Cargando…
Metabolic Strategies Shared by Basement Residents of the Lost City Hydrothermal Field
Alkaline fluids venting from chimneys of the Lost City hydrothermal field flow from a potentially vast microbial habitat within the seafloor where energy and organic molecules are released by chemical reactions within rocks uplifted from Earth’s mantle. In this study, we investigated hydrothermal fl...
Autores principales: | , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9469722/ https://www.ncbi.nlm.nih.gov/pubmed/35950875 http://dx.doi.org/10.1128/aem.00929-22 |
_version_ | 1784788700290351104 |
---|---|
author | Brazelton, William J. McGonigle, Julia M. Motamedi, Shahrzad Pendleton, H. Lizethe Twing, Katrina I. Miller, Briggs C. Lowe, William J. Hoffman, Alessandrina M. Prator, Cecilia A. Chadwick, Grayson L. Anderson, Rika E. Thomas, Elaina Butterfield, David A. Aquino, Karmina A. Früh-Green, Gretchen L. Schrenk, Matthew O. Lang, Susan Q. |
author_facet | Brazelton, William J. McGonigle, Julia M. Motamedi, Shahrzad Pendleton, H. Lizethe Twing, Katrina I. Miller, Briggs C. Lowe, William J. Hoffman, Alessandrina M. Prator, Cecilia A. Chadwick, Grayson L. Anderson, Rika E. Thomas, Elaina Butterfield, David A. Aquino, Karmina A. Früh-Green, Gretchen L. Schrenk, Matthew O. Lang, Susan Q. |
author_sort | Brazelton, William J. |
collection | PubMed |
description | Alkaline fluids venting from chimneys of the Lost City hydrothermal field flow from a potentially vast microbial habitat within the seafloor where energy and organic molecules are released by chemical reactions within rocks uplifted from Earth’s mantle. In this study, we investigated hydrothermal fluids venting from Lost City chimneys as windows into subseafloor environments where the products of geochemical reactions, such as molecular hydrogen (H(2)), formate, and methane, may be the only available sources of energy for biological activity. Our deep sequencing of metagenomes and metatranscriptomes from these hydrothermal fluids revealed a few key species of archaea and bacteria that are likely to play critical roles in the subseafloor microbial ecosystem. We identified a population of Thermodesulfovibrionales (belonging to phylum Nitrospirota) as a prevalent sulfate-reducing bacterium that may be responsible for much of the consumption of H(2) and sulfate in Lost City fluids. Metagenome-assembled genomes (MAGs) classified as Methanosarcinaceae and Candidatus Bipolaricaulota were also recovered from venting fluids and represent potential methanogenic and acetogenic members of the subseafloor ecosystem. These genomes share novel hydrogenases and formate dehydrogenase-like sequences that may be unique to hydrothermal environments where H(2) and formate are much more abundant than carbon dioxide. The results of this study include multiple examples of metabolic strategies that appear to be advantageous in hydrothermal and subsurface alkaline environments where energy and carbon are provided by geochemical reactions. IMPORTANCE The Lost City hydrothermal field is an iconic example of a microbial ecosystem fueled by energy and carbon from Earth’s mantle. Uplift of mantle rocks into the seafloor can trigger a process known as serpentinization that releases molecular hydrogen (H(2)) and creates unusual environmental conditions where simple organic carbon molecules are more stable than dissolved inorganic carbon. This study provides an initial glimpse into the kinds of microbes that live deep within the seafloor where serpentinization takes place, by sampling hydrothermal fluids exiting from the Lost City chimneys. The metabolic strategies that these microbes appear to be using are also shared by microbes that inhabit other sites of serpentinization, including continental subsurface environments and natural springs. Therefore, the results of this study contribute to a broader, interdisciplinary effort to understand the general principles and mechanisms by which serpentinization-associated processes can support life on Earth and perhaps other worlds. |
format | Online Article Text |
id | pubmed-9469722 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-94697222022-09-14 Metabolic Strategies Shared by Basement Residents of the Lost City Hydrothermal Field Brazelton, William J. McGonigle, Julia M. Motamedi, Shahrzad Pendleton, H. Lizethe Twing, Katrina I. Miller, Briggs C. Lowe, William J. Hoffman, Alessandrina M. Prator, Cecilia A. Chadwick, Grayson L. Anderson, Rika E. Thomas, Elaina Butterfield, David A. Aquino, Karmina A. Früh-Green, Gretchen L. Schrenk, Matthew O. Lang, Susan Q. Appl Environ Microbiol Geomicrobiology Alkaline fluids venting from chimneys of the Lost City hydrothermal field flow from a potentially vast microbial habitat within the seafloor where energy and organic molecules are released by chemical reactions within rocks uplifted from Earth’s mantle. In this study, we investigated hydrothermal fluids venting from Lost City chimneys as windows into subseafloor environments where the products of geochemical reactions, such as molecular hydrogen (H(2)), formate, and methane, may be the only available sources of energy for biological activity. Our deep sequencing of metagenomes and metatranscriptomes from these hydrothermal fluids revealed a few key species of archaea and bacteria that are likely to play critical roles in the subseafloor microbial ecosystem. We identified a population of Thermodesulfovibrionales (belonging to phylum Nitrospirota) as a prevalent sulfate-reducing bacterium that may be responsible for much of the consumption of H(2) and sulfate in Lost City fluids. Metagenome-assembled genomes (MAGs) classified as Methanosarcinaceae and Candidatus Bipolaricaulota were also recovered from venting fluids and represent potential methanogenic and acetogenic members of the subseafloor ecosystem. These genomes share novel hydrogenases and formate dehydrogenase-like sequences that may be unique to hydrothermal environments where H(2) and formate are much more abundant than carbon dioxide. The results of this study include multiple examples of metabolic strategies that appear to be advantageous in hydrothermal and subsurface alkaline environments where energy and carbon are provided by geochemical reactions. IMPORTANCE The Lost City hydrothermal field is an iconic example of a microbial ecosystem fueled by energy and carbon from Earth’s mantle. Uplift of mantle rocks into the seafloor can trigger a process known as serpentinization that releases molecular hydrogen (H(2)) and creates unusual environmental conditions where simple organic carbon molecules are more stable than dissolved inorganic carbon. This study provides an initial glimpse into the kinds of microbes that live deep within the seafloor where serpentinization takes place, by sampling hydrothermal fluids exiting from the Lost City chimneys. The metabolic strategies that these microbes appear to be using are also shared by microbes that inhabit other sites of serpentinization, including continental subsurface environments and natural springs. Therefore, the results of this study contribute to a broader, interdisciplinary effort to understand the general principles and mechanisms by which serpentinization-associated processes can support life on Earth and perhaps other worlds. American Society for Microbiology 2022-08-11 /pmc/articles/PMC9469722/ /pubmed/35950875 http://dx.doi.org/10.1128/aem.00929-22 Text en Copyright © 2022 Brazelton et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Geomicrobiology Brazelton, William J. McGonigle, Julia M. Motamedi, Shahrzad Pendleton, H. Lizethe Twing, Katrina I. Miller, Briggs C. Lowe, William J. Hoffman, Alessandrina M. Prator, Cecilia A. Chadwick, Grayson L. Anderson, Rika E. Thomas, Elaina Butterfield, David A. Aquino, Karmina A. Früh-Green, Gretchen L. Schrenk, Matthew O. Lang, Susan Q. Metabolic Strategies Shared by Basement Residents of the Lost City Hydrothermal Field |
title | Metabolic Strategies Shared by Basement Residents of the Lost City Hydrothermal Field |
title_full | Metabolic Strategies Shared by Basement Residents of the Lost City Hydrothermal Field |
title_fullStr | Metabolic Strategies Shared by Basement Residents of the Lost City Hydrothermal Field |
title_full_unstemmed | Metabolic Strategies Shared by Basement Residents of the Lost City Hydrothermal Field |
title_short | Metabolic Strategies Shared by Basement Residents of the Lost City Hydrothermal Field |
title_sort | metabolic strategies shared by basement residents of the lost city hydrothermal field |
topic | Geomicrobiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9469722/ https://www.ncbi.nlm.nih.gov/pubmed/35950875 http://dx.doi.org/10.1128/aem.00929-22 |
work_keys_str_mv | AT brazeltonwilliamj metabolicstrategiessharedbybasementresidentsofthelostcityhydrothermalfield AT mcgoniglejuliam metabolicstrategiessharedbybasementresidentsofthelostcityhydrothermalfield AT motamedishahrzad metabolicstrategiessharedbybasementresidentsofthelostcityhydrothermalfield AT pendletonhlizethe metabolicstrategiessharedbybasementresidentsofthelostcityhydrothermalfield AT twingkatrinai metabolicstrategiessharedbybasementresidentsofthelostcityhydrothermalfield AT millerbriggsc metabolicstrategiessharedbybasementresidentsofthelostcityhydrothermalfield AT lowewilliamj metabolicstrategiessharedbybasementresidentsofthelostcityhydrothermalfield AT hoffmanalessandrinam metabolicstrategiessharedbybasementresidentsofthelostcityhydrothermalfield AT pratorceciliaa metabolicstrategiessharedbybasementresidentsofthelostcityhydrothermalfield AT chadwickgraysonl metabolicstrategiessharedbybasementresidentsofthelostcityhydrothermalfield AT andersonrikae metabolicstrategiessharedbybasementresidentsofthelostcityhydrothermalfield AT thomaselaina metabolicstrategiessharedbybasementresidentsofthelostcityhydrothermalfield AT butterfielddavida metabolicstrategiessharedbybasementresidentsofthelostcityhydrothermalfield AT aquinokarminaa metabolicstrategiessharedbybasementresidentsofthelostcityhydrothermalfield AT fruhgreengretchenl metabolicstrategiessharedbybasementresidentsofthelostcityhydrothermalfield AT schrenkmatthewo metabolicstrategiessharedbybasementresidentsofthelostcityhydrothermalfield AT langsusanq metabolicstrategiessharedbybasementresidentsofthelostcityhydrothermalfield |