Mellon University, Pittsburgh, PA, USA.

Hannah Jeckel (H)

Max Planck Institute for Terrestrial Microbiology, Marburg, Germany.
Department of Physics, Philipps-Universität Marburg, Marburg, Germany.

Lisa Selinger (L)

Department of Ecophysiology, Max Planck Institute for Terrestrial Microbiology, Marburg, Germany.

Dimitrios Lampaki (D)

Department of Ecophysiology, Max Planck Institute for Terrestrial Microbiology, Marburg, Germany.
Max-Planck-Institut für Immunbiologie und Epigenetik, Freiburg, Germany.

Emma Eisemann (E)

Department of Ecophysiology, Max Planck Institute for Terrestrial Microbiology, Marburg, Germany.
James Madison University, Harrisonburg, VA, USA.

Ina Meuskens (I)

Department of Biosciences, University of Oslo, Oslo, Norway.

Dirk Linke (D)

Department of Biosciences, University of Oslo, Oslo, Norway.

Knut Drescher (K)

Max Planck Institute for Terrestrial Microbiology, Marburg, Germany.
Department of Physics, Philipps-Universität Marburg, Marburg, Germany.

Ulrike Endesfelder (U)

Max Planck Institute for Terrestrial Microbiology, Marburg, Germany.
Department of Physics, Mellon College of Science, Carnegie Mellon University, Pittsburgh, PA, USA.

Andreas Diepold (A)

Department of Ecophysiology, Max Planck Institute for Terrestrial Microbiology, Marburg, Germany. andreas.diepold@mpi-marburg.mpg.de.
SYNMIKRO, LOEWE Center for Synthetic Microbiology, Marburg, Germany. andreas.diepold@mpi-marburg.mpg.de.

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