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, OtherStart & end year
20232028Known Financial Commitments (USD)
$382,090Funder
National Institutes of Health (NIH)Principal Investigator
ASSISTANT PROFESSOR Jason PetersResearch Location
United States of AmericaLead Research Institution
UNIVERSITY OF WISCONSIN-MADISONResearch 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.