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Lysogenic bacteriophages encoding arsenic resistance determinants promote bacterial community adaptation to arsenic toxicity

Emerging evidence from genomics gives us a glimpse into the potential contribution of lysogenic bacteriophages (phages) to the environmental adaptability of their hosts. However, it is challenging to quantify this kind of contribution due to the lack of appropriate genetic markers and the associated...

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Autores principales: Tang, Xiang, Zhong, Linrui, Tang, Lin, Fan, Changzheng, Zhang, Baowei, Wang, Mier, Dong, Haoran, Zhou, Chengyun, Rensing, Christopher, Zhou, Shungui, Zeng, Guangming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10284793/
https://www.ncbi.nlm.nih.gov/pubmed/37161002
http://dx.doi.org/10.1038/s41396-023-01425-w
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author Tang, Xiang
Zhong, Linrui
Tang, Lin
Fan, Changzheng
Zhang, Baowei
Wang, Mier
Dong, Haoran
Zhou, Chengyun
Rensing, Christopher
Zhou, Shungui
Zeng, Guangming
author_facet Tang, Xiang
Zhong, Linrui
Tang, Lin
Fan, Changzheng
Zhang, Baowei
Wang, Mier
Dong, Haoran
Zhou, Chengyun
Rensing, Christopher
Zhou, Shungui
Zeng, Guangming
author_sort Tang, Xiang
collection PubMed
description Emerging evidence from genomics gives us a glimpse into the potential contribution of lysogenic bacteriophages (phages) to the environmental adaptability of their hosts. However, it is challenging to quantify this kind of contribution due to the lack of appropriate genetic markers and the associated controllable environmental factors. Here, based on the unique transformable nature of arsenic (the controllable environmental factor), a series of flooding microcosms was established to investigate the contribution of arsM-bearing lysogenic phages to their hosts’ adaptation to trivalent arsenic [As(III)] toxicity, where arsM is the marker gene associated with microbial As(III) detoxification. In the 15-day flooding period, the concentration of As(III) was significantly increased, and this elevated As(III) toxicity visibly inhibited the bacterial population, but the latter quickly adapted to As(III) toxicity. During the flooding period, some lysogenic phages re-infected new hosts after an early burst, while others persistently followed the productive cycle (i.e., lytic cycle). The unique phage-host interplay contributed to the rapid spread of arsM among soil microbiota, enabling the quick recovery of the bacterial community. Moreover, the higher abundance of arsM imparted a greater arsenic methylation capability to soil microbiota. Collectively, this study provides experimental evidence for lysogenic phages assisting their hosts in adapting to an extreme environment, which highlights the ecological perspectives on lysogenic phage-host mutualism. [Image: see text]
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spelling pubmed-102847932023-06-23 Lysogenic bacteriophages encoding arsenic resistance determinants promote bacterial community adaptation to arsenic toxicity Tang, Xiang Zhong, Linrui Tang, Lin Fan, Changzheng Zhang, Baowei Wang, Mier Dong, Haoran Zhou, Chengyun Rensing, Christopher Zhou, Shungui Zeng, Guangming ISME J Article Emerging evidence from genomics gives us a glimpse into the potential contribution of lysogenic bacteriophages (phages) to the environmental adaptability of their hosts. However, it is challenging to quantify this kind of contribution due to the lack of appropriate genetic markers and the associated controllable environmental factors. Here, based on the unique transformable nature of arsenic (the controllable environmental factor), a series of flooding microcosms was established to investigate the contribution of arsM-bearing lysogenic phages to their hosts’ adaptation to trivalent arsenic [As(III)] toxicity, where arsM is the marker gene associated with microbial As(III) detoxification. In the 15-day flooding period, the concentration of As(III) was significantly increased, and this elevated As(III) toxicity visibly inhibited the bacterial population, but the latter quickly adapted to As(III) toxicity. During the flooding period, some lysogenic phages re-infected new hosts after an early burst, while others persistently followed the productive cycle (i.e., lytic cycle). The unique phage-host interplay contributed to the rapid spread of arsM among soil microbiota, enabling the quick recovery of the bacterial community. Moreover, the higher abundance of arsM imparted a greater arsenic methylation capability to soil microbiota. Collectively, this study provides experimental evidence for lysogenic phages assisting their hosts in adapting to an extreme environment, which highlights the ecological perspectives on lysogenic phage-host mutualism. [Image: see text] Nature Publishing Group UK 2023-05-09 2023-07 /pmc/articles/PMC10284793/ /pubmed/37161002 http://dx.doi.org/10.1038/s41396-023-01425-w Text en © The Author(s) 2023, corrected publication 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 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/) .
spellingShingle Article
Tang, Xiang
Zhong, Linrui
Tang, Lin
Fan, Changzheng
Zhang, Baowei
Wang, Mier
Dong, Haoran
Zhou, Chengyun
Rensing, Christopher
Zhou, Shungui
Zeng, Guangming
Lysogenic bacteriophages encoding arsenic resistance determinants promote bacterial community adaptation to arsenic toxicity
title Lysogenic bacteriophages encoding arsenic resistance determinants promote bacterial community adaptation to arsenic toxicity
title_full Lysogenic bacteriophages encoding arsenic resistance determinants promote bacterial community adaptation to arsenic toxicity
title_fullStr Lysogenic bacteriophages encoding arsenic resistance determinants promote bacterial community adaptation to arsenic toxicity
title_full_unstemmed Lysogenic bacteriophages encoding arsenic resistance determinants promote bacterial community adaptation to arsenic toxicity
title_short Lysogenic bacteriophages encoding arsenic resistance determinants promote bacterial community adaptation to arsenic toxicity
title_sort lysogenic bacteriophages encoding arsenic resistance determinants promote bacterial community adaptation to arsenic toxicity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10284793/
https://www.ncbi.nlm.nih.gov/pubmed/37161002
http://dx.doi.org/10.1038/s41396-023-01425-w
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