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Anti-Neurotoxins from Micrurus mipartitus in the Development of Coral Snake Antivenoms

In Colombia, the genus Micrurus includes 30 species, of which M. mipartitus and M. dumerilii are the most widely distributed. Micrurus causes less than 3% of the approximately 5000 cases of snakebite per year. The elapid envenomation caused by the snakes from the Micrurus genus, are characterized by...

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Autores principales: Cardona-Ruda, Ana, Rey-Suárez, Paola, Núñez, Vitelbina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9027008/
https://www.ncbi.nlm.nih.gov/pubmed/35448874
http://dx.doi.org/10.3390/toxins14040265
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author Cardona-Ruda, Ana
Rey-Suárez, Paola
Núñez, Vitelbina
author_facet Cardona-Ruda, Ana
Rey-Suárez, Paola
Núñez, Vitelbina
author_sort Cardona-Ruda, Ana
collection PubMed
description In Colombia, the genus Micrurus includes 30 species, of which M. mipartitus and M. dumerilii are the most widely distributed. Micrurus causes less than 3% of the approximately 5000 cases of snakebite per year. The elapid envenomation caused by the snakes from the Micrurus genus, are characterized by the severity of their clinical manifestations, due to the venom neurotoxic components such as three-finger toxins (3FTx) and phospholipases (PLA(2)). The treatment for snakebites is the administration of specific antivenoms, however, some of them have limitations in their neutralizing ability. A strategy proposed to improve antivenoms is to produce antibodies against the main components of the venom. The aim of this work was to produce an antivenom, using an immunization protocol including the main 3FTx and PLA(2) responsible for M. mipartitus lethality. The antibody titers were determined by ELISA in rabbits’ serum. The immunized animals elicited a response against toxins and whole venom. The Immunoglobulin G (IgGs) obtained were able to neutralize the lethal effect of their homologous toxins. A combination of antivenom from M. mipartitus with antitoxins improved their neutralizing ability. In the same way, a mixture of anti 3FTx and PLA(2) protected the mice from a 1.5 median lethal dose (LD(50)) of M. mipartitus venom. The results showed that this might be a way to improve antibody titers specificity against the relevant toxins in M. mipartitus venom and indicated that there is a possibility to develop and use recombinant 3FTx and PLA(2) toxins as immunogens to produce antivenoms. Additionally, this represents an alternative to reduce the amount of venom used in anti-coral antivenom production.
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spelling pubmed-90270082022-04-23 Anti-Neurotoxins from Micrurus mipartitus in the Development of Coral Snake Antivenoms Cardona-Ruda, Ana Rey-Suárez, Paola Núñez, Vitelbina Toxins (Basel) Article In Colombia, the genus Micrurus includes 30 species, of which M. mipartitus and M. dumerilii are the most widely distributed. Micrurus causes less than 3% of the approximately 5000 cases of snakebite per year. The elapid envenomation caused by the snakes from the Micrurus genus, are characterized by the severity of their clinical manifestations, due to the venom neurotoxic components such as three-finger toxins (3FTx) and phospholipases (PLA(2)). The treatment for snakebites is the administration of specific antivenoms, however, some of them have limitations in their neutralizing ability. A strategy proposed to improve antivenoms is to produce antibodies against the main components of the venom. The aim of this work was to produce an antivenom, using an immunization protocol including the main 3FTx and PLA(2) responsible for M. mipartitus lethality. The antibody titers were determined by ELISA in rabbits’ serum. The immunized animals elicited a response against toxins and whole venom. The Immunoglobulin G (IgGs) obtained were able to neutralize the lethal effect of their homologous toxins. A combination of antivenom from M. mipartitus with antitoxins improved their neutralizing ability. In the same way, a mixture of anti 3FTx and PLA(2) protected the mice from a 1.5 median lethal dose (LD(50)) of M. mipartitus venom. The results showed that this might be a way to improve antibody titers specificity against the relevant toxins in M. mipartitus venom and indicated that there is a possibility to develop and use recombinant 3FTx and PLA(2) toxins as immunogens to produce antivenoms. Additionally, this represents an alternative to reduce the amount of venom used in anti-coral antivenom production. MDPI 2022-04-09 /pmc/articles/PMC9027008/ /pubmed/35448874 http://dx.doi.org/10.3390/toxins14040265 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Cardona-Ruda, Ana
Rey-Suárez, Paola
Núñez, Vitelbina
Anti-Neurotoxins from Micrurus mipartitus in the Development of Coral Snake Antivenoms
title Anti-Neurotoxins from Micrurus mipartitus in the Development of Coral Snake Antivenoms
title_full Anti-Neurotoxins from Micrurus mipartitus in the Development of Coral Snake Antivenoms
title_fullStr Anti-Neurotoxins from Micrurus mipartitus in the Development of Coral Snake Antivenoms
title_full_unstemmed Anti-Neurotoxins from Micrurus mipartitus in the Development of Coral Snake Antivenoms
title_short Anti-Neurotoxins from Micrurus mipartitus in the Development of Coral Snake Antivenoms
title_sort anti-neurotoxins from micrurus mipartitus in the development of coral snake antivenoms
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9027008/
https://www.ncbi.nlm.nih.gov/pubmed/35448874
http://dx.doi.org/10.3390/toxins14040265
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