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Strong genotype‐by‐genotype interactions between aphid‐defensive symbionts and parasitoids persist across different biotic environments

The dynamics of coevolution between hosts and parasites are influenced by their genetic interactions. Highly specific interactions, where the outcome of an infection depends on the precise combination of host and parasite genotypes (G × G interactions), have the potential to maintain genetic variati...

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Autores principales: Gimmi, Elena, Vorburger, Christoph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9298302/
https://www.ncbi.nlm.nih.gov/pubmed/34695269
http://dx.doi.org/10.1111/jeb.13953
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author Gimmi, Elena
Vorburger, Christoph
author_facet Gimmi, Elena
Vorburger, Christoph
author_sort Gimmi, Elena
collection PubMed
description The dynamics of coevolution between hosts and parasites are influenced by their genetic interactions. Highly specific interactions, where the outcome of an infection depends on the precise combination of host and parasite genotypes (G × G interactions), have the potential to maintain genetic variation by inducing negative frequency‐dependent selection. The importance of this effect also rests on whether such interactions are consistent across different environments or modified by environmental variation (G × G × E interaction). In the black bean aphid, Aphis fabae, resistance to its parasitoid Lysiphlebus fabarum is largely determined by the possession of a heritable bacterial endosymbiont, Hamiltonella defensa, with strong G × G interactions between H. defensa and L. fabarum. A key environmental factor in this system is the host plant on which the aphid feeds. Here, we exposed genetically identical aphids harbouring three different strains of H. defensa to three asexual genotypes of L. fabarum and measured parasitism success on three common host plants of A. fabae, namely Vicia faba, Chenopodium album and Beta vulgaris. As expected, we observed the pervasive G × G interaction between H. defensa and L. fabarum, but despite strong main effects of the host plants on average rates of parasitism, this interaction was not altered significantly by the host plant environment (no G × G × E interaction). The symbiont‐conferred specificity of resistance is thus likely to mediate the coevolution of A. fabae and L. fabarum, even when played out across diverse host plants of the aphid.
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spelling pubmed-92983022022-07-21 Strong genotype‐by‐genotype interactions between aphid‐defensive symbionts and parasitoids persist across different biotic environments Gimmi, Elena Vorburger, Christoph J Evol Biol Research Articles The dynamics of coevolution between hosts and parasites are influenced by their genetic interactions. Highly specific interactions, where the outcome of an infection depends on the precise combination of host and parasite genotypes (G × G interactions), have the potential to maintain genetic variation by inducing negative frequency‐dependent selection. The importance of this effect also rests on whether such interactions are consistent across different environments or modified by environmental variation (G × G × E interaction). In the black bean aphid, Aphis fabae, resistance to its parasitoid Lysiphlebus fabarum is largely determined by the possession of a heritable bacterial endosymbiont, Hamiltonella defensa, with strong G × G interactions between H. defensa and L. fabarum. A key environmental factor in this system is the host plant on which the aphid feeds. Here, we exposed genetically identical aphids harbouring three different strains of H. defensa to three asexual genotypes of L. fabarum and measured parasitism success on three common host plants of A. fabae, namely Vicia faba, Chenopodium album and Beta vulgaris. As expected, we observed the pervasive G × G interaction between H. defensa and L. fabarum, but despite strong main effects of the host plants on average rates of parasitism, this interaction was not altered significantly by the host plant environment (no G × G × E interaction). The symbiont‐conferred specificity of resistance is thus likely to mediate the coevolution of A. fabae and L. fabarum, even when played out across diverse host plants of the aphid. John Wiley and Sons Inc. 2021-11-02 2021-12 /pmc/articles/PMC9298302/ /pubmed/34695269 http://dx.doi.org/10.1111/jeb.13953 Text en © 2021 The Authors. Journal of Evolutionary Biology published by John Wiley & Sons Ltd on behalf of European Society for Evolutionary Biology https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Gimmi, Elena
Vorburger, Christoph
Strong genotype‐by‐genotype interactions between aphid‐defensive symbionts and parasitoids persist across different biotic environments
title Strong genotype‐by‐genotype interactions between aphid‐defensive symbionts and parasitoids persist across different biotic environments
title_full Strong genotype‐by‐genotype interactions between aphid‐defensive symbionts and parasitoids persist across different biotic environments
title_fullStr Strong genotype‐by‐genotype interactions between aphid‐defensive symbionts and parasitoids persist across different biotic environments
title_full_unstemmed Strong genotype‐by‐genotype interactions between aphid‐defensive symbionts and parasitoids persist across different biotic environments
title_short Strong genotype‐by‐genotype interactions between aphid‐defensive symbionts and parasitoids persist across different biotic environments
title_sort strong genotype‐by‐genotype interactions between aphid‐defensive symbionts and parasitoids persist across different biotic environments
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9298302/
https://www.ncbi.nlm.nih.gov/pubmed/34695269
http://dx.doi.org/10.1111/jeb.13953
work_keys_str_mv AT gimmielena stronggenotypebygenotypeinteractionsbetweenaphiddefensivesymbiontsandparasitoidspersistacrossdifferentbioticenvironments
AT vorburgerchristoph stronggenotypebygenotypeinteractionsbetweenaphiddefensivesymbiontsandparasitoidspersistacrossdifferentbioticenvironments