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Differential depth distribution of microbial function and putative symbionts through sediment-hosted aquifers in the deep terrestrial subsurface

An enormous diversity of previously unknown bacteria and archaea has been discovered recently, yet their functional capacities and distributions in the terrestrial subsurface remain uncertain. Here, we continually sampled a CO(2)-driven geyser (Colorado Plateau, Utah, USA) over its 5-day eruption cy...

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Autores principales: Probst, Alexander J., Ladd, Bethany, Jarett, Jessica K., Geller-McGrath, David E., Sieber, Christian M. K., Emerson, Joanne B., Anantharaman, Karthik, Thomas, Brian C., Malmstrom, Rex R., Stieglmeier, Michaela, Klingl, Andreas, Woyke, Tanja, Ryan, M. Cathryn, Banfield, Jillian F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6792436/
https://www.ncbi.nlm.nih.gov/pubmed/29379208
http://dx.doi.org/10.1038/s41564-017-0098-y
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author Probst, Alexander J.
Ladd, Bethany
Jarett, Jessica K.
Geller-McGrath, David E.
Sieber, Christian M. K.
Emerson, Joanne B.
Anantharaman, Karthik
Thomas, Brian C.
Malmstrom, Rex R.
Stieglmeier, Michaela
Klingl, Andreas
Woyke, Tanja
Ryan, M. Cathryn
Banfield, Jillian F.
author_facet Probst, Alexander J.
Ladd, Bethany
Jarett, Jessica K.
Geller-McGrath, David E.
Sieber, Christian M. K.
Emerson, Joanne B.
Anantharaman, Karthik
Thomas, Brian C.
Malmstrom, Rex R.
Stieglmeier, Michaela
Klingl, Andreas
Woyke, Tanja
Ryan, M. Cathryn
Banfield, Jillian F.
author_sort Probst, Alexander J.
collection PubMed
description An enormous diversity of previously unknown bacteria and archaea has been discovered recently, yet their functional capacities and distributions in the terrestrial subsurface remain uncertain. Here, we continually sampled a CO(2)-driven geyser (Colorado Plateau, Utah, USA) over its 5-day eruption cycle to test the hypothesis that stratified, sandstone-hosted aquifers sampled over three phases of the eruption cycle have microbial communities that differ both in membership and function. Genome-resolved metagenomics, single-cell genomics and geochemical analyses confirmed this hypothesis and linked microorganisms to groundwater compositions from different depths. Autotrophic Candidatus “Altiarchaeum sp.” and phylogenetically deep-branching nanoarchaea dominate the deepest groundwater. A nanoarchaeon with limited metabolic capacity is inferred to be a potential symbiont of the Ca. “Altiarchaeum”. Candidate Phyla Radiation bacteria are also present in the deepest groundwater and they are relatively abundant in water from intermediate depths. During the recovery phase of the geyser, microaerophilic Fe- and S-oxidizers have high in situ genome replication rates. Autotrophic Sulfurimonas sustained by aerobic sulfide oxidation and with the capacity for N(2) fixation dominate the shallow aquifer. Overall, 104 different phylum-level lineages are present in water from these subsurface environments, with uncultivated archaea and bacteria partitioned to the deeper subsurface.
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spelling pubmed-67924362019-10-17 Differential depth distribution of microbial function and putative symbionts through sediment-hosted aquifers in the deep terrestrial subsurface Probst, Alexander J. Ladd, Bethany Jarett, Jessica K. Geller-McGrath, David E. Sieber, Christian M. K. Emerson, Joanne B. Anantharaman, Karthik Thomas, Brian C. Malmstrom, Rex R. Stieglmeier, Michaela Klingl, Andreas Woyke, Tanja Ryan, M. Cathryn Banfield, Jillian F. Nat Microbiol Article An enormous diversity of previously unknown bacteria and archaea has been discovered recently, yet their functional capacities and distributions in the terrestrial subsurface remain uncertain. Here, we continually sampled a CO(2)-driven geyser (Colorado Plateau, Utah, USA) over its 5-day eruption cycle to test the hypothesis that stratified, sandstone-hosted aquifers sampled over three phases of the eruption cycle have microbial communities that differ both in membership and function. Genome-resolved metagenomics, single-cell genomics and geochemical analyses confirmed this hypothesis and linked microorganisms to groundwater compositions from different depths. Autotrophic Candidatus “Altiarchaeum sp.” and phylogenetically deep-branching nanoarchaea dominate the deepest groundwater. A nanoarchaeon with limited metabolic capacity is inferred to be a potential symbiont of the Ca. “Altiarchaeum”. Candidate Phyla Radiation bacteria are also present in the deepest groundwater and they are relatively abundant in water from intermediate depths. During the recovery phase of the geyser, microaerophilic Fe- and S-oxidizers have high in situ genome replication rates. Autotrophic Sulfurimonas sustained by aerobic sulfide oxidation and with the capacity for N(2) fixation dominate the shallow aquifer. Overall, 104 different phylum-level lineages are present in water from these subsurface environments, with uncultivated archaea and bacteria partitioned to the deeper subsurface. Nature Publishing Group UK 2018-01-29 2018 /pmc/articles/PMC6792436/ /pubmed/29379208 http://dx.doi.org/10.1038/s41564-017-0098-y Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Probst, Alexander J.
Ladd, Bethany
Jarett, Jessica K.
Geller-McGrath, David E.
Sieber, Christian M. K.
Emerson, Joanne B.
Anantharaman, Karthik
Thomas, Brian C.
Malmstrom, Rex R.
Stieglmeier, Michaela
Klingl, Andreas
Woyke, Tanja
Ryan, M. Cathryn
Banfield, Jillian F.
Differential depth distribution of microbial function and putative symbionts through sediment-hosted aquifers in the deep terrestrial subsurface
title Differential depth distribution of microbial function and putative symbionts through sediment-hosted aquifers in the deep terrestrial subsurface
title_full Differential depth distribution of microbial function and putative symbionts through sediment-hosted aquifers in the deep terrestrial subsurface
title_fullStr Differential depth distribution of microbial function and putative symbionts through sediment-hosted aquifers in the deep terrestrial subsurface
title_full_unstemmed Differential depth distribution of microbial function and putative symbionts through sediment-hosted aquifers in the deep terrestrial subsurface
title_short Differential depth distribution of microbial function and putative symbionts through sediment-hosted aquifers in the deep terrestrial subsurface
title_sort differential depth distribution of microbial function and putative symbionts through sediment-hosted aquifers in the deep terrestrial subsurface
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6792436/
https://www.ncbi.nlm.nih.gov/pubmed/29379208
http://dx.doi.org/10.1038/s41564-017-0098-y
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