The distribution, spatial clustering, and density of trapdoor spiders in two California coastal dune ecosystems

  The distribution, spatial clustering, and density of trapdoor spiders in two California coastal dune ecosystems Abstract Coastal dune ecosystems support endemic trapdoor spiders, yet population data for these species are limited. We conducted the first coastal dune trapdoor spider population estimation surveys at Moss Landing State Beach (California) and for Aptostichus stephencolberti Bond 2008 at Sunset State Beach using randomly selected 1m 2 quadrats across ~26,000 m 2 per site. Burrow densities were similar between sites (Sunset: 0.287 burrows/m 2 ; Moss: 0.453 burrows/m 2 ), yielding estimated population sizes of ~35,206 and ~30,959 individuals, respectively. However, spatial analyses revealed contrasting patterns of burrow distribution. At Sunset State Beach, burrow presence was strongly associated with vegetation and occurred closer to plants, despite vegetation being randomly distributed. In contrast, no vegetation–burrow association was detected at Moss Landing, alth...

Role of the complement system in kidney cell death induced by Loxosceles venom Sphingomyelinases D

 

Role of the complement system in kidney cell death induced by Loxosceles venom Sphingomyelinases D

Abstract

Envenomation by Loxosceles spiders can result in local and systemic pathologies. Systemic loxoscelism, which can lead to death, is characterized by intravascular hemolysis, platelet aggregation, and acute kidney injury. Sphingomyelinase D (SMase D) in Loxosceles spider venom is responsible for both local and systemic pathologies, and has been shown to induce metalloprotease activity. As the complement system is involved in many renal pathologies and is involved in hemolysis in systemic loxoscelism, the aim of this study was to investigate its role and the role of complement regulators and metalloproteases in an in vitro model of Loxosceles venom induced renal pathology. We investigated the effects of the venom/SMase D and the complement system on the HK-2 kidney cell line. Using cell viability assays, western blotting, and flow cytometry, we show that human serum, as a source of complement, enhanced the venom/SMase D induced cell death and the deposition of complement components and properdin. Inhibitors for ADAM-10 and ADAM-17 prevented the venom induced release of the of the complement regulator MCP/CD46 and reduced the venom/SMase D induced cell death. Our results show that the complement system can contribute to Loxosceles venom induced renal pathology. We therefore suggest that patients experiencing systemic loxoscelism may benefit from treatment with metalloproteinase inhibitors and complement inhibitors, but this proposition should be further analyzed in future pre-clinical and clinical assays.

Okamoto, C.K., van den Berg, C.W., Pohl, P.C. et al. Role of the complement system in kidney cell death induced by Loxosceles venom Sphingomyelinases D. Arch Toxicol (2024). https://doi.org/10.1007/s00204-024-03711-8