Abstract

Biofilms formed by Proteus mirabilis strains are a serious medical problem, especially in the case of urinary tract infections. Early stages of biofilm formation, such as reversible and irreversible adhesion, are essential for bacteria to form biofilm and avoid eradication by antibiotic therapy. Adhesion to solid surfaces is a complex process where numerous factors play a role, where hydrophobic and electrostatic interactions with solid surface seem to be substantial. Cell surface hydrophobicity and electrokinetic potential of bacterial cells depend on their surface composition and structure, where lipopolysaccharide, in Gram-negative bacteria, is prevailing. Our studies focused on clinical and laboratory P. mirabilis strains, where laboratory strains have determined LPS structures. Adherence and biofilm formation tests revealed significant differences between strains adhered in early stages of biofilm formation. Amounts of formed biofilm were expressed by the absorption of crystal violet. Higher biofilm amounts were formed by the strains with more negative values of zeta potential. In contrast, high cell surface hydrophobicity correlated with low biofilm amount.

Highlights

  • Proteus mirabilis is one of the causes of catheter-associated urinary tract infections (CAUTIs)

  • Cell surface hydrophobicity (CSH) is expressed as a percent of the cells excluded from the water phase (Fig. 1)

  • Tested strains differ in CSH value, but all strains were determined as hydrophilic, according to (Jones et al 1996)

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Summary

Introduction

Proteus mirabilis is one of the causes of catheter-associated urinary tract infections (CAUTIs). The first step, change of planktonic swimming cells to settled, adhered to solid surface, is crucial for biofilm formation. Unique environmental conditions in the biofilm matrix provide protection against antimicrobial agents and prevent eradication. The mechanism of this protection activity could be based on the properties of EPS, which hinder antibiotics diffusion, and changes in microorganisms’ metabolism and phenotype are observed (Stewart 2002; Czerwonka et al 2014). Microbial adhesion to solid surface plays a key role in biofilm formation. This process is mediated by bacterial cell wall surface structures like: lipopolysaccharide, pili, autotransporter adhesin, and other unique proteins (Hori and Matsumoto 2010). Cell surface hydrophobicity (CSH) participation in adhesion can be explained by the classical

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