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Environmental structure drives resistance to phages and antibiotics during phage therapy and to invading lysogens during colonisation

Microbial communities are shaped by bacteriophages through predation and lysogeny. A better understanding of the interactions between these processes across different types of environments is key to elucidate how phages mediate microbial competition and to design efficient phage therapies. We introd...

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Autores principales: Sousa, Jorge A. Moura de, Rocha, Eduardo P. C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6395636/
https://www.ncbi.nlm.nih.gov/pubmed/30816246
http://dx.doi.org/10.1038/s41598-019-39773-3
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author Sousa, Jorge A. Moura de
Rocha, Eduardo P. C.
author_facet Sousa, Jorge A. Moura de
Rocha, Eduardo P. C.
author_sort Sousa, Jorge A. Moura de
collection PubMed
description Microbial communities are shaped by bacteriophages through predation and lysogeny. A better understanding of the interactions between these processes across different types of environments is key to elucidate how phages mediate microbial competition and to design efficient phage therapies. We introduce an individual-based model (eVIVALDI) to investigate the role of environmental structure in the elimination of a population with a combined treatment of antibiotics and virulent phages, and in the invasion of a population of phage-sensitive bacteria by lysogens. We show that structured environments facilitate the emergence of double resistance, to antibiotics and phages, due to limited diffusion of phage particles and increased nutrient availability from dead cells. They also hinder phage amplification, thus decreasing the generation of phage genetic diversity and increasing the unpredictability of phage-bacteria arms-races. We used a machine learning approach to determine the variables most important for the invasion of sensitive populations by lysogens. They revealed that phage-associated traits and environmental structure are the key drivers of the process. Structured environments hinder invasions, and accounting for their existence improves the fit of the model to published in vivo experimental data. Our results underline environmental structure as key to understand in vivo phage-bacteria interactions.
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spelling pubmed-63956362019-03-04 Environmental structure drives resistance to phages and antibiotics during phage therapy and to invading lysogens during colonisation Sousa, Jorge A. Moura de Rocha, Eduardo P. C. Sci Rep Article Microbial communities are shaped by bacteriophages through predation and lysogeny. A better understanding of the interactions between these processes across different types of environments is key to elucidate how phages mediate microbial competition and to design efficient phage therapies. We introduce an individual-based model (eVIVALDI) to investigate the role of environmental structure in the elimination of a population with a combined treatment of antibiotics and virulent phages, and in the invasion of a population of phage-sensitive bacteria by lysogens. We show that structured environments facilitate the emergence of double resistance, to antibiotics and phages, due to limited diffusion of phage particles and increased nutrient availability from dead cells. They also hinder phage amplification, thus decreasing the generation of phage genetic diversity and increasing the unpredictability of phage-bacteria arms-races. We used a machine learning approach to determine the variables most important for the invasion of sensitive populations by lysogens. They revealed that phage-associated traits and environmental structure are the key drivers of the process. Structured environments hinder invasions, and accounting for their existence improves the fit of the model to published in vivo experimental data. Our results underline environmental structure as key to understand in vivo phage-bacteria interactions. Nature Publishing Group UK 2019-02-28 /pmc/articles/PMC6395636/ /pubmed/30816246 http://dx.doi.org/10.1038/s41598-019-39773-3 Text en © The Author(s) 2019 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/.
spellingShingle Article
Sousa, Jorge A. Moura de
Rocha, Eduardo P. C.
Environmental structure drives resistance to phages and antibiotics during phage therapy and to invading lysogens during colonisation
title Environmental structure drives resistance to phages and antibiotics during phage therapy and to invading lysogens during colonisation
title_full Environmental structure drives resistance to phages and antibiotics during phage therapy and to invading lysogens during colonisation
title_fullStr Environmental structure drives resistance to phages and antibiotics during phage therapy and to invading lysogens during colonisation
title_full_unstemmed Environmental structure drives resistance to phages and antibiotics during phage therapy and to invading lysogens during colonisation
title_short Environmental structure drives resistance to phages and antibiotics during phage therapy and to invading lysogens during colonisation
title_sort environmental structure drives resistance to phages and antibiotics during phage therapy and to invading lysogens during colonisation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6395636/
https://www.ncbi.nlm.nih.gov/pubmed/30816246
http://dx.doi.org/10.1038/s41598-019-39773-3
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