Literature DB >> 22564930

Development of a method for the detection of verotoxin-producing Escherichia coli in food.

Alexander Gill1, Amalia Martinez-Perez, Sarah McIlwham, Burton Blais.   

Abstract

The growing recognition of the role of non-O157 verotoxigenic Escherichia coli (VTEC) in foodborne illness underscores the importance of developing methods to detect it in the food supply. We describe here the development of a protocol for the detection, isolation, and characterization of VTEC from foods, designed for the serotype-independent enrichment, detection, and isolation of VTEC, in combination with rapid characterization of VTEC O157, O26, O103, O111, and O145. This study examined the inhibitory concentration of six antimicrobial agents used either singly or in combination for the optimal enrichment of a panel of 18 different O serogroups of VTEC in modified tryptic soy broth. Considerable variability in resistance to the different antimicrobials tested was noted among different VTEC strains. The combination enabling growth of strains of all 18 different O serogroups was vancomycin (10 μg/ml) and cefsulodin (3 μg/ml). A similar combination of antimicrobials formulated in agar plates was found beneficial in the recovery of VTEC strains from enrichment broth cultures. The efficacy of these media in the recovery of selected VTEC (O26, O103, O111, O145, and O157) from ground beef and O157 VTEC from lettuce, spinach, and apple cider was demonstrated. The selective enrichment media described herein would appear suitable for incorporation in methods for the recovery and detection of a wide range of VTEC serogroups.

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Year:  2012        PMID: 22564930     DOI: 10.4315/0362-028X.JFP-11-395

Source DB:  PubMed          Journal:  J Food Prot        ISSN: 0362-028X            Impact factor:   2.077


  5 in total

1.  Evaluation of a loop-mediated isothermal amplification suite for the rapid, reliable, and robust detection of Shiga toxin-producing Escherichia coli in produce.

Authors:  Fei Wang; Qianru Yang; Yinzhi Qu; Jianghong Meng; Beilei Ge
Journal:  Appl Environ Microbiol       Date:  2014-02-07       Impact factor: 4.792

2.  Use of clustered regularly interspaced short palindromic repeat sequence polymorphisms for specific detection of enterohemorrhagic Escherichia coli strains of serotypes O26:H11, O45:H2, O103:H2, O111:H8, O121:H19, O145:H28, and O157:H7 by real-time PCR.

Authors:  Sabine Delannoy; Lothar Beutin; Patrick Fach
Journal:  J Clin Microbiol       Date:  2012-10-03       Impact factor: 5.948

3.  Nationwide investigation of Shiga toxin-producing Escherichia coli among cattle in Japan revealed the risk factors and potentially virulent subgroups.

Authors:  K Lee; M Kusumoto; T Iwata; S Iyoda; M Akiba
Journal:  Epidemiol Infect       Date:  2017-03-06       Impact factor: 4.434

4.  GeneSippr: a rapid whole-genome approach for the identification and characterization of foodborne pathogens such as priority Shiga toxigenic Escherichia coli.

Authors:  Dominic Lambert; Catherine D Carrillo; Adam G Koziol; Paul Manninger; Burton W Blais
Journal:  PLoS One       Date:  2015-04-10       Impact factor: 3.240

5.  Multiplexed Single Intact Cell Droplet Digital PCR (MuSIC ddPCR) Method for Specific Detection of Enterohemorrhagic E. coli (EHEC) in Food Enrichment Cultures.

Authors:  Tanis C McMahon; Burton W Blais; Alex Wong; Catherine D Carrillo
Journal:  Front Microbiol       Date:  2017-03-02       Impact factor: 5.640

  5 in total

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