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Tension-activated channels in the mechanism of osmotic fitness in Pseudomonas aeruginosa

Pseudomonas aeruginosa (PA) is an opportunistic pathogen with an exceptional ability to adapt to a range of environments. Part of its adaptive potential is the ability to survive drastic osmolarity changes. Upon a sudden dilution of external medium, such as during exposure to rain, bacteria evade me...

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Autores principales: Çetiner, Uğur, Rowe, Ian, Schams, Anthony, Mayhew, Christina, Rubin, Deanna, Anishkin, Andriy, Sukharev, Sergei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5412531/
https://www.ncbi.nlm.nih.gov/pubmed/28424229
http://dx.doi.org/10.1085/jgp.201611699
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author Çetiner, Uğur
Rowe, Ian
Schams, Anthony
Mayhew, Christina
Rubin, Deanna
Anishkin, Andriy
Sukharev, Sergei
author_facet Çetiner, Uğur
Rowe, Ian
Schams, Anthony
Mayhew, Christina
Rubin, Deanna
Anishkin, Andriy
Sukharev, Sergei
author_sort Çetiner, Uğur
collection PubMed
description Pseudomonas aeruginosa (PA) is an opportunistic pathogen with an exceptional ability to adapt to a range of environments. Part of its adaptive potential is the ability to survive drastic osmolarity changes. Upon a sudden dilution of external medium, such as during exposure to rain, bacteria evade mechanical rupture by engaging tension-activated channels that act as osmolyte release valves. In this study, we compare fast osmotic permeability responses in suspensions of wild-type PA and Escherichia coli (EC) strains in stopped-flow experiments and provide electrophysiological descriptions of osmotic-release channels in PA. Using osmotic dilution experiments, we first show that PA tolerates a broader range of shocks than EC. We record the kinetics of cell equilibration reported by light scattering responses to osmotic up- and down-shocks. PA exhibits a lower water permeability and faster osmolyte release rates during large osmotic dilutions than EC, which correlates with better survival. To directly characterize the PA tension-activated channels, we generate giant spheroplasts from this microorganism and record current responses in excised patches. Unlike EC, which relies primarily on two types of channels, EcMscS and EcMscL, to generate a distinctive two-wave pressure ramp response, PA exhibits a more gradual response that is dominated by MscL-type channels. Genome analysis, cloning, and expression reveal that PA possesses one MscL-type (PaMscL) and two MscS-type (PaMscS-1 and 2) proteins. In EC spheroplasts, both PaMscS channels exhibit a slightly earlier activation by pressure compared with EcMscS. Unitary currents reveal that PaMscS-2 has a smaller conductance, higher anionic preference, stronger inactivation, and slower recovery compared with PaMscS-1. We conclude that PA relies on MscL as the major valve defining a high rate of osmolyte release sufficient to curb osmotic swelling under extreme shocks, but it still requires MscS-type channels with a strong propensity to inactivation to properly terminate massive permeability response.
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spelling pubmed-54125312017-11-01 Tension-activated channels in the mechanism of osmotic fitness in Pseudomonas aeruginosa Çetiner, Uğur Rowe, Ian Schams, Anthony Mayhew, Christina Rubin, Deanna Anishkin, Andriy Sukharev, Sergei J Gen Physiol Research Articles Pseudomonas aeruginosa (PA) is an opportunistic pathogen with an exceptional ability to adapt to a range of environments. Part of its adaptive potential is the ability to survive drastic osmolarity changes. Upon a sudden dilution of external medium, such as during exposure to rain, bacteria evade mechanical rupture by engaging tension-activated channels that act as osmolyte release valves. In this study, we compare fast osmotic permeability responses in suspensions of wild-type PA and Escherichia coli (EC) strains in stopped-flow experiments and provide electrophysiological descriptions of osmotic-release channels in PA. Using osmotic dilution experiments, we first show that PA tolerates a broader range of shocks than EC. We record the kinetics of cell equilibration reported by light scattering responses to osmotic up- and down-shocks. PA exhibits a lower water permeability and faster osmolyte release rates during large osmotic dilutions than EC, which correlates with better survival. To directly characterize the PA tension-activated channels, we generate giant spheroplasts from this microorganism and record current responses in excised patches. Unlike EC, which relies primarily on two types of channels, EcMscS and EcMscL, to generate a distinctive two-wave pressure ramp response, PA exhibits a more gradual response that is dominated by MscL-type channels. Genome analysis, cloning, and expression reveal that PA possesses one MscL-type (PaMscL) and two MscS-type (PaMscS-1 and 2) proteins. In EC spheroplasts, both PaMscS channels exhibit a slightly earlier activation by pressure compared with EcMscS. Unitary currents reveal that PaMscS-2 has a smaller conductance, higher anionic preference, stronger inactivation, and slower recovery compared with PaMscS-1. We conclude that PA relies on MscL as the major valve defining a high rate of osmolyte release sufficient to curb osmotic swelling under extreme shocks, but it still requires MscS-type channels with a strong propensity to inactivation to properly terminate massive permeability response. The Rockefeller University Press 2017-05-01 /pmc/articles/PMC5412531/ /pubmed/28424229 http://dx.doi.org/10.1085/jgp.201611699 Text en © 2017 Çetiner et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Research Articles
Çetiner, Uğur
Rowe, Ian
Schams, Anthony
Mayhew, Christina
Rubin, Deanna
Anishkin, Andriy
Sukharev, Sergei
Tension-activated channels in the mechanism of osmotic fitness in Pseudomonas aeruginosa
title Tension-activated channels in the mechanism of osmotic fitness in Pseudomonas aeruginosa
title_full Tension-activated channels in the mechanism of osmotic fitness in Pseudomonas aeruginosa
title_fullStr Tension-activated channels in the mechanism of osmotic fitness in Pseudomonas aeruginosa
title_full_unstemmed Tension-activated channels in the mechanism of osmotic fitness in Pseudomonas aeruginosa
title_short Tension-activated channels in the mechanism of osmotic fitness in Pseudomonas aeruginosa
title_sort tension-activated channels in the mechanism of osmotic fitness in pseudomonas aeruginosa
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5412531/
https://www.ncbi.nlm.nih.gov/pubmed/28424229
http://dx.doi.org/10.1085/jgp.201611699
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