Abstract |
We report here on the isolation of isogenic strains of Aeromonas hydrophila AB3 deleted for a segment of the aerolysin gene. All aer mutants obtained lacked the 49-kilodalton aerolysin gene product and were neither hemolytic for blood erythrocytes nor cytotoxic for Chinese hamster ovary tissue culture cells. One such mutant, AB3-5, was used in a mouse toxicity model to evaluate the role of aerolysin in the pathogenesis of A. hydrophila infections. The strain had a 50% lethal dose (LD50) of greater than 10(9) as compared with the parental strain which had an LD50 of 5 X 10(7). Reintegration of the deleted segment into AB3-5 resulted in an LD50 of 6 X 10(7) cells for this revertant. Furthermore, all mice injected with a sublethal dose of the parental strains developed necrotic lesions; this was never obtained with the aerolysin-deficient strain AB3-5. More importantly, specific neutralizing antibody to aerolysin was detected in mice surviving A. hydrophila infection, demonstrating that aerolysin is produced during the course of systemic A. hydrophila infections.
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Authors | T Chakraborty, B Huhle, H Hof, H Bergbauer, W Goebel |
Journal | Infection and immunity
(Infect Immun)
Vol. 55
Issue 9
Pg. 2274-80
(Sep 1987)
ISSN: 0019-9567 [Print] United States |
PMID | 3305370
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antibodies, Bacterial
- Bacterial Toxins
- DNA, Bacterial
- Hemolysin Proteins
- Pore Forming Cytotoxic Proteins
- aerolysin
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Topics |
- Aeromonas
(genetics, pathogenicity)
- Animals
- Antibodies, Bacterial
(analysis)
- Bacterial Toxins
(genetics, immunology)
- Chromosome Deletion
- DNA, Bacterial
(genetics)
- Genes, Bacterial
- Hemolysin Proteins
(genetics, immunology)
- Immunosorbent Techniques
- Lethal Dose 50
- Mice
- Mutation
- Pore Forming Cytotoxic Proteins
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