Neurophysiological action of centrally-acting spider toxin polypeptides derived from Hadronyche versuta and Tegenaria agrestis venoms

• Published in: Pesticide biochemistry and physiology 2023-05, Vol.192, p.105416-105416, Article 105416
• Main Authors: Bloomquist, J.R., Coquerel, Q.R.R., Hulbert, D., Norris, E.R.
• Format: Article
• Language: English
• Subjects: acetylcholine; adults; Animals; antagonism; antagonists; Australia; Blattodea; bungarotoxins; central nervous system; commercialization; Dipluridae; Drosophila melanogaster; Drosophila Proteins; GS-omega/kappa-Hxtx-Hv1a; Insect nicotinic acetylcholine receptor; larvae; Larval central nervous system; mechanism of action; Musca domestica; nerve tissue; neurophysiology; nicotine; Peptides - pharmacology; peripheral nervous system; pesticides; polypeptides; Scorpiones; Spider Venoms - toxicity; spiders; Tegenaria agrestes; toxins; U1-agatoxin-Ta1b-QA; α-Bungarotoxin
• ISSN: 0048-3575; 1095-9939
• DOI: 10.1016/j.pestbp.2023.105416

Established dogma concerning the action of insecticidal arthropod-derived peptides (e.g., scorpion toxins), was that they acted on the peripheral nervous system and were excluded from the central nervous system (CNS) by barrier systems. Initial evidence for a CNS-directed toxicological effect following parenteral administration was for a novel peptide from the Hobo spider, Tegeneria agrestis. This toxin was inactive on peripheral sensory and motor nerves, but had a potent excitatory effect on the CNS of larval Musca domestica. Recently, a commercialized formulation of GS-omega/kappa-Hxtx-Hv1a (HXTX), derived from the venom of the Australian blue mountain funnel web spider (Hadronyche versuta) was introduced for use in agriculture by Vestaron Corp. Its primary mode of action was found to be central neuroexcitation via positive allosteric modulation of nicotinic acetylcholine receptors (nAchR) of cockroach neurons. In the present study, this peptide showed hyperexcitation followed by a decrease in firing of the Drosophila melanogaster larval CNS that was prevented by co-exposure to 100 nM α-bungarotoxin (α-BGTX), a classical nAchR noncompetitive antagonist. This effect was mirrored in isobologram analysis, which showed clear antagonism between the two toxins when injected into adult houseflies. Interestingly, U1-agatoxin-Ta1b-QA derived from Tegeneria agrestis (VST-7304) had a similar biphasic action, but showed increased nerve discharge when co-exposed with 100 nM α-BGTX, and had additive effects when injected together with α-BGTX in isobologram analyses. Binary mixtures of HXTX or VST-7304 with 30 nM nicotine showed clear evidence of synergized nerve block, which was also observed for mixtures of HXTX and VST-7304. Taken together, these data suggest that HXTX and VST-7304 have somewhat different and complementary modes of action. [Display omitted] •GS-omega/kappa-Hxtx-Hv1a showed central hyperexcitation, then block•U1-agatoxin-Ta1b-QA had a similar biphasic action•These toxins had differential interactions in vivo and in vitro with α-bungarotoxin•Applying these 2 peptides together or each with nicotine caused synergized nerve block•HXTX and VST-7304 have somewhat different and complementary modes of action.