Combined Proteome and Toxicology Approach Reveals the Lethality of Venom Toxins from Jellyfish Cyanea nozakii.

Abstract

Jellyfish are a type of poisonous cnidarian invertebrate that secrete lethal venom for predation or defense. Human beings often become victims of jellyfish stings accidentally while swimming or fishing and suffer severe pain, itching, swelling, inflammation, shock, and even death. Jellyfish venom is composed of various toxins, and the lethal toxin is the most toxic and hazardous component of the venom, which is responsible for deaths caused by jellyfish stings and envenomation. Our previous study revealed many toxins in jellyfish venom, including phospholipase A2, metalloproteinase, and protease inhibitors. However, it is still unknown which type of toxin is lethal and how it works. Herein a combined toxicology analysis, proteome strategy, and purification approach was employed to investigate the lethality of the venom of the jellyfish Cyanea nozakii. Toxicity analysis revealed that cardiotoxicity including acute myocardial infarction and a significant decrease in both heart rate and blood pressure is the primary cause of death. Purified lethal toxin containing a fraction of jellyfish venom was subsequently subjected to proteome analysis and bioinformation analysis. A total of 316 and 374 homologous proteins were identified, including phospholipase A2-like toxins and metalloprotease-like toxins. Furthermore, we confirmed that the lethality of the jellyfish venom is related to metalloproteinase activity but without any phospholipase A2 activity or hemolytic activity. Altogether, this study not only provides a comprehensive understanding of the lethal mechanism of jellyfish venom but also provides very useful information for the therapeutic or rescue strategy for severe jellyfish stings.

• Authors: Rongfeng Li, Huahua Yu, Yang Yue, Pengcheng Li
• Journal: Journal of proteome research (J Proteome Res) Vol. 17 Issue 11 Pg. 3904-3913 (11 02 2018) ISSN: 1535-3907 [Electronic] United States
• PMID: 30223649 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Cnidarian Venoms
• Proteome
• Phospholipases A2
• Metalloproteases

Topics

• Animals
• Blood Pressure (drug effects)
• Brain (drug effects, physiopathology)
• Chromatography, Liquid
• Cnidarian Venoms (chemistry, toxicity)
• Female
• Gene Ontology
• Heart (drug effects, physiopathology)
• Heart Rate (drug effects)
• Kidney (drug effects, physiopathology)
• Liver (drug effects, physiopathology)
• Lung (drug effects, physiopathology)
• Male
• Mass Spectrometry
• Metalloproteases (chemistry, isolation & purification, toxicity)
• Mice
• Molecular Sequence Annotation
• Myocardial Infarction (chemically induced, physiopathology)
• Phospholipases A2 (chemistry, isolation & purification, toxicity)
• Proteome (chemistry, classification, isolation & purification, toxicity)
• Proteomics (methods)
• Scyphozoa (chemistry, pathogenicity, physiology)
• Spleen (drug effects, physiopathology)