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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
1989-4-27
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pubmed:abstractText |
A cytotoxin to Vero cells (Shiga-like toxin), which was neutralized by antibody against purified Shiga toxin produced by Shigella dysenteriae 1, was purified from Escherichia coli O157:H7, isolated from a patient with hemorrhagic colitis. The purification procedure consisted of ammonium sulfate fractionation, DEAE-cellulose column chromatography, chromatofocusing column chromatography and high performance liquid chromatography. About 200 micrograms of purified Shiga-like toxin was obtained from cell extracts of 14 liters of culture with a yield of about 15%. The purified Shiga-like toxin showed identical physicochemical, biological and immunological properties to those of Shiga toxin. Purified Shiga-like toxin and Shiga toxin also had the same mobilities on polyacrylamide disc gel electrophoresis and polyacrylamide gel isoelectrofocusing. On sodium dodecyl sulfate-polyacrylamide slab gel electrophoresis, purified Shiga-like toxin migrated as two bands corresponding to the A and B subunits, and these migrated to the same positions as A and B subunits of Shiga toxin. The amino acid composition of the purified Shiga-like toxin was also similar to that of Shiga toxin. The purified Shiga-like toxin showed various biological activities: lethal toxicity to mice when injected intraperitoneally, the LD50 being 30 ng per mouse; cytotoxicity to Vero cells, killing about 50% of the cells at 6 pg; and fluid accumulation in rabbit ileal loops at concentrations of more than 1.25 micrograms/loop. These values are comparable with those obtained with Shiga toxin. In an Ouchterlony double gel diffusion test, the lines formed by the purified Shiga-like toxin and Shiga toxin fused, indicating that the two toxins were immunologically identical.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0882-4010
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
2
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
339-49
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:3148810-Amino Acids,
pubmed-meshheading:3148810-Animals,
pubmed-meshheading:3148810-Bacterial Toxins,
pubmed-meshheading:3148810-Cell Survival,
pubmed-meshheading:3148810-Chromatography, DEAE-Cellulose,
pubmed-meshheading:3148810-Chromatography, High Pressure Liquid,
pubmed-meshheading:3148810-Colitis, Ulcerative,
pubmed-meshheading:3148810-Escherichia coli,
pubmed-meshheading:3148810-Humans,
pubmed-meshheading:3148810-Immunodiffusion,
pubmed-meshheading:3148810-Isoelectric Focusing,
pubmed-meshheading:3148810-Mice,
pubmed-meshheading:3148810-Mice, Inbred Strains,
pubmed-meshheading:3148810-Shiga Toxin 1,
pubmed-meshheading:3148810-Shiga Toxins,
pubmed-meshheading:3148810-Shigella dysenteriae,
pubmed-meshheading:3148810-Vero Cells
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pubmed:year |
1987
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pubmed:articleTitle |
Purification and some properties of Shiga-like toxin from Escherichia coli O157:H7 that is immunologically identical to Shiga toxin.
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pubmed:affiliation |
Department of Bacterial Infection, Institute of Medical Science, University of Tokyo, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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