Typing of human papillomavirus by pyrosequencing

被引:64
作者
Gharizadeh, B
Kalantari, M
Garcia, CA
Johansson, B
Nyrén, P
机构
[1] Royal Inst Technol, Dept Biotechnol, SE-10044 Stockholm, Sweden
[2] Huddinge Univ Hosp, Karolinska Inst, Dept Immunol Microbiol Pathol & Infect Dis, Div Clin Virol, S-14186 Huddinge, Sweden
关键词
D O I
10.1038/labinvest.3780276
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The possibility of using a new bioluminometric UNA sequencing technique, called pyrosequencing, for typing of human papillomaviruses (HPV) was investigated. A blinded pyrosequencing test was performed on an HPV test panel of 67 GP5+/GP6+ PCR-derived amplification products. The 67 clinical DNA samples were sequenced up to 25 bases and sequences were searched using BLAST. All of the samples were correctly genotyped by pyrosequencing and the results were unequivocally in accordance with the results obtained from conventional DNA sequencing. Pyrosequencing was found to be a fast and efficient tool for identifying individual HPV types. Furthermore, pyrosequencing has the capability of determining novel HPV types as well as HPV sequence variants harboring mutation(s). The method is robust and well suited for large-scale programs.
引用
收藏
页码:673 / 679
页数:7
相关论文
共 15 条
  • [1] ANALYSIS OF GENOMIC SEQUENCES OF 95 PAPILLOMAVIRUS TYPES - UNITING TYPING, PHYLOGENY, AND TAXONOMY
    CHAN, SY
    DELIUS, H
    HALPERN, AL
    BERNARD, HU
    [J]. JOURNAL OF VIROLOGY, 1995, 69 (05) : 3074 - 3083
  • [2] A population-based five-year follow-up study of cervical human papillomavirus infection
    Elfgren, K
    Kalantari, M
    Moberger, B
    Hagmar, B
    Dillner, J
    [J]. AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2000, 183 (03) : 561 - 567
  • [3] Amplification of human genomic sequences by human papillomaviruses universal consensus primers
    Fernández-Contreras, ME
    Sarriá, C
    Nieto, S
    Lazo, PA
    [J]. JOURNAL OF VIROLOGICAL METHODS, 2000, 87 (1-2) : 171 - 175
  • [4] Detection and identification of human papilloma viral DNA, types 16, 18, and 33, by a combination of polymerase chain reaction and a colorimetric solid phase capture hybridisation assay
    Godfroid, E
    Heinderyckx, M
    Mansy, F
    Fayt, I
    Noël, JC
    Thiry, L
    Bollen, A
    [J]. JOURNAL OF VIROLOGICAL METHODS, 1998, 75 (01) : 69 - 81
  • [5] Gravitt PE, 2000, J CLIN MICROBIOL, V38, P357
  • [6] HAGMAR B, 1995, ACTA CYTOL, V39, P741
  • [7] HUSMAN AMDR, 1995, J GEN VIROL, V76, P1057
  • [8] Production, purification, and luminometric analysis of recombinant Saccharomyces cerevisiae MET3 adenosine triphosphate sulfurylase expressed in Escherichia coli
    Karamohamed, S
    Nilsson, J
    Nourizad, K
    Ronaghi, M
    Pettersson, B
    Nyrén, P
    [J]. PROTEIN EXPRESSION AND PURIFICATION, 1999, 15 (03) : 381 - 388
  • [9] Poljak M, 1998, Adv Anat Pathol, V5, P216, DOI 10.1097/00125480-199807000-00002
  • [10] DETECTION AND TYPING OF HUMAN PAPILLOMAVIRUS IN ARCHIVAL CERVICAL-CANCER SPECIMENS BY DNA AMPLIFICATION WITH CONSENSUS PRIMERS
    RESNICK, RM
    CORNELISSEN, MTE
    WRIGHT, DK
    EICHINGER, GH
    FOX, HS
    TERSCHEGGET, J
    MANOS, MM
    [J]. JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1990, 82 (18): : 1477 - 1484