Characterization of biofilm formation in shigellosis
- Funded by National Institutes of Health (NIH)
- Total publications:0 publications
Grant number: 1R21AI193486-01A1
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Key facts
Disease
ShigellosisStart & end year
20262028Known Financial Commitments (USD)
$236,538Funder
National Institutes of Health (NIH)Principal Investigator
PROFESSOR HERVE AGAISSEResearch Location
United States of AmericaLead Research Institution
UNIVERSITY OF VIRGINIAResearch Priority Alignment
N/A
Research Category
Pathogen: natural history, transmission and diagnostics
Research Subcategory
Pathogen morphology, shedding & natural history
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
Abstract The intestinal pathogen Shigella flexneri is the causative agent of bacillary dysentery and is responsible for more than 250 million cases of dysentery annually, resulting in more than 200,000 deaths. S. flexneri is an intracellular pathogen that invade epithelial cells in the colon and spread from cell to cell. The dissemination process relies on a bacterial adaptor termed IcsA that recruits key components of the actin cytoskeleton and supports actin-based motility. We have recently discovered that in addition of its intracellular role in dissemination, IcsA also support bile salt-dependent biofilm formation. Here, we propose to characterize the structural determinants that support IcsA-mediated bile salts-dependent biofilm formation (Aim1) and the role of IcsA in extracellular and intracellular colonization in an infant rabbit model of shigellosis (Aim2). The characterization of the dual functions of IcsA will provide novel insights into the mechanisms supporting bacillary dysentery in humans.