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Identification of hydrolyzable tannins (punicalagin, punicalin and geraniin) as novel inhibitors of hepatitis B virus covalently closed circular DNA

机译:鉴定可水解的单宁(Punicalagin,Punicalin和Geraniin)作为乙型肝炎病毒的新抑制剂共价闭合圆形DNA

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摘要

The development of new agents to target HBV cccDNA is urgently needed because of the limitations of current available drugs for treatment of hepatitis B. By using a cell-based assay in which the production of HBeAg is in a cccDNA-dependent manner, we screened a compound library derived from Chinese herbal remedies for inhibitors against HBV cccDNA. Three hydrolyzable tannins, specifically punicalagin, punicalin and geraniin, emerged as novel anti-HBV agents. These compounds significantly reduced the production of secreted HBeAg and cccDNA in a dose-dependent manner in our assay, without dramatic alteration of viral DNA replication. Furthermore, punicalagin did not affect precore/core promoter activity, pgRNA transcription, core protein expression, or HBeAg secretion. By employing the cell-based cccDNA accumulation and stability assay, we found that these tannins significantly inhibited the establishment of cccDNA and modestly facilitated the degradation of preexisting cccDNA. Collectively, our results suggest that hydrolyzable tannins inhibit HBV cccDNA production via a dual mechanism through preventing the formation of cccDNA and promoting cccDNA decay, although the latter effect is rather minor. These hydrolyzable tannins may serve as lead compounds for the development of new agents to cure HBV infection. (C) 2016 Elsevier B.V. All rights reserved.
机译:迫切需要开发用于靶向HBV CCCDNA的靶向HBV CCCDNA,因为目前可用药物用于治疗乙型肝炎的局限性。通过使用基于细胞的测定,其中HBeAg的产生是CCCDNA依赖的方式,我们筛选了一个衍生自用于HBV CCCDNA抑制剂的中草药疗法的复合库。三种可水解的单宁,特别是Punicalicagin,瞳孔和Geraniin,作为新的抗HBV剂。这些化合物在我们的测定中显着降低了剂量依赖性方式的分泌的HBEAG和CCCDNA,而不会发生急剧改变病毒DNA复制。此外,PunicalAGIN不会影响预/核心启动子活性,PGRNA转录,核心蛋白表达或HBEAG分泌。通过采用基于细胞的CccDNA积累和稳定性测定,我们发现这些单宁显着抑制了CccDNA的建立,并且适度促进了预先存在的CccDNA的降解。统称,我们的结果表明,可水解的单宁通过双重机制抑制HBV CCCDNA生产,通过防止形成CccDNA并促进CCCDNA衰减,尽管后一种效果是不成分的。这些可水解的单宁可以用作用于制定新试剂以固化HBV感染的铅化合物。 (c)2016年Elsevier B.v.保留所有权利。

著录项

  • 来源
    《Antiviral Research》 |2016年第null期|共11页
  • 作者单位

    Chinese Acad Sci Wuhan Inst Virol State Key Lab Virol Wuhan 43001 Hubei Peoples R China;

    Indiana Univ Sch Med Dept Microbiol &

    Immunol 635 Barnhill Dr Indianapolis IN 46202 USA;

    Chinese Acad Sci Wuhan Inst Virol State Key Lab Virol Wuhan 43001 Hubei Peoples R China;

    Chinese Acad Sci Wuhan Inst Virol State Key Lab Virol Wuhan 43001 Hubei Peoples R China;

    Indiana Univ Sch Med Dept Microbiol &

    Immunol 635 Barnhill Dr Indianapolis IN 46202 USA;

    Indiana Univ Sch Med Dept Microbiol &

    Immunol 635 Barnhill Dr Indianapolis IN 46202 USA;

    Chinese Acad Sci Wuhan Inst Virol State Key Lab Virol Wuhan 43001 Hubei Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 医学微生物学(病原细菌学、病原微生物学);
  • 关键词

    HBV; Antiviral; cccDNA; Hydrolyzable tannins;

    机译:HBV;抗病毒;CCCDNA;可水解的单宁;

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