Preliminary analysis of a neotropical plant extract antiviral potential against Chikungunya and Mayaro viruses

Author:

Feitoza Pires Ellen CarolineORCID,da Silva Francini Pereira,Schallenberger Karoline,Hermann Bruna Saraiva,Mallmann Larissa,dos Santos Alini Godinho,Moura Wellington S.,de Oliveira Eugênio E.,Smagghe Guy,Ascêncio Sergio Donizeti,Santos Barbosa Robson dos,Mendes Ilsamar,Fleck Juliane DeiseORCID,Ribeiro Bergmann MoraisORCID,de Souza Aguiar Raimundo Wagner

Abstract

AbstractChikungunya and Mayaro fevers are viral infectious diseases, without vaccine or treatment, that causes fever and arthralgia. Establishing novel antiviral tools capable of preventing or treating Chikungunya virus (CHIKV), and Mayaro virus (MAYV) infections are needed. The use of plant-based compounds that affect the replication cycles of these viruses has been proposed as a promising strategy. Chiococca alba (L.) Hitchc. is a neotropical plant used by Yucatec Mayas traditional healers, mainly, as antipyretic and antirheumatic. To evaluate the potential of C. alba methanolic extracts against CHIKV and MAYV through preliminary analysis in vitro and in silico. The cytotoxicity profile of two C. alba roots methanolic extracts in Vero cells was performed by lysosomal viability using the neutral red assay, and the antiviral potential was determined by plaque assay. We further assessed, through in silico computational predictions, the possible interactions between the active site of the nsP2 proteases of these viruses with some secondary metabolites present in C. alba extracts, identified by High-Performance Liquid Chromatography (HPLC). Our partial phytochemical analysis revealed the presence of flavonoids, and phenolic acids in the C. alba extracts. Our in vitro assays showed that both C. alba extracts inhibited more than 70% of CHIKV and MAYV activities at 60 µg/mL concentration. Based on our in silico computational predictions, the flavonoids naringin and vitexin showed the greatest affinity energies with the CHIKV and MAYV nsP2 proteases, revealing the great potential of these compounds as viral inhibitors. The findings described here indicates that C. alba extracts, or their secondary metabolites, as a potential source of novel antiviral compounds.

Publisher

Cold Spring Harbor Laboratory

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