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Serpentinization-Influenced Groundwater Harbors Extremely Low Diversity Microbial Communities Adapted to High pH

Serpentinization is a widespread geochemical process associated with aqueous alteration of ultramafic rocks that produces abundant reductants (H(2) and CH(4)) for life to exploit, but also potentially challenging conditions, including high pH, limited availability of terminal electron acceptors, and...

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Autores principales: Twing, Katrina I., Brazelton, William J., Kubo, Michael D. Y., Hyer, Alex J., Cardace, Dawn, Hoehler, Tori M., McCollom, Tom M., Schrenk, Matthew O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5331062/
https://www.ncbi.nlm.nih.gov/pubmed/28298908
http://dx.doi.org/10.3389/fmicb.2017.00308
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author Twing, Katrina I.
Brazelton, William J.
Kubo, Michael D. Y.
Hyer, Alex J.
Cardace, Dawn
Hoehler, Tori M.
McCollom, Tom M.
Schrenk, Matthew O.
author_facet Twing, Katrina I.
Brazelton, William J.
Kubo, Michael D. Y.
Hyer, Alex J.
Cardace, Dawn
Hoehler, Tori M.
McCollom, Tom M.
Schrenk, Matthew O.
author_sort Twing, Katrina I.
collection PubMed
description Serpentinization is a widespread geochemical process associated with aqueous alteration of ultramafic rocks that produces abundant reductants (H(2) and CH(4)) for life to exploit, but also potentially challenging conditions, including high pH, limited availability of terminal electron acceptors, and low concentrations of inorganic carbon. As a consequence, past studies of serpentinites have reported low cellular abundances and limited microbial diversity. Establishment of the Coast Range Ophiolite Microbial Observatory (California, U.S.A.) allowed a comparison of microbial communities and physicochemical parameters directly within serpentinization-influenced subsurface aquifers. Samples collected from seven wells were subjected to a range of analyses, including solute and gas chemistry, microbial diversity by 16S rRNA gene sequencing, and metabolic potential by shotgun metagenomics, in an attempt to elucidate what factors drive microbial activities in serpentinite habitats. This study describes the first comprehensive interdisciplinary analysis of microbial communities in hyperalkaline groundwater directly accessed by boreholes into serpentinite rocks. Several environmental factors, including pH, methane, and carbon monoxide, were strongly associated with the predominant subsurface microbial communities. A single operational taxonomic unit (OTU) of Betaproteobacteria and a few OTUs of Clostridia were the almost exclusive inhabitants of fluids exhibiting the most serpentinized character. Metagenomes from these extreme samples contained abundant sequences encoding proteins associated with hydrogen metabolism, carbon monoxide oxidation, carbon fixation, and acetogenesis. Metabolic pathways encoded by Clostridia and Betaproteobacteria, in particular, are likely to play important roles in the ecosystems of serpentinizing groundwater. These data provide a basis for further biogeochemical studies of key processes in serpentinite subsurface environments.
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spelling pubmed-53310622017-03-15 Serpentinization-Influenced Groundwater Harbors Extremely Low Diversity Microbial Communities Adapted to High pH Twing, Katrina I. Brazelton, William J. Kubo, Michael D. Y. Hyer, Alex J. Cardace, Dawn Hoehler, Tori M. McCollom, Tom M. Schrenk, Matthew O. Front Microbiol Microbiology Serpentinization is a widespread geochemical process associated with aqueous alteration of ultramafic rocks that produces abundant reductants (H(2) and CH(4)) for life to exploit, but also potentially challenging conditions, including high pH, limited availability of terminal electron acceptors, and low concentrations of inorganic carbon. As a consequence, past studies of serpentinites have reported low cellular abundances and limited microbial diversity. Establishment of the Coast Range Ophiolite Microbial Observatory (California, U.S.A.) allowed a comparison of microbial communities and physicochemical parameters directly within serpentinization-influenced subsurface aquifers. Samples collected from seven wells were subjected to a range of analyses, including solute and gas chemistry, microbial diversity by 16S rRNA gene sequencing, and metabolic potential by shotgun metagenomics, in an attempt to elucidate what factors drive microbial activities in serpentinite habitats. This study describes the first comprehensive interdisciplinary analysis of microbial communities in hyperalkaline groundwater directly accessed by boreholes into serpentinite rocks. Several environmental factors, including pH, methane, and carbon monoxide, were strongly associated with the predominant subsurface microbial communities. A single operational taxonomic unit (OTU) of Betaproteobacteria and a few OTUs of Clostridia were the almost exclusive inhabitants of fluids exhibiting the most serpentinized character. Metagenomes from these extreme samples contained abundant sequences encoding proteins associated with hydrogen metabolism, carbon monoxide oxidation, carbon fixation, and acetogenesis. Metabolic pathways encoded by Clostridia and Betaproteobacteria, in particular, are likely to play important roles in the ecosystems of serpentinizing groundwater. These data provide a basis for further biogeochemical studies of key processes in serpentinite subsurface environments. Frontiers Media S.A. 2017-03-01 /pmc/articles/PMC5331062/ /pubmed/28298908 http://dx.doi.org/10.3389/fmicb.2017.00308 Text en Copyright © 2017 Twing, Brazelton, Kubo, Hyer, Cardace, Hoehler, McCollom and Schrenk. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Twing, Katrina I.
Brazelton, William J.
Kubo, Michael D. Y.
Hyer, Alex J.
Cardace, Dawn
Hoehler, Tori M.
McCollom, Tom M.
Schrenk, Matthew O.
Serpentinization-Influenced Groundwater Harbors Extremely Low Diversity Microbial Communities Adapted to High pH
title Serpentinization-Influenced Groundwater Harbors Extremely Low Diversity Microbial Communities Adapted to High pH
title_full Serpentinization-Influenced Groundwater Harbors Extremely Low Diversity Microbial Communities Adapted to High pH
title_fullStr Serpentinization-Influenced Groundwater Harbors Extremely Low Diversity Microbial Communities Adapted to High pH
title_full_unstemmed Serpentinization-Influenced Groundwater Harbors Extremely Low Diversity Microbial Communities Adapted to High pH
title_short Serpentinization-Influenced Groundwater Harbors Extremely Low Diversity Microbial Communities Adapted to High pH
title_sort serpentinization-influenced groundwater harbors extremely low diversity microbial communities adapted to high ph
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5331062/
https://www.ncbi.nlm.nih.gov/pubmed/28298908
http://dx.doi.org/10.3389/fmicb.2017.00308
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