Multiplex Polymerase Chain Reaction for Identification of Shigellae and FourShigellaSpecies Using Novel Genetic Markers Screened by Comparative Genomics

志贺氏菌 生物 聚合酶链反应 福氏志贺氏菌 痢疾志贺氏菌 博伊迪志贺氏菌 多重聚合酶链反应 底漆(化妆品) 基因组DNA 宋内志贺氏菌 微生物学 遗传学 大肠杆菌 基因 有机化学 化学
作者
Hyun‐Joong Kim,Ji-Oh Ryu,Jiyeon Song,Hae‐Yeong Kim
出处
期刊:Foodborne Pathogens and Disease [Mary Ann Liebert, Inc.]
卷期号:14 (7): 400-406 被引量:24
标识
DOI:10.1089/fpd.2016.2221
摘要

In the detection of Shigella species using molecular biological methods, previously known genetic markers for Shigella species were not sufficient to discriminate between Shigella species and diarrheagenic Escherichia coli. The purposes of this study were to screen for genetic markers of the Shigella genus and four Shigella species through comparative genomics and develop a multiplex polymerase chain reaction (PCR) for the detection of shigellae and Shigella species. A total of seven genomic DNA sequences from Shigella species were subjected to comparative genomics for the screening of genetic markers of shigellae and each Shigella species. The primer sets were designed from the screened genetic markers and evaluated using PCR with genomic DNAs from Shigella and other bacterial strains in Enterobacteriaceae. A novel Shigella quintuplex PCR, designed for the detection of Shigella genus, S. dysenteriae, S. boydii, S. flexneri, and S. sonnei, was developed from the evaluated primer sets, and its performance was demonstrated with specifically amplified results from each Shigella species. This Shigella multiplex PCR is the first to be reported with novel genetic markers developed through comparative genomics and may be a useful tool for the accurate detection of the Shigella genus and species from closely related bacteria in clinical microbiology and food safety.
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