Characterization of a putative new HPV genomic sequence from a cervical lesion using L1 consensus primers and restriction fragment length polymorphism

被引:25
作者
Astori, G [1 ]
Arzese, A [1 ]
Pipan, C [1 ]
deVilliers, EM [1 ]
Botta, GA [1 ]
机构
[1] UNIV UDINE, FAC MED, INST MICROBIOL, I-33100 UDINE, ITALY
关键词
new HPV type; sequencing; RFLP;
D O I
10.1016/S0168-1702(97)00054-3
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Various methods have been proposed for HPV detection and typing. Prevalence and distribution among types have varied depending upon the methods used and the populations studied. We have applied the polymerase chain reaction (PCR) followed by a Restriction Fragment Length Polymorphism (RFLP) analysis using the MY09/MY11 primers for detection of HPV in cervicovaginal lavages obtained from 323 patients who were referred to our Clinical Department either for genital complaints or an abnormal PAP smear. We assessed (i) the prevalence of HPV and (ii) the reliability of RFLP-typing. For the latter, 35 PCR-HPV products were sequenced. HPV-DNA was detected in 40/197 (20.3%) patients with normal cytology, 86/111 (77.5%) with LSIL and 11/15 (73.3%) with HSIL. HPV-16 was the most common type detected in normal cervical cytology samples (10/40, 25%), whereas HPV 16 and 18 were detected in 36/97 (37.1%) of the LSIL and HSIL patients, evidencing the presence of these high-risk HPV types not only in malignant conditions. Results obtained after partial nucleotide sequencing confirmed the results obtained by RFLP analysis. In this study, a putative new HPV fragment (GA6053) was identified. Its closest homology to other known HPV types is 73.8% to HPV-62, 73.0% to HPV-61 and 67.7% to HPV-18. The use of degenerate primers, in conjunction with RFLP, proved to be a reliable method for HPV detection and typing. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:57 / 63
页数:7
相关论文
共 23 条
  • [1] ASTORI G, 1995, MICROBIOLOGICA, V18, P143
  • [2] ASTORI G, 1994, ORAL COMM 2 SIMMOC N, P27
  • [3] IDENTIFICATION AND ASSESSMENT OF KNOWN AND NOVEL HUMAN PAPILLOMAVIRUSES BY POLYMERASE CHAIN-REACTION AMPLIFICATION, RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISMS, NUCLEOTIDE-SEQUENCE, AND PHYLOGENETIC ALGORITHMS
    BERNARD, HU
    CHAN, SY
    MANOS, MM
    ONG, CK
    VILLA, LL
    DELIUS, H
    PEYTON, CL
    BAUER, HM
    WHEELER, CM
    [J]. JOURNAL OF INFECTIOUS DISEASES, 1994, 170 (05) : 1077 - 1085
  • [4] ANALYSIS OF HUMAN PAPILLOMAVIRUS TYPES IN EXOPHYTIC CONDYLOMATA ACUMINATA BY HYBRID CAPTURE AND SOUTHERN BLOT TECHNIQUES
    BROWN, DR
    BRYAN, JT
    CRAMER, H
    FIFE, KH
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1993, 31 (10) : 2667 - 2673
  • [5] PHYLOGENETIC ANALYSIS OF 48 PAPILLOMAVIRUS TYPES AND 28 SUBTYPES AND VARIANTS - A SHOWCASE FOR THE MOLECULAR EVOLUTION OF DNA VIRUSES
    CHAN, SY
    BERNARD, HU
    ONG, CK
    CHAN, SP
    HOFMANN, B
    DELIUS, H
    [J]. JOURNAL OF VIROLOGY, 1992, 66 (10) : 5714 - 5725
  • [6] de Villiers E M, 1994, Curr Top Microbiol Immunol, V186, P1
  • [7] HETEROGENEITY OF THE HUMAN PAPILLOMAVIRUS GROUP
    DEVILLIERS, EM
    [J]. JOURNAL OF VIROLOGY, 1989, 63 (11) : 4898 - 4903
  • [8] TYPING OF HUMAN PAPILLOMAVIRUSES BY POLYMERASE CHAIN-REACTION AMPLIFICATION WITH L1 CONSENSUS PRIMERS AND RFLP ANALYSIS
    LUNGU, O
    WRIGHT, TC
    SILVERSTEIN, S
    [J]. MOLECULAR AND CELLULAR PROBES, 1992, 6 (02) : 145 - 152
  • [9] EPIDEMIOLOGY AND PARTIAL NUCLEOTIDE-SEQUENCE OF 4 NOVEL GENITAL HUMAN PAPILLOMAVIRUSES
    MANOS, MM
    WALDMAN, J
    ZHANG, TY
    GREER, CE
    EICHINGER, G
    SCHIFFMAN, MH
    WHEELER, CM
    [J]. JOURNAL OF INFECTIOUS DISEASES, 1994, 170 (05) : 1096 - 1099
  • [10] MANOS MM, 1989, CANCER CEL, V7, P209