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Hirsutine an Indole Alkaloid of Uncaria rhynchophylla Inhibits Late Step in Dengue Virus Lifecycle

机译:菱角钩藤的吲哚生物碱组长抑制登革热病毒生命周期的后期

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摘要

Dengue virus (DENV) is transmitted to humans by Aedes mosquitoes and is a public health issue worldwide. No antiviral drugs specific for treating dengue infection are currently available. To identify novel DENV inhibitors, we analyzed a library of 95 compounds and 120 extracts derived from crude drugs (herbal medicines). In the primary screening, A549 cells infected with DENV-1 were cultured in the presence of each compound and extract at a final concentration of 10 μM (compound) and 100 μg/mL (extract), and reduction of viral focus formation was assessed. Next, we eliminated compounds and extracts which were cytotoxic using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. Hirsutine, an indole alkaloid of Uncaria rhynchophylla, was identified as a potent anti-DENV compound exhibiting high efficacy and low cytotoxicity. Hirsutine showed antiviral activity against all DENV serotypes. Time-of-drug-addition and time-of-drug-elimination assays indicated that hirsutine inhibits the viral particle assembly, budding, or release step but not the viral translation and replication steps in the DENV lifecycle. A subgenomic replicon system was used to confirm that hirsutine does not restrict viral genome RNA replication. Hirsutine is a novel DENV inhibitor and potential candidate for treating dengue fever.
机译:登革热病毒(DENV)是由伊蚊传播给人类的,是世界范围内的公共卫生问题。当前没有可用于治疗登革热感染的抗病毒药物。为了鉴定新型的DENV抑制剂,我们分析了95种化合物和120种提取自粗制药物(草药)的提取物的库。在初次筛选中,在每种化合物的存在下培养感染DENV-1的A549细胞,并以10μM(化合物)和100μg/ mL(提取物)的终浓度提取,评估病毒灶形成的减少。接下来,我们使用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴化物测定法消除了具有细胞毒性的化合物和提取物。菱角钩藤的吲哚生物碱组氨酸被鉴定为有效的抗DENV化合物,具有高功效和低细胞毒性。 Hirsutine对所有DENV血清型均显示抗病毒活性。药物添加时间和药物去除时间分析表明,hirsutine抑制DENV生命周期中的病毒颗粒装配,萌芽或释放步骤,但不抑制病毒翻译和复制步骤。使用亚基因组复制子系统确认hirsutine不会限制病毒基因组RNA复制。 Hirsutine是一种新型的DENV抑制剂,是治疗登革热的潜在候选药物。

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