Wei Min, Guan Qi, Liang Hao, Chen Jianping, Chen Zhao, Hei Faxin, Feng Yi, Hong Kunxue, Huang Hailong, Xing Hui, Shao Yiming
Division of Virology and Immunology, National Center for AIDS/STD Prevention and Control, China Center for Disease Prevention and Control, Beijing, 100050 People's Republic of China.
J Clin Microbiol. 2004 Sep;42(9):4261-7. doi: 10.1128/JCM.42.9.4261-4267.2004.
After the initial development of a human immunodeficiency virus type 1 (HIV-1) subtype-screening tool by nested multiplex PCR, we further improve it through the redesign of subtype-specific primers based on subtype signature pattern (SSP) analyses and optimization of the PCR conditions. Extracted RNA from plasma samples was used in reverse transcription and the cDNA products were added to the first round PCR, in which universal primers in the gag region were used to detect HIV-1 M group isolates. In the second round of PCR, three pairs of subtype-specific primers, detecting subtypes B, C, and CRF01-AE, were added in one tube. Subtype determination was based on the different size of PCR products on the agarose gel electrophoresis. An additional set of primers detecting only the prevalent recombinant strains CRF07-BC and CRF08-BC was used to discriminate CRF07- and CRF08-BC from pure subtype C. Testing for all kinds of HIV subtype reference strains indicated that this assay was applicable. A panel of 252 HIV-positive samples and 30 HIV-negative samples was further used to evaluate and validate this assay. Compared to the assay of sequence-based phylogenetic analysis, the newly developed assay has an adequate designated subtype sensitivity, 93.2% (69 of 74) for subtype B, 95.1% (117 of 123) for subtype C, 94.0% (47 of 50) for CRF01-AE, and 95.0% (115 of 121) for CRF07-BC and CRF08-BC. Most importantly, the intersubtype specificity of the assay was found to be 100%. The assay specificity was also found to be 100% when used to test 30 HIV-negative samples. The average reproducibility was 96.0% for subtype B, 96.7% for subtype C, and 95.0% for CRF01-AE. We have developed a simple, rapid, and low cost assay for screening subtypes B, C, CRF01-AE, CRF07-BC, and CRF08-BC in China.
在通过巢式多重PCR初步开发出1型人类免疫缺陷病毒(HIV-1)亚型筛查工具后,我们基于亚型特征模式(SSP)分析重新设计亚型特异性引物并优化PCR条件,对该工具进行了进一步改进。从血浆样本中提取的RNA用于逆转录,cDNA产物被加入第一轮PCR,其中gag区域的通用引物用于检测HIV-1 M组毒株。在第二轮PCR中,将三对检测B、C和CRF01-AE亚型的亚型特异性引物加入同一管中。亚型的确定基于琼脂糖凝胶电泳上PCR产物的不同大小。另外一组仅检测流行重组毒株CRF07-BC和CRF08-BC的引物用于将CRF07-和CRF08-BC与纯C亚型区分开来。对所有类型的HIV亚型参考毒株进行检测表明该检测方法适用。进一步使用一组252份HIV阳性样本和30份HIV阴性样本对该检测方法进行评估和验证。与基于序列的系统发育分析检测方法相比,新开发的检测方法具有足够的指定亚型敏感性,B亚型为93.2%(74份中的69份),C亚型为95.1%(123份中的117份),CRF01-AE为94.0%(50份中的47份),CRF07-BC和CRF08-BC为95.0%(121份中的115份)。最重要的是,发现该检测方法的亚型间特异性为100%。当用于检测30份HIV阴性样本时,检测方法的特异性也为100%。B亚型的平均重复性为96.0%,C亚型为96.7%,CRF01-AE为95.0%。我们开发了一种简单、快速且低成本的检测方法,用于在中国筛查B、C、CRF01-AE、CRF07-BC和CRF08-BC亚型。