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Benzo[a]pyrene stress impacts adaptive strategies and ecological functions of earthworm intestinal viromes

The earthworm gut virome influences the structure and function of the gut microbiome, which in turn influences worm health and ecological functions. However, despite its ecological and soil quality implications, it remains elusive how earthworm intestinal phages respond to different environmental st...

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Autores principales: Xia, Rong, Sun, Mingming, Balcázar, José Luis, Yu, Pingfeng, Hu, Feng, Alvarez, Pedro J. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10284932/
https://www.ncbi.nlm.nih.gov/pubmed/37069233
http://dx.doi.org/10.1038/s41396-023-01408-x
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author Xia, Rong
Sun, Mingming
Balcázar, José Luis
Yu, Pingfeng
Hu, Feng
Alvarez, Pedro J. J.
author_facet Xia, Rong
Sun, Mingming
Balcázar, José Luis
Yu, Pingfeng
Hu, Feng
Alvarez, Pedro J. J.
author_sort Xia, Rong
collection PubMed
description The earthworm gut virome influences the structure and function of the gut microbiome, which in turn influences worm health and ecological functions. However, despite its ecological and soil quality implications, it remains elusive how earthworm intestinal phages respond to different environmental stress, such as soil pollution. Here we used metagenomics and metatranscriptomics to investigate interactions between the worm intestinal phages and their bacteria under different benzo[a]pyrene (BaP) concentrations. Low-level BaP (0.1 mg kg(−1)) stress stimulated microbial metabolism (1.74-fold to control), and enhanced the antiphage defense system (n = 75) against infection (8 phage-host pairs). Low-level BaP exposure resulted in the highest proportion of lysogenic phages (88%), and prophages expressed auxiliary metabolic genes (AMGs) associated with nutrient transformation (e.g., amino acid metabolism). In contrast, high-level BaP exposure (200 mg kg(−1)) disrupted microbial metabolism and suppressed the antiphage systems (n = 29), leading to the increase in phage-bacterium association (37 phage-host pairs) and conversion of lysogenic to lytic phages (lysogenic ratio declined to 43%). Despite fluctuating phage-bacterium interactions, phage-encoded AMGs related to microbial antioxidant and pollutant degradation were enriched, apparently to alleviate pollution stress. Overall, these findings expand our knowledge of complex phage-bacterium interactions in pollution-stressed worm guts, and deepen our understanding of the ecological and evolutionary roles of phages.
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spelling pubmed-102849322023-06-23 Benzo[a]pyrene stress impacts adaptive strategies and ecological functions of earthworm intestinal viromes Xia, Rong Sun, Mingming Balcázar, José Luis Yu, Pingfeng Hu, Feng Alvarez, Pedro J. J. ISME J Article The earthworm gut virome influences the structure and function of the gut microbiome, which in turn influences worm health and ecological functions. However, despite its ecological and soil quality implications, it remains elusive how earthworm intestinal phages respond to different environmental stress, such as soil pollution. Here we used metagenomics and metatranscriptomics to investigate interactions between the worm intestinal phages and their bacteria under different benzo[a]pyrene (BaP) concentrations. Low-level BaP (0.1 mg kg(−1)) stress stimulated microbial metabolism (1.74-fold to control), and enhanced the antiphage defense system (n = 75) against infection (8 phage-host pairs). Low-level BaP exposure resulted in the highest proportion of lysogenic phages (88%), and prophages expressed auxiliary metabolic genes (AMGs) associated with nutrient transformation (e.g., amino acid metabolism). In contrast, high-level BaP exposure (200 mg kg(−1)) disrupted microbial metabolism and suppressed the antiphage systems (n = 29), leading to the increase in phage-bacterium association (37 phage-host pairs) and conversion of lysogenic to lytic phages (lysogenic ratio declined to 43%). Despite fluctuating phage-bacterium interactions, phage-encoded AMGs related to microbial antioxidant and pollutant degradation were enriched, apparently to alleviate pollution stress. Overall, these findings expand our knowledge of complex phage-bacterium interactions in pollution-stressed worm guts, and deepen our understanding of the ecological and evolutionary roles of phages. Nature Publishing Group UK 2023-04-17 2023-07 /pmc/articles/PMC10284932/ /pubmed/37069233 http://dx.doi.org/10.1038/s41396-023-01408-x 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
Xia, Rong
Sun, Mingming
Balcázar, José Luis
Yu, Pingfeng
Hu, Feng
Alvarez, Pedro J. J.
Benzo[a]pyrene stress impacts adaptive strategies and ecological functions of earthworm intestinal viromes
title Benzo[a]pyrene stress impacts adaptive strategies and ecological functions of earthworm intestinal viromes
title_full Benzo[a]pyrene stress impacts adaptive strategies and ecological functions of earthworm intestinal viromes
title_fullStr Benzo[a]pyrene stress impacts adaptive strategies and ecological functions of earthworm intestinal viromes
title_full_unstemmed Benzo[a]pyrene stress impacts adaptive strategies and ecological functions of earthworm intestinal viromes
title_short Benzo[a]pyrene stress impacts adaptive strategies and ecological functions of earthworm intestinal viromes
title_sort benzo[a]pyrene stress impacts adaptive strategies and ecological functions of earthworm intestinal viromes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10284932/
https://www.ncbi.nlm.nih.gov/pubmed/37069233
http://dx.doi.org/10.1038/s41396-023-01408-x
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