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马尔堡病毒的基底外侧出芽:VP40将病毒糖蛋白GP重新定位到基底外侧表面。

Basolateral budding of Marburg virus: VP40 retargets viral glycoprotein GP to the basolateral surface.

作者信息

Kolesnikova Larissa, Ryabchikova Elena, Shestopalov Alexander, Becker Stephan

机构信息

Institute for Virology, Philipps-Universitat Marburg, Marburg, Germany.

出版信息

J Infect Dis. 2007 Nov 15;196 Suppl 2:S232-6. doi: 10.1086/520584.

Abstract

Virus budding from the basolateral domain of infected polarized cells could be one of the mechanisms underlying the quick systemic infection induced by Marburg virus (MARV). We found that MARV buds from the basolateral pole of hepatocytes and bile epithelial cells in infected guinea pigs, which leads to the release of infectious virus into the vascular system. Basolateral budding might be orchestrated by the basolaterally located MARV matrix protein VP40, which induces a partial relocalization of MARV glycoprotein from the apical to the basolateral plasma membrane. This redistribution is a prerequisite for budding of infectious virions from the basolateral domain.

摘要

从受感染的极化细胞基底外侧区域出芽的病毒可能是马尔堡病毒(MARV)引发快速全身感染的潜在机制之一。我们发现,在受感染的豚鼠中,MARV从肝细胞和胆管上皮细胞的基底外侧极出芽,这导致传染性病毒释放到血管系统中。基底外侧出芽可能由位于基底外侧的MARV基质蛋白VP40精心安排,该蛋白诱导MARV糖蛋白从顶端质膜部分重新定位到基底外侧质膜。这种重新分布是传染性病毒粒子从基底外侧区域出芽的先决条件。

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