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First crotoxin-like phospholipase A(2) complex from a New World non-rattlesnake species: nigroviriditoxin, from the arboreal Neotropical snake Bothriechis nigroviridis.
Lomonte, Bruno; Mora-Obando, Diana; Fernández, Julián; Sanz, Libia; Pla, Davinia; Gutiérrez, José María; Calvete, Juan J.
Afiliación
  • Lomonte B; Instituto Clodomiro Picado, Facultad de Microbiología, Universidad de Costa Rica, San José 11501, Costa Rica. Electronic address: bruno.lomonte@ucr.ac.cr.
  • Mora-Obando D; Instituto Clodomiro Picado, Facultad de Microbiología, Universidad de Costa Rica, San José 11501, Costa Rica.
  • Fernández J; Instituto Clodomiro Picado, Facultad de Microbiología, Universidad de Costa Rica, San José 11501, Costa Rica.
  • Sanz L; Instituto de Biomedicina de Valencia, CSIC, Jaume Roig 11, 46010 Valencia, Spain.
  • Pla D; Instituto de Biomedicina de Valencia, CSIC, Jaume Roig 11, 46010 Valencia, Spain.
  • Gutiérrez JM; Instituto Clodomiro Picado, Facultad de Microbiología, Universidad de Costa Rica, San José 11501, Costa Rica.
  • Calvete JJ; Instituto de Biomedicina de Valencia, CSIC, Jaume Roig 11, 46010 Valencia, Spain.
Toxicon ; 93: 144-54, 2015 Jan.
Article en En | MEDLINE | ID: mdl-25434534
ABSTRACT
Bothriechis nigroviridis is an arboreal Neotropical pitviper found in Costa Rica and Panamá. A previous proteomic profiling of its venom revealed the presence of proteins with homology to the A and B subunits of crotoxin/Mojave toxin, a heterodimeric phospholipase A2 (PLA2) complex only described in rattlesnake venoms (genera Crotalus and Sistrurus). The native crotoxin-like heterodimer, named nigroviriditoxin, and its A and B subunits were isolated in the present work, and the complete amino acid sequence of the B subunit was determined. The purified A and B components were demonstrated to form a complex when reconstituted under native conditions. Nigroviriditoxin presents features similar to crotoxin, albeit displaying lower toxicity the A component decreases the PLA2 activity of the B component, and increases its lethal potency in mice. Also in similarity to crotoxin B, nigroviriditoxin B induces myonecrosis. Its 122 amino acid sequence presents 81% identity with crotoxin B. Accordingly, nigroviriditoxin B was cross-recognized by equine antibodies from a Crotalus durissus terrificus antivenom. Phylogenetic analysis shows that the novel PLA2 from B. nigroviridis venom is basal to the branch including all the homologous PLA2 enzymes described in rattlesnakes, and more distant from PLA2s from Bothriechis species. Nigroviriditoxin is the first heterodimeric PLA2 complex found in a non-rattlesnake, Neotropical viperid venom, which displays structural, functional, and immunochemical similarities to crotoxin. The present findings are compatible with the existence of the particular structural trait of crotoxin-like molecules in New World pitvipers before the split of the Meso-South American and the Nearctic clades.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Modelos Moleculares / Viperidae / Crotoxina / Sustancias Macromoleculares / Fosfolipasas A2 Tipo de estudio: Prognostic_studies Límite: Animals País/Región como asunto: America central / Costa rica / Panama Idioma: En Revista: Toxicon Año: 2015 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Modelos Moleculares / Viperidae / Crotoxina / Sustancias Macromoleculares / Fosfolipasas A2 Tipo de estudio: Prognostic_studies Límite: Animals País/Región como asunto: America central / Costa rica / Panama Idioma: En Revista: Toxicon Año: 2015 Tipo del documento: Article