Jacobs M V, Snijders P J, van den Brule A J, Helmerhorst T J, Meijer C J, Walboomers J M
Department of Pathology, University Hospital Vrije Universiteit, Amsterdam, The Netherlands.
J Clin Microbiol. 1997 Mar;35(3):791-5. doi: 10.1128/jcm.35.3.791-795.1997.
Two cocktails of digoxigenin-labeled human papillomavirus (HPV) type-specific oligonucleotide probes and an enzyme immunoassay (EIA) were used as a basis to developed a group-specific detection method for 14 high-risk (types 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, and 68) and 6 low-risk (types 6, 11, 40, 42, 43, and 44) HPVs, following a general primer GP5+/bioGP6(+)-mediated PCR. The sensitivity of this high-risk/low-risk (HR/LR) HPV PCR-EIA ranged from 10 to 200 HPV copies, depending on the HPV type. Comparison of HR/LR HPV PCR-EIA with radioactive Southern blot hybridization using a general probe on the same PCR products derived from 417 cytomorphologically abnormal cervical scrapings resulted in an overall agreement of 96% between the two methods. Complete concordance between group-specific HR/LR detection and individual typing results for both single and multiple infections indicate the strong specificity of this HR/LR HPV PCR-EIA. Multiple infections could be predicted by comparing PCR-EIA optical density values of the cocktail probes with one of the individual oligonucleotide probes. This novel HR/LR PCR-EIA allows accurate and rapid identification of high-risk and low-risk HPV types in cervical scrapings and will facilitate HPV detection in HPV mass-screening programs.
以两种地高辛配体标记的人乳头瘤病毒(HPV)型特异性寡核苷酸探针混合物和酶免疫测定(EIA)为基础,在通用引物GP5+/bioGP6(+)-介导的聚合酶链反应(PCR)之后,开发了一种针对14种高危型(16、18、31、33、35、39、45、51、52、56、58、59、66和68型)和6种低危型(6、11、40、42、43和44型)HPV的组特异性检测方法。这种高危/低危(HR/LR)HPV PCR-EIA的灵敏度在10至200个HPV拷贝之间,具体取决于HPV的类型。对417份细胞形态学异常的宫颈刮片中相同PCR产物使用通用探针进行放射性Southern印迹杂交,并与HR/LR HPV PCR-EIA进行比较,结果两种方法的总体一致性为96%。对于单一和多重感染,组特异性HR/LR检测与个体分型结果之间的完全一致性表明这种HR/LR HPV PCR-EIA具有很强的特异性。通过比较混合探针与单个寡核苷酸探针之一的PCR-EIA光密度值,可以预测多重感染。这种新型的HR/LR PCR-EIA能够准确、快速地鉴定宫颈刮片中的高危和低危HPV类型,将有助于HPV大规模筛查项目中的HPV检测。