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Experimental immune challenges reduce the quality of male antennae and female pheromone output

Sexual signalling is a key feature of reproductive investment, yet the effects of immune system activation on investment into chemical signalling, and especially signal receiver traits such as antennae, are poorly understood. We explore how upregulation of juvenile immunity affects male antennal fun...

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Autores principales: Pham, Hieu T., Elgar, Mark A., van Lieshout, Emile, McNamara, Kathryn B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8897396/
https://www.ncbi.nlm.nih.gov/pubmed/35246550
http://dx.doi.org/10.1038/s41598-022-07100-y
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author Pham, Hieu T.
Elgar, Mark A.
van Lieshout, Emile
McNamara, Kathryn B.
author_facet Pham, Hieu T.
Elgar, Mark A.
van Lieshout, Emile
McNamara, Kathryn B.
author_sort Pham, Hieu T.
collection PubMed
description Sexual signalling is a key feature of reproductive investment, yet the effects of immune system activation on investment into chemical signalling, and especially signal receiver traits such as antennae, are poorly understood. We explore how upregulation of juvenile immunity affects male antennal functional morphology and female pheromone attractiveness in the gumleaf skeletonizer moth, Uraba lugens. We injected final-instar larvae with a high or low dose of an immune elicitor or a control solution and measured male antennal morphological traits, gonad investment and female pheromone attractiveness. Immune activation affected male and female signalling investment: immune challenged males had a lower density of antennal sensilla, and the pheromone of immune-challenged females was less attractive to males than their unchallenged counterparts. Immune challenge affected female investment into ovary development but not in a linear, dose-dependent manner. While there was no effect of immune challenge on testes size, there was a trade-off between male pre- and post-copulatory investment: male antennal length was negatively correlated with testes size. Our study highlights the costs of elaborate antennae and pheromone production and demonstrates the capacity for honest signalling in species where the costs of pheromone production were presumed to be trivial.
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spelling pubmed-88973962022-03-07 Experimental immune challenges reduce the quality of male antennae and female pheromone output Pham, Hieu T. Elgar, Mark A. van Lieshout, Emile McNamara, Kathryn B. Sci Rep Article Sexual signalling is a key feature of reproductive investment, yet the effects of immune system activation on investment into chemical signalling, and especially signal receiver traits such as antennae, are poorly understood. We explore how upregulation of juvenile immunity affects male antennal functional morphology and female pheromone attractiveness in the gumleaf skeletonizer moth, Uraba lugens. We injected final-instar larvae with a high or low dose of an immune elicitor or a control solution and measured male antennal morphological traits, gonad investment and female pheromone attractiveness. Immune activation affected male and female signalling investment: immune challenged males had a lower density of antennal sensilla, and the pheromone of immune-challenged females was less attractive to males than their unchallenged counterparts. Immune challenge affected female investment into ovary development but not in a linear, dose-dependent manner. While there was no effect of immune challenge on testes size, there was a trade-off between male pre- and post-copulatory investment: male antennal length was negatively correlated with testes size. Our study highlights the costs of elaborate antennae and pheromone production and demonstrates the capacity for honest signalling in species where the costs of pheromone production were presumed to be trivial. Nature Publishing Group UK 2022-03-04 /pmc/articles/PMC8897396/ /pubmed/35246550 http://dx.doi.org/10.1038/s41598-022-07100-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Pham, Hieu T.
Elgar, Mark A.
van Lieshout, Emile
McNamara, Kathryn B.
Experimental immune challenges reduce the quality of male antennae and female pheromone output
title Experimental immune challenges reduce the quality of male antennae and female pheromone output
title_full Experimental immune challenges reduce the quality of male antennae and female pheromone output
title_fullStr Experimental immune challenges reduce the quality of male antennae and female pheromone output
title_full_unstemmed Experimental immune challenges reduce the quality of male antennae and female pheromone output
title_short Experimental immune challenges reduce the quality of male antennae and female pheromone output
title_sort experimental immune challenges reduce the quality of male antennae and female pheromone output
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8897396/
https://www.ncbi.nlm.nih.gov/pubmed/35246550
http://dx.doi.org/10.1038/s41598-022-07100-y
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