Thailand-Japan Research Collaboration Center on Emerging and Re-emerging Infections (RCC-ERI), Department of Medical Sciences, Ministry of Public Health, Nonthaburi, Thailand.
Research Institute for Microbial Diseases (RIMD), Osaka University, Suita, Osaka, Japan.
Virus Res. 2019 Oct 15;272:197732. doi: 10.1016/j.virusres.2019.197732. Epub 2019 Aug 21.
To visually examine the early phase of chikungunya virus (CHIKV) infection in target cells, we constructed a virus-like particle (VLP) in which the envelope protein E1 is fused with green fluorescent protein (GFP). This chikungunya VLP-GFP (CHIK-VLP-EGFP), purified by density gradient fractionation, was observed as 60-70 nm-dia. particles and was detected as tiny puncta of fluorescence in the cells. CHIK-VLP-EGFP showed binding properties similar to those of the wild-type viruses. Most of the fluorescence signals that had bound on Vero cells disappeared within 30 min at 37 °C, but not in the presence of anti-CHIKV neutralizing serum or an endosomal acidification inhibitor (bafilomycin A1), suggesting that the loss of fluorescence signals is due to the disassembly of the viral envelope following the internalization of CHIK-VLP-EGFP. In addition to these results, the fluorescence signals disappeared in highly susceptible Vero and U251MG cells but not in poorly susceptible A549 cells. Thus, CHIK-VLP-EGFP is a useful tool to examine the effects of the CHIKV neutralizing antibodies and antiviral compounds that are effective in the entry phase of CHIKV.
为了直观地观察基孔肯雅病毒(CHIKV)在靶细胞中的早期感染阶段,我们构建了一种病毒样颗粒(VLP),其中包膜蛋白 E1 与绿色荧光蛋白(GFP)融合。这种基孔肯雅 VLP-GFP(CHIK-VLP-EGFP)通过密度梯度分级分离纯化,呈 60-70nm 直径的颗粒状,在细胞中呈现出微小的荧光斑点。CHIK-VLP-EGFP 表现出与野生型病毒相似的结合特性。在 37°C 下,大多数结合在 Vero 细胞上的荧光信号在 30 分钟内消失,但在存在抗 CHIKV 中和血清或内体酸化抑制剂(巴弗洛霉素 A1)的情况下不会消失,这表明荧光信号的丢失是由于 CHIK-VLP-EGFP 内化后病毒包膜的解体。除了这些结果外,荧光信号在高度易感的 Vero 和 U251MG 细胞中消失,但在不易感的 A549 细胞中不消失。因此,CHIK-VLP-EGFP 是一种有用的工具,可以研究 CHIKV 中和抗体和在 CHIKV 进入阶段有效的抗病毒化合物的作用。