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Antagonistic interactions peak at intermediate genetic distance in clinical and laboratory strains of Pseudomonas aeruginosa
BACKGROUND: Bacteria excrete costly toxins to defend their ecological niche. The evolution of such antagonistic interactions between individuals is expected to depend on both the social environment and the strength of resource competition. Antagonism is expected to be weak among highly similar genot...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3391984/ https://www.ncbi.nlm.nih.gov/pubmed/22439760 http://dx.doi.org/10.1186/1471-2180-12-40 |
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author | Schoustra, Sijmen E Dench, Jonathan Dali, Rola Aaron, Shawn D Kassen, Rees |
author_facet | Schoustra, Sijmen E Dench, Jonathan Dali, Rola Aaron, Shawn D Kassen, Rees |
author_sort | Schoustra, Sijmen E |
collection | PubMed |
description | BACKGROUND: Bacteria excrete costly toxins to defend their ecological niche. The evolution of such antagonistic interactions between individuals is expected to depend on both the social environment and the strength of resource competition. Antagonism is expected to be weak among highly similar genotypes because most individuals are immune to antagonistic agents and among dissimilar genotypes because these are unlikely to be competing for the same resources and antagonism should not yield much benefit. The strength of antagonism is therefore expected to peak at intermediate genetic distance. RESULTS: We studied the ability of laboratory strains of Pseudomonas aeruginosa to prevent growth of 55 different clinical P. aeruginosa isolates derived from cystic fibrosis patients. Genetic distance was determined using genetic fingerprints. We found that the strength of antagonism was maximal among genotypes of intermediate genetic distance and we show that genetic distance and resource use are linked. CONCLUSIONS: Our results suggest that the importance of social interactions like antagonism may be modulated by the strength of resource competition. |
format | Online Article Text |
id | pubmed-3391984 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-33919842012-07-10 Antagonistic interactions peak at intermediate genetic distance in clinical and laboratory strains of Pseudomonas aeruginosa Schoustra, Sijmen E Dench, Jonathan Dali, Rola Aaron, Shawn D Kassen, Rees BMC Microbiol Research Article BACKGROUND: Bacteria excrete costly toxins to defend their ecological niche. The evolution of such antagonistic interactions between individuals is expected to depend on both the social environment and the strength of resource competition. Antagonism is expected to be weak among highly similar genotypes because most individuals are immune to antagonistic agents and among dissimilar genotypes because these are unlikely to be competing for the same resources and antagonism should not yield much benefit. The strength of antagonism is therefore expected to peak at intermediate genetic distance. RESULTS: We studied the ability of laboratory strains of Pseudomonas aeruginosa to prevent growth of 55 different clinical P. aeruginosa isolates derived from cystic fibrosis patients. Genetic distance was determined using genetic fingerprints. We found that the strength of antagonism was maximal among genotypes of intermediate genetic distance and we show that genetic distance and resource use are linked. CONCLUSIONS: Our results suggest that the importance of social interactions like antagonism may be modulated by the strength of resource competition. BioMed Central 2012-03-22 /pmc/articles/PMC3391984/ /pubmed/22439760 http://dx.doi.org/10.1186/1471-2180-12-40 Text en Copyright ©2012 Schoustra et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Schoustra, Sijmen E Dench, Jonathan Dali, Rola Aaron, Shawn D Kassen, Rees Antagonistic interactions peak at intermediate genetic distance in clinical and laboratory strains of Pseudomonas aeruginosa |
title | Antagonistic interactions peak at intermediate genetic distance in clinical and laboratory strains of Pseudomonas aeruginosa |
title_full | Antagonistic interactions peak at intermediate genetic distance in clinical and laboratory strains of Pseudomonas aeruginosa |
title_fullStr | Antagonistic interactions peak at intermediate genetic distance in clinical and laboratory strains of Pseudomonas aeruginosa |
title_full_unstemmed | Antagonistic interactions peak at intermediate genetic distance in clinical and laboratory strains of Pseudomonas aeruginosa |
title_short | Antagonistic interactions peak at intermediate genetic distance in clinical and laboratory strains of Pseudomonas aeruginosa |
title_sort | antagonistic interactions peak at intermediate genetic distance in clinical and laboratory strains of pseudomonas aeruginosa |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3391984/ https://www.ncbi.nlm.nih.gov/pubmed/22439760 http://dx.doi.org/10.1186/1471-2180-12-40 |
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