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用于区分阪崎克罗诺杆菌和丙二酸克罗诺杆菌的双重实时聚合酶链反应方法

Duplex Real-Time PCR Method for the Differentiation of Cronobacter sakazakii and Cronobacter malonaticus.

作者信息

Li Xiaofang, Cui Jinghua, Du Xiaoli, Cui Zhigang, Huang Yibing, Kan Biao

机构信息

National Institute for Communicable Disease Control and Prevention and State Key Laboratory for Infectious Disease Prevention and Control, Chinese Center for Disease Control and Prevention, Beijing 102206, People's Republic of China.

Key Laboratory for Molecular Enzymology and Engineering of the Ministry of Education and School of Life Sciences, Jilin University, Changchun 130012, People's Republic of China.

出版信息

J Food Prot. 2017 Jan;80(1):50-56. doi: 10.4315/0362-028X.JFP-16-171.

Abstract

Cronobacter sakazakii and Cronobacter malonaticus are the most common species of Cronobacter , so it is necessary to detect the two species as soon as possible in surveillance programs. We developed a real-time PCR method for identifying C. sakazakii and C. malonaticus from the genus Cronobacter . In this study, the two pairs of primers and probes were designed, targeting 16S rRNA and fusA, respectively. The specificity of the real-time PCR assay was validated with 112 strains of Cronobacter , including 56 C. sakazakii , 32 C. malonaticus , 16 Cronobacter dublinensis , 6 Cronobacter turicensis , and 2 Cronobacter muytjensii . The results showed that C. sakazakii and C. malonaticus were all correctly identified, consistent with the results of another method by analyzing the clustering of the fusA sequence. The detection limit for pure culture was 10 CFU/ml and 10 CFU/g for artificially contaminated rehydrated powdered infant formula. Therefore, the developed real-time PCR was a rapid, sensitive, and reliable method for the identification of C. sakazakii and C. malonaticus .

摘要

阪崎克罗诺杆菌和丙二酸克罗诺杆菌是克罗诺杆菌属中最常见的菌种,因此在监测项目中尽快检测出这两种菌种很有必要。我们开发了一种实时荧光定量PCR方法,用于从克罗诺杆菌属中鉴定出阪崎克罗诺杆菌和丙二酸克罗诺杆菌。在本研究中,分别针对16S rRNA和fusA设计了两对引物和探针。利用112株克罗诺杆菌对实时荧光定量PCR检测方法的特异性进行了验证,其中包括56株阪崎克罗诺杆菌、32株丙二酸克罗诺杆菌、16株都柏林克罗诺杆菌、6株苏黎世克罗诺杆菌和2株穆氏克罗诺杆菌。结果表明,阪崎克罗诺杆菌和丙二酸克罗诺杆菌均被正确鉴定,通过分析fusA序列的聚类情况,这与另一种方法的结果一致。纯培养物的检测限为10 CFU/ml,人工污染的复原乳粉的检测限为10 CFU/g。因此,所开发的实时荧光定量PCR是一种快速、灵敏且可靠的阪崎克罗诺杆菌和丙二酸克罗诺杆菌鉴定方法。

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