This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Dean-Nystrom, E. A.
Right arrow Articles by O'Brien, A. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Dean-Nystrom, E. A.
Right arrow Articles by O'Brien, A. D.

 Previous Article  |  Next Article 

Infection and Immunity, September 1998, p. 4560-4563, Vol. 66, No. 9
0019-9567/98/$00.00+0

Escherichia coli O157:H7 Requires Intimin for Enteropathogenicity in Calves

Evelyn A. Dean-Nystrom,1,* Brad T. Bosworth,1 Harley W. Moon,2 and Alison D. O'Brien3

Enteric Diseases and Food Safety Research Unit, National Animal Disease Center, Agricultural Research Service, U.S. Department of Agriculture, Ames, Iowa 500101; Veterinary Medical Research Institute, College of Veterinary Medicine, Iowa State University, Ames, Iowa 500112; and Department of Microbiology and Immunology, F. Edward Hébert School of Medicine, Uniformed Services University of the Health Sciences, Bethesda, Maryland 208143

Received 8 April 1998/Returned for modification 15 May 1998/Accepted 26 June 1998

    ABSTRACT
Top
Abstract
Text
References

Enterohemorrhagic Escherichia coli (EHEC) strains require intimin to induce attaching and effacing (A/E) lesions in newborn piglets. Infection of newborn calves with intimin-positive or intimin-negative EHEC O157:H7 demonstrated that intimin is needed for colonization, A/E lesions, and disease in cattle. These results suggest that experiments to determine if intimin-based vaccines reduce O157:H7 levels in cattle are warranted.

    TEXT
Top
Abstract
Text
References

Enterohemorrhagic Escherichia coli (EHEC) strains of serotype O157:H7 are a major cause of bloody diarrhea in humans in the United States (20). Hemolytic uremic syndrome, a life-threatening complication of EHEC O157:H7 infection, is the primary cause of acute kidney failure in children in the United States and Canada (1). Other serotypes of EHEC have also been associated with outbreaks of bloody diarrhea and hemolytic uremic syndrome (2, 3, 19).

Cattle are important reservoirs of EHEC O157:H7 strains (20, 22). The majority of cases of EHEC disease recognized in the United States are associated with ingestion of undercooked, contaminated hamburger or raw milk. Outbreaks have also been associated with produce contaminated with bovine manure. Therefore, one strategy for reducing the risk of EHEC infections in humans is to reduce the prevalence of EHEC infections in cattle.

All EHEC strains are Shiga toxin-producing E. coli (STEC) strains. They produce cytotoxins, called Shiga toxins (Stx1 and Stx2) or verotoxins, that are considered essential for EHEC virulence in humans. EHEC strains are also characterized by the presence of a ~90-kb plasmid (12, 14, 21). Many EHEC strains have the capacity to attach intimately to host cell membranes and efface microvilli and cytoplasm in a characteristic pattern referred to as an attaching and effacing (A/E) lesion. EHEC strains cause A/E lesions in selected cell lines in vitro and in the intestines of experimental animals (13, 22).

EHEC-mediated A/E lesions are similar to those produced by enteropathogenic E. coli (EPEC) in humans and animals (13). In EPEC, the eae (for E. coli attaching and effacing; formerly called eaeA) chromosomal locus encodes an outer membrane adhesion protein called intimin (11). The eae gene is necessary, but not sufficient, for EPEC bacteria to cause A/E lesions (6, 7, 10). Some EHEC strains also carry an eae homolog that plays a critical role in the attachment of EHEC O157:H7 to human epithelial cells and the formation of A/E lesions in gnotobiotic pigs (8, 15, 16).

The objectives of the present study were to determine if intimin is required for EHEC-mediated enterocolitis and diarrhea in calves and to extend earlier studies showing its role in A/E lesion formation in neonatal piglets. We compared the pathogenicity of an intimin-negative eae mutant of EHEC O157:H7 (strain 86-24eaeDelta 10 [15]) with that of two isogenic intimin-positive (eae+) partners, one a wild-type EHEC isolate (strain 86-24) and the other the eae mutant complemented with the eae gene [strain 86-24eaeDelta 10(pEB310) (15)], in neonatal calves and cesarean-derived, colostrum-deprived (CDCD) piglets. We also tested the pathogenicity of an intimin-negative non-O157:H7 wild-type EHEC strain (B2F1) in neonatal calves.

                              
View this table:
[in this window]
[in a new window]
 
TABLE 1.   E. coli strains used in this study

The bacterial strains used in this study are described in Table 1. Each of 23 colostrum-deprived calves (18 holstein, 2 jersey, and 3 mixed breeds; 22 male and 1 female) was inoculated before it was 12 h old via suckling with milk replacer containing 1010 CFU of an EHEC strain that produces intimin (12 calves), an EHEC strain that does not produce intimin (8 calves), or the nonpathogenic control E. coli 123 (3 calves) as previously described (5). Calves were observed every 8 h for signs of disease and euthanatized with sodium pentobarbital at 18 or 42 h postinoculation.

At necropsy, rectal contents and sections from the rectum, colon, cecum, and ileum were collected and frozen at -80°C for bacteriological examination (5). Tissues from the rectum, colon, cecum, and ileum were fixed in formaldehyde, sectioned, and stained with hematoxylin and eosin or immunohistochemically with goat anti-O157:H7 as the primary antibody, biotinylated anti-goat immunoglobulin G (heavy and light chains) as the secondary antibody, and an avidin-biotin-peroxidase conjugate (5). Some sections were removed from formaldehyde and postfixed in glutaraldehyde for transmission electron microscopy (5).

Three of five calves inoculated with wild-type EHEC strain 86-24 developed watery diarrhea by 18 h postinoculation (Table 2). Two of three calves had blood-tinged diarrhea at 42 h postinoculation, and one of these calves died on day 2, about 2 h prior to the scheduled necropsy. Postmortem observations were compatible with enteritis as the cause of death. Similarly, two of seven calves inoculated with the complemented mutant strain 86-24eaeDelta 10(pEB310) developed diarrhea by 18 h, and three of four had diarrhea (blood tinged in two calves) by 42 h postinoculation. One such infected calf died on day 2, about 2 h prior to the scheduled necropsy. Again, postmortem observations were compatible with enteritis as the cause of death. In contrast, all calves inoculated with mutant strain 86-24eaeDelta 10, with B2F1, or with nonpathogenic control strain 123 remained healthy throughout the experiment.

                              
View this table:
[in this window]
[in a new window]
 
TABLE 2.   Clinical and histological findings in calves 18 and 42 h after inoculation with an eae+ EHEC strain [86-24 or 86-24eaeDelta 10(pEB310)], an eae mutant EHEC strain (86-24eaeDelta 10), or a strain lacking the eae gene (B2F1 or nonpathogenic E. coli 123)

Hyperemia, focal petechiae, and fibrinous exudates in the intestines were common postmortem observations in calves inoculated with strain 86-24 or 86-24eaeDelta 10(pEB310) but were not noted in any of the calves inoculated with mutant strain 86-24eaeDelta 10, strain B2F1, or control strain 123. A/E lesions containing O157:H7+ bacteria were identified by immunostaining in the ileum and large intestines of five of five calves inoculated with strain 86-24 and six of seven calves inoculated with strain 86-24eaeDelta 10(pEB310). In addition to A/E lesions, a diffuse mucosal neutrophil infiltration with accompanying hemorrhage, edema, atrophy of ileal villi, and fibrinous to fibrinohemorrhagic exudates in the intestinal lumen was noted in histologic sections from some of these calves. Neutrophil infiltrates also occurred in the one calf that had no A/E lesions. Examination of sections of ileum from two calves [18 and 42 h postinoculation with strain 86-24eaeDelta 10(pEB310)] by electron microscopy confirmed the in vivo A/E activity of the complemented mutant (Fig. 1). No A/E lesions or histopathological abnormalities were detected in any calf inoculated with mutant strain 86-24eaeDelta 10, strain B2F1, or control strain 123. However, there were patchy layers of O157:H7+ bacteria on the epithelium in the cecum, colon, and ileum of one calf necropsied 18 h after inoculation with mutant strain 86-24eaeDelta 10, but these bacteria were not associated with A/E lesions.


View larger version (209K):
[in this window]
[in a new window]
 
FIG. 1.   Electron micrograph of absorptive cells from the ileum of a calf 18 h after inoculation with EHEC O157:H7 strain 86-24eaeDelta 10(pEB310). This strain is an eae mutant which has been complemented with the eae gene. The intestinal lumen is to the left. Bacteria are intimately attached to absorptive-cell membranes with subjacent electron-dense filaments in absorptive-cell cytoplasm. Most of the absorptive-cell microvilli have been effaced. There are pedestals beneath bacteria to the upper left.

The numbers of the inoculated organisms (expressed as CFU per gram) recovered from tissues and feces of calves at 18 or 42 h postinoculation with eae+ or eae strains of E. coli are shown in Fig. 2. Sorbitol-negative EHEC O157:H7 bacteria were quantitated on sorbitol MacConkey agar containing 100 µg of streptomycin per ml (strain 86-24), 100 µg of streptomycin and 20 µg of nalidixic acid per ml (strain 86-24eaeDelta 10), or 100 µg of ampicillin and 34 µg of chloramphenicol per ml [strain 86-24eaeDelta 10(pEB310)]. Samples from which the inoculated strain were not recovered were recorded as having <103 CFU/g. Selected sorbitol-negative isolates were tested for O157:H7 antigen by a latex agglutination assay (5). Strain B2F1 (O91:H21) and strain 123 (O43:H28) bacteria were quantitated on MacConkey agar containing 100 µg of streptomycin or 20 µg of nalidixic acid per ml, respectively. Colonies were tested for O91 and O43 antigens to identify strains B2F1 and 123, respectively, by filter blot immunoperoxidase assay (4), using anti-O91 and anti-O43 sera (E. coli Reference Center, Pennsylvania State University, University Park) and peroxidase-conjugated anti-rabbit immunoglobulin G (heavy and light chains) (Kirkegaard and Perry Laboratories, Inc., Gaithersburg, Md.).


View larger version (40K):
[in this window]
[in a new window]
 
FIG. 2.   CFU of E. coli per gram of tissue or feces in necropsy samples from neonatal calves 18 h () or 42 h () after inoculation with eae+ EHEC strain 86-24 or 86-24eaeDelta 10(pEB310), eae mutant EHEC strain 86-24eaeDelta 10, strain B2F1, or nonpathogenic E. coli 123. Data are means ± standard deviations. See Table 2 for the number of calves in each group. Sp., spiral.

Greater numbers of the inoculated organisms were recovered from the intestines of calves inoculated with strain 86-24 or strain 86-24eaeDelta 10(pEB310) than from those of calves inoculated with strain 86-24eaeDelta 10, strain B2F1, or control strain 123 at 42 h postinoculation (Fig. 2). Because of the large degree of variation among animals and the small number of animals, there was no significant difference among the numbers of bacteria at the individual tissue level. However, when we took the group average for each tissue and treated the tissues as a block, the mean CFU per gram for all samples obtained at 42 h postinoculation from the group of calves inoculated with eae mutant strain 86-24eaeDelta 10 was lower (P < 0.05; analysis of variance and least significant difference test) than the means for calves inoculated with eae+ strain 86-24 or 86-24eaeDelta 10(pEB310). The only exception was that the one calf that did not develop clinical signs or have A/E lesions after inoculation with strain 86-24eaeDelta 10(pEB310) had bacterial levels comparable to those in calves inoculated with strains that lacked the eae gene. The numbers for strains 86-24eaeDelta 10 and B2F1 were similar to those for control strain 123. The number of strain 86-24eaeDelta 10 organisms recovered from feces was similar to that of the eae+ strains. The inoculum strain accounted for a larger percentage of the total number of coliforms isolated from calves inoculated with eae+ EHEC than from calves inoculated with eae mutant EHEC, strain B2F1, or the control E. coli strain (Fig. 3). The presence and severity of A/E lesions in tissues from calves inoculated with eae+ strains correlated with the number of inoculated bacteria recovered (data not shown). A/E lesions were only seen in tissues containing >= 106 CFU of eae+ EHEC/g of tissue.


View larger version (46K):
[in this window]
[in a new window]
 
FIG. 3.   Numbers of CFU of inoculated strain () and total coliforms () per gram of tissue or feces recovered at 42 h postinoculation from calves inoculated with eae+ EHEC strain 86-24 or 86-24eaeDelta 10(pEB310), eae mutant EHEC strain 86-24eaeDelta 10, strain B2F1, or E. coli control strain 123. Sp., spiral.

In earlier studies we showed that the histopathology of EHEC O157:H7 infection in neonatal calves is similar to that in CDCD piglets, but O157:H7 bacteria do not cause diarrhea in CDCD piglets by 18 h postinoculation (5). In this study, we compared the pathogenicity of isogenic eae+ and eae mutant derivatives of EHEC O157:H7 strain 86-24 in <8-h-old CDCD piglets (8). As shown in Table 3, CDCD piglets developed colonic edema and A/E lesions by 18 h after inoculation with the eae+ strain 86-24 or 86-24eaeDelta 10(pEB310) but not with the eae mutant. In contrast to calves, the A/E lesions occurred mainly in the ceca of the piglets. The numbers of inoculated bacteria recovered from the cecum or ileum at 18 h postinoculation were similar in all experimental groups (Table 3), and bacterial counts did not correlate with the presence or absence of A/E lesions. These results indicate that intimin plays a critical role in EHEC O157:H7 pathogenesis in CDCD piglets and extend the findings of earlier studies with these strains in gnotobiotic piglets (15).

                              
View this table:
[in this window]
[in a new window]
 
TABLE 3.   Findings in CDCD piglets at 18 h after inoculation with an eae+ [86-24 or 86-24eaeDelta 10(pEB310)] or an eae mutant (86-24eaeDelta 10) EHEC strain or nonpathogenic E. coli 123

In this study we have clearly demonstrated that the eae gene locus is required for E. coli O157:H7 strain 86-24 to intensively colonize the intestines and cause diarrhea and A/E lesions in neonatal calves and to cause colonic edema and A/E lesions in CDCD piglets. The eae mutant and B2F1 data indicate that eae-mediated adherence to the intestinal mucosa is critical for EHEC to cause fibrinohemorrhagic enterocolitis and diarrhea in calves. Similarly, the results confirm that eae-mediated colonization is necessary for intestinal lesion formation in CDCD piglets. These results suggest that anti-intimin vaccines might interfere with EHEC infections. Such vaccines could help reduce the levels of EHEC in cattle and thus reduce the number of EHEC infections in humans. The CDCD piglet EHEC infection model will be useful for preliminary experiments to test the efficacy of anti-intimin vaccines.

    ACKNOWLEDGMENTS

This work was partly supported by grant AI20148-15 from the National Institutes of Health to Alison D. O'Brien.

We thank M. I. Inbody, N. C. Lyon, R. W. Morgan, R. A. Schneider, R. J. Spaete, and J. A. Stasko for technical assistance.

    FOOTNOTES

* Corresponding author. Mailing address: USDA, ARS, National Animal Disease Center, P.O. Box 70, Ames, IA 50010-0070. Phone: (515) 239-8376. Fax: (515) 239-8458. E-mail: enystrom{at}nadc.ars.usda.gov.

Editor:   J. T. Barbieri

    REFERENCES
Top
Abstract
Text
References

1. Altekruse, S. F., M. L. Cohen, and D. L. Swerdlow. 1997. Emerging foodborne diseases. Emerg. Infect. Dis. 3:285-293[Medline].
2. Caprioli, A., A. E. Tozzi, G. Rizzoni, and H. Karch. 1997. Non-O157:H7 Shiga toxin-producing Escherichia coli infections in Europe. Emerg. Infect. Dis. 3:578-579[Medline]. (Letter.)
3. Centers for Disease Control and Prevention. 1995. Outbreak of acute gastroenteritis attributable to Escherichia coli serotype O104:H21---Helena, Montana 1994. Morbid. Mortal. Weekly Rep. 44:501-503[Medline].
4. Dean, E. A., S. C. Whipp, and H. W. Moon. 1989. Age-specific colonization of porcine intestinal epithelium by 987P-piliated enterotoxigenic Escherichia coli. Infect. Immun. 57:82-87[Abstract/Free Full Text].
5. Dean-Nystrom, E. A., B. T. Bosworth, W. C. Cray, Jr., and H. W. Moon. 1997. Pathogenicity of Escherichia coli O157:H7 in the intestines of neonatal calves. Infect. Immun. 65:1842-1848[Abstract].
6. Donnenberg, M. S., and J. B. Kaper. 1991. Construction of an eae deletion mutant of enteropathogenic Escherichia coli by using a positive-selection suicide vector. Infect. Immun. 59:4310-4317[Abstract/Free Full Text].
7. Donnenberg, M. S., and J. B. Kaper. 1992. Enteropathogenic Escherichia coli. Infect. Immun. 60:3953-3961[Free Full Text].
8. Donnenberg, M. S., S. Tzipori, M. L. McKee, A. D. O'Brien, J. Alroy, and J. B. Kaper. 1993. The role of the eae gene of enterohemorrhagic Escherichia coli in intimate attachment in vitro and in a porcine model. J. Clin. Invest. 92:1418-1424.
9. Ito, H., A. Terai, H. Kurazono, Y. Takeda, and M. Nishibuchi. 1990. Cloning and nucleotide sequencing of Vero toxin 2 varian genes from Escherichia coli O91:H21 isolated from a patient with the hemolytic uremic syndrome. Microb. Pathog. 8:47-60[Medline].
10. Jerse, A. E., and J. B. Kaper. 1991. The eae gene of enteropathogenic Escherichia coli encodes a 94-kilodalton membrane protein, the expression of which is influenced by the EAF plasmid. Infect. Immun. 59:4302-4309[Abstract/Free Full Text].
11. Jerse, A. E., J. Yu, B. D. Tall, and J. B. Kaper. 1990. A genetic locus of enteropathogenic Escherichia coli necessary for the production of attaching and effacing lesions on tissue culture cells. Proc. Natl. Acad. Sci. USA 87:7839-7843[Abstract/Free Full Text].
12. Johnson, W. M., H. Lior, and G. S. Bezanson. 1983. Cytotoxic Escherichia coli O157:H7 associated with haemorrhagic colitis in Canada. Lancet i:76.
13. Knutton, S. 1994. Attaching and effacing Escherichia coli, p. 567-591. In C. L. Gyles (ed.), Escherichia coli in domestic animals and humans. CAB International, Wallingford, United Kingdom.
14. Levine, M. M., J. Xu, J. B. Kaper, H. Lior, V. Prado, B. Tall, J. Nataro, H. Karch, and K. Wachsmuth. 1987. A DNA probe to identify enterohemorrhagic Escherichia coli of O157:H7 and other serotypes that cause hemorrhagic colitis and hemolytic uremic syndrome. J. Infect. Dis. 156:175-182[Medline].
15. McKee, M. L., A. R. Melton-Celsa, R. A. Moxley, D. H. Francis, and A. D. O'Brien. 1995. Enterohemorrhagic Escherichia coli O157:H7 requires intimin to colonize the gnotobiotic pig intestine and to adhere to HEp-2 cells. Infect. Immun. 63:3739-3744[Abstract].
16. McKee, M. L., and A. D. O'Brien. 1995. Investigation of enterohemorrhagic Escherichia coli O157:H7 adherence characteristics and invasion reveals a new attachment pattern shared by intestinal E. coli. Infect. Immun. 63:2070-2074[Abstract].
17. Melton-Celsa, A. R., S. C. Darnell, and A. D. O'Brien. 1996. Activation of Shiga-like toxins by mouse and human intestinal mucus correlates with virulence of enterohemorrhagic Escherichia coli O91:H21 isolates in orally infected, streptomycin-treated mice. Infect. Immun. 64:1569-1576[Abstract].
18. Moon, H. W., D. K. Sorensen, and J. H. Sautter. 1968. Experimental enteric colibacillosis in piglets. Can. J. Comp. Med. 32:493-497.
19. O'Brien, A. D., A. R. Melton, C. K. Schmitt, M. L. McKee, M. L. Batts, and D. E. Griffin. 1993. Profile of Escherichia coli O157:H7 pathogen responsible for hamburger-borne outbreak of hemorrhagic colitis and hemolytic uremic syndrome in Washington. J. Clin. Microbiol. 31:2799-2801[Abstract/Free Full Text].
20. Su, C., and L. J. Brandt. 1995. Escherichia coli O157:H7 infection in humans. Ann. Intern. Med. 123:698-714[Abstract/Free Full Text].
21. Wells, J. G., B. R. Davis, I. K. Wachsmuth, L. W. Riley, R. S. Remis, R. Sokolow, and G. K. Morris. 1983. Laboratory investigation of hemorrhagic colitis outbreaks associated with a rare Escherichia coli serotype. J. Clin. Microbiol. 18:512-520[Abstract/Free Full Text].
22. Whipp, S. C., M. A. Rasmussen, and W. C. Cray, Jr. 1994. Animals as a source of Escherichia coli pathogenic for human beings. J. Am. Vet. Med. Assoc. 204:1168-1175[Medline].


Infection and Immunity, September 1998, p. 4560-4563, Vol. 66, No. 9
0019-9567/98/$00.00+0



This article has been cited by other articles:

  • Hemrajani, C., Marches, O., Wiles, S., Girard, F., Dennis, A., Dziva, F., Best, A., Phillips, A. D., Berger, C. N., Mousnier, A., Crepin, V. F., Kruidenier, L., Woodward, M. J., Stevens, M. P., La Ragione, R. M., MacDonald, T. T., Frankel, G. (2008). Role of NleH, a Type III Secreted Effector from Attaching and Effacing Pathogens, in Colonization of the Bovine, Ovine, and Murine Gut. Infect. Immun. 76: 4804-4813 [Abstract] [Full Text]  
  • Stamm, I., Mohr, M., Bridger, P. S., Schropfer, E., Konig, M., Stoffregen, W. C., Dean-Nystrom, E. A., Baljer, G., Menge, C. (2008). Epithelial and Mesenchymal Cells in the Bovine Colonic Mucosa Differ in Their Responsiveness to Escherichia coli Shiga Toxin 1. Infect. Immun. 76: 5381-5391 [Abstract] [Full Text]  
  • Dean-Nystrom, E. A., Stoffregen, W. C., Bosworth, B. T., Moon, H. W., Pohlenz, J. F. (2008). Early Attachment Sites for Shiga-Toxigenic Escherichia coli O157:H7 in Experimentally Inoculated Weaned Calves. Appl. Environ. Microbiol. 74: 6378-6384 [Abstract] [Full Text]  
  • Kendall, M. M., Rasko, D. A., Sperandio, V. (2007). Global Effects of the Cell-to-Cell Signaling Molecules Autoinducer-2, Autoinducer-3, and Epinephrine in a luxS Mutant of Enterohemorrhagic Escherichia coli. Infect. Immun. 75: 4875-4884 [Abstract] [Full Text]  
  • Meltz Steinberg, K., Levin, B. R (2007). Grazing protozoa and the evolution of the Escherichia coli O157:H7 Shiga toxin-encoding prophage. Proc R Soc B 274: 1921-1929 [Abstract] [Full Text]  
  • Hoffman, M. A., Menge, C., Casey, T. A., Laegreid, W., Bosworth, B. T., Dean-Nystrom, E. A. (2006). Bovine Immune Response to Shiga-Toxigenic Escherichia coli O157:H7. CVI 13: 1322-1327 [Abstract] [Full Text]  
  • Sheng, H., Lim, J. Y., Knecht, H. J., Li, J., Hovde, C. J. (2006). Role of Escherichia coli O157:H7 Virulence Factors in Colonization at the Bovine Terminal Rectal Mucosa.. Infect. Immun. 74: 4685-4693 [Abstract] [Full Text]  
  • Low, A. S., Dziva, F., Torres, A. G., Martinez, J. L., Rosser, T., Naylor, S., Spears, K., Holden, N., Mahajan, A., Findlay, J., Sales, J., Smith, D. G. E., Low, J. C., Stevens, M. P., Gally, D. L. (2006). Cloning, Expression, and Characterization of Fimbrial Operon F9 from Enterohemorrhagic Escherichia coli O157:H7. Infect. Immun. 74: 2233-2244 [Abstract] [Full Text]  
  • Sinclair, J. F., Dean-Nystrom, E. A., O'Brien, A. D. (2006). The Established Intimin Receptor Tir and the Putative Eucaryotic Intimin Receptors Nucleolin and {beta}1 Integrin Localize at or near the Site of Enterohemorrhagic Escherichia coli O157:H7 Adherence to Enterocytes In Vivo. Infect. Immun. 74: 1255-1265 [Abstract] [Full Text]  
  • Vlisidou, I., Dziva, F., La Ragione, R. M., Best, A., Garmendia, J., Hawes, P., Monaghan, P., Cawthraw, S. A., Frankel, G., Woodward, M. J., Stevens, M. P. (2006). Role of Intimin-Tir Interactions and the Tir-Cytoskeleton Coupling Protein in the Colonization of Calves and Lambs by Escherichia coli O157:H7. Infect. Immun. 74: 758-764 [Abstract] [Full Text]  
  • Wang, J.-Y., Wang, S.-S., Yin, P.-Z. (2006). Haemolytic-uraemic syndrome caused by a non-O157 : H7 Escherichia coli strain in experimentally inoculated dogs. J Med Microbiol 55: 23-29 [Abstract] [Full Text]  
  • Naylor, S. W., Roe, A. J., Nart, P., Spears, K., Smith, David. G. E., Low, J. C., Gally, D. L. (2005). Escherichia coli O157 : H7 forms attaching and effacing lesions at the terminal rectum of cattle and colonization requires the LEE4 operon. Microbiology 151: 2773-2781 [Abstract] [Full Text]  
  • Ritchie, J. M., Waldor, M. K. (2005). The Locus of Enterocyte Effacement-Encoded Effector Proteins All Promote Enterohemorrhagic Escherichia coli Pathogenicity in Infant Rabbits. Infect. Immun. 73: 1466-1474 [Abstract] [Full Text]  
  • van Diemen, P. M., Dziva, F., Stevens, M. P., Wallis, T. S. (2005). Identification of Enterohemorrhagic Escherichia coli O26:H- Genes Required for Intestinal Colonization in Calves. Infect. Immun. 73: 1735-1743 [Abstract] [Full Text]  
  • Best, A., La Ragione, R. M., Sayers, A. R., Woodward, M. J. (2005). Role for Flagella but Not Intimin in the Persistent Infection of the Gastrointestinal Tissues of Specific-Pathogen-Free Chicks by Shiga Toxin-Negative Escherichia coli O157:H7. Infect. Immun. 73: 1836-1846 [Abstract] [Full Text]  
  • Jordan, D. M., Booher, S. L., Moon, H. W. (2005). Escherichia coli O157:H7 Does Not Require Intimin To Persist in Pigs. Infect. Immun. 73: 1865-1867 [Full Text]  
  • Torres, A. G., Zhou, X., Kaper, J. B. (2005). Adherence of Diarrheagenic Escherichia coli Strains to Epithelial Cells. Infect. Immun. 73: 18-29 [Full Text]  
  • Pohlenz, J. F., Winter, K. R., Dean-Nystrom, E. A. (2005). Shiga-Toxigenic Escherichia coli-Inoculated Neonatal Piglets Develop Kidney Lesions That Are Comparable to Those in Humans with Hemolytic-Uremic Syndrome. Infect. Immun. 73: 612-616 [Abstract] [Full Text]  
  • Dziva, F., van Diemen, P. M., Stevens, M. P., Smith, A. J., Wallis, T. S. (2004). Identification of Escherichia coli O157 : H7 genes influencing colonization of the bovine gastrointestinal tract using signature-tagged mutagenesis. Microbiology 150: 3631-3645 [Abstract] [Full Text]  
  • Jordan, D. M., Cornick, N., Torres, A. G., Dean-Nystrom, E. A., Kaper, J. B., Moon, H. W. (2004). Long Polar Fimbriae Contribute to Colonization by Escherichia coli O157:H7 In Vivo. Infect. Immun. 72: 6168-6171 [Abstract] [Full Text]  
  • Stevens, M. P., Roe, A. J., Vlisidou, I., van Diemen, P. M., La Ragione, R. M., Best, A., Woodward, M. J., Gally, D. L., Wallis, T. S. (2004). Mutation of toxB and a Truncated Version of the efa-1 Gene in Escherichia coli O157:H7 Influences the Expression and Secretion of Locus of Enterocyte Effacement-Encoded Proteins but not Intestinal Colonization in Calves or Sheep. Infect. Immun. 72: 5402-5411 [Abstract] [Full Text]  
  • Vlisidou, I., Lyte, M., van Diemen, P. M., Hawes, P., Monaghan, P., Wallis, T. S., Stevens, M. P. (2004). The Neuroendocrine Stress Hormone Norepinephrine Augments Escherichia coli O157:H7-Induced Enteritis and Adherence in a Bovine Ligated Ileal Loop Model of Infection. Infect. Immun. 72: 5446-5451 [Abstract] [Full Text]  
  • Cobbold, R. N., Rice, D. H., Szymanski, M., Call, D. R., Hancock, D. D. (2004). Comparison of Shiga-Toxigenic Escherichia coli Prevalences among Dairy, Feedlot, and Cow-Calf Herds in Washington State. Appl. Environ. Microbiol. 70: 4375-4378 [Abstract] [Full Text]  
  • Menge, C., Blessenohl, M., Eisenberg, T., Stamm, I., Baljer, G. (2004). Bovine Ileal Intraepithelial Lymphocytes Represent Target Cells for Shiga Toxin 1 from Escherichia coli. Infect. Immun. 72: 1896-1905 [Abstract] [Full Text]  
  • Deng, W., Puente, J. L., Gruenheid, S., Li, Y., Vallance, B. A., Vazquez, A., Barba, J., Ibarra, J. A., O'Donnell, P., Metalnikov, P., Ashman, K., Lee, S., Goode, D., Pawson, T., Finlay, B. B. (2004). Dissecting virulence: Systematic and functional analyses of a pathogenicity island. Proc. Natl. Acad. Sci. USA 101: 3597-3602 [Abstract] [Full Text]  
  • Judge, N. A., Mason, H. S., O'Brien, A. D. (2004). Plant Cell-Based Intimin Vaccine Given Orally to Mice Primed with Intimin Reduces Time of Escherichia coli O157:H7 Shedding in Feces. Infect. Immun. 72: 168-175 [Abstract] [Full Text]  
  • Ritchie, J. M., Thorpe, C. M., Rogers, A. B., Waldor, M. K. (2003). Critical Roles for stx2, eae, and tir in Enterohemorrhagic Escherichia coli-Induced Diarrhea and Intestinal Inflammation in Infant Rabbits. Infect. Immun. 71: 7129-7139 [Abstract] [Full Text]  
  • Dean-Nystrom, E. A., Melton-Celsa, A. R., Pohlenz, J. F. L., Moon, H. W., O'Brien, A. D. (2003). Comparative Pathogenicity of Escherichia coli O157 and Intimin-Negative Non-O157 Shiga Toxin-Producing E. coli Strains in Neonatal Pigs. Infect. Immun. 71: 6526-6533 [Abstract] [Full Text]  
  • Ramachandran, V., Brett, K., Hornitzky, M. A., Dowton, M., Bettelheim, K. A., Walker, M. J., Djordjevic, S. P. (2003). Distribution of Intimin Subtypes among Escherichia coli Isolates from Ruminant and Human Sources. J. Clin. Microbiol. 41: 5022-5032 [Abstract] [Full Text]  
  • Stevens, M. P., van Diemen, P. M., Dziva, F., Jones, P. W., Wallis, T. S. (2002). Options for the control of enterohaemorrhagic Escherichia coli in ruminants. Microbiology 148: 3767-3778 [Full Text]  
  • Stevens, M. P., van Diemen, P. M., Frankel, G., Phillips, A. D., Wallis, T. S. (2002). Efa1 Influences Colonization of the Bovine Intestine by Shiga Toxin-Producing Escherichia coli Serotypes O5 and O111. Infect. Immun. 70: 5158-5166 [Abstract] [Full Text]  
  • WALES, A. D., CLIFTON-HADLEY, F. A., COOKSON, A. L., DIBB-FULLER, M. P., LARAGIONE, R. M., PEARSON, G. R., WOODWARD, M. J. (2002). Production of attaching-effacing lesions in ligated large intestine loops of 6-month-old sheep by Escherichia coli O157:H7. J Med Microbiol 51: 755-763 [Abstract] [Full Text]  
  • Dean-Nystrom, E. A., Gansheroff, L. J., Mills, M., Moon, H. W., O'Brien, A. D. (2002). Vaccination of Pregnant Dams with IntiminO157 Protects Suckling Piglets from Escherichia coli O157:H7 Infection. Infect. Immun. 70: 2414-2418 [Abstract] [Full Text]  
  • Reece, S., Simmons, C. P., Fitzhenry, R. J., Batchelor, M., Hale, C., Matthews, S., Phillips, A. D., Dougan, G., Frankel, G. (2002). Mutagenesis of conserved tryptophan residues within the receptor-binding domain of intimin: influence on binding activity and virulence. Microbiology 148: 657-665 [Abstract] [Full Text]  
  • Stevens, M. P., Marches, O., Campbell, J., Huter, V., Frankel, G., Phillips, A. D., Oswald, E., Wallis, T. S. (2002). Intimin, Tir, and Shiga Toxin 1 Do Not Influence Enteropathogenic Responses to Shiga Toxin-Producing Escherichia coli in Bovine Ligated Intestinal Loops. Infect. Immun. 70: 945-952 [Abstract] [Full Text]  
  • Fitzhenry, R J, Pickard, D J, Hartland, E L, Reece, S, Dougan, G, Phillips, A D, Frankel, G (2002). Intimin type influences the site of human intestinal mucosal colonisation by enterohaemorrhagic Escherichia coli O157:H7. Gut 50: 180-185 [Abstract] [Full Text]  
  • Deng, W., Li, Y., Vallance, B. A., Finlay, B. B. (2001). Locus of Enterocyte Effacement from Citrobacter rodentium: Sequence Analysis and Evidence for Horizontal Transfer among Attaching and Effacing Pathogens. Infect. Immun. 69: 6323-6335 [Abstract] [Full Text]  
  • WALES, A. D., PEARSON, G. R., SKUSE, A. M., ROE, J. M., HAYES, C. M., COOKSON, A. L., WOODWARD, M. J. (2001). Attaching and effacing lesions caused by Escherichia coli O157:H7 in experimentally inoculated neonatal lambs. J Med Microbiol 50: 752-758 [Abstract] [Full Text]  
  • Cornick, N. A., Booher, S. L., Casey, T. A., Moon, H. W. (2000). Persistent Colonization of Sheep by Escherichia coli O157:H7 and Other E. coli Pathotypes. Appl. Environ. Microbiol. 66: 4926-4934 [Abstract] [Full Text]  
  • Krejany, E. O., Grant, T. H., Bennett-Wood, V., Adams, L. M., Robins-Browne, R. M. (2000). Contribution of Plasmid-Encoded Fimbriae and Intimin to Capacity of Rabbit-Specific Enteropathogenic Escherichia coli To Attach to and Colonize Rabbit Intestine. Infect. Immun. 68: 6472-6477 [Abstract] [Full Text]  
  • Phillips, A D, Navabpour, S, Hicks, S, Dougan, G, Wallis, T, Frankel, G (2000). Enterohaemorrhagic Escherichia coli O157:H7 target Peyer's patches in humans and cause attaching/effacing lesions in both human and bovine intestine. Gut 47: 377-381 [Abstract] [Full Text]  
  • Magnuson, B. A., Davis, M., Hubele, S., Austin, P. R., Kudva, I. T., Williams, C. J., Hunt, C. W., Hovde, C. J. (2000). Ruminant Gastrointestinal Cell Proliferation and Clearance of Escherichia coli O157:H7. Infect. Immun. 68: 3808-3814 [Abstract] [Full Text]  
  • Marches, O., Nougayrede, J.-P., Boullier, S., Mainil, J., Charlier, G., Raymond, I., Pohl, P., Boury, M., De Rycke, J., Milon, A., Oswald, E. (2000). Role of Tir and Intimin in the Virulence of Rabbit Enteropathogenic Escherichia coli Serotype O103:H2. Infect. Immun. 68: 2171-2182 [Abstract] [Full Text]  
  • Dean-Nystrom, E. A., Pohlenz, J. F. L., Moon, H. W., O'Brien, A. D. (2000). Escherichia coli O157:H7 Causes More-Severe Systemic Disease in Suckling Piglets than in Colostrum-Deprived Neonatal Piglets. Infect. Immun. 68: 2356-2358 [Abstract] [Full Text]  
  • Gansheroff, L. J., O'Brien, A. D. (2000). Escherichia coli O157:H7 in beef cattle presented for slaughter in the U.S.: Higher prevalence rates than previously estimated. Proc. Natl. Acad. Sci. USA 97: 2959-2961 [Full Text]  
  • Price, S. B., Cheng, C.-M., Kaspar, C. W., Wright, J. C., DeGraves, F. J., Penfound, T. A., Castanie-Cornet, M.-P., Foster, J. W. (2000). Role of rpoS in Acid Resistance and Fecal Shedding of Escherichia coli O157:H7. Appl. Environ. Microbiol. 66: 632-637 [Abstract] [Full Text]  
  • Oswald, E., Schmidt, H., Morabito, S., Karch, H., Marches, O., Caprioli, A. (2000). Typing of Intimin Genes in Human and Animal Enterohemorrhagic and Enteropathogenic Escherichia coli: Characterization of a New Intimin Variant. Infect. Immun. 68: 64-71 [Abstract] [Full Text]  
  • Gansheroff, L. J., Wachtel, M. R., O'Brien, A. D. (1999). Decreased Adherence of Enterohemorrhagic Escherichia coli to HEp-2 Cells in the Presence of Antibodies That Recognize the C-Terminal Region of Intimin. Infect. Immun. 67: 6409-6417 [Abstract] [Full Text]  
  • DeVinney, R., Stein, M., Reinscheid, D., Abe, A., Ruschkowski, S., Finlay, B. B. (1999). Enterohemorrhagic Escherichia coli O157:H7 Produces Tir, Which Is Translocated to the Host Cell Membrane but Is Not Tyrosine Phosphorylated. Infect. Immun. 67: 2389-2398 [Abstract] [Full Text]  
  • Sinclair, J. F., O'Brien, A. D. (2002). Cell Surface-localized Nucleolin Is a Eukaryotic Receptor for the Adhesin Intimin-gamma of Enterohemorrhagic Escherichia coli O157:H7. J. Biol. Chem. 277: 2876-2885 [Abstract] [Full Text]  

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Dean-Nystrom, E. A.
Right arrow Articles by O'Brien, A. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Dean-Nystrom, E. A.
Right arrow Articles by O'Brien, A. D.