Suppression of hepatitis C virus by the flavonoid quercetin is mediated by inhibition of NS3 protease activity

被引:160
作者
Bachmetov, L. [1 ]
Gal-Tanamy, M. [1 ]
Shapira, A. [2 ]
Vorobeychik, M. [1 ]
Giterman-Galam, T. [1 ]
Sathiyamoorthy, P. [3 ]
Golan-Goldhirsh, A. [4 ]
Benhar, I. [2 ]
Tur-Kaspa, R. [1 ,5 ,6 ]
Zemel, R. [1 ]
机构
[1] Tel Aviv Univ, Mol Hepatol Res Lab, Felsenstein Med Res Ctr, Sackler Sch Med, IL-49100 Petah Tiqwa, Israel
[2] Tel Aviv Univ, Dept Mol Microbiol & Biotechnol, George S Wise Fac Life Sci, Ramat, Aviv, Israel
[3] Gem Res Fdn, Madras, Tamil Nadu, India
[4] Ben Gurion Univ Negev, Blaustein Inst Desert Res, Sede Boqer, Israel
[5] Rabin Med Ctr, Dept Med D, Petah Tiqwa, Israel
[6] Rabin Med Ctr, Liver Inst, Petah Tiqwa, Israel
关键词
flavonoid; hepatitis C virus; NS3 serine protease; quercetin; HCVNS3; SERINE-PROTEASE; ANTIVIRAL ACTIVITY; EXPRESSION; INFECTION; RNA;
D O I
10.1111/j.1365-2893.2011.01507.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
. Phytochemicals exert antiviral activity and may play a potential therapeutic role in hepatitis C virus (HCV) infection. In this work, we aimed to isolate NS3 inhibitors from traditional Indian medicinal plants that were found, in our earlier study, to inhibit HCV NS3 protease activity and to evaluate their potential to inhibit HCV replication. A potent inhibitory effect of NS3 catalytic activity was obtained with Embelia ribes plant extracts. Quercetin, a ubiquitous plant flavonoid, was identified as the active substance in the fractioned extract. It was found to inhibit NS3 activity in a specific dose-dependent manner in an in vitro catalysis assay. Quercetin inhibited HCV RNA replication as analysed in the subgenomic HCV RNA replicon system. It also inhibited HCV infectious virus production in the HCV infectious cell culture system (HCVcc), as analysed by the focus-forming unit reduction assay and HCV RNA real-time PCR. The inhibitory effect of quercetin was also obtained when using a model system in which NS3 engineered substrates were introduced in NS3-expressing cells, providing evidence that inhibition in vivo could be directed to the NS3 and do not involve other HCV proteins. Our work demonstrates that quercetin has a direct inhibitory effect on the HCV NS3 protease. These results point to the potential of quercetin as a natural nontoxic anti-HCV agent reducing viral production by inhibiting both NS3 and heat shock proteins essential for HCV replication.
引用
收藏
页码:E81 / E88
页数:8
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