Cargando…

Expansion of Armatimonadota through marine sediment sequencing describes two classes with unique ecological roles

Marine sediments comprise one of the largest environments on the planet, and their microbial inhabitants are significant players in global carbon and nutrient cycles. Recent studies using metagenomic techniques have shown the complexity of these communities and identified novel microorganisms from t...

Descripción completa

Detalles Bibliográficos
Autores principales: Carlton, John D., Langwig, Marguerite V., Gong, Xianzhe, Aguilar-Pine, Emily J., Vázquez-Rosas-Landa, Mirna, Seitz, Kiley W., Baker, Brett J., De Anda, Valerie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10290634/
https://www.ncbi.nlm.nih.gov/pubmed/37355707
http://dx.doi.org/10.1038/s43705-023-00269-x
_version_ 1785062531591569408
author Carlton, John D.
Langwig, Marguerite V.
Gong, Xianzhe
Aguilar-Pine, Emily J.
Vázquez-Rosas-Landa, Mirna
Seitz, Kiley W.
Baker, Brett J.
De Anda, Valerie
author_facet Carlton, John D.
Langwig, Marguerite V.
Gong, Xianzhe
Aguilar-Pine, Emily J.
Vázquez-Rosas-Landa, Mirna
Seitz, Kiley W.
Baker, Brett J.
De Anda, Valerie
author_sort Carlton, John D.
collection PubMed
description Marine sediments comprise one of the largest environments on the planet, and their microbial inhabitants are significant players in global carbon and nutrient cycles. Recent studies using metagenomic techniques have shown the complexity of these communities and identified novel microorganisms from the ocean floor. Here, we obtained 77 metagenome-assembled genomes (MAGs) from the bacterial phylum Armatimonadota in the Guaymas Basin, Gulf of California, and the Bohai Sea, China. These MAGs comprise two previously undescribed classes within Armatimonadota, which we propose naming Hebobacteria and Zipacnadia. They are globally distributed in hypoxic and anoxic environments and are dominant members of deep-sea sediments (up to 1.95% of metagenomic raw reads). The classes described here also have unique metabolic capabilities, possessing pathways to reduce carbon dioxide to acetate via the Wood-Ljungdahl pathway (WLP) and generating energy through the oxidative branch of glycolysis using carbon dioxide as an electron sink, maintaining the redox balance using the WLP. Hebobacteria may also be autotrophic, not previously identified in Armatimonadota. Furthermore, these Armatimonadota may play a role in sulfur and nitrogen cycling, using the intermediate compounds hydroxylamine and sulfite. Description of these MAGs enhances our understanding of diversity and metabolic potential within anoxic habitats worldwide.
format Online
Article
Text
id pubmed-10290634
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-102906342023-06-26 Expansion of Armatimonadota through marine sediment sequencing describes two classes with unique ecological roles Carlton, John D. Langwig, Marguerite V. Gong, Xianzhe Aguilar-Pine, Emily J. Vázquez-Rosas-Landa, Mirna Seitz, Kiley W. Baker, Brett J. De Anda, Valerie ISME Commun Article Marine sediments comprise one of the largest environments on the planet, and their microbial inhabitants are significant players in global carbon and nutrient cycles. Recent studies using metagenomic techniques have shown the complexity of these communities and identified novel microorganisms from the ocean floor. Here, we obtained 77 metagenome-assembled genomes (MAGs) from the bacterial phylum Armatimonadota in the Guaymas Basin, Gulf of California, and the Bohai Sea, China. These MAGs comprise two previously undescribed classes within Armatimonadota, which we propose naming Hebobacteria and Zipacnadia. They are globally distributed in hypoxic and anoxic environments and are dominant members of deep-sea sediments (up to 1.95% of metagenomic raw reads). The classes described here also have unique metabolic capabilities, possessing pathways to reduce carbon dioxide to acetate via the Wood-Ljungdahl pathway (WLP) and generating energy through the oxidative branch of glycolysis using carbon dioxide as an electron sink, maintaining the redox balance using the WLP. Hebobacteria may also be autotrophic, not previously identified in Armatimonadota. Furthermore, these Armatimonadota may play a role in sulfur and nitrogen cycling, using the intermediate compounds hydroxylamine and sulfite. Description of these MAGs enhances our understanding of diversity and metabolic potential within anoxic habitats worldwide. Nature Publishing Group UK 2023-06-24 /pmc/articles/PMC10290634/ /pubmed/37355707 http://dx.doi.org/10.1038/s43705-023-00269-x Text en © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2023 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
Carlton, John D.
Langwig, Marguerite V.
Gong, Xianzhe
Aguilar-Pine, Emily J.
Vázquez-Rosas-Landa, Mirna
Seitz, Kiley W.
Baker, Brett J.
De Anda, Valerie
Expansion of Armatimonadota through marine sediment sequencing describes two classes with unique ecological roles
title Expansion of Armatimonadota through marine sediment sequencing describes two classes with unique ecological roles
title_full Expansion of Armatimonadota through marine sediment sequencing describes two classes with unique ecological roles
title_fullStr Expansion of Armatimonadota through marine sediment sequencing describes two classes with unique ecological roles
title_full_unstemmed Expansion of Armatimonadota through marine sediment sequencing describes two classes with unique ecological roles
title_short Expansion of Armatimonadota through marine sediment sequencing describes two classes with unique ecological roles
title_sort expansion of armatimonadota through marine sediment sequencing describes two classes with unique ecological roles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10290634/
https://www.ncbi.nlm.nih.gov/pubmed/37355707
http://dx.doi.org/10.1038/s43705-023-00269-x
work_keys_str_mv AT carltonjohnd expansionofarmatimonadotathroughmarinesedimentsequencingdescribestwoclasseswithuniqueecologicalroles
AT langwigmargueritev expansionofarmatimonadotathroughmarinesedimentsequencingdescribestwoclasseswithuniqueecologicalroles
AT gongxianzhe expansionofarmatimonadotathroughmarinesedimentsequencingdescribestwoclasseswithuniqueecologicalroles
AT aguilarpineemilyj expansionofarmatimonadotathroughmarinesedimentsequencingdescribestwoclasseswithuniqueecologicalroles
AT vazquezrosaslandamirna expansionofarmatimonadotathroughmarinesedimentsequencingdescribestwoclasseswithuniqueecologicalroles
AT seitzkileyw expansionofarmatimonadotathroughmarinesedimentsequencingdescribestwoclasseswithuniqueecologicalroles
AT bakerbrettj expansionofarmatimonadotathroughmarinesedimentsequencingdescribestwoclasseswithuniqueecologicalroles
AT deandavalerie expansionofarmatimonadotathroughmarinesedimentsequencingdescribestwoclasseswithuniqueecologicalroles