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1 ee datasets comprising approximately 250,000 enterohemorrhagic E. coli (EHEC), generic E. coli, and S
2  coli (2.4%), enteroinvasive E. coli (1.2%), enterohemorrhagic E. coli (0.6%), enteroaggregative E. c
3 cluding enteropathogenic E. coli 2 (EPEC 2), enterohemorrhagic E. coli 2 (EHEC 2), and EHEC-O121.
4        Enteropathogenic Escherichia coli and enterohemorrhagic E. coli cause an inflammatory colitis
5        Enteropathogenic Escherichia coli and enterohemorrhagic E. coli harbor highly homologous patho
6 sis of enteropathogenic Escherichia coli and enterohemorrhagic E. coli infection.
7 inase C-zeta by enteropathogenic E. coli and enterohemorrhagic E. coli may in part explain the less p
8 hogens enteropathogenic Escherichia coli and enterohemorrhagic E. coli, adheres to the apical membran
9  infection with enteropathogenic E. coli and enterohemorrhagic E. coli.
10 hogens enteropathogenic Escherichia coli and enterohemorrhagic E. coli.
11 Escherichia coli strains (enteroinvasive and enterohemorrhagic E. coli) show low survival whether inc
12 ll as enterotoxigenic, enteropathogenic, and enterohemorrhagic E. coli strains, behaved like avirulen
13 d effacing effect characteristic of EPEC and enterohemorrhagic E. coli and has been posited to play s
14 rains of enteropathogenic E. coli (EPEC) and enterohemorrhagic E. coli (EHEC) and in 6 strains origin
15 Enteropathogenic Escherichia coli (EPEC) and enterohemorrhagic E. coli (EHEC) are related intestinal
16 enteropathogenic Escherichia coli (EPEC) and enterohemorrhagic E. coli (EHEC) is incompletely underst
17 enteropathogenic Escherichia coli (EPEC) and enterohemorrhagic E. coli (EHEC) might contribute to hos
18 Enteropathogenic Escherichia coli (EPEC) and enterohemorrhagic E. coli (EHEC) possess a filamentous t
19 Enteropathogenic Escherichia coli (EPEC) and enterohemorrhagic E. coli are extracellular pathogens th
20 enteropathogenic Escherichia coli (EPEC) and enterohemorrhagic E. coli employ a type 3 secretion syst
21 Enteropathogenic Escherichia coli (EPEC) and enterohemorrhagic E. coli O157:H7 (EHEC) form characteri
22 E. coli K-12, EPEC serotypes H6 and H34, and enterohemorrhagic E. coli serotype H7 all induced IL-8 r
23 enteropathogenic E. coli (EPEC, O127:H6) and enterohemorrhagic E. coli (EHEC, O157:H7) strains.
24 Escherichia coli, Citrobacter rodentium, and enterohemorrhagic E. coli (EHEC) O157:H7 that mediate at
25 pervirulent E. coli subtypes of Shigella and enterohemorrhagic E. coli.
26 infant diarrhea in the developing world, and enterohemorrhagic E. coli (EHEC), which has caused large
27 higa-toxigenic E. coli (STEC), also known as enterohemorrhagic E. coli (EHEC).
28 timin is regulated by quorum sensing in both enterohemorrhagic E. coli and enteropathogenic E. coli.
29 was not better at preventing colonization by enterohemorrhagic E. coli EDL933.
30 tonin decreases virulence gene expression by enterohemorrhagic E. coli (EHEC) and Citrobacter rodenti
31  kinase C-zeta enzyme activity stimulated by enterohemorrhagic E. coli was transient and minor, and p
32 Stx)-producing Escherichia coli, also called enterohemorrhagic E. coli (EHEC), are important food-bor
33 A three-way genome comparison of the CFT073, enterohemorrhagic E. coli EDL933, and laboratory strain
34 te a Shiga toxin producing Escherichia coli (enterohemorrhagic E. coli) without harmful effects.
35 E. coli, including enteropathogenic E. coli, enterohemorrhagic E. coli, enterotoxigenic E. coli, and
36           Enteropathogenic Escherichia coli, enterohemorrhagic E. coli, and Citrobacter rodentium are
37           Enteropathogenic Escherichia coli, enterohemorrhagic E. coli, and Citrobacter rodentium are
38  strains can be further classified as either enterohemorrhagic E. coli (EHEC), typical enteropathogen
39 of enteropathogenic Escherichia coli (EPEC), enterohemorrhagic E. coli (EHEC) and Citrobacter rodenti
40                                          For enterohemorrhagic E. coli (EHEC) serotype O157:H7, we ha
41 ein also functions as an adhesion factor for enterohemorrhagic E. coli (EHEC) and Shiga toxin-produci
42 spC from enteropathogenic E. coli, EspP from enterohemorrhagic E. coli, Sat from uropathogenic E. col
43            One hundred percent of 75 O157:H7 enterohemorrhagic E. coli (EHEC), 41% of 227 EAggEC, 41%
44 Shiga toxin in the highly pathogenic O157:H7 enterohemorrhagic E. coli strain, also carries a gene en
45 cherichia coli (EPEC), human EPEC, and human enterohemorrhagic E. coli (EHEC) strains, identified cro
46                                           In enterohemorrhagic E. coli (EHEC), especially serotype O1
47  that an unidentified trans-acting factor in enterohemorrhagic E. coli (EHEC) is responsible for this
48  the toxin-induced renal injury occurring in enterohemorrhagic E. coli infection remains undefined.
49 ked other characteristics usually present in enterohemorrhagic E. coli constituted 8.4% of the isolat
50 species of Gram-negative bacteria, including enterohemorrhagic E. coli (EHEC), and as it is essential
51 se virulence in several pathogens, including enterohemorrhagic E. coli The mechanisms that allow path
52 egulated unique gene sets between intestinal enterohemorrhagic E. coli (EHEC) and extraintestinal uro
53 nt role in determining the infective dose of enterohemorrhagic E. coli.
54 s closely related to plasmid-encoded KatP of enterohemorrhagic E. coli O157:H7 (75% identity).
55                Within the O157:H7 lineage of enterohemorrhagic E. coli, strain-to-strain variation in
56  gene profile was similar to the profiles of enterohemorrhagic E. coli (EHEC) clones of E. coli: it i
57 herichia coli O157:H7 and other serotypes of enterohemorrhagic E. coli (EHEC).
58 enic E. coli are more profound than those of enterohemorrhagic E. coli.
59 yers infected by enteropathogenic E. coli or enterohemorrhagic E. coli were used for these studies.
60 styped as enteropathogenic E. coli (EPEC) or enterohemorrhagic E. coli (EHEC) owing to shared traits,
61 erence of Escherichia coli O157:H7 and other enterohemorrhagic E. coli (EHEC) strains to intestinal e
62 med that the related LEE-containing pathogen enterohemorrhagic E. coli (EHEC) lacks PerC-dependent ac
63 rowth of intestinal E. coli, both pathogenic enterohemorrhagic E. coli and commensal strains.
64 y enzyme immunoassay (EIA) (ImmunoCard STAT! enterohemorrhagic E. coli [EHEC]; Meridian Bioscience) a
65                                          The enterohemorrhagic E. coli NleH1 effector prevents the nu
66 urella haemolytica leukotoxin (LktA) and the enterohemorrhagic E. coli toxin (EhxA), were also examin
67 , katP, and espP, were acquired later by the enterohemorrhagic E. coli 1 complex in a stepwise manner
68 ion of virulence genes characteristic of the enterohemorrhagic E. coli, including intimin, translocat
69                                         This enterohemorrhagic E. coli toxin (Ehx) is a newly describ
70                                        Thus, enterohemorrhagic E. coli translocates 2 effectors that
71 ding uropathogenic E. coli CFT073 and UTI89, enterohemorrhagic E. coli O157:H7, and enterotoxigenic E
72 rotype is a recent precursor to the virulent enterohemorrhagic E. coli O157:H7.
73                 Pathogenesis associated with enterohemorrhagic E. coli involves direct delivery of vi
74 ) is clinically most closely associated with enterohemorrhagic E. coli O157:H7-mediated hemorrhagic c
75  we also studied C57BL/6J mice infected with enterohemorrhagic E. coli (EHEC) by gavage.
76          We observed similar phenotypes with enterohemorrhagic E. coli, showing that this is not a UP