Sreenivasan V, Ng K L, Ng M L
Department of Microbiology, National University of Singapore, Kent Ridge, Singapore.
J Virol Methods. 1993 Nov;45(1):1-17. doi: 10.1016/0166-0934(93)90135-e.
A fungal metabolite brefeldin A (BFA) was used to study virus-host interaction in glycoprotein processing in West Nile virus-infected Vero and C6/36 cells. The results indicated that as little as 1 microgram/ml of BFA resulted in complete breakdown in the Golgi organelle in infected Vero cells. This led to modifications of the glycoproteins which could not be efficiently used in infectious virion formation. In contrast, as much as 10 micrograms/ml of BFA in culture medium did not affect either glycoprotein formation or production of infectious particles in C6/36 cells. The results showed that in Vero cells, the transport of glycoproteins to the Golgi apparatus is important in West Nile virus infection. It also showed that BFA could be used as a tool to understand further the trafficking of glycoprotein from the ER to Golgi in flavivirus infection in Vero cells.
一种真菌代谢产物布雷菲德菌素A(BFA)被用于研究西尼罗河病毒感染的Vero细胞和C6/36细胞中糖蛋白加工过程中的病毒-宿主相互作用。结果表明,低至1微克/毫升的BFA会导致受感染的Vero细胞中高尔基体完全解体。这导致了糖蛋白的修饰,而这些修饰不能有效地用于感染性病毒粒子的形成。相比之下,培养基中高达10微克/毫升的BFA对C6/36细胞中的糖蛋白形成或感染性颗粒的产生均无影响。结果表明,在Vero细胞中,糖蛋白向高尔基体的转运在西尼罗河病毒感染中很重要。这也表明,BFA可作为一种工具,进一步了解黄病毒感染Vero细胞时糖蛋白从内质网到高尔基体的运输过程。