Porcine 2′, 5′-oligoadenylate synthetase 2 inhibits porcine reproductive and respiratory syndrome virus replication in vitro

被引:20
|
作者
Zhao, Mengmeng [1 ]
Wan, Bo [1 ]
Li, Huawei [2 ]
He, Jian [1 ]
Chen, Xinxin [2 ]
Wang, Linjian [2 ]
Wang, Yinbiao [2 ]
Xie, Sha [2 ]
Qiao, Songlin [2 ]
Zhang, Gaiping [1 ,2 ,3 ]
机构
[1] Henan Agr Univ, Coll Anim Husb & Vet Med, Zhengzhou 450002, Henan, Peoples R China
[2] Henan Acad Agr Sci, Key Lab Anim Immunol, Henan Prov Key Lab Anim Immunol, Minist Agr, Zhengzhou 450002, Henan, Peoples R China
[3] Jiangsu Coinnovat Ctr Prevent & Control Important, Yangzhou 225009, Jiangsu, Peoples R China
关键词
Porcine reproductive and respiratory syndrome virus; 2; 5 '-oligoadenylate synthetase; RIG-1; Replication; Porcine alveolar macrophages; RNase L; 2'-5'-OLIGOADENYLATE SYNTHETASE; ANTIVIRAL ACTIVITY; INNATE IMMUNITY; GENE FAMILY; CELL-LINE; PROTEIN; PATHOGENESIS; ACTIVATION; RESISTANCE; MECHANISM;
D O I
10.1016/j.micpath.2017.08.011
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Porcine reproductive and respiratory syndrome virus (PRRSV) is acknowledged a fulminating infectious pathogen affecting the pig farming industry, and current vaccines and drugs could hardly inhibit this virus. The 2', 5'-oligoadenylate synthetase (OASs) have antiviral activities, but the role(s) played by porcine OAS2 in protection against PRRSV infection are unknown. Here we found that endogenous expression of the porcine OAS2 gene could be promoted by interferon (IFN)-beta or PRRSV infection in porcine alveolar macrophages. Knockdown of porcine OAS2 led to increases in PRRSV replication, and OAS2 expression suppressed replication of PRRSV in a retinoic acid inducible gene I (RIG-I)-dependent manner, anti-PRRSV activity of porcine OAS2 would be lost if RNase L and OAS2 were both silenced. This discovery illustrates a pathway that porcine OAS2 responses to host anti-PRRSV function. (C) 2017 Published by Elsevier Ltd.
引用
收藏
页码:14 / 21
页数:8
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