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Harbouring public good mutants within a pathogen population can increase both fitness and virulence
Existing theory, empirical, clinical and field research all predict that reducing the virulence of individuals within a pathogen population will reduce the overall virulence, rendering disease less severe. Here, we show that this seemingly successful disease management strategy can fail with devasta...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5193496/ https://www.ncbi.nlm.nih.gov/pubmed/28029337 http://dx.doi.org/10.7554/eLife.18678 |
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author | Lindsay, Richard J Kershaw, Michael J Pawlowska, Bogna J Talbot, Nicholas J Gudelj, Ivana |
author_facet | Lindsay, Richard J Kershaw, Michael J Pawlowska, Bogna J Talbot, Nicholas J Gudelj, Ivana |
author_sort | Lindsay, Richard J |
collection | PubMed |
description | Existing theory, empirical, clinical and field research all predict that reducing the virulence of individuals within a pathogen population will reduce the overall virulence, rendering disease less severe. Here, we show that this seemingly successful disease management strategy can fail with devastating consequences for infected hosts. We deploy cooperation theory and a novel synthetic system involving the rice blast fungus Magnaporthe oryzae. In vivo infections of rice demonstrate that M. oryzae virulence is enhanced, quite paradoxically, when a public good mutant is present in a population of high-virulence pathogens. We reason that during infection, the fungus engages in multiple cooperative acts to exploit host resources. We establish a multi-trait cooperation model which suggests that the observed failure of the virulence reduction strategy is caused by the interference between different social traits. Multi-trait cooperative interactions are widespread, so we caution against the indiscriminant application of anti-virulence therapy as a disease-management strategy. DOI: http://dx.doi.org/10.7554/eLife.18678.001 |
format | Online Article Text |
id | pubmed-5193496 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-51934962017-01-03 Harbouring public good mutants within a pathogen population can increase both fitness and virulence Lindsay, Richard J Kershaw, Michael J Pawlowska, Bogna J Talbot, Nicholas J Gudelj, Ivana eLife Ecology Existing theory, empirical, clinical and field research all predict that reducing the virulence of individuals within a pathogen population will reduce the overall virulence, rendering disease less severe. Here, we show that this seemingly successful disease management strategy can fail with devastating consequences for infected hosts. We deploy cooperation theory and a novel synthetic system involving the rice blast fungus Magnaporthe oryzae. In vivo infections of rice demonstrate that M. oryzae virulence is enhanced, quite paradoxically, when a public good mutant is present in a population of high-virulence pathogens. We reason that during infection, the fungus engages in multiple cooperative acts to exploit host resources. We establish a multi-trait cooperation model which suggests that the observed failure of the virulence reduction strategy is caused by the interference between different social traits. Multi-trait cooperative interactions are widespread, so we caution against the indiscriminant application of anti-virulence therapy as a disease-management strategy. DOI: http://dx.doi.org/10.7554/eLife.18678.001 eLife Sciences Publications, Ltd 2016-12-28 /pmc/articles/PMC5193496/ /pubmed/28029337 http://dx.doi.org/10.7554/eLife.18678 Text en © 2016, Lindsay et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Ecology Lindsay, Richard J Kershaw, Michael J Pawlowska, Bogna J Talbot, Nicholas J Gudelj, Ivana Harbouring public good mutants within a pathogen population can increase both fitness and virulence |
title | Harbouring public good mutants within a pathogen population can increase both fitness and virulence |
title_full | Harbouring public good mutants within a pathogen population can increase both fitness and virulence |
title_fullStr | Harbouring public good mutants within a pathogen population can increase both fitness and virulence |
title_full_unstemmed | Harbouring public good mutants within a pathogen population can increase both fitness and virulence |
title_short | Harbouring public good mutants within a pathogen population can increase both fitness and virulence |
title_sort | harbouring public good mutants within a pathogen population can increase both fitness and virulence |
topic | Ecology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5193496/ https://www.ncbi.nlm.nih.gov/pubmed/28029337 http://dx.doi.org/10.7554/eLife.18678 |
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