MOV10 inhibits replication of porcine reproductive and respiratory syndrome virus by retaining viral nucleocapsid protein in the cytoplasm of Marc-145 cells

被引:24
作者
Zhao, Kuan [1 ]
Li, Li-Wei [1 ,2 ]
Zhang, Yu-Jiao [1 ]
Jiang, Yi-Feng [1 ,2 ]
Gao, Fei [1 ,2 ]
Li, Guo-Xin [1 ,2 ]
Yu, Ling-Xue [1 ,2 ]
Zhao, Wen-Ying [1 ]
Shan, Tong-Ling [1 ,2 ]
Zhou, Yan-Jun [1 ,2 ]
Tong, Guang-Zhi [1 ,2 ]
机构
[1] Chinese Acad Agr Sci, Shanghai Vet Res Inst, 518 Ziyue Rd, Shanghai 200241, Peoples R China
[2] Yangzhou Univ, Jiangsu Coinnovat Ctr Prevent & Control Important, Yangzhou 225009, Jiangsu, Peoples R China
基金
中国国家自然科学基金; 欧盟地平线“2020”;
关键词
Porcine reproductive and respiratory; syndrome virus; Moloney leukemia virus 10-like protein; Nucleocapsid protein; Viral replication; IN-VITRO; LOCALIZATION SIGNAL;
D O I
10.1016/j.bbrc.2018.08.148
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Porcine reproductive and respiratory syndrome virus (PRRSV) has been a major threat to global industrial pig farming ever since its emergence in the late 1980s. Identification of sustainable and effective control measures against PRRSV transmission is a pressing problem. The nucleocapsid (N) protein of PRRSV is specifically localized in the cytoplasm and nucleus of virus-infected cells which is important for PRRSV replication. In the current study, a new host restricted factor, Moloney leukemia virus 10-like protein (MOV10), was identified as an inhibitor of PRRSV replication. N protein levels and viral replication were significantly reduced in Marc-145 cells stably overexpressing MOV10 compared with those in wild-type Marc-145 cells. Adsorption experiments revealed that MOV10 did not affect the attachment and internalization of PRRSV. Co-immunoprecipitation and immunofluorescence co-localization analyses showed that MOV10 interacted and co-localized with the PRRSV N protein in the cytoplasm. Notably, MOV10 affected the distribution of N protein in the cytoplasm and nucleus, leading to the retention of N protein in the former. Taken together, these findings demonstrate for the first time that MOV10 inhibits PRRSV replication by restricting the nuclear import of N protein. These observations have great implications for the development of anti-PRRSV drugs and provide new insight into the role of N protein in PRRSV biology. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:157 / 163
页数:7
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