A polysaccharide fraction from medicinal herb Prunella vulgaris downregulates the expression of herpes simplex virus antigen in Vero cells

被引:75
作者
Chiu, LCM [1 ]
Zhu, W
Ooi, VEC
机构
[1] Chinese Univ Hong Kong, Dept Biol, Shatin, Hong Kong, Peoples R China
[2] Sichuan Univ, W China Hosp, Ctr Canc, Lab Lung Canc Mol Biol, Chengdu 610041, Sichuan, Peoples R China
关键词
Chinese medicine; antiviral; herpes simplex virus; Prunella vulgaris; flow cytometry;
D O I
10.1016/j.jep.2004.03.024
中图分类号
Q94 [植物学];
学科分类号
071001 [植物学];
摘要
Herpes simplex viruses (HSV) are pathogenic. With the emergence of drug-resistant strains of HSV, new antiviral agents, especially those with different modes of action, are urgently needed. Prunella vulgaris L. (Labiatae), a perennial plant commonly found in China and Europe, has long been used as a folk medicine to cure ailments. In this study, a polysaccharide fraction was prepared from Prunella vulgaris (PPV), and its effects on the expressions of HSV-1 and HSV-2 antigens in their host Vero cells were investigated with flow cytometry. The HSV antigen increased time-dependently in the infected cells, and PPV reduced its expression. The effective concentrations of PPV with 50% reductions of the HSV-1 and HSV-2 antigens were 20.6 and 20.1 mug/ml, respectively. The novelty of PPV is that it also reduces the antigen expression of acyclovir-resistant strain of HSV-1. After incubations with 25-100 mug/ml of PPV the HSV antigen-positive cells were reduced by 24.8-92.6%, respectively, showing that this polysaccharide fraction has a different mode of anti-HSV action from acyclovir. Results from this study show that PPV is effective against both the HSV-1 and HSV-2 infections, and flow cytometry offers a quantitative and highly reproducible anti-HSV drug-susceptibility assay. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:63 / 68
页数:6
相关论文
共 14 条
[1]
SULFATED POLYSACCHARIDES ARE POTENT AND SELECTIVE INHIBITORS OF VARIOUS ENVELOPED VIRUSES, INCLUDING HERPES-SIMPLEX VIRUS, CYTOMEGALO-VIRUS, VESICULAR STOMATITIS-VIRUS, AND HUMAN IMMUNODEFICIENCY VIRUS [J].
BABA, M ;
SNOECK, R ;
PAUWELS, R ;
DECLERCQ, E .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1988, 32 (11) :1742-1745
[2]
GLYCOPROTEIN C-DEPENDENT ATTACHMENT OF HERPES-SIMPLEX VIRUS TO SUSCEPTIBLE CELLS LEADING TO PRODUCTIVE INFECTION [J].
CAMPADELLIFIUME, G ;
STIRPE, D ;
BOSCARO, A ;
AVITABILE, E ;
FOATOMASI, L ;
BARKER, D ;
ROIZMAN, B .
VIROLOGY, 1990, 178 (01) :213-222
[3]
New therapeutic approaches to the alphaherpesvirus infections [J].
Cassady, KA ;
Whitley, RJ .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1997, 39 (02) :119-128
[4]
Herpes simplex virus-inhibitory sulfated xylogalactans from the red seaweed Nothogenia fastigiata [J].
Damonte, EB ;
Matulewicz, MC ;
Cerezo, AS ;
Coto, CE .
CHEMOTHERAPY, 1996, 42 (01) :57-64
[5]
FIELD AK, 1994, CLIN MICROBIOL REV, V7, P1
[6]
THE HERPES-SIMPLEX VIRUS TYPE-1 PARTICLE - STRUCTURE AND MOLECULAR FUNCTIONS [J].
HAARR, L ;
SKULSTAD, S .
APMIS, 1994, 102 (05) :321-346
[7]
Differences in the susceptibility of herpes simplex virus types 1 and 2 to modified heparin compounds suggest serotype differences in viral entry [J].
Herold, BC ;
Gerber, SI ;
Belval, BJ ;
Siston, AM ;
Shulman, N .
JOURNAL OF VIROLOGY, 1996, 70 (06) :3461-3469
[8]
ANTIMUTAGENIC ACTIVITY OF EXTRACTS FROM ANTICANCER DRUGS IN CHINESE-MEDICINE [J].
LEE, H ;
LIN, JY .
MUTATION RESEARCH, 1988, 204 (02) :229-234
[9]
Analysis of virus-infected cells by flow cytometry [J].
McSharry, JJ .
METHODS, 2000, 21 (03) :249-257
[10]
Flow cytometric analysis of herpes simplex virus type 1 susceptibility to acyclovir, ganciclovir, and foscarnet [J].
Pavic, I ;
Hartmann, A ;
Zimmermann, A ;
Michel, D ;
Hampl, W ;
Schleyer, I ;
Mertens, T .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (12) :2686-2692