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In vitro inhibition of the replication of classical swine fever virus by capsid-targeted virus inactivation.

机译:衣壳靶向病毒灭活体外抑制经典猪瘟病毒复制。

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Classical swine fever virus (CSFV) is the causative agent of classical swine fever (CSF), a highly contagious fatal disease of swine. Few effective antiviral drugs are currently available against CSFV infections. To explore the feasibility of using capsid-targeted viral inactivation (CTVI) as an antiviral strategy against CSFV infections, we expressed the CSFV capsid protein (Cap) fused with the nuclease of Staphylococcus aureus (SN) in Escherichia coli and investigated its effects on the replication of CSFV in PK-15 cells. The results indicated that the fusion protein Cap-SN showed a strong Ca(2+)-dependent nuclease activity and inhibited the replication of CSFV in a dose-dependent manner, with complete inhibition at a concentration of 15 microg/ml, whereas the Cap fused with an enzymatically inactive SN (Cap-SN*) showed no nuclease activity or antiviral effects. Thus, the CTVI approach might be applicable to CSFV inhibition as a novel antiviral strategy.
机译:古典猪瘟病毒(CSFV)是古典猪瘟(CSF)的病原体,这是一种高度传染性的致命性猪疾病。目前很少有有效的抗病毒药物可用于抵抗CSFV感染。为了探索使用以衣壳靶向的病毒灭活(CTVI)作为抗CSFV感染的抗病毒策略的可行性,我们在大肠杆菌中表达了融合有金黄色葡萄球菌(SN)核酸酶的CSFV衣壳蛋白(Cap),并研究了其对病毒感染的影响CSFV在PK-15细胞中的复制。结果表明,融合蛋白Cap-SN具有很强的Ca(2+)依赖性核酸酶活性,并以剂量​​依赖性方式抑制了CSFV的复制,在浓度为15μg/ ml时完全被抑制,而Cap与无酶活性的SN(Cap-SN *)融合显示无核酸酶活性或抗病毒作用。因此,CTVI方法可能适用于抑制CSFV作为一种新型抗病毒策略。

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