Lillsunde Larsson Gabriella, Carlsson Jessica, Karlsson Mats G, Helenius Gisela
Department of Laboratory Medicine, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.
Department of Urology, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.
J Mol Diagn. 2015 May;17(3):293-301. doi: 10.1016/j.jmoldx.2014.12.004. Epub 2015 Mar 16.
Human papillomavirus (HPV) testing and genotyping of FFPE tissue samples is important in epidemiological investigations. Here, we compare four different HPV genotyping methods for use in FFPE clinical samples. Comparative testing was performed on 99 samples with a clinical suspicion of HPV. Specimens were analyzed with Anyplex II HPV28 detecting 28 genotypes using real-time PCR and melting curve analysis, CLART HPV2 detecting 35 genotypes using PCR and microarray detection, and MGP5+/6+ consensus primer system together with pyrosequencing. Results were compared to a real-time PCR reference protocol detecting 14 genotypes. In total, 68% of the samples were positive for an HPV genotype using the reference protocol and MGP5+/6+ primer system. Anyplex II HPV28 analysis and CLART HPV2 had 82% and 72% positive samples, respectively. All four methods showed good agreement when comparing the 14 genotypes included in the reference protocol. When evaluating all genotypes, the Anyplex II HPV28 assay and the CLART assay changed the status of the sample (individually or together) from negative with respect to the reference protocol to positive for either a Group 1 (n = 4) or Group 2 (n = 6) genotype. We conclude from this study that for an extended genotyping approach with a high sensitivity for FFPE specimens, both the Anyplex II HPV28 and CLART HPV2 assays are suitable alternatives despite minor intra-assay differences.
福尔马林固定石蜡包埋(FFPE)组织样本的人乳头瘤病毒(HPV)检测和基因分型在流行病学调查中很重要。在此,我们比较了四种用于FFPE临床样本的不同HPV基因分型方法。对99例临床怀疑感染HPV的样本进行了对比检测。使用实时PCR和熔解曲线分析的Anyplex II HPV28检测28种基因型,使用PCR和微阵列检测的CLART HPV2检测35种基因型,以及MGP5+/6+共识引物系统结合焦磷酸测序对样本进行分析。将结果与检测14种基因型的实时PCR参考方案进行比较。使用参考方案和MGP5+/6+引物系统时,总共68%的样本HPV基因型呈阳性。Anyplex II HPV28分析和CLART HPV2的阳性样本分别为82%和72%。在比较参考方案中包含的14种基因型时,所有四种方法都显示出良好的一致性。在评估所有基因型时,Anyplex II HPV28检测和CLART检测(单独或一起)将样本相对于参考方案的状态从阴性变为1组(n = 4)或2组(n = 6)基因型中的阳性。我们从这项研究中得出结论,对于对FFPE样本具有高灵敏度的扩展基因分型方法,尽管检测内存在微小差异,但Anyplex II HPV28和CLART HPV2检测都是合适的替代方法。