Grupo de Inmunología Molecular GYMOL, Universidad del Quindío, Armenia 630001, Quindío, Colombia.
Grupo de Parasitología Molecular GEPAMOL, Universidad del Quindío, Armenia 630001, Quindío, Colombia.
Viruses. 2023 Jul 17;15(7):1563. doi: 10.3390/v15071563.
Dengue is an acute febrile illness caused by the Dengue virus (DENV), with a high number of cases worldwide. There is no available treatment that directly affects the virus or the viral cycle. The objective of this study was to identify a compound derived from natural products that interacts with the NS5 protein of the dengue virus through virtual screening and evaluate its antiviral effect on DENV-2. Molecular docking was performed on NS5 using AutoDock Vina software, and compounds with physicochemical and pharmacological properties of interest were selected. The preliminary antiviral effect was evaluated by the expression of the NS1 protein. The effect on viral genome replication and/or translation was determined by NS5 production using DENV-2 Huh-7 replicon through ELISA and viral RNA quantification using RT-qPCR. The strategy proved effective in finding a compound (M78) with an indole-like structure and with an effect on the replication cycle of DENV-2. Treatment at 50 µM reduced the expression of the NS5 protein by 70% and decreased viral RNA by 1.7 times. M78 is involved in the replication and/or translation of the viral genome.
登革热是由登革病毒(DENV)引起的急性发热性疾病,全球病例众多。目前尚无直接针对病毒或病毒周期的有效治疗方法。本研究的目的是通过虚拟筛选鉴定一种源自天然产物的化合物,该化合物与登革病毒的 NS5 蛋白相互作用,并评估其对 DENV-2 的抗病毒作用。使用 AutoDock Vina 软件对 NS5 进行分子对接,选择具有理化和药理学特性的化合物。通过 NS1 蛋白的表达评估初步抗病毒作用。通过 ELISA 检测 NS5 产生和使用 DENV-2 Huh-7 复制子进行 RT-qPCR 定量 RNA 来确定对病毒基因组复制和/或翻译的影响。该策略在寻找具有吲哚样结构并对 DENV-2 复制周期有影响的化合物(M78)方面证明是有效的。50 µM 浓度的处理使 NS5 蛋白的表达降低了 70%,病毒 RNA 减少了 1.7 倍。M78 参与病毒基因组的复制和/或翻译。