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1 Division of Gastroenterology and Nutrition, Research Institute, The Hospital for Sick Children, Toronto, Ontario M5G 1X8; 3 Gastrointestinal Research Group, University of Calgary, Calgary, Alberta T2N 4N1; 4 Newfoundland and Labrador Public Health Laboratory, St. John's, Newfoundland A1B 3T2; and Departments of 5 Pediatrics and 2 Molecular and Medical Genetics, University of Toronto, Toronto, Ontario, Canada M5G 1X8
Adhesion of bacterial enteropathogens to host mucosal surfaces is a critical primary step in the pathogenesis of diarrheal disease. We investigated the effects of altering the physical properties of eukaryotic cells on bacterial adhesion with the use of a series of three structurally dissimilar membrane fluidizers and several Escherichia coli as test strains. Lipid fluidity of the cell plasma membrane was measured by steady-state fluorescence anisotropy employing the probe 1-(4-trimethylammoniumphenyl)-6-phenyl-1,3,5-hexatriene. There was a dose-dependent and reversible inhibition of bacterial adhesion with increasing membrane fluidity. Time course experiments indicated that increasing membrane fluidity during the early stages of bacterial adhesion was essential for inhibition of attachment. None of the fluidizers affected the viability of either eukaryotic or prokaryotic cells. These findings demonstrate, for the first time, that changes in plasma membrane physical properties of epithelial cells can prevent microbial adhesion. This also suggests that altering the membrane properties of host cells could form a basis for novel strategies to prevent bacterial adhesion during infection in vivo.
lipid fluidity; Escherichia coli; O157:H7; O127:H6
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