Genetic variation at MHC class II loci influences both olfactory signals and scent discrimination in ring-tailed lemurs.

Published

Journal Article

BACKGROUND:Diversity at the Major Histocompatibility Complex (MHC) is critical to health and fitness, such that MHC genotype may predict an individual's quality or compatibility as a competitor, ally, or mate. Moreover, because MHC products can influence the components of bodily secretions, an individual's body odors may signal its MHC composition and influence partner identification or mate choice. Here, we investigated MHC-based signaling and recipient sensitivity by testing for odor-gene covariance and behavioral discrimination of MHC diversity and pairwise dissimilarity in a strepsirrhine primate, the ring-tailed lemur (Lemur catta). METHODS:First, we coupled genotyping of the MHC class II gene, DRB, with gas chromatography-mass spectrometry of genital gland secretions to investigate if functional genetic diversity is signaled by the chemical diversity of lemur scent secretions. We also assessed if the chemical similarity between individuals correlated with their MHC-DRB similarity. Next, we assessed if lemurs discriminated this chemically encoded, genetic information in opposite-sex conspecifics. RESULTS:We found that both sexes signaled overall MHC-DRB diversity and pairwise MHC-DRB similarity via genital secretions, but in a sex- and season-dependent manner. Additionally, the sexes discriminated absolute and relative MHC-DRB diversity in the genital odors of opposite-sex conspecifics, suggesting that lemur genital odors function to advertise genetic quality. CONCLUSIONS:In summary, genital odors of ring-tailed lemurs provide honest information about an individual's absolute and relative MHC quality. Complementing evidence in humans and Old World monkeys, we suggest that reliance on scent signals to communicate MHC quality may be important across the primate lineage.

Full Text

Duke Authors

Cited Authors

  • Grogan, KE; Harris, RL; Boulet, M; Drea, CM

Published Date

  • August 22, 2019

Published In

Volume / Issue

  • 19 / 1

Start / End Page

  • 171 -

PubMed ID

  • 31438845

Pubmed Central ID

  • 31438845

Electronic International Standard Serial Number (EISSN)

  • 1471-2148

International Standard Serial Number (ISSN)

  • 1471-2148

Digital Object Identifier (DOI)

  • 10.1186/s12862-019-1486-0

Language

  • eng