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基于交叉引物扩增法检测沙眼衣原体和淋病奈瑟菌

Detection of Chlamydia trachomatis and Neisseria gonorrhoeae based on cross-priming amplification.

作者信息

Yu B, An Y, Xu G, Shan H

机构信息

Department of Clinical Laboratory, College of Medicine, Sir Run Run Shaw Hospital, Zhejiang University, Hangzhou, Zhejiang, China.

Department of Gastroenterology, Yulin City first Hospital, Shaanxi, China.

出版信息

Lett Appl Microbiol. 2016 May;62(5):399-403. doi: 10.1111/lam.12560.

Abstract

UNLABELLED

Rapid, sensitive and specific isothermal nucleic acid amplification methods of Chlamydia trachomatis (C. trachomatis) and Neisseria gonorrhoeae (N. gonorrhoeae) have been developed based on cross-priming amplification (CPA). The amplicon of CPA can be detected by a disposable amplicon cross-contamination proof device. The whole assay takes 1-1·5 h from amplification to read out. Ten fold serial dilutions of quantified plasmids were used to test the CPA assay sensitivities, with the detection limits of 45 copies per reaction and 65 copies per reaction for C. trachomatis and N. gonorrhoeae respectively. The specificities of CPA assays for C. trachomatis and N. gonorrhoeae were tested by using total DNA extracted from nine other bacterial strains, and no cross-reactivity was detected. Eighty clinical cervical or vaginal swab specimens were tested by both CPA and real-time polymerase chain reaction (PCR) with the consistencies of 98·75% (79/80) and 97·5% (78/80) for C. trachomatis and N. gonorrhoeae respectively. Using real-time PCR as a reference standard, the clinical sensitivity (positive) and specificity (negative) of CPA was found to be 98·15% (53/54) and 100% (26/26) for C. trachomatis, and 93·75% (30/32) and 100% (48/48) for N. gonorrhoeae. Eight swab specimens tested positive for both C. trachomatis and N. gonorrhoeae simultaneously by real-time PCR and CPA assay. This study demonstrated that CPA is an affordable and accessible assay for C. trachomatis and N. gonorrhoeae detection, with high sensitivity and specificity.

SIGNIFICANCE AND IMPACT OF THE STUDY

Rapid and specific detection of the sexually transmitted pathogens Chlamydia trachomatis (C. trachomatis) and Neisseria gonorrhoeae (N. gonorrhoeae) would enable early treatment and management of their spread. Here, for the first time, a user friendly DNA isothermal amplification method named cross-priming amplification (CPA), was used to test C. trachomatis and N. gonorrhoeae with high sensitivity and specificity. The results indicate that CPA has great potential for improving C. trachomatis and N. gonorrhoeae diagnostics which could be particularly advantageous in resource-limited areas.

摘要

未标记

基于交叉引物扩增(CPA)开发了沙眼衣原体(C. trachomatis)和淋病奈瑟菌(N. gonorrhoeae)快速、灵敏且特异的等温核酸扩增方法。CPA的扩增产物可通过一次性防扩增产物交叉污染装置进行检测。整个检测过程从扩增到读出需1 - 1.5小时。使用定量质粒的十倍系列稀释液检测CPA检测的灵敏度,沙眼衣原体和淋病奈瑟菌的检测限分别为每个反应45个拷贝和65个拷贝。通过使用从其他9种细菌菌株中提取的总DNA来测试CPA检测对沙眼衣原体和淋病奈瑟菌的特异性,未检测到交叉反应。对80份临床宫颈或阴道拭子标本同时进行CPA和实时聚合酶链反应(PCR)检测,沙眼衣原体和淋病奈瑟菌的一致性分别为98.75%(79/80)和97.5%(78/80)。以实时PCR作为参考标准,发现CPA对沙眼衣原体的临床敏感性(阳性)和特异性(阴性)分别为98.15%(53/54)和100%(26/26),对淋病奈瑟菌分别为93.75%(30/32)和100%(48/48)。8份拭子标本通过实时PCR和CPA检测同时呈沙眼衣原体和淋病奈瑟菌阳性。本研究表明,CPA是一种用于检测沙眼衣原体和淋病奈瑟菌的经济且易于操作的检测方法,具有高灵敏度和特异性。

研究的意义和影响

快速且特异性地检测性传播病原体沙眼衣原体(C. trachomatis)和淋病奈瑟菌(N. gonorrhoeae)能够实现对其传播的早期治疗和管控。在此,首次使用一种名为交叉引物扩增(CPA)的用户友好型DNA等温扩增方法,以高灵敏度和特异性检测沙眼衣原体和淋病奈瑟菌。结果表明,CPA在改善沙眼衣原体和淋病奈瑟菌诊断方面具有巨大潜力,这在资源有限的地区可能特别有利。

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