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Development of physical forms of unintegrated retroviral DNA in mouse spinal cord tissue during ts1-induced spongiform encephalomyelopathy: elevated levels of a novel single-stranded form in paralyzed mice.在ts1诱导的海绵状脑脊髓病期间小鼠脊髓组织中未整合逆转录病毒DNA物理形式的发展:瘫痪小鼠中一种新型单链形式水平升高。
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本文引用的文献

1
Homologous superinfection of both producer and nonproducer HIV-infected cells is blocked at a late retrotranscription step.产生病毒和不产生病毒的HIV感染细胞的同源超感染在逆转录后期步骤被阻断。
Virology. 1993 Jun;194(2):441-52. doi: 10.1006/viro.1993.1283.
2
Integration of murine leukemia virus DNA depends on mitosis.鼠白血病病毒DNA的整合依赖于有丝分裂。
EMBO J. 1993 May;12(5):2099-108. doi: 10.1002/j.1460-2075.1993.tb05858.x.
3
Correlation of specific virus-astrocyte interactions and cytopathic effects induced by ts1, a neurovirulent mutant of Moloney murine leukemia virus.莫洛尼鼠白血病病毒神经毒力突变体ts1诱导的特定病毒-星形胶质细胞相互作用与细胞病变效应的相关性
J Virol. 1993 Mar;67(3):1137-47. doi: 10.1128/JVI.67.3.1137-1147.1993.
4
Toward an understanding of the molecular mechanisms of physiological cell death.迈向对生理性细胞死亡分子机制的理解。
Proc Natl Acad Sci U S A. 1993 Feb 1;90(3):786-9. doi: 10.1073/pnas.90.3.786.
5
Analysis of a temperature-sensitive mutation affecting the integration protein of Moloney murine leukemia virus.
Virology. 1993 Feb;192(2):673-8. doi: 10.1006/viro.1993.1086.
6
Distinct superinfection interference properties yet similar receptor utilization by cytopathic and noncytopathic feline leukemia viruses.细胞病变性和非细胞病变性猫白血病病毒具有不同的重叠感染干扰特性,但受体利用情况相似。
J Virol. 1993 Sep;67(9):5153-62. doi: 10.1128/JVI.67.9.5153-5162.1993.
7
Neurological disease induced in transgenic mice expressing the env gene of the Cas-Br-E murine retrovirus.在表达卡斯-布-埃氏鼠逆转录病毒env基因的转基因小鼠中诱发的神经疾病。
Proc Natl Acad Sci U S A. 1993 May 15;90(10):4538-42. doi: 10.1073/pnas.90.10.4538.
8
Expression of major histocompatibility complex antigens and serum neutralizing antibody in murine retroviral encephalitis.
J Neuropathol Exp Neurol. 1993 Mar;52(2):163-73. doi: 10.1097/00005072-199303000-00009.
9
The pathogenesis of murine retroviral infection of the central nervous system.
Brain Pathol. 1993 Apr;3(2):123-8. doi: 10.1111/j.1750-3639.1993.tb00736.x.
10
Temporal central and peripheral nervous system changes induced by a paralytogenic mutant of Moloney murine leukemia virus TB.莫洛尼鼠白血病病毒TB致瘫突变体引起的颞叶中枢和外周神经系统变化
Lab Invest. 1993 Dec;69(6):724-35.

在ts1诱导的海绵状脑脊髓病期间小鼠脊髓组织中未整合逆转录病毒DNA物理形式的发展:瘫痪小鼠中一种新型单链形式水平升高。

Development of physical forms of unintegrated retroviral DNA in mouse spinal cord tissue during ts1-induced spongiform encephalomyelopathy: elevated levels of a novel single-stranded form in paralyzed mice.

作者信息

Szurek P F, Brooks B R

机构信息

Neurology Service, William S. Middleton Memorial Veterans Affairs Hospital.

出版信息

J Virol. 1995 Jan;69(1):348-56. doi: 10.1128/JVI.69.1.348-356.1995.

DOI:10.1128/JVI.69.1.348-356.1995
PMID:7983729
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC188582/
Abstract

ts1 is a murine leukemia virus that causes rapidly evolving hindlimb paralysis in susceptible strains of mice. Following perinatal infection, three physical forms of unintegrated viral DNA were detected in the spinal cord by Southern blot hybridization. Linear and supercoiled closed-circle viral double-stranded DNAs were detected in both the central nervous system and non-central nervous system tissues. An elevated level of a novel minus-sense single-stranded form of viral DNA, which had a very high mobility in agarose gels, was correlated with the onset of symptoms of paralysis. As the severity of paralysis progressed, the level of this single-stranded form increased rapidly, with the highest level in the spinal cords of moribund mice. Since the virulence of a number of cytopathic retroviruses has been associated with the presence of increased amounts of unintegrated viral DNA in the tissues of the infected hosts, this novel form of highly mobile unintegrated single-stranded DNA may have a role in the neuropathogenesis of ts1.

摘要

ts1是一种鼠白血病病毒,可在易感小鼠品系中导致后肢迅速出现进行性麻痹。围产期感染后,通过Southern印迹杂交在脊髓中检测到三种未整合的病毒DNA物理形式。在中枢神经系统和非中枢神经系统组织中均检测到线性和超螺旋闭环病毒双链DNA。一种新型的负链单链病毒DNA水平升高,其在琼脂糖凝胶中具有非常高的迁移率,与麻痹症状的发作相关。随着麻痹严重程度的进展,这种单链形式的水平迅速增加,在濒死小鼠的脊髓中水平最高。由于许多细胞病变逆转录病毒的毒力与感染宿主组织中未整合病毒DNA数量的增加有关,这种新型的高度可移动未整合单链DNA形式可能在ts1的神经发病机制中起作用。