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The association of prokaryotic antiviral systems and symbiotic phage communities in drinking water microbiomes

Prokaryotic antiviral systems are important mediators for prokaryote-phage interactions, which have significant implications for the survival of prokaryotic community. However, the prokaryotic antiviral systems under environmental stress are poorly understood, limiting the understanding of microbial...

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Autores principales: Huang, Dan, Yuan, Mengting Maggie, Chen, Juhong, Zheng, Xiaoxuan, Wong, Dongsheng, Alvarez, Pedro J. J., Yu, Pingfeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10160068/
https://www.ncbi.nlm.nih.gov/pubmed/37142716
http://dx.doi.org/10.1038/s43705-023-00249-1
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author Huang, Dan
Yuan, Mengting Maggie
Chen, Juhong
Zheng, Xiaoxuan
Wong, Dongsheng
Alvarez, Pedro J. J.
Yu, Pingfeng
author_facet Huang, Dan
Yuan, Mengting Maggie
Chen, Juhong
Zheng, Xiaoxuan
Wong, Dongsheng
Alvarez, Pedro J. J.
Yu, Pingfeng
author_sort Huang, Dan
collection PubMed
description Prokaryotic antiviral systems are important mediators for prokaryote-phage interactions, which have significant implications for the survival of prokaryotic community. However, the prokaryotic antiviral systems under environmental stress are poorly understood, limiting the understanding of microbial adaptability. Here, we systematically investigated the profile of the prokaryotic antiviral systems at the community level and prokaryote-phage interactions in the drinking water microbiome. Chlorine disinfectant was revealed as the main ecological driver for the difference in prokaryotic antiviral systems and prokaryote-phage interactions. Specifically, the prokaryotic antiviral systems in the microbiome exhibited a higher abundance, broader antiviral spectrum, and lower metabolic burden under disinfectant stress. Moreover, significant positive correlations were observed between phage lysogenicity and enrichment of antiviral systems (e.g., Type IIG and IV restriction-modification (RM) systems, and Type II CRISPR-Cas system) in the presence of disinfection, indicating these antiviral systems might be more compatible with lysogenic phages and prophages. Accordingly, there was a stronger prokaryote-phage symbiosis in disinfected microbiome, and the symbiotic phages carried more auxiliary metabolic genes (AMGs) related to prokaryotic adaptability as well as antiviral systems, which might further enhance prokaryote survival in drinking water distribution systems. Overall, this study demonstrates that the prokaryotic antiviral systems had a close association with their symbiotic phages, which provides novel insights into prokaryote-phage interactions and microbial environmental adaptation.
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spelling pubmed-101600682023-05-06 The association of prokaryotic antiviral systems and symbiotic phage communities in drinking water microbiomes Huang, Dan Yuan, Mengting Maggie Chen, Juhong Zheng, Xiaoxuan Wong, Dongsheng Alvarez, Pedro J. J. Yu, Pingfeng ISME Commun Article Prokaryotic antiviral systems are important mediators for prokaryote-phage interactions, which have significant implications for the survival of prokaryotic community. However, the prokaryotic antiviral systems under environmental stress are poorly understood, limiting the understanding of microbial adaptability. Here, we systematically investigated the profile of the prokaryotic antiviral systems at the community level and prokaryote-phage interactions in the drinking water microbiome. Chlorine disinfectant was revealed as the main ecological driver for the difference in prokaryotic antiviral systems and prokaryote-phage interactions. Specifically, the prokaryotic antiviral systems in the microbiome exhibited a higher abundance, broader antiviral spectrum, and lower metabolic burden under disinfectant stress. Moreover, significant positive correlations were observed between phage lysogenicity and enrichment of antiviral systems (e.g., Type IIG and IV restriction-modification (RM) systems, and Type II CRISPR-Cas system) in the presence of disinfection, indicating these antiviral systems might be more compatible with lysogenic phages and prophages. Accordingly, there was a stronger prokaryote-phage symbiosis in disinfected microbiome, and the symbiotic phages carried more auxiliary metabolic genes (AMGs) related to prokaryotic adaptability as well as antiviral systems, which might further enhance prokaryote survival in drinking water distribution systems. Overall, this study demonstrates that the prokaryotic antiviral systems had a close association with their symbiotic phages, which provides novel insights into prokaryote-phage interactions and microbial environmental adaptation. Nature Publishing Group UK 2023-05-04 /pmc/articles/PMC10160068/ /pubmed/37142716 http://dx.doi.org/10.1038/s43705-023-00249-1 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
Huang, Dan
Yuan, Mengting Maggie
Chen, Juhong
Zheng, Xiaoxuan
Wong, Dongsheng
Alvarez, Pedro J. J.
Yu, Pingfeng
The association of prokaryotic antiviral systems and symbiotic phage communities in drinking water microbiomes
title The association of prokaryotic antiviral systems and symbiotic phage communities in drinking water microbiomes
title_full The association of prokaryotic antiviral systems and symbiotic phage communities in drinking water microbiomes
title_fullStr The association of prokaryotic antiviral systems and symbiotic phage communities in drinking water microbiomes
title_full_unstemmed The association of prokaryotic antiviral systems and symbiotic phage communities in drinking water microbiomes
title_short The association of prokaryotic antiviral systems and symbiotic phage communities in drinking water microbiomes
title_sort association of prokaryotic antiviral systems and symbiotic phage communities in drinking water microbiomes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10160068/
https://www.ncbi.nlm.nih.gov/pubmed/37142716
http://dx.doi.org/10.1038/s43705-023-00249-1
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