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Development of a serogroup-specific multiplex PCR assay to detect a set of Escherichia coli serogroups based on the identification of their O-antigen gene clusters
Authors:Quan Wang  Xiaojuan Ruan  Dongmei Wei  Zhidong Hu  Lixia Wu  Ting Yu  Lu Feng  Lei Wang
Institution:1. TEDA School of Biological Sciences and Biotechnology, Nankai University, 23 Hongda Street, TEDA, Tianjin 300457, China;2. Key Laboratory of Molecular Microbiology and Technology, Ministry of Education, Tianjin 300071, China;3. The Engineering and Research Center for Microbial Functional Genomics and Detection Technology, Ministry of Education, Tianjin 300071, China;4. Tianjin Medical University General Hospital, Tianjin 300052, China;5. Shenzhou Hospital of Shenyang Medical College, Liaoning Province 110002, China;6. The Second Hospital of Jilin University, Jilin Province 130041, China;7. Tianjin Key Laboratory of Microbial Functional Genomics, TEDA, Tianjin 300457, China;8. Tianjin Research Center for Functional Genomics and Biochip, TEDA, Tianjin 300457, China
Abstract:The Escherichia coli serogroups O115, O126, O137, O158, O165, and O173 are pathogenic strains associated with diarrhea. Molecular approaches such as PCR have been proven to be rapid, inexpensive, and accurate. The sequences of the O-antigen-processing genes wzx and wzy are specific for different O antigens and are generally used as the target genes for the detection and identification of E. coli strains belonging to different O serogroups. In this report, the O-antigen gene clusters of these 6 O serogroups were sequenced, and genes were identified on the basis of homology. By screening these sequences against all 186 E. coli and Shigella strains, we found that the sequences of the wzx and wzy genes were serogroup-specific, and 2 specific primer pairs for each serogroup were screened out. A multiplex PCR assay targeting all 6 serogroups was developed. Twenty-nine strains were used to validate the specificity of the assay. The detection sensitivity was 1 ng genomic DNA. As the assay was shown to be accurate and sensitive, it can be used for the identification and detection of strains belonging to these serogroups in stool and other environmental samples after being isolated by culture.
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