Jensen Jørgen Skov, Björnelius Eva, Dohn Birthe, Lidbrink Peter
Mycoplasma Laboratory, Department of Respiratory Infections, Meningitis, and Sexually Transmitted Infections, Statens Serum Institut, Copenhagen S, Denmark.
Sex Transm Dis. 2004 Aug;31(8):499-507. doi: 10.1097/01.olq.0000135992.98883.e4.
The objective of this study was to compare urogenital swab specimens and first void urine (FVU) specimens from male and female patients at a sexually transmitted disease clinic for the detection of Mycoplasma genitalium and Chlamydia trachomatis infections using in-house, inhibitor-controlled polymerase chain reaction (PCR).
Urethral swabs and FVU were collected from 1856 men and 753 women who also had a cervical swab collected. A positive diagnosis of infection was made if any 1 of the specimens tested positive and were confirmed in a second PCR assay targeting independent genes.
M. genitalium DNA and C. trachomatis DNA were detected in 126 (6.8%) and 246 (13.3%) of the male sample sets and in 51 (6.8%) and 73 (9.7%) of the female specimen sets, respectively. Using our in-house PCR and sample preparation methods, FVU was found to be the most sensitive diagnostic specimen for both pathogens, but for optimal sensitivity, it should be supplemented with a cervical specimen in women. In a small subset of female FVUs, storage at -20 degrees C led to false-negative M. genitalium PCR results in 27% of specimens found positive when a sample preparation was performed before freezing. The age-specific prevalence of M. genitalium in men was almost constant between 18 and 45 years of age in contrast to C. trachomatis infections, which were more common in younger men.
Urine appeared to be a better diagnostic specimen than the urethral swab for M. genitalium and C. trachomatis detection by PCR in this cohort of sexually transmitted disease clinic attendees but should be supplemented with a cervical specimen in women.
本研究的目的是比较性病门诊男性和女性患者的泌尿生殖拭子标本和首次晨尿(FVU)标本,使用内部抑制剂控制的聚合酶链反应(PCR)检测生殖支原体和沙眼衣原体感染。
从1856名男性和753名女性中收集尿道拭子和FVU,这些患者还采集了宫颈拭子。如果任何一份标本检测呈阳性,并在针对独立基因的第二次PCR检测中得到确认,则诊断为感染阳性。
在男性样本组中,分别在126例(6.8%)和246例(13.3%)中检测到生殖支原体DNA和沙眼衣原体DNA;在女性样本组中,分别在51例(6.8%)和73例(9.7%)中检测到。使用我们的内部PCR和样本制备方法,发现FVU是这两种病原体最敏感的诊断标本,但为了获得最佳敏感性,女性应补充宫颈标本。在一小部分女性FVU中,在-20℃下储存导致27%的标本在冷冻前进行样本制备时发现为阳性的生殖支原体PCR结果出现假阴性。与沙眼衣原体感染相比,男性生殖支原体的年龄特异性患病率在18至45岁之间几乎保持不变,沙眼衣原体感染在年轻男性中更为常见。
在这群性病门诊患者中,尿液似乎是比尿道拭子更好的用于通过PCR检测生殖支原体和沙眼衣原体的诊断标本,但女性应补充宫颈标本。