Stress sensing and processing by bacterial cytoplasmic megacomplexes

Information

  • Research Project
  • 10250481
  • ApplicationId
    10250481
  • Core Project Number
    R35GM138018
  • Full Project Number
    5R35GM138018-02
  • Serial Number
    138018
  • FOA Number
    PAR-17-190
  • Sub Project Id
  • Project Start Date
    9/15/2020 - 5 years ago
  • Project End Date
    8/31/2025 - 5 months ago
  • Program Officer Name
    GAILLARD, SHAWN R
  • Budget Start Date
    9/1/2021 - 4 years ago
  • Budget End Date
    8/31/2022 - 3 years ago
  • Fiscal Year
    2021
  • Support Year
    02
  • Suffix
  • Award Notice Date
    9/1/2021 - 4 years ago

Stress sensing and processing by bacterial cytoplasmic megacomplexes

PROJECT SUMMARY Bacteria can grow and divide in a remarkably wide range of quickly changing environments, adapting to harsh conditions by sensing external stressors and applying that information to mount an appropriate response. Stress- sensing processes are relevant to human health: pathogenic bacteria with activated stress responses are less susceptible to many antimicrobial treatments, and nearly 100,000 Americans die each year from infections with drug-resistant bacteria. Indeed, environmental antibiotics are one stressor (among many) to which bacterial cells readily respond. A persistent challenge has been that, although the molecular components of the environmental stress response system are well known, little has been discovered about the dynamics of these stress responses over time, particularly in individual cells. The PI has combined bacterial genetics with microfluidic technology to directly observe the responses of single-cell lineages under tightly controlled environmental stress conditions, revealing that the stress-response system is capable of eliciting several distinct responses with different dynamics that depend on which stress sensors are present in the cell. These results raise additional fundamental questions. How do stress-sensing proteins located in the cytoplasm effectively respond to the onset of stressors that are outside the cell? Which molecular features of stress-response proteins specify the stressors they respond to and the dynamic response patterns they instigate? How do different dynamic stress-response patterns contribute to cellular fitness and survival in adverse conditions? The proposed studies tackle these questions by taking advantage of the bacterium Bacillus subtilis as a highly tractable model for environmental stress. By bringing together classical bacterial genetics, molecular techniques, fluorescence microscopy, and microfluidic technology, these studies will yield a new and more mechanistic understanding of the principles that govern how bacterial cells sense environmental stress, process those sensory inputs, and produce an effective response. The results will have broad implications for understanding the general features of stress responses across many biological systems. They will also furnish knowledge that will be useful for devising antimicrobial treatment strategies that interfere with environmental stress sensing.

IC Name
NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
  • Activity
    R35
  • Administering IC
    GM
  • Application Type
    5
  • Direct Cost Amount
    233879
  • Indirect Cost Amount
    110256
  • Total Cost
    344135
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    859
  • Ed Inst. Type
    SCHOOLS OF ARTS AND SCIENCES
  • Funding ICs
    NIGMS:344135\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    OKLAHOMA STATE UNIVERSITY STILLWATER
  • Organization Department
    MICROBIOLOGY/IMMUN/VIROLOGY
  • Organization DUNS
    049987720
  • Organization City
    STILLWATER
  • Organization State
    OK
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    740781016
  • Organization District
    UNITED STATES