Inhibition of multiplication of herpes simplex virus by caffeic acid

被引:117
作者
Ikeda, Keiko [1 ,2 ]
Tsujimoto, Kazuko [1 ]
Uozaki, Misao [1 ]
Nishide, Mitsunori [1 ]
Suzuki, Yukiko [2 ]
Koyama, A. Hajime [1 ]
Yamasaki, Hisashi [1 ]
机构
[1] Wakayama Med Univ, Div Virol, Dept Cellular & Mol Med, Grad Sch Med, Wakayama 6410011, Japan
[2] Wakayama Med Univ, Sch Nursing & Hlth Sci, Wakayama 6410011, Japan
关键词
caffeic acid; herpes simplex virus type 1; coffee; antiviral; RNA VIRUSES; COFFEE EXTRACTS; OCTYL GALLATE; VERO CELLS; IN-VITRO; DNA; EXPRESSION; TYPE-1;
D O I
10.3892/ijmm.2011.739
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
Hot water extracts of coffee grinds and commercial instant coffee solutions have been shown to exhibit marked antiviral and virucidal activities against herpes simplex virus type 1 (HSV-1). Specifically, it has been shown that caffeine and N-methyl-pyridinium formate inhibit the multiplication of HSV-1 in HEp-2 cells. The present study examined the virological properties and the antiviral activity of caffeic acid against HSV-1. Caffeic acid inhibited the multiplication of HSV-1 in vitro, while chlorogenic acid, a caffeic acid ester with quinic acid, did not. These reagents did not have a direct virucidal effect. The one-step growth curve of HSV-1 showed that the addition of caffeic acid at 8 h post infection (h p.i.) did not significantly affect the formation of progeny viruses. An analysis of the influence of the time of caffeic acid addition, revealed that addition at an early time post infection remarkably inhibited the formation of progeny infectious virus in the infected cells, but its addition after 6 h p.i. (i.e., the time of the completion of viral genome replication) did not efficiently inhibit this process. These results indicate that caffeic acid inhibits HSV-1 multiplication mainly before the completion of viral DNA replication, but not thereafter. Although caffeic acid showed some cytotoxicity by prolonged incubation, the observed antiviral activity is likely not the secondary result of the cytotoxic effect of the reagent, because the inhibition of the virus multiplication was observed before appearance of the notable cytotoxicity.
引用
收藏
页码:595 / 598
页数:4
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