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Rapid Experimental Evolution of Pesticide Resistance in C. elegans Entails No Costs and Affects the Mating System
Pesticide resistance is a major concern in natural populations and a model trait to study adaptation. Despite the importance of this trait, the dynamics of its evolution and of its ecological consequences remain largely unstudied. To fill this gap, we performed experimental evolution with replicated...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2580027/ https://www.ncbi.nlm.nih.gov/pubmed/19011681 http://dx.doi.org/10.1371/journal.pone.0003741 |
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author | Lopes, Patricia C. Sucena, Élio Santos, M. Emília Magalhães, Sara |
author_facet | Lopes, Patricia C. Sucena, Élio Santos, M. Emília Magalhães, Sara |
author_sort | Lopes, Patricia C. |
collection | PubMed |
description | Pesticide resistance is a major concern in natural populations and a model trait to study adaptation. Despite the importance of this trait, the dynamics of its evolution and of its ecological consequences remain largely unstudied. To fill this gap, we performed experimental evolution with replicated populations of Caenorhabditis elegans exposed to the pesticide Levamisole during 20 generations. Exposure to Levamisole resulted in decreased survival, fecundity and male frequency, which declined from 30% to zero. This was not due to differential susceptibility of males. Rather, the drug affected mobility, resulting in fewer encounters, probably leading to reduced outcrossing rates. Adaptation, i.e., increased survival and fecundity, occurred within 10 and 20 generations, respectively. Male frequency also increased by generation 20. Adaptation costs were undetected in the ancestral environment and in presence of Ivermectin, another widely-used pesticide with an opposite physiological effect. Our results demonstrate that pesticide resistance can evolve at an extremely rapid pace. Furthermore, we unravel the effects of behaviour on life-history traits and test the environmental dependence of adaptation costs. This study establishes experimental evolution as a powerful tool to tackle pesticide resistance, and paves the way to further investigations manipulating environmental and/or genetic factors underlying adaptation to pesticides. |
format | Text |
id | pubmed-2580027 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-25800272008-11-17 Rapid Experimental Evolution of Pesticide Resistance in C. elegans Entails No Costs and Affects the Mating System Lopes, Patricia C. Sucena, Élio Santos, M. Emília Magalhães, Sara PLoS One Research Article Pesticide resistance is a major concern in natural populations and a model trait to study adaptation. Despite the importance of this trait, the dynamics of its evolution and of its ecological consequences remain largely unstudied. To fill this gap, we performed experimental evolution with replicated populations of Caenorhabditis elegans exposed to the pesticide Levamisole during 20 generations. Exposure to Levamisole resulted in decreased survival, fecundity and male frequency, which declined from 30% to zero. This was not due to differential susceptibility of males. Rather, the drug affected mobility, resulting in fewer encounters, probably leading to reduced outcrossing rates. Adaptation, i.e., increased survival and fecundity, occurred within 10 and 20 generations, respectively. Male frequency also increased by generation 20. Adaptation costs were undetected in the ancestral environment and in presence of Ivermectin, another widely-used pesticide with an opposite physiological effect. Our results demonstrate that pesticide resistance can evolve at an extremely rapid pace. Furthermore, we unravel the effects of behaviour on life-history traits and test the environmental dependence of adaptation costs. This study establishes experimental evolution as a powerful tool to tackle pesticide resistance, and paves the way to further investigations manipulating environmental and/or genetic factors underlying adaptation to pesticides. Public Library of Science 2008-11-17 /pmc/articles/PMC2580027/ /pubmed/19011681 http://dx.doi.org/10.1371/journal.pone.0003741 Text en Lopes 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Lopes, Patricia C. Sucena, Élio Santos, M. Emília Magalhães, Sara Rapid Experimental Evolution of Pesticide Resistance in C. elegans Entails No Costs and Affects the Mating System |
title | Rapid Experimental Evolution of Pesticide Resistance in C. elegans Entails No Costs and Affects the Mating System |
title_full | Rapid Experimental Evolution of Pesticide Resistance in C. elegans Entails No Costs and Affects the Mating System |
title_fullStr | Rapid Experimental Evolution of Pesticide Resistance in C. elegans Entails No Costs and Affects the Mating System |
title_full_unstemmed | Rapid Experimental Evolution of Pesticide Resistance in C. elegans Entails No Costs and Affects the Mating System |
title_short | Rapid Experimental Evolution of Pesticide Resistance in C. elegans Entails No Costs and Affects the Mating System |
title_sort | rapid experimental evolution of pesticide resistance in c. elegans entails no costs and affects the mating system |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2580027/ https://www.ncbi.nlm.nih.gov/pubmed/19011681 http://dx.doi.org/10.1371/journal.pone.0003741 |
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