Ultrastructural analysis of the interaction between F-actin and respiratory syncytial virus during virus assembly

被引:51
|
作者
Jeffree, Chris E.
Brown, Gaie
Aitken, Jim
Su-Yin, Dawn Yeo
Tan, Boon-Huan
Sugrue, Richard J.
机构
[1] Nanyang Technol Univ, Sch Biol Sci, Singapore 637551, Singapore
[2] Univ Edinburgh, Sch Biol Sci, Edinburgh EH9 3JH, Midlothian, Scotland
[3] Inst Virol, MRC Virol Unit, Glasgow G11 5JR, Lanark, Scotland
[4] DSO Natl Labs, Def Med & Environm Res Inst, Detect & Diagnost Lab, Singapore 117510, Singapore
基金
英国医学研究理事会;
关键词
respiratory syncytial virus; virus assembly; F-actin; phosphatidyl-3-kinase; Rac GTPase;
D O I
10.1016/j.virol.2007.08.007
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
During respiratory syncytial virus (RSV) infection there is a close physical interaction between the filamentous actin (F-actin) and the virus, involving both inclusion bodies and the virus filaments. This interaction appears to occur relatively early in the replication cycle, and can be detected from 8 h post-infection. Furthermore, during virus assembly we obtained evidence for the participation of an F-actin-associated signalling pathway involving phosphatidyl-3-kinase (PI3K). Treatment with the PI3K inhibitor LY294002 prevented the formation of virus filaments, although no effect was observed either on virus protein expression, or on trafficking of the virus glycoproteins to the cell surface. Inhibition of the activity of Rac GTPase, a down-stream effector of PI3K, by treatment with the Rac-specific inhibitor NSC23766 gave similar results. These data suggest that an intimate interaction occurs between actin and RSV, and that actin-associated signalling pathway, involving PI3K and Rac GTPase, may play an important role during virus assembly. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:309 / 323
页数:15
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