Ellis Laura C, Koralnik Igor J
Division of Neurovirology, Department of Neurology, Beth Israel Deaconess Medical Center, Harvard Medical School, E/CLS-1005, 330 Brookline Avenue, Boston, MA, 02215, USA.
Center for Virology and Vaccine Research, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
J Neurovirol. 2015 Dec;21(6):671-8. doi: 10.1007/s13365-014-0278-y. Epub 2014 Aug 21.
JC virus (JCV) infection of the brain can cause progressive multifocal leukoencephalopathy, JCV granule cell neuronopathy, and JCV encephalopathy (JCVE). JCVCPN, isolated from the brain of a patient with JCVE, is a naturally occurring strain of JCV with a 143-base pair deletion in the agnogene. Cell culture studies of JCVCPN have shown that the loss of these nucleotides in the agnogene results in impaired expression of VP1 and infectious virion production. To better understand the role of this DNA sequence in JCV replication, we generated a series of deletions in the agnogene on the backbone of a virus which has a mutated agnoprotein start codon preventing agnoprotein expression. We found that deletion of nucleotides 376-396 results in decreased levels of viral DNA replication and a lack of VP1 expression. These results indicate that these nucleotides play a crucial role in JCV replication.
脑部的JC病毒(JCV)感染可导致进行性多灶性白质脑病、JCV颗粒细胞神经元病和JCV脑病(JCVE)。从一名JCVE患者脑部分离出的JCVCPN是一种自然存在的JCV毒株,其agnogene中有一个143个碱基对的缺失。对JCVCPN的细胞培养研究表明,agnogene中这些核苷酸的缺失导致VP1表达受损和传染性病毒粒子产生减少。为了更好地理解这段DNA序列在JCV复制中的作用,我们在一种病毒的骨干上的agnogene中产生了一系列缺失,该病毒的agnoprotein起始密码子发生了突变,从而阻止了agnoprotein的表达。我们发现,删除核苷酸376 - 396会导致病毒DNA复制水平降低以及VP1表达缺失。这些结果表明,这些核苷酸在JCV复制中起着关键作用。