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Global Biodiversity of Aquatic Ammonia-Oxidizing Archaea is Partitioned by Habitat

Archaea play an important role in nitrification and are, thus, inextricably linked to the global carbon and nitrogen cycles. Since the initial discovery of an ammonia monooxygenase α-subunit (amoA) gene associated with an archaeal metagenomic fragment, archaeal amoA sequences have been detected in a...

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Autores principales: Biller, Steven J., Mosier, Annika C., Wells, George F., Francis, Christopher A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3399221/
https://www.ncbi.nlm.nih.gov/pubmed/22826704
http://dx.doi.org/10.3389/fmicb.2012.00252
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author Biller, Steven J.
Mosier, Annika C.
Wells, George F.
Francis, Christopher A.
author_facet Biller, Steven J.
Mosier, Annika C.
Wells, George F.
Francis, Christopher A.
author_sort Biller, Steven J.
collection PubMed
description Archaea play an important role in nitrification and are, thus, inextricably linked to the global carbon and nitrogen cycles. Since the initial discovery of an ammonia monooxygenase α-subunit (amoA) gene associated with an archaeal metagenomic fragment, archaeal amoA sequences have been detected in a wide variety of nitrifying environments. Recent sequencing efforts have revealed extensive diversity of archaeal amoA sequences within different habitats. In this study, we have examined over 8000 amoA sequences from the literature and public databases in an effort to understand the ecological factors influencing the distribution and diversity of ammonia-oxidizing archaea (AOA), with a particular focus on sequences from aquatic habitats. This broad survey provides strong statistical support for the hypothesis that different environments contain distinct clusters of AOA amoA sequences, as surprisingly few sequences are found in more than one habitat type. Within aquatic environments, salinity, depth in the water column, and temperature were significantly correlated with the distribution of sequence types. These findings support the existence of multiple distinct aquatic AOA populations in the environment and suggest some possible selective pressures driving the partitioning of AOA amoA diversity.
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spelling pubmed-33992212012-07-23 Global Biodiversity of Aquatic Ammonia-Oxidizing Archaea is Partitioned by Habitat Biller, Steven J. Mosier, Annika C. Wells, George F. Francis, Christopher A. Front Microbiol Microbiology Archaea play an important role in nitrification and are, thus, inextricably linked to the global carbon and nitrogen cycles. Since the initial discovery of an ammonia monooxygenase α-subunit (amoA) gene associated with an archaeal metagenomic fragment, archaeal amoA sequences have been detected in a wide variety of nitrifying environments. Recent sequencing efforts have revealed extensive diversity of archaeal amoA sequences within different habitats. In this study, we have examined over 8000 amoA sequences from the literature and public databases in an effort to understand the ecological factors influencing the distribution and diversity of ammonia-oxidizing archaea (AOA), with a particular focus on sequences from aquatic habitats. This broad survey provides strong statistical support for the hypothesis that different environments contain distinct clusters of AOA amoA sequences, as surprisingly few sequences are found in more than one habitat type. Within aquatic environments, salinity, depth in the water column, and temperature were significantly correlated with the distribution of sequence types. These findings support the existence of multiple distinct aquatic AOA populations in the environment and suggest some possible selective pressures driving the partitioning of AOA amoA diversity. Frontiers Research Foundation 2012-07-18 /pmc/articles/PMC3399221/ /pubmed/22826704 http://dx.doi.org/10.3389/fmicb.2012.00252 Text en Copyright © 2012 Biller, Mosier, Wells and Francis. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Microbiology
Biller, Steven J.
Mosier, Annika C.
Wells, George F.
Francis, Christopher A.
Global Biodiversity of Aquatic Ammonia-Oxidizing Archaea is Partitioned by Habitat
title Global Biodiversity of Aquatic Ammonia-Oxidizing Archaea is Partitioned by Habitat
title_full Global Biodiversity of Aquatic Ammonia-Oxidizing Archaea is Partitioned by Habitat
title_fullStr Global Biodiversity of Aquatic Ammonia-Oxidizing Archaea is Partitioned by Habitat
title_full_unstemmed Global Biodiversity of Aquatic Ammonia-Oxidizing Archaea is Partitioned by Habitat
title_short Global Biodiversity of Aquatic Ammonia-Oxidizing Archaea is Partitioned by Habitat
title_sort global biodiversity of aquatic ammonia-oxidizing archaea is partitioned by habitat
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3399221/
https://www.ncbi.nlm.nih.gov/pubmed/22826704
http://dx.doi.org/10.3389/fmicb.2012.00252
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