Oleszak E L, Knisley K, Rodkey L S, Leibowitz J L
Department of Pathology and Laboratory Medicine, University of Texas Health Science Center, Houston 77030.
J Virol Methods. 1992 Jul;38(1):103-12. doi: 10.1016/0166-0934(92)90173-b.
Mouse hepatitis virus (MHV) strain JHM (MHV-JHM) is a neurotropic coronavirus that causes acute fatal encephalomyelitis in 75-99% of infected mice. The surviving animals may subsequently develop demyelinating disease. We compared the S peplomer protein of the wild type (wt) and five temperature-sensitive (ts) mutants of MHV-JHM. In contrast with the wt, none of these five cause fatal disease (mortality less than 10%). Three of these ts mutants did not induce any demyelinating disease, a fourth caused demyelinating disease in 5% of the animals and a fifth, designated ts8, exhibited strong demyelinating properties and caused demyelination in 99% of the animals. SDS-PAGE analysis revealed no differences in the molecular weight of S peplomer protein of wt or ts MHV-JHM mutants. However, isoelectric focusing of the S protein of these five ts mutants and the wt MHV-JHM, followed by transfer to nitrocellulose sheets and immunoblotting with anti-S specific antibody revealed significant differences in the microheterogeneity of the S protein.
小鼠肝炎病毒(MHV)JHM株(MHV-JHM)是一种嗜神经冠状病毒,可在75%-99%的感染小鼠中引起急性致命性脑脊髓炎。存活的动物随后可能会发展为脱髓鞘疾病。我们比较了野生型(wt)和MHV-JHM的五个温度敏感(ts)突变体的S刺突蛋白。与野生型不同,这五个突变体均不会导致致命疾病(死亡率低于10%)。其中三个ts突变体不会诱发任何脱髓鞘疾病,第四个在5%的动物中引起脱髓鞘疾病,第五个称为ts8,具有很强的脱髓鞘特性,在99%的动物中引起脱髓鞘。SDS-PAGE分析显示,野生型或ts MHV-JHM突变体的S刺突蛋白分子量没有差异。然而,对这五个ts突变体和野生型MHV-JHM的S蛋白进行等电聚焦,然后转移到硝酸纤维素膜上,并用抗S特异性抗体进行免疫印迹,结果显示S蛋白的微观异质性存在显著差异。