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Alternative strategies of nutrient acquisition and energy conservation map to the biogeography of marine ammonia-oxidizing archaea

Ammonia-oxidizing archaea (AOA) are among the most abundant and ubiquitous microorganisms in the ocean, exerting primary control on nitrification and nitrogen oxides emission. Although united by a common physiology of chemoautotrophic growth on ammonia, a corresponding high genomic and habitat varia...

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Autores principales: Qin, Wei, Zheng, Yue, Zhao, Feng, Wang, Yulin, Urakawa, Hidetoshi, Martens-Habbena, Willm, Liu, Haodong, Huang, Xiaowu, Zhang, Xinxu, Nakagawa, Tatsunori, Mende, Daniel R., Bollmann, Annette, Wang, Baozhan, Zhang, Yao, Amin, Shady A., Nielsen, Jeppe L., Mori, Koji, Takahashi, Reiji, Virginia Armbrust, E., Winkler, Mari-K.H., DeLong, Edward F., Li, Meng, Lee, Po-Heng, Zhou, Jizhong, Zhang, Chuanlun, Zhang, Tong, Stahl, David A., Ingalls, Anitra E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7490402/
https://www.ncbi.nlm.nih.gov/pubmed/32636492
http://dx.doi.org/10.1038/s41396-020-0710-7
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author Qin, Wei
Zheng, Yue
Zhao, Feng
Wang, Yulin
Urakawa, Hidetoshi
Martens-Habbena, Willm
Liu, Haodong
Huang, Xiaowu
Zhang, Xinxu
Nakagawa, Tatsunori
Mende, Daniel R.
Bollmann, Annette
Wang, Baozhan
Zhang, Yao
Amin, Shady A.
Nielsen, Jeppe L.
Mori, Koji
Takahashi, Reiji
Virginia Armbrust, E.
Winkler, Mari-K.H.
DeLong, Edward F.
Li, Meng
Lee, Po-Heng
Zhou, Jizhong
Zhang, Chuanlun
Zhang, Tong
Stahl, David A.
Ingalls, Anitra E.
author_facet Qin, Wei
Zheng, Yue
Zhao, Feng
Wang, Yulin
Urakawa, Hidetoshi
Martens-Habbena, Willm
Liu, Haodong
Huang, Xiaowu
Zhang, Xinxu
Nakagawa, Tatsunori
Mende, Daniel R.
Bollmann, Annette
Wang, Baozhan
Zhang, Yao
Amin, Shady A.
Nielsen, Jeppe L.
Mori, Koji
Takahashi, Reiji
Virginia Armbrust, E.
Winkler, Mari-K.H.
DeLong, Edward F.
Li, Meng
Lee, Po-Heng
Zhou, Jizhong
Zhang, Chuanlun
Zhang, Tong
Stahl, David A.
Ingalls, Anitra E.
author_sort Qin, Wei
collection PubMed
description Ammonia-oxidizing archaea (AOA) are among the most abundant and ubiquitous microorganisms in the ocean, exerting primary control on nitrification and nitrogen oxides emission. Although united by a common physiology of chemoautotrophic growth on ammonia, a corresponding high genomic and habitat variability suggests tremendous adaptive capacity. Here, we compared 44 diverse AOA genomes, 37 from species cultivated from samples collected across diverse geographic locations and seven assembled from metagenomic sequences from the mesopelagic to hadopelagic zones of the deep ocean. Comparative analysis identified seven major marine AOA genotypic groups having gene content correlated with their distinctive biogeographies. Phosphorus and ammonia availabilities as well as hydrostatic pressure were identified as selective forces driving marine AOA genotypic and gene content variability in different oceanic regions. Notably, AOA methylphosphonate biosynthetic genes span diverse oceanic provinces, reinforcing their importance for methane production in the ocean. Together, our combined comparative physiological, genomic, and metagenomic analyses provide a comprehensive view of the biogeography of globally abundant AOA and their adaptive radiation into a vast range of marine and terrestrial habitats.
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spelling pubmed-74904022020-10-01 Alternative strategies of nutrient acquisition and energy conservation map to the biogeography of marine ammonia-oxidizing archaea Qin, Wei Zheng, Yue Zhao, Feng Wang, Yulin Urakawa, Hidetoshi Martens-Habbena, Willm Liu, Haodong Huang, Xiaowu Zhang, Xinxu Nakagawa, Tatsunori Mende, Daniel R. Bollmann, Annette Wang, Baozhan Zhang, Yao Amin, Shady A. Nielsen, Jeppe L. Mori, Koji Takahashi, Reiji Virginia Armbrust, E. Winkler, Mari-K.H. DeLong, Edward F. Li, Meng Lee, Po-Heng Zhou, Jizhong Zhang, Chuanlun Zhang, Tong Stahl, David A. Ingalls, Anitra E. ISME J Article Ammonia-oxidizing archaea (AOA) are among the most abundant and ubiquitous microorganisms in the ocean, exerting primary control on nitrification and nitrogen oxides emission. Although united by a common physiology of chemoautotrophic growth on ammonia, a corresponding high genomic and habitat variability suggests tremendous adaptive capacity. Here, we compared 44 diverse AOA genomes, 37 from species cultivated from samples collected across diverse geographic locations and seven assembled from metagenomic sequences from the mesopelagic to hadopelagic zones of the deep ocean. Comparative analysis identified seven major marine AOA genotypic groups having gene content correlated with their distinctive biogeographies. Phosphorus and ammonia availabilities as well as hydrostatic pressure were identified as selective forces driving marine AOA genotypic and gene content variability in different oceanic regions. Notably, AOA methylphosphonate biosynthetic genes span diverse oceanic provinces, reinforcing their importance for methane production in the ocean. Together, our combined comparative physiological, genomic, and metagenomic analyses provide a comprehensive view of the biogeography of globally abundant AOA and their adaptive radiation into a vast range of marine and terrestrial habitats. Nature Publishing Group UK 2020-07-07 2020-10 /pmc/articles/PMC7490402/ /pubmed/32636492 http://dx.doi.org/10.1038/s41396-020-0710-7 Text en © The Author(s) 2020 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
Qin, Wei
Zheng, Yue
Zhao, Feng
Wang, Yulin
Urakawa, Hidetoshi
Martens-Habbena, Willm
Liu, Haodong
Huang, Xiaowu
Zhang, Xinxu
Nakagawa, Tatsunori
Mende, Daniel R.
Bollmann, Annette
Wang, Baozhan
Zhang, Yao
Amin, Shady A.
Nielsen, Jeppe L.
Mori, Koji
Takahashi, Reiji
Virginia Armbrust, E.
Winkler, Mari-K.H.
DeLong, Edward F.
Li, Meng
Lee, Po-Heng
Zhou, Jizhong
Zhang, Chuanlun
Zhang, Tong
Stahl, David A.
Ingalls, Anitra E.
Alternative strategies of nutrient acquisition and energy conservation map to the biogeography of marine ammonia-oxidizing archaea
title Alternative strategies of nutrient acquisition and energy conservation map to the biogeography of marine ammonia-oxidizing archaea
title_full Alternative strategies of nutrient acquisition and energy conservation map to the biogeography of marine ammonia-oxidizing archaea
title_fullStr Alternative strategies of nutrient acquisition and energy conservation map to the biogeography of marine ammonia-oxidizing archaea
title_full_unstemmed Alternative strategies of nutrient acquisition and energy conservation map to the biogeography of marine ammonia-oxidizing archaea
title_short Alternative strategies of nutrient acquisition and energy conservation map to the biogeography of marine ammonia-oxidizing archaea
title_sort alternative strategies of nutrient acquisition and energy conservation map to the biogeography of marine ammonia-oxidizing archaea
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7490402/
https://www.ncbi.nlm.nih.gov/pubmed/32636492
http://dx.doi.org/10.1038/s41396-020-0710-7
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