Rapid homogeneous PCR assay for the detection of Chlamydia trachomatis in urine samples

被引:10
|
作者
Lehmusvuori, Ari [1 ]
Juntunen, Etvi [1 ]
Tapio, Antti-Heikki [1 ]
Rantakokko-Jalava, Kaisu [2 ]
Soukka, Tero [1 ]
Lovgren, Timo [1 ]
机构
[1] Univ Turku, Dept Biotechnol, FIN-20520 Turku, Finland
[2] Turku Univ Hosp, Clin Microbiol Lab, Turku 20521, Finland
关键词
Chlamydia trachomatis; Non-invasive sampling; Fast homogenous DNA assay; Time-resolved fluorometry; Lanthanide chelate; ACID AMPLIFICATION TESTS; NEISSERIA-GONORRHOEAE; REAL-TIME; COMPETITIVE HYBRIDIZATION; PERFORMANCE; DIAGNOSTICS; FLUOROMETRY; CHEMISTRY; SPECIMENS; PLASMID;
D O I
10.1016/j.mimet.2010.09.018
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Chlamydia trachomatis infection is the most common bacterial sexually transmitted disease and a major public health problem worldwide. Fast and sensitive point-of-care diagnostics including non-invasive sample collection would be of value for the prevention of C trachomatis transmission. The aim of this study was to develop a fast, reliable, non-invasive and easy-to-use homogenous PCR assay for the detection of C. trachomatis. Bacteria were concentrated from urine by a simple and fast centrifugation-based urine pretreatment method. Novel automated GenomEra technology was utilized for the rapid closed-tube PCR including time-resolved fluorometric detection of the target using lanthanide chelate labeled probes. We have developed a rapid C trachomatis assay which provides qualitative results in 1 h with diagnostic sensitivity and specificity of 98.7% and 97.3%, respectively. The novel assay can be performed with minimal laboratory expertise and without sophisticated DNA-extraction devices and has performance comparable to current gold standard assays. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:302 / 306
页数:5
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