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Geomicrobiology of sublacustrine thermal vents in Yellowstone Lake: geochemical controls on microbial community structure and function

Yellowstone Lake (Yellowstone National Park, WY, USA) is a large high-altitude (2200 m), fresh-water lake, which straddles an extensive caldera and is the center of significant geothermal activity. The primary goal of this interdisciplinary study was to evaluate the microbial populations inhabiting...

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Autores principales: Inskeep, William P., Jay, Zackary J., Macur, Richard E., Clingenpeel, Scott, Tenney, Aaron, Lovalvo, David, Beam, Jacob P., Kozubal, Mark A., Shanks, W. C., Morgan, Lisa A., Kan, Jinjun, Gorby, Yuri, Yooseph, Shibu, Nealson, Kenneth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4620420/
https://www.ncbi.nlm.nih.gov/pubmed/26579074
http://dx.doi.org/10.3389/fmicb.2015.01044
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author Inskeep, William P.
Jay, Zackary J.
Macur, Richard E.
Clingenpeel, Scott
Tenney, Aaron
Lovalvo, David
Beam, Jacob P.
Kozubal, Mark A.
Shanks, W. C.
Morgan, Lisa A.
Kan, Jinjun
Gorby, Yuri
Yooseph, Shibu
Nealson, Kenneth
author_facet Inskeep, William P.
Jay, Zackary J.
Macur, Richard E.
Clingenpeel, Scott
Tenney, Aaron
Lovalvo, David
Beam, Jacob P.
Kozubal, Mark A.
Shanks, W. C.
Morgan, Lisa A.
Kan, Jinjun
Gorby, Yuri
Yooseph, Shibu
Nealson, Kenneth
author_sort Inskeep, William P.
collection PubMed
description Yellowstone Lake (Yellowstone National Park, WY, USA) is a large high-altitude (2200 m), fresh-water lake, which straddles an extensive caldera and is the center of significant geothermal activity. The primary goal of this interdisciplinary study was to evaluate the microbial populations inhabiting thermal vent communities in Yellowstone Lake using 16S rRNA gene and random metagenome sequencing, and to determine how geochemical attributes of vent waters influence the distribution of specific microorganisms and their metabolic potential. Thermal vent waters and associated microbial biomass were sampled during two field seasons (2007–2008) using a remotely operated vehicle (ROV). Sublacustrine thermal vent waters (circa 50–90°C) contained elevated concentrations of numerous constituents associated with geothermal activity including dissolved hydrogen, sulfide, methane and carbon dioxide. Microorganisms associated with sulfur-rich filamentous “streamer” communities of Inflated Plain and West Thumb (pH range 5–6) were dominated by bacteria from the Aquificales, but also contained thermophilic archaea from the Crenarchaeota and Euryarchaeota. Novel groups of methanogens and members of the Korarchaeota were observed in vents from West Thumb and Elliot's Crater (pH 5–6). Conversely, metagenome sequence from Mary Bay vent sediments did not yield large assemblies, and contained diverse thermophilic and nonthermophilic bacterial relatives. Analysis of functional genes associated with the major vent populations indicated a direct linkage to high concentrations of carbon dioxide, reduced sulfur (sulfide and/or elemental S), hydrogen and methane in the deep thermal ecosystems. Our observations show that sublacustrine thermal vents in Yellowstone Lake support novel thermophilic communities, which contain microorganisms with functional attributes not found to date in terrestrial geothermal systems of YNP.
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spelling pubmed-46204202015-11-17 Geomicrobiology of sublacustrine thermal vents in Yellowstone Lake: geochemical controls on microbial community structure and function Inskeep, William P. Jay, Zackary J. Macur, Richard E. Clingenpeel, Scott Tenney, Aaron Lovalvo, David Beam, Jacob P. Kozubal, Mark A. Shanks, W. C. Morgan, Lisa A. Kan, Jinjun Gorby, Yuri Yooseph, Shibu Nealson, Kenneth Front Microbiol Microbiology Yellowstone Lake (Yellowstone National Park, WY, USA) is a large high-altitude (2200 m), fresh-water lake, which straddles an extensive caldera and is the center of significant geothermal activity. The primary goal of this interdisciplinary study was to evaluate the microbial populations inhabiting thermal vent communities in Yellowstone Lake using 16S rRNA gene and random metagenome sequencing, and to determine how geochemical attributes of vent waters influence the distribution of specific microorganisms and their metabolic potential. Thermal vent waters and associated microbial biomass were sampled during two field seasons (2007–2008) using a remotely operated vehicle (ROV). Sublacustrine thermal vent waters (circa 50–90°C) contained elevated concentrations of numerous constituents associated with geothermal activity including dissolved hydrogen, sulfide, methane and carbon dioxide. Microorganisms associated with sulfur-rich filamentous “streamer” communities of Inflated Plain and West Thumb (pH range 5–6) were dominated by bacteria from the Aquificales, but also contained thermophilic archaea from the Crenarchaeota and Euryarchaeota. Novel groups of methanogens and members of the Korarchaeota were observed in vents from West Thumb and Elliot's Crater (pH 5–6). Conversely, metagenome sequence from Mary Bay vent sediments did not yield large assemblies, and contained diverse thermophilic and nonthermophilic bacterial relatives. Analysis of functional genes associated with the major vent populations indicated a direct linkage to high concentrations of carbon dioxide, reduced sulfur (sulfide and/or elemental S), hydrogen and methane in the deep thermal ecosystems. Our observations show that sublacustrine thermal vents in Yellowstone Lake support novel thermophilic communities, which contain microorganisms with functional attributes not found to date in terrestrial geothermal systems of YNP. Frontiers Media S.A. 2015-10-26 /pmc/articles/PMC4620420/ /pubmed/26579074 http://dx.doi.org/10.3389/fmicb.2015.01044 Text en Copyright © 2015 Inskeep, Jay, Macur, Clingenpeel, Tenney, Lovalvo, Beam, Kozubal, Shanks, Morgan, Kan, Gorby, Yooseph and Nealson. 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
Inskeep, William P.
Jay, Zackary J.
Macur, Richard E.
Clingenpeel, Scott
Tenney, Aaron
Lovalvo, David
Beam, Jacob P.
Kozubal, Mark A.
Shanks, W. C.
Morgan, Lisa A.
Kan, Jinjun
Gorby, Yuri
Yooseph, Shibu
Nealson, Kenneth
Geomicrobiology of sublacustrine thermal vents in Yellowstone Lake: geochemical controls on microbial community structure and function
title Geomicrobiology of sublacustrine thermal vents in Yellowstone Lake: geochemical controls on microbial community structure and function
title_full Geomicrobiology of sublacustrine thermal vents in Yellowstone Lake: geochemical controls on microbial community structure and function
title_fullStr Geomicrobiology of sublacustrine thermal vents in Yellowstone Lake: geochemical controls on microbial community structure and function
title_full_unstemmed Geomicrobiology of sublacustrine thermal vents in Yellowstone Lake: geochemical controls on microbial community structure and function
title_short Geomicrobiology of sublacustrine thermal vents in Yellowstone Lake: geochemical controls on microbial community structure and function
title_sort geomicrobiology of sublacustrine thermal vents in yellowstone lake: geochemical controls on microbial community structure and function
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4620420/
https://www.ncbi.nlm.nih.gov/pubmed/26579074
http://dx.doi.org/10.3389/fmicb.2015.01044
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