Asymmetry in reproduction strategies drives evolution of resistance in biological control systems
The success of biological control may depend on the control agent co-evolving with its target pest species, precluding the emergence of resistance that often undermines chemical control. However, recent evidence of a decline in attack rates of a sexual pest weevil by its asexual parasitoid suggests...
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Published in | PloS one Vol. 13; no. 12; p. e0207610 |
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Language | English |
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19.12.2018
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Abstract | The success of biological control may depend on the control agent co-evolving with its target pest species, precluding the emergence of resistance that often undermines chemical control. However, recent evidence of a decline in attack rates of a sexual pest weevil by its asexual parasitoid suggests that evolutionary arms races may not prevent the emergence of resistance if the host and parasitoid do not have reproductive strategies that generate equal amounts of genetic variation. To understand how these asymmetries in reproductive strategies may drive the emergence of resistance, we combined life history data from two pest weevils and their parasitoids (one sexual and one asexual) in the New Zealand pastoral ecosystem, with a population dynamic model that allows the coevolution of hosts and parasitoids. We found that the ratio of the genetic variance of hosts to parasitoids was a key determinant of the emergence of resistance. Host resistance eventually occurred unless the parasitoids had considerably greater additive genetic variance than their host. The higher reproductive rate of asexual parasitoids did little to offset the cost of reduced additive genetic variance. The model predictions were congruent with long-term parasitism rates observed in the field for both of the pests considered (one with a sexual and one with an asexual parasitoid). We then explored the consequences of introducing two parasitoids with different reproductive strategies that attack the same sexual host. The model showed that the sexually reproducing parasitoid always out-competed the asexually reproducing one. Our study shows that any asymmetry in reproductive strategies is extremely important for predicting the long-term success of biological control agents. Fortunately, introduction of sexually reproducing individuals after an initial introduction of asexual strains may overcome the problems of host resistance. We conclude that evolution must be considered when evaluating the long-term outcomes of importation biological control. |
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AbstractList | The success of biological control may depend on the control agent co-evolving with its target pest species, precluding the emergence of resistance that often undermines chemical control. However, recent evidence of a decline in attack rates of a sexual pest weevil by its asexual parasitoid suggests that evolutionary arms races may not prevent the emergence of resistance if the host and parasitoid do not have reproductive strategies that generate equal amounts of genetic variation. To understand how these asymmetries in reproductive strategies may drive the emergence of resistance, we combined life history data from two pest weevils and their parasitoids (one sexual and one asexual) in the New Zealand pastoral ecosystem, with a population dynamic model that allows the coevolution of hosts and parasitoids. We found that the ratio of the genetic variance of hosts to parasitoids was a key determinant of the emergence of resistance. Host resistance eventually occurred unless the parasitoids had considerably greater additive genetic variance than their host. The higher reproductive rate of asexual parasitoids did little to offset the cost of reduced additive genetic variance. The model predictions were congruent with long-term parasitism rates observed in the field for both of the pests considered (one with a sexual and one with an asexual parasitoid). We then explored the consequences of introducing two parasitoids with different reproductive strategies that attack the same sexual host. The model showed that the sexually reproducing parasitoid always out-competed the asexually reproducing one. Our study shows that any asymmetry in reproductive strategies is extremely important for predicting the long-term success of biological control agents. Fortunately, introduction of sexually reproducing individuals after an initial introduction of asexual strains may overcome the problems of host resistance. We conclude that evolution must be considered when evaluating the long-term outcomes of importation biological control. The success of biological control may depend on the control agent co-evolving with its target pest species, precluding the emergence of resistance that often undermines chemical control. However, recent evidence of a decline in attack rates of a sexual pest weevil by its asexual parasitoid suggests that evolutionary arms races may not prevent the emergence of resistance if the host and parasitoid do not have reproductive strategies that generate equal amounts of genetic variation. To understand how these asymmetries in reproductive strategies may drive the emergence of resistance, we combined life history data from two pest weevils and their parasitoids (one sexual and one asexual) in the New Zealand pastoral ecosystem, with a population dynamic model that allows the coevolution of hosts and parasitoids. We found that the ratio of the genetic variance of hosts to parasitoids was a key determinant of the emergence of resistance. Host resistance eventually occurred unless the parasitoids had considerably greater additive genetic variance than their host. The higher reproductive rate of asexual parasitoids did little to offset the cost of reduced additive genetic variance. The model predictions were congruent with long-term parasitism rates observed in the field for both of the pests considered (one with a sexual and one with an asexual parasitoid). We then explored the consequences of introducing two parasitoids with different reproductive strategies that attack the same sexual host. The model showed that the sexually reproducing parasitoid always out-competed the asexually reproducing one. Our study shows that any asymmetry in reproductive strategies is extremely important for predicting the long-term success of biological control agents. Fortunately, introduction of sexually reproducing individuals after an initial introduction of asexual strains may overcome the problems of host resistance. We conclude that evolution must be considered when evaluating the long-term outcomes of importation biological control.The success of biological control may depend on the control agent co-evolving with its target pest species, precluding the emergence of resistance that often undermines chemical control. However, recent evidence of a decline in attack rates of a sexual pest weevil by its asexual parasitoid suggests that evolutionary arms races may not prevent the emergence of resistance if the host and parasitoid do not have reproductive strategies that generate equal amounts of genetic variation. To understand how these asymmetries in reproductive strategies may drive the emergence of resistance, we combined life history data from two pest weevils and their parasitoids (one sexual and one asexual) in the New Zealand pastoral ecosystem, with a population dynamic model that allows the coevolution of hosts and parasitoids. We found that the ratio of the genetic variance of hosts to parasitoids was a key determinant of the emergence of resistance. Host resistance eventually occurred unless the parasitoids had considerably greater additive genetic variance than their host. The higher reproductive rate of asexual parasitoids did little to offset the cost of reduced additive genetic variance. The model predictions were congruent with long-term parasitism rates observed in the field for both of the pests considered (one with a sexual and one with an asexual parasitoid). We then explored the consequences of introducing two parasitoids with different reproductive strategies that attack the same sexual host. The model showed that the sexually reproducing parasitoid always out-competed the asexually reproducing one. Our study shows that any asymmetry in reproductive strategies is extremely important for predicting the long-term success of biological control agents. Fortunately, introduction of sexually reproducing individuals after an initial introduction of asexual strains may overcome the problems of host resistance. We conclude that evolution must be considered when evaluating the long-term outcomes of importation biological control. |
Audience | Academic |
Author | Tylianakis, Jason M. Casanovas, Paula Goldson, Stephen L. |
AuthorAffiliation | 3 AgResearch Ltd., Christchurch, New Zealand 4 Department of Life Sciences, Imperial College London, Silwood Park Campus, Ascot, Berkshire, United Kingdom 2 Bio-Protection Research Centre, Lincoln University, Lincoln, New Zealand 1 Bio-Protection Research Centre, School of Biological Sciences, University of Canterbury, Christchurch, New Zealand University of Minnesota, UNITED STATES |
AuthorAffiliation_xml | – name: 1 Bio-Protection Research Centre, School of Biological Sciences, University of Canterbury, Christchurch, New Zealand – name: 2 Bio-Protection Research Centre, Lincoln University, Lincoln, New Zealand – name: 3 AgResearch Ltd., Christchurch, New Zealand – name: 4 Department of Life Sciences, Imperial College London, Silwood Park Campus, Ascot, Berkshire, United Kingdom – name: University of Minnesota, UNITED STATES |
Author_xml | – sequence: 1 givenname: Paula orcidid: 0000-0002-4462-139X surname: Casanovas fullname: Casanovas, Paula – sequence: 2 givenname: Stephen L. orcidid: 0000-0003-0057-6969 surname: Goldson fullname: Goldson, Stephen L. – sequence: 3 givenname: Jason M. surname: Tylianakis fullname: Tylianakis, Jason M. |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/30566468$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1007_s10526_021_10104_8 crossref_primary_10_1017_S0007485321000547 crossref_primary_10_1093_jisesa_ieaa018 crossref_primary_10_1038_s41559_020_1184_8 crossref_primary_10_1016_j_ibmb_2022_103897 crossref_primary_10_3389_fevo_2022_923248 crossref_primary_10_3390_insects11070441 crossref_primary_10_3389_fpls_2022_923237 crossref_primary_10_1080_00288233_2024_2425071 crossref_primary_10_1186_s12864_023_09538_4 crossref_primary_10_1186_s12864_024_10215_3 crossref_primary_10_1016_j_tplants_2022_04_002 crossref_primary_10_1016_j_tree_2024_04_002 |
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ContentType | Journal Article |
Copyright | COPYRIGHT 2018 Public Library of Science 2018 Casanovas et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. 2018 Casanovas et al 2018 Casanovas et al |
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SubjectTerms | Animal behavior Animals Asymmetry Biological control Biological evolution Biology and Life Sciences Chemical attack Chemical control Coevolution Control systems Dynamic models Ecology and Environmental Sciences Ecosystems Emergence Evolution Evolution (Biology) Evolution, Molecular Genetic diversity Genetic variance Genetic Variation Host-Parasite Interactions Importation Laws, regulations and rules Life history Medicine and Health Sciences Models, Biological Organic chemistry Parasitism Pest Control, Biological Pesticides Pests Physiological regulation Population Predictive control Reproduction Reproduction (biology) Reproduction, Asexual Weevils - parasitology Weevils - physiology |
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Title | Asymmetry in reproduction strategies drives evolution of resistance in biological control systems |
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