Bartholomeusz Angeline, Tehan Benjamin G, Chalmers David K
Victorian Infectious Diseases Reference Laboratory, North Melbourne, Victoria, Australia.
Antivir Ther. 2004 Apr;9(2):149-60.
The antiviral treatment of chronic hepatitis B is limited by the selection of antiviral resistance mutations. Primary resistance to lamivudine occurs at rtM2041/V in the C Domain of the polymerase. Recently, resistance to adefovir has also been described in the D Domain at rtN236T. The treatment of patients with resistant virus without complete suppression can lead to the further selection of compensatory mutations. Thus, to gain an understanding of the hepatitis B virus (HBV) polymerase and also mutations associated with resistance, a three-dimensional model of the HBV reverse transcriptase core region based on homology with human immunodeficiency virus (HIV) was created. A comparative analysis of the HIV polymerase and the model of HBV polymerase was performed. In addition, the antiviral resistance mutations including potential compensatory mutations were mapped to determine their effect on the HBV polymerase model, especially in the nucleotide binding site.
慢性乙型肝炎的抗病毒治疗受到抗病毒耐药突变选择的限制。对拉米夫定的原发性耐药发生在聚合酶C结构域的rtM204I/V处。最近,在D结构域的rtN236T处也发现了对阿德福韦的耐药性。对病毒耐药但未完全抑制的患者进行治疗可能会导致进一步选择补偿性突变。因此,为了了解乙型肝炎病毒(HBV)聚合酶以及与耐药相关的突变,基于与人类免疫缺陷病毒(HIV)的同源性构建了HBV逆转录酶核心区域的三维模型。对HIV聚合酶和HBV聚合酶模型进行了比较分析。此外,对抗病毒耐药突变(包括潜在的补偿性突变)进行了定位,以确定它们对HBV聚合酶模型的影响,特别是在核苷酸结合位点的影响。