Literature DB >> 1850950

Diagnostic sensitivity of polymerase chain reaction and Southern blot hybridization for the detection of human papillomavirus DNA in biopsy specimens from cervical lesions.

K M Tham1, V T Chow, P Singh, E P Tock, K C Ching, S K Lim-Tan, I T Sng, H U Bernard.   

Abstract

Human papillomaviruses (HPVs) are associated with benign and malignant neoplasms of the cervix. One of the criteria for their etiologic role requires an assessment of whether virtually all or only a small fraction of lesions contain viral genomes. DNA preparations from colposcopically directed punch biopsies of cervical lesions were analyzed by Southern blot hybridization and the polymerase chain reaction (PCR) for the presence of HPV DNA. The biopsy specimens represented different pathologic entities (koilocytosis, condyloma, cervical intraepithelial neoplasia, and invasive carcinoma). In Southern blot hybridization with radioactive probes for HPV 11, 16, 18, 31, and 33, HPV DNA was detected in 74% of the biopsy specimens (42 of 57 cases), with the predominant types being HPV 16 and HPV 18. In contrast, after PCR amplification with primers yielding fragments of characteristic size for HPV 11, 16, and 18, the analysis of the same 57 biopsy specimens revealed that all samples were positive for at least one HPV type. To exclude false-positive PCR results, controls without HPV DNA were interspersed at regular intervals, and results were evaluated only if these controls remained HPV negative. To exclude false-negative results due to failure of the reaction, a target sequence within the c-Ha-ras-1 gene was used as an internal control. All HPV typing results obtained by Southern blot hybridization were in agreement with HPV typing by PCR. The higher number of positive samples in the latter analysis stems from the increased sensitivity of PCR, which was which was effective in identifying as few as 10-100 HPV DNA molecules; in contrast, the sensitivity of Southern blot hybridization was 1 pg, or approximately 10(5) molecules of HPV DNA. The authors conclude that, with sufficiently sensitive diagnostic methods, HPV DNA can be detected in most, if not all, neoplastic cervical lesions.

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Year:  1991        PMID: 1850950     DOI: 10.1093/ajcp/95.5.638

Source DB:  PubMed          Journal:  Am J Clin Pathol        ISSN: 0002-9173            Impact factor:   2.493


  10 in total

1.  Detection of chicken anaemia agent DNA sequences by the polymerase chain reaction.

Authors:  K M Tham; W L Stanislawek
Journal:  Arch Virol       Date:  1992       Impact factor: 2.574

2.  Sequence variants of human papillomavirus type 16 in clinical samples permit verification and extension of epidemiological studies and construction of a phylogenetic tree.

Authors:  L Ho; S Y Chan; V Chow; T Chong; S K Tay; L L Villa; H U Bernard
Journal:  J Clin Microbiol       Date:  1991-09       Impact factor: 5.948

3.  Use of NS3 consensus primers for the polymerase chain reaction amplification and sequencing of dengue viruses and other flaviviruses.

Authors:  V T Chow; C L Seah; Y C Chan
Journal:  Arch Virol       Date:  1993       Impact factor: 2.574

4.  The novel human MOST-1 (C8orf17) gene exhibits tissue specific expression, maps to chromosome 8q24.2, and is overexpressed/amplified in high grade cancers of the breast and prostate.

Authors:  J M M Tan; E P C Tock; V T K Chow
Journal:  Mol Pathol       Date:  2003-04

5.  Inverse modulation of intraepithelial Langerhans' cells and stromal macrophage/dendrocyte populations in human papillomavirus-associated squamous intraepithelial lesions of the cervix.

Authors:  W al-Saleh; P Delvenne; J E Arrese; A F Nikkels; G E Piérard; J Boniver
Journal:  Virchows Arch       Date:  1995       Impact factor: 4.064

6.  Polymerase chain reaction amplification of wildebeest-associated and cervine-derived malignant catarrhal fever virus DNA.

Authors:  K M Tham; K Ng; L W Young
Journal:  Arch Virol       Date:  1994       Impact factor: 2.574

7.  Detection of human papillomavirus 16 and 18 DNA in epithelial lesions of the lower genital tract by in situ hybridization and polymerase chain reaction: cervical scrapes are not substitutes for biopsies.

Authors:  N Margall; X Matias-Guiu; M Chillon; P Coll; M Alejo; V Nunes; M Quilez; N Rabella; G Prats; J Prat
Journal:  J Clin Microbiol       Date:  1993-04       Impact factor: 5.948

8.  Comparison of dot filter hybridization, Southern transfer hybridization, and polymerase chain reaction amplification for diagnosis of anal human papillomavirus infection.

Authors:  J M Kuypers; C W Critchlow; P E Gravitt; D A Vernon; J B Sayer; M M Manos; N B Kiviat
Journal:  J Clin Microbiol       Date:  1993-04       Impact factor: 5.948

9.  Variation of human papillomavirus type 6 (HPV-6) and HPV-11 genomes sampled throughout the world.

Authors:  P A Heinzel; S Y Chan; L Ho; M O'Connor; P Balaram; M S Campo; K Fujinaga; N Kiviat; J Kuypers; H Pfister
Journal:  J Clin Microbiol       Date:  1995-07       Impact factor: 5.948

10.  Polymerase chain reaction amplification of latent Aujeszky's disease virus in dexamethasone treated pigs.

Authors:  K M Tham; M X Motha; G W Horner; J C Ralston
Journal:  Arch Virol       Date:  1994       Impact factor: 2.574

  10 in total

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