Kluytmans J A, Niesters H G, Mouton J W, Quint W G, Ijpelaar J A, Van Rijsoort-Vos J H, Habbema L, Stolz E, Michel M F, Wagenvoort J H
Department of Clinical Microbiology, University Hospital Rotterdam Dijkzigt, The Netherlands.
J Clin Microbiol. 1991 Dec;29(12):2685-9. doi: 10.1128/jcm.29.12.2685-2689.1991.
The Gen-Probe PACE 2 assay (GP), a nonisotopic DNA probe, was evaluated by using cell culture as the method of reference. Specimens were collected from 260 men and 482 women visiting the outpatient department for sexually transmitted diseases at the University Hospital in Rotterdam, The Netherlands. The prevalences of Chlamydia culture-positive men and women were 13.2 and 8.6%, respectively. Sensitivity values for the male and female patients were 70.6 and 92.7%, respectively. Specificity values for these groups were 98.2 and 97.7%, respectively. Sensitivity was significantly lower when the number of inclusions in cell culture was low. Samples which showed a discordance between cell culture and GP results were retested by the polymerase chain reaction. If the results of the polymerase chain reaction were considered as the points of reference, the sensitivity and specificity of both GP and cell culture could be calculated. The performance of GP for females was comparable to that of cell culture. In males, the sensitivity of GP was considerably lower than that of cell culture (77.2 versus 91.4%), while specificity was somewhat higher (99.6 versus 99.1%). Compared with cell culture, the GP is a relatively simple and rapid test that is suitable for diagnosing Chlamydia infections in urogenital specimens.
采用细胞培养作为参考方法,对Gen-Probe PACE 2检测法(GP)这一非同位素DNA探针进行了评估。标本取自荷兰鹿特丹大学医院性病门诊的260名男性和482名女性。衣原体培养阳性的男性和女性患病率分别为13.2%和8.6%。男性和女性患者的敏感度值分别为70.6%和92.7%。这些组别的特异度值分别为98.2%和97.7%。当细胞培养中的包涵体数量较少时,敏感度显著降低。对细胞培养和GP检测结果不一致的样本,通过聚合酶链反应进行重新检测。如果将聚合酶链反应的结果视为参考标准,则可以计算出GP和细胞培养的敏感度和特异度。GP对女性的检测性能与细胞培养相当。在男性中,GP的敏感度显著低于细胞培养(77.2%对91.4%),而特异度则略高(99.6%对99.1%)。与细胞培养相比,GP是一种相对简单、快速的检测方法,适用于诊断泌尿生殖系统标本中的衣原体感染。