A strategy combining human papillomavirus general primer (mainly the PGMY primers)-directed PCR sequencing and type-specific PCR is presented. DNA samples were first tested in general primer-mediated PCR. The amplified fragments of positive samples after ethidium bromide-stained DNA gel analysis were further sequenced, and corresponding DNA samples were further analyzed by PCR using type-specific primers for human papillomavirus ( It is now well accepted that all cervical carcinomas contain at least one of the "high-risk" types of human papillomavirus (HPV) DNA (41). Over 100 HPV genotypes have been isolated to date. Among these more than 40 have been shown to infect the genital tract, and 15 of them (genotypes 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 68, 73, and 82) have been found to be associated with cervical cancer or high-grade cervical intraepithelial neoplasia and therefore classified as high-risk types (31). In contrast, some HPV genotypes (6,11,40,42,43, 44, 54, 61, 70, 72, 81, and CP6108) are classified as low-risk types (31). Three additional types were classified as probable high risk (26, 53, and 66) while the risk of those previously undetected remains undetermined (31). Differences in geographic distribution of HPV types have been reported to exist between countries (10).Multiple concurrent and sequential infections with different oncogenic types of HPV are common, usually transient, and disappear spontaneously without clinical lesion. Only persistent high-risk HPV infection induces higher risk for the development of a high-grade precancerous lesion or cervical cancer (14,41,43). Since the absence of HPV infection means that the risk of cervical cancer is negligible, testing for HPV has now been incorporated into screening programs that previously relied only on cytology (6). HPV DNA analysis has shown encouraging results when used in conjunction with cytological analysis in primary screening for cervical cancer in women 30 years of age or older (5, 23). As a result of large randomized clinical trials, testing for HPV DNA is now recommended for most women with equivocal findings on cervical cytological analysis (atypical squamous cells of undetermined significance, also called ASCUS) (1, 28). Furthermore, HPV DNA testing provides a unique advantage for early detection of treatment failure (3,9,33,42). Recently, encouraging results with prophylactic HPV vaccines have been reported. These vaccines are believed to be effective against four different HPV types, including the most frequently encountered type, HPV-16. This further emphasizes the need for HPV DNA testing, which will be useful to guide vaccination and to monitor the frequency and the severity of infection by unaffected HPV types (15,20,21).Highly sensitive HPV DNA tests have been developed that rely on molecular biology techniques. For example, the FDA approved the HPV detection kit of Digene/Hybrid Capture 2 (HC2) manufactured by DiGene (MD). Within this test, genotype-specific RNA probes are mixed in a highrisk or a low-risk...