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Metagenomes from High-Temperature Chemotrophic Systems Reveal Geochemical Controls on Microbial Community Structure and Function

The Yellowstone caldera contains the most numerous and diverse geothermal systems on Earth, yielding an extensive array of unique high-temperature environments that host a variety of deeply-rooted and understudied Archaea, Bacteria and Eukarya. The combination of extreme temperature and chemical con...

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Autores principales: Inskeep, William P., Rusch, Douglas B., Jay, Zackary J., Herrgard, Markus J., Kozubal, Mark A., Richardson, Toby H., Macur, Richard E., Hamamura, Natsuko, Jennings, Ryan deM., Fouke, Bruce W., Reysenbach, Anna-Louise, Roberto, Frank, Young, Mark, Schwartz, Ariel, Boyd, Eric S., Badger, Jonathan H., Mathur, Eric J., Ortmann, Alice C., Bateson, Mary, Geesey, Gill, Frazier, Marvin
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2841643/
https://www.ncbi.nlm.nih.gov/pubmed/20333304
http://dx.doi.org/10.1371/journal.pone.0009773
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author Inskeep, William P.
Rusch, Douglas B.
Jay, Zackary J.
Herrgard, Markus J.
Kozubal, Mark A.
Richardson, Toby H.
Macur, Richard E.
Hamamura, Natsuko
Jennings, Ryan deM.
Fouke, Bruce W.
Reysenbach, Anna-Louise
Roberto, Frank
Young, Mark
Schwartz, Ariel
Boyd, Eric S.
Badger, Jonathan H.
Mathur, Eric J.
Ortmann, Alice C.
Bateson, Mary
Geesey, Gill
Frazier, Marvin
author_facet Inskeep, William P.
Rusch, Douglas B.
Jay, Zackary J.
Herrgard, Markus J.
Kozubal, Mark A.
Richardson, Toby H.
Macur, Richard E.
Hamamura, Natsuko
Jennings, Ryan deM.
Fouke, Bruce W.
Reysenbach, Anna-Louise
Roberto, Frank
Young, Mark
Schwartz, Ariel
Boyd, Eric S.
Badger, Jonathan H.
Mathur, Eric J.
Ortmann, Alice C.
Bateson, Mary
Geesey, Gill
Frazier, Marvin
author_sort Inskeep, William P.
collection PubMed
description The Yellowstone caldera contains the most numerous and diverse geothermal systems on Earth, yielding an extensive array of unique high-temperature environments that host a variety of deeply-rooted and understudied Archaea, Bacteria and Eukarya. The combination of extreme temperature and chemical conditions encountered in geothermal environments often results in considerably less microbial diversity than other terrestrial habitats and offers a tremendous opportunity for studying the structure and function of indigenous microbial communities and for establishing linkages between putative metabolisms and element cycling. Metagenome sequence (14–15,000 Sanger reads per site) was obtained for five high-temperature (>65°C) chemotrophic microbial communities sampled from geothermal springs (or pools) in Yellowstone National Park (YNP) that exhibit a wide range in geochemistry including pH, dissolved sulfide, dissolved oxygen and ferrous iron. Metagenome data revealed significant differences in the predominant phyla associated with each of these geochemical environments. Novel members of the Sulfolobales are dominant in low pH environments, while other Crenarchaeota including distantly-related Thermoproteales and Desulfurococcales populations dominate in suboxic sulfidic sediments. Several novel archaeal groups are well represented in an acidic (pH 3) Fe-oxyhydroxide mat, where a higher O(2) influx is accompanied with an increase in archaeal diversity. The presence or absence of genes and pathways important in S oxidation-reduction, H(2)-oxidation, and aerobic respiration (terminal oxidation) provide insight regarding the metabolic strategies of indigenous organisms present in geothermal systems. Multiple-pathway and protein-specific functional analysis of metagenome sequence data corroborated results from phylogenetic analyses and clearly demonstrate major differences in metabolic potential across sites. The distribution of functional genes involved in electron transport is consistent with the hypothesis that geochemical parameters (e.g., pH, sulfide, Fe, O(2)) control microbial community structure and function in YNP geothermal springs.
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spelling pubmed-28416432010-03-24 Metagenomes from High-Temperature Chemotrophic Systems Reveal Geochemical Controls on Microbial Community Structure and Function Inskeep, William P. Rusch, Douglas B. Jay, Zackary J. Herrgard, Markus J. Kozubal, Mark A. Richardson, Toby H. Macur, Richard E. Hamamura, Natsuko Jennings, Ryan deM. Fouke, Bruce W. Reysenbach, Anna-Louise Roberto, Frank Young, Mark Schwartz, Ariel Boyd, Eric S. Badger, Jonathan H. Mathur, Eric J. Ortmann, Alice C. Bateson, Mary Geesey, Gill Frazier, Marvin PLoS One Research Article The Yellowstone caldera contains the most numerous and diverse geothermal systems on Earth, yielding an extensive array of unique high-temperature environments that host a variety of deeply-rooted and understudied Archaea, Bacteria and Eukarya. The combination of extreme temperature and chemical conditions encountered in geothermal environments often results in considerably less microbial diversity than other terrestrial habitats and offers a tremendous opportunity for studying the structure and function of indigenous microbial communities and for establishing linkages between putative metabolisms and element cycling. Metagenome sequence (14–15,000 Sanger reads per site) was obtained for five high-temperature (>65°C) chemotrophic microbial communities sampled from geothermal springs (or pools) in Yellowstone National Park (YNP) that exhibit a wide range in geochemistry including pH, dissolved sulfide, dissolved oxygen and ferrous iron. Metagenome data revealed significant differences in the predominant phyla associated with each of these geochemical environments. Novel members of the Sulfolobales are dominant in low pH environments, while other Crenarchaeota including distantly-related Thermoproteales and Desulfurococcales populations dominate in suboxic sulfidic sediments. Several novel archaeal groups are well represented in an acidic (pH 3) Fe-oxyhydroxide mat, where a higher O(2) influx is accompanied with an increase in archaeal diversity. The presence or absence of genes and pathways important in S oxidation-reduction, H(2)-oxidation, and aerobic respiration (terminal oxidation) provide insight regarding the metabolic strategies of indigenous organisms present in geothermal systems. Multiple-pathway and protein-specific functional analysis of metagenome sequence data corroborated results from phylogenetic analyses and clearly demonstrate major differences in metabolic potential across sites. The distribution of functional genes involved in electron transport is consistent with the hypothesis that geochemical parameters (e.g., pH, sulfide, Fe, O(2)) control microbial community structure and function in YNP geothermal springs. Public Library of Science 2010-03-19 /pmc/articles/PMC2841643/ /pubmed/20333304 http://dx.doi.org/10.1371/journal.pone.0009773 Text en Inskeep et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Inskeep, William P.
Rusch, Douglas B.
Jay, Zackary J.
Herrgard, Markus J.
Kozubal, Mark A.
Richardson, Toby H.
Macur, Richard E.
Hamamura, Natsuko
Jennings, Ryan deM.
Fouke, Bruce W.
Reysenbach, Anna-Louise
Roberto, Frank
Young, Mark
Schwartz, Ariel
Boyd, Eric S.
Badger, Jonathan H.
Mathur, Eric J.
Ortmann, Alice C.
Bateson, Mary
Geesey, Gill
Frazier, Marvin
Metagenomes from High-Temperature Chemotrophic Systems Reveal Geochemical Controls on Microbial Community Structure and Function
title Metagenomes from High-Temperature Chemotrophic Systems Reveal Geochemical Controls on Microbial Community Structure and Function
title_full Metagenomes from High-Temperature Chemotrophic Systems Reveal Geochemical Controls on Microbial Community Structure and Function
title_fullStr Metagenomes from High-Temperature Chemotrophic Systems Reveal Geochemical Controls on Microbial Community Structure and Function
title_full_unstemmed Metagenomes from High-Temperature Chemotrophic Systems Reveal Geochemical Controls on Microbial Community Structure and Function
title_short Metagenomes from High-Temperature Chemotrophic Systems Reveal Geochemical Controls on Microbial Community Structure and Function
title_sort metagenomes from high-temperature chemotrophic systems reveal geochemical controls on microbial community structure and function
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2841643/
https://www.ncbi.nlm.nih.gov/pubmed/20333304
http://dx.doi.org/10.1371/journal.pone.0009773
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