Interferon-inducible cell-autonomous immunity to cytosolic bacterial pathogens

NIH RePORTER · NIH · R01 · $540,532 · view on reporter.nih.gov ↗

Abstract

Human cells including epithelial cells are equipped with cell-autonomous host defense programs providing protection against intracellular pathogens. These host protective programs are controlled in a temporal and spatial manner and respond to extracellular cues including pro-inflammatory cytokines released by professional immune cells. Arguably, the most potent inducer of antibacterial cell-autonomous host defense is lymphocyte- derived interferon-gamma (IFN). IFN-receptor signaling in human epithelial cells induces the expression of hundreds of IFN-stimulated genes (ISGs) encoding antimicrobial proteins. While a few ISGs have been studied in much detail, our understanding of most ISGs and their functions in host defense is limited. We recently discovered a critical role for IFN-inducible guanylate binding proteins (GBPs) in cell-autonomous immunity to Gram-negative bacterial pathogens invading the host cell cytosol. Human GBP1 is a cytosolically localized member this GBP family and able to directly detect a central building block of the Gram-negative bacterial outer membrane, i.e. lipopolysaccharide (LPS). Our previous work showed that GBP1, through these LPS interactions, forms a multimeric microcapsule or coatomer surrounding Gram-negatives invading the host cell cytosol. However, GBP1 binding to the bacterial surface on its own is neither bactericidal nor bacteriostatic, implicating other GBP1-dependent co-factors required for sterilizing cell-autonomous immunity. Aim1 of our proposal will explore a novel GBP1-dependent pathway that results in bacterial ubiquitylation, a well-established ‘eat-me’ signal that marks cytosolic microbial invaders for destruction. Our studies are multidisciplinary and include biochemical approaches levering a novel in vitro GBP1-bacteria binding assay that we established. Using this assay, we will directly assess how GBP1 promotes the recruitment of IFN-inducible host ubiquitin E3 ligases to the surface of the Gram-negative cytosol-invading bacterial pathogen Shigella flexneri. S. flexneri is a human- adapted enteric pathogen that causes dysentery and diarrheal deaths, especially in children in low- and middle- income countries. Our preliminary data demonstrate that wildtype S. flexneri is resistant to GBP1-dependent and -independent host-driven bacterial ubiquitylation. Therefore, in our second aim we will identify and characterize a network of virulence factors used by S. flexneri to escape IFN-induced ubiquitylation and associated host defenses. To define the physiological relevance of these antagonistic relationships between antibacterial ISGs and counter-acting bacterial virulence mechanisms employed by S. flexneri, we will exploit a novel mouse model of intestinal S. flexneri infections. Using ISG-deficient mouse lines established in our lab and, reciprocally, infecting with S. flexneri mutants defective for virulence effectors targeting the same ISGs, we will determine the physiological importance of G...

Key facts

NIH application ID
10871750
Project number
2R01AI139425-05A1
Recipient
DUKE UNIVERSITY
Principal Investigator
Joern Coers
Activity code
R01
Funding institute
NIH
Fiscal year
2024
Award amount
$540,532
Award type
2
Project period
2019-09-01 → 2028-11-30