4.7 Article

Cranberry changes the physicochemical surface properties of E. coli and adhesion with uroepithelial cells

期刊

COLLOIDS AND SURFACES B-BIOINTERFACES
卷 65, 期 1, 页码 35-42

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ELSEVIER SCIENCE BV
DOI: 10.1016/j.colsurfb.2008.02.012

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atomic force microscopy; bacterial adhesion; cranberry; natural products; thermodynamic model; interfacial free energy; urinary tract infection

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Cranberries have been suggested to decrease the attachment of bacteria to uroepithelial cells (UC), thus preventing urinary tract infections, although the mechanisms are not well understood. A thermodynamic approach was used to calculate the Gibbs free energy of adhesion changes (Delta G(adh)) for bacteria-UC interactions, based on measuring contact angles with three probe liquids. Interfacial tensions and Delta G(adh) values were calculated for Escherichia coli HB101pDC1 (P-fimbriated) and HB101 (non-fimbriated) exposed to cranberry juice (0-27 wt.%). HB101 pDC1 can form strong bonds with the Gal-Gal disaccharide receptor on uroepithelial cells, while HB101-UC interactions are only non-specific. For HB101 interacting with UC, Delta G(adh) was always negative, suggesting favorable adhesion, and the values were insensitive to cranberry juice concentration. For the HB101 pDC1-UC system, Delta G(adh) became positive at 27 wt.% cranberry juice, suggesting that adhesion was unfavorable. Acid-base (AB) interactions dominated the interfacial tensions, compared to Lifshitz-van der Waals (M) interactions. Exposure to cranberry juice increased the AB component of the interfacial tension of HB101 pDC1. LW interactions were small and insensitive to cranberry-juice concentration. The number of bacteria attached to UC was quantified in batch adhesion assays and quantitatively correlated with Delta G(adh). Since the thermodynamic approach should not agree with the experimental results when specific interactions are present, such as HB101 pDC-UC ligand-receptor bonds, our results may suggest that cranberry juice disrupts bacterial ligand-UC receptor binding. These results help form the mechanistic explanation of how cranberry products can be used to prevent bacterial attachment to host tissue, and may lead to the development of better therapies based on natural products. (C) 2008 Elsevier B.V. All rights reserved.

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