Cargando…

Molecular chaperone accumulation as a function of stress evidences adaptation to high hydrostatic pressure in the piezophilic archaeon Thermococcus barophilus

The accumulation of mannosyl-glycerate (MG), the salinity stress response osmolyte of Thermococcales, was investigated as a function of hydrostatic pressure in Thermococcus barophilus strain MP, a hyperthermophilic, piezophilic archaeon isolated from the Snake Pit site (MAR), which grows optimally a...

Descripción completa

Detalles Bibliográficos
Autores principales: Cario, Anaïs, Jebbar, Mohamed, Thiel, Axel, Kervarec, Nelly, Oger, Phil M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4932500/
https://www.ncbi.nlm.nih.gov/pubmed/27378270
http://dx.doi.org/10.1038/srep29483
_version_ 1782441066828398592
author Cario, Anaïs
Jebbar, Mohamed
Thiel, Axel
Kervarec, Nelly
Oger, Phil M.
author_facet Cario, Anaïs
Jebbar, Mohamed
Thiel, Axel
Kervarec, Nelly
Oger, Phil M.
author_sort Cario, Anaïs
collection PubMed
description The accumulation of mannosyl-glycerate (MG), the salinity stress response osmolyte of Thermococcales, was investigated as a function of hydrostatic pressure in Thermococcus barophilus strain MP, a hyperthermophilic, piezophilic archaeon isolated from the Snake Pit site (MAR), which grows optimally at 40 MPa. Strain MP accumulated MG primarily in response to salinity stress, but in contrast to other Thermococcales, MG was also accumulated in response to thermal stress. MG accumulation peaked for combined stresses. The accumulation of MG was drastically increased under sub-optimal hydrostatic pressure conditions, demonstrating that low pressure is perceived as a stress in this piezophile, and that the proteome of T. barophilus is low-pressure sensitive. MG accumulation was strongly reduced under supra-optimal pressure conditions clearly demonstrating the structural adaptation of this proteome to high hydrostatic pressure. The lack of MG synthesis only slightly altered the growth characteristics of two different MG synthesis deletion mutants. No shift to other osmolytes was observed. Altogether our observations suggest that the salinity stress response in T. barophilus is not essential and may be under negative selective pressure, similarly to what has been observed for its thermal stress response.
format Online
Article
Text
id pubmed-4932500
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-49325002016-07-06 Molecular chaperone accumulation as a function of stress evidences adaptation to high hydrostatic pressure in the piezophilic archaeon Thermococcus barophilus Cario, Anaïs Jebbar, Mohamed Thiel, Axel Kervarec, Nelly Oger, Phil M. Sci Rep Article The accumulation of mannosyl-glycerate (MG), the salinity stress response osmolyte of Thermococcales, was investigated as a function of hydrostatic pressure in Thermococcus barophilus strain MP, a hyperthermophilic, piezophilic archaeon isolated from the Snake Pit site (MAR), which grows optimally at 40 MPa. Strain MP accumulated MG primarily in response to salinity stress, but in contrast to other Thermococcales, MG was also accumulated in response to thermal stress. MG accumulation peaked for combined stresses. The accumulation of MG was drastically increased under sub-optimal hydrostatic pressure conditions, demonstrating that low pressure is perceived as a stress in this piezophile, and that the proteome of T. barophilus is low-pressure sensitive. MG accumulation was strongly reduced under supra-optimal pressure conditions clearly demonstrating the structural adaptation of this proteome to high hydrostatic pressure. The lack of MG synthesis only slightly altered the growth characteristics of two different MG synthesis deletion mutants. No shift to other osmolytes was observed. Altogether our observations suggest that the salinity stress response in T. barophilus is not essential and may be under negative selective pressure, similarly to what has been observed for its thermal stress response. Nature Publishing Group 2016-07-05 /pmc/articles/PMC4932500/ /pubmed/27378270 http://dx.doi.org/10.1038/srep29483 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Cario, Anaïs
Jebbar, Mohamed
Thiel, Axel
Kervarec, Nelly
Oger, Phil M.
Molecular chaperone accumulation as a function of stress evidences adaptation to high hydrostatic pressure in the piezophilic archaeon Thermococcus barophilus
title Molecular chaperone accumulation as a function of stress evidences adaptation to high hydrostatic pressure in the piezophilic archaeon Thermococcus barophilus
title_full Molecular chaperone accumulation as a function of stress evidences adaptation to high hydrostatic pressure in the piezophilic archaeon Thermococcus barophilus
title_fullStr Molecular chaperone accumulation as a function of stress evidences adaptation to high hydrostatic pressure in the piezophilic archaeon Thermococcus barophilus
title_full_unstemmed Molecular chaperone accumulation as a function of stress evidences adaptation to high hydrostatic pressure in the piezophilic archaeon Thermococcus barophilus
title_short Molecular chaperone accumulation as a function of stress evidences adaptation to high hydrostatic pressure in the piezophilic archaeon Thermococcus barophilus
title_sort molecular chaperone accumulation as a function of stress evidences adaptation to high hydrostatic pressure in the piezophilic archaeon thermococcus barophilus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4932500/
https://www.ncbi.nlm.nih.gov/pubmed/27378270
http://dx.doi.org/10.1038/srep29483
work_keys_str_mv AT carioanais molecularchaperoneaccumulationasafunctionofstressevidencesadaptationtohighhydrostaticpressureinthepiezophilicarchaeonthermococcusbarophilus
AT jebbarmohamed molecularchaperoneaccumulationasafunctionofstressevidencesadaptationtohighhydrostaticpressureinthepiezophilicarchaeonthermococcusbarophilus
AT thielaxel molecularchaperoneaccumulationasafunctionofstressevidencesadaptationtohighhydrostaticpressureinthepiezophilicarchaeonthermococcusbarophilus
AT kervarecnelly molecularchaperoneaccumulationasafunctionofstressevidencesadaptationtohighhydrostaticpressureinthepiezophilicarchaeonthermococcusbarophilus
AT ogerphilm molecularchaperoneaccumulationasafunctionofstressevidencesadaptationtohighhydrostaticpressureinthepiezophilicarchaeonthermococcusbarophilus