Wen-Jun Shi,
Han-Xiao Sun ,
Xue-Mei Mo,
Shi-Yu Li,
Xiu-Ying Li,
Guang Zhang,
Hong-Ai Liu
Institute of Genomic Medicine, College of Pharmacy, Jinan University, Guangzhou, 510632, China;
For correspondence:- Han-Xiao Sun
Email: sunhanxiao5@gmail.com
Received: 1 December 2012
Accepted: 19 June 2013
Published: 23 August 2013
Citation:
Shi W, Sun H, Mo X, Li S, Li X, Zhang G, et al.
Development of a Broad-Spectrum Antiviral Agent with Activity Against Herpesvirus Replication and Gene expression. Trop J Pharm Res 2013; 12(4):541-547
doi:
10.4314/tjpr.v12i4.15
© 2013 The authors.
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Abstract
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.
Keywords: Antagonist, Trapping receptor/ligand, Broad-spectrum, Anti-herpesvirus, H9 peptide, Gene ex
pression