Development of real-time PCR assay for differential detection of Bordetella bronchiseptica and Bordetella parapertussis

被引:17
作者
Tizolova, Anette [1 ,2 ,3 ]
Brun, Delphine [2 ,3 ]
Guiso, Nicole [2 ,3 ]
Guillot, Sophie [2 ,3 ]
机构
[1] Inst Chem Technol, Dept Biochem & Microbiol, CR-16628 Prague 6, Czech Republic
[2] Inst Pasteur, Unite Prevent & Therapie Mol Malad Humaines, F-75015 Paris, France
[3] CNRS, URA 3012, Paris, France
关键词
Bordetella bronchiseptica; Bordetella parapertussis; Real-time PCR; Diagnosis; POLYMERASE-CHAIN-REACTION; ACID AMPLIFICATION TESTS; IMMUNOCOMPETENT INFANT; PERTUSSIS; INFECTION; HOLMESII; PNEUMONIA; PATHOGENS; PATIENT; COUGH;
D O I
10.1016/j.diagmicrobio.2013.12.020
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Bordetella parapertussis is a causative agent of whooping cough in humans, and B. bronchiseptica is causing wide variety of respiratory infections in mammals, including humans. Specific diagnostic tests are not currently available. Our first objective was to develop a real-time PCR test for the specific detection of B. bronchiseptica based on the previously described end-point PCR, targeting an intergenomic sequence of the fla gene locus, but it has not been reached. However, there is cross-reactivity between B. parapertussis and B. bronchiseptica. Therefore, the targeted region of several clinical isolates of both species was sequenced, and alignment of the sequences allowed the development of a 2-step real-time PCR assay. The first PCR assay detected the DNA of all clinical isolates of both B. bronchiseptica and B. parapertussis tested. The second PCR assay detected only the DNA of B. parapertussis clinical isolates, thereby allowing discrimination between B. parapertussis and B. bronchiseptica. (c) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:347 / 351
页数:5
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