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Escherichia coli O157:H7 adherence to HEp-2 cells is implicated with curli expression and outer membrane integrity
Author(s) -
Sang Hyun Kim,
Yong Hwan Kim
Publication year - 2004
Publication title -
journal of veterinary science
Language(s) - English
Resource type - Journals
eISSN - 1976-555X
pISSN - 1229-845X
DOI - 10.4142/jvs.2004.5.2.119
Subject(s) - escherichia coli , bacterial outer membrane , fimbria , microbiology and biotechnology , biology , bacteria , strain (injury) , biofilm , population , congo red , mutant , enterobacteriaceae , chemistry , gene , biochemistry , genetics , organic chemistry , anatomy , adsorption , demography , sociology
Escherichia coli (E. coli) has ability to express thin aggregative fimbriae, known as curli, on the cell surface. Previously, a few example of curli expression in serogroup O157:H7 of enterohemorrhagic E. coli (EHEC) were reported, compared to other E. coli groups. However, significance of curliation in the EHEC pathobiology has not been described well in the literature. A highly curliated O157:H7 strain was used in this study in order to elucidate role of curliation in EHEC adherence to cultured HEp-2 cells. The expression of curli in the EHEC isolate was consistent with strong positive indication of Congo-red (CR) binding and formation of clumps in the bottom of the tube containing Luria-Bertani (LB) broth when cultured overnight at 37 degrees C. A few CR-binding negative (CR-) colonies occurred spontaneously within the population of CR+ isolate. The CR+ EHEC showed massive aggregative adhesion pattern, whereas the spontaneous CR- strain showed typical localized adherence on HEp-2 cells. Electron microscopy confirmed highly curliated bacteria in the CR+ EHEC sample. Interestingly, the curliation disappeared in a msbB1 and msbB2 double mutant derived from the CR+ EHEC. These results suggest that the compromised outer membrane integrity caused by msbB mutations may abrogate curli production in the CR+ EHEC harbouring penta-acylated lipid A structure in their outer membrane.

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