Open AccessNegative relationships between cellular immune response, Mhc class II heterozygosity and secondary sexual trait in the montane water vole
Author(s) -
Charbonnel Nathalie,
Bryja Josef,
Galan Maxime,
Deter Julie,
Tollenaere Charlotte,
Chaval Yannick,
Morand Serge,
Cosson JeanFrançois
Publication year - 2010
Publication title -
evolutionary applications
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.776
H-Index - 68
ISSN - 1752-4571
DOI - 10.1111/j.1752-4571.2009.00108.x
Subject(s) - biology , major histocompatibility complex , phytohaemagglutinin , genetics , allotype , loss of heterozygosity , heterozygote advantage , immune system , mhc class i , immunocompetence , trait , evolutionary biology , genotype , gene , allele , computer science , programming language
Heterogeneities in immune responsiveness may affect key epidemiological parameters and the dynamics of pathogens. The roles of immunogenetics in these variations remain poorly explored. We analysed the influence of Major histocompatibility complex (Mhc) genes and epigamic traits on the response to phytohaemagglutinin in males from cyclic populations of the montane water vole ( Arvicola scherman) . Besides, we tested the relevance of lateral scent glands as honest signals of male quality. Our results did not corroborate neither the hypotheses of genome‐wide heterozygosity‐fitness correlation nor the Mhc heterozygote advantage. We found a negative relationship between Mhc hetetozygosity and response to phytohaemagglutinin, mediated by a specific Mhc homozygous genotype. Our results therefore support the hypothesis of the Arte‐Dqa‐05 homozygous genotype being a ‘good’ Mhc variant in terms of immunogenetic quality. The development of the scent glands seems to be an honest signal for mate choice as it is negatively correlated with helminth load. The ‘good gene’ hypothesis was not validated as Arte‐Dqa‐05 homozygous males did not exhibit larger glands. Besides, the negative relationship observed between the size of these glands and the response to phytohaemagglutinin, mainly for Mhc homozygotes, corroborates the immunocompetence handicap hypothesis. The Mhc variants associated with larger glands remain yet to be determined.