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Viral community-wide auxiliary metabolic genes differ by lifestyles, habitats, and hosts

BACKGROUND: Viral-encoded auxiliary metabolic genes (AMGs) are important toolkits for modulating their hosts’ metabolisms and the microbial-driven biogeochemical cycles. Although the functions of AMGs have been extensively reported in numerous environments, we still know little about the drivers tha...

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Autores principales: Luo, Xiao-Qing, Wang, Pandeng, Li, Jia-Ling, Ahmad, Manzoor, Duan, Li, Yin, Ling-Zi, Deng, Qi-Qi, Fang, Bao-Zhu, Li, Shan-Hui, Li, Wen-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9636769/
https://www.ncbi.nlm.nih.gov/pubmed/36333738
http://dx.doi.org/10.1186/s40168-022-01384-y
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author Luo, Xiao-Qing
Wang, Pandeng
Li, Jia-Ling
Ahmad, Manzoor
Duan, Li
Yin, Ling-Zi
Deng, Qi-Qi
Fang, Bao-Zhu
Li, Shan-Hui
Li, Wen-Jun
author_facet Luo, Xiao-Qing
Wang, Pandeng
Li, Jia-Ling
Ahmad, Manzoor
Duan, Li
Yin, Ling-Zi
Deng, Qi-Qi
Fang, Bao-Zhu
Li, Shan-Hui
Li, Wen-Jun
author_sort Luo, Xiao-Qing
collection PubMed
description BACKGROUND: Viral-encoded auxiliary metabolic genes (AMGs) are important toolkits for modulating their hosts’ metabolisms and the microbial-driven biogeochemical cycles. Although the functions of AMGs have been extensively reported in numerous environments, we still know little about the drivers that shape the viral community-wide AMG compositions in natural ecosystems. Exploring the drivers of viral community-wide AMG compositions is critical for a deeper understanding of the complex interplays among viruses, hosts, and the environments. RESULTS: Here, we investigated the impact of viral lifestyles (i.e., lytic and lysogenic), habitats (i.e., water, particle, and sediment), and prokaryotic hosts on viral AMG profiles by utilizing metagenomic and metatranscriptomic techniques. We found that viral lifestyles were the most important drivers, followed by habitats and host identities. Specifically, irrespective of what habitats viruses came from, lytic viruses exhibited greater AMG diversity and tended to encode AMGs for chaperone biosynthesis, signaling proteins, and lipid metabolism, which could boost progeny reproduction, whereas temperate viruses were apt to encode AMGs for host survivability. Moreover, the lytic and temperate viral communities tended to mediate the microbial-driven biogeochemical cycles, especially nitrogen metabolism, in different manners via AMGs. When focusing on each lifestyle, we further found clear dissimilarity in AMG compositions between water and sediment, as well the divergent AMGs encoded by viruses infecting different host orders. CONCLUSIONS: Overall, our study provides a first systematic characterization of the drivers of viral community-wide AMG compositions and further expands our knowledge of the distinct interactions of lytic and temperate viruses with their prokaryotic hosts from an AMG perspective, which is critical for understanding virus-host-environment interactions in natural conditions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01384-y.
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spelling pubmed-96367692022-11-06 Viral community-wide auxiliary metabolic genes differ by lifestyles, habitats, and hosts Luo, Xiao-Qing Wang, Pandeng Li, Jia-Ling Ahmad, Manzoor Duan, Li Yin, Ling-Zi Deng, Qi-Qi Fang, Bao-Zhu Li, Shan-Hui Li, Wen-Jun Microbiome Research BACKGROUND: Viral-encoded auxiliary metabolic genes (AMGs) are important toolkits for modulating their hosts’ metabolisms and the microbial-driven biogeochemical cycles. Although the functions of AMGs have been extensively reported in numerous environments, we still know little about the drivers that shape the viral community-wide AMG compositions in natural ecosystems. Exploring the drivers of viral community-wide AMG compositions is critical for a deeper understanding of the complex interplays among viruses, hosts, and the environments. RESULTS: Here, we investigated the impact of viral lifestyles (i.e., lytic and lysogenic), habitats (i.e., water, particle, and sediment), and prokaryotic hosts on viral AMG profiles by utilizing metagenomic and metatranscriptomic techniques. We found that viral lifestyles were the most important drivers, followed by habitats and host identities. Specifically, irrespective of what habitats viruses came from, lytic viruses exhibited greater AMG diversity and tended to encode AMGs for chaperone biosynthesis, signaling proteins, and lipid metabolism, which could boost progeny reproduction, whereas temperate viruses were apt to encode AMGs for host survivability. Moreover, the lytic and temperate viral communities tended to mediate the microbial-driven biogeochemical cycles, especially nitrogen metabolism, in different manners via AMGs. When focusing on each lifestyle, we further found clear dissimilarity in AMG compositions between water and sediment, as well the divergent AMGs encoded by viruses infecting different host orders. CONCLUSIONS: Overall, our study provides a first systematic characterization of the drivers of viral community-wide AMG compositions and further expands our knowledge of the distinct interactions of lytic and temperate viruses with their prokaryotic hosts from an AMG perspective, which is critical for understanding virus-host-environment interactions in natural conditions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01384-y. BioMed Central 2022-11-05 /pmc/articles/PMC9636769/ /pubmed/36333738 http://dx.doi.org/10.1186/s40168-022-01384-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Luo, Xiao-Qing
Wang, Pandeng
Li, Jia-Ling
Ahmad, Manzoor
Duan, Li
Yin, Ling-Zi
Deng, Qi-Qi
Fang, Bao-Zhu
Li, Shan-Hui
Li, Wen-Jun
Viral community-wide auxiliary metabolic genes differ by lifestyles, habitats, and hosts
title Viral community-wide auxiliary metabolic genes differ by lifestyles, habitats, and hosts
title_full Viral community-wide auxiliary metabolic genes differ by lifestyles, habitats, and hosts
title_fullStr Viral community-wide auxiliary metabolic genes differ by lifestyles, habitats, and hosts
title_full_unstemmed Viral community-wide auxiliary metabolic genes differ by lifestyles, habitats, and hosts
title_short Viral community-wide auxiliary metabolic genes differ by lifestyles, habitats, and hosts
title_sort viral community-wide auxiliary metabolic genes differ by lifestyles, habitats, and hosts
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9636769/
https://www.ncbi.nlm.nih.gov/pubmed/36333738
http://dx.doi.org/10.1186/s40168-022-01384-y
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