Chambers Thomas J, Jiang Xiaoshan, Droll Deborah A, Liang Yan, Wold William S M, Nickells Janice
Department of Molecular Microbiology and Immunology, St Louis University School of Medicine, 1402 South Grand Avenue, St Louis, MO 63104, USA.
J Gen Virol. 2006 Nov;87(Pt 11):3131-3140. doi: 10.1099/vir.0.81909-0.
A molecular clone of Japanese encephalitis virus (JE virus) was derived from the JE virus Nakayama strain and used to produce infectious JE virus in cell culture. The engineered JE virus resembled the parental JE virus in cell-culture properties and was related closely to other JE virus strains based on nucleotide sequence analysis. The JE virus clone was used as a genetic background for construction of a chimeric virus containing the structural proteins prM and E of Dengue virus, serotype 2. The chimeric JE/dengue 2 virus generated authentic dengue 2 structural proteins as assessed by immunoassays for the dengue E protein. It exhibited a small plaque size and less efficient growth in various cell lines than the parental JE virus. JE/dengue 2 virus was non-neuroinvasive for young adult mice, but displayed partial neurovirulence at doses up to 4 log p.f.u. given intracerebrally. Immunization of 3-week-old mice with JE/dengue 2 virus yielded neutralizing-antibody titres against dengue 2 virus and conferred protection against dengue encephalitis caused by neuroadapted dengue 2 virus. A rise in post-challenge neutralizing-antibody titres against dengue 2 virus in surviving mice suggests that immunization is associated with establishment of a memory antibody response in this model. This study demonstrates the capacity of JE virus to serve as a vector for expression of heterologous flavivirus structural proteins. Similar to previous studies with other chimeric flaviviruses, this approach may be useful as a genetic system for engineering experimental vaccines against Dengue virus and other medically important flaviviruses.
日本脑炎病毒(JE病毒)的一个分子克隆源自JE病毒中山株,并用于在细胞培养中产生传染性JE病毒。经基因工程改造的JE病毒在细胞培养特性方面与亲代JE病毒相似,并且根据核苷酸序列分析,与其他JE病毒株密切相关。该JE病毒克隆被用作构建一种嵌合病毒的遗传背景,该嵌合病毒含有2型登革病毒的结构蛋白prM和E。通过针对登革病毒E蛋白的免疫测定评估,嵌合JE/登革2病毒产生了正宗的登革2结构蛋白。与亲代JE病毒相比,它在各种细胞系中表现出较小的蚀斑大小和较低的生长效率。JE/登革2病毒对成年小鼠无神经侵袭性,但在脑内接种高达4 log p.f.u.的剂量时表现出部分神经毒力。用JE/登革2病毒免疫3周龄小鼠可产生针对登革2病毒的中和抗体滴度,并能预防由神经适应的登革2病毒引起的登革脑炎。存活小鼠中针对登革2病毒的攻击后中和抗体滴度升高表明,在该模型中免疫与记忆抗体反应的建立有关。本研究证明了JE病毒作为表达异源黄病毒结构蛋白载体的能力。与之前对其他嵌合黄病毒的研究类似,这种方法可能作为一种遗传系统,用于构建针对登革病毒和其他医学上重要的黄病毒的实验性疫苗。