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Biofilm Formation and Immunomodulatory Activity of Proteus mirabilis Clinically Isolated Strains.

Biofilm Formation and Immunomodulatory Activity of Proteus mirabilis Clinically Isolated Strains.
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Fusco A, Coretti L, Savio V, Buommino E, Lembo F, Donnarumma G,


Fusco A, Coretti L, Savio V, Buommino E, Lembo F, Donnarumma G, (click to view)

Fusco A, Coretti L, Savio V, Buommino E, Lembo F, Donnarumma G,

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International journal of molecular sciences 2017 02 1518(2) pii E414
Abstract

Urinary tract infections (UTIs) and catheter-associated UTIs (CAUTIs) are the principal hospital-acquired infections. Proteus mirabilis is characterized by several virulence factors able to promote adhesion and biofilm formation and ameliorate the colonization of urinary tract and the formation of crystalline biofilms on the abiotic surface of the urinary catheters. Since, to date, the role of P. mirabilis in the etiopathogenesis of different types of urinary tract infections is not well established, in this study we sought to characterize two different clinically isolated strains of P. mirabilis (PM1 and PM2) with distinctive phenotypes and analyzed various virulence factors possibly implicated in the ability to induce UTIs and CAUTIs. In particular, we analyzed motility, biofilm formation both on abiotic and biotic surfaces of PM1 and PM2 and paralleled these parameters with the ability to induce an inflammatory response in an epithelial cell model. Results showed that PM1 displayed major motility and a capacity to form biofilm and was associated with an anti-inflammatory response of host cells. Conversely, PM2 exhibited lack motility and a had slower organization in biofilm but promoted an increase of proinflammatory cytokine expression in infected epithelial cells. Our study provides data useful to start uncovering the pathologic basis of P. mirabilis-associated urinary infections. The evidence of different virulence factors expressed by PM1 and PM2 highlights the possibility to use precise and personalized therapies targeting specific virulence pathways.

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