Nematodes use an extensive chemical language based on glycosides of the dideoxysugar ascarylose for developmental regulation (dauer formation), male sex attraction, aggregation, and dispersal. However, no examples of a female-or hermaphrodite-specific sex attractant have been identified to date. In this study, we investigated the pheromone system of the gonochoristic sour paste nematode Panagrellus redivivus, which produces sex-specific attractants of the opposite sex. Activity-guided fractionation of the P. redivivus exometabolome revealed that males are strongly attracted to ascr#1 (also known as daumone), an ascaroside previously identified from Caenorhabditis elegans hermaphrodites. Female P. redivivus are repelled by high concentrations of ascr#1 but are specifically attracted to a previously unknown ascaroside that we named dhas#18, a dihydroxy derivative of the known ascr#18 and an ascaroside that features extensive functionalization of the lipid-derived side chain. Targeted profiling of the P. redivivus exometabolome revealed several additional ascarosides that did not induce strong chemotaxis. We show that P. redivivus females, but not males, produce the male-attracting ascr#1, whereas males, but not females, produce the female-attracting dhas#18. These results show that ascaroside biosynthesis in P. redivivus is highly sex-specific. Furthermore, the extensive side chain functionalization in dhas#18, which is reminiscent of polyketide-derived natural products, indicates unanticipated biosynthetic capabilities in nematodes.hemical communication plays an important role in the biology of many free-living and parasitic nematodes (1). Recent studies have shown that a family of small-molecule signals, the ascarosides, control sexual attraction (2-5), aggregation (6, 7), olfactory plasticity (8), dauer formation (9-12), and dispersal (13) in the model organism Caenorhabditis elegans. Ascarosides ( Fig. 1) are glycolipids derived from the dideoxysugar ascarylose, which in some cases, bear additional moieties, such as para-aminobenzoic acid and indole carboxy-or p-hydroxybenzoyl groups. The diversity of behavioral effects modulated by ascarosides in C. elegans is paralleled by complexity of ascaroside structures. Targeted metabolomicsbased analysis of wild-type C. elegans exudates (i.e., the exometabolome) resulted in the detection of over 50 ascaroside components, many of which have no known function (14). Using LC-MS analysis, we have previously shown that ascaroside signaling is not restricted to C. elegans and is widely conserved among nematodes (15). Many free-living and parasitic nematode species were shown to release ascarosides. However, the species-specific functions of the identified ascarosides remain largely unknown. Moreover, this targeted analysis focused exclusively on ascarosides previously identified from C. elegans, and it seems likely that other nematode species produce additional ascarosides not present in C. elegans.In this study, we used activity-guided fractionation to isolate both male-an...