1990 Fiscal Year Final Research Report Summary
Molecular Genetic Analysis and Mechanism of Action of Bacterial Cytolysins
| Project/Area Number |
01304033
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| Research Category |
Grant-in-Aid for Co-operative Research (A)
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| Allocation Type | Single-year Grants |
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| Research Field |
細菌学
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| Research Institution | Okayama University |
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Principal Investigator |
SHINODA Sumio Okayama University, Faculty of Pharmaceutcal Sciences, Professor, 薬学部, 教授 (50029782)
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| Co-Investigator(Kenkyū-buntansha) |
HONDA Takesh Osaka University, Research Insititute for Microbial Diseases, Associate Professo, 微生物病研究所, 助教授 (60029808)
NAKAZAWA Teruko Yamaguchi University, School of Medicine, Professor, 医学部, 教授 (40053053)
MIZUGUCHI Yasuo Univercity of Occupational and Environmental Health, School of Medicine, Profess, 医学部, 教授 (10072919)
SAKURAI Jun Tokushima Bunri University, Faculty of Pharmaceutical Sciences, Professor, 薬学部, 教授 (80029800)
NODA Masatoshi Chiba University, School of Medicne, Professor, 医学部, 教授 (60164703)
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| Project Period (FY) |
1989 – 1990
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| Keywords | Hemolysin / Cytolysin / Erythrocytes / Vibrio parahaemolyticus / ibrio vulnificus / Staphylococcus aureus / Clostridium perfringens / Pseudomonas cepatia |
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| Research Abstract |
This research projiects was organized to accumulate the information of property of various bacterial cytolysisns and to understand their exact role in infection. Shinoda purified Vibrio vulnificus hemolysin (VVH) and studied its property. Sensitivity of erythrocytes to VVH varied with the animal species because of difference of their ability to bind VVH. Some strains produced immunologically different VVH. Katoh and Noda studied the mechanism of cytolytic action of alpha-toxin and leukocidin of Staphylococcus aureus and found that their NAD-ribosylation activity was important to the lytic action. They also showed the exact role of S- and F-fragment of leukocidin. Sakurai found that active center for hemolytic activity and phospholipase of alpha-toxin of Clostridium perfrigens located on different sites of the toxin molecule. Furthermore, he showed change of phospholipid metabolism in action of the toxin on contraction of blood vessel smooth muscle. Honda studied structure and function of V. parahaemolyticus thermostable direct hemolysin (TDH). He isolated a mutant producing a TDH-related molecule which did non show hemolytic actibity and found that glycine residue at 90th was replaced with asparagine in the mutant hemolysin. Mizuguchi isolated a transformant which had gene encoding a hemolysin (delta-VPH) of V. parahaemolyticus. Delta-VPH was not produced by usual cultivation of V. parahaemolyticus. However, challenge of delta-VPH preparation to animal model suggested that the toxin was one of the pathogenic factor of the vibrio. Nakazawa found a new hemolysin of Pseudomonas cepatia The hemolysin was noon-proteinic and showed antimycotic activity. These results presented the important information for general understanding of the mechanism of action of bacterial cytolysins.
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[Publications] Hoashi, K., Ogata, K., Taniguchi, H., Yamashiya, H., Tsuji, K., Mizuguchi, Y. and Ohtomo. N.: "Pathogenesis of Vibrio parahaemolyticus : Intraperitoneal and orgastric challenge experiments in mice." Microbiol. Immunol.,. 34. 355-366 (1990)
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「研究成果報告書概要(欧文)」より
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[Publications] Honda, T., Ni, Y., Hori, S., Takakura, H., Tsunasawa, S., Sakiyma, F. and T. Miwatani.: "A mutant hemolysin with lower biological activity produced by a mutant Vibrio parahaemolyticus." FEMS Microbiol. Lett.,. 61. 95-100 (1989)
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「研究成果報告書概要(欧文)」より
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[Publications] Taniguchi, H., Kubomura, S., Hirano, H., Mizue, K., Ogawa, M. and Mizuguchi, Y.: "Cloning and characterization of a gene encoding a new thermostable hemolysin from Vibrio parahaemolyticus." FEMS Microbiol. Lett.,. 67. 339-346 (1990)
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「研究成果報告書概要(欧文)」より
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[Publications] Yamanaka, H., Shimatani, S., Tanaka, M., Katsu, T., Ono, B. and Shinoda, S.: "Susceptibility of erythrocytes from several animal species to Vibrio vulnificus hemolysin." FEMS Microbiol. Lett.61. 251-256 (1989)
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「研究成果報告書概要(欧文)」より
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