Kaposi's sarcoma-associated herpesvirus viral interferon regulatory factor

被引:142
作者
Li, MT
Lee, H
Guo, J
Neipel, F
Fleckenstein, B
Ozato, K
Jung, JU
机构
[1] Harvard Univ, New England Reg Primate Res Ctr, Sch Med, Southborough, MA 01772 USA
[2] Univ Erlangen Nurnberg, Inst Klin & Mol Virol, D-8520 Erlangen, Germany
[3] NICHHD, Lab Mol Growth Regulat, Bethesda, MD 20892 USA
关键词
D O I
10.1128/JVI.72.7.5433-5440.1998
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Interferons (IFNs) are a family of multifunctional cytokines with antiviral activities. The K9 open reading frame of Kaposi's sarcoma-associated herpesvirus (KSHV) exhibits significant homology with cellular IFN regulatory factors (IRFs). We have investigated the functional consequence of K9 expression in IFN-mediated signal transduction. Expression of K9 dramatically repressed transcriptional activation induced by IFN-alpha, -beta, and -gamma. Further, it induced transformation of NIH 3T3 cells, resulting in morphologic changes, focus formation, and growth in reduced-serum conditions. The expression of antisense K9 in KSHV-infected BCBL-1 cells consistently increased IFN-mediated transcriptional activation but drastically decreased the expression of certain KSHV genes. Thus, the K9 gene of KSHV encodes the first virus-encoded IRF (v-IRF) which functions as a repressor for cellular IFN-mediated signal transduction. In addition, v-IRF likely plays an important role in regulating KSHV gene expression. These results suggest that KSHV employs an unique mechanism to antagonize IPN-mediated antiviral activity by harboring a functional v-IRF.
引用
收藏
页码:5433 / 5440
页数:8
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