Rapid and permanent cytotoxic effects of venom from Chiropsella bronzie and Malo maxima on human skeletal and cardiac muscle cells
Toxicon, ISSN: 0041-0101, Vol: 233, Page: 107250
2023
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Article Description
Jellyfish envenomation is a global public health risk; Cubozoans (box jellyfish) are a prevalent jellyfish class with some species causing potent and potentially fatal envenomation in tropical Australian waters. Previous studies have explored the mechanism of action of venom from the lethal Cubozoan Chironex fleckeri and from C arukia barnesi (which causes “Irukandji syndrome”), but mechanistic knowledge to develop effective treatment is still limited. This study performed an in-vitro cytotoxic examination of the venoms of Chiropsella bronzie and Malo maxima, two understudied species that are closely related to Chironex fleckeri and Carukia barnesi respectively. Venom was applied to human skeletal muscle cells and human cardiomyocytes while monitoring with the xCELLigence system. Chiropsella bronzie caused rapid cytotoxicity at concentrations as low as 58.8 μg/mL. Malo maxima venom caused a notable increase in cell index, a measure of cell viability, followed by cytotoxicity after 24-h venom exposure at ≥11.2 μg/mL on skeletal muscle cells. In contrast, the cardiomyocytes mostly showed significant increased cell index at the higher M. maxima concentrations tested. These findings show that these venoms can exert cytotoxic effects and Malo maxima venom mainly caused a sustained increase in cell index across both human cell lines, suggesting a different mode of action to Chiropsella bronzie. As these venoms show different real-world envenomation symptoms, the different cellular toxicity profiles provide a first step towards developing improved understanding of mechanistic pathways and novel envenomation treatment.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0041010123002362; http://dx.doi.org/10.1016/j.toxicon.2023.107250; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85169554438&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/37572796; https://linkinghub.elsevier.com/retrieve/pii/S0041010123002362; https://dx.doi.org/10.1016/j.toxicon.2023.107250
Elsevier BV
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