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Aphid symbionts and endogenous resistance traits mediate competition between rival parasitoids
Insects use endogenous mechanisms and infection with protective symbionts to thwart attacks from natural enemies. Defenses that target specific enemies, however, potentially mediate competition between rivals and thereby impact community composition. Following its introduction to North America to co...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5507255/ https://www.ncbi.nlm.nih.gov/pubmed/28700614 http://dx.doi.org/10.1371/journal.pone.0180729 |
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author | Kraft, Laura J. Kopco, James Harmon, Jason P. Oliver, Kerry M. |
author_facet | Kraft, Laura J. Kopco, James Harmon, Jason P. Oliver, Kerry M. |
author_sort | Kraft, Laura J. |
collection | PubMed |
description | Insects use endogenous mechanisms and infection with protective symbionts to thwart attacks from natural enemies. Defenses that target specific enemies, however, potentially mediate competition between rivals and thereby impact community composition. Following its introduction to North America to control pea aphids (Acyrthosiphon pisum), the parasitoid Aphidius ervi competitively displaced other parasitoids, except for the native Praon pequodorum. The pea aphid exhibits tremendous clonal variation in resistance to A. ervi, primarily through infection with the heritable bacterial symbiont Hamiltonella defensa, although some symbiont-free aphid genotypes encode endogenous resistance. Interestingly, H. defensa strains and aphid genotypes that protect against A. ervi, provide no protection against the closely related, P. pequodorum. Given the specificity of aphid defenses, we hypothesized that aphid resistance traits may contribute to the continued persistence of P. pequodorum. We conducted multiparasitism assays to determine whether aphid resistance traits mediate internal competition between these two solitary parasitoid species, but found this was not the case; P. pequodorum was the successful internal competitor across lines varying in susceptibility to A. ervi. Next, to determine whether resistance traits influence competitive interactions resulting in the stable persistence of P. pequodorum, we established replicated cages varying in the proportion of resistant aphids and recorded successful parasitism for each wasp species over time. As expected, A. ervi outcompeted P. pequodorum in cages containing only susceptible aphids. However, P. pequodorum not only persisted, but was the superior competitor in populations containing any proportion (20–100%) of resistant aphids (20–100%). Smaller scale, better replicated competition cage studies corroborated this finding, and no-competition and behavioral assays provide insight into the processes mediating competition. Genetic variation, including that acquired via infection with protective symbionts, may provide a supply of hosts susceptible only to particular enemies, mediating competition with effects on community richness and stability. |
format | Online Article Text |
id | pubmed-5507255 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-55072552017-07-25 Aphid symbionts and endogenous resistance traits mediate competition between rival parasitoids Kraft, Laura J. Kopco, James Harmon, Jason P. Oliver, Kerry M. PLoS One Research Article Insects use endogenous mechanisms and infection with protective symbionts to thwart attacks from natural enemies. Defenses that target specific enemies, however, potentially mediate competition between rivals and thereby impact community composition. Following its introduction to North America to control pea aphids (Acyrthosiphon pisum), the parasitoid Aphidius ervi competitively displaced other parasitoids, except for the native Praon pequodorum. The pea aphid exhibits tremendous clonal variation in resistance to A. ervi, primarily through infection with the heritable bacterial symbiont Hamiltonella defensa, although some symbiont-free aphid genotypes encode endogenous resistance. Interestingly, H. defensa strains and aphid genotypes that protect against A. ervi, provide no protection against the closely related, P. pequodorum. Given the specificity of aphid defenses, we hypothesized that aphid resistance traits may contribute to the continued persistence of P. pequodorum. We conducted multiparasitism assays to determine whether aphid resistance traits mediate internal competition between these two solitary parasitoid species, but found this was not the case; P. pequodorum was the successful internal competitor across lines varying in susceptibility to A. ervi. Next, to determine whether resistance traits influence competitive interactions resulting in the stable persistence of P. pequodorum, we established replicated cages varying in the proportion of resistant aphids and recorded successful parasitism for each wasp species over time. As expected, A. ervi outcompeted P. pequodorum in cages containing only susceptible aphids. However, P. pequodorum not only persisted, but was the superior competitor in populations containing any proportion (20–100%) of resistant aphids (20–100%). Smaller scale, better replicated competition cage studies corroborated this finding, and no-competition and behavioral assays provide insight into the processes mediating competition. Genetic variation, including that acquired via infection with protective symbionts, may provide a supply of hosts susceptible only to particular enemies, mediating competition with effects on community richness and stability. Public Library of Science 2017-07-10 /pmc/articles/PMC5507255/ /pubmed/28700614 http://dx.doi.org/10.1371/journal.pone.0180729 Text en © 2017 Kraft 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Kraft, Laura J. Kopco, James Harmon, Jason P. Oliver, Kerry M. Aphid symbionts and endogenous resistance traits mediate competition between rival parasitoids |
title | Aphid symbionts and endogenous resistance traits mediate competition between rival parasitoids |
title_full | Aphid symbionts and endogenous resistance traits mediate competition between rival parasitoids |
title_fullStr | Aphid symbionts and endogenous resistance traits mediate competition between rival parasitoids |
title_full_unstemmed | Aphid symbionts and endogenous resistance traits mediate competition between rival parasitoids |
title_short | Aphid symbionts and endogenous resistance traits mediate competition between rival parasitoids |
title_sort | aphid symbionts and endogenous resistance traits mediate competition between rival parasitoids |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5507255/ https://www.ncbi.nlm.nih.gov/pubmed/28700614 http://dx.doi.org/10.1371/journal.pone.0180729 |
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