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PMID: 65205 Published · ppublish English Comparative Study Journal Article

Response of cultured mammalian cells to the exotoxins of Pseudomonas aeruginosa and Corynebacterium diphtheriae: differential cytotoxicity.

Canadian journal of microbiology ·Vol. 23 ·No. 2 ·1977-02-00 ·Pages 183-9

Middlebrook JL, Dorland RB

Abstract

The sensitivities of 21 mammalian cell lines to the exotoxins of Pseudomonas aeruginosa and Corynebacterium diphtheriae were measured. Each line exhibited 1-4 log differences in sensitivities to the two toxins. No species-specific sensitivities were noted for Pseudomonas exotoxin while diphtheria exotoxin was most potent in cells of monkey origin, followed by human and hamster cells. Rat- and mouse-derived cell lines were very insensitive to diphtheria exotoxin. The rates of cellular intoxication by both toxins exhibited apparent first-order kinetics and were indistinguishable from one another when equipotent doses were used. Our preparation of diphtheria exotoxin appeared to have a slightly higher ADP-ribosylating efficiency than did Pseudomonas toxin. However, neither toxin exhibited cell line-specific differences in ribosylating efficiencies which could have explained the wide range in potencies for intact cells. Our results suggest that there are significant differences in the mechanisms of cellular intoxication by Pseudomonas and diphtheria exotoxins and that these differences probably exist in the attachment or internalization stages of toxin action.

MeSH Terms
Animals Bacterial Toxins/pharmacology Cell Line Cells, Cultured/drug effects Cytotoxicity Tests, Immunologic Diphtheria Toxin/pharmacology Epitopes Humans Mammals Pseudomonas aeruginosa Species Specificity
Chemicals
Bacterial Toxins Diphtheria Toxin Epitopes
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Middlebrook J L
Dorland R B
Article Info
Journal
Canadian journal of microbiology
Abbr.
Can J Microbiol
ISSN
0008-4166
Published
1977-02-00
Pages
183-9
Language
English
Region
Canada
NLM ID
0372707
Subset
IM
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