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Antivenomics of Atropoides mexicanus and Atropoides picadoi snake venoms: Relationship to the neutralization of toxic and enzymatic activities

Authors :
Antúnez, José
Fernández, Julián
Lomonte, Bruno
Angulo, Yamileth
Sanz, Libia
Pérez, Alicia
Calvete, Juan J.
Gutiérrez, José María
Source :
Journal of Venom Research; Volumen 1. 2010, Kérwá, Universidad de Costa Rica, instacron:UCR, Journal of Venom Research, Digital.CSIC. Repositorio Institucional del CSIC, instname
Publication Year :
2010

Abstract

11 pages, 3 figures, 3 tables. PMID:21544177[PubMed] PMCID: PMC3086187<br />Viperid snakes of the genus Atropoides are distributed in Mexico and Central America and, owing to their size and venom yield, are capable of provoking severe envenomings in humans. This study evaluated, using an 'antivenomics' approach, the ability of a polyspecific (polyvalent) antivenom manufactured in Costa Rica to recognize the proteins of Atropoides mexicanus and A. picadoi venoms, which are not included in the immunization mixture. In addition, the neutralization of lethal, hemorrhagic, myotoxic, coagulant, proteinase and phospholipase A(2) (PLA(2)) activities of these venoms by the antivenom was assessed. The antivenom was highly-effective in immunodepleting many venom components, particularly high molecular mass P-III metalloproteinases (SVMPs), L-amino acid oxidases, and some serine proteinases and P-I SVMPs. In contrast, PLA(2)s, certain serine proteinases and P-I SVMPs, and a C type lectin-like protein were only partially immunodepleted, and two PLA(2) molecules were not depleted at all. The antivenom was able to neutralize all toxic and enzymatic activities tested, although neutralization of lethality by A. nummifer venom was achieved when a challenge dose of 3 LD(50)s of venom was used, but was iffective when 4 LD(50)s were used. These results, and previously obtained evidence on the immunoreactivity of this antivenom towards homologous and heterologous venoms, revealed the low immunogenicity of a number of venom components (PLA(2)s, CRISPs, P-I SVMPs, and some serine proteinases), underscoring the need to search for innovative immunization protocols to improve the immune response to these antigens.<br />This study was supported by projects from the Vicerrectoría de Investigación, Universidad de Costa Rica (741-A7- 611), CRUSA-CSIC (2007CR0004), CONARE, and grants BFU2007-61563 and BFU2010-17373 from the Ministerio de Ciencia e Innovación, Madrid, Spain

Details

Language :
English
Database :
OpenAIRE
Journal :
Journal of Venom Research; Volumen 1. 2010, Kérwá, Universidad de Costa Rica, instacron:UCR, Journal of Venom Research, Digital.CSIC. Repositorio Institucional del CSIC, instname
Accession number :
edsair.pmid.dedup....a0a8c419b22943fd05a4f2af5b24e63e