Lavi E, Gilden D H, Wroblewska Z, Rorke L B, Weiss S R
Neurology. 1984 May;34(5):597-603. doi: 10.1212/wnl.34.5.597.
Intracerebral inoculation of 4- to 6-week-old C57BL/6 mice with the A59 strain of mouse hepatitis virus (MHV), a murine coronavirus, produced biphasic disease. Acute hepatitis and mild meningoencephalitis were followed by subacute spastic paralysis with demyelinating lesions in the brain and spinal cord as determined by Epon-embedded toluidine-blue-stained sections and by electronmicroscopy. MHV-A59 was cultured by plaque assay from the blood, brain, spinal cord, and liver of infected mice during the acute phase, but not in the chronic stage. MHV-A59 antigen was detected by immunofluorescence (IF) until 3 months postinfection (PI). Serum anti-MHV-A59 antibodies were detected from 7 days to 5 months PI. The induction of demyelination by MHV-A59 provides a suitable system to study virus-induced demyelination further.
用鼠冠状病毒小鼠肝炎病毒(MHV)的A59株对4至6周龄的C57BL / 6小鼠进行脑内接种,会引发双相性疾病。急性肝炎和轻度脑膜脑炎之后会出现亚急性痉挛性麻痹,并伴有大脑和脊髓的脱髓鞘病变,这通过环氧树脂包埋、甲苯胺蓝染色切片以及电子显微镜检查得以确定。在急性期,通过噬斑测定法可从感染小鼠的血液、大脑、脊髓和肝脏中培养出MHV - A59,但在慢性期则无法培养。通过免疫荧光(IF)在感染后(PI)3个月内均可检测到MHV - A59抗原。在感染后7天至5个月可检测到血清抗MHV - A59抗体。MHV - A59诱导的脱髓鞘为进一步研究病毒诱导的脱髓鞘提供了一个合适的系统。