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传染性法氏囊病病毒的 VP5 蛋白促进感染细胞中的病毒粒子释放,而不参与细胞死亡。

The VP5 protein of infectious bursal disease virus promotes virion release from infected cells and is not involved in cell death.

机构信息

Key Laboratory of Animal Epidemic Etiology & Immunological Prevention, Ministry of Agriculture, Zhejiang University, Zhejiang, People's Republic of China.

出版信息

Arch Virol. 2009;154(12):1873-82. doi: 10.1007/s00705-009-0524-4. Epub 2009 Oct 20.

Abstract

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.

摘要

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。

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