Peking University People's Hospital, Peking University Hepatology Institute, Beijing Key Laboratory of Hepatitis C and Immunotherapy for Liver Diseases, Peking University, Beijing, China.
State Key Laboratory of Anti-Infective Drug Development, Sunshine Lake Pharma Co., Ltd., Dong Guan, China.
J Med Virol. 2017 Oct;89(10):1804-1810. doi: 10.1002/jmv.24830. Epub 2017 May 23.
Heteroaryldihydropyrimidine (HAP) compounds inhibit HBV replication by binding to a hydrophobic pocket at the interface between hepatitis B virus core protein (HBcAg) dimer, which interrupts capsid assembly by changing the kinetics and thermodynamics during this process. Structure biological studies have identified several amino acids in HBcAg crucial for compound binding. Here, we investigated the polymorphisms of T109 and V124 amino acids in HBV sequences submitted to GenBank database. Naturally occurring T109 and V124 and/or possible compensatory mutations in neighbored amino acids were introduced into HBV-expressing plasmids. Viral replication competence and sensitivity to GLS4, a HAP compound, were evaluated using transient transfection and in vitro infection cell models. All tested mutations in these amino acids led to decreasing viral DNA replication at different levels. Specially, T109N and all V124 mutants caused severe deficiencies in viral plus-strand DNA synthesis. T109I single mutation and all T109S/M/C/N mutations impaired HBeAg secretion. T109I showed modestly decreased sensitivities with IC50 3.3- to 6.8-folds higher than wild-type virus. In vitro infection assay showed T109N and all V124 mutants failed to synthesize cccDNA and following viral proteins. The other mutants, however, produced functional cccDNA pools as wild-type virus did. Taken together, we profiled the competences of viral replication and sensitivities to capsid inhibitor of naturally existing mutations in T109 and V124. This will help to understand the possible antiviral resistance issues in future clinical applications of capsid inhibitors.
杂芳基二氢嘧啶 (HAP) 化合物通过与乙型肝炎病毒核心蛋白 (HBcAg) 二聚体之间的疏水性口袋结合来抑制 HBV 复制,从而通过改变该过程中的动力学和热力学来中断衣壳组装。结构生物学研究已经确定了 HBcAg 中几个对化合物结合至关重要的氨基酸。在这里,我们研究了提交给 GenBank 数据库的 HBV 序列中 T109 和 V124 氨基酸的多态性。天然存在的 T109 和 V124 以及相邻氨基酸的可能补偿性突变被引入到 HBV 表达质粒中。使用瞬时转染和体外感染细胞模型评估病毒复制能力和对 HAP 化合物 GLS4 的敏感性。这些氨基酸中的所有测试突变都导致病毒 DNA 复制水平不同程度地降低。特别是,T109N 和所有 V124 突变体导致病毒正链 DNA 合成严重缺陷。T109I 单突变和所有 T109S/M/C/N 突变均损害 HBeAg 分泌。T109I 显示出适度降低的敏感性,IC50 比野生型病毒高 3.3-6.8 倍。体外感染试验表明,T109N 和所有 V124 突变体无法合成 cccDNA 和随后的病毒蛋白。然而,其他突变体产生了与野生型病毒一样功能的 cccDNA 池。总之,我们对天然存在于 T109 和 V124 中的突变体的病毒复制能力和对衣壳抑制剂的敏感性进行了分析。这将有助于了解未来在临床应用衣壳抑制剂时可能出现的抗病毒耐药问题。