Synergism of in vitro plasmodicidal activity of phospholipase A2 isoforms isolated from panamanian Bothrops asper venom

dc.contributor.authorSilva, Simoes R.
dc.contributor.authorAlfonso Ruiz Díaz, Jorge Javier
dc.contributor.authorGómez Garay, Ana Fidelina
dc.contributor.authorSobrinho, Juliana C.
dc.contributor.authorKayano, Anderson Makoto
dc.contributor.authorMedeiros, Daniel Sol de
dc.contributor.authorTeles, Carolina Bioni Garcia
dc.contributor.authorQuintero Rueda, Aristides
dc.contributor.authorFuly, Andre
dc.contributor.authorGómez, Celeste Vega
dc.contributor.authorPereira, Soraya S.
dc.contributor.authorDa Silva, Saulo Luis
dc.contributor.authorStábeli, Rodrigo Guerino
dc.contributor.authorSoares, Andreimar M.
dc.date.accessioned2022-02-02T19:34:06Z
dc.date.available2022-02-02T19:34:06Z
dc.date.issued2021
dc.description.abstractBothrops 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 The findings indicated the isolation of five unpublished isoforms, four Asp49-PLA, corresponding to the group of acidic isoforms, and one Lys49-PLA2-like.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
dc.identifier.doi10.1016/j.cbi.2021.109581
dc.identifier.issn0009-2797
dc.identifier.urihttps://www.scopus.com/record/display.uri?eid=2-s2.0-85111259832&doi=10.1016%2fj.cbi.2021.109581&origin=inward&txGid=d393d08d099e7a610e7a19ba800e31a0
dc.language.isoes_ES
dc.sourceChemico-Biological Interactions
dc.subjectAntiparasitic activity
dc.subjectBothrops asper
dc.subjectPhospholipases A2
dc.subjectSnake venom
dc.subjectSynergism
dc.titleSynergism of in vitro plasmodicidal activity of phospholipase A2 isoforms isolated from panamanian Bothrops asper venom
dc.typeARTÍCULO
dc.ucuenca.afiliacionSilva, S., Fundacao Oswaldo Cruz de Rondonia (Fiocruz Rondonia), Porto Velho, Brasil
dc.ucuenca.afiliacionAlfonso, J., Centro para el Desarrollo de la Investigación Científica (CEDIC), Asunción, Paraguay
dc.ucuenca.afiliacionGómez, A., Fundacao Oswaldo Cruz de Rondonia (Fiocruz Rondonia), Porto Velho, Brasil
dc.ucuenca.afiliacionSobrinho, J., Fundacao Oswaldo Cruz de Rondonia (Fiocruz Rondonia), Porto Velho, Brasil
dc.ucuenca.afiliacionKayano, A., Fundacao Oswaldo Cruz de Rondonia (Fiocruz Rondonia), Porto Velho, Brasil
dc.ucuenca.afiliacionMedeiros, D., Fundacao Oswaldo Cruz de Rondonia (Fiocruz Rondonia), Porto Velho, Brasil
dc.ucuenca.afiliacionTeles, C., Fundacao Oswaldo Cruz de Rondonia (Fiocruz Rondonia), Porto Velho, Brasil
dc.ucuenca.afiliacionQuintero, A., Universidad Autónoma de Chiriquí (UNACHI), Chiriquí, Panama
dc.ucuenca.afiliacionFuly, A., Universidade Federal Fluminense, Niterói, Brasil
dc.ucuenca.afiliacionGómez, C., Centro para el Desarrollo de la Investigación Científica (CEDIC), Asunción, Paraguay
dc.ucuenca.afiliacionPereira, S., Fundacao Oswaldo Cruz de Rondonia (Fiocruz Rondonia), Porto Velho, Brasil
dc.ucuenca.afiliacionDa, S., Universidad de Cuenca, Facultad de Ciencias Químicas, Cuenca, Ecuador
dc.ucuenca.afiliacionStábeli, R., Fundacao Oswaldo Cruz de Rondonia (Fiocruz Rondonia), Porto Velho, Brasil
dc.ucuenca.afiliacionSoares, A., Fundacao Oswaldo Cruz de Rondonia (Fiocruz Rondonia), Porto Velho, Brasil
dc.ucuenca.areaconocimientofrascatiamplio1. Ciencias Naturales y Exactas
dc.ucuenca.areaconocimientofrascatidetallado1.6.4 Bioquímica y Biología Molecular
dc.ucuenca.areaconocimientofrascatiespecifico1.6 Ciencias Biológicas
dc.ucuenca.areaconocimientounescoamplio05 - Ciencias Físicas, Ciencias Naturales, Matemáticas y Estadísticas
dc.ucuenca.areaconocimientounescodetallado0511 - Biología
dc.ucuenca.areaconocimientounescoespecifico051 - Ciencias Biológicas y Afines
dc.ucuenca.correspondenciaSoares, Andreimar M., andreimar.soares@fiocruz.br
dc.ucuenca.cuartilQ2
dc.ucuenca.factorimpacto0.943
dc.ucuenca.idautorSRGP-4943-01
dc.ucuenca.idautor0000-0003-3189-0037
dc.ucuenca.idautor0000-0003-3737-7015
dc.ucuenca.idautorSGRP-4943-04
dc.ucuenca.idautorSGRP-4943-05
dc.ucuenca.idautorSGRP-4943-07
dc.ucuenca.idautor0000-0002-4529-2137
dc.ucuenca.idautor0000-0001-5400-7978
dc.ucuenca.idautor0000-0002-5265-5258
dc.ucuenca.idautorSGRP-4943-10
dc.ucuenca.idautorSRGP-4943-11
dc.ucuenca.idautor1757872526
dc.ucuenca.idautor0000-0002-5746-8152
dc.ucuenca.idautor0000-0003-1032-2188
dc.ucuenca.indicebibliograficoSCOPUS
dc.ucuenca.numerocitaciones0
dc.ucuenca.urifuentehttps://www.journals.elsevier.com/chemico-biological-interactions
dc.ucuenca.versionVersión publicada
dc.ucuenca.volumenVolumen 346

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