Monaco M C, Jensen P N, Hou J, Durham L C, Major E O
Laboratory of Molecular Medicine and Neuroscience, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, 20892, USA.
J Virol. 1998 Dec;72(12):9918-23. doi: 10.1128/JVI.72.12.9918-9923.1998.
Progressive multifocal leukoencephalopathy is a demyelinating disease of the human central nervous system that results from lytic infection of oligodendrocytes by the polyomavirus JC (JCV). Originally, JCV was thought to replicate exclusively in human glial cells, specifically oligodendrocytes. However, we have recently shown that JCV can replicate in cells of lymphoid origin such as hematopoietic precursor cells, B lymphocytes, and tonsillar stromal cells. To determine whether tonsils harbor JCV, we tested a total of 54 tonsils, 38 from children and 16 from adult donors. Nested PCRs with primer sets specific for the viral T protein and regulatory regions were used for the detection of JCV DNA. JCV DNA was detected in 21 of 54 tonsil tissues, or 39% (15 of 38 children and 6 of 16 adults) by using regulatory-region primers and in 19 of 54 tonsil tissues, or 35% (13 of 38 children and 6 of 16 adults) by using the T-protein primers. The DNA extracted from children's nondissected tonsil tissue, isolated tonsillar lymphocytes, and isolated stromal cells that demonstrated PCR amplification of the JCV regulatory region underwent cloning and nucleotide sequencing. Of the regulatory-region sequences obtained, nearly all contained tandem repeat arrangements. Clones originating from nondissected tonsil tissue and tonsillar lymphocytes were found to have sequences predominantly of the Mad-1 prototype strain, whereas the majority of clones from the DNA of tonsillar stromal cells had sequences characteristic of the Mad-8br strain of JCV. A few clones demonstrated structures other than tandem repeats but were isolated only from tonsillar lymphocytes. These data provide the first evidence of the JCV genome in tonsil tissue and suggest that tonsils may serve as an initial site of viral infection.
进行性多灶性白质脑病是一种人类中枢神经系统脱髓鞘疾病,由多瘤病毒JC(JCV)对少突胶质细胞的溶解性感染引起。最初,JCV被认为仅在人类神经胶质细胞,特别是少突胶质细胞中复制。然而,我们最近发现JCV可以在淋巴来源的细胞中复制,如造血前体细胞、B淋巴细胞和扁桃体基质细胞。为了确定扁桃体是否携带JCV,我们总共检测了54个扁桃体,其中38个来自儿童,16个来自成年供体。使用针对病毒T蛋白和调控区的引物对进行巢式PCR检测JCV DNA。使用调控区引物在54个扁桃体组织中的21个(即39%,38个儿童中的15个和16个成年人中的6个)检测到JCV DNA,使用T蛋白引物在54个扁桃体组织中的19个(即35%,38个儿童中的13个和16个成年人中的6个)检测到JCV DNA。从儿童未解剖的扁桃体组织、分离的扁桃体淋巴细胞和分离的基质细胞中提取的DNA,若显示JCV调控区PCR扩增,则进行克隆和核苷酸测序。在获得的调控区序列中,几乎所有序列都包含串联重复排列。发现来自未解剖扁桃体组织和扁桃体淋巴细胞的克隆序列主要是Mad-1原型株,而来自扁桃体基质细胞DNA的大多数克隆具有JCV Mad-8br株的特征序列。少数克隆显示出串联重复以外的结构,但仅从扁桃体淋巴细胞中分离得到。这些数据提供了扁桃体组织中存在JCV基因组的首个证据,并表明扁桃体可能是病毒感染的初始部位。