Hasenkrug K J, Robertson S J, Porti J, McAtee F, Nishio J, Chesebro B
Laboratory of Persistent Viral Diseases, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, Hamilton, Montana 59840, USA. Kim
J Virol. 1996 Jul;70(7):4825-8. doi: 10.1128/JVI.70.7.4825-4828.1996.
The major determinants involved in neurological disease induction by polytropic murine leukemia virus FMCF98 are encoded by the envelope gene. To map these determinants further, we produced four chimeras which contained neurovirulent FMCF98 envelope sequences combined with envelope sequences from the closely related nonneurovirulent polytropic virus FMCF54. Surprisingly, two chimeric viruses containing completely separate envelope regions from FMCF98 could both induce neurological disease. Clinical signs caused by both neurovirulent chimeras appeared to be indistinguishable from those caused by FMCF98, although the incubation periods were longer. One neurovirulence determinant mapped to the N-terminal portion of gp7O, which contains the VRA and VRB receptor-binding regions, while the other determinant mapped downstream of both of the variable regions. Western blot (immunoblot) analyses and immunohistochemical staining of tissue sections indicated that the variations in neurovirulence of these viruses could not be explained by differences in either the quantitative level or the location of virus expression in the brain.
多嗜性鼠白血病病毒FMCF98诱发神经疾病的主要决定因素由包膜基因编码。为了进一步定位这些决定因素,我们构建了四个嵌合体,它们包含神经毒性FMCF98包膜序列,并与密切相关的非神经毒性多嗜性病毒FMCF54的包膜序列相结合。令人惊讶的是,两个含有来自FMCF98完全不同包膜区域的嵌合病毒都能诱发神经疾病。尽管潜伏期较长,但两种神经毒性嵌合体引起的临床症状似乎与FMCF98引起的症状无法区分。一个神经毒力决定因素定位于gp7O的N端部分,该部分包含VRA和VRB受体结合区域,而另一个决定因素定位于两个可变区域的下游。蛋白质免疫印迹分析和组织切片的免疫组织化学染色表明,这些病毒神经毒力的差异无法用大脑中病毒表达的定量水平或位置差异来解释。