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The P. aeruginosa effector Tse5 forms membrane pores disrupting the membrane potential of intoxicated bacteria

The type VI secretion system (T6SS) of Pseudomonas aeruginosa injects effector proteins into neighbouring competitors and host cells, providing a fitness advantage that allows this opportunistic nosocomial pathogen to persist and prevail during the onset of infections. However, despite the high clin...

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Autores principales: González-Magaña, Amaia, Altuna, Jon, Queralt-Martín, María, Largo, Eneko, Velázquez, Carmen, Montánchez, Itxaso, Bernal, Patricia, Alcaraz, Antonio, Albesa-Jové, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9637101/
https://www.ncbi.nlm.nih.gov/pubmed/36335275
http://dx.doi.org/10.1038/s42003-022-04140-y
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author González-Magaña, Amaia
Altuna, Jon
Queralt-Martín, María
Largo, Eneko
Velázquez, Carmen
Montánchez, Itxaso
Bernal, Patricia
Alcaraz, Antonio
Albesa-Jové, David
author_facet González-Magaña, Amaia
Altuna, Jon
Queralt-Martín, María
Largo, Eneko
Velázquez, Carmen
Montánchez, Itxaso
Bernal, Patricia
Alcaraz, Antonio
Albesa-Jové, David
author_sort González-Magaña, Amaia
collection PubMed
description The type VI secretion system (T6SS) of Pseudomonas aeruginosa injects effector proteins into neighbouring competitors and host cells, providing a fitness advantage that allows this opportunistic nosocomial pathogen to persist and prevail during the onset of infections. However, despite the high clinical relevance of P. aeruginosa, the identity and mode of action of most P. aeruginosa T6SS-dependent effectors remain to be discovered. Here, we report the molecular mechanism of Tse5-CT, the toxic auto-proteolytic product of the P. aeruginosa T6SS exported effector Tse5. Our results demonstrate that Tse5-CT is a pore-forming toxin that can transport ions across the membrane, causing membrane depolarisation and bacterial death. The membrane potential regulates a wide range of essential cellular functions; therefore, membrane depolarisation is an efficient strategy to compete with other microorganisms in polymicrobial environments.
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spelling pubmed-96371012022-11-07 The P. aeruginosa effector Tse5 forms membrane pores disrupting the membrane potential of intoxicated bacteria González-Magaña, Amaia Altuna, Jon Queralt-Martín, María Largo, Eneko Velázquez, Carmen Montánchez, Itxaso Bernal, Patricia Alcaraz, Antonio Albesa-Jové, David Commun Biol Article The type VI secretion system (T6SS) of Pseudomonas aeruginosa injects effector proteins into neighbouring competitors and host cells, providing a fitness advantage that allows this opportunistic nosocomial pathogen to persist and prevail during the onset of infections. However, despite the high clinical relevance of P. aeruginosa, the identity and mode of action of most P. aeruginosa T6SS-dependent effectors remain to be discovered. Here, we report the molecular mechanism of Tse5-CT, the toxic auto-proteolytic product of the P. aeruginosa T6SS exported effector Tse5. Our results demonstrate that Tse5-CT is a pore-forming toxin that can transport ions across the membrane, causing membrane depolarisation and bacterial death. The membrane potential regulates a wide range of essential cellular functions; therefore, membrane depolarisation is an efficient strategy to compete with other microorganisms in polymicrobial environments. Nature Publishing Group UK 2022-11-05 /pmc/articles/PMC9637101/ /pubmed/36335275 http://dx.doi.org/10.1038/s42003-022-04140-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
González-Magaña, Amaia
Altuna, Jon
Queralt-Martín, María
Largo, Eneko
Velázquez, Carmen
Montánchez, Itxaso
Bernal, Patricia
Alcaraz, Antonio
Albesa-Jové, David
The P. aeruginosa effector Tse5 forms membrane pores disrupting the membrane potential of intoxicated bacteria
title The P. aeruginosa effector Tse5 forms membrane pores disrupting the membrane potential of intoxicated bacteria
title_full The P. aeruginosa effector Tse5 forms membrane pores disrupting the membrane potential of intoxicated bacteria
title_fullStr The P. aeruginosa effector Tse5 forms membrane pores disrupting the membrane potential of intoxicated bacteria
title_full_unstemmed The P. aeruginosa effector Tse5 forms membrane pores disrupting the membrane potential of intoxicated bacteria
title_short The P. aeruginosa effector Tse5 forms membrane pores disrupting the membrane potential of intoxicated bacteria
title_sort p. aeruginosa effector tse5 forms membrane pores disrupting the membrane potential of intoxicated bacteria
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9637101/
https://www.ncbi.nlm.nih.gov/pubmed/36335275
http://dx.doi.org/10.1038/s42003-022-04140-y
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