Host-Pathogen Interactions and M.tb Drug Resistance

Information

  • Research Project
  • 7102431
  • ApplicationId
    7102431
  • Core Project Number
    R01AI066046
  • Full Project Number
    1R01AI066046-01A1
  • Serial Number
    66046
  • FOA Number
  • Sub Project Id
  • Project Start Date
    8/15/2006 - 17 years ago
  • Project End Date
    12/18/2006 - 17 years ago
  • Program Officer Name
    SIZEMORE, CHRISTINE F.
  • Budget Start Date
    8/15/2006 - 17 years ago
  • Budget End Date
    12/18/2006 - 17 years ago
  • Fiscal Year
    2006
  • Support Year
    1
  • Suffix
    A1
  • Award Notice Date
    8/14/2006 - 17 years ago

Host-Pathogen Interactions and M.tb Drug Resistance

[unreadable] DESCRIPTION (provided by applicant): Tuberculosis (TB) remains the leading infectious cause of mortality in the world today. Both treatment and control of this deadly disease are increasingly hampered by the emergence of multidrug resistant (MDR) strains of M. tuberculosis. While poor compliance and/or inadequate TB therapy clearly provides the selection pressure driving the evolution of drug resistant strains, the process is complex, likely involving both host and mycobacterial determinants as well. We hypothesize that interactions between selected mycobacterial properties that interfere with the induction of the host immune response or resist the effects of this response can act to increase bacillary growth and survival and thus the propensity of acquiring drug resistance. The consequence of this occurring over time will be an enrichment of specific strains among the drug resistant cases within communities where TB is endemic. Our overall goal in these studies is to define determinants in M. tuberculosis that can contribute to develop drug resistance in human populations. We propose to 1) Carry out a carefully designed case-control study to characterize the natural distribution of MDR-TB and non-MDR-TB M. tuberculosis strains circulating in a defined human population with high endemic TB; 2) Test the hypothesis that an M. tuberculosis phenol glycolipid (PGL-tb), which induces a host immune response that fails to control bacillary growth efficiently, is therefore associated with an increased resistance in the host; and 3) Examine the interaction between host oxidative stress and DNA repair mechanisms in the acquisition of drug resistance in M. tuberculosis. Because a multidisciplinary approach is required to achieve these objectives, we have assembled a team of collaborators with a range of expertise to enable us to tease apart the many facets of this complex infectious disease problem. [unreadable] [unreadable] Multidrug-resistant tuberculosis (MDR TB) is associated with high morbidity and mortality, prolonged treatment to cure, and increased risk of spread in the community. We will test the hypothesis that some naturally occurring strains of M. tuberculosis are more prone to develop drug resistance than others. Results of these studies can contribute to improved TB control strategies aimed at reducing the emergence of MDR- TB and the development of new therapeutic approaches for combating this deadly disease. [unreadable] [unreadable] [unreadable]

IC Name
NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES
  • Activity
    R01
  • Administering IC
    AI
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    102386
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    855
  • Ed Inst. Type
  • Funding ICs
    NIAID:102386\
  • Funding Mechanism
  • Study Section
    HIBP
  • Study Section Name
    Host Interactions with Bacterial Pathogens Study Section
  • Organization Name
    PUBLIC HEALTH RESEARCH INSTITUTE
  • Organization Department
  • Organization DUNS
  • Organization City
    NEWARK
  • Organization State
    NJ
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    071033535
  • Organization District
    UNITED STATES