Abstract
The mechanism by which smooth lipopolysaccharide (LPS) protects Salmonella typhimurium C5 from the lethal action of specific antibody and complement has been investigated. Tris(hydroxymethyl)aminomethane (Tris) and ethylenediaminetetraacetate (EDTA), which sensitize S. typhimurium C5 to the bactericidal action of immune serum, were shown to cause appreciable structural modification of the smooth LPS associated with these cells. Mg(2+) was shown to reverse the sensitization of C5 by Tris, but this divalent cation was unable to reverse the sensitizing effect of Tris plus EDTA, which, unlike Tris, caused relatively large amounts of O-antigenic components to be released from the C5 cell wall. The possibility that smooth LPS blocks the interaction of activated complement components with receptors on the cell wall is discussed.
MeSH Terms
Animals
Antibodies, Bacterial
Blood Bactericidal Activity
Cell Wall/immunology
Complement System Proteins
Edetic Acid/pharmacology
Erythrocytes/immunology
Glycopeptides/metabolism
Hemagglutination Inhibition Tests
Hemagglutination Tests
Lipopolysaccharides/analysis,isolation & purification,metabolism
Magnesium/pharmacology
Microscopy, Electron
Polysaccharides, Bacterial
Salmonella typhimurium/analysis,drug effects,immunology,metabolism
Sheep/immunology
Structure-Activity Relationship
Tritium
Viscosity
Chemicals
Antibodies, Bacterial
Glycopeptides
Lipopolysaccharides
Polysaccharides, Bacterial
Tritium
Complement System Proteins
Edetic Acid
Magnesium
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Reynolds B L
Pruul H
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