Characterization of Potential Drug Targets Farnesyl Diphosphate Synthase and Geranylgeranyl Diphosphate Synthase in Schistosoma mansoni

ABSTRACT Schistosomiasis affects over 200 million people worldwide, with over 200,000 deaths annually. Currently, praziquantel is the only drug available against schistosomiasis. We report here that Schistosoma mansoni farnesyl diphosphate synthase ( Sm FPPS) and geranylgeranyl diphosphate synthase ( Sm GGPPS) are potential drug targets for the treatment of schistosomiasis. We expressed active, recombinant Sm FPPS and Sm GGPPS for subsequent kinetic characterization and testing against a variety of bisphosphonate inhibitors. Recombinant Sm FPPS was found to be a soluble 44.2-kDa protein, while Sm GGPPS was a soluble 38.3-kDa protein. Characterization of the substrate utilization of the two enzymes indicates that they have overlapping substrate specificities. Against Sm FPPS, several bisphosphonates had 50% inhibitory concentrations (IC 50 s) in the low micromolar to nanomolar range; these inhibitors had significantly less activity against Sm GGPPS. Several lipophilic bisphosphonates were active against ex vivo adult worms, with worm death occurring over 4 to 6 days. These results indicate that FPPS and GGPPS could be of interest in the context of the emerging resistance to praziquantel in schistosomiasis therapy.