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泰勒氏鼠脑脊髓炎病毒3D RNA聚合酶:其在中枢神经系统中的表达以及持续感染小鼠所产生的特异性免疫反应。

Theiler's murine encephalomyelitis virus 3D RNA polymerase: its expression in the CNS and the specific immune response generated in persistently infected mice.

作者信息

Johnston I C, Usherwood E J, Nash A A, Brown T D

机构信息

Department of Pathology, University of Cambridge, UK.

出版信息

J Gen Virol. 1995 Nov;76 ( Pt 11):2765-77. doi: 10.1099/0022-1317-76-11-2765.

Abstract

Intracerebral inoculation of the neurotropic murine picornavirus, Theiler's murine encephalomyelitis virus (TMEV), results either in an acute encephalitis (GDVII strain) or in the establishment of a persistent infection with the development of demyelinating lesions (BeAn strain). In this article, the expression of the viral RNA polymerase was studied in the central nervous system of both acutely and persistently infected mice and in infected cells in tissue culture. Similar numbers of acutely infected glial cells (80-85%) expressed both viral polymerase and structural proteins in vitro while a much smaller proportion of persistently infected glial cells (0.6-0.9%) expressed these proteins. Following infection of mice with GDVII, many cells in the brain were found to express polymerase. However, in the spinal cord of mice persistently infected with BeAn, very few cells were found to express the polymerase while many more cells showed the presence of viral structural proteins. This suggests that a restriction in viral replication, possibly at the level of polymerase expression, may be a feature of the persistent infection. However, enough polymerase was expressed to maintain a polymerase-specific antibody response in a number of infected animals as late as 21 months post-infection. Mechanisms that may be involved in the establishment and maintenance of TMEV persistence are discussed with reference to these findings.

摘要

向小鼠脑内接种嗜神经的小鼠微小核糖核酸病毒——泰勒氏小鼠脑脊髓炎病毒(TMEV),会引发急性脑炎(GDVII毒株),或者导致持续性感染并伴有脱髓鞘病变的发展(BeAn毒株)。在本文中,研究了病毒RNA聚合酶在急性和持续性感染小鼠的中枢神经系统以及组织培养中的感染细胞中的表达情况。在体外,数量相似的急性感染神经胶质细胞(80 - 85%)表达病毒聚合酶和结构蛋白,而持续性感染的神经胶质细胞中表达这些蛋白的比例要小得多(0.6 - 0.9%)。用GDVII感染小鼠后,发现脑中许多细胞表达聚合酶。然而,在持续感染BeAn的小鼠脊髓中,发现很少有细胞表达聚合酶,而更多细胞显示存在病毒结构蛋白。这表明病毒复制的限制,可能在聚合酶表达水平,可能是持续性感染的一个特征。然而,表达了足够的聚合酶,以在一些感染动物中维持聚合酶特异性抗体反应,直至感染后21个月。参照这些发现,讨论了可能参与TMEV持续性感染建立和维持的机制。

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