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The evolution of antibiotic production rate in a spatial model of bacterial competition

We consider competition between antibiotic producing bacteria, non-producers (or cheaters), and sensitive cells in a two-dimensional lattice model. Previous work has shown that these three cell types can survive in spatial models due to the presence of spatial patterns, whereas coexistence is not po...

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Autores principales: Kosakowski, Jakub, Verma, Prateek, Sengupta, Supratim, Higgs, Paul G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6209167/
https://www.ncbi.nlm.nih.gov/pubmed/30379843
http://dx.doi.org/10.1371/journal.pone.0205202
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author Kosakowski, Jakub
Verma, Prateek
Sengupta, Supratim
Higgs, Paul G.
author_facet Kosakowski, Jakub
Verma, Prateek
Sengupta, Supratim
Higgs, Paul G.
author_sort Kosakowski, Jakub
collection PubMed
description We consider competition between antibiotic producing bacteria, non-producers (or cheaters), and sensitive cells in a two-dimensional lattice model. Previous work has shown that these three cell types can survive in spatial models due to the presence of spatial patterns, whereas coexistence is not possible in a well-mixed system. We extend this to consider the evolution of the antibiotic production rate, assuming that the cost of antibiotic production leads to a reduction in growth rate of the producers. We find that coexistence occurs for an intermediate range of antibiotic production rate. If production rate is too high or too low, only sensitive cells survive. When evolution of production rate is allowed, a mixture of cell types arises in which there is a dominant producer strain that produces sufficient to limit the growth of sensitive cells and which is able to withstand the presence of cheaters in its own species. The mixture includes a range of low-rate producers and non-producers, none of which could survive without the presence of the dominant producer strain. We also consider the case of evolution of antibiotic resistance within the sensitive species. In order for the resistant cells to survive, they must grow faster than both the non-producers and the producers. However, if the resistant cells grow too rapidly, the producing species is eliminated, after which the resistance mutation is no longer useful, and sensitive cells take over the system. We show that there is a range of growth rates of the resistant cells where the two species coexist, and where the production mechanism is maintained as a polymorphism in the producing species and the resistance mechanism is maintained as a polymorphism in the sensitive species.
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spelling pubmed-62091672018-11-19 The evolution of antibiotic production rate in a spatial model of bacterial competition Kosakowski, Jakub Verma, Prateek Sengupta, Supratim Higgs, Paul G. PLoS One Research Article We consider competition between antibiotic producing bacteria, non-producers (or cheaters), and sensitive cells in a two-dimensional lattice model. Previous work has shown that these three cell types can survive in spatial models due to the presence of spatial patterns, whereas coexistence is not possible in a well-mixed system. We extend this to consider the evolution of the antibiotic production rate, assuming that the cost of antibiotic production leads to a reduction in growth rate of the producers. We find that coexistence occurs for an intermediate range of antibiotic production rate. If production rate is too high or too low, only sensitive cells survive. When evolution of production rate is allowed, a mixture of cell types arises in which there is a dominant producer strain that produces sufficient to limit the growth of sensitive cells and which is able to withstand the presence of cheaters in its own species. The mixture includes a range of low-rate producers and non-producers, none of which could survive without the presence of the dominant producer strain. We also consider the case of evolution of antibiotic resistance within the sensitive species. In order for the resistant cells to survive, they must grow faster than both the non-producers and the producers. However, if the resistant cells grow too rapidly, the producing species is eliminated, after which the resistance mutation is no longer useful, and sensitive cells take over the system. We show that there is a range of growth rates of the resistant cells where the two species coexist, and where the production mechanism is maintained as a polymorphism in the producing species and the resistance mechanism is maintained as a polymorphism in the sensitive species. Public Library of Science 2018-10-31 /pmc/articles/PMC6209167/ /pubmed/30379843 http://dx.doi.org/10.1371/journal.pone.0205202 Text en © 2018 Kosakowski et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Kosakowski, Jakub
Verma, Prateek
Sengupta, Supratim
Higgs, Paul G.
The evolution of antibiotic production rate in a spatial model of bacterial competition
title The evolution of antibiotic production rate in a spatial model of bacterial competition
title_full The evolution of antibiotic production rate in a spatial model of bacterial competition
title_fullStr The evolution of antibiotic production rate in a spatial model of bacterial competition
title_full_unstemmed The evolution of antibiotic production rate in a spatial model of bacterial competition
title_short The evolution of antibiotic production rate in a spatial model of bacterial competition
title_sort evolution of antibiotic production rate in a spatial model of bacterial competition
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6209167/
https://www.ncbi.nlm.nih.gov/pubmed/30379843
http://dx.doi.org/10.1371/journal.pone.0205202
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