Nakano Kazushi, Nishinaka Kazuko, Tanaka Tatsuya, Ohshima Atsushi, Sugimoto Nakaba, Isegawa Yuji
Department of Infectious Disease Control, G-5, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
J Virol Methods. 2009 Nov;161(2):223-30. doi: 10.1016/j.jviromet.2009.06.016. Epub 2009 Jun 25.
A denaturing high-performance liquid chromatography (dHPLC) assay was developed to detect antiviral drug-resistance mutations of human herpesvirus 6 (HHV-6). Recombinant baculoviruses were created that contained wild-type and mutant forms of the HHV-6 U69 gene, which determines sensitivity to the antiviral drug ganciclovir (GCV). The mutations causing GCV resistance in HHV-6 U69 were single-base mutations adapted from known GCV-resistant DNA sequences of HCMV, and their ability to confer GCV resistance on recombinant baculoviruses was confirmed. Six characterized mutant sequences, including one reported previously that encodes a GCV-sensitive kinase-activity mutant, were used. DNA was extracted, and the levels of homoduplex and heteroduplex DNA in the PCR products from mixed wild-type and mutant viral DNAs were determined using dHPLC. The optimized assay could distinguish the different mutants, and could detect mutants representing only 10% of the DNAs. The new assay with dHPLC readout permitted the rapid (4 h), objective, and reproducible detection of HHV-6 drug-resistance mutations.
开发了一种变性高效液相色谱(dHPLC)检测方法,用于检测人疱疹病毒6型(HHV-6)的抗病毒药物耐药性突变。构建了含有HHV-6 U69基因野生型和突变型形式的重组杆状病毒,该基因决定了对抗病毒药物更昔洛韦(GCV)的敏感性。导致HHV-6 U69对GCV耐药的突变是从已知的人巨细胞病毒(HCMV)GCV耐药DNA序列中改编的单碱基突变,并且证实了它们赋予重组杆状病毒GCV耐药性的能力。使用了六个已鉴定的突变序列,包括先前报道的一个编码GCV敏感激酶活性突变体的序列。提取DNA,并使用dHPLC测定来自野生型和突变型病毒DNA混合物的PCR产物中同型双链和异型双链DNA的水平。优化后的检测方法可以区分不同的突变体,并且可以检测仅占DNA 10%的突变体。采用dHPLC读数的新检测方法能够快速(4小时)、客观且可重复地检测HHV-6药物耐药性突变。