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Spatial structure affects phage efficacy in infecting dual-strain biofilms of Pseudomonas aeruginosa

Bacterial viruses, or phage, are key members of natural microbial communities. Yet much research on bacterial-phage interactions has been conducted in liquid cultures involving single bacterial strains. Here we explored how bacterial diversity affects the success of lytic phage in structured communi...

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Autores principales: Testa, Samuele, Berger, Sarah, Piccardi, Philippe, Oechslin, Frank, Resch, Grégory, Mitri, Sara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6828766/
https://www.ncbi.nlm.nih.gov/pubmed/31701033
http://dx.doi.org/10.1038/s42003-019-0633-x
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author Testa, Samuele
Berger, Sarah
Piccardi, Philippe
Oechslin, Frank
Resch, Grégory
Mitri, Sara
author_facet Testa, Samuele
Berger, Sarah
Piccardi, Philippe
Oechslin, Frank
Resch, Grégory
Mitri, Sara
author_sort Testa, Samuele
collection PubMed
description Bacterial viruses, or phage, are key members of natural microbial communities. Yet much research on bacterial-phage interactions has been conducted in liquid cultures involving single bacterial strains. Here we explored how bacterial diversity affects the success of lytic phage in structured communities. We infected a sensitive Pseudomonas aeruginosa strain PAO1 with a lytic phage Pseudomonas 352 in the presence versus absence of an insensitive P. aeruginosa strain PA14, in liquid culture versus colonies on agar. We found that both in liquid and in colonies, inter-strain competition reduced resistance evolution in the susceptible strain and decreased phage population size. However, while all sensitive bacteria died in liquid, bacteria in colonies could remain sensitive yet escape phage infection, due mainly to reduced growth in colony centers. In sum, spatial structure can protect bacteria against phage infection, while the presence of competing strains reduces the evolution of resistance to phage.
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spelling pubmed-68287662019-11-07 Spatial structure affects phage efficacy in infecting dual-strain biofilms of Pseudomonas aeruginosa Testa, Samuele Berger, Sarah Piccardi, Philippe Oechslin, Frank Resch, Grégory Mitri, Sara Commun Biol Article Bacterial viruses, or phage, are key members of natural microbial communities. Yet much research on bacterial-phage interactions has been conducted in liquid cultures involving single bacterial strains. Here we explored how bacterial diversity affects the success of lytic phage in structured communities. We infected a sensitive Pseudomonas aeruginosa strain PAO1 with a lytic phage Pseudomonas 352 in the presence versus absence of an insensitive P. aeruginosa strain PA14, in liquid culture versus colonies on agar. We found that both in liquid and in colonies, inter-strain competition reduced resistance evolution in the susceptible strain and decreased phage population size. However, while all sensitive bacteria died in liquid, bacteria in colonies could remain sensitive yet escape phage infection, due mainly to reduced growth in colony centers. In sum, spatial structure can protect bacteria against phage infection, while the presence of competing strains reduces the evolution of resistance to phage. Nature Publishing Group UK 2019-11-04 /pmc/articles/PMC6828766/ /pubmed/31701033 http://dx.doi.org/10.1038/s42003-019-0633-x 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
Testa, Samuele
Berger, Sarah
Piccardi, Philippe
Oechslin, Frank
Resch, Grégory
Mitri, Sara
Spatial structure affects phage efficacy in infecting dual-strain biofilms of Pseudomonas aeruginosa
title Spatial structure affects phage efficacy in infecting dual-strain biofilms of Pseudomonas aeruginosa
title_full Spatial structure affects phage efficacy in infecting dual-strain biofilms of Pseudomonas aeruginosa
title_fullStr Spatial structure affects phage efficacy in infecting dual-strain biofilms of Pseudomonas aeruginosa
title_full_unstemmed Spatial structure affects phage efficacy in infecting dual-strain biofilms of Pseudomonas aeruginosa
title_short Spatial structure affects phage efficacy in infecting dual-strain biofilms of Pseudomonas aeruginosa
title_sort spatial structure affects phage efficacy in infecting dual-strain biofilms of pseudomonas aeruginosa
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6828766/
https://www.ncbi.nlm.nih.gov/pubmed/31701033
http://dx.doi.org/10.1038/s42003-019-0633-x
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