Dal Canto M C, Rabinowitz S G, Johnson T C, Hughes J V
Infect Immun. 1979 Apr;24(1):276-81. doi: 10.1128/iai.24.1.276-281.1979.
Ultrastructural immunoperoxidase studies were done in spinal cords of mice infected with wild type vesicular stomatitis virus or its temperature-sensitive (ts) mutant G31. Infected neurons showed subplasmalemmal staining of viral antigen and staining of viral particles budding from the neuronal membrane in wild-type vesicular stomatitis virus infection, whereas diffuse membrane and cytoplasmic staining with no budding virus was observed in ts G31 infection. Such findings suggest rapid viral assembly and release of viral particles from cells infected with wild-type virus. In contrast, maturation of ts G31 appears defective, and this would lead to accumulation of viral antigen in the cytoplasm of infected cells. These results correlate with studies in neuroblastoma cells which investigated the growth cycles of wild type, ts G31, and the spinal cord isolate of ts G31 as well as the viral protein-synthetic capacity of these viruses.
对感染野生型水疱性口炎病毒或其温度敏感(ts)突变体G31的小鼠脊髓进行了超微结构免疫过氧化物酶研究。在野生型水疱性口炎病毒感染中,受感染的神经元显示出病毒抗原的膜下染色以及从神经元膜出芽的病毒颗粒的染色,而在ts G31感染中观察到弥漫性膜和细胞质染色,但没有出芽病毒。这些发现表明野生型病毒感染的细胞中病毒快速组装并释放病毒颗粒。相比之下,ts G31的成熟似乎存在缺陷,这将导致病毒抗原在受感染细胞的细胞质中积累。这些结果与神经母细胞瘤细胞的研究相关,该研究调查了野生型、ts G31以及ts G31的脊髓分离株的生长周期以及这些病毒的病毒蛋白合成能力。