MRC-University of Glasgow, Centre for Virus Research, Glasgow, UK.
Laboratory of Virology and Infectious Disease, The Rockefeller University, New York, NY, USA.
Antiviral Res. 2020 Nov;183:104939. doi: 10.1016/j.antiviral.2020.104939. Epub 2020 Sep 24.
Yellow fever virus (YFV), a member of the Flaviviridae family, is an arthropod-borne virus that can cause severe disease in humans with a lethality rate of up to 60%. Since 2017, increases in YFV activity in areas of South America and Africa have been described. Although a vaccine is available, named strain 17D (Theiler and Smith, 1937), it is contraindicated for use in the elderly, expectant mothers, immunocompromised people, among others. To this day there is no antiviral treatment against YFV to reduce the severity of viral infection. Here, we used a circular polymerase extension reaction (CPER)-based reverse genetics approach to generate a full-length reporter virus (YFVhb) by introducing a small HiBit tag in the NS1 protein. The reporter virus replicates at a similar rate to the parental YFV in HuH-7 cells. Using YFVhb, we designed a high throughput antiviral screening luciferase-based assay to identify inhibitors that target any step of the viral replication cycle. We validated our assay by using a range of inhibitors including drugs, immune sera and neutralizing single chain variable fragments (scFv). In light of the recent upsurge in YFV and a potential spread of the virus, this assay is a further tool in the development of antiviral therapy against YFV.
黄热病病毒(YFV)属于黄病毒科,是一种节肢动物传播的病毒,可导致人类罹患重病,致死率高达 60%。自 2017 年以来,在南美洲和非洲的一些地区,YFV 的活动有所增加。虽然有一种名为 17D 株(Theiler 和 Smith,1937)的疫苗可用,但它不适用于老年人、孕妇、免疫功能低下者等人群。迄今为止,尚无针对 YFV 的抗病毒治疗方法来减轻病毒感染的严重程度。在这里,我们使用基于环聚合酶延伸反应(CPER)的反向遗传学方法,通过在 NS1 蛋白中引入一个小的 HiBit 标签,生成全长报告病毒(YFVhb)。报告病毒在 HuH-7 细胞中的复制速度与亲本 YFV 相似。使用 YFVhb,我们设计了一种高通量抗病毒筛选基于荧光素酶的测定法,以鉴定针对病毒复制周期任何步骤的抑制剂。我们使用一系列抑制剂(包括药物、免疫血清和中和单链可变片段(scFv))验证了我们的测定法。鉴于最近 YFV 的爆发以及该病毒传播的潜在风险,该测定法是针对 YFV 开发抗病毒治疗的又一工具。