Microbial pathogens have evolved many ingenious ways to infect their hosts
and cause disease, including the subversion and exploitation of target host
cells. One such subversive microbe is enteropathogenic Escherichia coil (E
PEC), A major cause of infantile diarrhea in developing countries, EPEC pos
es a significant health threat to children worldwide, Central to EPEC-media
ted disease is its colonization of the intestinal epithelium. After initial
adherence, EPEC causes the localized effacement of microvilli and intimate
ly attaches to the host cell surface, forming characteristic attaching and
effacing (A/E) lesions. Considered the prototype for a family of A/E lesion
-causing bacteria, recent in vitro studies of EPEC have revolutionized our
understanding of how these pathogens infect their hosts and cause disease,
Intimate attachment requires the type Ill-mediated secretion of bacterial p
roteins, several of which are translocated directly into the infected cell,
including the bacteria's own receptor (Tir). Binding to this membrane-boun
d, pathogen-derived protein permits EPEC to intimately attach to mammalian
cells, The translocated EPEC proteins also activate signaling pathways with
in the underlying cell, causing the reorganization of the host actin cytosk
eleton and the formation of pedestal-like structures beneath the adherent b
acteria, This review explores what is known about EPEC's subversion of mamm
alian cell functions and how this knowledge has provided novel insights int
o bacterial pathogenesis and microbe-host interactions, Future studies of A
/E pathogens in animal models should provide further insights into how EPEC
exploits not only epithelial cells but other host cells, including those o
f the immune system, to cause diarrheal disease.