Purification and characterization of lipopolysaccharides from six strains of non-O157 Shiga toxin-producing Escherichia coli

Journal Article · Thu Jun 18 00:00:00 EDT 2015 · Journal of Microbiological Methods

DOI:https://doi.org/10.1016/j.mimet.2015.06.008· OSTI ID:1492572

Stromberg, Loreen R. ^[1]; Stromberg, Zachary R. ^[2]; Banisadr, Afsheen ^[3]; Graves, Steven W. ^[4]; Moxley, Rodney A. ^[2]; Mukundan, Harshini ^[5]

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1. Los Alamos National Lab. (LANL), Los Alamos, NM (United States); The New Mexico Consortium, Los Alamos, NM (United States); Univ. of New Mexico, Albuquerque, NM (United States)
2. Univ. of Nebraska, Lincoln, NE (United States)
3. Los Alamos National Lab. (LANL), Los Alamos, NM (United States)
4. The New Mexico Consortium, Los Alamos, NM (United States); Univ. of New Mexico, Albuquerque, NM (United States)
5. Los Alamos National Lab. (LANL), Los Alamos, NM (United States); The New Mexico Consortium, Los Alamos, NM (United States)

Certain Shiga toxin-producing Escherichia coli (STEC) are virulent human pathogens that are most often acquired through contaminated food. The United States Department of Agriculture, Food Safety and Inspection Service has declared several serogroups of STEC as adulterants in non-intact raw beef products. Hence, sensitive and specific tests for the detection of these STEC are a necessity for implementation in food safety programs. E. coli serogroups are identified by their respective O-antigen moiety on the lipopolysaccharide (LPS) macromolecule. We propose that the development of O-antigen-specific immunological assays can facilitate simple and rapid discriminatory detection of STEC in beef. However, the resources (antigens and antibodies) required for such development are not readily available. To overcome this, we extracted and characterized LPS and O-antigen from six STEC strains. Using hot phenol extraction, we isolated the LPS component from each strain and purified it using a series of steps to eliminate proteins, nucleic acids, and lipid A antigens. Antigens and crude LPS extracts were characterized using gel electrophoresis, immunoblotting, and modified Western blotting with commercially available antibodies, thus assessing the serogroup specificity and sensitivity of available ligands as well. The results indicate that, while many commercially available antibodies bind LPS, their activities and specificities are highly variable, and often not as specific as those required for serogroup discrimination. This variability could be minimized by the production of antibodies specific for the O-antigen. Additionally, the antigens generated from this study provide a source of characterized LPS and O-antigen standards for six serogroups of STEC.

• Research Organization: Los Alamos National Laboratory (LANL), Los Alamos, NM (United States)
• Sponsoring Organization: USDA; USDOE
• Grant/Contract Number: 89233218CNA000001
• OSTI ID: 1492572
• Report Number(s): LA-UR-15-21477
• Journal Information: Journal of Microbiological Methods, Vol. 116, Issue C; ISSN 0167-7012
• Publisher: Elsevier
• Country of Publication: United States
• Language: English

Related Subjects

59 BASIC BIOLOGICAL SCIENCES
Biological Science
E. coli
LPS
antibody specificity
O-Antigen
serotyping
Shiga Toxin-Producing E. coli
STEC