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Caveolae Restrict Tiger Frog Virus Release in HepG2 cells and Caveolae-Associated Proteins Incorporated into Virus Particles

机译:小窝限制了HepG2细胞中的虎蛙病毒的释放以及被整合到病毒颗粒中的小窝相关蛋白

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Caveolae are flask-shaped invaginations of the plasma membrane. Caveolae play important roles in the process of viruses entry into host cells, but the roles of caveolae at the late stage of virus infection were not completely understood. Tiger frog virus (TFV) has been isolated from the diseased tadpoles of the frog, Rana tigrina rugulosa, and causes high mortality of tiger frog tadpoles cultured in Southern China. In the present study, the roles of caveolae at the late stage of TFV infection were investigated. We showed that TFV virions were localized with the caveolae at the late stage of infection in HepG2 cells. Disruption of caveolae by methyl-β-cyclodextrinystatin or knockdown of caveolin-1 significantly increase the release of TFV. Moreover, the interaction between caveolin-1 and TFV major capsid protein was detected by co-immunoprecipitation. Those results suggested that caveolae restricted TFV release from the HepG2 cells. Caveolae-associated proteins (caveolin-1, caveolin-2, cavin-1, and cavin-2) were selectively incorporated into TFV virions. Different combinations of proteolytic and/or detergent treatments with virions showed that caveolae-associated proteins were located in viral capsid of TFV virons. Taken together, caveolae might be a restriction factor that affects virus release and caveolae-associated proteins were incorporated in TFV virions.
机译:小窝是质膜的烧瓶状内陷。小窝蛋白在病毒进入宿主细胞的过程中起着重要的作用,但是小窝蛋白在病毒感染后期的作用尚不完全清楚。虎蛙病毒(TFV)已从患病的tRana tigrina rugulosa的isolated中分离出来,并导致在中国南方养殖的tiger蛙的高死亡率。在本研究中,调查了小窝在TFV感染后期的作用。我们显示,TFV病毒粒子在HepG2细胞感染的晚期被定位于小窝。甲基-β-环糊精/制霉菌素破坏小窝或降低小窝蛋白-1可以显着增加TFV的释放。此外,通过共免疫沉淀检测caveolin-1和TFV主要衣壳蛋白之间的相互作用。这些结果表明,海绵体限制了TFV从HepG2细胞中的释放。与小窝相关的蛋白(caveolin-1,caveolin-2,cavin-1和cavin-2)被选择性地整合到TFV病毒粒子中。蛋白体的蛋白水解和/或去污剂处理的不同组合显示,海绵窝相关蛋白位于TFV病毒体的病毒衣壳中。总体而言,小窝蛋白可能是影响病毒释放的限制因素,并且与小窝蛋白相关的蛋白质已掺入TFV病毒粒子中。

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