Samiotaki M, Kwiatkowski M, Ylitalo N, Landegren U
The Beijer Laboratory, Uppsala University, Uppsala, Sweden.
Anal Biochem. 1997 Nov 15;253(2):156-61. doi: 10.1006/abio.1997.2387.
Identification of human papilloma virus (HPV) types is important in order to determine the risk of cervical carcinoma in women. This requires a technique to probe individual samples for multiple virus specificities. Here we describe simultaneous multicolor analysis of amplification products for any of seven amplified HPV types 16, 18, 31, 33, 35, 39, and 45, associated with cancer of the cervix. A seminested polymerase chain reaction was performed in a single tube using a biotinylated inner primer. Sets of amplification products, immobilized on a 96-pronged manifold solid support, were rendered single stranded and probed with a mix of seven type-specific, differentially labeled oligonucleotides. These probes contained 10 or 20 lanthanide chelates at the 5' ends with seven distinct combinations of europium, terbium, and samarium ions. The seven viral strains were correctly identified by time-resolved fluorescence measurement of the specifically hybridized probes. Using this assay format, simultaneous detection of any of seven or even more target variants is possible.
鉴定人乳头瘤病毒(HPV)类型对于确定女性患宫颈癌的风险很重要。这需要一种能够针对多种病毒特异性对单个样本进行检测的技术。在此,我们描述了对与宫颈癌相关的七种HPV类型(16、18、31、33、35、39和45型)中的任何一种的扩增产物进行同时多色分析的方法。使用生物素化的内引物在单个管中进行半巢式聚合酶链反应。固定在96针歧管固体支持物上的扩增产物集被转化为单链,并用七种类型特异性、不同标记的寡核苷酸混合物进行检测。这些探针在5'端含有10或20个镧系螯合物,具有铕、铽和钐离子的七种不同组合。通过对特异性杂交探针的时间分辨荧光测量,正确鉴定了七种病毒株。使用这种检测形式,可以同时检测七种甚至更多的目标变体。