Varikkodan Muhammed Muhsin, Chen Chun-Chung, Wu Tzong-Yuan
Department of Chemistry, Chung Yuan Christian University, Chungli 320, Taiwan.
Department of Bioscience Technology, Chung Yuan Christian University, Chungli 320, Taiwan.
Int J Mol Sci. 2021 Jul 23;22(15):7891. doi: 10.3390/ijms22157891.
Chikungunya virus (CHIKV) is a mosquito-transmitted infectious agent that causes an endemic or epidemic outbreak(s) of Chikungunya fever that is reported in almost all countries. This virus is an intense global threat, due to its high rate of contagion and the lack of effective remedies. In this study, we developed two baculovirus expression vector system (BEVS)-based approaches for the screening of anti-CHIKV drugs in insect (Sf21) cells and U-2OS cells. First, structural protein of CHIKV was co-expressed through BEVS and thereby induced cell fusion in Sf21 cells. We used an internal ribosome entry site (IRES) to co-express the green fluorescent protein (EGFP) for identifying these fusion events. The EGFP-positive Sf21 cells fused with each other and with uninfected cells to form syncytia. We identified that ursolic acid has potential anti-CHIKV activity in vitro, by using this approach. Second, BacMam virus-based gene delivery has been successfully applied for the transient expression of non-structural proteins with a subgenomic promoter-EGFP (SP-EGFP) cassette in U-2OS cells to act as an in vitro CHIKV replicon system. Our BacMam-based screening system has identified that the potential effects of baicalin and baicalein phytocompounds can inhibit the replicon activity of CHIKV in U-2OS cells. In conclusion, our results suggested that BEVS can be a potential tool for screening drugs against CHIKV.
基孔肯雅病毒(CHIKV)是一种通过蚊子传播的感染因子,可引发基孔肯雅热的地方性或流行性疫情,几乎在所有国家都有报告。由于其高传染率和缺乏有效治疗方法,这种病毒对全球构成了严重威胁。在本研究中,我们开发了两种基于杆状病毒表达载体系统(BEVS)的方法,用于在昆虫(Sf21)细胞和U-2OS细胞中筛选抗CHIKV药物。首先,通过BEVS共表达CHIKV的结构蛋白,从而在Sf21细胞中诱导细胞融合。我们使用内部核糖体进入位点(IRES)共表达绿色荧光蛋白(EGFP)以识别这些融合事件。EGFP阳性的Sf21细胞相互融合,并与未感染的细胞融合形成多核巨细胞。通过这种方法,我们确定熊果酸在体外具有潜在的抗CHIKV活性。其次,基于BacMam病毒的基因递送已成功应用于在U-2OS细胞中用亚基因组启动子-EGFP(SP-EGFP)盒瞬时表达非结构蛋白,以作为体外CHIKV复制子系统。我们基于BacMam的筛选系统已确定黄芩苷和黄芩素植物化合物的潜在作用可抑制CHIKV在U-2OS细胞中的复制子活性。总之,我们的结果表明BEVS可能是筛选抗CHIKV药物的潜在工具。