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Development of multiplex real-time quantitative PCR for simultaneous detection of Chlamydia trachomatis and Ureaplasma parvum
被引:13
|作者:
Wei, Hong-bo
[1
,2
]
Zou, She-xiao
[2
]
Yang, Xiao-lin
[2
]
Yang, Dai-qin
[2
]
Chen, Xiang-dong
[1
]
机构:
[1] Wuhan Univ, Coll Life Sci, State Key Lab Virol, Wuhan 430072, Peoples R China
[2] Yangtze Univ, Coll Anim Sci, Jinzhou 434000, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Chlamydia trachomatis;
Multiplex real-time quantitative PCR;
Standard curves;
Ureaplasma parvum;
POLYMERASE-CHAIN-REACTION;
DNA AMPLIFICATION;
UREALYTICUM;
QUANTIFICATION;
IDENTIFICATION;
D O I:
10.1016/j.clinbiochem.2012.03.010
中图分类号:
R446 [实验室诊断];
R-33 [实验医学、医学实验];
学科分类号:
1001 ;
摘要:
Objectives: Chlamydia trachomatis and Ureaplasma urealyticum are common pathogens of sexually transmitted diseases. The majority of human ureaplasma isolates belong to the new species U. parvum. Clinically, C trachomatis and U. parvum usually double infect in the nongonococcal urethritis patients. A novel method for simultaneous detection of C. trachomatis and U. parvum was set up in the present work. Design and methods: Multiple real-time quantitative PCR was developed to allow for rapid, sensitive, specific and quantitative detection of C. trachomatis and U. parvum, simultaneously. To evaluate the applicability of the multiplex real-time quantitative PCR assay to clinical specimens, 64 samples of cervical swabs collected were studied. Results: Compared to the results obtained from single real-time quantitative PCR of C trachomatis and U. parvum, the specificity, sensitivity and quantitative detection results of multiple real-time quantitative PCR are approximately identical with those of the former. Conclusions: This assay will be of great value in the simultaneous and rapid diagnosis of C trachomatis and U. parvum in the future. (C) 2012 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved.
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页码:663 / 667
页数:5
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