Cross-species Analysis of Bacterial Gene Networks

  • Funded by National Institutes of Health (NIH)
  • Total publications:0 publications

Grant number: 5R35GM150487-02

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Key facts

  • Disease

    Bacterial infection caused by Klebsiella pneumonia, Other
  • Start & end year

    2023
    2028
  • Known Financial Commitments (USD)

    $382,090
  • Funder

    National Institutes of Health (NIH)
  • Principal Investigator

    ASSISTANT PROFESSOR Jason Peters
  • Research Location

    United States of America
  • Lead Research Institution

    UNIVERSITY OF WISCONSIN-MADISON
  • Research Priority Alignment

    N/A
  • Research Category

    Clinical characterisation and management

  • Research Subcategory

    Disease pathogenesis

  • Special Interest Tags

    N/A

  • Study Type

    Non-Clinical

  • Clinical Trial Details

    N/A

  • Broad Policy Alignment

    Pending

  • Age Group

    Not Applicable

  • Vulnerable Population

    Not applicable

  • Occupations of Interest

    Not applicable

Abstract

PROJECT SUMMARY/ABSTRACT Rationale: Gene networks underpin all aspects of bacterial physiology. These networks mitigate antibiotic induced stress in the context of antibiotic resistance, and drive microbe-microbe and microbe-host interactions in the context of the human microbiome. Despite the central role of gene networks in maintaining viability and organizing stress responses, there have been few studies that systematically compare gene networks across bacterial species. Patterns in chemical-gene, gene-gene, and gene-promoter interactions will provide clues to gene functions, pathways, and regulons, broadening our understanding of how the genetic backgrounds of strains alter network connectivity. Objective: Here we propose a cross-species comparison of genetic and regulatory networks in three enteric species relevant to human health: Escherichia coli, Enterobacter cloacae, and Klebsiella pneumoniae. Comparisons to the well-studied model, E. coli K-12, will drive gene function discovery in E. cloacae and K. pneumoniae, as well as provide a test bed for future cross species comparisons. To facilitate these analyses, we have developed CRISPR-based tools that are easily portable across species and can be used to investigate gene function and regulation at the genome scale. We seek to uncover fundamental mechanisms of homeostasis and stress responses by identifying conserved pathways. Our basic research approach could inform strategies that target weak points in gene networks of bacterial pathogens or could be applied to examine host-modified networks in the context of the human microbiome.