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Parasites and infectious diseases represent ecological forces shaping animal social evolution. Although empirical studies supporting this link abound in various vertebrate orders, both the study of the dynamics and impact of parasite infections and infectious diseases in strepsirrhine primates have received little empirical attention. We conducted a longitudinal parasitological study on four groups of wild red-fronted lemurs (Eulemur fulvus rufus) at Kirindy Forest, Madagascar, during two field seasons in consecutive years to investigate i) the degree of gastrointestinal parasite infection on population and individual levels and ii) factors potentially determining individual infection risk. Using a comprehensive dataset with multiple individually assignable parasite samples as well as information on age, sex, group size, social rank, and endocrine status (fecal androgen and glucocorticoid), we examined parasite infection patterns and host traits that may affect individual infection risk. In addition, we examined whether parasite infection affects mating and reproductive success. Our results indicated high variability in parasite infection on individual and population levels. Time of year and group size was important determinants of variability in parasite infection. Variation in hormone levels was also associated with parasite species richness and parasite infection intensity. Differences in parasite infection between years indicate a potential immune-enhancing function of steroid hormones on nematode infections, which has not been reported before from other vertebrates studied under natural conditions. Male mating and reproductive success were not correlated to any measure of parasite infection, which suggests a nonfunctional role of the parasites we examined in primate sexual selection. Am J Phys Anthropol 142:441-452, 2010. [c]2010 Wiley-Liss, Inc. KEY WORDS primates; helminth; protozoa; hormones; reproductive success DOI 10.1002/ajpa.21243

To link to full-text access for this article, visit this link: http://dx.doi.org/10.1016/j.anbehav.2008.08.032 Byline: Markus Port (a)(b), Dagmar Clough (a)(b), Peter M. Kappeler (a)(b) Abstract: Social grooming is a commonly observed affiliative behaviour in primates. Grooming has been suggested to represent a service in a biological marketplace, exchanged either for grooming or for other social commodities or services. Accordingly, grooming is predicted to be approximately reciprocated within a dyad when no other services are being exchanged, but it should be more asymmetrical if partners have different quantities of other services to offer. We analysed 412 grooming bouts observed in four groups of free-ranging redfronted lemurs to test this prediction. Grooming in this species seems to take place in a highly reciprocal manner because partners usually alternate in the roles of groomer and gromee within a grooming bout. However, within dyads there were asymmetries in the duration of grooming given and received. In both sexes, more grooming was directed from low-ranking towards high-ranking individuals than vice versa, and in males this asymmetry became more pronounced as the number of subordinates per group increased. Grooming in bisexual dyads was generally skewed in favour of males, but patterns of grooming between the sexes were less clear than within the sexes. In addition, aggression occurred at high frequencies between classes of individuals that were characterized by nonreciprocal grooming, suggesting that grooming may serve as a means to reduce aggression in dyads with a high potential for conflicts. Taken together, our results indicate that a strict reciprocation of grooming can be offset by power differentials between partners, where grooming appears to be traded by subordinates in exchange for the tolerance of dominants. Author Affiliation: (a) Department of Behavioral Ecology and Sociobiology, German Primate Center, Germany (b) Department of Sociobiology/Anthropology, University of Gottingen, Germany Article History: Received 21 May 2008; Revised 2 July 2008; Accepted 29 August 2008 Article Note: (miscellaneous) MS. number: 08-00337

Abstract Background Susceptibility to parasite infection affects fitness-related processes, such as mate choice and survival, yet its genetic regulation remains poorly understood. Interleukin-4 (IL4) plays a central role in the humoral immune defence against nematode parasite infections, inducing IgE switch and regulation of worm expulsion from the intestines. The evolutionary and functional significance of single nucleotide polymorphisms (SNPs) in IL4-genes is known, yet empirical information on the effect of IL4 SNPs on gastro-intestinal infections is lacking. Using samples from a population of wild red-fronted lemurs (Eulemur fulvus rufus, Primates: Lemuridae), from western Madagascar, we explored the association of IL4-gene promoter polymorphisms with nematode infections and investigated a possible functional role of the IL4 polymorphism on male reproductive success. Results Using sequence analyses of lemur DNA we detected a new SNP in the IL4 gene promoter area. Carriers of the genotype T/T showed higher nematode infection intensities than individuals of genotypes C/T and C/C. Genetic population analyses using data from more than 10 years, suggested higher reproductive success of T/T males than expected. Conclusions Our results suggest a regulatory effect of an IL4 gene promoter polymorphism on the intensity of parasite infections in a natural population of red-fronted lemurs, with a seemingly disadvantageous genotype represented in low frequencies. Long-term population analyses, however, point in the direction of a negative frequency-dependent association, giving a fitness advantage to the rare genotype. Due to low frequencies of the genotype in question conclusive evidence of a functional role of IL4 polymorphism cannot be drawn here; still, we suggest the use of IL4 polymorphism as a new molecular tool for quick assessment of individual genetic constitution with regard to nematode infection intensities, contributing to a better understanding of the actual components of the immune response that mediate protection against gastro-intestinal parasites.