Gaydos C A, Howell M R, Quinn T C, Gaydos J C, McKee K T
Infectious Disease Division, The Johns Hopkins University, Baltimore, MD 21205, USA.
J Clin Microbiol. 1998 May;36(5):1300-4. doi: 10.1128/JCM.36.5.1300-1304.1998.
Ligase chain reaction (LCR) (Abbott Laboratories, Abbott Park, Ill.) with first-catch urine specimens was used to detect Chlamydia trachomatis infections in 465 asymptomatic military women attending clinics for routine Papanicolaou smear tests. Results were compared to results of cervical culture to determine the sensitivity of the urine LCR and the possible presence of inhibitors of amplification in pregnant and nonpregnant women. Discrepant results for LCR and culture were resolved by direct fluorescent antibody staining of culture sediments, two different PCR assays, and LCR for the outer membrane protein 1 gene. The prevalence of Chlamydia in specimens by urine LCR was 7.3% compared to 5% by culture. For 434 women with matching specimens, there were 11 more specimens positive by LCR than were positive by culture, of which all but one were determined to be true positives. There were four culture-positive, LCR-negative specimens, all from nonpregnant women. The sensitivity, specificity, and positive and negative predictive values of urine LCR after discrepant results were resolved were 88.6, 99.7, 96.9, and 99.0%, respectively. The sensitivity of culture was 71.4%. From the 148 pregnant women (prevalence by LCR, 6.8%), there were no patients who were cervical culture positive and urine LCR negative to indicate the presence in pregnant women of inhibitors of LCR. Additionally, a subset of 55 of the LCR-negative frozen urine specimens from pregnant women that had been previously processed in LCR buffer were inoculated with 5 cell culture inclusion forming units of C. trachomatis each and retested by LCR; all tested positive, indicating the absence of inhibitors of LCR in urine from these pregnant women. The use of LCR testing of urine specimens from asymptomatic women, whether pregnant or not, offers a sensitive and easy method to detect C. trachomatis infection in women.
采用连接酶链反应(LCR)(雅培实验室,伊利诺伊州雅培公园)检测465名因常规巴氏涂片检查而就诊的无症状军中女性首次晨尿标本中的沙眼衣原体感染。将结果与宫颈培养结果进行比较,以确定尿液LCR的敏感性以及孕妇和非孕妇中可能存在的扩增抑制剂。LCR和培养结果不一致的情况通过对培养沉淀物进行直接荧光抗体染色、两种不同的聚合酶链反应(PCR)检测以及外膜蛋白1基因的LCR检测来解决。尿液LCR检测标本中衣原体的患病率为7.3%,而培养法为5%。对于434名有匹配标本的女性,LCR检测阳性的标本比培养法多11份,其中除一份外均被确定为真阳性。有4份培养阳性、LCR阴性的标本,均来自非孕妇。在解决结果不一致的问题后,尿液LCR的敏感性、特异性、阳性预测值和阴性预测值分别为88.6%、99.7%、96.9%和99.0%。培养法的敏感性为71.4%。在148名孕妇中(LCR患病率为6.8%),没有宫颈培养阳性而尿液LCR阴性的患者,这表明孕妇中不存在LCR的抑制剂。此外,从之前在LCR缓冲液中处理过的55份孕妇LCR阴性冷冻尿液标本中选取一部分,每份接种5个沙眼衣原体细胞培养包涵体形成单位,然后用LCR重新检测;所有检测均为阳性,表明这些孕妇尿液中不存在LCR抑制剂。对无症状女性尿液标本进行LCR检测,无论其是否怀孕,都为检测女性沙眼衣原体感染提供了一种敏感且简便的方法。