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The effects of spatial structure, frequency dependence and resistance evolution on the dynamics of toxin-mediated microbial invasions

Recent evidence suggests that interference competition between bacteria shapes the distribution of the opportunistic pathogen Staphylococcus aureus in the lower nasal airway of humans, either by preventing colonization or by driving displacement. This competition within the nasal microbial community...

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Autores principales: Libberton, Ben, Horsburgh, Malcolm J, Brockhurst, Michael A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4516424/
https://www.ncbi.nlm.nih.gov/pubmed/26240609
http://dx.doi.org/10.1111/eva.12284
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author Libberton, Ben
Horsburgh, Malcolm J
Brockhurst, Michael A
author_facet Libberton, Ben
Horsburgh, Malcolm J
Brockhurst, Michael A
author_sort Libberton, Ben
collection PubMed
description Recent evidence suggests that interference competition between bacteria shapes the distribution of the opportunistic pathogen Staphylococcus aureus in the lower nasal airway of humans, either by preventing colonization or by driving displacement. This competition within the nasal microbial community would add to known host factors that affect colonization. We tested the role of toxin-mediated interference competition in both structured and unstructured environments, by culturing S. aureus with toxin-producing or nonproducing Staphylococcus epidermidis nasal isolates. Toxin-producing S. epidermidis invaded S. aureus populations more successfully than nonproducers, and invasion was promoted by spatial structure. Complete displacement of S. aureus was prevented by the evolution of toxin resistance. Conversely, toxin-producing S. epidermidis restricted S. aureus invasion. Invasion of toxin-producing S. epidermidis populations by S. aureus resulted from the evolution of toxin resistance, which was favoured by high initial frequency and low spatial structure. Enhanced toxin production also evolved in some invading populations of S. epidermidis. Toxin production therefore promoted invasion by, and constrained invasion into, populations of producers. Spatial structure enhanced both of these invasion effects. Our findings suggest that manipulation of the nasal microbial community could be used to limit colonization by S. aureus, which might limit transmission and infection rates.
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spelling pubmed-45164242015-08-03 The effects of spatial structure, frequency dependence and resistance evolution on the dynamics of toxin-mediated microbial invasions Libberton, Ben Horsburgh, Malcolm J Brockhurst, Michael A Evol Appl Original Articles Recent evidence suggests that interference competition between bacteria shapes the distribution of the opportunistic pathogen Staphylococcus aureus in the lower nasal airway of humans, either by preventing colonization or by driving displacement. This competition within the nasal microbial community would add to known host factors that affect colonization. We tested the role of toxin-mediated interference competition in both structured and unstructured environments, by culturing S. aureus with toxin-producing or nonproducing Staphylococcus epidermidis nasal isolates. Toxin-producing S. epidermidis invaded S. aureus populations more successfully than nonproducers, and invasion was promoted by spatial structure. Complete displacement of S. aureus was prevented by the evolution of toxin resistance. Conversely, toxin-producing S. epidermidis restricted S. aureus invasion. Invasion of toxin-producing S. epidermidis populations by S. aureus resulted from the evolution of toxin resistance, which was favoured by high initial frequency and low spatial structure. Enhanced toxin production also evolved in some invading populations of S. epidermidis. Toxin production therefore promoted invasion by, and constrained invasion into, populations of producers. Spatial structure enhanced both of these invasion effects. Our findings suggest that manipulation of the nasal microbial community could be used to limit colonization by S. aureus, which might limit transmission and infection rates. John Wiley & Sons, Ltd 2015-08 2015-07-16 /pmc/articles/PMC4516424/ /pubmed/26240609 http://dx.doi.org/10.1111/eva.12284 Text en © 2015 The Authors. Evolutionary Applications published by John Wiley & Sons Ltd. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Libberton, Ben
Horsburgh, Malcolm J
Brockhurst, Michael A
The effects of spatial structure, frequency dependence and resistance evolution on the dynamics of toxin-mediated microbial invasions
title The effects of spatial structure, frequency dependence and resistance evolution on the dynamics of toxin-mediated microbial invasions
title_full The effects of spatial structure, frequency dependence and resistance evolution on the dynamics of toxin-mediated microbial invasions
title_fullStr The effects of spatial structure, frequency dependence and resistance evolution on the dynamics of toxin-mediated microbial invasions
title_full_unstemmed The effects of spatial structure, frequency dependence and resistance evolution on the dynamics of toxin-mediated microbial invasions
title_short The effects of spatial structure, frequency dependence and resistance evolution on the dynamics of toxin-mediated microbial invasions
title_sort effects of spatial structure, frequency dependence and resistance evolution on the dynamics of toxin-mediated microbial invasions
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4516424/
https://www.ncbi.nlm.nih.gov/pubmed/26240609
http://dx.doi.org/10.1111/eva.12284
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