He Jian-Hui, Yan Muting, Zuo Hongliang, Niu Shengwen, Yuan Jia, Weng Shao-Ping, He Jianguo, Xu Xiaopeng
MOE Key Laboratory of Aquatic Product Safety / State Key Laboratory of Biocontrol, School of Life Sciences, Sun Yat-sen University, Guangzhou, PR China; Institute of Aquatic Economic Animals and Guangdong Provice Key Laboratory for Aquatic Economic Animals, Sun Yat-sen University, Guangzhou, PR China.
MOE Key Laboratory of Aquatic Product Safety / State Key Laboratory of Biocontrol, School of Life Sciences, Sun Yat-sen University, Guangzhou, PR China; Institute of Aquatic Economic Animals and Guangdong Provice Key Laboratory for Aquatic Economic Animals, Sun Yat-sen University, Guangzhou, PR China; School of Marine Sciences, Sun Yat-sen University, Guangzhou, PR China; South China Sea Resource Exploitation and Protection Collaborative Innovation Center (SCS-REPIC), Guangzhou, PR China.
Vet Microbiol. 2017 Aug;207:19-24. doi: 10.1016/j.vetmic.2017.05.024. Epub 2017 Jun 1.
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.
传染性脾肾坏死病毒(ISKNV)是虹彩病毒科巨细胞病毒属的模式种。鱼类组织中被ISKNV感染的细胞会被淋巴管内皮细胞(LEC)附着,这是ISKNV感染的一种独特病理现象。病毒蛋白VP23R和VP08R以及宿主蛋白巢蛋白-1在被感染细胞的膜上构成病毒模拟基底膜(VMBM),为LEC提供附着位点。VP08R可通过分子间二硫键形成交联多聚体,使VMBM成为紧密且坚固的结构。一个问题是,当病毒粒子成熟时,它们如何穿透VMBM从细胞中释放出来?在本研究中,对ISKNV感染细胞中的氧化还原状态进行了研究。我们证明,在ISKNV感染的细胞中,还原型/氧化型谷胱甘肽(GSH/GSSG)的比例显著升高,表明还原能力增强。在许多谷胱甘肽代谢酶的活性以及NADPH/NADP的比例方面也观察到了显著变化。我们进一步证明,高比例的GSH/GSSG在体外可导致VP08R多聚体降解。这些可能表明,感染细胞中高比例的GSH/GSSG可能作用于VP08R多聚体,以促进病毒成熟后VMBM的解体。