Sex and hatching order modulate the association between MHC-II diversity and fitness in early-life stages of a wild seabird.


Journal

Molecular ecology
ISSN: 1365-294X
Titre abrégé: Mol Ecol
Pays: England
ID NLM: 9214478

Informations de publication

Date de publication:
09 2020
Historique:
received: 11 09 2019
revised: 04 07 2020
accepted: 06 07 2020
pubmed: 13 7 2020
medline: 22 6 2021
entrez: 13 7 2020
Statut: ppublish

Résumé

Genes of the major histocompatibility complex (MHC) play a pivotal role in parasite resistance, and their allelic diversity has been associated with fitness variations in several taxa. However, studies report inconsistencies in the direction of this association, with either positive, quadratic or no association being described. These discrepancies may arise because the fitness costs and benefits of MHC diversity differ among individuals depending on their exposure and immune responses to parasites. Here, we investigated in black-legged kittiwake (Rissa tridactyla) chicks whether associations between MHC class-II diversity and fitness vary with sex and hatching order. MHC-II diversity was positively associated with growth and tick clearance in female chicks, but not in male chicks. Our data also revealed a positive association between MHC-II diversity and survival in second-hatched female chicks (two eggs being the typical clutch size). These findings may result from condition-dependent parasite infections differentially impacting sexes in relation to hatching order. We thus suggest that it may be important to account for individual heterogeneities in traits that potentially exert selective pressures on MHC diversity in order to properly predict MHC-fitness associations.

Identifiants

pubmed: 32654215
doi: 10.1111/mec.15551
doi:

Substances chimiques

Histocompatibility Antigens Class II 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3316-3329

Informations de copyright

© 2020 John Wiley & Sons Ltd.

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Auteurs

Maxime Pineaux (M)

Laboratoire Évolution & Diversité Biologique (EDB UMR 5174), CNRS, IRD, Université Fédérale de Toulouse Midi-Pyrénées, Toulouse, France.

Thomas Merkling (T)

Laboratoire Évolution & Diversité Biologique (EDB UMR 5174), CNRS, IRD, Université Fédérale de Toulouse Midi-Pyrénées, Toulouse, France.

Etienne Danchin (E)

Laboratoire Évolution & Diversité Biologique (EDB UMR 5174), CNRS, IRD, Université Fédérale de Toulouse Midi-Pyrénées, Toulouse, France.

Scott Hatch (S)

Institute for Seabird Research and Conservation, Anchorage, AK, USA.

David Duneau (D)

Laboratoire Évolution & Diversité Biologique (EDB UMR 5174), CNRS, IRD, Université Fédérale de Toulouse Midi-Pyrénées, Toulouse, France.

Pierrick Blanchard (P)

Laboratoire Évolution & Diversité Biologique (EDB UMR 5174), CNRS, IRD, Université Fédérale de Toulouse Midi-Pyrénées, Toulouse, France.

Sarah Leclaire (S)

Laboratoire Évolution & Diversité Biologique (EDB UMR 5174), CNRS, IRD, Université Fédérale de Toulouse Midi-Pyrénées, Toulouse, France.

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