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High reduced/oxidized glutathione ratio in infectious spleen and kidney necrosis virus-infected cells contributes to degradation of VP08R multimers

机译:感染性脾脏和肾脏坏死病毒感染细胞的高降低/氧化谷胱甘肽比率有助于降解VP08R多方数

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Infectious spleen and kidney necrosis virus (ISKNV) is the type species of the genus Megalocytivirus, family Iridoviridae. The ISKNV-infected cells in fish tissues are attached by lymphatic endothelial cells (LECs), which is a unique pathological phenomenon of ISKNV infection. The viral proteins VP23R and VP08R and the host protein nidogen-1 constitute the virus-mock basement membrane (VMBM) on the membrane of infected cells to provide attaching sites for LECs. VP08R can form cross-linked multimers via intermolecular disulfide bonds to make VMBM a compact and strong structure. A question is that when the virions mature, how do they penetrate VMBMs to be released from the cells? In this study, the redox state in ISKNV-infected cells was investigated. We demonstrated that the ratio of reduced/oxidized glutathione (GSH/GSSG) was significantly elevated in ISKNV-infected cells, suggesting the increasing of reducing power. Remarkable changes were also observed in activities of many GSH metabolic enzymes and in the ratio of NADPH/NADP. We further exhibited that the high ratio of GSH/GSSG could lead to degradation of the VP08R multimer in vitro. These may suggest that the high GSH/GSSG ratio in infected cells could act on the VP08R multimer to facilitate the disassembly of VMBMs after virus maturation.
机译:感染性脾脏和肾脏坏死病毒(Isknv)是兆胞嘧啶属的类型,伊米多维尿基因。鱼类组织中的IsknV感染细胞由淋巴内皮细胞(LECs)附着,这是ISKNV感染的独特病理现象。病毒蛋白VP23R和VP08R和宿主蛋白氮原蛋白-1构成感染细胞膜上的病毒 - 模拟基底膜(VMBM),以提供LEC的附着位点。 VP08R可以通过分子间二硫键形成交联的多聚体,使VMBM具有紧凑且强的结构。一个问题是,当病毒群岛成熟时,它们如何穿透vmbms从细胞中释放?在该研究中,研究了IsknV感染细胞中的氧化还原状态。我们证明,Isknv感染细胞中,减少/氧化谷胱甘肽(GSH / GSSG)的比例显着升高,表明减少功率的增加。在许多GSH代谢酶的活动和NADPH / NADP之比中也观察到显着变化。我们进一步表现出GSH / GSSG的高比率可能导致VP08R多聚体在体外降解。这些可能表明感染细胞中的高GSH / GSSG比可以作用于VP08R多聚体,以便于病毒成熟后促进VMBMS的拆卸。

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