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Culexarchaeia, a novel archaeal class of anaerobic generalists inhabiting geothermal environments
Geothermal environments, including terrestrial hot springs and deep-sea hydrothermal sediments, often contain many poorly understood lineages of archaea. Here, we recovered ten metagenome-assembled genomes (MAGs) from geothermal sediments and propose that they constitute a new archaeal class within...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723716/ https://www.ncbi.nlm.nih.gov/pubmed/37938354 http://dx.doi.org/10.1038/s43705-022-00175-8 |
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author | Kohtz, Anthony J. Jay, Zackary J. Lynes, Mackenzie M. Krukenberg, Viola Hatzenpichler, Roland |
author_facet | Kohtz, Anthony J. Jay, Zackary J. Lynes, Mackenzie M. Krukenberg, Viola Hatzenpichler, Roland |
author_sort | Kohtz, Anthony J. |
collection | PubMed |
description | Geothermal environments, including terrestrial hot springs and deep-sea hydrothermal sediments, often contain many poorly understood lineages of archaea. Here, we recovered ten metagenome-assembled genomes (MAGs) from geothermal sediments and propose that they constitute a new archaeal class within the TACK superphylum, “Candidatus Culexarchaeia”, named after the Culex Basin in Yellowstone National Park. Culexarchaeia harbor distinct sets of proteins involved in key cellular processes that are either phylogenetically divergent or are absent from other closely related TACK lineages, with a particular divergence in cell division and cytoskeletal proteins. Metabolic reconstruction revealed that Culexarchaeia have the capacity to metabolize a wide variety of organic and inorganic substrates. Notably, Culexarchaeia encode a unique modular, membrane associated, and energy conserving [NiFe]-hydrogenase complex that potentially interacts with heterodisulfide reductase (Hdr) subunits. Comparison of this [NiFe]-hydrogenase complex with similar complexes from other archaea suggests that interactions between membrane associated [NiFe]-hydrogenases and Hdr may be more widespread than previously appreciated in both methanogenic and non-methanogenic lifestyles. The analysis of Culexarchaeia further expands our understanding of the phylogenetic and functional diversity of lineages within the TACK superphylum and the ecology, physiology, and evolution of these organisms in extreme environments. |
format | Online Article Text |
id | pubmed-9723716 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-97237162023-01-04 Culexarchaeia, a novel archaeal class of anaerobic generalists inhabiting geothermal environments Kohtz, Anthony J. Jay, Zackary J. Lynes, Mackenzie M. Krukenberg, Viola Hatzenpichler, Roland ISME Commun Article Geothermal environments, including terrestrial hot springs and deep-sea hydrothermal sediments, often contain many poorly understood lineages of archaea. Here, we recovered ten metagenome-assembled genomes (MAGs) from geothermal sediments and propose that they constitute a new archaeal class within the TACK superphylum, “Candidatus Culexarchaeia”, named after the Culex Basin in Yellowstone National Park. Culexarchaeia harbor distinct sets of proteins involved in key cellular processes that are either phylogenetically divergent or are absent from other closely related TACK lineages, with a particular divergence in cell division and cytoskeletal proteins. Metabolic reconstruction revealed that Culexarchaeia have the capacity to metabolize a wide variety of organic and inorganic substrates. Notably, Culexarchaeia encode a unique modular, membrane associated, and energy conserving [NiFe]-hydrogenase complex that potentially interacts with heterodisulfide reductase (Hdr) subunits. Comparison of this [NiFe]-hydrogenase complex with similar complexes from other archaea suggests that interactions between membrane associated [NiFe]-hydrogenases and Hdr may be more widespread than previously appreciated in both methanogenic and non-methanogenic lifestyles. The analysis of Culexarchaeia further expands our understanding of the phylogenetic and functional diversity of lineages within the TACK superphylum and the ecology, physiology, and evolution of these organisms in extreme environments. Nature Publishing Group UK 2022-09-20 /pmc/articles/PMC9723716/ /pubmed/37938354 http://dx.doi.org/10.1038/s43705-022-00175-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Kohtz, Anthony J. Jay, Zackary J. Lynes, Mackenzie M. Krukenberg, Viola Hatzenpichler, Roland Culexarchaeia, a novel archaeal class of anaerobic generalists inhabiting geothermal environments |
title | Culexarchaeia, a novel archaeal class of anaerobic generalists inhabiting geothermal environments |
title_full | Culexarchaeia, a novel archaeal class of anaerobic generalists inhabiting geothermal environments |
title_fullStr | Culexarchaeia, a novel archaeal class of anaerobic generalists inhabiting geothermal environments |
title_full_unstemmed | Culexarchaeia, a novel archaeal class of anaerobic generalists inhabiting geothermal environments |
title_short | Culexarchaeia, a novel archaeal class of anaerobic generalists inhabiting geothermal environments |
title_sort | culexarchaeia, a novel archaeal class of anaerobic generalists inhabiting geothermal environments |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723716/ https://www.ncbi.nlm.nih.gov/pubmed/37938354 http://dx.doi.org/10.1038/s43705-022-00175-8 |
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