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Sci Adv. 2017 Apr 7;3(4):e1601721. doi: 10.1126/sciadv.1601721. eCollection 2017 Apr.

Mandrills use olfaction to socially avoid parasitized conspecifics.

Author information

1
Centre d'Ecologie Fonctionnelle et Evolutive (CEFE)-CNRS, UMR 5175, 1919 Route de Mende, 34293 Montpellier Cedex 5, France.
2
Institut des Sciences de l'Evolution de Montpellier (ISEM), UMR 5554, Place Eugène Bataillon, 34095 Montpellier Cedex 5, France.
3
CNRS, Université de Lille-Sciences et Technologies, UMR 8198, Evo-Eco-Paléo, F-59655 Villeneuve d'Ascq, France.
4
Centre de Primatologie, Centre International de Recherches Médicales de Franceville (CIRMF), BP 769, Franceville, Gabon.
5
Projet Mandrillus, Société d'exploitation du Parc de Lékédi (SODEPAL), BP 52, Bakoumba, Gabon.
6
Behavioral Ecology and Sociobiology Unit, German Primate Center, Kellnerweg 4, 37077 Göttingen, Germany.

Abstract

The evolutionary transition from a solitary to a social lifestyle entails an elevated parasite cost because the social proximity associated with group living favors parasite transmission. Despite this cost, sociality is widespread in a large range of taxonomic groups. In this context, hosts would be expected to have evolved behavioral mechanisms to reduce the risk of parasite infection. Few empirical studies have focused on the influence of pathogen-mediated selection on the evolution of antiparasitic behavior in wild vertebrates. We report an adaptive functional relationship between parasitism and social behavior in mandrills, associated with evidence that they are able to gauge parasite status of their group members. Using long-term observations, controlled experiments, and chemical analyses, we show that (i) wild mandrills avoid grooming conspecifics infected with orofecally transmitted parasites; (ii) mandrills receive significantly more grooming after treatment that targets these parasites; (iii) parasitism influences the host's fecal odors; and (iv) mandrills selectively avoid fecal material from parasitized conspecifics. These behavioral adaptations reveal that selecting safe social partners may help primates to cope with parasite-mediated costs of sociality and that "behavioral immunity" plays a crucial role in the coevolutionary dynamics between hosts and their parasites.

KEYWORDS:

anti-parasitic strategy; olfactory-guided mechanism; primate; social avoidance

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