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Ecophysiology of an uncultivated lineage of Aigarchaeota from an oxic, hot spring filamentous ‘streamer' community

The candidate archaeal phylum ‘Aigarchaeota' contains microorganisms from terrestrial and subsurface geothermal ecosystems. The phylogeny and metabolic potential of Aigarchaeota has been deduced from several recent single-cell amplified genomes; however, a detailed description of their metaboli...

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Autores principales: Beam, Jacob P, Jay, Zackary J, Schmid, Markus C, Rusch, Douglas B, Romine, Margaret F, M Jennings, Ryan de, Kozubal, Mark A, Tringe, Susannah G, Wagner, Michael, Inskeep, William P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4681859/
https://www.ncbi.nlm.nih.gov/pubmed/26140529
http://dx.doi.org/10.1038/ismej.2015.83
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author Beam, Jacob P
Jay, Zackary J
Schmid, Markus C
Rusch, Douglas B
Romine, Margaret F
M Jennings, Ryan de
Kozubal, Mark A
Tringe, Susannah G
Wagner, Michael
Inskeep, William P
author_facet Beam, Jacob P
Jay, Zackary J
Schmid, Markus C
Rusch, Douglas B
Romine, Margaret F
M Jennings, Ryan de
Kozubal, Mark A
Tringe, Susannah G
Wagner, Michael
Inskeep, William P
author_sort Beam, Jacob P
collection PubMed
description The candidate archaeal phylum ‘Aigarchaeota' contains microorganisms from terrestrial and subsurface geothermal ecosystems. The phylogeny and metabolic potential of Aigarchaeota has been deduced from several recent single-cell amplified genomes; however, a detailed description of their metabolic potential and in situ transcriptional activity is absent. Here, we report a comprehensive metatranscriptome-based reconstruction of the in situ metabolism of Aigarchaeota in an oxic, hot spring filamentous ‘streamer' community. Fluorescence in situ hybridization showed that these newly discovered Aigarchaeota are filamentous, which is consistent with the presence and transcription of an actin-encoding gene. Aigarchaeota filaments are intricately associated with other community members, which include both bacteria (for example, filamentous Thermocrinis spp.) and archaea. Metabolic reconstruction of genomic and metatranscriptomic data suggests that this aigarchaeon is an aerobic, chemoorganoheterotroph with autotrophic potential. A heme copper oxidase complex was identified in the environmental genome assembly and highly transcribed in situ. Potential electron donors include acetate, fatty acids, amino acids, sugars and aromatic compounds, which may originate from extracellular polymeric substances produced by other microorganisms shown to exist in close proximity and/or autochthonous dissolved organic carbon (OC). Transcripts related to genes specific to each of these potential electron donors were identified, indicating that this aigarchaeon likely utilizes several OC substrates. Characterized members of this lineage cannot synthesize heme, and other cofactors and vitamins de novo, which suggests auxotrophy. We propose the name Candidatus ‘Calditenuis aerorheumensis' for this aigarchaeon, which describes its filamentous morphology and its primary electron acceptor, oxygen.
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spelling pubmed-46818592016-01-01 Ecophysiology of an uncultivated lineage of Aigarchaeota from an oxic, hot spring filamentous ‘streamer' community Beam, Jacob P Jay, Zackary J Schmid, Markus C Rusch, Douglas B Romine, Margaret F M Jennings, Ryan de Kozubal, Mark A Tringe, Susannah G Wagner, Michael Inskeep, William P ISME J Original Article The candidate archaeal phylum ‘Aigarchaeota' contains microorganisms from terrestrial and subsurface geothermal ecosystems. The phylogeny and metabolic potential of Aigarchaeota has been deduced from several recent single-cell amplified genomes; however, a detailed description of their metabolic potential and in situ transcriptional activity is absent. Here, we report a comprehensive metatranscriptome-based reconstruction of the in situ metabolism of Aigarchaeota in an oxic, hot spring filamentous ‘streamer' community. Fluorescence in situ hybridization showed that these newly discovered Aigarchaeota are filamentous, which is consistent with the presence and transcription of an actin-encoding gene. Aigarchaeota filaments are intricately associated with other community members, which include both bacteria (for example, filamentous Thermocrinis spp.) and archaea. Metabolic reconstruction of genomic and metatranscriptomic data suggests that this aigarchaeon is an aerobic, chemoorganoheterotroph with autotrophic potential. A heme copper oxidase complex was identified in the environmental genome assembly and highly transcribed in situ. Potential electron donors include acetate, fatty acids, amino acids, sugars and aromatic compounds, which may originate from extracellular polymeric substances produced by other microorganisms shown to exist in close proximity and/or autochthonous dissolved organic carbon (OC). Transcripts related to genes specific to each of these potential electron donors were identified, indicating that this aigarchaeon likely utilizes several OC substrates. Characterized members of this lineage cannot synthesize heme, and other cofactors and vitamins de novo, which suggests auxotrophy. We propose the name Candidatus ‘Calditenuis aerorheumensis' for this aigarchaeon, which describes its filamentous morphology and its primary electron acceptor, oxygen. Nature Publishing Group 2016-01 2015-07-03 /pmc/articles/PMC4681859/ /pubmed/26140529 http://dx.doi.org/10.1038/ismej.2015.83 Text en Copyright © 2016 International Society for Microbial Ecology http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Original Article
Beam, Jacob P
Jay, Zackary J
Schmid, Markus C
Rusch, Douglas B
Romine, Margaret F
M Jennings, Ryan de
Kozubal, Mark A
Tringe, Susannah G
Wagner, Michael
Inskeep, William P
Ecophysiology of an uncultivated lineage of Aigarchaeota from an oxic, hot spring filamentous ‘streamer' community
title Ecophysiology of an uncultivated lineage of Aigarchaeota from an oxic, hot spring filamentous ‘streamer' community
title_full Ecophysiology of an uncultivated lineage of Aigarchaeota from an oxic, hot spring filamentous ‘streamer' community
title_fullStr Ecophysiology of an uncultivated lineage of Aigarchaeota from an oxic, hot spring filamentous ‘streamer' community
title_full_unstemmed Ecophysiology of an uncultivated lineage of Aigarchaeota from an oxic, hot spring filamentous ‘streamer' community
title_short Ecophysiology of an uncultivated lineage of Aigarchaeota from an oxic, hot spring filamentous ‘streamer' community
title_sort ecophysiology of an uncultivated lineage of aigarchaeota from an oxic, hot spring filamentous ‘streamer' community
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4681859/
https://www.ncbi.nlm.nih.gov/pubmed/26140529
http://dx.doi.org/10.1038/ismej.2015.83
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