학술논문

Increased adherence and actin pedestal formation by dam-deficient enterohaemorrhagic Escherichia coli O157:H7.
Document Type
Article
Source
Molecular Microbiology. Mar2007, Vol. 63 Issue 5, p1468-1481. 14p. 5 Diagrams, 1 Chart, 4 Graphs.
Subject
*ESCHERICHIA coli
*PATHOGENIC microorganisms
*EPITHELIAL cells
*CELL membranes
*GENES
*GENETIC mutation
Language
ISSN
0950-382X
Abstract
Enterohaemorrhagic Escherichia coli (EHEC) are highly infectious pathogens capable of causing severe diarrhoeal illnesses. As a critical step during their colonization, EHEC adhere intimately to intestinal epithelial cells and generate F-actin ‘pedestal’ structures that elevate them above surrounding cell surfaces. Intimate adhesion and pedestal formation result from delivery of the EHEC type III secretion system (TTSS) effector proteins Tir and EspFU into the host cell and expression of the bacterial outer membrane adhesin, intimin. To investigate a role for DNA methylation during the regulation of adhesion and pedestal formation in EHEC, we deleted the dam ( NA denine ethyltransferase) gene from EHEC O157:H7 and demonstrate that this mutation results in increased interactions with cultured host cells. EHECΔ dam exhibits dramatically elevated levels of adherence and pedestal formation when compared with wild-type EHEC, and expresses significantly higher protein levels of intimin, Tir and EspFU. Analyses of GFP fusions, Northern blotting, reverse transcription polymerase chain reaction, and microarray experiments indicate that the abundance of Tir in the dam mutant is not due to increased transcription levels, raising the possibility that Dam methylation can indirectly control protein expression by a post-transcriptional mechanism. In contrast to other dam-deficient pathogens, EHECΔ dam is capable of robust intestinal colonization of experimentally infected animals. [ABSTRACT FROM AUTHOR]