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Protistan predation selects for antibiotic resistance in soil bacterial communities

Understanding how antibiotic resistance emerges and evolves in natural habitats is critical for predicting and mitigating antibiotic resistance in the context of global change. Bacteria have evolved antibiotic production as a strategy to fight competitors, predators and other stressors, but how pred...

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Autores principales: Nguyen, Thi Bao-Anh, Bonkowski, Michael, Dumack, Kenneth, Chen, Qing-Lin, He, Ji-Zheng, Hu, Hang-Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10689782/
https://www.ncbi.nlm.nih.gov/pubmed/37794244
http://dx.doi.org/10.1038/s41396-023-01524-8
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author Nguyen, Thi Bao-Anh
Bonkowski, Michael
Dumack, Kenneth
Chen, Qing-Lin
He, Ji-Zheng
Hu, Hang-Wei
author_facet Nguyen, Thi Bao-Anh
Bonkowski, Michael
Dumack, Kenneth
Chen, Qing-Lin
He, Ji-Zheng
Hu, Hang-Wei
author_sort Nguyen, Thi Bao-Anh
collection PubMed
description Understanding how antibiotic resistance emerges and evolves in natural habitats is critical for predicting and mitigating antibiotic resistance in the context of global change. Bacteria have evolved antibiotic production as a strategy to fight competitors, predators and other stressors, but how predation pressure of their most important consumers (i.e., protists) affects soil antibiotic resistance genes (ARGs) profiles is still poorly understood. To address this gap, we investigated responses of soil resistome to varying levels of protistan predation by inoculating low, medium and high concentrations of indigenous soil protist suspensions in soil microcosms. We found that an increase in protistan predation pressure was strongly associated with higher abundance and diversity of soil ARGs. High protist concentrations significantly enhanced the abundances of ARGs encoding multidrug (oprJ and ttgB genes) and tetracycline (tetV) efflux pump by 608%, 724% and 3052%, respectively. Additionally, we observed an increase in the abundance of numerous bacterial genera under high protistan pressure. Our findings provide empirical evidence that protistan predation significantly promotes antibiotic resistance in soil bacterial communities and advances our understanding of the biological driving forces behind the evolution and development of environmental antibiotic resistance.
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spelling pubmed-106897822023-12-02 Protistan predation selects for antibiotic resistance in soil bacterial communities Nguyen, Thi Bao-Anh Bonkowski, Michael Dumack, Kenneth Chen, Qing-Lin He, Ji-Zheng Hu, Hang-Wei ISME J Article Understanding how antibiotic resistance emerges and evolves in natural habitats is critical for predicting and mitigating antibiotic resistance in the context of global change. Bacteria have evolved antibiotic production as a strategy to fight competitors, predators and other stressors, but how predation pressure of their most important consumers (i.e., protists) affects soil antibiotic resistance genes (ARGs) profiles is still poorly understood. To address this gap, we investigated responses of soil resistome to varying levels of protistan predation by inoculating low, medium and high concentrations of indigenous soil protist suspensions in soil microcosms. We found that an increase in protistan predation pressure was strongly associated with higher abundance and diversity of soil ARGs. High protist concentrations significantly enhanced the abundances of ARGs encoding multidrug (oprJ and ttgB genes) and tetracycline (tetV) efflux pump by 608%, 724% and 3052%, respectively. Additionally, we observed an increase in the abundance of numerous bacterial genera under high protistan pressure. Our findings provide empirical evidence that protistan predation significantly promotes antibiotic resistance in soil bacterial communities and advances our understanding of the biological driving forces behind the evolution and development of environmental antibiotic resistance. Nature Publishing Group UK 2023-10-04 2023-12 /pmc/articles/PMC10689782/ /pubmed/37794244 http://dx.doi.org/10.1038/s41396-023-01524-8 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 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
Nguyen, Thi Bao-Anh
Bonkowski, Michael
Dumack, Kenneth
Chen, Qing-Lin
He, Ji-Zheng
Hu, Hang-Wei
Protistan predation selects for antibiotic resistance in soil bacterial communities
title Protistan predation selects for antibiotic resistance in soil bacterial communities
title_full Protistan predation selects for antibiotic resistance in soil bacterial communities
title_fullStr Protistan predation selects for antibiotic resistance in soil bacterial communities
title_full_unstemmed Protistan predation selects for antibiotic resistance in soil bacterial communities
title_short Protistan predation selects for antibiotic resistance in soil bacterial communities
title_sort protistan predation selects for antibiotic resistance in soil bacterial communities
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10689782/
https://www.ncbi.nlm.nih.gov/pubmed/37794244
http://dx.doi.org/10.1038/s41396-023-01524-8
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