Shankar V, Dietzschold B, Koprowski H
Wistar Institute of Anatomy and Biology, Philadelphia, Pennsylvania 19104-4268.
J Virol. 1991 May;65(5):2736-8. doi: 10.1128/JVI.65.5.2736-2738.1991.
Rabies virus pathogenesis was studied in a mouse model by inoculation of the masseter muscle. At different intervals, the masseter muscle, trigeminal ganglia, and brain were analyzed for virus-specific RNA with a polymerase chain reaction assay, which revealed that as early as 18 h postinfection (p.i.), virus-specific RNA was present in the trigeminal ganglia, and at 24 h p.i., viral RNA was identified in the brain stem. Analysis of the masseter muscle demonstrated virus at 1 h p.i. but no virus-specific RNA between 6 and 30 h p.i., indicating that virus invaded the nerve ending directly, without prior replication in the muscle. At 36 h p.i., viral RNA was detected again in the masseter muscle. Selective amplification of plus- and minus-strand RNA isolated from the masseter muscle at 96 h p.i. revealed that the majority of the rabies virus-specific RNA was in the positive sense, suggesting virus replication in muscle tissue during late stages of infection.
通过将狂犬病毒接种到咬肌,在小鼠模型中研究了狂犬病毒的发病机制。在不同时间间隔,采用聚合酶链反应分析法对咬肌、三叉神经节和脑进行病毒特异性RNA分析,结果显示,感染后(p.i.)最早在18小时,三叉神经节中就存在病毒特异性RNA,在感染后24小时,在脑干中鉴定出病毒RNA。咬肌分析显示在感染后1小时有病毒,但在感染后6至30小时没有病毒特异性RNA,这表明病毒直接侵入神经末梢,而没有先在肌肉中复制。在感染后36小时,在咬肌中再次检测到病毒RNA。对感染后96小时从咬肌分离的正链和负链RNA进行选择性扩增,结果显示,大多数狂犬病毒特异性RNA为正链,提示在感染后期病毒在肌肉组织中复制。