Sicarius rugosus, the only member of the genus that inhabits Central America, is phylogenetically related to South American Sicarius spiders. These originated from a common ancestor with sister African species. Like Loxosceles, Sicarius exhibits venom phospholipase D activity due to a group of toxins known collectively as SicTox. A gel-assisted, bottom-up, proteomic analysis was performed to characterize the venom composition of S. rugosus. Hyaluronidase activity was determined using zymography. We identified several SicTox sequences, all classified as β-clade paralogs and sharing unique peptides with proteins from S. patagonicus, S. peruensis, and other species. Enzymes such as metalloproteinases, including putative astacins, carboxypeptidases, and angiotensin-converting enzymes, were detected in the venom. We also identified probable serine proteinases and a toxin-processing peptidylglycine α-hydroxylating monooxygenase, which may participate in venom peptide maturation. The venom displays in vitro hyaluronidase activity. Some likely peptide toxins were also identified, including a sicaritoxin, which preferentially targets insects. This represents the first proteomic study of the rare six-eyed sand spider, S. rugosus, from the dry forest of Costa Rica, confirming the presence of sequences similar to phospholipases D of other Sicarius and Loxosceles species, as well as venom neuropeptides and enzymes characteristic of the family Sicariidae, which may participate in tissue spreading and processing of other venom constituents.
Díaz et al. (Sun,) studied this question.