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Rapid evolution of symbiont‐mediated resistance compromises biological control of aphids by parasitoids

There is growing interest in biological control as a sustainable and environmentally friendly way to control pest insects. Aphids are among the most detrimental agricultural pests worldwide, and parasitoid wasps are frequently employed for their control. The use of asexual parasitoids may improve th...

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Autores principales: Käch, Heidi, Mathé‐Hubert, Hugo, Dennis, Alice B., Vorburger, Christoph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5775498/
https://www.ncbi.nlm.nih.gov/pubmed/29387157
http://dx.doi.org/10.1111/eva.12532
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author Käch, Heidi
Mathé‐Hubert, Hugo
Dennis, Alice B.
Vorburger, Christoph
author_facet Käch, Heidi
Mathé‐Hubert, Hugo
Dennis, Alice B.
Vorburger, Christoph
author_sort Käch, Heidi
collection PubMed
description There is growing interest in biological control as a sustainable and environmentally friendly way to control pest insects. Aphids are among the most detrimental agricultural pests worldwide, and parasitoid wasps are frequently employed for their control. The use of asexual parasitoids may improve the effectiveness of biological control because only females kill hosts and because asexual populations have a higher growth rate than sexuals. However, asexuals may have a reduced capacity to track evolutionary change in their host populations. We used a factorial experiment to compare the ability of sexual and asexual populations of the parasitoid Lysiphlebus fabarum to control caged populations of black bean aphids (Aphis fabae) of high and low clonal diversity. The aphids came from a natural population, and one‐third of the aphid clones harbored Hamiltonella defensa, a heritable bacterial endosymbiont that increases resistance to parasitoids. We followed aphid and parasitoid population dynamics for 3 months but found no evidence that the reproductive mode of parasitoids affected their effectiveness as biocontrol agents, independent of host clonal diversity. Parasitoids failed to control aphids in most cases, because their introduction resulted in strong selection for clones protected by H. defensa. The increasingly resistant aphid populations escaped control by parasitoids, and we even observed parasitoid extinctions in many cages. The rapid evolution of symbiont‐conferred resistance in turn imposed selection on parasitoids. In cages where asexual parasitoids persisted until the end of the experiment, they became dominated by a single genotype able to overcome the protection provided by H. defensa. Thus, there was evidence for parasitoid counteradaptation, but it was generally too slow for parasitoids to regain control over aphid populations. It appears that when pest aphids possess defensive symbionts, the presence of parasitoid genotypes able to overcome symbiont‐conferred resistance is more important for biocontrol success than their reproductive mode.
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spelling pubmed-57754982018-01-31 Rapid evolution of symbiont‐mediated resistance compromises biological control of aphids by parasitoids Käch, Heidi Mathé‐Hubert, Hugo Dennis, Alice B. Vorburger, Christoph Evol Appl Original Articles There is growing interest in biological control as a sustainable and environmentally friendly way to control pest insects. Aphids are among the most detrimental agricultural pests worldwide, and parasitoid wasps are frequently employed for their control. The use of asexual parasitoids may improve the effectiveness of biological control because only females kill hosts and because asexual populations have a higher growth rate than sexuals. However, asexuals may have a reduced capacity to track evolutionary change in their host populations. We used a factorial experiment to compare the ability of sexual and asexual populations of the parasitoid Lysiphlebus fabarum to control caged populations of black bean aphids (Aphis fabae) of high and low clonal diversity. The aphids came from a natural population, and one‐third of the aphid clones harbored Hamiltonella defensa, a heritable bacterial endosymbiont that increases resistance to parasitoids. We followed aphid and parasitoid population dynamics for 3 months but found no evidence that the reproductive mode of parasitoids affected their effectiveness as biocontrol agents, independent of host clonal diversity. Parasitoids failed to control aphids in most cases, because their introduction resulted in strong selection for clones protected by H. defensa. The increasingly resistant aphid populations escaped control by parasitoids, and we even observed parasitoid extinctions in many cages. The rapid evolution of symbiont‐conferred resistance in turn imposed selection on parasitoids. In cages where asexual parasitoids persisted until the end of the experiment, they became dominated by a single genotype able to overcome the protection provided by H. defensa. Thus, there was evidence for parasitoid counteradaptation, but it was generally too slow for parasitoids to regain control over aphid populations. It appears that when pest aphids possess defensive symbionts, the presence of parasitoid genotypes able to overcome symbiont‐conferred resistance is more important for biocontrol success than their reproductive mode. John Wiley and Sons Inc. 2017-09-03 /pmc/articles/PMC5775498/ /pubmed/29387157 http://dx.doi.org/10.1111/eva.12532 Text en © 2017 The Authors. Evolutionary Applications published by John Wiley & Sons Ltd This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Käch, Heidi
Mathé‐Hubert, Hugo
Dennis, Alice B.
Vorburger, Christoph
Rapid evolution of symbiont‐mediated resistance compromises biological control of aphids by parasitoids
title Rapid evolution of symbiont‐mediated resistance compromises biological control of aphids by parasitoids
title_full Rapid evolution of symbiont‐mediated resistance compromises biological control of aphids by parasitoids
title_fullStr Rapid evolution of symbiont‐mediated resistance compromises biological control of aphids by parasitoids
title_full_unstemmed Rapid evolution of symbiont‐mediated resistance compromises biological control of aphids by parasitoids
title_short Rapid evolution of symbiont‐mediated resistance compromises biological control of aphids by parasitoids
title_sort rapid evolution of symbiont‐mediated resistance compromises biological control of aphids by parasitoids
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5775498/
https://www.ncbi.nlm.nih.gov/pubmed/29387157
http://dx.doi.org/10.1111/eva.12532
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