In Vitro Screening for Compounds Derived from Traditional Chinese Medicines with Antiviral Activities Against Porcine Reproductive and Respiratory Syndrome Virus

被引:30
作者
Cheng, Jia [1 ]
Sun, Na [1 ]
Zhao, Xin [1 ]
Niu, Li [1 ]
Song, Meiqin [1 ]
Sun, Yaogui [1 ]
Jiang, Junbing [1 ]
Guo, Jianhua [2 ]
Bai, Yuansheng [3 ]
He, Junping [1 ]
Li, Hongquan [1 ]
机构
[1] Shanxi Agr Univ, Coll Anim Sci & Vet Med, Taigu 030801, Shanxi, Peoples R China
[2] Texas A&M Univ, Coll Vet Med, Dept Pathobiol, College Stn, TX 77843 USA
[3] Shanxi Prov Ecol & Livestock Ind Management Stn, Taiyuan 030801, Shanxi, Peoples R China
关键词
Natural compound; traditional Chinese medicine; antiviral activity; PRRSV; Marc-145; cell; HEPATITIS-B-VIRUS; EXTRACTS; ACID; REPLICATION; MACROPHAGES; SCUTELLARIN; MECHANISM; PLANTS; PRRSV;
D O I
10.4014/jmb.1303.03074
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Seventeen compounds derived from traditional Chinese medicines (TCMs) were tested for their antiviral activity against porcine reproductive and respiratory syndrome virus (PRRSV) in vitro. Visualization with the cytopathologic effect (CPE) assay and the 3-(4, 5-dimethyithiazol-2-yl)-2,5-diphenyltetrazolium bromide test were used to determine the 50% cytotoxic concentration (CC50) and 50% effective concentration (EC50) in cultured Marc-145 cells. Among the tested compounds, chlorogenic acid and scutellarin showed potential anti-PRRSV activity. The EC50 values were 270.8 +/- 14.6 mu g/ml and 28.21 +/- 26.0 mu g/ml and the selectivity indexes were >5.54 and 35.5, respectively. The time-of-addition and virucidal assay indicated that the anti-PRRSV activity of the two compounds could be due to their inhibiting the early stage of virus replication and/or inactivating the virus directly. The inhibition of the virus attachment was not observed in the adsorption inhibition assay. The inhibition ratios of chlorogenic acid and scutellarin were, respectively, 90.8% and 61.1% at the maximum non-cytotoxic concentrations. The results have provided a basis for further exploration of their antiviral properties and mechanisms in vivo. We believe that the chlorogenic acid and scutellarin have a great potential to be developed as new anti-PRRSV drugs for clinical application.
引用
收藏
页码:1076 / 1083
页数:8
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