Shifts in sex-specific immune gene expression in a beetle with parental care

Abstract Males and females generally differ in resource investment strategies in order to maximise reproductive output. These strategies involve the control of important systemic processes such as self-maintenance and immune activity, which in turn could be traded-off against aspects of reproduction...

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Main Authors: Nikoletta A. Nagy, José O. Valdebenito, Johanna Lévai-Kiss, Zoltán Rádai, András Kosztolányi, Tamás Székely, Zoltán Barta
Format: Article
Language:English
Published: Nature Portfolio 2025-03-01
Series:Scientific Reports
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Online Access:https://doi.org/10.1038/s41598-025-95268-4
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author Nikoletta A. Nagy
José O. Valdebenito
Johanna Lévai-Kiss
Zoltán Rádai
András Kosztolányi
Tamás Székely
Zoltán Barta
author_facet Nikoletta A. Nagy
José O. Valdebenito
Johanna Lévai-Kiss
Zoltán Rádai
András Kosztolányi
Tamás Székely
Zoltán Barta
author_sort Nikoletta A. Nagy
collection DOAJ
description Abstract Males and females generally differ in resource investment strategies in order to maximise reproductive output. These strategies involve the control of important systemic processes such as self-maintenance and immune activity, which in turn could be traded-off against aspects of reproduction in a sex-specific manner. While some aspects of this immunomodulation have been previously shown in domestic animals, sex-specific immune modulation using repeated sampling over the breeding period has rarely been tested in the wild. Here we used Lethrus apterus, a sexually dimorphic beetle with parental care, to investigate the association between sex roles (e.g. offspring provisioning) and sex-specific immune gene expression. By determining the immune gene activation of males and females at five successive moments within the active season, we found that their sex-specific immune gene expression varies substantially across the active season, alternating between male bias to female bias and vice versa. Though, when pooling all sampling dates together, there was no overall difference in the number of up-regulated immune genes between the sexes. Sex roles in this beetle are associated with energetically demanding behaviours that could potentially explain our results. We highlight the importance of successive sampling protocols to understand ecological dynamics in the wild.
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spelling doaj-art-7d353844f77d4e7fae5d2c2f044ac5a52025-08-20T02:49:32ZengNature PortfolioScientific Reports2045-23222025-03-0115111110.1038/s41598-025-95268-4Shifts in sex-specific immune gene expression in a beetle with parental careNikoletta A. Nagy0José O. Valdebenito1Johanna Lévai-Kiss2Zoltán Rádai3András Kosztolányi4Tamás Székely5Zoltán Barta6Department of Evolutionary Zoology and Human Biology, University of DebrecenDepartment of Evolutionary Zoology and Human Biology, University of DebrecenHUN-REN-UD Behavioural Ecology Research Group, Department of Evolutionary Zoology, University of DebrecenOne Health Institute, Faculty of Health Sciences, University of DebrecenDepartment of Zoology, University of Veterinary Medicine BudapestDepartment of Evolutionary Zoology and Human Biology, University of DebrecenDepartment of Evolutionary Zoology and Human Biology, University of DebrecenAbstract Males and females generally differ in resource investment strategies in order to maximise reproductive output. These strategies involve the control of important systemic processes such as self-maintenance and immune activity, which in turn could be traded-off against aspects of reproduction in a sex-specific manner. While some aspects of this immunomodulation have been previously shown in domestic animals, sex-specific immune modulation using repeated sampling over the breeding period has rarely been tested in the wild. Here we used Lethrus apterus, a sexually dimorphic beetle with parental care, to investigate the association between sex roles (e.g. offspring provisioning) and sex-specific immune gene expression. By determining the immune gene activation of males and females at five successive moments within the active season, we found that their sex-specific immune gene expression varies substantially across the active season, alternating between male bias to female bias and vice versa. Though, when pooling all sampling dates together, there was no overall difference in the number of up-regulated immune genes between the sexes. Sex roles in this beetle are associated with energetically demanding behaviours that could potentially explain our results. We highlight the importance of successive sampling protocols to understand ecological dynamics in the wild.https://doi.org/10.1038/s41598-025-95268-4GeotrupidaeLethrus apterusTranscriptomicsSexual selectionSex-biasImmunoecology
spellingShingle Nikoletta A. Nagy
José O. Valdebenito
Johanna Lévai-Kiss
Zoltán Rádai
András Kosztolányi
Tamás Székely
Zoltán Barta
Shifts in sex-specific immune gene expression in a beetle with parental care
Scientific Reports
Geotrupidae
Lethrus apterus
Transcriptomics
Sexual selection
Sex-bias
Immunoecology
title Shifts in sex-specific immune gene expression in a beetle with parental care
title_full Shifts in sex-specific immune gene expression in a beetle with parental care
title_fullStr Shifts in sex-specific immune gene expression in a beetle with parental care
title_full_unstemmed Shifts in sex-specific immune gene expression in a beetle with parental care
title_short Shifts in sex-specific immune gene expression in a beetle with parental care
title_sort shifts in sex specific immune gene expression in a beetle with parental care
topic Geotrupidae
Lethrus apterus
Transcriptomics
Sexual selection
Sex-bias
Immunoecology
url https://doi.org/10.1038/s41598-025-95268-4
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