Screening of specific nucleic acid targets for Cronobacter sakazakii and visual detection by loop-mediated isothermal amplification and lateral flow dipstick method in powdered infant formula

Author:

Fu Shiqian,Qin Xue,Wang Zhenghui,Yang Xinyan,Chen SihanORCID,Yang Tao,Jin Haonan,Man ChaoxinORCID,Jiang YujunORCID

Publisher

American Dairy Science Association

Subject

Genetics,Animal Science and Zoology,Food Science

Reference50 articles.

1. The speciation and genotyping of Cronobacter isolates from hospitalised patients;Alsonosi;Eur. J. Clin. Microbiol. Infect. Dis.,2015

2. Rapid detection and simultaneous genotyping of Cronobacter spp. (formerly Enterobacter sakazakii) in powdered infant formula using real-time PCR and high resolution melting (HRM) analysis;Cai;PLoS One,2013

3. Multiplex PCR assay targeting a diguanylate cyclase-encoding gene, cgcA, to differentiate species within the genus Cronobacter.;Carter;Appl. Environ. Microbiol.,2013

4. Comparison of three chromogenic media and evaluation of two molecular-based identification systems for the detection of Enterobacter sakazakii from environmental samples from infant formulae factories;Derzelle;J. Food Prot.,2007

5. Loop-mediated isothermal amplification of DNA (LAMP): A new diagnostic tool lights the world of diagnosis of animal and human pathogens: A review;Dhama;Pak. J. Biol. Sci.,2014

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