Inhibition of herpes simplex virus type 1 with the modified green tea polyphenol palmitoyl-epigallocatechin gallate

被引:48
作者
de Oliveira, Aline [1 ]
Adams, Sandra D. [2 ]
Lee, Lee H. [2 ]
Murray, Sean R. [3 ]
Hsu, Stephen D. [4 ]
Hammond, Jeffrey R. [3 ]
Dickinson, Douglas [4 ]
Chen, Ping [5 ]
Chu, Tin-Chun [1 ]
机构
[1] Seton Hall Univ, Dept Biol Sci, S Orange, NJ 07079 USA
[2] Montclair State Univ, Dept Biol & Mol Biol, Montclair, NJ USA
[3] Calif State Univ Northridge, Dept Biol, Ctr Canc & Dev Biol, Northridge, CA 91330 USA
[4] Georgia Hlth Sci, Dept Oral Biol & Maxillofacial Pathol, Augusta, GA USA
[5] Zhejiang Univ, Dept Chem, Catalyst Res Inst, Hangzhou 310003, Zhejiang, Peoples R China
关键词
HSV-1; Vero cells; EGCG; Palmitoyl-EGCG; IN-VITRO CYTOTOXICITY; HUMAN ORAL-CAVITY; NORMAL-CELLS; VIRAL ENTRY; REPLICATION; HSV-1; (-)-EPIGALLOCATECHIN-3-GALLATE; INFECTIONS; STABILITY; CATECHINS;
D O I
10.1016/j.fct.2012.11.006
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Green tea polyphenol epigallocatechin gallate (EGCG) is a strong antioxidant that has previously been shown to reduce the number of plaques in HIV-infected cultured cells. Modified EGCG, palmitoyl-EGCG (p-EGCG), is of interest as a topical antiviral agent for herpes simplex virus (HSV-1) infections. This study evaluated the effect of p-EGCG on HSV-infected Vero cells. Results of cell viability and cell proliferation assays indicate that p-EGCG is not toxic to cultured Vero cells and show that modification of the green tea polyphenol epigallocatechin gallate (EGCG) with palmitate increases the effectiveness of EGCG as an antiviral agent. Furthermore, p-EGCG is a more potent inhibitor of herpes simplex virus I (HSV-1) than EGCG and can be topically applied to skin, one of the primary tissues infected by HSV. Viral binding assay, plaque forming assay, PCR, real-time PCR, and fluorescence microscopy were used to demonstrate that p-EGCG concentrations of 50 mu M and higher block the production of infectious HSV-1 particles. p-EGCG was found to inhibit HSV-1 adsorption to Vero cells. Thus, p-EGCG may provide a novel treatment for HSV-1 infections. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:207 / 215
页数:9
相关论文
共 45 条
[1]   Viral entry mechanisms: cellular and viral mediators of herpes simplex virus entry [J].
Akhtar, Jihan ;
Shukla, Deepak .
FEBS JOURNAL, 2009, 276 (24) :7228-7236
[2]   Multiple Peptides Homologous to Herpes Simplex Virus Type 1 Glycoprotein B Inhibit Viral Infection [J].
Akkarawongsa, Radeekorn ;
Pocaro, Nina E. ;
Case, Gary ;
Kolb, Aaron W. ;
Brandt, Curtis R. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2009, 53 (03) :987-996
[3]   Differential in vitro cytotoxicity of (-)-epicatechin gallate (ECG) to cancer and normal cells from the human oral cavity [J].
Babich, H ;
Krupka, ME ;
Nissim, HA ;
Zuckerbraun, HL .
TOXICOLOGY IN VITRO, 2005, 19 (02) :231-242
[4]   Efficacy Results of a Trial of a Herpes Simplex Vaccine [J].
Belshe, Robert B. ;
Leone, Peter A. ;
Bernstein, David I. ;
Wald, Anna ;
Levin, Myron J. ;
Stapleton, Jack T. ;
Gorfinkel, Iris ;
Morrow, Rhoda L. Ashley ;
Ewell, Marian G. ;
Stokes-Riner, Abbie ;
Dubin, Gary ;
Heineman, Thomas C. ;
Schulte, Joann M. ;
Deal, Carolyn D. .
NEW ENGLAND JOURNAL OF MEDICINE, 2012, 366 (01) :34-43
[5]   Herpes simplex virus vaccines [J].
Bernstein, DI ;
Stanberry, LR .
VACCINE, 1999, 17 (13-14) :1681-1689
[6]   Treatment of herpes simplex virus infections [J].
Brady, RC ;
Bernstein, DI .
ANTIVIRAL RESEARCH, 2004, 61 (02) :73-81
[7]   Herpes simplex virus glycoprotein D bound to the human receptor HveA [J].
Carfí, A ;
Willis, SH ;
Whitbeck, JC ;
Krummenacher, C ;
Cohen, GH ;
Eisenberg, RJ ;
Wiley, DC .
MOLECULAR CELL, 2001, 8 (01) :169-179
[8]  
Chen P., 2009, HDB GREEN TEA HLTH R, P500
[9]  
Chen Ping, 2003, J Zhejiang Univ Sci, V4, P714, DOI 10.1631/jzus.2003.0714
[10]   The Green Tea Polyphenol, Epigallocatechin-3-Gallate, Inhibits Hepatitis C Virus Entry [J].
Ciesek, Sandra ;
von Hahn, Thomas ;
Colpitts, Che C. ;
Schang, Luis M. ;
Friesland, Martina ;
Steinmann, Joerg ;
Manns, Michael P. ;
Ott, Michael ;
Wedemeyer, Heiner ;
Meuleman, Philip ;
Pietschmann, Thomas ;
Steinmann, Eike .
HEPATOLOGY, 2011, 54 (06) :1947-1955