Lin H J, Wu P C, Lai C L
J Virol Methods. 1987 Feb;15(2):139-49. doi: 10.1016/0166-0934(87)90057-7.
A novel and practical assay for the detection of hepatitis B virus (HBV) DNA in serum is described that utilizes as probe a 21-nucleotide sequence 5'-d (CTTCGCTTCACCTCTGCACGT) labelled at the 3'-end with [32P]ddAMP. The oligonucleotide probe sequence occurs in all known HBV genomes and is complementary to a region near the end of the single-stranded gap. It includes the 11-nucleotide direct repeat 5'-d(TTCACCTCTGC). The method was tested on 988 serum HBsAg-positive or -negative specimens and compared to results with HBV DNA probe, with over 98% concordance between the methods. The sensitivity of the two assays was comparable. The assay was developed for testing serum samples fixed to nylon or nitrocellulose membranes. Hybridization time could be shortened to a few hours as compared to 16 h for HBV DNA probes. Immaculate backgrounds were obtained by using a hybridization medium containing polyethylene glycol, heparin and pyrophosphate, and a particular washing procedure.
本文描述了一种用于检测血清中乙肝病毒(HBV)DNA的新颖实用的检测方法,该方法使用一条21个核苷酸的序列5'-d(CTTCGCTTCACCTCTGCACGT)作为探针,其3'-末端用[32P]ddAMP标记。该寡核苷酸探针序列存在于所有已知的HBV基因组中,并且与单链缺口末端附近的一个区域互补。它包含11个核苷酸的直接重复序列5'-d(TTCACCTCTGC)。该方法在988份血清HBsAg阳性或阴性标本上进行了测试,并与HBV DNA探针的检测结果进行了比较,两种方法的一致性超过98%。两种检测方法的灵敏度相当。该检测方法是为检测固定在尼龙或硝酸纤维素膜上的血清样本而开发的。与HBV DNA探针的16小时杂交时间相比,杂交时间可缩短至数小时。通过使用含有聚乙二醇、肝素和焦磷酸的杂交介质以及特定的洗涤程序,可获得纯净的背景。