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Novel, Deep-Branching Heterotrophic Bacterial Populations Recovered from Thermal Spring Metagenomes

Thermal spring ecosystems are a valuable resource for the discovery of novel hyperthermophilic Bacteria and Archaea, and harbor deeply-branching lineages that provide insight regarding the nature of early microbial life. We characterized bacterial populations in two circumneutral (pH ~8) Yellowstone...

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Autores principales: Colman, Daniel R., Jay, Zackary J., Inskeep, William P., Jennings, Ryan deM., Maas, Kendra R., Rusch, Douglas B., Takacs-Vesbach, Cristina D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4791363/
https://www.ncbi.nlm.nih.gov/pubmed/27014227
http://dx.doi.org/10.3389/fmicb.2016.00304
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author Colman, Daniel R.
Jay, Zackary J.
Inskeep, William P.
Jennings, Ryan deM.
Maas, Kendra R.
Rusch, Douglas B.
Takacs-Vesbach, Cristina D.
author_facet Colman, Daniel R.
Jay, Zackary J.
Inskeep, William P.
Jennings, Ryan deM.
Maas, Kendra R.
Rusch, Douglas B.
Takacs-Vesbach, Cristina D.
author_sort Colman, Daniel R.
collection PubMed
description Thermal spring ecosystems are a valuable resource for the discovery of novel hyperthermophilic Bacteria and Archaea, and harbor deeply-branching lineages that provide insight regarding the nature of early microbial life. We characterized bacterial populations in two circumneutral (pH ~8) Yellowstone National Park thermal (T ~80°C) spring filamentous “streamer” communities using random metagenomic DNA sequence to investigate the metabolic potential of these novel populations. Four de novo assemblies representing three abundant, deeply-branching bacterial phylotypes were recovered. Analysis of conserved phylogenetic marker genes indicated that two of the phylotypes represent separate groups of an uncharacterized phylum (for which we propose the candidate phylum name “Pyropristinus”). The third new phylotype falls within the proposed Calescamantes phylum. Metabolic reconstructions of the “Pyropristinus” and Calescamantes populations showed that these organisms appear to be chemoorganoheterotrophs and have the genomic potential for aerobic respiration and oxidative phosphorylation via archaeal-like V-type, and bacterial F-type ATPases, respectively. A survey of similar phylotypes (>97% nt identity) within 16S rRNA gene datasets suggest that the newly described organisms are restricted to terrestrial thermal springs ranging from 70 to 90°C and pH values of ~7–9. The characterization of these lineages is important for understanding the diversity of deeply-branching bacterial phyla, and their functional role in high-temperature circumneutral “streamer” communities.
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spelling pubmed-47913632016-03-24 Novel, Deep-Branching Heterotrophic Bacterial Populations Recovered from Thermal Spring Metagenomes Colman, Daniel R. Jay, Zackary J. Inskeep, William P. Jennings, Ryan deM. Maas, Kendra R. Rusch, Douglas B. Takacs-Vesbach, Cristina D. Front Microbiol Microbiology Thermal spring ecosystems are a valuable resource for the discovery of novel hyperthermophilic Bacteria and Archaea, and harbor deeply-branching lineages that provide insight regarding the nature of early microbial life. We characterized bacterial populations in two circumneutral (pH ~8) Yellowstone National Park thermal (T ~80°C) spring filamentous “streamer” communities using random metagenomic DNA sequence to investigate the metabolic potential of these novel populations. Four de novo assemblies representing three abundant, deeply-branching bacterial phylotypes were recovered. Analysis of conserved phylogenetic marker genes indicated that two of the phylotypes represent separate groups of an uncharacterized phylum (for which we propose the candidate phylum name “Pyropristinus”). The third new phylotype falls within the proposed Calescamantes phylum. Metabolic reconstructions of the “Pyropristinus” and Calescamantes populations showed that these organisms appear to be chemoorganoheterotrophs and have the genomic potential for aerobic respiration and oxidative phosphorylation via archaeal-like V-type, and bacterial F-type ATPases, respectively. A survey of similar phylotypes (>97% nt identity) within 16S rRNA gene datasets suggest that the newly described organisms are restricted to terrestrial thermal springs ranging from 70 to 90°C and pH values of ~7–9. The characterization of these lineages is important for understanding the diversity of deeply-branching bacterial phyla, and their functional role in high-temperature circumneutral “streamer” communities. Frontiers Media S.A. 2016-03-15 /pmc/articles/PMC4791363/ /pubmed/27014227 http://dx.doi.org/10.3389/fmicb.2016.00304 Text en Copyright © 2016 Colman, Jay, Inskeep, Jennings, Maas, Rusch and Takacs-Vesbach. 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
Colman, Daniel R.
Jay, Zackary J.
Inskeep, William P.
Jennings, Ryan deM.
Maas, Kendra R.
Rusch, Douglas B.
Takacs-Vesbach, Cristina D.
Novel, Deep-Branching Heterotrophic Bacterial Populations Recovered from Thermal Spring Metagenomes
title Novel, Deep-Branching Heterotrophic Bacterial Populations Recovered from Thermal Spring Metagenomes
title_full Novel, Deep-Branching Heterotrophic Bacterial Populations Recovered from Thermal Spring Metagenomes
title_fullStr Novel, Deep-Branching Heterotrophic Bacterial Populations Recovered from Thermal Spring Metagenomes
title_full_unstemmed Novel, Deep-Branching Heterotrophic Bacterial Populations Recovered from Thermal Spring Metagenomes
title_short Novel, Deep-Branching Heterotrophic Bacterial Populations Recovered from Thermal Spring Metagenomes
title_sort novel, deep-branching heterotrophic bacterial populations recovered from thermal spring metagenomes
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4791363/
https://www.ncbi.nlm.nih.gov/pubmed/27014227
http://dx.doi.org/10.3389/fmicb.2016.00304
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