Antiviral Effect of Epigallocatechin Gallate on Enterovirus 71

被引:124
作者
Ho, Hung-Yao [1 ,2 ]
Cheng, Mei-Ling [1 ,2 ]
Weng, Shiue-Fen [1 ,2 ]
Leu, Yann-Lii [3 ]
Chiu, Daniel Tsun-Yee [1 ,2 ]
机构
[1] Chang Gung Univ, Grad Inst Med Biotechnol, Tao Yuan, Taiwan
[2] Chang Gung Univ, Dept Med Biotechnol & Lab Sci, Tao Yuan, Taiwan
[3] Chang Gung Univ, Grad Inst Nat Prod, Tao Yuan, Taiwan
关键词
EGCG; enterovirus; 71; G6PD deficiency; TEA POLYPHENOL (-)-EPIGALLOCATECHIN-3-GALLATE; GREEN TEA; OXIDATIVE STRESS; INFLUENZA-VIRUS; INFECTION; INHIBITION; CATECHINS; DISEASE; TAIWAN; BIOAVAILABILITY;
D O I
10.1021/jf901128u
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Oxidative stress is known to be a determinant of a host's Susceptibility to pathogens. Natural compounds with antioxidant activity may provide a preventive measure against infection. Tea polyphenols were evaluated for their ability to inhibit enterovirus 71 (EV71) replication in Vero cell culture. Among the polyphenolic compounds tested, epigallocatechin gallate (EGCG) and gallocatechin gallate (GCG) potently inhibited replication of EV71. EGCG and GCG reduced the titer of infectious progeny virus by 95%. Quantitative RT-PCR analysis also revealed that EGCG suppressed replication of genomic RNA. It was accompanied by an increased cytoprotective effect. EGCG and GCG caused 5-fold increase in the viability of EV71-infected cells. The viral inhibitory effect correlated well with the antioxidant capacity of polyphenol. Mechanistically, EV71 infection led to increased oxidative stress, as shown by increased dichlorofluorescein and MitoSOX Red fluorescence. Upon EGCG treatment, reactive oxygen species (ROS) generation was significantly reduced. Consistent with this, EV71 replication was enhanced in glucose-6-phosphate dehydrogenase deficient cells, and such enhancement was largely reversed by EGCG. These findings suggest that EGCG may suppress viral replication via modulation of cellular redox milieu.
引用
收藏
页码:6140 / 6147
页数:8
相关论文
共 50 条
[31]   DIFFERENTIAL INHIBITORY EFFECTS OF SOME CATECHIN DERIVATIVES ON THE ACTIVITIES OF HUMAN-IMMUNODEFICIENCY-VIRUS REVERSE-TRANSCRIPTASE AND CELLULAR DEOXYRIBONUCLEIC AND RIBONUCLEIC-ACID POLYMERASES [J].
NAKANE, H ;
ONO, K .
BIOCHEMISTRY, 1990, 29 (11) :2841-2845
[32]   INHIBITION OF THE INFECTIVITY OF INFLUENZA-VIRUS BY TEA POLYPHENOLS [J].
NAKAYAMA, M ;
SUZUKI, K ;
TODA, M ;
OKUBO, S ;
HARA, Y ;
SHIMAMURA, T .
ANTIVIRAL RESEARCH, 1993, 21 (04) :289-299
[33]   INHIBITION OF INFLUENZA-VIRUS INFECTION BY TEA [J].
NAKAYAMA, M ;
TODA, M ;
OKUBO, S ;
SHIMAMURA, T .
LETTERS IN APPLIED MICROBIOLOGY, 1990, 11 (01) :38-40
[34]   Scavenging effects of tea catechins and their derivatives on 1,1-diphenyl-2-picrylhydrazyl radical [J].
Nanjo, F ;
Goto, K ;
Seto, R ;
Suzuki, M ;
Sakai, M ;
Hara, Y .
FREE RADICAL BIOLOGY AND MEDICINE, 1996, 21 (06) :895-902
[35]  
NODA M, 1994, JPN J BACTERIOL, V49, P117
[36]  
Racaniello V.R., 2001, FIELDS VIROLOGY, V1, P685
[37]  
RYU E, 1980, INT J ZOONOSES, V7, P164
[38]   POLYPHENOLIC FLAVANOLS AS SCAVENGERS OF AQUEOUS-PHASE RADICALS AND AS CHAIN-BREAKING ANTIOXIDANTS [J].
SALAH, N ;
MILLER, NJ ;
PAGANGA, G ;
TIJBURG, L ;
BOLWELL, GP ;
RICEEVANS, C .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1995, 322 (02) :339-346
[39]   APPARENTLY NEW ENTEROVIRUS ISOLATED FROM PATIENTS WITH DISEASE OF CENTRAL NERVOUS-SYSTEM [J].
SCHMIDT, NJ ;
LENNETTE, EH ;
HO, HH .
JOURNAL OF INFECTIOUS DISEASES, 1974, 129 (03) :304-309
[40]   Antiviral effect of catechins in green tea on influenza virus [J].
Song, JM ;
Lee, KH ;
Seong, BL .
ANTIVIRAL RESEARCH, 2005, 68 (02) :66-74