| Summary: | <p>Abstract</p> <p>Background</p> <p><it>Pseudomonas fluorescens </it>has long been considered as a psychrotrophic microorganism. Recently, we have shown that clinical strains of <it>P. fluorescens </it>(biovar 1) are able to adapt at a growth temperature of 37°C or above and induce a specific inflammatory response. Interestingly, a highly specific antigen of <it>P. fluorescens</it>, I2, is detected in the serum of patients with Crohn's disease but the possible role of this bacterium in the disease has not yet been explored. In the present study, we examined the ability of a psychrotrophic and a clinical strain of <it>P. fluorescens </it>to modulate the permeability of a Caco-2/TC7 intestinal epithelial model, reorganize the actin cytoskeleton, invade the target cells and translocate across the epithelium. The behaviour of these two strains was compared to that of the well known opportunistic pathogen <it>P. aeruginosa </it>PAO1.</p> <p>Results</p> <p>Both strains of <it>P. fluorescens </it>were found to decrease the transepithelial resistance (TER) of Caco-2/TC7 differentiated monolayers. This was associated with an increase in paracellular permeability and F-actin microfilaments rearrangements. Moreover, the invasion and translocation tests demonstrated that the two strains used in this study can invade and translocate across the differentiated Caco-2/TC7 cell monolayers.</p> <p>Conclusions</p> <p>The present work shows for the first time, that <it>P. fluorescens </it>is able to alter the intestinal epithelial barrier function by disorganizing the F-actin microfilament network. Moreover, we reveal that independently of their origins, the two <it>P. fluorescens </it>strains can translocate across differentiated Caco-2/TC7 cell monolayers by using the transcellular pathway. These findings could, at least in part, explain the presence of the <it>P. fluorescens </it>specific I2 antigen in the serum of patients with Crohn's disease.</p>
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