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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2018
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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. |
format | Online Article Text |
id | pubmed-6792436 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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