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Mesophilic and thermophilic viruses are associated with nutrient cycling during hyperthermophilic composting
While decomposition of organic matter by bacteria plays a major role in nutrient cycling in terrestrial ecosystems, the significance of viruses remains poorly understood. Here we combined metagenomics and metatranscriptomics with temporal sampling to study the significance of mesophilic and thermoph...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10202948/ https://www.ncbi.nlm.nih.gov/pubmed/37031344 http://dx.doi.org/10.1038/s41396-023-01404-1 |
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author | Liao, Hanpeng Liu, Chen Ai, Chaofan Gao, Tian Yang, Qiu-E Yu, Zhen Gao, Shaoming Zhou, Shungui Friman, Ville-Petri |
author_facet | Liao, Hanpeng Liu, Chen Ai, Chaofan Gao, Tian Yang, Qiu-E Yu, Zhen Gao, Shaoming Zhou, Shungui Friman, Ville-Petri |
author_sort | Liao, Hanpeng |
collection | PubMed |
description | While decomposition of organic matter by bacteria plays a major role in nutrient cycling in terrestrial ecosystems, the significance of viruses remains poorly understood. Here we combined metagenomics and metatranscriptomics with temporal sampling to study the significance of mesophilic and thermophilic bacteria and their viruses on nutrient cycling during industrial-scale hyperthermophilic composting (HTC). Our results show that virus-bacteria density dynamics and activity are tightly coupled, where viruses specific to mesophilic and thermophilic bacteria track their host densities, triggering microbial community succession via top-down control during HTC. Moreover, viruses specific to mesophilic bacteria encoded and expressed several auxiliary metabolic genes (AMGs) linked to carbon cycling, impacting nutrient turnover alongside bacteria. Nutrient turnover correlated positively with virus–host ratio, indicative of a positive relationship between ecosystem functioning, viral abundances, and viral activity. These effects were predominantly driven by DNA viruses as most detected RNA viruses were associated with eukaryotes and not associated with nutrient cycling during the thermophilic phase of composting. Our findings suggest that DNA viruses could drive nutrient cycling during HTC by recycling bacterial biomass through cell lysis and by expressing key AMGs. Viruses could hence potentially be used as indicators of microbial ecosystem functioning to optimize productivity of biotechnological and agricultural systems. |
format | Online Article Text |
id | pubmed-10202948 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-102029482023-05-24 Mesophilic and thermophilic viruses are associated with nutrient cycling during hyperthermophilic composting Liao, Hanpeng Liu, Chen Ai, Chaofan Gao, Tian Yang, Qiu-E Yu, Zhen Gao, Shaoming Zhou, Shungui Friman, Ville-Petri ISME J Article While decomposition of organic matter by bacteria plays a major role in nutrient cycling in terrestrial ecosystems, the significance of viruses remains poorly understood. Here we combined metagenomics and metatranscriptomics with temporal sampling to study the significance of mesophilic and thermophilic bacteria and their viruses on nutrient cycling during industrial-scale hyperthermophilic composting (HTC). Our results show that virus-bacteria density dynamics and activity are tightly coupled, where viruses specific to mesophilic and thermophilic bacteria track their host densities, triggering microbial community succession via top-down control during HTC. Moreover, viruses specific to mesophilic bacteria encoded and expressed several auxiliary metabolic genes (AMGs) linked to carbon cycling, impacting nutrient turnover alongside bacteria. Nutrient turnover correlated positively with virus–host ratio, indicative of a positive relationship between ecosystem functioning, viral abundances, and viral activity. These effects were predominantly driven by DNA viruses as most detected RNA viruses were associated with eukaryotes and not associated with nutrient cycling during the thermophilic phase of composting. Our findings suggest that DNA viruses could drive nutrient cycling during HTC by recycling bacterial biomass through cell lysis and by expressing key AMGs. Viruses could hence potentially be used as indicators of microbial ecosystem functioning to optimize productivity of biotechnological and agricultural systems. Nature Publishing Group UK 2023-04-08 2023-06 /pmc/articles/PMC10202948/ /pubmed/37031344 http://dx.doi.org/10.1038/s41396-023-01404-1 Text en © The Author(s) 2023 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 Liao, Hanpeng Liu, Chen Ai, Chaofan Gao, Tian Yang, Qiu-E Yu, Zhen Gao, Shaoming Zhou, Shungui Friman, Ville-Petri Mesophilic and thermophilic viruses are associated with nutrient cycling during hyperthermophilic composting |
title | Mesophilic and thermophilic viruses are associated with nutrient cycling during hyperthermophilic composting |
title_full | Mesophilic and thermophilic viruses are associated with nutrient cycling during hyperthermophilic composting |
title_fullStr | Mesophilic and thermophilic viruses are associated with nutrient cycling during hyperthermophilic composting |
title_full_unstemmed | Mesophilic and thermophilic viruses are associated with nutrient cycling during hyperthermophilic composting |
title_short | Mesophilic and thermophilic viruses are associated with nutrient cycling during hyperthermophilic composting |
title_sort | mesophilic and thermophilic viruses are associated with nutrient cycling during hyperthermophilic composting |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10202948/ https://www.ncbi.nlm.nih.gov/pubmed/37031344 http://dx.doi.org/10.1038/s41396-023-01404-1 |
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