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Propagation of viral genomes by replicating ammonia-oxidising archaea during soil nitrification
Ammonia-oxidising archaea (AOA) are a ubiquitous component of microbial communities and dominate the first stage of nitrification in some soils. While we are beginning to understand soil virus dynamics, we have no knowledge of the composition or activity of those infecting nitrifiers or their potent...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9859776/ https://www.ncbi.nlm.nih.gov/pubmed/36414709 http://dx.doi.org/10.1038/s41396-022-01341-5 |
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author | Lee, Sungeun Sieradzki, Ella T. Nicol, Graeme W. Hazard, Christina |
author_facet | Lee, Sungeun Sieradzki, Ella T. Nicol, Graeme W. Hazard, Christina |
author_sort | Lee, Sungeun |
collection | PubMed |
description | Ammonia-oxidising archaea (AOA) are a ubiquitous component of microbial communities and dominate the first stage of nitrification in some soils. While we are beginning to understand soil virus dynamics, we have no knowledge of the composition or activity of those infecting nitrifiers or their potential to influence processes. This study aimed to characterise viruses having infected autotrophic AOA in two nitrifying soils of contrasting pH by following transfer of assimilated CO(2)-derived (13)C from host to virus via DNA stable-isotope probing and metagenomic analysis. Incorporation of (13)C into low GC mol% AOA and virus genomes increased DNA buoyant density in CsCl gradients but resulted in co-migration with dominant non-enriched high GC mol% genomes, reducing sequencing depth and contig assembly. We therefore developed a hybrid approach where AOA and virus genomes were assembled from low buoyant density DNA with subsequent mapping of (13)C isotopically enriched high buoyant density DNA reads to identify activity of AOA. Metagenome-assembled genomes were different between the two soils and represented a broad diversity of active populations. Sixty-four AOA-infecting viral operational taxonomic units (vOTUs) were identified with no clear relatedness to previously characterised prokaryote viruses. These vOTUs were also distinct between soils, with 42% enriched in (13)C derived from hosts. The majority were predicted as capable of lysogeny and auxiliary metabolic genes included an AOA-specific multicopper oxidase suggesting infection may augment copper uptake essential for central metabolic functioning. These findings indicate virus infection of AOA may be a frequent process during nitrification with potential to influence host physiology and activity. |
format | Online Article Text |
id | pubmed-9859776 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-98597762023-01-22 Propagation of viral genomes by replicating ammonia-oxidising archaea during soil nitrification Lee, Sungeun Sieradzki, Ella T. Nicol, Graeme W. Hazard, Christina ISME J Brief Communication Ammonia-oxidising archaea (AOA) are a ubiquitous component of microbial communities and dominate the first stage of nitrification in some soils. While we are beginning to understand soil virus dynamics, we have no knowledge of the composition or activity of those infecting nitrifiers or their potential to influence processes. This study aimed to characterise viruses having infected autotrophic AOA in two nitrifying soils of contrasting pH by following transfer of assimilated CO(2)-derived (13)C from host to virus via DNA stable-isotope probing and metagenomic analysis. Incorporation of (13)C into low GC mol% AOA and virus genomes increased DNA buoyant density in CsCl gradients but resulted in co-migration with dominant non-enriched high GC mol% genomes, reducing sequencing depth and contig assembly. We therefore developed a hybrid approach where AOA and virus genomes were assembled from low buoyant density DNA with subsequent mapping of (13)C isotopically enriched high buoyant density DNA reads to identify activity of AOA. Metagenome-assembled genomes were different between the two soils and represented a broad diversity of active populations. Sixty-four AOA-infecting viral operational taxonomic units (vOTUs) were identified with no clear relatedness to previously characterised prokaryote viruses. These vOTUs were also distinct between soils, with 42% enriched in (13)C derived from hosts. The majority were predicted as capable of lysogeny and auxiliary metabolic genes included an AOA-specific multicopper oxidase suggesting infection may augment copper uptake essential for central metabolic functioning. These findings indicate virus infection of AOA may be a frequent process during nitrification with potential to influence host physiology and activity. Nature Publishing Group UK 2022-11-21 2023-02 /pmc/articles/PMC9859776/ /pubmed/36414709 http://dx.doi.org/10.1038/s41396-022-01341-5 Text en © The Author(s) 2022 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 | Brief Communication Lee, Sungeun Sieradzki, Ella T. Nicol, Graeme W. Hazard, Christina Propagation of viral genomes by replicating ammonia-oxidising archaea during soil nitrification |
title | Propagation of viral genomes by replicating ammonia-oxidising archaea during soil nitrification |
title_full | Propagation of viral genomes by replicating ammonia-oxidising archaea during soil nitrification |
title_fullStr | Propagation of viral genomes by replicating ammonia-oxidising archaea during soil nitrification |
title_full_unstemmed | Propagation of viral genomes by replicating ammonia-oxidising archaea during soil nitrification |
title_short | Propagation of viral genomes by replicating ammonia-oxidising archaea during soil nitrification |
title_sort | propagation of viral genomes by replicating ammonia-oxidising archaea during soil nitrification |
topic | Brief Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9859776/ https://www.ncbi.nlm.nih.gov/pubmed/36414709 http://dx.doi.org/10.1038/s41396-022-01341-5 |
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