A low molecular weight outer-membrane protein of Escherichia coli O157:H7 associated with adherence to INT407 cells and chicken caeca

References

1. Griffin P. M., Tauxe R. V. The epidemiology of infections caused by Escherichia coli O157:H7, other enterohemorrhagic E. coli, and the associated hemolytic uremic syndrome. Epidemiol Rev 1991; 13:60–98
   [Google Scholar]
2. Padhye N. V., Doyle M. P. Escherichia coli O157:H7: epidemiology, pathogenesis, and methods for detection in food. J Food Prot 1992; 55:555–565
   [Google Scholar]
3. O’Brien A. D., Holmes R. K. Shiga and Shiga-like toxins. Microbiol Rev 1987; 51:206–220
   [Google Scholar]
4. Donnenberg M. S., Tzipori S., McKee M. L., O’Brien A. D., Alroy J., Kaper J. B. The role of the eae gene of enterohemorrhagic Escherichia coli in intimate attachment in vitro and in a porcine model. J Clin Invest 1993; 92:1418–1224
   [Google Scholar]
5. Dytoc M., Soni R., Cockerill F. Multiple determinants of verotoxin-producing Escherichia coli O157:H7 attachmenteffacement. Infect Immun 1993; 61:3382–3391
   [Google Scholar]
6. Sherman P., Soni R. Adherence of verocytotoxin-producing Escherichia coli of serotype O157:H7 to human epithelial cells in tissue culture: role of outer membranes as bacterial adhesins. J Med Microbiol 1988; 26:11–17
   [Google Scholar]
7. Karch H., Heesemann J., Laufs R., O’Brien A. D., Tacket C. O., Levine M. M. A plasmid of enterohemorrhagic Escherichia coli O157:H7 is required for expression of a new fimbrial antigen and for adhesion to epithelial cells. Infect Immun 1987; 55:455–461
   [Google Scholar]
8. Louie M., De Azavedo J. C. S., Handelsman M. Y. C. Expression and characterization of the eaeA gene product of Escherichia coli serotype O157:H7. Infect Immun 1993; 61:4085–4092
   [Google Scholar]
9. Sherman P., Cockerill F., Soni R., Brunton J. Outer membranes are competitive inhibitors of Escherichia coli O157:H7 adherence to epithelial cells. Infect Immun 1991; 59:890–899
   [Google Scholar]
10. Toth I., Cohen M. L., Rumschlag H. S. Influence of the 60-megadalton plasmid on adherence of Escherichia coli 0157-H7 and genetic derivatives. Infect Immun 1990; 58:1223–1231
    [Google Scholar]
11. Tzipori S., Gibson R., Montanaro J. Nature and distribution of mucosal lesions associated with enteropathogenic and enterohemorrhagic Escherichia coli in piglets and the role of plasmid-mediated factors. Infect Immun 1989; 57:1142–1150
    [Google Scholar]
12. Tzipori S., Karch H., Wachsmuth K. I. 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. Infect Immun 1987; 55:3117–3125
    [Google Scholar]
13. Beebakhee G., Louie M., De Azavedo J., Brunton J. Cloning and nucleotide sequence of the eae gene homologue from enterohemorrhagic Escherichia coli serotype O157:H7. FEMS Microbiol Lett 1992; 91:63–68
    [Google Scholar]
14. Yu J., Kaper J. B. Cloning and characterization of the eae gene of enterohemorrhagic Escherichia coli O157:H7. Mol Microbiol 1992; 6:411–417
    [Google Scholar]
15. Padhye N. V., Doyle M. P. Production and characterization of a monoclonal antibody specific for enterohemorrhagic Escherichia coli of serotypes O157:H7 and O26:H11. J Clin Microbiol 1991; 29:99–103
    [Google Scholar]
16. Clark C. G., Johnson S., Johnson R. P. Further characterisation of a monoclonal antibody reactive with Escherichia coli O157:H7. J Med Microbiol 1995; 43:262–269
    [Google Scholar]
17. Hoffman C. S., Wright A. Fusion of secreted proteins to alkaline phosphatase: an approach for studying protein secretion. Proc Natl Acad Sci USA 1985; 82:5107–5111
    [Google Scholar]
18. Manoil C., Beckwith J. TnphoA: A transposon probe for protein export signals. Proc Natl Acad Sci USA 1985; 82:8129–8133
    [Google Scholar]
19. Donnenberg M. S., Calderwood S. B., Donohue-Rolfe A., Keusch G. T., Kaper J. B. Construction and analysis of TnphoA mutants of enteropathogenic Escherichia coli unable to invade HEp-2 cells. Infect Immun 1990; 58:1565–1571
    [Google Scholar]
20. Jerse A. E., Kaper J. B. The eae gene of enteropathogenic Escherichia coli encodes a 94-kilodalton membrane protein, the expression of which is influenced by EAF plasmid. Infect Immun 1991; 59:4302–4309
    [Google Scholar]
21. Taylor R. K., Manoil C., Mekalanos J. J. Broad-host-range vectors for delivery of TnphoA: use in genetic analysis of secreted virulence determinants of Vibrio cholerae. J Bacterial 1989; 171:1870–1878
    [Google Scholar]
22. Hj elmland L. M., Chrambach A. Solubilization of functional membrane-bound receptors. In Venter J. C., Harrison L. C. (eds) Membrane, detergents and receptors solubilization New York: Alan R. Liss; 198435–46
    [Google Scholar]
23. Schagger H., van Jagow G. Tricine-sodium dodecyl sulfatepolyacrylamide gel electrophoresis for the separation of proteins in the range from 1-100 kDa. Anal Biochem 1987; 166:368–379
    [Google Scholar]
24. Lech K., Brent R. Minipreps of plasmid DNA. In Ausubel F.M., Brent R., Kingston R.E. (eds) Short protocols in molecular biology—a compendium of methods from Current Protocols in Molecular Biology New York: John Wiley and Sons; 198919–20
    [Google Scholar]
25. Wilson K. Preparation of genomic DNA from bacteria. In Ausubel F. M., Brent R., Kingston R. E. (eds) Short protocols in molecular biology—a compendium of methods from Current Protocols in Molecular Biology New York: John Wiley and Sons; 198961–63
    [Google Scholar]
26. Feinberg A. P., Vbgelstein B. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Anal Biochem 1983; 132:6–13
    [Google Scholar]
27. Junkins A. D., Doyle M. P. Comparison of adherence properties ofEscherichia coli O157:H7 and a 60-megadalton plasmid-cured derivative. Curr Microbiol 1989; 19:21–27
    [Google Scholar]
28. Daniel W. W. Hypothesis testing. In Daniel W. W. (ed) Biostatistics: a foundation for analysis in the health sciences New York: John Wiley and Sons; 1987188–272
    [Google Scholar]
29. Berry J. T., Doyle M. P., Schoeni J. L. Colonization of chicken cecae by Escherichia coli associated with hemorrhagic colitis. Appl Environ Microbiol 1985; 49:310–315
    [Google Scholar]
30. Ashkenazi S., May L., LaRocco M., Lopez E. L., Cleary T. G. The effect of postnatal age on the adherence of enterohemorrhagic Escherichia coli to rabbit intestinal cells. Pediatr Res 1991; 29:14–19
    [Google Scholar]
31. Leroy S. M., Lesage, M-C., Chaslus-Dancla E., Lafont J. P. Presence of eaeA sequences in pathogenic and non-pathogenic Escherichia coli strains isolated from weaned rabbits. J Med Microbiol 1994; 40:90–94
    [Google Scholar]
32. McDaniel T. K., Jarvis K. G., Donnenberg M. S., Kaper J. B. A genetic locus of enterocyte effacement conserved among diverse enterobacterial pathogens. Proc Natl Acad Sci USA 1995; 92:1664–1668
    [Google Scholar]
33. Jarvis K. G., Giron J. A., Jerse A. E., McDaniel T. K., Donnenberg M. S., Kaper J. B. Enteropathogenic Escherichia coli contains a putative type III secretion system necessary for the export of proteins involved in attaching and effacing lesion formation. Proc Natl Acad Sci USA 1995; 92:7996–8000
    [Google Scholar]
34. Rocque W. J., Coughlin R. T., McGroarty E. J. Lipopolysaccharide tightly bound to porin monomers and trimers from Escherichia coli K-12. J Bacteriol 1987; 169:4003–4010
    [Google Scholar]
35. Wu M.-C., Heath E. C. Isolation and characterization of lipopolysaccharide protein from Escherichia coli. Proc Natl Acad Sci USA 1973; 70:2572–2576
    [Google Scholar]
36. Bilge S. S., Varu J. C., Potter K., Dowell S. F., Tarr P. L. Escherichia coli O157:H7 lipopolysaccharide mutants are hyperadherent, abstr. B-2. Abstracts of the 95th Annual Meeting of the American Society for Microbiology; Washington, DC, USA: 1995166
    [Google Scholar]