College of Veterinary Medicine, Yangzhou University, Yangzhou, 225009, Jiangsu, China; Comparative Medicine Research Institute, Yangzhou University, Yangzhou, 225009, Jiangsu, China; Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou, 225009, Jiangsu, China; State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute of the Chinese Academy of Agricultural Sciences, Harbin, 150069, China.
College of Veterinary Medicine, Yangzhou University, Yangzhou, 225009, Jiangsu, China; Comparative Medicine Research Institute, Yangzhou University, Yangzhou, 225009, Jiangsu, China; Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou, 225009, Jiangsu, China.
Antiviral Res. 2022 Jan;197:105233. doi: 10.1016/j.antiviral.2021.105233. Epub 2021 Dec 30.
Japanese encephalitis virus (JEV) belongs to a zoonotic flavivirus and is the main cause of viral encephalitis in humans throughout Asia. During the past two decades, both genotypes I (G) and III (GIII) JEVs co-existed in many Asian countries, and the prevalent strains have shifted from GIII to GI. Since all licensed JE vaccines are derived from GIII strains and no specific treatment is available, the development of novel vaccines and specific antiviral drugs against both genotypes is urgently required. To solve the unstable issue of the JEV infectious cDNA clone and establish a reliable antiviral screening assay, we established the yeast artificial chromosome (YAC)-based reverse genetics systems for GI and GIII JEV strains through transformation-associated recombination (TAR) technology in yeast. The YAC-based infectious clones of GI and GIII JEV exhibited high genetic stability both in yeast and E. coli. Using these reverse genetics systems, recombinant EGFP-reporter viruses were generated and remained stable for at least 10 passages in vitro. An image-based antiviral assay for JEV was developed with the EGFP-reporter viruses, and two drugs were identified to have a broad-spectrum inhibitory effect on GI and GIII JEV replication, which provide potential new therapeutic for the treatment of multiple genotypes JEV infection.
日本脑炎病毒 (JEV) 属于人畜共患的黄病毒,是亚洲各地人类病毒性脑炎的主要病因。在过去的二十年中,两种基因型 I (G) 和 III (GIII) JEV 在许多亚洲国家共存,流行株已从 GIII 转变为 GI。由于所有许可的 JE 疫苗均源自 GIII 株,且尚无特效治疗方法,因此迫切需要针对两种基因型的新型疫苗和特效抗病毒药物。为了解决 JEV 感染性 cDNA 克隆的不稳定性问题并建立可靠的抗病毒筛选检测方法,我们通过酵母中的转化相关重组 (TAR) 技术,为 GI 和 GIII JEV 株建立了基于酵母人工染色体 (YAC) 的反向遗传学系统。GI 和 GIII JEV 的基于 YAC 的感染性克隆在酵母和大肠杆菌中均表现出很高的遗传稳定性。使用这些反向遗传学系统,生成了重组 EGFP 报告病毒,并且在体外至少稳定传代 10 次。使用 EGFP 报告病毒开发了基于图像的 JEV 抗病毒检测方法,并鉴定出两种药物对 GI 和 GIII JEV 复制具有广谱抑制作用,为治疗多种基因型 JEV 感染提供了潜在的新疗法。