Antibody-mediated neutralization and binding-reversal studies on alpha-neurotoxins from Micrurus nigrocinctus nigrocinctus (coral snake) venom.
Abstract: An ELISA based, non-radioactive acetylcholine receptor (AchR) binding assay was used to detect the alpha-neurotoxins present in Micrurus nigrocinctus nigrocinctus venom. Sera from horses hyperimmunized against M. nigrocinctus venom contain antibodies which inhibit the binding of M. n. nigrocinctus alpha-neurotoxins to AchR and reverse the binding of toxins already complexed with the receptor. This result supports the importance of using antivenom therapeutically in M. n. nigrocinctus envenomations even after the onset of neurological symptoms. M. nigrocinctus antivenoms cross-reacted in an ELISA with several elapid alpha-neurotoxins and inhibited the binding of Bungarus multicinctus alpha-bungarotoxin and Naja naja oxiana neurotoxin II to AchR in vitro, suggesting the presence of short-chain and long-chain alpha-neurotoxins in M. nigrocinctus venom. In vivo neutralization experiments with M. nigrocinctus antivenom demonstrate that M. nigrocinctus venom contains short-chain alpha-neurotoxin(s) which share common neutralizing epitope(s) with Naja naja oxiana neurotoxin II.
Publication Date: 1996-03-01 PubMed ID: 8730930DOI: 10.1016/0041-0101(95)00126-3Google Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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The research study explores the effect of antibodies in neutralizing and reversing the binding of alpha-neurotoxins, derived from the venom of Micrurus nigrocinctus nigrocinctus (coral snake), to the acetylcholine receptor (AchR). The study also emphasizes the therapeutic value of antivenom in treating envenomations even after neurological symptoms kickstart.
Methodology
- The researchers used a non-radioactive acetylcholine receptor (AchR) binding assay rooted in ELISA (Enzyme-Linked Immunosorbent Assay) to detect the alpha-neurotoxins in Micrurus nigrocinctus nigrocinctus venom.
- A hyperimmunization process was carried out on horses against the venom to produce vital antibodies.
Key Findings
- The research discovered that the sera from horses hyperimmunized against the venom comprises of antibodies that both inhibit the binding of alpha-neurotoxins to AchR and reverse the binding of toxins already complexed with the receptor.
- These findings underline the significant role of antivenom in treating M. n. nigrocinctus envenomations, especially after the start of neurological symptoms, differing from any presumptions that might assume antivenom to be ineffective after symptom onset.
- This efficacious impact of antivenom proceeds from its capacity to cross-react with several elapid alpha-neurotoxins and inhibit the binding of Bungarus multicinctus alpha-bungarotoxin and Naja naja oxiana neurotoxin II to AchR in vitro.
Identification of Toxins in Venom
- This cross-reactivity recommended the existence of both short-chain and long-chain alpha-neurotoxins in the venom of M. nigrocinctus.
- Moreover, in vivo neutralization experiments with M. nigrocinctus antivenom substantiated that the venom contains short-chain alpha-neurotoxin(s), which share common neutralizing epitope(s) with Naja naja oxiana neurotoxin II.
Implications
- The findings accentuate the need for comprehensive understanding of venom toxins to develop more efficient treatments against envenomations.
- The observations of how antibodies counteract these toxins open up possibilities for insights into the design and refinement of therapeutic strategies against various neurotoxic envenomations in the future.
Cite This Article
APA
Alape-Giron A, Stiles BG, Gutierrez JM.
(1996).
Antibody-mediated neutralization and binding-reversal studies on alpha-neurotoxins from Micrurus nigrocinctus nigrocinctus (coral snake) venom.
Toxicon, 34(3), 369-380.
https://doi.org/10.1016/0041-0101(95)00126-3 Publication
Researcher Affiliations
- Instituto Clodomiro Picado, Facultad de Microbiologia, Universidad de Costa Rica, San José, Costa Rica.
MeSH Terms
- Animals
- Antibodies / immunology
- Antivenins / administration & dosage
- Antivenins / immunology
- Binding, Competitive
- Cross Reactions
- Dose-Response Relationship, Drug
- Elapid Venoms / immunology
- Elapid Venoms / metabolism
- Elapid Venoms / toxicity
- Elapidae
- Enzyme-Linked Immunosorbent Assay
- Guinea Pigs
- Horses
- Immune Sera / immunology
- Immunization
- Mice
- Neurotoxins / immunology
- Neurotoxins / metabolism
- Neurotoxins / toxicity
- Neutralization Tests
- Receptors, Cholinergic / drug effects
- Receptors, Cholinergic / metabolism
Citations
This article has been cited 6 times.- Knudsen C, Jürgensen JA, Føns S, Haack AM, Friis RUW, Dam SH, Bush SP, White J, Laustsen AH. Snakebite Envenoming Diagnosis and Diagnostics.. Front Immunol 2021;12:661457.
- Castillo-Beltrán MC, Hurtado-Gómez JP, Corredor-Espinel V, Ruiz-Gómez FJ. A polyvalent coral snake antivenom with broad neutralization capacity.. PLoS Negl Trop Dis 2019 Mar;13(3):e0007250.
- Silva A, Hodgson WC, Isbister GK. Antivenom for Neuromuscular Paralysis Resulting From Snake Envenoming.. Toxins (Basel) 2017 Apr 19;9(4).
- Camargo TM, de Roodt AR, da Cruz-Höfling MA, Rodrigues-Simioni L. The neuromuscular activity of Micrurus pyrrhocryptus venom and its neutralization by commercial and specific coral snake antivenoms.. J Venom Res 2011;2:24-31.
- Gutiérrez JM, León G, Lomonte B. Pharmacokinetic-pharmacodynamic relationships of immunoglobulin therapy for envenomation.. Clin Pharmacokinet 2003;42(8):721-41.
- Heard K, O'Malley GF, Dart RC. Antivenom therapy in the Americas.. Drugs 1999 Jul;58(1):5-15.
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