Venom Evolution Laboratory, School of Biological Sciences, The University of Queensland, St. Lucia, QLD, 4072, Australia.
Venom Evolution Laboratory, School of Biological Sciences, The University of Queensland, St. Lucia, QLD, 4072, Australia.
Toxicol Lett. 2021 Aug 1;346:16-22. doi: 10.1016/j.toxlet.2021.04.007. Epub 2021 Apr 17.
The reef stonefish (Synanceia verrucosa) is a venomous fish which causes excruciatingly painful envenomations. While some research on the pathophysiology and functions of the venom have been conducted, there are still some gaps in the understanding of the venom effects due to the extreme lability of fish venom toxins and the lack of available testing platforms. Here we set out to assess new functions of the venom whilst also attempting to address some unclear pathophysiological effects from previous literature. Utilising a biolayer interferometry assay, our results highlight that the venom binds to the orthosteric site of the α-1 nicotinic acetylcholine receptor as well as the domain IV of voltage-gated Ca (Ca1.2) channel mimotopes. Both these results add some clarity to the previously ambiguous literature. We further assessed the coagulotoxic effects of the venom using thromboelastography and Stago STA-R Max coagulation analyser assays. We reveal that the venom produced anticoagulant activity and significantly delayed time until clot formation of recalcified human plasma which is likely through the degradation of phospholipids. There was a difference between fresh and lyophilised venom activity toward the nicotinic acetylcholine receptor mimotopes and coagulation assays, whilst no difference was observed in the activity toward the domain IV of Ca1.2 mimotopes. This research adds further insights into the neglected area of fish venom whilst also highlighting the extreme labile nature of fish venom toxins.
石斑鱼(Synanceia verrucosa)是一种有毒鱼类,其毒液会引起极其疼痛的中毒反应。尽管已经对毒液的病理生理学和功能进行了一些研究,但由于鱼类毒液毒素的极端不稳定性以及缺乏可用的测试平台,对毒液作用的理解仍存在一些空白。在这里,我们旨在评估毒液的新功能,同时尝试解决以前文献中一些不清楚的病理生理学效应。我们利用生物层干涉测定法,结果表明毒液与α-1 烟碱型乙酰胆碱受体的正构结合位点以及电压门控 Ca(Ca1.2)通道模拟肽的域 IV 结合。这两个结果都为以前模棱两可的文献提供了一些清晰度。我们进一步使用血栓弹性描记术和 Stago STA-R Max 凝血分析仪评估了毒液的凝血毒性作用。我们发现,毒液产生抗凝活性,并显著延迟了复钙人血浆的凝血形成时间,这可能是通过磷脂的降解实现的。新鲜毒液和冻干毒液在烟碱型乙酰胆碱受体模拟肽和凝血测定中的活性存在差异,而在 Ca1.2 模拟肽的域 IV 中的活性则没有差异。这项研究进一步深入了解了被忽视的鱼类毒液领域,同时也强调了鱼类毒液毒素的极端不稳定性。