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Pseudorabies Virus DNA Polymerase Processivity Factor UL42 Inhibits Type I IFN Response by Preventing ISGF3-ISRE Interaction

文献类型： 外文期刊

作者： Zhang, Rui 1 ; Chen, Shifan 1 ; Zhang, Ying 1 ; Wang, Mengdong 1 ; Qin, Chao 1 ; Yu, Cuilian 1 ; Zhang, Yunfan 1 ; Li, Yue 1 ; Chen, Liankai 1 ; Zhang, Xinrui 1 ; Yuan, Xiufang 2 ; Tang, Jun 1 ;

作者机构： 1.China Agr Univ, Coll Vet Med, 2 Yuanmingyuan West Rd, Beijing 100193, Peoples R China

2.Zhejiang Acad Agr Sci, Inst Anim Husb & Vet Sci, 145 Shiqiao Rd, Hangzhou 310022, Peoples R China

期刊名称：JOURNAL OF IMMUNOLOGY （ 影响因子：5.426； 五年影响因子：6.178 ）

ISSN： 0022-1767

年卷期： 2021 年 207 卷 2 期

页码：

收录情况： SCI

摘要： Alphaherpesviruses are large dsDNA viruses with an ability to establish persistent infection in hosts, which rely partly on their ability to evade host innate immune responses, notably the type I IFN response. However, the relevant molecular mechanisms are not well understood. In this study, we report the UL42 proteins of alphaherpesvirus pseudorabies virus (PRV) and HSV type 1 (HSV1) as a potent antagonist of the IFN-I-induced JAK-STAT signaling pathway. We found that ectopic expression of UL42 in porcine macrophage CRL and human HeLa cells significantly suppresses IFN-alpha-mediated activation of the IFN-stimulated response element (ISRE), leading to a decreased transcription and expression of IFN-stimulated genes (ISGs). Mechanistically, UL42 directly interacts with ISRE and interferes with ISG factor 3 (ISGF3) from binding to ISRE for efficient gene transcription, and four conserved DNA-binding sites of UL42 are required for this interaction. The substitution of these DNA-binding sites with alanines results in reduced ISRE-binding ability of UL42 and impairs for PRV to evade the IFN response. Knockdown of UL42 in PRV remarkably attenuates the antagonism of virus to IFN in porcine kidney PK15 cells. Our results indicate that the UL42 protein of alphaherpesviruses possesses the ability to suppress IFN-I signaling by preventing the association of ISGF3 and ISRE, thereby contributing to immune evasion. This finding reveals UL42 as a potential antiviral target.

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