Caste, sex, and parasitism influence brain plasticity in a social wasp

Abstract

Phenotypic plasticity is the capacity of a single genotype to exhibit different phenotypes, and can be an adaptive response to specific environmental and social conditions. Social insects are particularly well-suited to study plasticity, because the division of labor amongst females and the different life histories of males and females are associated with specific sensory needs. Here, we take advantage of the social wasp Polistes dominula to explore if brain plasticity is influenced by caste and sex, and the exploitation by the parasite Xenos vesparum. Within sexes, males had proportionally larger optic lobes, while females, regardless of caste, had larger antennal lobes, which is consistent with sensory needs of sex-specific life histories. Within castes, reproductive females had larger calyces, as predicted by their sensory needs for extensive within-colony interactions and forming winter aggregations, than workers who spend more time foraging for nest material and prey. Surprisingly, parasites had different effects on female and male hosts. Female workers were castrated and behaviorally manipulated by female or male parasites, but only showed moderate differences in relative allocation of different brain tissue compared to non-parasitized workers. In contrast, the testes and behavior of parasitized males were essentially unaffected, but they had smaller brains and greater relative volume of most sensory brain regions than non-parasitized males. Our results are consistent with caste and sex mediating brain plasticity in P. dominula and that the parasites manipulation can also drive differential allocation of brain regions depending on host sex.