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Children and Snakebite: Snake Venom Effects on Adult and Paediatric Plasma
Christina N Zdenek1, Caroline F B Rodrigues2, Lachlan A Bourke1
1Venom Evolution Lab, School of Biological Sciences, The University of Queensland, St. Lucia, QLD 4072, Australia.
Insights
Snakebite venom affects adults and children differently. Russell's Viper venom is more potent in children, while Mulga Snake and Many-horned Adder venoms are more potent in adults.
Area of Science:
- Toxicology
- Hematology
- Herpetology
Background:
- Snakebite envenoming is a neglected tropical disease, primarily causing coagulation disturbances.
- Age-related variations in human plasma are known, but their impact on snakebite pathology is understudied.
Purpose of the Study:
- To investigate age-related differences in human plasma susceptibility to snake venom coagulotoxicity.
- To compare the in vivo clotting effects of diverse snake venoms on adult versus pediatric plasma.
Main Methods:
- Tested venoms from 15 medically significant snake species globally.
- Assessed venom coagulotoxicity by measuring clotting time in adult (18+) and pediatric (median 3.3 years) human plasma.
- Compared venom effects to spontaneous plasma clotting times.
Main Results:
- Russell's Viper (procoagulant) venom showed significantly higher potency in pediatric plasma.
- Mulga Snake and Many-horned Adder (anticoagulant) venoms were significantly more potent in adult plasma.
- Other procoagulant and all pseudo-procoagulant venoms exhibited similar potency across both age groups.
Conclusions:
- Preliminary findings highlight age-dependent variations in plasma response to snake venoms.
- Results may guide future research on snakebite pathophysiology in different age demographics.
- Understanding these differences could help reduce the global burden of snakebite envenoming.
Abstract:
Snakebite is a globally neglected tropical disease, with coagulation disturbances being the primary pathology of many deadly snake venoms. Age-related differences in human plasma have been abundantly reported, yet the effect that these differences pose regarding snakebite is largely unknown. We tested for differences in coagulotoxic effects (via clotting time) of multiple snake venoms upon healthy human adult (18+) and paediatric (median 3.3 years old) plasma in vivo and compared these effects to the time it takes the plasmas to clot without the addition of venom (the spontaneous clotting time). We tested venoms from 15 medically significant snake species (from 13 genera) from around the world with various mechanisms of coagulotoxic actions, across the three broad categories of procoagulant, pseudo-procoagulant, and anticoagulant, to identify any differences between the two plasmas in their relative pathophysiological vulnerability to snakebite. One procoagulant venom (Daboia russelii, Russell's Viper) produced significantly greater potency on paediatric plasma compared with adult plasma. In contrast, the two anticoagulant venoms (Pseudechis australis, Mulga Snake; and Bitis cornuta, Many-horned Adder) were significantly more potent on adult plasma. All other procoagulant venoms and all pseudo-procoagulant venoms displayed similar potency across both plasmas. Our preliminary results may inform future studies on the effect of snake venoms upon plasmas from different age demographics and hope to reduce the burden of snakebite upon society.
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