Marquardt M T, Kielian M
Department of Cell Biology, Albert Einstein College of Medicine, Bronx, New York 10461, USA.
Virology. 1996 Oct 1;224(1):198-205. doi: 10.1006/viro.1996.0521.
Semliki Forest virus (SFV), an enveloped alphavirus, Infects cells by endocytosis followed by low pH-triggered fusion of the virus and endocytic vesicle membranes. Progeny virus is released by budding from the cell plasma membrane. In vitro, SFV fusion with artificial liposomes is triggered by low pH and is dependent on the presence of cholesterol and sphingolipid in the target liposome membrane. In tissue culture, both SFV fusion and virus exit are strongly cholesterol-dependent when assayed in cholesterol-depleted insect cells. We here describe the preparation of insect cells that while not containing detectable amounts of cholesterol, have adapted to sterol-depleted conditions, resulting in a more permissive phenotype for SFV infection. Although still less efficient at supporting SFV infection than control cholesterol-containing cells, the adapted cells show a 45-fold increase in primary infection by SFV, increased release of progeny virus, and enhanced virus growth kinetics compared to nonadapted cholesterol-depleted cells. The adapted cells are also about 85-fold more permissive for low pH-induced fusion of SFV with the plasma membrane, suggesting that adaptation correlates with a change in the cell membrane.
塞姆利基森林病毒(SFV)是一种有包膜的甲病毒,通过内吞作用感染细胞,随后在低pH值触发下病毒与内吞囊泡膜融合。子代病毒通过从细胞质膜出芽释放。在体外,SFV与人工脂质体的融合由低pH值触发,并且依赖于靶脂质体膜中胆固醇和鞘脂的存在。在组织培养中,当在缺乏胆固醇的昆虫细胞中进行检测时,SFV融合和病毒释放都强烈依赖胆固醇。我们在此描述了昆虫细胞的制备方法,这些细胞虽然不含可检测量的胆固醇,但已适应了无甾醇条件,从而产生了对SFV感染更易感染的表型。尽管与含胆固醇的对照细胞相比,在支持SFV感染方面仍然效率较低,但与未适应的缺乏胆固醇的细胞相比,适应后的细胞在SFV初次感染时增加了45倍,子代病毒释放增加,病毒生长动力学增强。适应后的细胞对低pH诱导的SFV与质膜融合的敏感性也高出约85倍,这表明适应与细胞膜的变化相关。