Wang J J, Liao C L, Yang C I, Lin Y L, Chiou C T, Chen L K
Institute of Biology and Anatomy, NDMC Taipei, Taiwan, Republic of China.
Arch Virol. 1998;143(12):2353-69. doi: 10.1007/s007050050466.
Infection with a mutant Japanese encephalitis virus (JEV) strain RP-2ms showed reduced neurovirulence than wild type or RP-9 strains after inoculation in BALB/c mice. However, higher intracellular viral titer was detected in Rp-2ms infected cultured cells. Localizations of non-structural 3 (NS3) and envelope (E) proteins were demonstrated by immunocytochemistry. NS3 protein was primarily found in the pyramidal neurons in cerebrum, in the molecular and granular layers of cerebellum. Neither E nor NS3 protein was detected in Purkinje cells of the cerebellum. Immunoelectron microscopic observations showed that E and NS3 proteins were positive in JEV-induced membranous systems, mainly hypertrophic rough endoplasmic reticulum (rER) and membrane vesicle structure (MVS) but not smooth membrane structure. Virus particles were seen in the Golgi apparatus, rER, nuclear envelope, MVS and cytoplasmic vacuoles. Different mechanisms of intracellular trapping in vivo provide a possible basis for attenuation of RP-2ms strains of JEV.
在BALB/c小鼠中接种后,感染突变型日本脑炎病毒(JEV)株RP-2ms显示出比野生型或RP-9株更低的神经毒力。然而,在Rp-2ms感染的培养细胞中检测到更高的细胞内病毒滴度。通过免疫细胞化学证实了非结构3(NS3)蛋白和包膜(E)蛋白的定位。NS3蛋白主要存在于大脑的锥体神经元、小脑的分子层和颗粒层。在小脑的浦肯野细胞中未检测到E蛋白和NS3蛋白。免疫电子显微镜观察表明,E蛋白和NS3蛋白在JEV诱导的膜系统中呈阳性,主要是肥大的粗面内质网(rER)和膜泡结构(MVS),而不是光滑膜结构。在高尔基体、rER、核膜、MVS和细胞质空泡中可见病毒颗粒。体内细胞内捕获的不同机制为JEV的RP-2ms株减毒提供了可能的基础。