Key Laboratory of Animal Epidemic Etiology & Immunological Prevention, Ministry of Agriculture, Zhejiang University, Zhejiang, People's Republic of China.
Arch Virol. 2009;154(12):1873-82. doi: 10.1007/s00705-009-0524-4. Epub 2009 Oct 20.
The VP5 protein of infectious bursal disease virus (IBDV) was shown in previous reports to be involved in the cytopathogenicity of IBDV. Here, using a rescued VP5-deficient IBDV infectious clone, it was demonstrated that a lack of VP5 expression significantly hinders the release of viral progeny from infected cells but does not block intracellular virus production. Monoclonal VP5-expressing Vero cells did not exhibit induction of cell death. Using VP5-specific mAbs generated in our laboratory as a tool, it was shown by flow cytometry analysis that VP5 was detectable on the surface of IBDV-infected and monoclonal VP5-expressing Vero cells and bursal cells in IBDV-infected chickens. Taken together, these data suggest that the VP5 protein is involved in regulation of the release of intracellular IBDV virions and may be used as a cell-surface marker for detecting IBDV-infected cells in FCM analysis. This study contributes to the further characterization of the VP5 protein, which will allow a better understanding of the mechanism of IBDV pathogenicity.
传染性法氏囊病病毒(IBDV)的 VP5 蛋白先前的报告显示其参与了 IBDV 的细胞病变作用。在这里,使用拯救的 VP5 缺失 IBDV 感染性克隆,证明缺乏 VP5 表达显著阻碍了感染细胞中病毒后代的释放,但并不阻止细胞内病毒的产生。表达单克隆 VP5 的 Vero 细胞未表现出诱导细胞死亡。使用我们实验室中产生的 VP5 特异性 mAb 作为工具,通过流式细胞术分析表明,VP5 可在 IBDV 感染的细胞和表达单克隆 VP5 的 Vero 细胞以及 IBDV 感染的鸡的法氏囊中检测到。总之,这些数据表明 VP5 蛋白参与调节细胞内 IBDV 病毒粒子的释放,并且可以用作 FCM 分析中检测 IBDV 感染细胞的表面标志物。本研究有助于进一步表征 VP5 蛋白,这将有助于更好地理解 IBDV 致病性的机制。