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Genomic inference of the metabolism and evolution of the archaeal phylum Aigarchaeota
Microbes of the phylum Aigarchaeota are widely distributed in geothermal environments, but their physiological and ecological roles are poorly understood. Here we analyze six Aigarchaeota metagenomic bins from two circumneutral hot springs in Tengchong, China, to reveal that they are either strict o...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6053391/ https://www.ncbi.nlm.nih.gov/pubmed/30026532 http://dx.doi.org/10.1038/s41467-018-05284-4 |
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author | Hua, Zheng-Shuang Qu, Yan-Ni Zhu, Qiyun Zhou, En-Min Qi, Yan-Ling Yin, Yi-Rui Rao, Yang-Zhi Tian, Ye Li, Yu-Xian Liu, Lan Castelle, Cindy J. Hedlund, Brian P. Shu, Wen-Sheng Knight, Rob Li, Wen-Jun |
author_facet | Hua, Zheng-Shuang Qu, Yan-Ni Zhu, Qiyun Zhou, En-Min Qi, Yan-Ling Yin, Yi-Rui Rao, Yang-Zhi Tian, Ye Li, Yu-Xian Liu, Lan Castelle, Cindy J. Hedlund, Brian P. Shu, Wen-Sheng Knight, Rob Li, Wen-Jun |
author_sort | Hua, Zheng-Shuang |
collection | PubMed |
description | Microbes of the phylum Aigarchaeota are widely distributed in geothermal environments, but their physiological and ecological roles are poorly understood. Here we analyze six Aigarchaeota metagenomic bins from two circumneutral hot springs in Tengchong, China, to reveal that they are either strict or facultative anaerobes, and most are chemolithotrophs that can perform sulfide oxidation. Applying comparative genomics to the Thaumarchaeota and Aigarchaeota, we find that they both originated from thermal habitats, sharing 1154 genes with their common ancestor. Horizontal gene transfer played a crucial role in shaping genetic diversity of Aigarchaeota and led to functional partitioning and ecological divergence among sympatric microbes, as several key functional innovations were endowed by Bacteria, including dissimilatory sulfite reduction and possibly carbon monoxide oxidation. Our study expands our knowledge of the possible ecological roles of the Aigarchaeota and clarifies their evolutionary relationship to their sister lineage Thaumarchaeota. |
format | Online Article Text |
id | pubmed-6053391 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60533912018-07-25 Genomic inference of the metabolism and evolution of the archaeal phylum Aigarchaeota Hua, Zheng-Shuang Qu, Yan-Ni Zhu, Qiyun Zhou, En-Min Qi, Yan-Ling Yin, Yi-Rui Rao, Yang-Zhi Tian, Ye Li, Yu-Xian Liu, Lan Castelle, Cindy J. Hedlund, Brian P. Shu, Wen-Sheng Knight, Rob Li, Wen-Jun Nat Commun Article Microbes of the phylum Aigarchaeota are widely distributed in geothermal environments, but their physiological and ecological roles are poorly understood. Here we analyze six Aigarchaeota metagenomic bins from two circumneutral hot springs in Tengchong, China, to reveal that they are either strict or facultative anaerobes, and most are chemolithotrophs that can perform sulfide oxidation. Applying comparative genomics to the Thaumarchaeota and Aigarchaeota, we find that they both originated from thermal habitats, sharing 1154 genes with their common ancestor. Horizontal gene transfer played a crucial role in shaping genetic diversity of Aigarchaeota and led to functional partitioning and ecological divergence among sympatric microbes, as several key functional innovations were endowed by Bacteria, including dissimilatory sulfite reduction and possibly carbon monoxide oxidation. Our study expands our knowledge of the possible ecological roles of the Aigarchaeota and clarifies their evolutionary relationship to their sister lineage Thaumarchaeota. Nature Publishing Group UK 2018-07-19 /pmc/articles/PMC6053391/ /pubmed/30026532 http://dx.doi.org/10.1038/s41467-018-05284-4 Text en © The Author(s) 2018 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/. |
spellingShingle | Article Hua, Zheng-Shuang Qu, Yan-Ni Zhu, Qiyun Zhou, En-Min Qi, Yan-Ling Yin, Yi-Rui Rao, Yang-Zhi Tian, Ye Li, Yu-Xian Liu, Lan Castelle, Cindy J. Hedlund, Brian P. Shu, Wen-Sheng Knight, Rob Li, Wen-Jun Genomic inference of the metabolism and evolution of the archaeal phylum Aigarchaeota |
title | Genomic inference of the metabolism and evolution of the archaeal phylum Aigarchaeota |
title_full | Genomic inference of the metabolism and evolution of the archaeal phylum Aigarchaeota |
title_fullStr | Genomic inference of the metabolism and evolution of the archaeal phylum Aigarchaeota |
title_full_unstemmed | Genomic inference of the metabolism and evolution of the archaeal phylum Aigarchaeota |
title_short | Genomic inference of the metabolism and evolution of the archaeal phylum Aigarchaeota |
title_sort | genomic inference of the metabolism and evolution of the archaeal phylum aigarchaeota |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6053391/ https://www.ncbi.nlm.nih.gov/pubmed/30026532 http://dx.doi.org/10.1038/s41467-018-05284-4 |
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