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Biotic interactions govern genetic adaptation to toxicants

The genetic recovery of resistant populations released from pesticide exposure is accelerated by the presence of environmental stressors. By contrast, the relevance of environmental stressors for the spread of resistance during pesticide exposure has not been studied. Moreover, the consequences of i...

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Detalles Bibliográficos
Autores principales: Becker, Jeremias Martin, Liess, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4426622/
https://www.ncbi.nlm.nih.gov/pubmed/25833856
http://dx.doi.org/10.1098/rspb.2015.0071
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author Becker, Jeremias Martin
Liess, Matthias
author_facet Becker, Jeremias Martin
Liess, Matthias
author_sort Becker, Jeremias Martin
collection PubMed
description The genetic recovery of resistant populations released from pesticide exposure is accelerated by the presence of environmental stressors. By contrast, the relevance of environmental stressors for the spread of resistance during pesticide exposure has not been studied. Moreover, the consequences of interactions between different stressors have not been considered. Here we show that stress through intraspecific competition accelerates microevolution, because it enhances fitness differences between adapted and non-adapted individuals. By contrast, stress through interspecific competition or predation reduces intraspecific competition and thereby delays microevolution. This was demonstrated in mosquito populations (Culex quinquefasciatus) that were exposed to the pesticide chlorpyrifos. Non-selective predation through harvesting and interspecific competition with Daphnia magna delayed the selection for individuals carrying the ace-1(R) resistance allele. Under non-toxic conditions, susceptible individuals without ace-1(R) prevailed. Likewise, predation delayed the reverse adaptation of the populations to a non-toxic environment, while the effect of interspecific competition was not significant. Applying a simulation model, we further identified how microevolution is generally determined by the type and degree of competition and predation. We infer that interactions with other species—especially strong in ecosystems with high biodiversity—can delay the development of pesticide resistance.
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spelling pubmed-44266222015-05-21 Biotic interactions govern genetic adaptation to toxicants Becker, Jeremias Martin Liess, Matthias Proc Biol Sci Research Articles The genetic recovery of resistant populations released from pesticide exposure is accelerated by the presence of environmental stressors. By contrast, the relevance of environmental stressors for the spread of resistance during pesticide exposure has not been studied. Moreover, the consequences of interactions between different stressors have not been considered. Here we show that stress through intraspecific competition accelerates microevolution, because it enhances fitness differences between adapted and non-adapted individuals. By contrast, stress through interspecific competition or predation reduces intraspecific competition and thereby delays microevolution. This was demonstrated in mosquito populations (Culex quinquefasciatus) that were exposed to the pesticide chlorpyrifos. Non-selective predation through harvesting and interspecific competition with Daphnia magna delayed the selection for individuals carrying the ace-1(R) resistance allele. Under non-toxic conditions, susceptible individuals without ace-1(R) prevailed. Likewise, predation delayed the reverse adaptation of the populations to a non-toxic environment, while the effect of interspecific competition was not significant. Applying a simulation model, we further identified how microevolution is generally determined by the type and degree of competition and predation. We infer that interactions with other species—especially strong in ecosystems with high biodiversity—can delay the development of pesticide resistance. The Royal Society 2015-05-07 /pmc/articles/PMC4426622/ /pubmed/25833856 http://dx.doi.org/10.1098/rspb.2015.0071 Text en http://creativecommons.org/licenses/by/4.0/ © 2015 The Authors. Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Research Articles
Becker, Jeremias Martin
Liess, Matthias
Biotic interactions govern genetic adaptation to toxicants
title Biotic interactions govern genetic adaptation to toxicants
title_full Biotic interactions govern genetic adaptation to toxicants
title_fullStr Biotic interactions govern genetic adaptation to toxicants
title_full_unstemmed Biotic interactions govern genetic adaptation to toxicants
title_short Biotic interactions govern genetic adaptation to toxicants
title_sort biotic interactions govern genetic adaptation to toxicants
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4426622/
https://www.ncbi.nlm.nih.gov/pubmed/25833856
http://dx.doi.org/10.1098/rspb.2015.0071
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