Debrus S, Sadzot-Delvaux C, Nikkels A F, Piette J, Rentier B
Laboratory of Fundamental Virology, Institute of Pathology, University of Liège, Belgium.
J Virol. 1995 May;69(5):3240-5. doi: 10.1128/JVI.69.5.3240-3245.1995.
Varicella-zoster virus (VZV) gene 63 encodes a protein with a predicted molecular mass of 30.5 kDa which has amino acid similarities with the immediate-early (IE) protein 22 (ICP-22) of herpes simplex virus type 1. In order to study the expression of this protein during lytic and latent infection, gene 63 was cloned in frame and downstream from the glutathione-S-transferase gene, expressed as a fusion protein, and purified. In VZV-infected Vero cells, antibodies directed against this protein detect two polypeptides of 45 and 38 kDa which are localized both in the cytoplasm and in the nucleus. Using a sequential combination of transcription and protein synthesis inhibitors (actinomycin D and cycloheximide, respectively), we demonstrated the immediate-early nature of this protein, which can thus be named IE63. Using a rat model of VZV latency, we showed that IE63 is heavily expressed, essentially in neurons, during latency. IE63 can also be detected in the skin of patients showing early herpes zoster symptoms.
水痘带状疱疹病毒(VZV)基因63编码一种预测分子量为30.5 kDa的蛋白质,该蛋白质与单纯疱疹病毒1型的立即早期(IE)蛋白22(ICP-22)具有氨基酸相似性。为了研究该蛋白在裂解性感染和潜伏性感染期间的表达情况,将基因63与谷胱甘肽-S-转移酶基因框内并在其下游进行克隆,表达为融合蛋白并进行纯化。在VZV感染的Vero细胞中,针对该蛋白的抗体可检测到两条分子量分别为45 kDa和38 kDa的多肽,它们定位于细胞质和细胞核中。通过分别使用转录抑制剂放线菌素D和蛋白质合成抑制剂环己酰亚胺的顺序组合,我们证明了该蛋白的立即早期性质,因此可将其命名为IE63。使用VZV潜伏的大鼠模型,我们发现IE63在潜伏期间大量表达,主要在神经元中。在出现早期带状疱疹症状的患者皮肤中也可检测到IE63。