Literature DB >> 22564929

Latex agglutination assays for detection of non-O157 Shiga toxin-producing Escherichia coli serogroups O26, O45, O103, O111, O121, and O145.

Marjorie B Medina1, Weilin L Shelver, Pina M Fratamico, Laurie Fortis, Glenn Tillman, Neelam Narang, William C Cray, Emilio Esteban, Andchitrita Debroy.   

Abstract

Latex agglutination assays utilizing polyclonal antibodies were developed for the top six non-O157 Shiga toxin-producing Escherichia coli (STEC) serogroups. Rabbit antisera were affinity purified through protein A/G columns, and the isolated immunoglobulins (IgGs) were covalently immobilized onto polystyrene latex particles. The resulting latex-IgG complex had a protein (IgG) load of 0.20 to 0.28 mg/ml in a 1% latex suspension. Optimum conditions for the agglutination assay consisted of utilizing 20 μm l of latex-IgG reagent containing 2.0 to 2.8 μm g IgG in a 0.5% latex suspension. Agglutination or flocculation was observed almost instantly after mixing the colonies with the latex-IgG, indicating STEC strains. More than 100 target and nontarget strains were tested in more than 3,000 test replicates. All target organisms produced positive results, but three antisera (anti-O26, anti-O103, and anti-O145) cross-reacted with some other STECs. The anti-O103 and anti-O145 latex reagents cross-reacted with O26 strains, and the anti-O26 cross-reacted with O103 strains. The latex-IgG reagents are stable for at least 1 year and are easy to prepare. These agglutination assays can be used for identification of presumptive non-O157 STEC colonies from agar media. The techniques used to prepare the latex reagents also can be utilized for testing other STEC serogroups, other E. coli serotypes, or other pathogens to ensure safe foods to consumers.

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Year:  2012        PMID: 22564929     DOI: 10.4315/0362-028X.JFP-11-430

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


  5 in total

1.  Genomic diversity and virulence profiles of historical Escherichia coli O157 strains isolated from clinical and environmental sources.

Authors:  Lydia V Rump; Narjol Gonzalez-Escalona; Wenting Ju; Fei Wang; Guojie Cao; Sean Meng; Jianghong Meng
Journal:  Appl Environ Microbiol       Date:  2014-11-07       Impact factor: 4.792

2.  Phenotypic and genotypic characterization of biofilm forming capabilities in non-O157 Shiga toxin-producing Escherichia coli strains.

Authors:  Chin-Yi Chen; Christopher S Hofmann; Bryan J Cottrell; Terence P Strobaugh; George C Paoli; Ly-Huong Nguyen; Xianghe Yan; Gaylen A Uhlich
Journal:  PLoS One       Date:  2013-12-27       Impact factor: 3.240

3.  A high-throughput antibody-based microarray typing platform.

Authors:  Andrew Gehring; Charles Barnett; Ted Chu; Chitrita DebRoy; Doris D'Souza; Shannon Eaker; Pina Fratamico; Barbara Gillespie; Narasimha Hegde; Kevin Jones; Jun Lin; Stephen Oliver; George Paoli; Ashan Perera; Joseph Uknalis
Journal:  Sensors (Basel)       Date:  2013-05-03       Impact factor: 3.576

4.  Detection of Shiga toxin-producing Escherichia coli (STEC) O157:H7, O26, O45, O103, O111, O121, and O145, and Salmonella in retail raw ground beef using the DuPont™ BAX® system.

Authors:  Jamie L Wasilenko; Pina M Fratamico; Christopher Sommers; Daniel R DeMarco; Stephen Varkey; Kyle Rhoden; George Tice
Journal:  Front Cell Infect Microbiol       Date:  2014-06-18       Impact factor: 5.293

5.  Comparison of O-Antigen Gene Clusters of All O-Serogroups of Escherichia coli and Proposal for Adopting a New Nomenclature for O-Typing.

Authors:  Chitrita DebRoy; Pina M Fratamico; Xianghe Yan; GianMarco Baranzoni; Yanhong Liu; David S Needleman; Robert Tebbs; Catherine D O'Connell; Adam Allred; Michelle Swimley; Michael Mwangi; Vivek Kapur; Juan A Raygoza Garay; Elisabeth L Roberts; Robab Katani
Journal:  PLoS One       Date:  2016-01-29       Impact factor: 3.240

  5 in total

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