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Título : Bothrops atrox from Ecuadorian Amazon: Initial analyses of venoms from individuals
Autor : Palma Patiño, Ricardo Sebastián
Salazar Valenzuela, David
Medina Villamizar, Evencio
Mendes, Bruno
Proaño Bolaños, Carolina
da Silva, Saulo L.
de Almeida, José R.
Palabras clave : Antivenom
Enzymatic
Lethality
Phenotype
Toxicological.
Fecha de publicación : 2021
Editorial : Scopus
Citación : Patiño RSP, Salazar-Valenzuela D, Medina-Villamizar E, Mendes B, Proaño-Bolaños C, da Silva SL, Almeida JR. Bothrops atrox from Ecuadorian Amazon: Initial analyses of venoms from individuals. Toxicon. 2021 Jan 24;193:63-72. doi: 10.1016/j.toxicon.2021.01.007. Epub ahead of print. PMID: 33503404.
Citación : PRODUCCIÒN CIENTÍFICA - ARTÍCULO CIENTÍFICO;A-IKIAM-000304
Resumen : Bothrops atrox is the most clinically relevant snake species within the Amazon region, which includes Ecuadorian territories. It comprises a large distribution, which could contribute to the genetic and venomic variation identified in the species. The high variability and protein isoform diversity of its venom are of medical interest, since it can influence the clinical manifestations caused by envenomation and its treatment. However, in Ecuador there is insufficient information on the diversity of venomic phenotypes, even of relevant species such as B. atrox. Here, we characterized the biochemical and toxicological profiles of the venom of six B. atrox individuals from the Ecuadorian Amazon. Differences in catalytic activities of toxins, elution profiles in liquid chromatography, electrophoretic patterns, and toxic effects among the analyzed samples were identified. Nonetheless, in the preclinical testing of antivenom, two samples from Mera (Pastaza) required a higher dose to achieve total neutralization of lethality and hemorrhage. Taken together, these data highlight the importance of analyzing individual venoms in studies focused on the outcomes of envenoming.
URI : https://doi.org/10.1016/j.toxicon.2021.01.007
http://repositorio.ikiam.edu.ec/jspui/handle/RD_IKIAM/424
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