BMC Complementary and Alternative Medicine | |
Effect of black tea extract on herpes simplex virus-1 infection of cultured cells | |
Sandra D Adams1  Daniel Traum1  Sade D Randall1  Anthony Cantatore1  | |
[1] Department of Biology and Molecular Biology, Montclair State University, Montclair, NJ 07043, USA | |
关键词: Antiviral; Theaflavins; Black tea extract; Herpes simplex virus-1; | |
Others : 1229451 DOI : 10.1186/1472-6882-13-139 |
|
received in 2013-01-16, accepted in 2013-06-14, 发布年份 2013 |
【 摘 要 】
Background
The purpose of this investigation was to determine if black tea extract (BTE), consisting primarily of flavanol compounds called theaflavins, could inhibit herpes simplex virus type-1 (HSV-1) infection in cultured A549 (human epithelial) and Vero cells.
Methods
The effect of BTE both on A549 and Vero cultured cells and on HSV-1 was assessed by using phase contrast and fluorescent microscopy, and cell viability and proliferation assays. After establishing the maximum non-cytotoxic concentration of BTE, A549 and Vero cells and HSV-1 virions were treated with varying concentrations of BTE, respectively. A549 and Vero cells were infected with HSV-1 with green fluorescent protein (GFP) insert at the UL46 gene. The effect of infectivity was determined by viral DNA extraction followed by PCR, plaque assays, adsorption assays, and electrophoresis of PCR products.
Results
BTE was not cytotoxic to A549 and Vero cells, as confirmed by cell viability and proliferation assays, in which BTE treated groups paralleled the positive control group. For both cell lines, plaque assays and fluorescent microscopy indicated an inverse relationship between BTE concentration (from 0.14 μM – 1.4 mM) and HSV-1 infectivity. Specifically, PCR and electrophoresis showed a reduction in the viral genome following treatment with BTE. In addition, there was a noticeable decrease in the amount of viral plaques for BTE treated samples in the adsorption assays.
Conclusions
BTE consisting primarily of theaflavins is not cytotoxic and can reduce or block the production of infectious HSV-1 virions in cultured A549 and Vero cells, thus inhibiting the infectivity of the virus by interfering in the attachment, penetration and viral DNA replication of HSV-1 particles. These findings indicate that BTE enriched with theaflavins has the potential to be developed as a safe, therapeutic antiviral agent to prevent the spread of HSV-1.
【 授权许可】
2013 Cantatore et al.; licensee BioMed Central Ltd.
Files | Size | Format | View |
---|---|---|---|
Figure 6. | 90KB | Image | download |
Figure 5. | 64KB | Image | download |
Figure 4. | 103KB | Image | download |
Figure 3. | 42KB | Image | download |
Figure 2. | 30KB | Image | download |
Figure 1. | 25KB | Image | download |
Figure 6. | 90KB | Image | download |
Figure 5. | 64KB | Image | download |
Figure 4. | 103KB | Image | download |
Figure 3. | 42KB | Image | download |
Figure 2. | 30KB | Image | download |
Figure 1. | 25KB | Image | download |
【 图 表 】
Figure 1.
Figure 2.
Figure 3.
Figure 4.
Figure 5.
Figure 6.
Figure 1.
Figure 2.
Figure 3.
Figure 4.
Figure 5.
Figure 6.
【 参考文献 】
- [1]Mettenleiter TC, Klupp BG, Granzow H: Herpesvirus assembly: an update. Virus Res 2009, 143:222-234.
- [2]Roizman B, Baines J: The diversity and unity of herpesviridae. Comp Immunol Microbiol Infect Dis 1991, 14:63-79.
- [3]Akhtar J, Shukla D: Viral entry mechanisms: cellular and viral mediators of herpes simplex virus entry. Federation of European Biochemical Societies Journal 2009, 276:7228-7236.
- [4]Garner JA: Herpes simplex virion entry into and intracellular transport within mammalian cells. Adv Drug Deliv Rev 2003, 55:1497-1513.
- [5]O'Donnell CD, Kovacs M, Akhtar J, Valyi-Nagy T, Shukla D: Expanding the role of 3-O sulfated heparan sulfate in herpes simplex virus type-1 entry. Virology 2010, 397:389-398.
- [6]Bonnely S, Davis AL, Lewis JR, Astill C: A model oxidation system to study oxidised phenolic compounds present in black tea. Food Chem 2003, 83:485-492.
- [7]Cheng TO: All teas are not created equal: the Chinese green tea and cardiovascular health. Int J Cardiol 2006, 108:301-308.
- [8]Luczaj W, Skrzydlewska E: Antioxidative properties of black tea. Preventative Medicine 2005, 40:910-918.
- [9]Yang Z, Tu Y, Xia H, Jie G, Chen X, He P: Suppression of free-radicals and protection against H2O2-induced oxidative damage in HPF-1 cell by oxidized phenolic compounds present in black tea. Food Chem 2007, 105:1349-1356.
- [10]Kundu T, Dey S, Roy M, Siddiqi M, Bhattacharya RK: Induction of apoptosis in human leukemia cells by black tea and its polyphenol theaflavin. Cancer Lett 2005, 230:111-121.
- [11]Clark KJ, Grant PG, Sarr AB, Belakere JR, Swaggerty CL, Phillips TD, Woode GN: An in vitro study of theaflavins extracted from black tea to neutralize bovine rotavirus and bovine coronavirus infections. Vet Microbiol 1998, 63:147-157.
- [12]Liu S, Lu H, Zhao Q, He Y, Niu J, Debnath AK, Wu S, Jiang S: Theaflavin derivatives in black tea and catechin derivatives in green tea inhibit HIV-1 entry by targeting gp41. Biochim Biophys Acta 2005, 1723:270-281.
- [13]Yang J, Li L, Tan S, Jin H, Qiu J, Mao Q, Li R, Xia C, Jiang X-H, Jiang S, Liu S: A natural theaflavins preparaton inhibits HIV-1 infection by targeting the entry step: potential applications for preventing HIV-1 infection. Fitoterapia 2012, 83:348-355.
- [14]Zu M, Yang F, Zhou W, Liu A, Du G, Zheng L: In vitro anti-influenza virus and anti-inflammatory activities of theaflavin derivatives. Antiviral Res 2012, 94:217-224.
- [15]Oliveira A, Adams SD, Lee L, Murray SR, Hsu SD, Hammond JR, Dickinson D, Chen P, Chu TC: Inhibition of herpes simplex virus type 1 with the modified green tea polyphenol palmitoyl-epigallocatechin gallate. Food Chem Toxicol 2012, 52:207-215.
- [16]Thompson KD: Herbal extracts and compounds active against herpes simplex virus. Advances in Phytomedicine 2006, 2:65-86.
- [17]Fukuchi K, Sakagami H, Okuda T, Hatano T, Tanuma S, Kitajima K, Inoue Y, Inoue S, Ichikawa S, Nonoyama M, Konno K: Inhibition of herpes simplex virus infection by tannins and related compounds. Antiviral Res 1989, 11:285-297.
- [18]Willard M: Rapid directional translocations in virus replication. J Virol 2002, 76:5220-5232.
- [19]Khan MTH, Ather A, Thompson KD, Gambari R: Extracts and molecules from medicinal plants against herpes simplex viruses. Antiviral Res 2005, 67:107-119.
- [20]Wang C, Li Y: Research progress on property and application of theaflavins. African Journal of Biotechnology 2006, 5:213-218.
- [21]Fatahzadeh M, Schwartz RA: Human herpes simplex virus infections: epidemiology, pathogenesis, symptomatology, diagnosis, and management. J Am Acad Dermatol 2007, 57:737-763.
- [22]Whitley RJ, Roizman B: Herpes simplex virus infections. Lancet 2001, 357:1513-1518.
- [23]Babich H, Pinsky SM, Muskin ET, Zuckerbraun HL: In vitro cytotoxicity of a theaflavin mixture from black tea to malignant, immortalized, and normal cells from the human oral cavity. Toxicity in Vitro 2006, 20:677-688.
- [24]Isaacs CE, Wen GY, Xu W, Jia JH, Rohan L, Corbo C, DiMaggio V, Jenkins EC Jr, Hillier S: Epigallocatechin gallate inactivates clinical isolates of herpes simplex virus. Antimicrob Agents Chemother 2008, 52:962-970.
- [25]Su YL, Leung LK, Huang Y, Chen ZY: Stability of tea theaflavins and catechins. Food Chem 2003, 83:189-195.
- [26]Henning SM, Choo JJ, Heber D: Nongallated compared with gallated flavan-3-ols in green and black tea are more bioavailable. J Nutr 2008, 138:1529S-1534S.
- [27]Isaacs CE, Merz G, Hillier S, Rohan L, Wen GY: Digallate dimmers of (−)- epigallocatechin gallate inactivate herpes simplex virus. Antimicrob Agents Chemother 2011, 55:5646-5653.