The arylsulfatase- and phospholipase-rich venom of the plutoniumid centipede Theatops posticus

Toxicon. 2023 Sep:233:107231. doi: 10.1016/j.toxicon.2023.107231. Epub 2023 Jul 28.

Abstract

Research on centipede venoms has led to the discovery of a diverse array of novel proteins and peptides, including those with homology to previously discovered toxin families (e.g., phospholipase A2s and pM12a metalloproteases) and novel toxin families not previously detected in venoms (e.g., β-pore forming toxins and scoloptoxins). Most of this research has focused on centipedes in the order Scolopendromorpha, particularly those in the families Scolopendridae, Cryptopidae, and Scolopocryptopidae. To generate the first high-throughput venom characterization for a centipede in the scolopendromorph family Plutoniumidae, we performed venom-gland transcriptomics and venom proteomics on two Theatops posticus. We identified a total of 64 venom toxins, 60 of which were detected in both the venom-gland transcriptome and venom proteome and four of which were only detected transcriptomically. We detected a single highly abundant arylsulfatase B (ARSB) toxin, the first ARSB toxin identified from centipede venoms. As ARSBs have been detected in other venomous species (e.g., scorpions), ARSBs in T. posticus highlights a new case of convergent evolution across venoms. Theatops posticus venom also contained a much higher abundance and diversity of phospholipase A2 toxins compared to other characterized centipede venoms. Conversely, we detected other common centipedes toxins, such as CAPs and scoloptoxins, at relatively low abundances and diversities. Our observation of a diverse set of toxins from T. posticus venom, including those from novel toxin families, emphasizes the importance of studying unexplored centipede taxonomic groups and the continued potential of centipede venoms for novel toxin discovery and unraveling the molecular mechanisms underlying trait evolution.

Keywords: Arylsulfatase B; Centipede; Plutoniumidae; Theatops; Venom.

MeSH terms

  • Animals
  • Arthropod Venoms* / chemistry
  • Arthropods* / chemistry
  • Arylsulfatases / metabolism
  • Chilopoda / metabolism
  • Phospholipases / metabolism
  • Transcriptome

Substances

  • Arylsulfatases
  • Phospholipases
  • Arthropod Venoms