Pseudomonas Aeruginosa Strains with Lipopolysaccharide Defects Exhibit Reduced Intracellular Viability After Invasion of Corneal Epithelial Cells
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Pseudomonas aeruginosa is a leading cause of infectious keratitis. Many ocular isolates of this bacterium invade corneal epithelial cells in vitro and in vivo. Antibiotic survival assays have shown that a complete core lipopolysaccharide is required for full epithelial invasion by P. aeruginosa. In this study, we show that P. aeruginosa mutants with defects in their lipopolysaccharide core and O antigen exhibited reduced viability after internalization by corneal epithelial cells. Restoration of lipopolysaccharide core and O antigen expression by complementation with the plasmid pLPS1 restored intracellular survival. P. aeruginosa strains with a complete lipopolysaccharide survived and replicated within the cells. The data suggest that lipopolysaccharide is involved in the intracellular survival and/or replication of P. aeruginosa, indicating an additional mechanism by which this important virulence factor may contribute to the pathogenesis of corneal infection.
An Organ System-Based Synopsis of Virulence.
Morin C, Deziel E, Gauthier J, Levesque R, Lau G Virulence. 2021; 12(1):1469-1507.
PMID: 34180343 PMC: 8237970. DOI: 10.1080/21505594.2021.1926408.
Contact lens-related corneal infection: Intrinsic resistance and its compromise.
Fleiszig S, Kroken A, Nieto V, Grosser M, Wan S, Metruccio M Prog Retin Eye Res. 2019; 76:100804.
PMID: 31756497 PMC: 7237316. DOI: 10.1016/j.preteyeres.2019.100804.
Buyck J, Tulkens P, Van Bambeke F Antimicrob Agents Chemother. 2013; 57(5):2310-8.
PMID: 23478951 PMC: 3632903. DOI: 10.1128/AAC.02609-12.
Angus A, Evans D, Barbieri J, Fleiszig S Infect Immun. 2010; 78(11):4500-10.
PMID: 20732998 PMC: 2976358. DOI: 10.1128/IAI.00417-10.
Jiang S, Liu M, Teng L, Wang W, Hsueh P, Liaw S Antimicrob Agents Chemother. 2010; 54(4):1564-71.
PMID: 20123999 PMC: 2849355. DOI: 10.1128/AAC.01219-09.