Literature DB >> 1650785

A general primer pair for amplification and detection of genital human papillomavirus types.

M Evander1, G Wadell.   

Abstract

A general primer pair localized in the E7 and E1 regions was identified and used for the detection of genital human papillomaviruses (HPVs). The genital HPV types 6b, 11, 16, 18, 31 and 33 were amplified and detected by the polymerase chain reaction (PCR) performed at a high stringency annealing temperature (60 degrees C). HPV-2, -3, -7, -13 and -30 were amplified only at lower temperatures. Twelve biopsies from women with invasive cancer in the cervix were analysed with the general primer pair. The amplification product specific for the general primer pair was detected in 11 of the 12 biopsies. The eleven HPV DNA positive specimens were shown to contain HPV-6b, HPV-16 and/or HPV-18 by Southern blot hybridization of the PCR products. The general primers were also used for analysis of 57 cervical scrapes from women with normal cytology, condyloma or CIN. By ethidium bromide staining after agarose gel electrophoresis we could detect 21 positives. Slot-blot analysis of the amplification products from all 57 scrapes confirmed the specificity of the 21 positives and revealed 5 additional positives. Among the 57 scrapes, 15/21 CIN scrapes, 10/21 condyloma scrapes and 1/15 normal scrapes contained HPV DNA. Eight different HPV types were detected. The general primer pair from the E7/E1 region is thus a powerful tool for the detection of HPV in clinical samples. The amplimer obtained offers a possibility for further typing by slot-blot hybridization using HPV-type specific probes.

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Year:  1991        PMID: 1650785     DOI: 10.1016/0166-0934(91)90162-s

Source DB:  PubMed          Journal:  J Virol Methods        ISSN: 0166-0934            Impact factor:   2.014


  6 in total

1.  A novel and rapid PCR-based method for genotyping human papillomaviruses in clinical samples.

Authors:  J H Nelson; G A Hawkins; K Edlund; M Evander; L Kjellberg; G Wadell; J Dillner; T Gerasimova; A L Coker; L Pirisi; D Petereit; P F Lambert
Journal:  J Clin Microbiol       Date:  2000-02       Impact factor: 5.948

2.  Genital human papillomavirus infection among patients attending an STD clinic.

Authors:  A Strand; E Rylander; M Evander; G Wadell
Journal:  Genitourin Med       Date:  1993-12

3.  Detection of genital human papillomavirus by single-tube nested PCR and type-specific oligonucleotide hybridization.

Authors:  N Ylitalo; T Bergström; U Gyllensten
Journal:  J Clin Microbiol       Date:  1995-07       Impact factor: 5.948

4.  Comparison of a one-step and a two-step polymerase chain reaction with degenerate general primers in a population-based study of human papillomavirus infection in young Swedish women.

Authors:  M Evander; K Edlund; E Bodén; A Gustafsson; M Jonsson; R Karlsson; E Rylander; G Wadell
Journal:  J Clin Microbiol       Date:  1992-04       Impact factor: 5.948

5.  High-risk human papillomavirus types in cytologically normal cervical scrapes from Kenya.

Authors:  J Czeglédy; K O Rogo; M Evander; G Wadell
Journal:  Med Microbiol Immunol       Date:  1992       Impact factor: 3.402

6.  Group-specific differentiation between high- and low-risk human papillomavirus genotypes by general primer-mediated PCR and two cocktails of oligonucleotide probes.

Authors:  M V Jacobs; A M de Roda Husman; A J van den Brule; P J Snijders; C J Meijer; J M Walboomers
Journal:  J Clin Microbiol       Date:  1995-04       Impact factor: 5.948

  6 in total

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