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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 |
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 |
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
86-24eae
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
86-24eae
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.
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 86-24eae
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
86-24eae
10, with B2F1, or with nonpathogenic control strain 123 remained healthy throughout the experiment.
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TABLE 2.
Clinical and histological findings in calves 18 and
42 h after inoculation with an eae+ EHEC
strain [86-24 or 86-24eae 10(pEB310)], an
eae mutant EHEC strain (86-24eae 10), or a
strain lacking the eae gene (B2F1 or nonpathogenic E. coli 123)
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Hyperemia, focal petechiae, and fibrinous exudates in the intestines
were common postmortem observations in calves inoculated with strain
86-24 or 86-24eae
10(pEB310) but were not noted in any of
the calves inoculated with mutant strain 86-24eae
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
86-24eae
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 86-24eae
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
86-24eae
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 86-24eae
10, but these bacteria were not associated with
A/E lesions.

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FIG. 1.
Electron micrograph of absorptive cells from the ileum
of a calf 18 h after inoculation with EHEC O157:H7 strain
86-24eae 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.
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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 86-24eae
10), or 100 µg of ampicillin and 34 µg of chloramphenicol per ml
[strain 86-24eae
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.).

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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 86-24eae 10(pEB310), eae mutant EHEC
strain 86-24eae 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.
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Greater numbers of the inoculated organisms were recovered from the
intestines of calves inoculated with strain 86-24 or strain 86-24eae
10(pEB310) than from those of calves inoculated
with strain 86-24eae
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
86-24eae
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
86-24eae
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 86-24eae
10(pEB310) had bacterial levels comparable to those in calves inoculated with strains that lacked the eae gene. The numbers for strains
86-24eae
10 and B2F1 were similar to those for control
strain 123. The number of strain 86-24eae
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.

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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 86-24eae 10(pEB310), eae
mutant EHEC strain 86-24eae 10, strain B2F1, or E. coli control strain 123. Sp., spiral.
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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
86-24eae
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).
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TABLE 3.
Findings in CDCD piglets at 18 h after inoculation
with an eae+ [86-24 or
86-24eae 10(pEB310)] or an eae mutant
(86-24eae 10) EHEC strain or nonpathogenic E. coli 123
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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
 |
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0019-9567/98/$00.00+0
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Jordan, D. M., Booher, S. L., Moon, H. W.
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Jordan, D. M., Cornick, N., Torres, A. G., Dean-Nystrom, E. A., Kaper, J. B., Moon, H. W.
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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.
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Vlisidou, I., Lyte, M., van Diemen, P. M., Hawes, P., Monaghan, P., Wallis, T. S., Stevens, M. P.
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Cobbold, R. N., Rice, D. H., Szymanski, M., Call, D. R., Hancock, D. D.
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Judge, N. A., Mason, H. S., O'Brien, A. D.
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Dean-Nystrom, E. A., Melton-Celsa, A. R., Pohlenz, J. F. L., Moon, H. W., O'Brien, A. D.
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WALES, A. D., CLIFTON-HADLEY, F. A., COOKSON, A. L., DIBB-FULLER, M. P., LARAGIONE, R. M., PEARSON, G. R., WOODWARD, M. J.
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Dean-Nystrom, E. A., Gansheroff, L. J., Mills, M., Moon, H. W., O'Brien, A. D.
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Stevens, M. P., Marches, O., Campbell, J., Huter, V., Frankel, G., Phillips, A. D., Oswald, E., Wallis, T. S.
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