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采用一种新的聚合酶链反应分析法快速检测结膜、咽部和尿道标本中的沙眼衣原体。

Rapid detection of Chlamydia trachomatis in conjunctival, pharyngeal, and urethral specimens with a new polymerase chain reaction assay.

作者信息

Kessler H H, Pierer K, Stuenzner D, Auer-Grumbach P, Haller E M, Marth E

机构信息

Department of Hygiene, KF-University, Graz, Austria.

出版信息

Sex Transm Dis. 1994 Jul-Aug;21(4):191-5. doi: 10.1097/00007435-199407000-00002.

Abstract

GOAL OF THIS STUDY

The Amplicor polymerase chain reaction (PCR) assay for the detection of Chlamydia trachomatis (Roche Molecular Systems, Branchburg, NJ) was evaluated on conjunctival, pharyngeal, and urethral swabs.

STUDY DESIGN

A total of 515 conjunctival, pharyngeal, and urethral swabs. The reference system was culture with McCoy cells in shell vials with fluorescent immunostaining. One swab was used for both cell culture and the molecular assay. Initial storage took place in 2-SP medium. After transfer to Amplicor specimen transport medium the molecular assay was done using the Amplicor Chlamydia trachomatis amplification and detection kits.

RESULTS

The total positive rate was 6.6%. Specificity of culture was 100%. The evaluated molecular assay gave a specificity of 99.8%. Sensitivities of PCR and culture were 100% and 85.3%, respectively.

CONCLUSIONS

Because of the high sensitivity, specificity, and ease of use, the molecular assay was found to be a good alternative to culture for detection of C. trachomatis in conjunctival, pharyngeal, and urethral specimens.

摘要

本研究目的

对用于检测沙眼衣原体的Amplicor聚合酶链反应(PCR)检测法(罗氏分子系统公司,新泽西州布兰奇堡)在结膜、咽和尿道拭子上进行评估。

研究设计

共515份结膜、咽和尿道拭子。参考系统是在带荧光免疫染色的壳瓶中用McCoy细胞进行培养。一份拭子用于细胞培养和分子检测。最初保存在2 - SP培养基中。转移到Amplicor标本转运培养基后,使用Amplicor沙眼衣原体扩增和检测试剂盒进行分子检测。

结果

总阳性率为6.6%。培养的特异性为100%。所评估的分子检测法特异性为99.8%。PCR和培养的敏感性分别为100%和85.3%。

结论

由于具有高敏感性、特异性且使用方便,分子检测法被认为是在结膜、咽和尿道标本中检测沙眼衣原体时替代培养的良好方法。

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