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Vertebrate host phylogeny influences gut archaeal diversity

Commonly used 16S rRNA gene primers do not detect the full range of archaeal diversity present in the vertebrate gut. As a result, several questions regarding the archaeal component of the gut microbiota remain, including which Archaea are host-associated, the specificities of such associations and...

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Autores principales: Youngblut, Nicholas D., Reischer, Georg H., Dauser, Silke, Maisch, Sophie, Walzer, Chris, Stalder, Gabrielle, Farnleitner, Andreas H., Ley, Ruth E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8556154/
https://www.ncbi.nlm.nih.gov/pubmed/34702978
http://dx.doi.org/10.1038/s41564-021-00980-2
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author Youngblut, Nicholas D.
Reischer, Georg H.
Dauser, Silke
Maisch, Sophie
Walzer, Chris
Stalder, Gabrielle
Farnleitner, Andreas H.
Ley, Ruth E.
author_facet Youngblut, Nicholas D.
Reischer, Georg H.
Dauser, Silke
Maisch, Sophie
Walzer, Chris
Stalder, Gabrielle
Farnleitner, Andreas H.
Ley, Ruth E.
author_sort Youngblut, Nicholas D.
collection PubMed
description Commonly used 16S rRNA gene primers do not detect the full range of archaeal diversity present in the vertebrate gut. As a result, several questions regarding the archaeal component of the gut microbiota remain, including which Archaea are host-associated, the specificities of such associations and the major factors influencing archaeal diversity. Using 16S rRNA gene amplicon sequencing with primers that specifically target Archaea, we obtained sufficient sequence data from 185 gastrointestinal samples collected from 110 vertebrate species that span five taxonomic classes (Mammalia, Aves, Reptilia, Amphibia and Actinopterygii), of which the majority were wild. We provide evidence for previously undescribed Archaea–host associations, including Bathyarchaeia and Methanothermobacter, the latter of which was prevalent among Aves and relatively abundant in species with higher body temperatures, although this association could not be decoupled from host phylogeny. Host phylogeny explained archaeal diversity more strongly than diet, while specific taxa were associated with both factors, and cophylogeny was significant and strongest for mammalian herbivores. Methanobacteria was the only class predicted to be present in the last common ancestors of mammals and all host species. Further analysis indicated that Archaea–Bacteria interactions have a limited effect on archaeal diversity. These findings expand our current understanding of Archaea–vertebrate associations.
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spelling pubmed-85561542021-11-04 Vertebrate host phylogeny influences gut archaeal diversity Youngblut, Nicholas D. Reischer, Georg H. Dauser, Silke Maisch, Sophie Walzer, Chris Stalder, Gabrielle Farnleitner, Andreas H. Ley, Ruth E. Nat Microbiol Article Commonly used 16S rRNA gene primers do not detect the full range of archaeal diversity present in the vertebrate gut. As a result, several questions regarding the archaeal component of the gut microbiota remain, including which Archaea are host-associated, the specificities of such associations and the major factors influencing archaeal diversity. Using 16S rRNA gene amplicon sequencing with primers that specifically target Archaea, we obtained sufficient sequence data from 185 gastrointestinal samples collected from 110 vertebrate species that span five taxonomic classes (Mammalia, Aves, Reptilia, Amphibia and Actinopterygii), of which the majority were wild. We provide evidence for previously undescribed Archaea–host associations, including Bathyarchaeia and Methanothermobacter, the latter of which was prevalent among Aves and relatively abundant in species with higher body temperatures, although this association could not be decoupled from host phylogeny. Host phylogeny explained archaeal diversity more strongly than diet, while specific taxa were associated with both factors, and cophylogeny was significant and strongest for mammalian herbivores. Methanobacteria was the only class predicted to be present in the last common ancestors of mammals and all host species. Further analysis indicated that Archaea–Bacteria interactions have a limited effect on archaeal diversity. These findings expand our current understanding of Archaea–vertebrate associations. Nature Publishing Group UK 2021-10-26 2021 /pmc/articles/PMC8556154/ /pubmed/34702978 http://dx.doi.org/10.1038/s41564-021-00980-2 Text en © The Author(s) 2021 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
Youngblut, Nicholas D.
Reischer, Georg H.
Dauser, Silke
Maisch, Sophie
Walzer, Chris
Stalder, Gabrielle
Farnleitner, Andreas H.
Ley, Ruth E.
Vertebrate host phylogeny influences gut archaeal diversity
title Vertebrate host phylogeny influences gut archaeal diversity
title_full Vertebrate host phylogeny influences gut archaeal diversity
title_fullStr Vertebrate host phylogeny influences gut archaeal diversity
title_full_unstemmed Vertebrate host phylogeny influences gut archaeal diversity
title_short Vertebrate host phylogeny influences gut archaeal diversity
title_sort vertebrate host phylogeny influences gut archaeal diversity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8556154/
https://www.ncbi.nlm.nih.gov/pubmed/34702978
http://dx.doi.org/10.1038/s41564-021-00980-2
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