| Abstrakt: |
A microtiter plate-based method to detect amplified DNA was developed. The method uses one biotin-labeled primer in the polymerase chain reaction (PCR) mixture. The labeled amplicon is bound to streptavidin-coated microtiter plates, denatured and hybridized to a digoxigenin-labeled probe. The specificity of the hybridization reaction was optimized by varying the temperature of the subsequent washing step and adding urea to the washing buffer. The digoxigenin label was detected using an enzyme immunoassay (EIA). This PCR-EIA was compared with a standard PCR assay that uses gel electrophoresis, blotting and hybridization to detect the amplicon, with isolation in cell culture, and with an antigen detection EIA (Chlamydiazyme) in the diagnosis ofChlamydia trachomatis infection in 309 female patients attending a sexually transmitted diseases outpatient clinic. The prevalence ofChlamydia trachomatis infection as determined by isolation in cell culture, EIA, PCR-EIA and standard PCR assay was 9.1 %, 8.7 %, 12.3 %, and 12.9 %, respectively. Compared with results of a reference set of confirmed-positive cases (defined by a positive result in two or more independent assays after analysis of discrepancies), the sensitivity and specificity was 71.1 % and 99.6 % for cell culture, 65.8 % and 99.3 % for the EIA, 92.1 % and 98.9 % for the PCR-EIA, and 97.4 % and 98.9 % for the standard PCR assay. It is concluded that the PCR-EIA described is a fast, sensitive and specific method for detectingChlamydia trachomatis in clinical specimens. |
Full text from SpringerLink