High-throughput detection, genotyping and quantification of the human papillomavirus using real-time PCR

作者：Micalessi Isabel M^*; Boulet Gaelle A V; Bogers Johannes J; Benoy Ina H; Depuydt Christophe E

来源：Clinical Chemistry and Laboratory Medicine, 2012, 50(4): 655-661.

DOI：10.1515/CCLM.2011.835

• cervical screening
• genotype
• human papillomavirus
• real-time PCR
• viral load

Background: The establishment of the causal relationship between high-risk human papillomavirus (HR-HPV) infection and cervical cancer and its precursors has resulted in the development of HPV DNA detection systems. Currently, real-time PCR assays for the detection of HPV, such as the RealTime High Risk (HR) HPV assay (Abbott) and the cobas (R) 4800 HPV Test (Roche Molecular Diagnostics) are commercially available. However, none of them enables the detection and typing of all HR-HPV types in a clinical high-throughput setting. This paper describes the laboratory workflow and the validation of a type-specific real-time quantitative PCR (qPCR) assay for high-throughput HPV detection, genotyping and quantification. This assay is routinely applied in a liquid-based cytology screening setting (700 samples in 24 h) and was used in many epidemiological and clinical studies. %26lt;br%26gt;Methods: The TaqMan-based qPCR assay enables the detection of 17 HPV genotypes and beta-globin in seven multiplex reactions. These HPV types include all 12 high-risk types (HPV16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59), three probably high-risk types (HPV53, 66 and 68), one low-risk type (HPV6) and one undetermined risk type (HPV67). %26lt;br%26gt;Results: An analytical sensitivity of %26lt;= 100 copies was obtained for all the HPV types. The analytical specificity of each primer pair was 100% and an intra- and inter-run variability of %26lt;6.4% was observed. %26lt;br%26gt;Conclusions: The type-specific real-time PCR approach enables detection of 17 HPV types, identification of the HPV type and determination of the viral load in a single sensitive assay suitable for high-throughput screening.

• 出版日期2012