Long Live the Queen: Eusociality is often considered to have arisen, at least in part, due to the inclusive fitness that workers gain through helping their queen sister to raise her offspring.
Van Oystaeyen
et al. (p. 287 ; see the Perspective by Chapuisat ) characterized the sterility-inducing queen pheromone across three distantly related eusocial hymenopterans (a wasp, a bumblebee, and a desert ant) and synthesized data across 69 other species. Queen pheromones appear to be remarkably conserved, which suggests that reproductive manipulation has ancient roots.
Eusocial insects use cuticular hydrocarbons as components of pheromones that mediate social behaviours, such as caste and nestmate recognition, and regulation of reproduction. In ants such as Harpegnathos saltator, the queen produces a pheromone which suppresses the development of workers’ ovaries and if she is removed, workers can transition to a reproductive state known as gamergate. Here we functionally characterize a subfamily of odorant receptors (Ors) with a nine-exon gene structure that have undergone a massive expansion in ants and other eusocial insects. We deorphanize 22 representative members and find they can detect cuticular hydrocarbons from different ant castes, with one (HsOr263) that responds strongly to gamergate extract and a candidate queen pheromone component. After systematic testing with a diverse panel of hydrocarbons, we find that most Harpegnathos saltator Ors are narrowly tuned, suggesting that several receptors must contribute to detection and discrimination of different cuticular hydrocarbons important in mediating eusocial behaviour.
1 July 2012 in Insect Biochemistry and Molecular Biology
▪ Abstract Polyene hydrocarbons and epoxides are used as pheromone components and sex attractants by four macrolepidopteran families: the Geometridae, Noctuidae, Arctiidae, and Lymantriidae. They constitute a second major class of lepidopteran pheromones, different from the C10-C18 acetates, alcohols, and aldehydes commonly found in other species. They are biosynthesized from diet-derived linoleic or linolenic acids and are characterized by C17-C23 straight chains, 1-3 cis double bonds separated by methylene groups, and 0, 1, or 2 epoxide functions. Pheromone blends are created from components with different chain lengths, numbers of double bonds, and functional groups, or from mixtures of epoxide regioisomers or enantiomers, with several examples of synergism between enantiomers. Behavioral antagonists also limit interspecific attraction, with numerous examples of antagonism by enantiomers. This review summarizes the taxonomic distribution, mechanisms used to generate unique pheromone blends, and the identification, synthesis, and biosynthesis of these compounds.