TARGETING AN ESSENTIAL METHYLASE IN PATHOGENIC BACTERIA

Information

  • Research Project
  • 2642829
  • ApplicationId
    2642829
  • Core Project Number
    R41AI041775
  • Full Project Number
    1R41AI041775-01A1
  • Serial Number
    41775
  • FOA Number
  • Sub Project Id
  • Project Start Date
    8/1/1998 - 25 years ago
  • Project End Date
    2/28/1999 - 25 years ago
  • Program Officer Name
  • Budget Start Date
    8/1/1998 - 25 years ago
  • Budget End Date
    2/28/1999 - 25 years ago
  • Fiscal Year
    1998
  • Support Year
    1
  • Suffix
    A1
  • Award Notice Date
    7/22/1998 - 25 years ago

TARGETING AN ESSENTIAL METHYLASE IN PATHOGENIC BACTERIA

The objective of this research is to discover drugs that prevent infection caused by a variety of clinically and economically important disease causing bacteria. Recent work by Dr. David Low~s group has shown that the expression of fimbraie involved in the pathogenesis of urinary tract infections (UTIs) and diarrheal disease caused by a number of organisms is controlled by a methylation- dependent phase variation mechanism. This methylation-dependent regulatory mechanism is controlled by a number of proteins including deoxyadenosine methylase (Dam). Small perturbations in the levels of Dam abrogate the expression of Pap fimbraie (involved in UTI), and presumably, due to conservation in the regulation mechanism, the other methylation-regulated fimbraie. Dr. Low has developed an assay to measure Dam activity. We propose to modify this assay to utilize a Scintillation Proximity Assay (SPA) format in order to perform high- throughput screening of combinatorial compounds. We propose to screen 10,000 compounds to identify a compound that perturbs Dam activity. These compounds will be investigated for their ability to abrogate fimbraie expression. Compounds that affect Dam levels, and hence abrogate fimbraie expression by these pathogenic bacteria, will potentially cause these organisms to lose their ability to adhere to cells of the gut, ureter, and bladder. These non-adherent cells could then be flushed from these areas by normal clearance mechanisms. PROPOSED COMMERCIAL APPLICATION: Compounds identified by this work would be effective against UTI- causing E.coli. About 35% of the nosocomial infections are UTI~s and 25% of those are caused by E.coli. E.coli is the causative agent of about 75% of the community derived UTI~s and UTI causing E.coli are responsible for about 20% of community-acquired bacteremias. It is likely that an inhibitor of Dam would have broad spectrum activity. Dam is involved in normal bacterial replication and the Dam controlled phase variation mechanism used by uropathogenic E.coli is also used by other fimbrial expression systems associated with clinically and economically important pathogens.

IC Name
NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES
  • Activity
    R41
  • Administering IC
    AI
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    856
  • Ed Inst. Type
  • Funding ICs
  • Funding Mechanism
  • Study Section
    ZRG5
  • Study Section Name
  • Organization Name
    ISIS PHARMACEUTICALS, INC.
  • Organization Department
  • Organization DUNS
  • Organization City
    CARLSBAD
  • Organization State
    CA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    920087208
  • Organization District
    UNITED STATES