Portis J L, Czub S, Robertson S, McAtee F, Chesebro B
Laboratory of Persistent Viral Diseases, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, Hamilton, Montana 59840, USA.
J Virol. 1995 Dec;69(12):8070-5. doi: 10.1128/JVI.69.12.8070-8075.1995.
A variety of ecotropic murine leukemia viruses cause neurodegenerative disease. We describe here the clinical and histopathological features of a neurologic disease induced by a polytropic murine leukemia virus, FMCF98. Clinical disease was dominated by hyperexcitability and ataxia, and the histopathology was characterized primarily by astrocytosis and astrocytic degeneration. The viral envelope gene harbored the determinants of neurovirulence, since the chimeric virus Fr98E, which contained the envelope gene of FMCF98 on a background of the nonneurovirulent virus FB29, caused a similar disease. The disease caused by Fr98E differed from that induced by the coisogenic neurovirulent ecotropic virus FrCasE in clinical presentation, histopathology, and distribution of virus in the central nervous system. Since Fr98E contains a polytropic envelope gene and FrCasE contains an ecotropic envelope gene, these phenotypic differences appeared to be determined by envelope sequences and may reflect differences in virus receptor usage in the central nervous system.
多种嗜亲性鼠白血病病毒可引发神经退行性疾病。我们在此描述由一种多嗜性鼠白血病病毒FMCF98诱发的神经系统疾病的临床和组织病理学特征。临床疾病主要表现为过度兴奋和共济失调,组织病理学主要特征为星形细胞增生和星形细胞变性。病毒包膜基因携带神经毒力的决定因素,因为嵌合病毒Fr98E(其在非神经毒力病毒FB29的背景上含有FMCF98的包膜基因)可引发类似疾病。由Fr98E引起的疾病在临床表现、组织病理学以及病毒在中枢神经系统中的分布方面与同基因神经毒力嗜亲性病毒FrCasE诱发的疾病不同。由于Fr98E含有多嗜性包膜基因而FrCasE含有嗜亲性包膜基因,这些表型差异似乎由包膜序列决定,并且可能反映中枢神经系统中病毒受体使用情况的差异。