Molden Tor, Kraus Irene, Skomedal Hanne, Nordstrøm Trine, Karlsen Frank
Institute of Pathology, Rikshospitalet University Hospital, 0027 Oslo, Norway.
J Virol Methods. 2007 Jun;142(1-2):204-12. doi: 10.1016/j.jviromet.2007.01.036. Epub 2007 Mar 26.
Monitoring human papillomavirus (HPV) E6/E7 mRNA expression may provide an accurate and informative diagnostic approach for detection of oncogene activity related to the development of severe dysplasia or cervical carcinoma. A multiplex nucleic acid sequence based amplification (NASBA) assay, utilizing molecular beacon probes for real-time detection was developed for the identification of E6/E7 mRNA from HPV types 16, 18, 31, 33 and 45. The assay is called PreTect HPV-Proofer and this report describes the development and the analytical performance of the assay. The reproducibility of PreTect HPV-Proofer with regard to a positive result was found to be between 96 and 100%, depending on HPV type. The melting temperature for the different molecular beacons was in the range of 48-55 degrees C, indicating conformational stability, i.e. the molecular beacons will not get activated by the 41 degrees C annealing temperature, but will be activated by the annealing to the target itself. The limit of detection for HPV 16 was ten SiHa or CaSki cells and for HPV 18 one HeLa cell. No cross reactivity was observed with E6/E7 mRNA from the other tested HPV types. mRNA from cervical cells was also successfully amplified after more than one year of storage. In conclusion, the PreTect HPV-Proofer assay, individually identifying E6/E7 mRNA expression from five carcinogenic HPV types, is a reproducible assay that may serve as a valuable tool in monitoring HPV infections producing proteins with a transforming potential.
监测人乳头瘤病毒(HPV)E6/E7 mRNA表达可为检测与严重发育异常或宫颈癌发生相关的癌基因活性提供一种准确且信息丰富的诊断方法。我们开发了一种基于多重核酸序列扩增(NASBA)的检测方法,利用分子信标探针进行实时检测,以鉴定16、18、31、33和45型HPV的E6/E7 mRNA。该检测方法称为PreTect HPV-Proofer,本报告描述了该检测方法的开发过程及其分析性能。PreTect HPV-Proofer检测阳性结果的重现性在96%至100%之间,具体取决于HPV类型。不同分子信标的解链温度在48 - 55摄氏度范围内,表明其构象稳定性,即分子信标不会因41摄氏度的退火温度而被激活,但会因与靶标自身退火而被激活。HPV 16的检测限为10个SiHa或CaSki细胞,HPV 18的检测限为1个HeLa细胞。未观察到与其他检测的HPV类型的E6/E7 mRNA有交叉反应。宫颈细胞的mRNA在储存一年多后也成功扩增。总之,PreTect HPV-Proofer检测方法能够单独鉴定五种致癌HPV类型的E6/E7 mRNA表达,是一种可重现的检测方法,可作为监测产生具有转化潜能蛋白质的HPV感染的有价值工具。