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Título : Synergism of in vitro plasmodicidal activity of phospholipase A2 isoforms isolated from panamanian Bothrops asper venom
Autor: Silva, Simoes R.
Alfonso Ruiz Díaz, Jorge Javier
Gómez Garay, Ana Fidelina
Sobrinho, Juliana C.
Kayano, Anderson Makoto
Medeiros, Daniel Sol de
Teles, Carolina Bioni Garcia
Quintero Rueda, Aristides
Fuly, Andre
Gómez, Celeste Vega
Pereira, Soraya S.
Da Silva, Saulo Luis
Stábeli, Rodrigo Guerino
Soares, Andreimar M.
Correspondencia: Soares, Andreimar M., andreimar.soares@fiocruz.br
Palabras clave : Antiparasitic activity
Bothrops asper
Phospholipases A2
Snake venom
Synergism
Área de conocimiento FRASCATI amplio: 1. Ciencias Naturales y Exactas
Área de conocimiento FRASCATI detallado: 1.6.4 Bioquímica y Biología Molecular
Área de conocimiento FRASCATI específico: 1.6 Ciencias Biológicas
Área de conocimiento UNESCO amplio: 05 - Ciencias Físicas, Ciencias Naturales, Matemáticas y Estadísticas
ÁArea de conocimiento UNESCO detallado: 0511 - Biología
Área de conocimiento UNESCO específico: 051 - Ciencias Biológicas y Afines
Fecha de publicación : 2021
Volumen: Volumen 346
Fuente: Chemico-Biological Interactions
metadata.dc.identifier.doi: 10.1016/j.cbi.2021.109581
Tipo: ARTÍCULO
Abstract: 
Bothrops asper is one of the most important snake species in Central America, mainly because of its medical importance in countries like Ecuador, Panama and Costa Rica, where this species causes a high number of snakebite accidents. Several basic phospholipases A2 (PLA2s) have been previously characterized from B. asper venom, but few studies have been carried out with its acidic isoforms. In addition, since snake venom is a rich source of bioactive substances, it is necessary to investigate the biotechnological potential of its components. In this context, this study aimed to carry out the biochemical characterization of PLA2 isoforms isolated from B. asper venom and to evaluate the antiparasitic potential of these toxins. The venom and key fractions were subjected to different chromatographic steps, obtaining nine PLA2s, four acidic ones (BaspAc-I, BaspAc-II, BaspAc-III and BaspAc-IV) and five basic ones (BaspB-I, BaspB-II, BaspB-III, BaspB-IV and BaspB-V). The isoelectric points of the acidic PLA2s were also determined, which presented values ranging between 4.5 and 5. The findings indicated the isolation of five unpublished isoforms, four Asp49-PLA, corresponding to the group of acidic isoforms, and one Lys49-PLA2-like. Acidic PLA2s catalyzed the degradation of all substrates evaluated; however, for the basic PLA2s, there was a preference for phosphatidylglycerol and phosphatidic acid. The antiparasitic potential of the toxins was evaluated, and the acidic PLA2s demonstrated action against the epimastigote forms of T. cruzi and promastigote forms of L. infantum, while the basic PLA2s BaspB-II and BaspB-IV showed activity against P. falciparum. The results indicated an increase of up to 10 times in antiplasmodial activity, when the Asp49-PLA2 and Lys49-PLA2 were associated with one another, denoting synergistic action between these PLA2 isoforms. These findings correspond to the first report of synergistic antiplasmodial action for svPLA2s, demonstrating that these molecules may be important targets in the search for new antiparasitic agents
URI : https://www.scopus.com/record/display.uri?eid=2-s2.0-85111259832&doi=10.1016%2fj.cbi.2021.109581&origin=inward&txGid=d393d08d099e7a610e7a19ba800e31a0
URI Fuente: https://www.journals.elsevier.com/chemico-biological-interactions
ISSN : 0009-2797
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