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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
1994-1-6
pubmed:abstractText
Seventeen strains of Escherichia coli serotype O157:H7 producing Shiga-like toxin were examined for the presence of plasmids and for the ability to adhere to HEp-2 and Intestine 407 cells. All of the strains possessed a common 60-MDa plasmid. To determine the role of the 60-MDa plasmid, plasmid-cured strains were compared with the parent strains for their ability to produce pili and to adhere to epithelial cells in culture. The total cell lysate protein and outer-membrane protein (OMP) profiles were also compared. Both the parent strains and their plasmid-cured derivatives produced pili. Immunofluorescence assay results indicated that the plasmid-cured and parent strains adhered equally well to HEp-2 and Intestine 407 cells; overall adherence was greater with intestinal cells than HEp-2 cells. SDS-PAGE of polypeptides synthesised in an E. coli system in vitro showed that plasmid DNA encodes c. 35 proteins. SDS-PAGE of OMP preparations demonstrated that the 60-MDa plasmid appears to be involved in the synthesis of a 33-kDa OMP. Two strains cured of the 60-MDa plasmid, one that possessed no plasmids and one that still contained a 2.2-MDa plasmid, produced exopolysaccharide (EPS) when cultured on solid medium at 25 degrees C. Two other strains, which were cured of the 60-MDa plasmid but contained a 4.5-MDa plasmid, did not produce visible amounts of EPS. Gas chromatography analysis showed that the EPS consisted of fucose, glucose and galactose in an approximate molar ratio of 2.0:0.9:1.1 and also had 7% of a uronic acid sugar as part of its structure.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0022-2615
pubmed:author
pubmed:issnType
Print
pubmed:volume
39
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
371-81
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:7902442-Bacterial Adhesion, pubmed-meshheading:7902442-Bacterial Outer Membrane Proteins, pubmed-meshheading:7902442-Bacterial Proteins, pubmed-meshheading:7902442-Bacterial Toxins, pubmed-meshheading:7902442-Chromatography, Gas, pubmed-meshheading:7902442-Colitis, pubmed-meshheading:7902442-Cytotoxins, pubmed-meshheading:7902442-DNA, Bacterial, pubmed-meshheading:7902442-Escherichia coli, pubmed-meshheading:7902442-Escherichia coli Infections, pubmed-meshheading:7902442-Fimbriae, Bacterial, pubmed-meshheading:7902442-Fluorescent Antibody Technique, pubmed-meshheading:7902442-Food Microbiology, pubmed-meshheading:7902442-Gastrointestinal Hemorrhage, pubmed-meshheading:7902442-Humans, pubmed-meshheading:7902442-Microscopy, Electron, Scanning, pubmed-meshheading:7902442-Plasmids, pubmed-meshheading:7902442-Polysaccharides, Bacterial, pubmed-meshheading:7902442-Shiga Toxin 1, pubmed-meshheading:7902442-Virulence
pubmed:year
1993
pubmed:articleTitle
Studies on Escherichia coli serotype O157:H7 strains containing a 60-MDa plasmid and on 60-MDa plasmid-cured derivatives.
pubmed:affiliation
Microbial Food Safety Research Unit, US Department of Agriculture, Philadelphia, PA 19118.
pubmed:publicationType
Journal Article