Kitano T, Suzuki K, Yamaguchi T
J Virol. 1974 Sep;14(3):631-9. doi: 10.1128/JVI.14.3.631-639.1974.
Three morphologically distinct structures, inner core, envelope, and surface projections, were observed in purified Japanese encephalitis virus virions by electron microscopy. The average diameter of each structure was 29.8 +/- 2.5, 44.8 +/- 3.2, and 53.1 +/- 4.5 nm, respectively. Double staining with uranyl acetate and phosphotungstic acid preserved these structures well. Treatment of virions with proteolytic enzymes resulted in the loss of hemagglutinating activity, surface projections, and the major polypeptide band in polyacrylamide gel electrophoresis, which corresponds to glycoprotein, one of the three virion polypeptides. Surface projections were purified by cesium chloride density gradient centrifugation after treatment of virions with Nonidet P-40. The purified materials had a density of 1.256 g/cm(3) and were composed of only glycoprotein, as revealed by polyacrylamide gel electrophoresis. Purified surface projections carried hemagglutinating activity, as well as neutralizing antibody-blocking activity, and induced neutralizing antibody in mice.
通过电子显微镜观察纯化的日本脑炎病毒粒子,发现了三种形态上不同的结构,即内核、包膜和表面突起。每种结构的平均直径分别为29.8±2.5、44.8±3.2和53.1±4.5纳米。用醋酸铀和磷钨酸进行双重染色能很好地保存这些结构。用蛋白水解酶处理病毒粒子会导致血凝活性、表面突起以及聚丙烯酰胺凝胶电泳中的主要多肽带丧失,该多肽带对应于三种病毒粒子多肽之一的糖蛋白。在用Nonidet P - 40处理病毒粒子后,通过氯化铯密度梯度离心法纯化表面突起。纯化后的物质密度为1.256 g/cm³,聚丙烯酰胺凝胶电泳显示其仅由糖蛋白组成。纯化的表面突起具有血凝活性以及中和抗体阻断活性,并能在小鼠体内诱导中和抗体。