Crotchfelt K A, Welsh L E, DeBonville D, Rosenstraus M, Quinn T C
Division of Infectious Diseases, Johns Hopkins University, Baltimore, Maryland 21205, USA.
J Clin Microbiol. 1997 Jun;35(6):1536-40. doi: 10.1128/jcm.35.6.1536-1540.1997.
A coamplification PCR test for the direct detection of Neisseria gonorrhoeae and Chlamydia trachomatis in urethral and endocervical swabs and urine samples from men and women was compared to standard culture techniques. Processed specimens were amplified in single reaction tubes containing primers for both organisms, and PCR products were detected by a colorimetric microwell plate hybridization assay specific for each pathogen. Of 344 specimens from men, 45 (13.1%) urine specimens were PCR positive for C. trachomatis, 51 (14.8%) urethral swab specimens were PCR positive, and 29 urethral swab specimens (8.4%) were culture positive. After analysis of discrepancies, the resolved sensitivity and specificity of PCR for C. trachomatis were 96.2 and 99.3%, respectively, in urethral swab specimens, compared to 88.2 and 98.6% for urine specimens. Of the 192 specimens from women, 28 (14.6%) urine specimens were PCR positive for C. trachomatis, 32 (16.7%) endocervical specimens were PCR positive, and 19 (9.9%) endocervical specimens were culture positive. After analysis of discrepancies, the resolved sensitivity and specificity of PCR for C. trachomatis for endocervical specimens were both 100% compared to 100 and 99.4%, respectively, for urine specimens from women. In men, 68 (19.8%) urine specimens were PCR positive for N. gonorrhoeae, 73 (21.2%) urethral swabs were PCR positive, and 59 (17.2%) urethral swabs were culture positive. After analysis of discrepancies, the resolved sensitivity and specificity of PCR for N. gonorrhoeae were 97.3 and 97.0%, respectively, for urethral specimens compared to 94.4 and 98.5% for urine specimens. In women, 18 (9.4%) urine specimens were PCR positive for N. gonorrhoeae, 23 (12.0%) were endocervical swab PCR positive, and 15 (7.8%) endocervical specimens were culture positive. After analysis of discrepancies, the resolved sensitivity and specificity of PCR for N. gonorrhoeae were 100 and 99.4%, respectively, for endocervical specimens compared to 90.0 and 95.9% for female urine specimens. These results indicate that a multiplex PCR is highly sensitive for detecting both C. trachomatis and N. gonorrhoeae from a single urine or genital swab, providing a more cost-effective way of screening multiple pathogens.
将一种用于直接检测男性和女性尿道及宫颈拭子以及尿液样本中淋病奈瑟菌和沙眼衣原体的共扩增聚合酶链反应(PCR)检测方法与标准培养技术进行了比较。处理后的标本在含有两种病原体引物的单个反应管中进行扩增,PCR产物通过针对每种病原体的比色微孔板杂交试验进行检测。在344份男性标本中,45份(13.1%)尿液标本沙眼衣原体PCR检测呈阳性,51份(14.8%)尿道拭子标本PCR检测呈阳性,29份尿道拭子标本(8.4%)培养呈阳性。在分析差异后,尿道拭子标本中PCR检测沙眼衣原体的分辨率敏感性和特异性分别为96.2%和99.3%,而尿液标本分别为88.2%和98.6%。在192份女性标本中,28份(14.6%)尿液标本沙眼衣原体PCR检测呈阳性,32份(16.7%)宫颈标本PCR检测呈阳性,19份(9.9%)宫颈标本培养呈阳性。在分析差异后,宫颈标本中PCR检测沙眼衣原体的分辨率敏感性和特异性均为100%,而女性尿液标本分别为100%和99.4%。在男性中,68份(19.8%)尿液标本淋病奈瑟菌PCR检测呈阳性,73份(21.2%)尿道拭子PCR检测呈阳性,59份(17.2%)尿道拭子培养呈阳性。在分析差异后,尿道标本中PCR检测淋病奈瑟菌的分辨率敏感性和特异性分别为97.3%和97.0%,而尿液标本分别为94.4%和98.5%。在女性中,18份(9.4%)尿液标本淋病奈瑟菌PCR检测呈阳性,23份(12.0%)宫颈拭子PCR检测呈阳性,15份(7.8%)宫颈标本培养呈阳性。在分析差异后,宫颈标本中PCR检测淋病奈瑟菌的分辨率敏感性和特异性分别为100%和99.4%,而女性尿液标本分别为90.0%和95.9%。这些结果表明,多重PCR对从单一尿液或生殖器拭子中检测沙眼衣原体和淋病奈瑟菌具有高度敏感性,为筛查多种病原体提供了一种更具成本效益的方法。