Human papillomavirus detection and typing using a nested-PCR-RFLP assay

Brazilian Journal of Infectious Diseases

Ikuta, Nilo¹  Coser, Janaina¹  Boeira, Thaís da Rocha²  Lunge, Vagner Ricardo¹  Fonseca, André Salvador Kazantzi² 

[1]Universidade Luterana do Brasil, Canoas, Brazil

[2]Simbios Biotecnologia, Canoas, Brazil

关键词: DNA probes;    HPV;    polymerase chain reaction;    polymorphism;    restriction;    fragment length.;   

DOI  :  10.1590/S1413-86702011000500009

来源: Contexto

【 摘 要 】

BACKGROUND: It is clinically important to detect and type human papillomavirus (HPV) in a sensitive and specific manner.
OBJECTIVES: Development of a nested-polymerase chain reaction-restriction fragment length polymorphism (nested-PCR-RFLP) assay to detect and type HPV based on the analysis of L1 gene.
METHODS: Analysis of published DNA sequence of mucosal HPV types to select sequences of new primers. Design of an original nested-PCR assay using the new primers pair selected and classical MY09/11 primers. HPV detection and typing in cervical samples using the nested-PCR-RFLP assay.
RESULTS: The nested-PCR-RFLP assay detected and typed HPV in cervical samples. Of the total of 128 clinical samples submitted to simple PCR and nested-PCR for detection of HPV, 37 (28.9%) were positive for the virus by both methods and 25 samples were positive only by nested-PCR (67.5% increase in detection rate compared with single PCR). All HPV positive samples were effectively typed by RFLP assay.
CONCLUSION: The method of nested-PCR proved to be an effective diagnostic tool for HPV detection and typing.

【 授权许可】

CC BY-NC-ND