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Development of a disposable cartridge real-time PCR test for detection of Chlamydia trachomatis directly from urine
被引:2
|作者:
Brennan, Desmond
[1
]
O'Connor, Louise
[2
]
Cormican, Martin
[3
]
Kileen, James
[3
]
Clancy, Eoin
[2
]
Smith, Terry J.
[2
]
Galvin, Paul
[1
]
机构:
[1] Univ Coll Cork, Tyndall Natl Inst, Life Sci Interface Grp, Cork, Ireland
[2] Natl Univ Ireland, Mol Diagnost Res Grp, Galway, Ireland
[3] Hlth Serv Execut, Dublin, Ireland
关键词:
Duplex PCR;
Microfluidics;
Fluorescence detection;
Chlamydia trachomatis;
MICROARRAY HYBRIDIZATION;
MICROFLUIDIC DEVICE;
RAPID DETECTION;
GENOMIC DNA;
AMPLIFICATION;
INFECTION;
SYSTEM;
POINT;
D O I:
10.1016/j.snb.2021.129873
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
We present a PCR assay screening Chlamydia trachomatis directly from urine without pre-amplification or sample clean-up and demonstrate suitability for implementation on a disposable cartridge system. Primers and probes were designed to detect all Chlamydia trachomatis serovars with a high degree of sensitivity and specificity. The assay also incorporated a synthetic internal amplification control to monitor inhibition of the PCR reaction. The assay protocol worked directly on urine samples with initial heating to 85 ?C for ten minutes, followed by a duplex realtime PCR (95 ?C, 55 ?C, 45 cycles) on resulting urine lysate. The test cartridge incorporated heating and liquid manipulation using pinch valves and a compressible blister pouch. Lyophilised PCR reagents were incorporated into the cartridge and were re-suspended by a 40 ?L aliquot of the urine lysate. Primers were designed to screen for all Chlamydia trachomatis serovars with a high degree of sensitivity and specificity. Evaluation of the newly developed PCR assay was carried out on the LightCyclerTM using urine samples previously confirmed positive or negative for the target pathogen, using the ABBOTT real-time PCR Cobas CT/NG test at a local hospital.
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