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1 reports connecting quorum sensing to TTS in enterohemorrhagic and enteropathogenic Escherichia coli
2 protein required for intimate attachment of enterohemorrhagic and enteropathogenic Escherichia coli
7 hanisms for enterotoxigenic, enteroadherent, enterohemorrhagic, and enteroinvasive Escherichia coli.
10 Germany, Escherichia coli O104:H4 caused the enterohemorrhagic E coli (EHEC) outbreak with the highes
11 coli (2.4%), enteroinvasive E. coli (1.2%), enterohemorrhagic E. coli (0.6%), enteroaggregative E. c
13 of enteropathogenic Escherichia coli (EPEC), enterohemorrhagic E. coli (EHEC) and Citrobacter rodenti
14 tonin decreases virulence gene expression by enterohemorrhagic E. coli (EHEC) and Citrobacter rodenti
15 egulated unique gene sets between intestinal enterohemorrhagic E. coli (EHEC) and extraintestinal uro
16 rains of enteropathogenic E. coli (EPEC) and enterohemorrhagic E. coli (EHEC) and in 6 strains origin
17 ein also functions as an adhesion factor for enterohemorrhagic E. coli (EHEC) and Shiga toxin-produci
19 Enteropathogenic Escherichia coli (EPEC) and enterohemorrhagic E. coli (EHEC) are related intestinal
21 gene profile was similar to the profiles of enterohemorrhagic E. coli (EHEC) clones of E. coli: it i
24 enteropathogenic Escherichia coli (EPEC) and enterohemorrhagic E. coli (EHEC) is incompletely underst
25 that an unidentified trans-acting factor in enterohemorrhagic E. coli (EHEC) is responsible for this
26 med that the related LEE-containing pathogen enterohemorrhagic E. coli (EHEC) lacks PerC-dependent ac
28 enteropathogenic Escherichia coli (EPEC) and enterohemorrhagic E. coli (EHEC) might contribute to hos
29 Escherichia coli, Citrobacter rodentium, and enterohemorrhagic E. coli (EHEC) O157:H7 that mediate at
30 styped as enteropathogenic E. coli (EPEC) or enterohemorrhagic E. coli (EHEC) owing to shared traits,
31 Enteropathogenic Escherichia coli (EPEC) and enterohemorrhagic E. coli (EHEC) possess a filamentous t
34 erence of Escherichia coli O157:H7 and other enterohemorrhagic E. coli (EHEC) strains to intestinal e
35 cherichia coli (EPEC), human EPEC, and human enterohemorrhagic E. coli (EHEC) strains, identified cro
37 species of Gram-negative bacteria, including enterohemorrhagic E. coli (EHEC), and as it is essential
38 Stx)-producing Escherichia coli, also called enterohemorrhagic E. coli (EHEC), are important food-bor
40 ee datasets comprising approximately 250,000 enterohemorrhagic E. coli (EHEC), generic E. coli, and S
41 strains can be further classified as either enterohemorrhagic E. coli (EHEC), typical enteropathogen
42 infant diarrhea in the developing world, and enterohemorrhagic E. coli (EHEC), which has caused large
46 , katP, and espP, were acquired later by the enterohemorrhagic E. coli 1 complex in a stepwise manner
47 cluding enteropathogenic E. coli 2 (EPEC 2), enterohemorrhagic E. coli 2 (EHEC 2), and EHEC-O121.
48 y enzyme immunoassay (EIA) (ImmunoCard STAT! enterohemorrhagic E. coli [EHEC]; Meridian Bioscience) a
50 timin is regulated by quorum sensing in both enterohemorrhagic E. coli and enteropathogenic E. coli.
51 d effacing effect characteristic of EPEC and enterohemorrhagic E. coli and has been posited to play s
52 overall sequences of GlnZ from E. coli K-12, Enterohemorrhagic E. coli and Salmonella enterica have s
53 Enteropathogenic Escherichia coli (EPEC) and enterohemorrhagic E. coli are extracellular pathogens th
55 ked other characteristics usually present in enterohemorrhagic E. coli constituted 8.4% of the isolat
56 A three-way genome comparison of the CFT073, enterohemorrhagic E. coli EDL933, and laboratory strain
58 enteropathogenic Escherichia coli (EPEC) and enterohemorrhagic E. coli employ a type 3 secretion syst
60 the toxin-induced renal injury occurring in enterohemorrhagic E. coli infection remains undefined.
63 inase C-zeta by enteropathogenic E. coli and enterohemorrhagic E. coli may in part explain the less p
66 Enteropathogenic Escherichia coli (EPEC) and enterohemorrhagic E. coli O157:H7 (EHEC) form characteri
67 ding uropathogenic E. coli CFT073 and UTI89, enterohemorrhagic E. coli O157:H7, and enterotoxigenic E
68 ) is clinically most closely associated with enterohemorrhagic E. coli O157:H7-mediated hemorrhagic c
70 E. coli K-12, EPEC serotypes H6 and H34, and enterohemorrhagic E. coli serotype H7 all induced IL-8 r
71 Shiga toxin in the highly pathogenic O157:H7 enterohemorrhagic E. coli strain, also carries a gene en
73 ll as enterotoxigenic, enteropathogenic, and enterohemorrhagic E. coli strains, behaved like avirulen
74 se virulence in several pathogens, including enterohemorrhagic E. coli The mechanisms that allow path
76 urella haemolytica leukotoxin (LktA) and the enterohemorrhagic E. coli toxin (EhxA), were also examin
78 kinase C-zeta enzyme activity stimulated by enterohemorrhagic E. coli was transient and minor, and p
79 yers infected by enteropathogenic E. coli or enterohemorrhagic E. coli were used for these studies.
80 Escherichia coli strains (enteroinvasive and enterohemorrhagic E. coli) show low survival whether inc
82 hogens enteropathogenic Escherichia coli and enterohemorrhagic E. coli, adheres to the apical membran
85 E. coli, including enteropathogenic E. coli, enterohemorrhagic E. coli, enterotoxigenic E. coli, and
86 ion of virulence genes characteristic of the enterohemorrhagic E. coli, including intimin, translocat
87 spC from enteropathogenic E. coli, EspP from enterohemorrhagic E. coli, Sat from uropathogenic E. col
95 -based PCR assay was evaluated using various enterohemorrhagic (EHEC) and Shiga-like toxin-producing
98 ion of the attaching and effacing lesions by enterohemorrhagic Escherichia coli (EHEC) and enteropath
110 s of Vibrio cholerae, Vibrio vulnificus, and enterohemorrhagic Escherichia coli (EHEC) GspG were eluc
126 ocus of enterocyte effacement (LEE) genes in enterohemorrhagic Escherichia coli (EHEC) is regulated b
127 2 Salmonella species, 39 Shigella species, 3 enterohemorrhagic Escherichia coli (EHEC) isolates, 2 Ye
128 or Shiga toxins in parallel with the Premier enterohemorrhagic Escherichia coli (EHEC) kit (Meridian
130 la, Campylobacter, and Shiga toxin-producing enterohemorrhagic Escherichia coli (EHEC) O157 in seeded
131 The StcE zinc metalloprotease is secreted by enterohemorrhagic Escherichia coli (EHEC) O157:H7 and co
136 suckling neonatal piglets are susceptible to enterohemorrhagic Escherichia coli (EHEC) O157:H7 diseas
141 pression of the long polar fimbriae (LPF) of enterohemorrhagic Escherichia coli (EHEC) O157:H7 is con
142 ing infection in the gastrointestinal tract, enterohemorrhagic Escherichia coli (EHEC) O157:H7 is exp
145 yte effacement (LEE) pathogenicity island of enterohemorrhagic Escherichia coli (EHEC) O157:H7 posses
150 important reservoir of Shiga toxin-producing enterohemorrhagic Escherichia coli (EHEC) O157:H7 strain
153 ntimin-gamma is an outer membrane protein of enterohemorrhagic Escherichia coli (EHEC) O157:H7 that i
155 operons (LEE1 through LEE4 and tir), enables enterohemorrhagic Escherichia coli (EHEC) O157:H7 to pro
157 various pathogens and specifically focus on enterohemorrhagic Escherichia coli (EHEC) O157:H7, Salmo
167 emic effects of the Shiga toxins produced by enterohemorrhagic Escherichia coli (EHEC) require toxin
173 established how the sensing and response of enterohemorrhagic Escherichia coli (EHEC) to d-serine (d
177 Enteropathogenic Escherichia coli (EPEC) and enterohemorrhagic Escherichia coli (EHEC) utilize a macr
179 erved among the attaching/effacing pathogens enterohemorrhagic Escherichia coli (EHEC), enteropathoge
181 airy manure containing Campylobacter jejuni, enterohemorrhagic Escherichia coli (EHEC), or Salmonella
182 n predominantly associated with infection by enterohemorrhagic Escherichia coli (EHEC), such as E. co
183 on during the course of infection, including enterohemorrhagic Escherichia coli (EHEC), which utilize
190 oded regulator (Ler) of enteropathogenic and enterohemorrhagic Escherichia coli (EPEC and EHEC) funct
191 The human pathogens enteropathogenic and enterohemorrhagic Escherichia coli (EPEC and EHEC) share
194 related human pathogens enteropathogenic and enterohemorrhagic Escherichia coli (EPEC and EHEC, respe
195 homologues of EspJ from enteropathogenic and enterohemorrhagic Escherichia coli (EPEC and EHEC, respe
196 III secretion system of enteropathogenic and enterohemorrhagic Escherichia coli (EPEC and EHEC, respe
197 for the isolation and identification of the enterohemorrhagic Escherichia coli (serotype O157:H7) in
198 tected sRNAs for three predicted toxins from enterohemorrhagic Escherichia coli and Bacillus subtilis
199 dentium is used to model the human pathogens enterohemorrhagic Escherichia coli and enteropathogenic
200 re in children, often follows infection with enterohemorrhagic Escherichia coli and is mediated by th
203 tein (RIP) related to Shiga-like toxins from enterohemorrhagic Escherichia coli and that Howardula ri
204 nterica, Shigella spp., enteropathogenic and enterohemorrhagic Escherichia coli and their murine equi
205 produced by Shigella dysenteriae type 1 and enterohemorrhagic Escherichia coli are the most common c
208 Shiga toxin 1 (Stx-1) and Stx-2 produced by enterohemorrhagic Escherichia coli cause the diarrhea-as
213 II secretion systems of enteropathogenic and enterohemorrhagic Escherichia coli Furthermore, we have
215 nding B subunit of verotoxin VT-1 (VTB) from enterohemorrhagic Escherichia coli in association with t
221 incipal virulence factor of human pathogenic enterohemorrhagic Escherichia coli is Shiga toxin (Stx).
227 Intimin, the product of the eaeA gene in enterohemorrhagic Escherichia coli O157:H7 (EHEC), is re
230 briae) is one of the few adhesive factors of enterohemorrhagic Escherichia coli O157:H7 associated wi
231 ly, the effacement effector protein Tir from enterohemorrhagic Escherichia coli O157:H7 expressed in
234 y was performed to estimate the frequency of enterohemorrhagic Escherichia coli O157:H7 or O157:nonmo
235 enterocyte effacement (LEE) from EDL933, an enterohemorrhagic Escherichia coli O157:H7 serovar origi
238 copy structures for flagellar filaments from enterohemorrhagic Escherichia coli O157:H7, enteropathog
241 ) is associated with intestinal infection by enterohemorrhagic Escherichia coli strains that produce
242 is perceived to be an important property of enterohemorrhagic Escherichia coli strains, enabling the
243 tcE(E447D) is a pan-mucin stain derived from enterohemorrhagic Escherichia coli that is tolerant to a
244 QseC is a membrane sensor kinase shown in enterohemorrhagic Escherichia coli to respond to host an
245 hesis of the AI-3 autoinducer that activates enterohemorrhagic Escherichia coli virulence genes.
246 ), one of the principal virulence factors of enterohemorrhagic Escherichia coli, is encoded by 933W,
247 However, the TTSS of enteropathogenic and enterohemorrhagic Escherichia coli, two important human
260 with a benign Escherichia coli (G58-1) or a enterohemorrhagic strain (933D) derived from O157:H7, an