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The P. aeruginosa effector Tse5 forms membrane pores disrupting the membrane potential of intoxicated bacteria
dc.contributor.author | González Magaña, Amaia | |
dc.contributor.author | Altuna, Jon | |
dc.contributor.author | Queralt-Martín, María | |
dc.contributor.author | Largo, Eneko | |
dc.contributor.author | Velázquez, Carmen | |
dc.contributor.author | Montánchez, Itxaso | |
dc.contributor.author | Bernal, Patricia | |
dc.contributor.author | Alcaraz, Antonio | |
dc.contributor.author | Albesa-Jové, David | |
dc.date.accessioned | 2023-04-19T09:34:10Z | |
dc.date.available | 2023-04-19T09:34:10Z | |
dc.date.issued | 2022 | |
dc.identifier.citation | González-Magaña, A., Altuna, J., Queralt-Martín, M. et al. The P. aeruginosa effector Tse5 forms membrane pores disrupting the membrane potential of intoxicated bacteria. Commun Biol 5, 1189 (2022). https://doi.org/10.1038/s42003-022-04140-y | ca_CA |
dc.identifier.issn | 2399-3642 | |
dc.identifier.uri | http://hdl.handle.net/10234/202202 | |
dc.description.abstract | 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. | ca_CA |
dc.format.extent | 15 p. | ca_CA |
dc.format.mimetype | application/pdf | ca_CA |
dc.language.iso | eng | ca_CA |
dc.publisher | Nature Research | ca_CA |
dc.relation | Estudio biofísico de los mecanismos de permeabilización de membranas inducidos por canales iónicos | ca_CA |
dc.relation.isPartOf | Communications Biology, 2022, vol. 5, no 1 | ca_CA |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | ca_CA |
dc.subject | VI secretion system | ca_CA |
dc.subject | crystal structure | ca_CA |
dc.subject | structural insights | ca_CA |
dc.subject | nucleotide sequence | ca_CA |
dc.subject | RHS proteins | ca_CA |
dc.subject | colicin-B | ca_CA |
dc.title | The P. aeruginosa effector Tse5 forms membrane pores disrupting the membrane potential of intoxicated bacteria | ca_CA |
dc.type | info:eu-repo/semantics/article | ca_CA |
dc.identifier.doi | https://doi.org/10.1038/s42003-022-04140-y | |
dc.rights.accessRights | info:eu-repo/semantics/openAccess | ca_CA |
dc.relation.publisherVersion | https://www.nature.com/articles/s42003-022-04140-y | ca_CA |
dc.description.sponsorship | We gratefully acknowledge the Laboratories of Dr. Daniel Ladant (Institut Pasteur, Paris) and Dr. Victor de Lorenzo (Centro Nacional de Biotecnología, Madrid) for the plasmids received (pKTop and pSEVA plasmids, respectively). Also, we would like to acknowledge the Laboratory of Dr. Joseph Mougous for the P. aeruginosa strains received. The technical assistance from Cristina Civantos and Adrian Ruiz is also very much appreciated. We acknowledge the FGCZ for the mass spectrometry analyses and the technical support (Functional Genomics Center Zurich (FGCZ), University/ETH Zurich). D.A.-J. acknowledges support by the MINECO Contracts CTQ2016-76941-R and PID2021-127816NB-I00, Fundación Biofísica Bizkaia, the Basque Excellence Research Centre (BERC) programme, and IT709-13 and IT1745-22 of the Basque Government, and Fundación BBVA. A.G.-M. acknowledges the financial support received from the Spanish Ministry of Universities and the Grants for the requalification of the Spanish university system for 2021–2023, financed by the European Union-Next Generation EU-Margarita Salas Modality. A.A. acknowledges support from the Spanish Ministry of Science and Innovation (Project 2019-108434GB-I00 funded by MCIN/AEI/10.13039/501100011033), Generalitat Valenciana (project AICO/2020/066) and Universitat Jaume I (project UJI-B2018-53). M.Q.-M. acknowledges support from the Spanish Ministry of Science and Innovation (Project IJC2018-035283-I funded by MCIN/AEI/10.13039/501100011033) and Universitat Jaume I (project UJI-A2020–21). P.B acknowledges the financial support received from the Spanish Ministry of Science and Innovation through the Ramón y Cajal Programme (contract RYC2019-026551-I). | |
dc.type.version | info:eu-repo/semantics/publishedVersion | ca_CA |
project.funder.identifier | http://dx.doi.org/10.13039/501100003329 | ca_CA |
project.funder.identifier | http://dx.doi.org/10.13039/501100004837 | |
project.funder.identifier | http://dx.doi.org/10.13039/501100011033 | |
project.funder.name | Ministerio de Economía y Competitividad (España) | ca_CA |
project.funder.name | Ministerio de Ciencia e Innovación | ca_CA |
project.funder.name | Gobierno Vasco | ca_CA |
project.funder.name | Ministerio de Ciencia, Innovación y Universidades | ca_CA |
project.funder.name | Generalitat Valenciana | ca_CA |
project.funder.name | Universitat Jaume I | ca_CA |
oaire.awardNumber | MINECO/CTQ2016-76941-R | ca_CA |
oaire.awardNumber | MICINN/PID2021-127816NB-I00 | ca_CA |
oaire.awardNumber | IT709-13 | ca_CA |
oaire.awardNumber | IT1745-22 | ca_CA |
oaire.awardNumber | MICIU/ICTI2017-2020/PID2021-127816NB-I00 | ca_CA |
oaire.awardNumber | AICO/2020/066 | ca_CA |
oaire.awardNumber | UJI-B2018-53 | ca_CA |
oaire.awardNumber | MICIU/IJC2018-035283-I | ca_CA |
oaire.awardNumber | UJI-A2020–21 | ca_CA |
oaire.awardNumber | MICINN/RYC2019-026551-I | ca_CA |
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