Giuliani Laura, Coletti Anna, Syrjänen Kari, Favalli Cartesio, Ciotti Marco
Laboratory of Clinical Microbiology and Virology, University Hospital Tor Vergata, Rome, Italy.
Anticancer Res. 2006 Sep-Oct;26(5B):3939-41.
Human papillomavirus (HPV) is the etiological agent of cervical cancer. HPV genotyping is important to determine the presence of high-risk types. Recently, a new HPV genotyping method, the Roche Linear array genotyping test, was introduced and is compared here with a sequencing-based HPV genotyping system.
A series of 102 women (age range 30-55 years) shown to be HPV DNA-positive by PCR were typed by sequencing and the Linear array genotyping assay.
The sequence analysis revealed the presence of 80 single high-risk types and 22 single low-risk types. With the Linear array, single infections were found in 46 cases, double infections in 37 cases, triple infections in 12 cases, and more than three in 6 cases. One case positive by sequencing gave a negative result by Linear array. Altogether, a concordant single genotype was found in 93 (91.2%) out of the 102 cases and the single-type concordance between the two assays was significant (Spearman rho = 0.849, p = 0.0001; intraclass correlation coefficient (ICC) (ICC = 0.924, 95% CI 0.888-0.949) (p = 0.0001). The majority of the disparate results were due to the detection of multiple types by the Linear array.
The Roche Linear array is a highly accurate assay for HPV genotyping. This is particularly true in the presence of multiple infections which DNA sequencing is unable to resolve.
人乳头瘤病毒(HPV)是宫颈癌的病原体。HPV基因分型对于确定高危型别的存在很重要。最近,一种新的HPV基因分型方法——罗氏线性阵列基因分型检测被引入,并在此与基于测序的HPV基因分型系统进行比较。
通过聚合酶链反应(PCR)显示为HPV DNA阳性的102名女性(年龄范围30 - 55岁),采用测序和线性阵列基因分型检测进行分型。
序列分析显示存在80种单一高危型别和22种单一低危型别。采用线性阵列检测,发现46例为单一感染,37例为双重感染,12例为三重感染,6例为三种以上感染。1例测序阳性的样本经线性阵列检测结果为阴性。在102例样本中,共发现93例(91.2%)两种检测方法的单一基因型结果一致,两种检测方法的单一型别一致性具有显著性(Spearman秩相关系数rho = 0.849,p = 0.0001;组内相关系数(ICC)(ICC = 0.924,95%可信区间0.888 - 0.949)(p = 0.0001)。大多数不一致的结果是由于线性阵列检测出多种型别。
罗氏线性阵列是一种用于HPV基因分型的高度准确的检测方法。在存在多种感染而DNA测序无法分辨的情况下尤其如此。