• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to project page

1999 Fiscal Year Final Research Report Summary

MOLECULAR MECHANISM OF VIRULENT FACTOR PRODUCTION IN GRAM POSITIVE BACTERIA

Research Project

Project/Area Number 08407010
Research Category

Grant-in-Aid for Scientific Research (A)

Allocation TypeSingle-year Grants
Section一般
Research Field Bacteriology (including Mycology)
Research InstitutionUniversity of Tsukuba

Principal Investigator

HAYASHI Hideo  INSTITUTE OF BASIC MEDICAL SCIENCES, UNIVERSITY OF TSUKUBA, PROFESSOR, 基礎医学系, 教授 (40033203)

Co-Investigator(Kenkyū-buntansha) SHIMIZU Tohru  INSTITUTE OF BASIC MEDICAL SCIENCES, UNIVERSITY OF TSUKUBA, ASSOCIATE PROFESSOR, 基礎医学系, 助教授 (80235655)
OHTA Toshiko  MEDICAL TECHNOLOGY, UNIVERSITY OF TSUKUBA, PROFESSOR, 医療短期大学, 教授 (40233134)
NAKAMURA Shinichi  DEPARTMENT OF MICROBIOLOGY, KANAZAWA UNIVERSITY, PROFESSOR, 医学部, 教授 (90019620)
KURAZONO Hisao  HEALTH SCIENCES, OKAYAMA UNIVERSITY, PROFESSOR, 医学部, 教授 (90186487)
Project Period (FY) 1996 – 1999
KeywordsGram Positive bacteria / Stress response mechanism / Heat shock / Transcription factors / Staphylococcus aureus / Clostridium / Antibiotics / 抗菌剤
Research Abstract

Molecular mechanism of production of toxins and the other virulence factors in Gram positive bacteria has been investigated to develop novel infection control measures for Gram positive bacteria which produce variety of virulence factors to cause desease in human.
1. The production of toxins and enzymes was regulated by the environmental factors.
The production of toxins (α, β, γ, ε, θ, etc, in Clostridium perfringens, toxin A and B in C. difficile, soluble and surface virulent factors in Staphylococcus aureus) was regulated by the growth phase, density/population of bacteria (quoram sensing), carbon source and nutritional substrate, inter-cellular factors (like pheromon). Under the stressful condition for bacteria, ie ; heat, extream pH, in the presence of heavy metals, antibiotics, the bacteria induced the stress responsible genes including virulent genes.
2. Specific receptors for sensing environmental factors.
Each bacterium has a certain specific receptors for environmental factors, i … More .e., the most common one is the sensor component of two-component system. In C. perfringens, several systems have been identified, among which one for activation and the other for inhibition of production of toxin. In S. aureus, the receptors for zinc, alkaline, β-lactams were mostly identified.
3. Information transmitting network in bacteria.
Along with genomic analysis of C. perfringens, and that of Staphylococci, molecular basis of information transmitting system in bacteria has been made clear from receptor to effecter production as an sequential "molecular net work" with global regulatory system. This information is useful for the design of antibiotics in future.
4. Regulation at the level of transcription, translation, post translation and secretion from cell.
On basing upon those results, molecular net work of virulent factor production has been more clearly confirmed and the results will contribute to those who are looking for more specific effective anti-infection drugs and preventive measures. Less

  • Research Products

    (24 results)

All Other

All Publications (24 results)

  • [Publications] Kuroda M.et al.: "Chromosome-determined Zinc Responsible Operon czr in Staphylococcus aureus"Microbiol.Immunol.. 43. 115-125 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Kato H.et al.: "Deletion in the repeating sequences of the toxin-A gene of toxin A-negative, toxin B-positive Ctostridium difficile strains"FEMS Microbiology Lett.. 175. 197-203 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Yamakawa K.et al.: "Inhibition of the enhanced toxin production by Clostridium difficile in biotin-limitedconditions"J.Med.Microbiol.. 47. 767-771 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Kozaki S.et al.: "Characterization of Clostridium botulium type B neurotoxin associated with infant botulism in Japan"Infect.Immun.. 66. 4811-4816 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Aoki Y.et al.: "Characterization of small colony variants of methicillin-resistant Staphylococcus regrown in the presence of Arbekacin"J.Infect Cehmother.. 4. 107-11 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Banu S.et al.: "Identification of novel VirR/VirS-regulated genes in Clostridium perfrihgens"Mol.Microbiol.. 35. 1-12 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Shimizu, T., K. Ohtani, W. Ba-Thein, S. Inui, S. Nakamura, and H. Hayashi: "Characterization of a toxin-deficient Clostridium perfringens strain, KZ1340."Microbiol. Immunol.. 40. 141-145 (1996)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Ba-thein, W., M. Lyristis, K. Ohtani, I. T. Nisbet, H. Hayashi, J. I. Rood and T. Shimizu: "The virR/virS locus regulates the transcription of genes encoding extra cellular toxin production in clostridium perfringens."J. Bacteriol. 178. 2514-2520 (1996)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Ohtani, K., M. Bando, T. Swe, S. Banu, M. Ooe, H. Hayashi, and T. Shimizu: "Collagenase gene (colA) is located in the 3'-flanking of the perfringolysin O (pfoA) locus in Clostridium perfringens."FEMS Microbiol. Lett.. 146. 155-160 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] William Ba-Thein, S. Inui, T. Shimizu, Tint Swe, Sayera Banu, K. Ohtani, M. Oe, N. Sakurai, S. Nakakura, and H. Hayashi: "Genomic Diversity in the pfoA region of theta-toxin-deficient strains of Clostridium perfringens"Microbiol. Immunol.. 41. 629-631 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Banu, Syera, Ohtani, K., Yaguchi, H., Sew, Tint, Cole, S. T., Hayashi, H. and Shimizu, T.: "Identification of novel VirR/VirS-regulated genes in Clostridium perfringens"Mol. Microbiol. 35. 1-12 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Ohatani, K., Takamura, H., Yaguchi, H., Hayashi, H. and Shimizu, T.: "Genetidc analysis of the ycgJ-metB-cycK-ygaG operon negatively regulated by the VirR/VirS system in Clostridium perfringens."Microbiol. Immunol.. (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Ohta T., Nettikadan S., Tokumasu F., Ideno H., Ohta T., Nettikadan S., Tokumasu F., Ideno H., Abe Y., Kuroda M., Hayashi H., and Takeyasu K.: "Atomic Force Microscopy proposes a novel model for stem-loop structure that binds a heat shock protein in the Staphylococcus aureus HSP70 operon."Biochem. Biophys. Res. Commun.. 226. 730-734 (1996)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Aoki, Y., Yamauchi, Y., Hayashi, H., Takayama, Y. and tsuji, A.: "Characterization of samll colony variants of methicillin-resistant Staphylococcus aureus regrown in the presence of Arbekacin."J. Infect Cehmother.. 4. 107-111 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Kuroda, Makoto, Daisuke Kobayashi, Kyoko Honda, Hideo Hayashi and Toshiko Ohta.: "The hsp operon is repressed by the hrc37 of the hsp70 operon in Staphylococcus aureus."Microbiol. Immunol.. 43. 19-27 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Kuroda M., Hayashi H., and Ohta T.: "Chromosome-determined Zinc Responsible Operon czr in Staphylococcus aureus."Microbiology and Immunology. 43(2). 115-125 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Murakami H., Matsumaru H., Kanamori M., Hayashi H., and Ohta T.: "Cell wall-affectingÅ@antibiotics induce expression of a novel gene drp35 in Staphylococcus aureus. Biochem."Biophys. Res. Commun.. 264(2). 348-351 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] H. Kato, N. Kato, S. Katow, T. Maegawa, S. Nakamura and D. M. Lyerly.: "Deletion in the repeating sequences of the toxin A gene of toxin A- negative, toxin B-positive Clostridium difficile_strains"FEMS Microbiology Letters. 175. 197-203 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] D. Ikeda, T. Karasawa, K. Yamakawa, R. Tanaka, M. Namiki and S. Nakamura.: "Effect of isoleucine on toxin production by Clostridium difficile_in a defined medium Zbl."Bakt.. 287. 375-386 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] K. Yamakawa, T. Karasawa, T. Ohta, H. Hayashi and S. Nakamura.: "Inhibition of the enhanced toxin production by Clostridium difficile in biotin-limited conditions"J. Med. Microbiol. 47. 767-771 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] S. Kozai, Y. Kamata, T-I. Nishiki, H. Kakinuma, H. Maruyama, H. Takahashi, T. Karasawa, K. Yamakawa and sS. Nakamura.: "Characterization of Clostridium botulinum type B neurotoxin associated with infant botulism in Japan."Infect. Immun.. 66(10). 4811-4816 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] X. Meng, T. Karasawa, K. Zou, X. Kuang, X. Wang, C. Lu, C. Wang, K. Yamakawa and S. Nakamura: "Characterization of a neurotoxigenic Clostridium butyricum strain isolated from the food implicated in an outbreak of food-borne type E botulism"J. Clin. Microbiol.. 35(8). 2160-2162 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] T. Karasawa, T. Maegawa, T. Nojiri, K. Yamakawa and S. Nakamura: "Effect of Arginine on Toxin Production by Clostridium difficile in Defined Medium Microbiol."Immunol.. 41(8). 581-585 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] S. Kamiya, T. Yamamoto-Osaki, H. Taguchi, H. Yamaguchi, A. Ozawa and S. Nakamura: "Growth kinetics and pathogenicity of Clostridium difficile in continuous flow culture and mouse intestine."(eds) A. R. Eley and K. W. Bennett In Anaerobic pathogens, Sheffield Academic Press, Sheffield, England. 77-83 (1997)

    • Description
      「研究成果報告書概要(欧文)」より

URL: 

Published: 2001-10-23  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi