Institute for Molecular Bioscience, The University of Queensland, St Lucia, Queensland, 4072, Australia.
Centre for Advanced Imaging, The University of Queensland, St Lucia, Queensland 4072, Australia.
J Proteomics. 2019 Jun 15;201:12-26. doi: 10.1016/j.jprot.2019.04.002. Epub 2019 Apr 4.
The Estuarine stonefish (Synanceia horrida) is recognised as one of the most venomous fish species in the world but the overall venom composition has yet to be investigated using in-depth transcriptomic and proteomic methods. To date, known venom components are restricted to a hyaluronidase and a large, pore-forming toxin known as Stonustoxin (SNTX). Transcriptomic sequencing of the venom gland resulted in over 170,000 contigs with only 0.4% that were homologous to putative venom proteins. Integration of the transcriptomic data with proteomic data from the S. horrida venom confirmed the hyaluronidase and SNTX to be present, together with several other protein families including major contributions from C-type lectins. Other protein families observed included peroxiredoxin and several minor protein families such as Golgi-associated plant pathogenesis related proteins, tissue pathway factor inhibitors, and Kazal-type serine protease inhibitors that, although not putative venom proteins, may contribute to the venom's adverse effects. BIOLOGICAL SIGNIFICANCE: Proteomic analysis of milked Synanceia horrida venom, paired with transcriptomic analysis of the venom gland tissue revealed for the first time the composition of one of the world's most dangerous fish venoms. The results demonstrate that the venom is relatively less complex compared to other well-studied venomous animals with a number of unique proteins not previously found in animal venoms.
石斑鱼(Synanceia horrida)被认为是世界上最毒的鱼类之一,但迄今为止,尚未采用深入的转录组学和蛋白质组学方法来研究其整体毒液成分。目前,已知的毒液成分仅限于透明质酸酶和一种称为石斑鱼毒素(SNTX)的大型孔形成毒素。毒液腺的转录组测序产生了超过 170000 个连续序列,其中只有 0.4%与假定的毒液蛋白具有同源性。将转录组数据与 S. horrida 毒液的蛋白质组数据整合,证实了透明质酸酶和 SNTX 的存在,此外还有其他几个蛋白家族,包括 C 型凝集素的主要贡献。观察到的其他蛋白家族包括过氧化物酶和几种较小的蛋白家族,如高尔基相关植物发病相关蛋白、组织途径因子抑制剂和 Kazal 型丝氨酸蛋白酶抑制剂,尽管它们不是假定的毒液蛋白,但可能有助于毒液的不良影响。生物学意义:从挤奶的 Synanceia horrida 毒液进行蛋白质组分析,并与毒液腺组织的转录组分析相结合,首次揭示了世界上最危险的鱼类毒液之一的成分。结果表明,与其他研究充分的有毒动物相比,毒液的相对复杂性较低,并且存在一些以前在动物毒液中未发现的独特蛋白质。