Paramyxovirus fusion: Real-time measurement of parainfluenza virus 5 virus-cell fusion

被引:19
作者
Connolly, Sarah A.
Lamb, Robert A.
机构
[1] Northwestern Univ, Dept Biochem Mol Biol & Cell Biol, Evanston, IL 60208 USA
[2] Northwestern Univ, Howard Hughes Med Inst, Evanston, IL 60208 USA
关键词
R18; paramyxovirus membrane fusion; parainfluenza virus 5; Simian virus 5; pyrene; virus entry; flourescence;
D O I
10.1016/j.virol.2006.07.021
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Although cell-cell fusion assays are useful surrogate methods for studying virus fusion, differences between cell-cell and virus-cell fusion exist. To examine paramyxovirus fusion in real time, we labeled viruses with fluorescent lipid probes and monitored virus-cell fusion by fluorimetry. Two parainfluenza virus 5 (PIV5) isolates (W3A and SER) and PIV5 containing mutations within the fusion protein (F) were studied. Fusion was specific and temperature-dependent. Compared to many low pH-dependent viruses, the kinetics of PIV5 fusion was slow, approaching completion within several minutes. As predicted from cell-cell fusion assays, virus containing an F protein with an extended cytoplasmic tail (rSV5 F551) had reduced fusion compared to wild-type virus (W3A). In contrast, virus-cell fusion for SER occurred at near wild-type levels, despite the fact that this isolate exhibits a severely reduced cell-cell fusion phenotype. These results support the notion that virus-cell and cell-cell fusion have significant differences. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:203 / 212
页数:10
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