Investigation into the role of bacteria in aging and development

Information

  • Research Project
  • 7306014
  • ApplicationId
    7306014
  • Core Project Number
    R15AG027749
  • Full Project Number
    1R15AG027749-01A1
  • Serial Number
    27749
  • FOA Number
    PA-06-42
  • Sub Project Id
  • Project Start Date
    9/15/2007 - 17 years ago
  • Project End Date
    8/31/2010 - 14 years ago
  • Program Officer Name
    MURTHY, MAHADEV
  • Budget Start Date
    9/15/2007 - 17 years ago
  • Budget End Date
    8/31/2010 - 14 years ago
  • Fiscal Year
    2007
  • Support Year
    1
  • Suffix
    A1
  • Award Notice Date
    9/5/2007 - 17 years ago
Organizations

Investigation into the role of bacteria in aging and development

[unreadable] DESCRIPTION (provided by applicant): In many animals, bacteria modulate nutrition, gut development, immune system maturation, and longevity. In Drosophila melanogaster, bacteria enhance longevity but their effects on vertebrate aging are unknown. The long-term goal of this proposal is to determine the role that bacteria play during the aging process in the well-characterized Drosophila model system. Several lines of evidence suggest that these studies may also provide a basis for the mechanism by which bacteria affect longevity in humans, as well as tools for promoting human longevity. First, as all animals evolved in the presence of bacteria and most are colonized by them, it is likely that conserved methods for detecting and modulating bacterial flora exist across species. In addition, genes involved in the regulation of aging are conserved across diverse phyla and some of these, when mutated, produce both long life, and altered responses to bacteria. Furthermore, genes regulating both the fly immune system and human innate immune system are highly similar suggesting that pathways involved in the sensing and interaction with bacteria are highly conserved. Characterization of DJ817, a novel mutation that extends Drosophila longevity only when bacteria are present, will be performed to specifically address the role of bacteria in aging. Initial experiments will identify the gene involved via excision analysis as well as RNA interference-mediated assays to eliminate the gene function in subsets of tissues in which it is normally expressed in order to determine the spatial-temporal requirement of the gene. Further characterization will include identifying and characterizing the bacteria involved in longevity extension by using metabolic fingerprinting, a substrate utilization assay that measures metabolic capacity based upon the ability of bacteria to utilize a panel of different carbon substrate sources. Beneficial bacteria and their components will be identified and screened in assays based upon the observation that bacteria can increase the rate of development in flies by 50% relative to flies lacking bacteria. [unreadable] [unreadable] [unreadable] [unreadable]

IC Name
NATIONAL INSTITUTE ON AGING
  • Activity
    R15
  • Administering IC
    AG
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    165713
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    866
  • Ed Inst. Type
    SCHOOLS OF ARTS AND SCIENCES
  • Funding ICs
    NIA:165713\
  • Funding Mechanism
  • Study Section
    CMAD
  • Study Section Name
    Cellular Mechanisms in Aging and Development Study Section
  • Organization Name
    LONG ISLAND UNIVERSITY C. W. POST CENTER
  • Organization Department
    BIOLOGY
  • Organization DUNS
  • Organization City
    GREENVALE
  • Organization State
    NY
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    115481326
  • Organization District
    UNITED STATES