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一种从尿液中分离沙眼衣原体的新型自动化方法消除了抑制作用,并提高了核酸扩增检测(NAAT)系统的稳健性。

A new automated method for isolation of Chlamydia trachomatis from urine eliminates inhibition and increases robustness for NAAT systems.

作者信息

Anglès d'Auriac Marc, Refseth Unn Hilde, Espelund Mari, Moi Harald, Størvold Gunnar, Jeansson Stig

机构信息

Genpoint AS, Frysjaveien 40, Oslo, N-0884, Norway.

出版信息

J Microbiol Methods. 2007 Sep;70(3):416-23. doi: 10.1016/j.mimet.2007.05.017. Epub 2007 May 31.

DOI:10.1016/j.mimet.2007.05.017
PMID:17610971
Abstract

Chlamydia trachomatis is a leading cause of sexually transmitted infection. Diagnostic methods with easy non-invasive sample collection are important to increase testing and hence to reduce the spread of this infection. To enable more use of urine samples in C. trachomatis diagnostics, automation is an absolute requirement since obtaining high-quality DNA from urine specimens involves extensive processing. Here, we present a study in which a new automated sample preparation method, BUGS'n BEADS STI (BnB STI), was used up-front of the BDProbeTec ET end point analysis and compared with the full BDProbeTec ET method to analyze C. trachomatis in 1002 urine samples. The BnB STI system represents a new concept within magnetic sample preparation in which bacteria are first isolated from the sample material followed by purification of bacterial nucleic acid using the same magnetic particles. Similar sensitivity and specificity were obtained with both methods. None of the samples processed with BnB STI inhibited the BDProbeTec ET test whereas 1.8% showed inhibition when processed according to the manual BDProbeTect ET DNA preparation method. Moreover, the average MOTA scores obtained with the BnB STI system were 48% higher for all amplification controls and 57% higher for positive samples, compared to the manual sample preparation. Based on these results and the significant reduction in hands-on-time for urine sample processing, the automated BnB STI sample preparation method was implemented for routine analysis of C. trachomatis from urine samples.

摘要

沙眼衣原体是性传播感染的主要病因。具有简便无创样本采集的诊断方法对于增加检测从而减少这种感染的传播至关重要。为了在沙眼衣原体诊断中更多地使用尿液样本,自动化是绝对必要的,因为从尿液标本中获取高质量DNA需要大量处理。在此,我们展示一项研究,其中一种新的自动化样本制备方法,即BUGS'n BEADS STI(BnB STI),在BDProbeTec ET终点分析之前使用,并与完整的BDProbeTec ET方法进行比较,以分析1002份尿液样本中的沙眼衣原体。BnB STI系统代表了磁性样本制备中的一个新概念,其中首先从样本材料中分离细菌,然后使用相同的磁性颗粒纯化细菌核酸。两种方法获得了相似的灵敏度和特异性。用BnB STI处理的样本均未抑制BDProbeTec ET检测,而按照手动BDProbeTect ET DNA制备方法处理时,有1.8%的样本显示出抑制作用。此外,与手动样本制备相比,BnB STI系统对所有扩增对照获得的平均MOTA分数高48%,对阳性样本高57%。基于这些结果以及尿液样本处理的实际操作时间显著减少,自动化的BnB STI样本制备方法被用于尿液样本沙眼衣原体的常规分析。

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A new automated method for isolation of Chlamydia trachomatis from urine eliminates inhibition and increases robustness for NAAT systems.一种从尿液中分离沙眼衣原体的新型自动化方法消除了抑制作用,并提高了核酸扩增检测(NAAT)系统的稳健性。
J Microbiol Methods. 2007 Sep;70(3):416-23. doi: 10.1016/j.mimet.2007.05.017. Epub 2007 May 31.
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Use of pooled urine samples and automated DNA isolation to achieve improved sensitivity and cost-effectiveness of large-scale testing for Chlamydia trachomatis in pregnant women.使用混合尿液样本和自动化DNA提取以提高孕妇沙眼衣原体大规模检测的灵敏度和成本效益。
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[DNA amplification in the diagnosis of urogenital Chlamydia trachomatis infection].[DNA扩增技术在泌尿生殖系统沙眼衣原体感染诊断中的应用]
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Screening for Chlamydia trachomatis infection using the BDProbeTec ET Chlamydia trachomatis amplified DNA assay on urine in a GUM clinic setting: a simple, fast and cost-effective alternative.在性健康诊所环境中,使用BDProbeTec ET沙眼衣原体扩增DNA检测法对尿液进行沙眼衣原体感染筛查:一种简单、快速且经济高效的替代方法。
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引用本文的文献

1
Systematic screening with information and home sampling for genital Chlamydia trachomatis infections in young men and women in Norway: a randomized controlled trial.挪威对年轻男女进行生殖道沙眼衣原体感染的信息和家庭采样的系统筛查:一项随机对照试验。
BMC Infect Dis. 2013 Jan 23;13:30. doi: 10.1186/1471-2334-13-30.
2
Population based study of genital Chlamydia trachomatis prevalence and associated factors in Norway: a cross sectional study.基于人群的挪威生殖道沙眼衣原体流行率及相关因素的研究:一项横断面研究。
BMC Infect Dis. 2012 Jul 2;12:150. doi: 10.1186/1471-2334-12-150.