Development of a Broad-Spectrum Antiviral Agent with Activity Against Herpesvirus Replication and Gene Expression

被引:1
|
作者
Shi, Wen-Jun [1 ]
Sun, Han-Xiao [1 ]
Mo, Xue-Mei [1 ]
Li, Shi-Yu [1 ]
Li, Xiu-Ying [1 ]
Zhang, Guang [1 ]
Liu, Hong-Ai [1 ]
机构
[1] Jinan Univ, Coll Pharm, Inst Genom Med, Guangzhou 510632, Peoples R China
基金
美国国家科学基金会;
关键词
Antagonist; Trapping receptor/ligand; Broad-spectrum; Anti-herpesvirus; H9; peptide; Gene expression; TRAPPING LIGAND ANTAGONIST; RECEPTOR; ACTIVATION; SIGNAL; CELLS; US28;
D O I
10.4314/tjpr.v12i4.15
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Purpose: To evaluate the broad-spectrum antiviral activity of peptide H9 (H9) in vitro in order to gain insight into its underlying molecular mechanisms. Method: Antiviral activity against Herpes simplex virus type 1 (HSV-1) was determined using thiazolyl blue (MTT) assay. Polymerase Chain Reaction (PCR) was employed to assay H9 antiviral activity against human cytomegalovirus (HCMV) and Epstein-Barr virus (EBV). The inhibitory effect of H9 on the replication of these viral genes including early genes was assayed by real time-Ppolymerase chain reaction (RT-PCR) and Western blot. Results: H9 possessed significant inhibitory effect on the four different herpesviruses with 50 % inhibitory concentration (IC50) of 1.21 ng/mL (HSV-1). AD169 infection was strongly inhibited with an EC50 value of 0.46 ng/ml. The anti-herpesviral activity of H9 was dose-dependent. The peptide acted primarily during the early stage of infection by detection of the early genes. Conclusion: The results demonstrate that H9 can inhibit the infection of HSV-1, EBV and HCMV. Furthermore, H9 has a broad-spectrum anti-herpesviral effect in vitro based on targeted killing of infected cells expressing genes.
引用
收藏
页码:541 / 547
页数:7
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