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Hormonal modulation of reproduction and fertility signaling in polistine wasps

In social insects, it has been suggested that reproduction and the production of particular fertility-linked cuticular hydrocarbons (CHC) may be under shared juvenile hormone (JH) control, and this could have been key in predisposing such cues to later evolve into full-fledged queen pheromone signal...

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Autores principales: Oi, Cintia Akemi, da Silva, Rafael Carvalho, Stevens, Ian, Ferreira, Helena Mendes, Nascimento, Fabio Santos, Wenseleers, Tom
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8489163/
https://www.ncbi.nlm.nih.gov/pubmed/34616950
http://dx.doi.org/10.1093/cz/zoab026
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author Oi, Cintia Akemi
da Silva, Rafael Carvalho
Stevens, Ian
Ferreira, Helena Mendes
Nascimento, Fabio Santos
Wenseleers, Tom
author_facet Oi, Cintia Akemi
da Silva, Rafael Carvalho
Stevens, Ian
Ferreira, Helena Mendes
Nascimento, Fabio Santos
Wenseleers, Tom
author_sort Oi, Cintia Akemi
collection PubMed
description In social insects, it has been suggested that reproduction and the production of particular fertility-linked cuticular hydrocarbons (CHC) may be under shared juvenile hormone (JH) control, and this could have been key in predisposing such cues to later evolve into full-fledged queen pheromone signals. However, to date, only few studies have experimentally tested this “hormonal pleiotropy” hypothesis. Here, we formally test this hypothesis using data from four species of Polistine wasps, Polistes dominula, Polistes satan, Mischocyttarus metathoracicus, and Mischocyttarus cassununga, and experimental treatments with JH using the JH analogue methoprene and the anti-JH precocene. In line with reproduction being under JH control, our results show that across these four species, precocene significantly decreased ovary development when compared with both the acetone solvent-only control and the methoprene treatment. Consistent with the hormonal pleiotropy hypothesis, these effects on reproduction were further matched by subtle shifts in the CHC profiles, with univariate analyses showing that in P. dominula and P. satan the abundance of particular linear alkanes and mono-methylated alkanes were affected by ovary development and our hormonal treatments. The results indicate that in primitively eusocial wasps, and particularly in Polistes, reproduction and the production of some CHC cues are under joint JH control. We suggest that pleiotropic links between reproduction and the production of such hydrocarbon cues have been key enablers for the origin of true fertility and queen signals in more derived, advanced eusocial insects.
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spelling pubmed-84891632021-10-05 Hormonal modulation of reproduction and fertility signaling in polistine wasps Oi, Cintia Akemi da Silva, Rafael Carvalho Stevens, Ian Ferreira, Helena Mendes Nascimento, Fabio Santos Wenseleers, Tom Curr Zool Special Column: Uncovering Variation in Social Insect Communication In social insects, it has been suggested that reproduction and the production of particular fertility-linked cuticular hydrocarbons (CHC) may be under shared juvenile hormone (JH) control, and this could have been key in predisposing such cues to later evolve into full-fledged queen pheromone signals. However, to date, only few studies have experimentally tested this “hormonal pleiotropy” hypothesis. Here, we formally test this hypothesis using data from four species of Polistine wasps, Polistes dominula, Polistes satan, Mischocyttarus metathoracicus, and Mischocyttarus cassununga, and experimental treatments with JH using the JH analogue methoprene and the anti-JH precocene. In line with reproduction being under JH control, our results show that across these four species, precocene significantly decreased ovary development when compared with both the acetone solvent-only control and the methoprene treatment. Consistent with the hormonal pleiotropy hypothesis, these effects on reproduction were further matched by subtle shifts in the CHC profiles, with univariate analyses showing that in P. dominula and P. satan the abundance of particular linear alkanes and mono-methylated alkanes were affected by ovary development and our hormonal treatments. The results indicate that in primitively eusocial wasps, and particularly in Polistes, reproduction and the production of some CHC cues are under joint JH control. We suggest that pleiotropic links between reproduction and the production of such hydrocarbon cues have been key enablers for the origin of true fertility and queen signals in more derived, advanced eusocial insects. Oxford University Press 2021-03-15 /pmc/articles/PMC8489163/ /pubmed/34616950 http://dx.doi.org/10.1093/cz/zoab026 Text en © The Author(s) (2021). Published by Oxford University Press on behalf of Editorial Office, Current Zoology. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Special Column: Uncovering Variation in Social Insect Communication
Oi, Cintia Akemi
da Silva, Rafael Carvalho
Stevens, Ian
Ferreira, Helena Mendes
Nascimento, Fabio Santos
Wenseleers, Tom
Hormonal modulation of reproduction and fertility signaling in polistine wasps
title Hormonal modulation of reproduction and fertility signaling in polistine wasps
title_full Hormonal modulation of reproduction and fertility signaling in polistine wasps
title_fullStr Hormonal modulation of reproduction and fertility signaling in polistine wasps
title_full_unstemmed Hormonal modulation of reproduction and fertility signaling in polistine wasps
title_short Hormonal modulation of reproduction and fertility signaling in polistine wasps
title_sort hormonal modulation of reproduction and fertility signaling in polistine wasps
topic Special Column: Uncovering Variation in Social Insect Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8489163/
https://www.ncbi.nlm.nih.gov/pubmed/34616950
http://dx.doi.org/10.1093/cz/zoab026
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