首页> 外文期刊>Journal of Food Safety >Detection of Cronobacter on gluB Gene and Differentiation of Four Cronobacter Species by Polymerase Chain Reaction-Restriction Fragment Length Polymorphism Typing
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Detection of Cronobacter on gluB Gene and Differentiation of Four Cronobacter Species by Polymerase Chain Reaction-Restriction Fragment Length Polymorphism Typing

机译:聚合酶链反应-限制性片段长度多态性分型检测gluB基因上的克罗诺杆菌并区分四种克罗诺杆菌

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摘要

Cronobacter species are foodborne pathogens associated with neonatal meningitis, sepsis and necrotizing enterocolitis through consumption of contaminated powdered milk. However, there are no specific targets used for differentiating Cronobacter species. The DNA-based assay and polyphasic analysis have facilitated the detection and typing of Cronobacter species in foodborne outbreaks. In this study, polymerase chain reaction (PCR) and dot hybridization for detecting Cronobacter spp. was developed targeting gluB gene, then one PCR-restriction fragment length polymorphism (RFLP) typing assay with TaqI digestion was applied for four species differentiation within Cronobacter. Results indicated that the gluB gene is a specific target for detecting Cronobacter and the PCR-RFLP typing assay could conveniently and rapidly differentiate Cronobactermalonaticus, C.dublinensis, C.sakazakii and C.muytjensii.
机译:克罗诺杆菌是通过食用受污染的奶粉与新生儿脑膜炎,败血症和坏死性小肠结肠炎相关的食源性病原体。但是,没有用于区分Cronobacter物种的特定目标。基于DNA的测定和多相分析促进了食源性暴发中克罗诺杆菌种类的检测和分型。在这项研究中,聚合酶链反应(PCR)和斑点杂交检测克氏杆菌。以gluB基因为靶基因进行了克隆,然后用一种TaqI酶切的PCR酶切限制性片段长度多态性(RFLP)分型法对克罗诺杆菌进行了四种分化。结果表明,gluB基因是检测克罗诺杆菌的特异性靶标,PCR-RFLP分型分析可以方便,快速地区分克罗诺杆菌,杜氏梭菌,阪崎氏梭菌和穆氏梭菌。

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