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Bacteriophages affect evolution of bacterial communities in spatially distributed habitats: a simulation study

BACKGROUND: Bacteriophages are known to be one of the driving forces of bacterial evolution. Besides promoting horizontal transfer of genes between cells, they may induce directional selection of cells (for instance, according to more or less resistance to phage infection). Switching between lysogen...

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Autores principales: Klimenko, Alexandra Igorevna, Matushkin, Yury Georgievich, Kolchanov, Nikolay Alexandrovich, Lashin, Sergey Alexandrovich
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4895265/
https://www.ncbi.nlm.nih.gov/pubmed/26823184
http://dx.doi.org/10.1186/s12866-015-0620-4
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author Klimenko, Alexandra Igorevna
Matushkin, Yury Georgievich
Kolchanov, Nikolay Alexandrovich
Lashin, Sergey Alexandrovich
author_facet Klimenko, Alexandra Igorevna
Matushkin, Yury Georgievich
Kolchanov, Nikolay Alexandrovich
Lashin, Sergey Alexandrovich
author_sort Klimenko, Alexandra Igorevna
collection PubMed
description BACKGROUND: Bacteriophages are known to be one of the driving forces of bacterial evolution. Besides promoting horizontal transfer of genes between cells, they may induce directional selection of cells (for instance, according to more or less resistance to phage infection). Switching between lysogenic and lytic pathways results in various types of (co)evolution in host-phage systems. Spatial (more generally, ecological) organization of the living environment is another factor affecting evolution. In this study, we have simulated and analyzed a series of computer models of microbial communities evolving in spatially distributed environments under the pressure of phage infection. RESULTS: We modeled evolving microbial communities living in spatially distributed flowing environments. Non-specific nutrient supplied in the only spatial direction, resulting in its non-uniform distribution in environment. We varied the time and the location of initial phage infestation of cells as well as switched chemotaxis on and off. Simulations were performed with the Haploid evolutionary constructor software (http://evol-constructor.bionet.nsc.ru/). CONCLUSION: Simulations have shown that the spatial location of initial phage invasion may lead to different evolutionary scenarios. Phage infection decreases the speciation rate by more than one order as far as intensified selection blocks the origin of novel viable populations/species, which could carve out potential ecological niches. The dependence of speciation rate on the invasion node location varied on the time of invasion. Speciation rate was found to be lower when the phage invaded fully formed community of sedentary cells (at middle and late times) at the species-rich regions. This is especially noticeable in the case of late-time invasion. Our simulation study has shown that phage infection affects evolution of microbial community slowing down speciation and stabilizing the system as a whole. This influencing varied in its efficiency depending on spatially-ecological factors as well as community state at the moment of phage invasion. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12866-015-0620-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-48952652016-06-10 Bacteriophages affect evolution of bacterial communities in spatially distributed habitats: a simulation study Klimenko, Alexandra Igorevna Matushkin, Yury Georgievich Kolchanov, Nikolay Alexandrovich Lashin, Sergey Alexandrovich BMC Microbiol Research BACKGROUND: Bacteriophages are known to be one of the driving forces of bacterial evolution. Besides promoting horizontal transfer of genes between cells, they may induce directional selection of cells (for instance, according to more or less resistance to phage infection). Switching between lysogenic and lytic pathways results in various types of (co)evolution in host-phage systems. Spatial (more generally, ecological) organization of the living environment is another factor affecting evolution. In this study, we have simulated and analyzed a series of computer models of microbial communities evolving in spatially distributed environments under the pressure of phage infection. RESULTS: We modeled evolving microbial communities living in spatially distributed flowing environments. Non-specific nutrient supplied in the only spatial direction, resulting in its non-uniform distribution in environment. We varied the time and the location of initial phage infestation of cells as well as switched chemotaxis on and off. Simulations were performed with the Haploid evolutionary constructor software (http://evol-constructor.bionet.nsc.ru/). CONCLUSION: Simulations have shown that the spatial location of initial phage invasion may lead to different evolutionary scenarios. Phage infection decreases the speciation rate by more than one order as far as intensified selection blocks the origin of novel viable populations/species, which could carve out potential ecological niches. The dependence of speciation rate on the invasion node location varied on the time of invasion. Speciation rate was found to be lower when the phage invaded fully formed community of sedentary cells (at middle and late times) at the species-rich regions. This is especially noticeable in the case of late-time invasion. Our simulation study has shown that phage infection affects evolution of microbial community slowing down speciation and stabilizing the system as a whole. This influencing varied in its efficiency depending on spatially-ecological factors as well as community state at the moment of phage invasion. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12866-015-0620-4) contains supplementary material, which is available to authorized users. BioMed Central 2016-01-27 /pmc/articles/PMC4895265/ /pubmed/26823184 http://dx.doi.org/10.1186/s12866-015-0620-4 Text en © Klimenko et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Klimenko, Alexandra Igorevna
Matushkin, Yury Georgievich
Kolchanov, Nikolay Alexandrovich
Lashin, Sergey Alexandrovich
Bacteriophages affect evolution of bacterial communities in spatially distributed habitats: a simulation study
title Bacteriophages affect evolution of bacterial communities in spatially distributed habitats: a simulation study
title_full Bacteriophages affect evolution of bacterial communities in spatially distributed habitats: a simulation study
title_fullStr Bacteriophages affect evolution of bacterial communities in spatially distributed habitats: a simulation study
title_full_unstemmed Bacteriophages affect evolution of bacterial communities in spatially distributed habitats: a simulation study
title_short Bacteriophages affect evolution of bacterial communities in spatially distributed habitats: a simulation study
title_sort bacteriophages affect evolution of bacterial communities in spatially distributed habitats: a simulation study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4895265/
https://www.ncbi.nlm.nih.gov/pubmed/26823184
http://dx.doi.org/10.1186/s12866-015-0620-4
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