Iltis J P, Vette J, Castellano G A, Madden D L, Sever J L
Infect Immun. 1982 Jul;37(1):350-8. doi: 10.1128/iai.37.1.350-358.1982.
Varicella-zoster virus (VZV) has been found to persistently infect the human rhabdomyosarcoma cell line A204. Infectious center assays and fluorescent antibody staining demonstrated continuous production of infectious VZV and viral antigen. The level of infection determined by fluorescent antibody staining was variable, and usually only a small percentage of the cells were capable of producing plaques in permissive fibroblasts. The extent of infection was similar in cell cultures passaged at split ratios of 1:2 or 1:10 and grown at 33 or 37 degrees C. VZV recovered from A204 cells several months after establishment of the persistent infection had markedly increased syncytia-forming activity as compared with the parental VZV grown in human diploid fibroblast cells and the three monkey kidney-derived cell lines Vero, CV-1, and MA104. The expression of this altered phenotype continued after serial passage of the cell-associated virus in human diploid fibroblast and Vero cells. Consequently, we designated the reisolated VZV as plaque variant A. The buoyant densities of VZV plaque variant A and VZV DNAs in CsCl gradients were indistinguishable.
已发现水痘-带状疱疹病毒(VZV)可持续感染人横纹肌肉瘤细胞系A204。感染中心试验和荧光抗体染色显示有传染性的VZV和病毒抗原持续产生。通过荧光抗体染色确定的感染水平各不相同,通常只有一小部分细胞能够在允许生长的成纤维细胞中形成噬斑。在以1:2或1:10的分裂比传代并在33℃或37℃下培养的细胞培养物中,感染程度相似。与在人二倍体成纤维细胞以及三种猴肾来源的细胞系Vero、CV-1和MA104中生长的亲本VZV相比,在建立持续感染数月后从A204细胞中回收的VZV具有明显增强的形成多核巨细胞的活性。在细胞相关病毒在人二倍体成纤维细胞和Vero细胞中连续传代后,这种改变的表型仍持续存在。因此,我们将重新分离的VZV命名为噬斑变体A。VZV噬斑变体A和VZV DNA在氯化铯梯度中的浮力密度没有区别。