Simultaneous amplification and identification of 25 human papillomavirus types with Templex technology

被引:84
作者
Han, Jian
Swan, David C.
Smith, Sharon J.
Lum, Shanjuan H.
Sefers, Susan E.
Unger, Elizabeth R.
Tang, Yi-Wei
机构
[1] Genaco Biomed Prod Inc, Huntsville, AL 35805 USA
[2] Ctr Dis Control & Prevent, Natl Ctr Infect Dis, Atlanta, GA 30333 USA
[3] Vanderbilt Univ, Dept Pathol, Sch Med, Nashville, TN 37232 USA
[4] Vanderbilt Univ, Dept Med, Sch Med, Nashville, TN 37232 USA
关键词
D O I
10.1128/JCM.01762-06
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The majority of existing human papillomavirus (HPV) genotyping assays are based on multiplex PCR using consensus or degenerate primers. We developed a Templex HPV assay that simultaneously detects and identifies 25 common HPV genotypes in a single-tube reaction using type-specific primers for the HPV-specific E6 and E7 genes. The analytical sensitivities of the Templex assay for HPV type 16 (HPV-16), -18, and -56 were 20, 100, and 20 copies per reaction mixture, respectively. The Templex assay provides semiquantitative information on each type when multiple HPV types coexist in one reaction. We tested 109 clinical cervical specimens previously evaluated with the Digene HC2 high-risk HPV DNA test and found 95.4% concordance between the assay results. The Templex assay provided type-specific results and found multiple types in 29.2% (14 of 48) of high-risk HPV-positive samples. The entire Templex procedure, including DNA extraction, can be completed within 5 hours, providing a rapid and reliable diagnostic tool for HPV detection and typing that is amenable to automation.
引用
收藏
页码:4157 / 4162
页数:6
相关论文
共 27 条
  • [1] The causal relation between human papillomavirus and cervical cancer
    Bosch, FX
    Lorincz, A
    Muñoz, N
    Meijer, CJLM
    Shah, KV
    [J]. JOURNAL OF CLINICAL PATHOLOGY, 2002, 55 (04) : 244 - 265
  • [2] Current methods of testing for human papillomavirus
    Davies, P
    Kornegay, J
    Iftner, T
    [J]. BEST PRACTICE & RESEARCH CLINICAL OBSTETRICS & GYNAECOLOGY, 2001, 15 (05) : 677 - 700
  • [3] Fletcher R.H., 1996, CLIN EPIDEMIOLOGY ES, V3rd
  • [4] Genotyping of 27 human papillomavirus types by using L1 consensus PCR products by a single-hybridization, reverse line blot detection method
    Gravitt, PE
    Peyton, CL
    Apple, RJ
    Wheeler, CM
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (10) : 3020 - 3027
  • [5] Gravitt PE, 2000, J CLIN MICROBIOL, V38, P357
  • [6] Efficacy of a bivalent L1 virus-like particle vaccine in prevention of infection with human papillomavirus types 16 and 18 in young women: a randomised controlled trial
    Harper, DM
    Franco, EL
    Wheeler, C
    Ferris, DG
    Jenkins, D
    Schuind, A
    Zahaf, T
    Innis, B
    Naud, P
    De Carvalho, NS
    Roteli-Martins, CM
    Teixeira, J
    Blatter, MM
    Korn, AP
    Quint, W
    Dubin, G
    [J]. LANCET, 2004, 364 (9447) : 1757 - 1765
  • [7] GROUP-SPECIFIC DIFFERENTIATION BETWEEN HIGH- AND LOW-RISK HUMAN PAPILLOMAVIRUS GENOTYPES BY GENERAL PRIMER-MEDIATED PCR AND 2 COCKTAILS OF OLIGONUCLEOTIDE PROBES
    JACOBS, MV
    HUSMAN, AMD
    VANDENBRULE, AJC
    SNIJDERS, PJF
    MEIJER, CJLM
    WALBOOMERS, JMM
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (04) : 901 - 905
  • [8] Detection of human papillomaviruses in cervical neoplasias using multiple sets of generic polymerase chain reaction primers
    Kado, S
    Kawamata, Y
    Shino, Y
    Kasai, T
    Kubota, K
    Iwasaki, H
    Fukazawa, I
    Takano, H
    Nunoyama, T
    Mitsuhashi, A
    Sekiya, S
    Shirasawa, H
    [J]. GYNECOLOGIC ONCOLOGY, 2001, 81 (01) : 47 - 52
  • [9] Human papillomavirus type 16 status in cervical carcinoma cell DNA assayed by multiplex PCR
    Lukaszuk, K
    Liss, J
    Wozniak, I
    Emerich, J
    Wójcikowski, C
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (02) : 608 - 612
  • [10] MULDREW KL, IN PRESS AM J CLIN P