Gilead Sciences, Foster City, CA, USA.
I. Medical Clinic and Polyclinic, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Methods Mol Biol. 2024;2837:113-124. doi: 10.1007/978-1-0716-4027-2_10.
HBV covalently closed circular DNA (cccDNA) plays an important role in the persistence of hepatitis B virus (HBV) infection by serving as the template for transcription of viral RNAs. To cure HBV infection, it is expected that cccDNA needs either to be eliminated or silenced. Hence, precise cccDNA quantification is essential. Sample preparation is crucial to specifically detect cccDNA. Southern blot is regarded as the "gold standard" for specific cccDNA detection but lacks sensitivity. Here, we describe a rapid and reliable modified kit-based, HBV protein-free DNA extraction method as well as a novel enhanced sensitivity Southern blot that uses branched DNA technology to detect HBV DNA in cell culture and liver tissue samples. It is useful for both HBV molecular biology and antiviral research.
HBV 共价闭合环状 DNA(cccDNA)作为病毒 RNA 转录的模板,在乙型肝炎病毒(HBV)感染的持续存在中起着重要作用。为了治愈 HBV 感染,预计 cccDNA 需要被消除或沉默。因此,精确的 cccDNA 定量是必不可少的。样品制备对于特异性检测 cccDNA 至关重要。Southern 印迹被认为是特异性检测 cccDNA 的“金标准”,但缺乏灵敏度。在这里,我们描述了一种快速可靠的改良试剂盒,无 HBV 蛋白 DNA 提取方法,以及一种新的增强敏感性 Southern 印迹,该印迹使用分支 DNA 技术检测细胞培养物和肝组织样本中的 HBV DNA。它对 HBV 分子生物学和抗病毒研究都很有用。