Molecular beacon-based real-time PCR method for detection of 15 high-risk and 5 low-risk HPV types

被引:32
作者
Takacs, Tibor [3 ]
Jeney, Csaba [1 ,3 ]
Kovacs, Laura [3 ]
Mozes, Johanna [3 ]
Benczik, Marta [3 ]
Sebe, Attila [2 ]
机构
[1] Semmelweis Univ, Dept Microbiol, H-1089 Budapest, Hungary
[2] Semmelweis Univ, Dept Pathophysiol, H-1089 Budapest, Hungary
[3] GenolD Ltd, H-1399 Budapest, Hungary
关键词
molecular beacon; multiplex real-time PCR; HPV detection;
D O I
10.1016/j.jviromet.2007.12.009
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Detection of HPV infections requires a robust time-effective single-step method for efficient screening. A molecular beacon-based one-step multiplex real-time PCR system was developed to detect 15 high-risk (HPV types 16, 18, 26, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, 68) and 5 low-risk HPV types (HPV types 6, 11, 42, 43, 44). Molecular beacons detecting high-risk types are 5'-FAM-3'-DABCYL-labelled, molecular beacons for low-risk detection are 5'-TET-3'-DABCYL-labelled, while the internal control added before sample DNA extraction is detected by a 5'-FAM-TexasRed-3'-DABCYL wavelength-shifting molecular beacon. Accordingly, fluorescent data for HPV detection are collected at 530 nm for high-risk types, 560nm in case of low-risk types and the reaction internal control is detected at 610nm on a Roche LightCycler 2.0 instrument. The sensitivity for detected types varies between 22 and 700 copies/reaction. The clinical performance was tested on 161 clinical sample DNAs. The MB-RT PCR results were compared to the typing results obtained by the LIF/L1R PCR and hybridization-based system described previously, and the concordance rate between the two systems was 89.44%. The favorable characteristics shown by this multiplex single-step real-time HPV detection system make this promising approach worthy for further development and application for clinical screening. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:153 / 162
页数:10
相关论文
共 32 条
[1]   Clinical utility of HPV-DNA detection: Triage of minor cervical lesions, follow-up of women treated for high-grade CIN: An update of pooled evidence [J].
Arbyn, M ;
Paraskevaidis, E ;
Martin-Hirsch, P ;
Prendiville, W ;
Dillner, J .
GYNECOLOGIC ONCOLOGY, 2005, 99 (03) :S7-S11
[2]   Overview of the European and North American studies on HPV testing in primary cervical cancer screening [J].
Cuzick, Jack ;
Clavel, Christine ;
Petry, Karl-Ulrich ;
Meijer, Chris J. L. M. ;
Hoyer, Heike ;
Ratnam, Samuel ;
Szarewski, Anne ;
Birembaut, Philippe ;
Kulasingam, Shalini ;
Sasieni, Peter ;
Iftner, Thomas .
INTERNATIONAL JOURNAL OF CANCER, 2006, 119 (05) :1095-1101
[3]   Classification of papillomaviruses [J].
de Villiers, EM ;
Fauquet, C ;
Broker, TR ;
Bernard, HU ;
zur Hausen, H .
VIROLOGY, 2004, 324 (01) :17-27
[4]   Reproducibility of HPV 16 and HPV 18 viral load quantitation using TaqMan real-time PCR assays [J].
Gravitt, PE ;
Peyton, C ;
Wheeler, C ;
Apple, R ;
Higuchi, R ;
Shah, KV .
JOURNAL OF VIROLOGICAL METHODS, 2003, 112 (1-2) :23-33
[5]   Novel method for detection, typing, and quantification of human papillomaviruses in clinical samples [J].
Hart, KW ;
Williams, OM ;
Thelwell, N ;
Flander, AN ;
Brown, T ;
Borysiewicz, LK ;
Gelder, CM .
JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (09) :3204-3212
[6]   Real time quantitative PCR [J].
Heid, CA ;
Stevens, J ;
Livak, KJ ;
Williams, PM .
GENOME RESEARCH, 1996, 6 (10) :986-994
[7]  
Hubbard RA, 2003, ARCH PATHOL LAB MED, V127, P940
[8]   A simple and reliable protocol for the detection of apple stem grooving virus by RT-PCR and in a multiplex PCR assay [J].
James, D .
JOURNAL OF VIROLOGICAL METHODS, 1999, 83 (1-2) :1-9
[9]   Detection and typing of 46 genital human papillomaviruses by the L1F/L1R primer system based multiplex PCR and hybridization [J].
Jeney, Csaba ;
Takacz, Tibor ;
Sebe, Attila ;
Schaff, Zsuzsa .
JOURNAL OF VIROLOGICAL METHODS, 2007, 140 (1-2) :32-42
[10]   Amplification with molecular beacon primers and reverse line blotting for the detection and typing of human papillomaviruses [J].
Jordens, JZ ;
Lanham, S ;
Pickett, MA ;
Amarasekara, S ;
Abeywickrema, I ;
Watt, PJ .
JOURNAL OF VIROLOGICAL METHODS, 2000, 89 (1-2) :29-37