EVALUATION OF CLEARVIEW AND MAGIC LITE TESTS, POLYMERASE CHAIN-REACTION, AND CELL-CULTURE FOR DETECTION OF CHLAMYDIA-TRACHOMATIS IN UROGENITAL SPECIMENS

Citation
Jajw. Kluytmans et al., EVALUATION OF CLEARVIEW AND MAGIC LITE TESTS, POLYMERASE CHAIN-REACTION, AND CELL-CULTURE FOR DETECTION OF CHLAMYDIA-TRACHOMATIS IN UROGENITAL SPECIMENS, Journal of clinical microbiology, 31(12), 1993, pp. 3204-3210
Citations number
28
Categorie Soggetti
Microbiology
ISSN journal
00951137
Volume
31
Issue
12
Year of publication
1993
Pages
3204 - 3210
Database
ISI
SICI code
0095-1137(1993)31:12<3204:EOCAML>2.0.ZU;2-O
Abstract
The Clearview Chlamydia test (CV; Unipath Ltd., Bedford, United Kingdo m), the Magic Lite Chlamydia test (ML; CIBA Corning, Medfield, Mass.), a polymerase chain reaction (PCR), and cell culture (CC) were evaluat ed for detection of Chlamydia trachomatis in urogenital specimens. Spe cimens were collected from 283 men and 724 women visiting the outpatie nt clinic for Sexually Transmitted Diseases at the University Hospital Rotterdam, Rotterdam, The Netherlands. ML, PCR, and CC were all perfo rmed on the same sample to prevent swab-to-swab variability. CV was pe rformed on a separate sample. Analysis of discordant results was perfo rmed by application of the following confirmatory assays: first, PCR o n the CC, second, ML was repeated, and third, PCR was repeated by usin g a different DNA extraction protocol. ff more than one test was posit ive, the sample was considered true positive. If only one test was pos itive, which was confirmed by the confirmatory assay, the sample was a lso considered true positive. By using these interpretations, the foll owing results were obtained. The sensitivity and specificity of CV for samples from men were 60.4 and 86.3%, respectively. For samples from women, these values were 62.3 and 99.7%, respectively. The low specifi city for samples from men was caused by unidentified substances in the swab that was used. The use of CV on samples from men is not recommen ded by the manufacturer. For samples from women, the specificity of CV was high, but the low sensitivity of CV limits its use for diagnostic purposes. The sensitivities of ML were low for samples from both men and women (68.8 and 50.9% respectively), while specificities were exce llent for samples from both groups (100 and 99.9%, respectively). The low sensitivity of ML limits its diagnostic value. The PCR technique w as highly specific for samples from both men (99.6%) and women (99.9%) . The sensitivity of PCR, however, was unexpectedly low for samples fr om both groups (men, 87.5%; women, 79.2%), most likely because of the sample treatment method used. The sensitivity and specificity values o f CC for samples from men were 95.8 and 100%, respectively. For sample s from women, these values were 100 and 99.9%, respectively. In the pr esent study, CC was the most reliable technique for the detection of C . trachomatis.