Systematic identification of type I and type II interferon-induced antiviral factors

被引:386
作者
Liu, Su-Yang [1 ]
Sanchez, David Jesse [2 ]
Aliyari, Roghiyh [1 ]
Lu, Sun [3 ]
Cheng, Genhong [1 ]
机构
[1] Univ Calif Los Angeles, Dept Microbiol Immunol & Mol Genet, Los Angeles, CA 90095 USA
[2] Western Univ Hlth Sci, Dept Pharmaceut Sci, Pomona, CA 91766 USA
[3] Guangzhou FulenGen Co Ltd, Guangzhou 510663, Guangdong, Peoples R China
基金
美国国家卫生研究院;
关键词
interferon stimulated genes; antiviral effectors; murine gammaherpes virus 68; MURINE GAMMAHERPESVIRUS 68; PEPTIDE-LOADING COMPLEX; SIGNALING PATHWAY; GAMMA; GENE; REPLICATION; VIRUS; MICE; TRANSCRIPTION; RECEPTORS;
D O I
10.1073/pnas.1114981109
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Type I and type II interferons (IFNs) are cytokines that establish the cellular antiviral state through the induction of IFN-stimulated genes (ISGs). We sought to understand the basis of the antiviral activity induced by type I and II IFNs in relation to the functions of their ISGs. Based on gene expression studies, we systematically identified antiviral ISGs by performing blinded, functional screens on 288 type I and type II ISGs. We assessed and validated the antiviral activity of these ISGs against an RNA virus, vesicular stomatitis virus (VSV), and a DNA virus, murine gammaherpes virus (MHV-68). Overall, we identified 34 ISGs that elicited an antiviral effect on the replication of either one or both viruses. Fourteen ISGs have uncharacterized antiviral functions. We further defined ISGs that affect critical life-cycle processes in expression of VSV protein and MHV-68 immediate-early genes. Two previously undescribed antiviral ISGs, TAP1 and BMP2, were further validated. TAP1-deficient fibroblasts were more susceptible to VSV infection but less so to MHV-68 infection. On the other hand, exogenous BMP2 inhibits MHV-68 lytic growth but did not affect VSV growth. These results delineate common and distinct sets of type I and type II IFN-induced genes as well as identify unique ISGs that have either broad or specific antiviral effects on these viruses.
引用
收藏
页码:4239 / 4244
页数:6
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