Herpes simplex virus type 1 suppresses the interferon signaling pathway by inhibiting phosphorylation of STATs and janus kinases during an early infection stage

被引:73
作者
Yokota, S
Yokosawa, N
Kubota, T
Suzutani, T
Yoshida, I
Miura, S
Jimbow, K
Fujii, N [1 ]
机构
[1] Sapporo Med Univ, Sch Med, Dept Microbiol, Chuo Ku, Sapporo, Hokkaido 0608556, Japan
[2] Sapporo Med Univ, Sch Med, Dept Dermatol, Chuo Ku, Sapporo, Hokkaido 0608556, Japan
[3] Asahikawa Med Coll, Dept Microbiol, Asahikawa, Hokkaido 0788510, Japan
关键词
herpes simplex virus type 1; interferon; JAK/STAT pathway; STAT1; STAT2; Jak1; Jak2; Tyk2; tyrosine phosphorylation;
D O I
10.1006/viro.2001.0941
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We examined the influence on the interferon (IFN) signaling pathway of infection with herpes simplex virus type 1 (HSV-1 strain VR3. Data from reporter gene assays showed that expression of both type I and type II IFN-inducible genes was dramatically suppressed during the early stage of HSV-1 infection (2 to 3 h postinfection). During these periods, phosphorylation levels of janus kinases (JAKs) and STATs did not increase after treatment of HSV-1-infected FL cells with IFN-alpha or IFN-gamma, although cellular protein levels of the JAKs and the sTATs were not significantly changed. In contrast, the inhibitory effect of HSV-1 on phosphorylation of STAT1 was not observed in U937 cells, which show resistance to steady-state accumulation of RNA for HSV-1 immediate-early genes. The phosphorylation of STAT1 in FL cells was not inhibited by infection with a UV-inactivated virus. These results indicate that Viral gene expression or viral protein production is necessary for the inhibition of phosphorylation by HSV-1. (C) 2001 Academic Press.
引用
收藏
页码:119 / 124
页数:6
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