Distinct binding properties of eaeA-negative verocytotoxin-producing Escherichia coli of serotype O113:H21

Infection of humans with verotoxin-producing Escherichia coli (VTEC) O113:H21 is associated with clinical features comparable to those associated with infection with attaching and effacing VTEC strains including those of serotype O157:H7. We have shown previously that the adhesion phenotype of VTEC O157:H7 is influenced by the presence of a homolog of the chromosomal eaeA (for E. coli attaching and effacing) gene. In contrast, by colony blot hybridization, VTEC O113:H21 is negative for the eaeA gene. Therefore, the aim of this study was to define the adhesion phenotype of VTEC O113:H21 strain CL-15 to both cultured epithelial cells (HEp-2) and rabbit intestine in vivo. Under transmission electron microscopy, areas of microvillus effacement were observed in regions directly beneath the organism in CL-15-infected cells both in vitro and in vivo. However, F-actin adhesion pedestals on the host plasma membrane were absent. Failure of CL-15 to induce polymerization of actin was confirmed by using staining of F-actin with fluorescein-labeled phalloidin. Under indirect immunofluorescence microscopy, CL-15-infected HEp-2 cells also failed to demonstrate the recruitment of another cytoskeletal element, alpha-actinin, below foci of bacterial adhesion. In contrast, VTEC O157:H7 infection of HEp-2 cells was associated with increased alpha-actinin immunofluorescence. These findings suggest that bacterial factors distinct from those of EaeA are necessary for the adhesion phenotype of VTEC O113:H21.

[1]  A. Borczyk,et al.  Sequence heterogeneity of the eae gene and detection of verotoxin-producing Escherichia coli using serotype-specific primers , 1994, Epidemiology and Infection.

[2]  P. Sherman,et al.  Signal transduction in human epithelial cells infected with attaching and effacing Escherichia coli in vitro. , 1994, Gastroenterology.

[3]  M. McKee,et al.  The role of the eae gene of enterohemorrhagic Escherichia coli in intimate attachment in vitro and in a porcine model. , 1993, The Journal of clinical investigation.

[4]  M. Levine,et al.  Role of the eaeA gene in experimental enteropathogenic Escherichia coli infection. , 1993, The Journal of clinical investigation.

[5]  P. Sherman,et al.  Multiple determinants of verotoxin-producing Escherichia coli O157:H7 attachment-effacement , 1993, Infection and immunity.

[6]  B. Finlay,et al.  Enteropathogenic Escherichia coli decreases the transepithelial electrical resistance of polarized epithelial monolayers , 1993, Infection and immunity.

[7]  S. Falkow,et al.  Attaching and effacing locus of a Citrobacter freundii biotype that causes transmissible murine colonic hyperplasia , 1993, Infection and immunity.

[8]  S. Faruque,et al.  Sharing of virulence-associated properties at the phenotypic and genetic levels between enteropathogenic Escherichia coli and Hafnia alvei. , 1992, Journal of medical microbiology.

[9]  B. Finlay,et al.  Signal transduction between enteropathogenic Escherichia coli (EPEC) and epithelial cells: EPEC induces tyrosine phosphorylation of host cell proteins to initiate cytoskeletal rearrangement and bacterial uptake. , 1992, The EMBO journal.

[10]  B. Finlay,et al.  Cytoskeletal composition of attaching and effacing lesions associated with enteropathogenic Escherichia coli adherence to HeLa cells , 1992, Infection and immunity.

[11]  V. L. Tesh,et al.  Adherence and colonization mechanisms of enteropathogenic and enterohemorrhagic Escherichia coli. , 1992, Microbial pathogenesis.

[12]  P. Williams,et al.  Intestinal epithelial cell protein phosphorylation in enteropathogenic Escherichia coli diarrhoea , 1992, The Lancet.

[13]  P. Williams,et al.  Elevation of intracellular free calcium levels in HEp-2 cells infected with enteropathogenic Escherichia coli , 1991, Infection and immunity.

[14]  S. Tzipori,et al.  Hafnia alvei, a probable cause of diarrhea in humans , 1991, Infection and immunity.

[15]  P. Sherman,et al.  Outer membranes are competitive inhibitors of Escherichia coli O157:H7 adherence to epithelial cells , 1991, Infection and immunity.

[16]  J. Yu,et al.  A genetic locus of enteropathogenic Escherichia coli necessary for the production of attaching and effacing lesions on tissue culture cells. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[17]  J. H. Carr,et al.  Influence of the 60-megadalton plasmid on adherence of Escherichia coli O157:H7 and genetic derivatives , 1990, Infection and immunity.

[18]  P. Williams,et al.  Protein phosphorylation by protein kinase C in HEp-2 cells infected with enteropathogenic Escherichia coli , 1990, Infection and immunity.

[19]  M. Donowitz,et al.  Elevated intracellular Ca2+ acts through protein kinase C to regulate rabbit ileal NaCl absorption. Evidence for sequential control by Ca2+/calmodulin and protein kinase C. , 1989, The Journal of clinical investigation.

[20]  J. Cook,et al.  Viability measurements in mammalian cell systems. , 1989, Analytical biochemistry.

[21]  P. Williams,et al.  Actin accumulation at sites of bacterial adhesion to tissue culture cells: basis of a new diagnostic test for enteropathogenic and enterohemorrhagic Escherichia coli , 1989, Infection and immunity.

[22]  M. Karmali,et al.  Infection by verocytotoxin-producing Escherichia coli , 1989, Clinical Microbiology Reviews.

[23]  P. Sherman,et al.  Attaching and effacing adherence of Vero cytotoxin-producing Escherichia coli to rabbit intestinal epithelium in vivo , 1988, Infection and immunity.

[24]  S. Tzipori,et al.  Role of a 60-megadalton plasmid and Shiga-like toxins in the pathogenesis of infection caused by enterohemorrhagic Escherichia coli O157:H7 in gnotobiotic piglets , 1987, Infection and immunity.

[25]  P. Sherman,et al.  Surface properties of the Vero cytotoxin-producing Escherichia coli O157:H7 , 1987, Infection and immunity.

[26]  M. Levine Escherichia coli that cause diarrhea: enterotoxigenic, enteropathogenic, enteroinvasive, enterohemorrhagic, and enteroadherent. , 1987, The Journal of infectious diseases.

[27]  M. Levine,et al.  Attaching and effacing activities of rabbit and human enteropathogenic Escherichia coli in pig and rabbit intestines , 1983, Infection and immunity.

[28]  E. Beachey,et al.  Bacterial adherence: adhesin-receptor interactions mediating the attachment of bacteria to mucosal surface. , 1981, The Journal of infectious diseases.

[29]  E. Wulf,et al.  Fluorescent phallotoxin, a tool for the visualization of cellular actin. , 1979, Proceedings of the National Academy of Sciences of the United States of America.

[30]  Daniel S Waterman,et al.  ESCHERICHIA COLI STRAINS THAT CAUSE DIARRHŒA BUT DO NOT PRODUCE HEAT-LABILE OR HEAT-STABLE ENTEROTOXINS AND ARE NON-INVASIVE , 1978, The Lancet.

[31]  J. Kvittingen [Enteropathogenic Escherichia coli]. , 1966, Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke.

[32]  C. Clark,et al.  Expression and characterization of the eaeA gene product of Escherichia coli serotype O157:H7 , 1993, Infection and immunity.

[33]  M. Welsh,et al.  Ca2+ and cyclic AMP in regulation of intestinal Na, K, and Cl transport. , 1986, Annual review of physiology.

[34]  H. Lior,et al.  The association between idiopathic hemolytic uremic syndrome and infection by verotoxin-producing Escherichia coli. , 1985, The Journal of infectious diseases.