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Effect of endotoxin on cells and on their response to infection by polioviruses.

Murphy, W. H. (The University of Michigan, Ann Arbor) and C. Wisner. Effect of endotoxin on cells and on their response to infection by polioviruses. J. Bacteriol. 83:649-662. 1962.-The effect of lipopolysaccharide on HeLa-S3, HeLa-Gey, Chang-liver, Maben, and L strain mouse fibroblasts was studied. The liminal dose of endotoxin for the human epithelial cell strains was approximately 250 mug/ml, and their order of sensitivity to endotoxin was: Chang-liver, HeLa-Gey, HeLa-S3, and Maben, the latter being the most resistant. Endotoxin at concentrations exceeding 100 mug/ml was cytotoxic to the L strain of mouse fibroblasts and caused them to markedly agglutinate. Cytotoxic response of cells to endotoxin was not characterized by cell lysis, but by distinctive nuclear changes. In an attempt to demonstrate the metabolic induction of the latent infection of cell cultures by a noncytopathic variant of poliovirus, endotoxin was added at maximal subliminal concentration to cell cultures totally, partially, or fully susceptible to virus. Endotoxin caused a slight but consistent accelerative cytopathic response of cells to infection by cytopathic poliovirus, but failed to induce cytopathic response to infection by submoderate (noncytopathic) poliovirus. Although endotoxin slightly suppressed yields of poliovirus from cells, it did not affect the plating efficiency of virus on cell monolayers.

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PREPARATION AND ASSAY OF THE INTERNATIONAL STANDARDS FOR CLOSTRIDIUM BOTULINUM TYPES A, B, C, D AND E ANTITOXINS.

The National Institute for Medical Research, London, was authorized in 1962 by the WHO Expert Committee on Biological Standardization to establish the International Standards for Clostridium botulinum Types A, B, C, D and E Antitoxins and to define the International Units. For this purpose use was made of the material accepted in 1954 as the British reference preparations and reconstituted in 1960 for establishment as the first British standards.The author describes the methods of preparation of this material and results of examinations, including estimates of the quality of the antitoxins (assessed as an "efficiency ratio") and of the specificity of the sera.The International Unit is defined as the specific activity contained in a known weight of dried antitoxin of each Cl. botulinum type: for Type A, 0.1360 mg; for Type B, 0.1740 mg; for Type C, 0.0800 mg; for Type D, 0.0121 mg; and for Type E, 0.0691 mg.

Animals↗