In vitro inhibition of the replication of classical swine fever virus by porcine Mx1 protein

被引:35
|
作者
He, Dan-ni [1 ]
Zhang, Xiao-min [1 ]
Liu, Ke [1 ]
Pang, Ran [1 ]
Zhao, Jin [1 ]
Zhou, Bin [1 ]
Chen, Pu-yan [1 ]
机构
[1] Nanjing Agr Univ, Coll Vet Med, Nanjing 210095, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Classical swine fever virus (CSFV); Porcine Mx1 (poMx1); Antiviral activity; BOVINE VIRAL DIARRHEA; MOLECULAR-CLONING; EXPRESSION; FAMILY; TARGET;
D O I
10.1016/j.antiviral.2014.01.020
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Classical swine fever virus (CSFV) is the causative pathogen of classical swine fever (CSF), a highly contagious disease of swine. Mx proteins are interferon-induced dynamin-like GTPases present in all vertebrates with a wide range of antiviral activities. Although Zhao et al. (2011) have reported that human MxA can inhibit CSFV replication, whether porcine Mxl (poMx1) has anti-CSFV activity remains unknown. In this study, we generated a cell line designated PK-15/EGFP-poMx1 which expressed porcine Mxl protein constitutively, and we observed that the proliferation of progeny virus in this cell line was significantly inhibited as measured by virus titration, indirect immune fluorescence assay, Q-PCR and Western blot. Furthermore, when PTD-poMx1 fusion protein expressed in Escherichia coli (Zhang et al., 2013) was used to treat CSFV-infected PK-15 cells, the results showed that PTD-poMx1 inhibited CSFV replication in a dose-dependent manner. Additionally, the proliferation of progeny virus was inhibited as measured by virus titration and Q-PCR. Overall, the results demonstrated that poMx1 effectively inhibited CSFV replication, suggesting that poMx1 may be a valuable therapeutic agent against CSFV infection. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:128 / 135
页数:8
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