A spatiotemporally controlled recombinant cccDNA mouse model for studying HBV and developing drugs against the virus

cccDNA 乙型肝炎病毒 病毒学 生物 强力霉素 转基因 病毒 病毒血症 重组DNA 转基因小鼠 基因 分子生物学 乙型肝炎表面抗原 遗传学 抗生素
作者
Zhongmin Zhou,Cong Li,Zexi Tan,Guoliang Sun,Xiaozhong Peng,Tengfei Ren,Jiabei He,Yixue Wang,Yinyan Sun,Fengchao Wang,Wenhui Li
出处
期刊:Antiviral Research [Elsevier BV]
卷期号:216: 105642-105642 被引量:2
标识
DOI:10.1016/j.antiviral.2023.105642
摘要

Covalently closed circular (ccc) DNA is the template for hepatitis B virus (HBV) replication. The lack of small animal models for characterizing chronic HBV infection has hampered research progress in HBV pathogenesis and drug development. Here, we generated a spatiotemporally controlled recombinant cccDNA (rcccDNA) mouse model by combining Cre/loxP-mediated DNA recombination with the liver-specific "Tet-on/Cre" system. The mouse model harbors three transgenes: a single copy of the HBV genome (integrated at the Rosa26 locus, RHBV), H11-albumin-rtTA (spatiotemporal conditional module), and (tetO)7-Cre (tetracycline response element), and is named as RHTC mouse. By supplying the RHTC mice with doxycycline (DOX)-containing drinking water for two days, the animals generate rcccDNA in hepatocytes, and the rcccDNA supports active HBV gene expression and can maintain HBV viremia persistence for over 60 weeks. Persistent HBV gene expression induces intrahepatic inflammation, fibrosis, and dysplastic pathology, which closely mirrors the disease progression in clinical patients. Bepirovirsen, an antisense oligonucleotide (ASO) targeting all HBV RNA species, showed dose-dependent antiviral effects in the RHTC mouse model. The spatiotemporally controlled rcccDNA mouse is convenient and reliable, providing versatile small animal model for studying cccDNA-centric HBV biology as well as evaluating antiviral therapeutics.
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