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1 ndrome secretes blended virulence factors of enterohaemorrhagic and enteroaggregative E. coli, but th
2 tes virulence gene expression and attenuates enterohaemorrhagic and uropathogenic Escherichia coli (E
3 Enteropathogenic Escherichia coli (EPEC) and enterohaemorrhagic E. coli (EHEC) each promote the reorg
4                                         Only enterohaemorrhagic E. coli (EHEC) possess a sequence var
5                                              Enterohaemorrhagic E. coli (EHEC) utilises the pathogeni
6 e pathobiont Enterococcus faecalis increases enterohaemorrhagic E. coli (EHEC) virulence by upregulat
7    EspF(U), a protein secreted by pathogenic enterohaemorrhagic E. coli (EHEC), activates N-WASp/WASp
8 , including enteropathogenic E. coli (EPEC), enterohaemorrhagic E. coli (EHEC), enteroinvasive E. col
9 y islands in uropathogenic Escherichia coli, enterohaemorrhagic E. coli and Salmonella enterica.
10 ulence factors (stx, bfpA) that characterize enterohaemorrhagic E. coli and typical EPEC, respectivel
11                       We show that pnrf from enterohaemorrhagic E. coli is more active than its K-12
12                                          The enterohaemorrhagic E. coli O157:H7 (EHEC) Tir molecule i
13  The hallmark of enteropathogenic (EPEC) and enterohaemorrhagic (EHEC) Escherchia coli adhesion to ho
14 ically significant enteric pathogens such as enterohaemorrhagic Escherichia coli (EHEC) and enteropat
15 ization of their ruminant reservoir hosts by enterohaemorrhagic Escherichia coli (EHEC) and might als
16  been observed only in few strains including Enterohaemorrhagic Escherichia coli (EHEC) and their ind
17                                              Enterohaemorrhagic Escherichia coli (EHEC) are highly in
18                                              Enterohaemorrhagic Escherichia coli (EHEC) colonizes the
19                                              Enterohaemorrhagic Escherichia coli (EHEC) comprise a gr
20                  Enteropathogenic (EPEC) and enterohaemorrhagic Escherichia coli (EHEC) constitute a
21                                              Enterohaemorrhagic Escherichia coli (EHEC) employs a typ
22                                              Enterohaemorrhagic Escherichia coli (EHEC) has emerged a
23                  Attachment to host cells by enterohaemorrhagic Escherichia coli (EHEC) is associated
24 Colonization of the intestinal epithelium by enterohaemorrhagic Escherichia coli (EHEC) is characteri
25                                              Enterohaemorrhagic Escherichia coli (EHEC) O157:H7 as we
26                The gastrointestinal pathogen enterohaemorrhagic Escherichia coli (EHEC) relies on int
27                                              Enterohaemorrhagic Escherichia coli (EHEC) serotype O157
28 ve identified and characterized a protein of enterohaemorrhagic Escherichia coli (EHEC) serotype O157
29 st against enteric pathogens(1-3), including enterohaemorrhagic Escherichia coli (EHEC) serotype O157
30                            During infection, enterohaemorrhagic Escherichia coli (EHEC) takes over th
31 ative pathogens, enteropathogenic (EPEC) and enterohaemorrhagic Escherichia coli (EHEC) use a macromo
32         Here, we explored the role of Hfq in enterohaemorrhagic Escherichia coli (EHEC), a group of n
33 t is widely encoded by the zoonotic pathogen enterohaemorrhagic Escherichia coli (EHEC), required for
34                  We previously reported that enterohaemorrhagic Escherichia coli (EHEC), which is res
35 ting virulence gene expression in pathogenic enterohaemorrhagic Escherichia coli (EHEC).
36 he course of infection, enteropathogenic and enterohaemorrhagic Escherichia coli (EPEC and EHEC, resp
37                         Enteropathogenic and enterohaemorrhagic Escherichia coli (EPEC/EHEC) manipula
38                           Here, we show that enterohaemorrhagic Escherichia coli and Citrobacter rode
39 ins of intimin (Int) of enteropathogenic and enterohaemorrhagic Escherichia coli and invasin (Inv) of
40                         Enteropathogenic and enterohaemorrhagic Escherichia coli are closely related
41                                              Enterohaemorrhagic Escherichia coli attaches to the inte
42                                              Enterohaemorrhagic Escherichia coli harbours a pathogeni
43 d during infection with enteropathogenic and enterohaemorrhagic Escherichia coli inhibiting host cell
44  the locus of enterocyte effacement (LEE) in enterohaemorrhagic Escherichia coli is primarily co-ordi
45 ied horizontally acquired genomic regions of enterohaemorrhagic Escherichia coli O157:H7 that regulat
46                         Here we identify the enterohaemorrhagic Escherichia coli O157:H7 type III eff
47 ga toxin genes that enhance pathogenicity of enterohaemorrhagic Escherichia coli strain O157:H7, also
48  intimate attachment of enteropathogenic and enterohaemorrhagic Escherichia coli to mammalian host ce
49  attaching and effacing enteropathogenic and enterohaemorrhagic Escherichia coli, impairs the charact
50 key virulence factor of enteropathogenic and enterohaemorrhagic Escherichia coli, playing roles in ba
51                      In enteropathogenic and enterohaemorrhagic Escherichia coli, SepL and SepD are e
52 ogens such as Salmonella, Vibrio cholerae or enterohaemorrhagic Escherichia coli.
53 ic pathogens, including enteropathogenic and enterohaemorrhagic Escherichia coli.
54  to plant tissue for the foodborne pathogen, enterohaemorrhagic Escherichia coli.
55        In contrast, the efeUOB operon of the enterohaemorrhagic strain, O157:H7, lacks any frameshift
56 unds: enteropathogenic E. coli E2348-69, and enterohaemorrhagic strains Sakai and NCTC12900.
57 e 3 secretion system synonymous with typical enterohaemorrhagic strains.