Beneficial ureolytic microbes and urea nitrogen salvage: examinations in an extreme animal model

Information

  • Research Project
  • 9171910
  • ApplicationId
    9171910
  • Core Project Number
    R15DK110784
  • Full Project Number
    1R15DK110784-01
  • Serial Number
    110784
  • FOA Number
    PA-13-313
  • Sub Project Id
  • Project Start Date
    9/21/2016 - 7 years ago
  • Project End Date
    8/31/2018 - 5 years ago
  • Program Officer Name
    MARUVADA, PADMA
  • Budget Start Date
    9/21/2016 - 7 years ago
  • Budget End Date
    8/31/2018 - 5 years ago
  • Fiscal Year
    2016
  • Support Year
    01
  • Suffix
  • Award Notice Date
    9/20/2016 - 7 years ago

Beneficial ureolytic microbes and urea nitrogen salvage: examinations in an extreme animal model

Urea-nitrogen salvage occurs when urea, generated in the liver and passed to the bloodstream, diffuses into the gut where it is hydrolyzed by ureolytic microbes into NH3 and CO2. Microbially-liberated urea-N can then be utilized in biosynthesis by gut microbes as well as the host. Although long-understood to be important in ruminants, UNS in non-ruminants is not well described; however, it has recently been implicated in protein conservation in monogastric mammals, including humans, especially under conditions of dietary nitrogen deficiency or increased host nitrogen demand. While these studies suggest an important role for ureolytic microbes and UNS in human health, little is known about the degree to which UNS contributes to host biosynthetic processes, or about beneficial ureolytic microbes in the gut. Therefore, the goal of this study is to exploit the extreme phenotype of the arctic ground squirrel to discover interrelationships between host physiology and the gut microbial community important for host nitrogen metabolism. The hypotheses for this investigation are that 1) reliance upon UNS to meet nitrogen needs varies with dietary nitrogen content and host nitrogen demand and across the annual cycle of hibernation and activity, and that 2) the gut microbial community contains active ureolytic microbes that contribute significantly to host nitrogen homeostasis via UNS. The proposed experimental approach 1) utilizes injections of 13C/15N labeled urea to assess ureolytic activity and UNS in vivo via measurements of 13CO2 in breath (evidence of ureolysis in the gut) and 15N in tissues (evidence of use of microbially-liberated urea-N in host biosynthetic processes), 2) links phylogenic and functional diversity of the gut microbiota using next generation sequencing techniques (metagenomics and metatranscriptomics) and 3) specifically examines the abundance and activity of ureolytic bacteria in the gut using qPCR and qRT-PCR of microbial urease genes, respectively. Through comparison of relative changes in ?15N of tissues of hibernating arctic ground squirrels injected with labeled or unlabeled urea, studies in Specific Aim 1 will demonstrate the degree to which microbially-liberated urea-N is incorporated into host tissues under a long term fast. In Specific Aim 2, manipulation of dietary protein content will be used to determine the degree to which euthermic animals rely upon UNS for protein conservation under conditions of protein insufficiency. Similar diet manipulations in gestating and lactating squirrels will be conducted to evaluate the influence of dietary protein content and high nitrogen demand on the incorporation of microbially-liberated urea-N in mothers and pups in Specific Aim 3. Our experiments promise to yield an increased knowledge about interrelationships between the gut microbial community and host nitrogen homeostasis, ultimately contributing to our understanding of the relationship between the gut microbial community and human health, in particular under states of compromised nutrition (starvation, low dietary protein) and elevated N demand (gestation and lactation).

IC Name
NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES
  • Activity
    R15
  • Administering IC
    DK
  • Application Type
    1
  • Direct Cost Amount
    315507
  • Indirect Cost Amount
    138898
  • Total Cost
    454405
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    847
  • Ed Inst. Type
    SCHOOLS OF ARTS AND SCIENCES
  • Funding ICs
    NIDDK:454405\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    MCE
  • Study Section Name
    Molecular and Cellular Endocrinology Study Section
  • Organization Name
    UNIVERSITY OF ALASKA ANCHORAGE
  • Organization Department
    BIOLOGY
  • Organization DUNS
    076664986
  • Organization City
    ANCHORAGE
  • Organization State
    AK
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    995084614
  • Organization District
    UNITED STATES