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Antileishmanial effects of γCdcPLI, a phospholipase A(2) inhibitor from Crotalus durissus collilineatus snake serum, on Leishmania (Leishmania) amazonensis

BACKGROUND: Leishmaniasis, a neglected disease caused by the parasite Leishmania, is treated with drugs associated with high toxicity and limited efficacy, in addition to constant reports of the emergence of resistant parasites. In this context, snake serums emerge as good candidates since they are...

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Detalles Bibliográficos
Autores principales: Gonçalves, Marina Neves, Lopes, Daiana Silva, Teixeira, Samuel Cota, Teixeira, Thaise Lara, de Freitas, Vitor, Costa, Tássia Rafaella, Gimenes, Sarah Natalie Cirilo, de Camargo, Isabella Mitie, de Souza, Guilherme, da Silva, Marcelo Santos, Azevedo, Fernanda Van Petten de Vasconcelos, Grego, Kathleen Fernandes, Santos, Luísa Carregosa, Oliveira, Vinícius Queiroz, da Silva, Claudio Vieira, Rodrigues, Renata Santos, Yoneyama, Kelly Aparecida Geraldo, Clissa, Patricia Bianca, Rodrigues, Veridiana de Melo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Instituto Oswaldo Cruz, Ministério da Saúde 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10690931/
https://www.ncbi.nlm.nih.gov/pubmed/38018570
http://dx.doi.org/10.1590/0074-02760220225
Descripción
Sumario:BACKGROUND: Leishmaniasis, a neglected disease caused by the parasite Leishmania, is treated with drugs associated with high toxicity and limited efficacy, in addition to constant reports of the emergence of resistant parasites. In this context, snake serums emerge as good candidates since they are natural sources with the potential to yield novel drugs. OBJECTIVES: We aimed to show the antileishmanial effects of γCdcPLI, a phospholipase A(2) inhibitor from Crotalus durissus collilineatus snake serum, against Leishmania (Leishmania) amazonensis. METHODS: Promastigotes forms were exposed to γCdcPLI, and we assessed the parasite viability and cell cycle, as well as invasion and proliferation assays. FINDINGS: Despite the low cytotoxicity effect on macrophages, our data indicate that γCdcPLI has a direct effect on parasites promoting an arrest in the G1 phase and reduction in the G2/M phase at the highest dose tested. Moreover, this PLA(2) inhibitor reduced the parasite infectivity when promastigotes were pre-treated. Also, we demonstrated that the γCdcPLI treatment modulated the host cell environment impairing early and late steps of the parasitism. MAIN CONCLUSIONS: γCdcPLI is an interesting tool for the discovery of new essential targets on the parasite, as well as an alternative compound to improve the effectiveness of the leishmaniasis treatment.