P. Mcnicol et al., VARIABILITY OF POLYMERASE CHAIN REACTION-BASED DETECTION OF HUMAN PAPILLOMAVIRUS DNA IS ASSOCIATED WITH THE COMPOSITION OF VAGINAL MICROBIAL-FLORA, Journal of medical virology, 43(2), 1994, pp. 194-200
The results of repeated human papillomavirus (HPV) DNA testing were co
mpared to changes in cervical pathology and the composition of vaginal
microorganisms. A cohort of 19 women with HPV cervical infections in
the absence of cervical intraepithelial neoplasia at enrollment was re
ex amined on average at 7.3-month intervals over a 2-year period. At e
ach follow-up visit, cytological and colposcopic examinations were don
e and vaginal microorganisms were assessed quantitatively by Gram stai
ning of secretions, and anaerobic and aerobic culture. HPV genotypes 6
, 11, 16, and 18 were detected by polymerase chain reaction analysis u
sing DNA isolated from exfoliated cervical cells. The detection of HPV
DNA was significantly associated with carriage of Grade II flora (P <
0.001), isolation of Gardner ella vaginalis (P = 0.03), Ureaplasma ur
ealyti cum (P = 0.04), Candida albicans (P = 0.01), Bacteroides specie
s (P = 0.01), and overgrowth by anaerobes (P = 0.004). Normal vaginal
flora, characterised by the predominance of Lactobacillus species, was
significantly associated (P < 0.001) with a negative HPV test. The de
tection of HPV DNA is associated with the composition of microorganism
s present in the vagina at the time of testing. (C) 1994 Wiley-Liss, I
nc.