基于交叉引物扩增的EasyNAT CT/NG快速简便检测沙眼衣原体和淋病奈瑟菌

IF 3 3区 医学 Q2 INFECTIOUS DISEASES
Qing Wu, Hongxiang Tu, Yingjie Dai, Yumin Wang, Lijuan Hu
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引用次数: 0

摘要

目的:沙眼衣原体(CT)和淋病奈瑟菌(NG)是最常见的性传播病原体。快速筛选和检测这些细菌对于减少后遗症和预防传播至关重要。本研究评估了EasyNAT CT/NG检测方法的有效性,该方法利用交叉引物扩增(CPA)技术快速同时检测多种生殖道标本中的CT和NG,在30分钟内实现诊断。方法:使用198个临床样本评估EasyNAT CT/NG检测CT和NG的临床性能,并将结果与传统的室内实时荧光定量PCR进行比较,以确定一致性。通过连续稀释定量质粒来测量灵敏度,并通过纳入18种常见STI病原体的DNA来评估特异性。根据目标产品简介(TPPs)中概述的标准,评估了该方法作为护理点检测(POCT)工具的适用性。结果:EasyNAT CT/NG检测结果与Real-Time PCR结果高度一致,CT阳性率为98.5%,NG阳性率为99.0%。尿样CT和NG的符合率分别为98.6%和100%,宫颈拭子CT和NG的符合率均为97.7%;阴道和尿道拭子对这两种病原体的检测均达到100%。198份样本中,有1份尿样CT Real-Time PCR检测为阴性,但EasyNAT CT/NG检测为阳性,造父变星Xpert CT/NG检测证实为阳性。两份宫颈拭子的CT和NG均为Real-Time PCR阴性,EasyNAT CT/NG检测结果无效,但造父变星Xpert CT/NG检测结果为CT和NG阴性。EasyNAT CT/NG测定在浑浊标本中可靠地检测出CT和NG,但在严重溶血标本中可能失败。检出限为400拷贝/mL,与其他18种病原菌无交叉反应。结论:EasyNAT CT/NG检测快速、灵敏、特异,对感染筛查和早期诊断具有重要价值。作为一种快速POCT方法,它显示出了良好的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rapid and simple detection of Chlamydia trachomatis and Neisseria gonorrhoeae using the EasyNAT CT/NG assay based on cross-priming amplification.

Purpose: Chlamydia trachomatis (CT) and Neisseria gonorrhoeae (NG) rank among the most common sexually transmitted pathogens. Rapid screening and detection of these bacteria are essential to reduce sequelae and prevent transmission. This study evaluated the efficacy of the EasyNAT CT/NG assay, which utilizes cross-priming amplification (CPA) technique for the rapid and simultaneous detection of CT and NG in diverse reproductive tract specimens, achieving diagnosis within 30 min.

Methods: The clinical performance of the EasyNAT CT/NG assay in detecting CT and NG was assessed using 198 clinical samples, with results compared to those of conventional in-house Real-Time PCR to determine concordance. Sensitivity was measured using serial dilutions of quantified plasmids and specificity was evaluated by incorporating DNA from 18 common STI pathogens. The assay's suitability as a point-of-care testing (POCT) tool was evaluated with the criteria outlined in Target Product Profiles (TPPs).

Results: The EasyNAT CT/NG assay demonstrated high concordance with Real-Time PCR, with rates of 98.5% for CT and 99.0% for NG. Concordance in urine samples reached 98.6% for CT and 100% for NG, while cervical swabs showed both 97.7% for CT and NG; vaginal and urethral swabs achieved 100% for both pathogens. Among the 198 samples, one urine specimen tested negative for CT by Real-Time PCR but positive by the EasyNAT CT/NG assay, a positive result confirmed by the Cepheid Xpert CT/NG assay. Two cervical swabs, negative for CT and NG by Real-Time PCR, yielded invalid results with the EasyNAT CT/NG assay but were confirmed negative or CT and NG by the Cepheid Xpert CT/NG assay. The EasyNAT CT/NG assay reliably detected CT and NG in turbid specimens, though it may fail with severely hemolytic samples. Its detection limit was 400 copies/mL, with no cross-reactivity observed across 18 other pathogens.

Conclusion: The EasyNAT CT/NG assay offers rapid, sensitive, and specific detection of CT and NG, proving valuable for infection screening and early diagnosis. It shows promise as a rapid POCT method.

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来源期刊
CiteScore
10.40
自引率
2.20%
发文量
138
审稿时长
1 months
期刊介绍: EJCMID is an interdisciplinary journal devoted to the publication of communications on infectious diseases of bacterial, viral and parasitic origin.
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