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The mechanoelectrical response of the cytoplasmic membrane of Vibrio cholerae
Persistence of Vibrio cholerae in waters of fluctuating salinity relies on the capacity of this facultative enteric pathogen to adapt to varying osmotic conditions. In an event of osmotic downshift, osmolytes accumulated inside the bacterium can be quickly released through tension-activated channels...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3691451/ https://www.ncbi.nlm.nih.gov/pubmed/23797422 http://dx.doi.org/10.1085/jgp.201310985 |
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author | Rowe, Ian Elahi, Merina Huq, Anwar Sukharev, Sergei |
author_facet | Rowe, Ian Elahi, Merina Huq, Anwar Sukharev, Sergei |
author_sort | Rowe, Ian |
collection | PubMed |
description | Persistence of Vibrio cholerae in waters of fluctuating salinity relies on the capacity of this facultative enteric pathogen to adapt to varying osmotic conditions. In an event of osmotic downshift, osmolytes accumulated inside the bacterium can be quickly released through tension-activated channels. With the newly established procedure of giant spheroplast preparation from V. cholerae, we performed the first patch-clamp characterization of its cytoplasmic membrane and compared tension-activated currents with those in Esherichia coli. Saturating pressure ramps revealed two waves of activation belonging to the ∼1-nS mechanosensitive channel of small conductance (MscS)-like channels and ∼3-nS mechanosensitive channel of large conductance (MscL)-like channels, with a pressure midpoint ratio p(0.5)MscS/p(0.5)MscL of 0.48. We found that MscL-like channels in V. cholerae present at a density three times higher than in E. coli, and yet, these vibrios were less tolerant to large osmotic downshocks. The Vibrio MscS-like channels exhibit characteristic inward rectification and subconductive states at depolarizing voltages; they also adapt and inactivate at subsaturating tensions and recover within 2 s upon tension release, just like E. coli MscS. Trehalose, a compatible internal osmolyte accumulated under hypertonic conditions, significantly shifts activation curves of both MscL- and MscS-like channels toward higher tensions, yet does not freely partition into the channel pore. Direct electrophysiology of V. cholerae offers new avenues for the in situ analysis of membrane components critical for osmotic survival and electrogenic transport in this pathogen. |
format | Online Article Text |
id | pubmed-3691451 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-36914512014-01-01 The mechanoelectrical response of the cytoplasmic membrane of Vibrio cholerae Rowe, Ian Elahi, Merina Huq, Anwar Sukharev, Sergei J Gen Physiol Communication Persistence of Vibrio cholerae in waters of fluctuating salinity relies on the capacity of this facultative enteric pathogen to adapt to varying osmotic conditions. In an event of osmotic downshift, osmolytes accumulated inside the bacterium can be quickly released through tension-activated channels. With the newly established procedure of giant spheroplast preparation from V. cholerae, we performed the first patch-clamp characterization of its cytoplasmic membrane and compared tension-activated currents with those in Esherichia coli. Saturating pressure ramps revealed two waves of activation belonging to the ∼1-nS mechanosensitive channel of small conductance (MscS)-like channels and ∼3-nS mechanosensitive channel of large conductance (MscL)-like channels, with a pressure midpoint ratio p(0.5)MscS/p(0.5)MscL of 0.48. We found that MscL-like channels in V. cholerae present at a density three times higher than in E. coli, and yet, these vibrios were less tolerant to large osmotic downshocks. The Vibrio MscS-like channels exhibit characteristic inward rectification and subconductive states at depolarizing voltages; they also adapt and inactivate at subsaturating tensions and recover within 2 s upon tension release, just like E. coli MscS. Trehalose, a compatible internal osmolyte accumulated under hypertonic conditions, significantly shifts activation curves of both MscL- and MscS-like channels toward higher tensions, yet does not freely partition into the channel pore. Direct electrophysiology of V. cholerae offers new avenues for the in situ analysis of membrane components critical for osmotic survival and electrogenic transport in this pathogen. The Rockefeller University Press 2013-07 /pmc/articles/PMC3691451/ /pubmed/23797422 http://dx.doi.org/10.1085/jgp.201310985 Text en © 2013 Rowe et al. 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 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Communication Rowe, Ian Elahi, Merina Huq, Anwar Sukharev, Sergei The mechanoelectrical response of the cytoplasmic membrane of Vibrio cholerae |
title | The mechanoelectrical response of the cytoplasmic membrane of Vibrio cholerae |
title_full | The mechanoelectrical response of the cytoplasmic membrane of Vibrio cholerae |
title_fullStr | The mechanoelectrical response of the cytoplasmic membrane of Vibrio cholerae |
title_full_unstemmed | The mechanoelectrical response of the cytoplasmic membrane of Vibrio cholerae |
title_short | The mechanoelectrical response of the cytoplasmic membrane of Vibrio cholerae |
title_sort | mechanoelectrical response of the cytoplasmic membrane of vibrio cholerae |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3691451/ https://www.ncbi.nlm.nih.gov/pubmed/23797422 http://dx.doi.org/10.1085/jgp.201310985 |
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