Expression of attaching effacing activity by enteropathogenic Escherichia coli depends on growth phase, temperature, and protein synthesis upon contact with epithelial cells
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Rosenshine, I
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UNIV BRITISH COLUMBIA, BIOTECHNOL LAB, VANCOUVER, BC V6T 1Z3, CANADAUNIV BRITISH COLUMBIA, BIOTECHNOL LAB, VANCOUVER, BC V6T 1Z3, CANADA
Rosenshine, I
[1
]
Ruschkowski, S
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UNIV BRITISH COLUMBIA, BIOTECHNOL LAB, VANCOUVER, BC V6T 1Z3, CANADAUNIV BRITISH COLUMBIA, BIOTECHNOL LAB, VANCOUVER, BC V6T 1Z3, CANADA
Ruschkowski, S
[1
]
Finlay, BB
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UNIV BRITISH COLUMBIA, BIOTECHNOL LAB, VANCOUVER, BC V6T 1Z3, CANADAUNIV BRITISH COLUMBIA, BIOTECHNOL LAB, VANCOUVER, BC V6T 1Z3, CANADA
Finlay, BB
[1
]
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[1] UNIV BRITISH COLUMBIA, BIOTECHNOL LAB, VANCOUVER, BC V6T 1Z3, CANADA
Enteropathogenic Escherichia coli (EPEC) induces tyrosine phosphorylation of a 90-kDa protein (Hp90) in infected epithelial cells. This in turn facilitates intimate binding of EPEC via the outer membrane protein intimin, effacement of host cell microvilli, cytoskeletal rearrangement, and bacterial uptake. This phenotype has been commonly referred to as attaching/effacing (A/E). The ability of EPEC to induce A/E lesions was de-pendent on bacterial growth phase acid temperature. Early-logarithmic-phase EPEC grown at 37 degrees C elicits strong A/E activity within minutes after infection of HeLa epithelial cells, EPEC de nova protein synthesis du:ring the first minutes of interaction with the host cell was required to elicit A/E lesions, However, once formed, bacterial viability was not needed to maintain A/E lesions, The type of growth media and partial O-2 pressure Level do nut seem to affect the ability of EPEC to cause A/E lesions, The results indicates that the A/E activity of EPEC is tightly regulated by environmental and host factors.
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UNIV FED RIO DE JANEIRO, INST MICROBIOL, MICROSCOPIA ELECTRON LAB, BR-21941 RIO DE JANEIRO, RJ, BRAZILUNIV FED RIO DE JANEIRO, INST MICROBIOL, MICROSCOPIA ELECTRON LAB, BR-21941 RIO DE JANEIRO, RJ, BRAZIL
ANDRADE, JRC
DAVEIGA, VF
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UNIV FED RIO DE JANEIRO, INST MICROBIOL, MICROSCOPIA ELECTRON LAB, BR-21941 RIO DE JANEIRO, RJ, BRAZILUNIV FED RIO DE JANEIRO, INST MICROBIOL, MICROSCOPIA ELECTRON LAB, BR-21941 RIO DE JANEIRO, RJ, BRAZIL
DAVEIGA, VF
ROSA, MRD
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UNIV FED RIO DE JANEIRO, INST MICROBIOL, MICROSCOPIA ELECTRON LAB, BR-21941 RIO DE JANEIRO, RJ, BRAZILUNIV FED RIO DE JANEIRO, INST MICROBIOL, MICROSCOPIA ELECTRON LAB, BR-21941 RIO DE JANEIRO, RJ, BRAZIL
ROSA, MRD
SUASSUNA, I
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UNIV FED RIO DE JANEIRO, INST MICROBIOL, MICROSCOPIA ELECTRON LAB, BR-21941 RIO DE JANEIRO, RJ, BRAZILUNIV FED RIO DE JANEIRO, INST MICROBIOL, MICROSCOPIA ELECTRON LAB, BR-21941 RIO DE JANEIRO, RJ, BRAZIL
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UNIV FED RIO DE JANEIRO, INST MICROBIOL, MICROSCOPIA ELECTRON LAB, BR-21941 RIO DE JANEIRO, RJ, BRAZILUNIV FED RIO DE JANEIRO, INST MICROBIOL, MICROSCOPIA ELECTRON LAB, BR-21941 RIO DE JANEIRO, RJ, BRAZIL
ANDRADE, JRC
DAVEIGA, VF
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UNIV FED RIO DE JANEIRO, INST MICROBIOL, MICROSCOPIA ELECTRON LAB, BR-21941 RIO DE JANEIRO, RJ, BRAZILUNIV FED RIO DE JANEIRO, INST MICROBIOL, MICROSCOPIA ELECTRON LAB, BR-21941 RIO DE JANEIRO, RJ, BRAZIL
DAVEIGA, VF
ROSA, MRD
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UNIV FED RIO DE JANEIRO, INST MICROBIOL, MICROSCOPIA ELECTRON LAB, BR-21941 RIO DE JANEIRO, RJ, BRAZILUNIV FED RIO DE JANEIRO, INST MICROBIOL, MICROSCOPIA ELECTRON LAB, BR-21941 RIO DE JANEIRO, RJ, BRAZIL
ROSA, MRD
SUASSUNA, I
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UNIV FED RIO DE JANEIRO, INST MICROBIOL, MICROSCOPIA ELECTRON LAB, BR-21941 RIO DE JANEIRO, RJ, BRAZILUNIV FED RIO DE JANEIRO, INST MICROBIOL, MICROSCOPIA ELECTRON LAB, BR-21941 RIO DE JANEIRO, RJ, BRAZIL