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The Polar Legionella Icm/Dot T4SS Establishes Distinct Contact Sites with the Pathogen Vacuole Membrane

Legionella pneumophila, the causative agent of Legionnaires’ disease, is a facultative intracellular pathogen that survives inside phagocytic host cells by establishing a protected replication niche, termed the “Legionella-containing vacuole” (LCV). To form an LCV and subvert pivotal host pathways,...

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Autores principales: Böck, Désirée, Hüsler, Dario, Steiner, Bernhard, Medeiros, João M., Welin, Amanda, Radomska, Katarzyna A., Hardt, Wolf-Dietrich, Pilhofer, Martin, Hilbi, Hubert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8510526/
https://www.ncbi.nlm.nih.gov/pubmed/34634944
http://dx.doi.org/10.1128/mBio.02180-21
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author Böck, Désirée
Hüsler, Dario
Steiner, Bernhard
Medeiros, João M.
Welin, Amanda
Radomska, Katarzyna A.
Hardt, Wolf-Dietrich
Pilhofer, Martin
Hilbi, Hubert
author_facet Böck, Désirée
Hüsler, Dario
Steiner, Bernhard
Medeiros, João M.
Welin, Amanda
Radomska, Katarzyna A.
Hardt, Wolf-Dietrich
Pilhofer, Martin
Hilbi, Hubert
author_sort Böck, Désirée
collection PubMed
description Legionella pneumophila, the causative agent of Legionnaires’ disease, is a facultative intracellular pathogen that survives inside phagocytic host cells by establishing a protected replication niche, termed the “Legionella-containing vacuole” (LCV). To form an LCV and subvert pivotal host pathways, L. pneumophila employs a type IV secretion system (T4SS), which translocates more than 300 different effector proteins into the host cell. The L. pneumophila T4SS complex has been shown to span the bacterial cell envelope at the bacterial poles. However, the interactions between the T4SS and the LCV membrane are not understood. Using cryo-focused ion beam milling, cryo-electron tomography, and confocal laser scanning fluorescence microscopy, we show that up to half of the intravacuolar L. pneumophila bacteria tether their cell pole to the LCV membrane. Tethering coincides with the presence and function of T4SSs and likely promotes the establishment of distinct contact sites between T4SSs and the LCV membrane. Contact sites are characterized by indentations in the limiting LCV membrane and localize juxtaposed to T4SS machineries. The data are in agreement with the notion that effector translocation occurs by close membrane contact rather than by an extended pilus. Our findings provide novel insights into the interactions of the L. pneumophila T4SS with the LCV membrane in situ.
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spelling pubmed-85105262021-10-20 The Polar Legionella Icm/Dot T4SS Establishes Distinct Contact Sites with the Pathogen Vacuole Membrane Böck, Désirée Hüsler, Dario Steiner, Bernhard Medeiros, João M. Welin, Amanda Radomska, Katarzyna A. Hardt, Wolf-Dietrich Pilhofer, Martin Hilbi, Hubert mBio Research Article Legionella pneumophila, the causative agent of Legionnaires’ disease, is a facultative intracellular pathogen that survives inside phagocytic host cells by establishing a protected replication niche, termed the “Legionella-containing vacuole” (LCV). To form an LCV and subvert pivotal host pathways, L. pneumophila employs a type IV secretion system (T4SS), which translocates more than 300 different effector proteins into the host cell. The L. pneumophila T4SS complex has been shown to span the bacterial cell envelope at the bacterial poles. However, the interactions between the T4SS and the LCV membrane are not understood. Using cryo-focused ion beam milling, cryo-electron tomography, and confocal laser scanning fluorescence microscopy, we show that up to half of the intravacuolar L. pneumophila bacteria tether their cell pole to the LCV membrane. Tethering coincides with the presence and function of T4SSs and likely promotes the establishment of distinct contact sites between T4SSs and the LCV membrane. Contact sites are characterized by indentations in the limiting LCV membrane and localize juxtaposed to T4SS machineries. The data are in agreement with the notion that effector translocation occurs by close membrane contact rather than by an extended pilus. Our findings provide novel insights into the interactions of the L. pneumophila T4SS with the LCV membrane in situ. American Society for Microbiology 2021-10-12 /pmc/articles/PMC8510526/ /pubmed/34634944 http://dx.doi.org/10.1128/mBio.02180-21 Text en Copyright © 2021 Böck et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Böck, Désirée
Hüsler, Dario
Steiner, Bernhard
Medeiros, João M.
Welin, Amanda
Radomska, Katarzyna A.
Hardt, Wolf-Dietrich
Pilhofer, Martin
Hilbi, Hubert
The Polar Legionella Icm/Dot T4SS Establishes Distinct Contact Sites with the Pathogen Vacuole Membrane
title The Polar Legionella Icm/Dot T4SS Establishes Distinct Contact Sites with the Pathogen Vacuole Membrane
title_full The Polar Legionella Icm/Dot T4SS Establishes Distinct Contact Sites with the Pathogen Vacuole Membrane
title_fullStr The Polar Legionella Icm/Dot T4SS Establishes Distinct Contact Sites with the Pathogen Vacuole Membrane
title_full_unstemmed The Polar Legionella Icm/Dot T4SS Establishes Distinct Contact Sites with the Pathogen Vacuole Membrane
title_short The Polar Legionella Icm/Dot T4SS Establishes Distinct Contact Sites with the Pathogen Vacuole Membrane
title_sort polar legionella icm/dot t4ss establishes distinct contact sites with the pathogen vacuole membrane
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8510526/
https://www.ncbi.nlm.nih.gov/pubmed/34634944
http://dx.doi.org/10.1128/mBio.02180-21
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