Tenser R B, Sommerville K W, Mummaw J G, Frisque R J
J Neurol Sci. 1986 Feb;72(2-3):243-54. doi: 10.1016/0022-510x(86)90012-2.
Brain tissue from a patient with progressive multifocal leukoencephalopathy (PML) was analyzed by molecular biological and electron-microscopic techniques. Viral DNA was isolated directly from brain tissue, cloned into a plasmid vector, and subjected to restriction endonuclease analysis. The pattern of restriction fragments identified by gel electrophoresis was almost indistinguishable from that of prototype JC virus. By this procedure the etiologic agent of PML in this patient was identified without the isolation of infectious virus. After centrifugal clarification of brain homogenates, high speed centrifugal pellets were studied by electron microscopy. Large numbers of 9-nm polygonal particles, sometimes in paracrystalline arrays, were observed. It was thought likely that these particles were capsomer subunits of 41-43 nm JC virus virions. That the particles were capsomers was supported by negative stain electron microscopy, including reconstruction studies with simian virus 40.
采用分子生物学和电子显微镜技术对一名进行性多灶性白质脑病(PML)患者的脑组织进行了分析。病毒DNA直接从脑组织中分离出来,克隆到质粒载体中,并进行限制性内切酶分析。通过凝胶电泳鉴定的限制性片段模式与原型JC病毒的模式几乎无法区分。通过该程序,在未分离出感染性病毒的情况下确定了该患者PML的病原体。在对脑匀浆进行离心澄清后,通过电子显微镜研究高速离心沉淀物。观察到大量9纳米的多边形颗粒,有时呈准晶体排列。据认为,这些颗粒可能是41 - 43纳米JC病毒粒子的衣壳亚基。负染色电子显微镜,包括用猿猴病毒40进行的重建研究,支持了这些颗粒是衣壳的观点。