Chiou Shyan-Song, Chen Wei-June
Graduate Institute of Veterinary Public Health, National Chung Hsing University, Taichung 40227, Taiwan.
Vaccine. 2007 Dec 21;26(1):15-23. doi: 10.1016/j.vaccine.2007.10.047. Epub 2007 Nov 9.
Live attenuated strains of the Japanese encephalitis (JE) virus are known to form in various cultured cells. In this study, we selected attenuated JE virus variants by passing the parent virus strains once through Neuro-2a cells, showing that the selection intensity ranged 2-1000-fold after infection for 3d. The selection of attenuated variants appeared in association with mutations on the envelope (E) glycoprotein. This is likely determined by the differential binding abilities of specific E proteins with highly sulfated glycosaminoglycans on the cell surface. A plaque-purification method showed that Neuro-2a-selected variants were usually less neurovirulent, leading to a longer survival time of intracerebrally inoculated mice. Specific selected variants (mostly with the small-plaque phenotype) were shown to be more efficient at replication in Vero cells and less virulent, particularly those with substitution of the E-138 (Glu-->Lys) residue. As a result, most, if not all, low-virulent variants were generated in a relatively short time, all which have the potential to be live-attenuated vaccine candidates of the JE virus.
已知日本脑炎(JE)病毒的减毒活毒株可在多种培养细胞中形成。在本研究中,我们通过将亲本病毒株传代一次Neuro-2a细胞来选择减毒的JE病毒变体,结果表明感染3天后选择强度范围为2至1000倍。减毒变体的选择似乎与包膜(E)糖蛋白上的突变有关。这可能是由特定E蛋白与细胞表面高度硫酸化的糖胺聚糖的不同结合能力决定的。噬斑纯化方法表明,Neuro-2a选择的变体通常神经毒性较小,导致脑内接种小鼠的存活时间更长。特定选择的变体(大多具有小噬斑表型)在Vero细胞中的复制效率更高且毒性更低,特别是那些E-138(Glu→Lys)残基发生取代的变体。结果,大多数(如果不是全部)低毒力变体在相对较短的时间内产生,所有这些变体都有可能成为JE病毒的减毒活疫苗候选株。