Fontaine Véronique, Mascaux Corinne, Weyn Christine, Bernis Aurore, Celio Nathalie, Lefèvre Philippe, Kaufman Leonard, Garbar Christian
Laboratory of Molecular Virology, ISP/Institut Pasteur, rue Engeland 642, 1180 Brussels, Belgium.
J Clin Microbiol. 2007 Mar;45(3):928-34. doi: 10.1128/JCM.02098-06. Epub 2007 Jan 17.
A strategy combining human papillomavirus general primer (mainly the PGMY primers)-directed PCR sequencing and type-specific PCR is presented. DNA samples were first tested in general primer-mediated PCR. The amplified fragments of positive samples after ethidium bromide-stained DNA gel analysis were further sequenced, and corresponding DNA samples were further analyzed by PCR using type-specific primers for human papillomavirus (HPV) types 16, 18, 31, and 52. The comparison of the results of 157 samples analyzed by this strategy in parallel with the Hybrid Capture 2 tests and with the HPV INNO-LiPA (Innogenetics line probe assay) shows that this method is suitable for HPV detection and genotyping in cervical cell samples. Although the PCR sequencing method is as sensitive as the HPV INNO-LiPA for HPV detection, our method allows the identification of a broader range of HPV types. In contrast, the HPV INNO-LiPA was less time-consuming and better identified coinfections.
本文提出了一种将人乳头瘤病毒通用引物(主要是PGMY引物)引导的PCR测序与型特异性PCR相结合的策略。首先对DNA样本进行通用引物介导的PCR检测。经溴化乙锭染色的DNA凝胶分析后,对阳性样本的扩增片段进行进一步测序,并用针对人乳头瘤病毒(HPV)16、18、31和52型的型特异性引物通过PCR对相应的DNA样本进行进一步分析。通过该策略对157个样本进行分析,并与杂交捕获2试验和HPV INNO-LiPA(Innogenetics线性探针分析)并行比较,结果表明该方法适用于宫颈细胞样本中的HPV检测和基因分型。虽然PCR测序方法在HPV检测方面与HPV INNO-LiPA一样敏感,但我们的方法能够鉴定出更广泛的HPV类型。相比之下,HPV INNO-LiPA耗时较少,且能更好地鉴定合并感染。