摘要：Chikungunya virus (CHIKV) is the etiologic agent of Chikungunya fever, a globally spreading mosquito-borne disease. There is no approved antiviral or vaccine against CHIKV, highlighting an urgent need for novel therapies. In this context, snake venom proteins have demonstrated antiviral activity against several viruses, including arboviruses which are relevant to public health. In particular, the phospholipase A2
CB (PLA2
CB), a protein isolated from the venom of
Crotalus durissus terrificus was previously shown to possess anti-inflammatory, antiparasitic, antibacterial and antiviral activities. In this study, we investigated the multiple effects of PLA2
CB on the CHIKV replicative cycle in BHK-21 cells using CHIKV-
nanoluc, a marker virus carrying
nanoluciferase reporter. The results demonstrated that PLA2
CB possess a strong anti-CHIKV activity with a selectivity index of 128. We identified that PLA2
CB treatment protected cells against CHIKV infection, strongly impairing virus entry by reducing adsorption and post-attachment stages. Moreover, PLA2
CB presented a modest yet significant activity towards post-entry stages of CHIKV replicative cycle. Molecular docking calculations indicated that PLA2
CB may interact with CHIKV glycoproteins, mainly with E1 through hydrophobic interactions. In addition, infrared spectroscopy measurements indicated interactions of PLA2
CB and CHIKV glycoproteins, corroborating with data from in silico analyses. Collectively, this data demonstrated the multiple antiviral effects of PLA2
CB on the CHIKV replicative cycle, and suggest that PLA2
CB interacts with CHIKV glycoproteins and that this interaction blocks binding of CHIKV virions to the host cells.
