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Comprehensive phylogenomic analyses re-write the evolution of parasitism within cynipoid wasps

BACKGROUND: Parasitoidism, a specialized life strategy in which a parasite eventually kills its host, is frequently found within the insect order Hymenoptera (wasps, ants and bees). A parasitoid lifestyle is one of two dominant life strategies within the hymenopteran superfamily Cynipoidea, with the...

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Autores principales: Blaimer, Bonnie B., Gotzek, Dietrich, Brady, Seán G., Buffington, Matthew L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7686688/
https://www.ncbi.nlm.nih.gov/pubmed/33228574
http://dx.doi.org/10.1186/s12862-020-01716-2
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author Blaimer, Bonnie B.
Gotzek, Dietrich
Brady, Seán G.
Buffington, Matthew L.
author_facet Blaimer, Bonnie B.
Gotzek, Dietrich
Brady, Seán G.
Buffington, Matthew L.
author_sort Blaimer, Bonnie B.
collection PubMed
description BACKGROUND: Parasitoidism, a specialized life strategy in which a parasite eventually kills its host, is frequently found within the insect order Hymenoptera (wasps, ants and bees). A parasitoid lifestyle is one of two dominant life strategies within the hymenopteran superfamily Cynipoidea, with the other being an unusual plant-feeding behavior known as galling. Less commonly, cynipoid wasps exhibit inquilinism, a strategy where some species have adapted to usurp other species’ galls instead of inducing their own. Using a phylogenomic data set of ultraconserved elements from nearly all lineages of Cynipoidea, we here generate a robust phylogenetic framework and timescale to understand cynipoid systematics and the evolution of these life histories. RESULTS: Our reconstructed evolutionary history for Cynipoidea differs considerably from previous hypotheses. Rooting our analyses with non-cynipoid outgroups, the Paraulacini, a group of inquilines, emerged as sister-group to the rest of Cynipoidea, rendering the gall wasp family Cynipidae paraphyletic. The families Ibaliidae and Liopteridae, long considered archaic and early-branching parasitoid lineages, were found nested well within the Cynipoidea as sister-group to the parasitoid Figitidae. Cynipoidea originated in the early Jurassic around 190 Ma. Either inquilinism or parasitoidism is suggested as the ancestral and dominant strategy throughout the early evolution of cynipoids, depending on whether a simple (three states: parasitoidism, inquilinism and galling) or more complex (seven states: parasitoidism, inquilinism and galling split by host use) model is employed. CONCLUSIONS: Our study has significant impact on understanding cynipoid evolution and highlights the importance of adequate outgroup sampling. We discuss the evolutionary timescale of the superfamily in relation to their insect hosts and host plants, and outline how phytophagous galling behavior may have evolved from entomophagous, parasitoid cynipoids. Our study has established the framework for further physiological and comparative genomic work between gall-making, inquiline and parasitoid lineages, which could also have significant implications for the evolution of diverse life histories in other Hymenoptera.
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spelling pubmed-76866882020-11-25 Comprehensive phylogenomic analyses re-write the evolution of parasitism within cynipoid wasps Blaimer, Bonnie B. Gotzek, Dietrich Brady, Seán G. Buffington, Matthew L. BMC Evol Biol Research Article BACKGROUND: Parasitoidism, a specialized life strategy in which a parasite eventually kills its host, is frequently found within the insect order Hymenoptera (wasps, ants and bees). A parasitoid lifestyle is one of two dominant life strategies within the hymenopteran superfamily Cynipoidea, with the other being an unusual plant-feeding behavior known as galling. Less commonly, cynipoid wasps exhibit inquilinism, a strategy where some species have adapted to usurp other species’ galls instead of inducing their own. Using a phylogenomic data set of ultraconserved elements from nearly all lineages of Cynipoidea, we here generate a robust phylogenetic framework and timescale to understand cynipoid systematics and the evolution of these life histories. RESULTS: Our reconstructed evolutionary history for Cynipoidea differs considerably from previous hypotheses. Rooting our analyses with non-cynipoid outgroups, the Paraulacini, a group of inquilines, emerged as sister-group to the rest of Cynipoidea, rendering the gall wasp family Cynipidae paraphyletic. The families Ibaliidae and Liopteridae, long considered archaic and early-branching parasitoid lineages, were found nested well within the Cynipoidea as sister-group to the parasitoid Figitidae. Cynipoidea originated in the early Jurassic around 190 Ma. Either inquilinism or parasitoidism is suggested as the ancestral and dominant strategy throughout the early evolution of cynipoids, depending on whether a simple (three states: parasitoidism, inquilinism and galling) or more complex (seven states: parasitoidism, inquilinism and galling split by host use) model is employed. CONCLUSIONS: Our study has significant impact on understanding cynipoid evolution and highlights the importance of adequate outgroup sampling. We discuss the evolutionary timescale of the superfamily in relation to their insect hosts and host plants, and outline how phytophagous galling behavior may have evolved from entomophagous, parasitoid cynipoids. Our study has established the framework for further physiological and comparative genomic work between gall-making, inquiline and parasitoid lineages, which could also have significant implications for the evolution of diverse life histories in other Hymenoptera. BioMed Central 2020-11-23 /pmc/articles/PMC7686688/ /pubmed/33228574 http://dx.doi.org/10.1186/s12862-020-01716-2 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Blaimer, Bonnie B.
Gotzek, Dietrich
Brady, Seán G.
Buffington, Matthew L.
Comprehensive phylogenomic analyses re-write the evolution of parasitism within cynipoid wasps
title Comprehensive phylogenomic analyses re-write the evolution of parasitism within cynipoid wasps
title_full Comprehensive phylogenomic analyses re-write the evolution of parasitism within cynipoid wasps
title_fullStr Comprehensive phylogenomic analyses re-write the evolution of parasitism within cynipoid wasps
title_full_unstemmed Comprehensive phylogenomic analyses re-write the evolution of parasitism within cynipoid wasps
title_short Comprehensive phylogenomic analyses re-write the evolution of parasitism within cynipoid wasps
title_sort comprehensive phylogenomic analyses re-write the evolution of parasitism within cynipoid wasps
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7686688/
https://www.ncbi.nlm.nih.gov/pubmed/33228574
http://dx.doi.org/10.1186/s12862-020-01716-2
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