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2 function revealed a coordinated response to enterotoxigenic and enteropathogenic E. coli infections.
3 diarrheagenic Escherichia coli, particularly enterotoxigenic and enteropathogenic E. coli, rotavirus,
6 A multiplex PCR was developed to identify enterotoxigenic, attaching and effacing, and Shiga toxin
7 the entire B. fragilis toxin gene (bft) from enterotoxigenic B. fragilis (ETBF) 86-5443-2-2 is report
8 des fragilis pathogenicity island (BfPAI) in enterotoxigenic B. fragilis (ETBF) strain 86-5443-2-2 an
10 and sensitive assay can be used to identify enterotoxigenic B. fragilis and may be used clinically t
12 fragilis associated with diarrheal disease (enterotoxigenic B. fragilis) produce a 20-kDa zinc-depen
13 associated with diarrhea in children (termed enterotoxigenic B. fragilis, or ETBF) produce a heat-lab
16 n cancer-spared regions is the prevalence of enterotoxigenic bacteria associated with diarrheal disea
17 Infectious diarrhea caused by viruses plus enterotoxigenic bacteria is often more severe than diarr
24 t of gastrointestinal disease, the bacterium enterotoxigenic Bacteroides fragilis (ETBF) is a signifi
30 ed enteric pathogens, Arcobacter species and enterotoxigenic Bacteroides fragilis (ETBF), in 201 U.S.
31 p) (c+/-) mice with the human gut bacterium, enterotoxigenic Bacteroides fragilis (ETBF), to investig
36 rigenesis-including Fusobacterium nucleatum, enterotoxigenic Bacteroides fragilis, and colibactin-pro
37 ingens type A food poisoning, is produced by enterotoxigenic C. perfringens type A isolates when thes
41 ths), and 0.3 versus 0.1 (24-59 months); for enterotoxigenic E coli encoding heat-stable toxin was 4.
42 h typical enteropathogenic Escherichia coli, enterotoxigenic E coli encoding heat-stable toxin, enter
44 rventions targeting rotavirus, Shigella spp, enterotoxigenic E coli producing heat-stable toxin, and
46 teropathogenic Escherichia coli, heat-stable enterotoxigenic E coli, rotavirus, Shigella spp and ente
48 egorized as enteropathogenic E. coli (1.8%), enterotoxigenic E. coli (2.4%), enteroinvasive E. coli (
50 li (EHEC), enteroinvasive E. coli (EIEC) and enterotoxigenic E. coli (ETEC) are major causes of food
51 nteroaggregative Escherichia coli (EAEC) and enterotoxigenic E. coli (ETEC) infection was studied amo
53 rt LT-IIc, a new type II HLT encoded from an enterotoxigenic E. coli (ETEC) strain isolated from an a
54 For comparison, we also sequenced a human enterotoxigenic E. coli (ETEC) strain of the same ST23 s
56 , enteroaggregative Escherichia coli (EAEC), enterotoxigenic E. coli (ETEC), enteropathogenic E. coli
57 or enteropathogenic Escherichia coli (EPEC), enterotoxigenic E. coli (ETEC), Shiga toxin-producing E.
58 tity to proteins of the type IV COF pilus of enterotoxigenic E. coli (ETEC), the toxin co-regulated p
62 oli [EAEC], enteropathogenic E. coli [EPEC], enterotoxigenic E. coli [ETEC], enteroinvasive E. coli,
63 including enteroaggregative E. coli [EAEC], enterotoxigenic E. coli [ETEC], enteropathogenic E. coli
64 rrheogenic E. coli, 4 of 43 sauces contained enterotoxigenic E. coli and 14 of 32 contained enteroagg
65 ibodies that recognize antigens expressed by enterotoxigenic E. coli and other Enterobacteriaceae spe
66 ing those encoding the CS2 and CFA/I pili of enterotoxigenic E. coli and the global regulator virB of
68 ive, attenuated Salmonella vector-expressing enterotoxigenic E. coli fimbriae, colonization factor Ag
69 individuals per compound, the prevalence of enterotoxigenic E. coli genes on child hands was lower i
72 high morbidity and mortality associated with enterotoxigenic E. coli infection, little is known of th
75 monstrate by multilocus sequence typing that enterotoxigenic E. coli isolates are present in all phyl
77 TI89, enterohemorrhagic E. coli O157:H7, and enterotoxigenic E. coli O78:H11, compared to the parent
78 previously associated with the virulence of enterotoxigenic E. coli revealed that they were not abun
81 ion of the cmlA gene among diverse hemolytic enterotoxigenic E. coli strains demonstrates its broad d
82 to protect against human diarrhea caused by enterotoxigenic E. coli strains that have serologically
83 hemolysin would reduce the ability of F4(+) enterotoxigenic E. coli to cause septicemia in swine fol
84 hought to be essential for the attachment of enterotoxigenic E. coli to the human small intestine ear
87 (STb) in neonatal porcine diarrhea caused by enterotoxigenic E. coli was examined by comparing adhere
88 ization factor antigen I (CFA/I) fimbriae of enterotoxigenic E. coli was proposed to proceed via the
89 at the results obtained here for CS1 pili in enterotoxigenic E. coli will help develop an understandi
90 herichia coli, enteropathogenic E. coli, and enterotoxigenic E. coli), 137 (94.5%) follow-up tests an
91 ), a doughnut-shaped oligomeric protein from enterotoxigenic E. coli, activates the TLR2/TLR1 heterod
92 thogenic E. coli, enterohemorrhagic E. coli, enterotoxigenic E. coli, and uropathogenic E. coli, in d
93 eroaggregative E. coli, stIa/stIb and lt for enterotoxigenic E. coli, eaeA for enteropathogenic E. co
94 que features of three unsequenced pathovars, enterotoxigenic E. coli, enteropathogenic E. coli, and e
95 trate that EtpA, a TPS exoprotein adhesin of enterotoxigenic E. coli, mimics and interacts with highl
96 h enteroaggregative Escherichia coli (EAEC), enterotoxigenic E. coli, or Salmonella or Shigella speci
97 Bentero containing epitopes from antigens of enterotoxigenic E. coli, S. typhimurium, and V. parahaem
98 i O157, other Shiga toxin-producing E. coli, enterotoxigenic E. coli, Salmonella, Shigella, Vibrio, a
99 gregative E. coli, enteropathogenic E. coli, enterotoxigenic E. coli, Shiga-like toxin-producing E. c
104 Heat-stable enterotoxin (STa), elaborated by enterotoxigenic Echerichia coli, is a worldwide cause of
105 ultiplex polymerase chain reaction assay for enterotoxigenic, enteroaggregative, and enteropathogenic
106 ly, including Hly- EAggEC strains as well as enterotoxigenic, enteropathogenic, and enterohemorrhagic
107 es screened, as well as lower proportions of enterotoxigenic, enteropathogenic, enterohemorrhagic, an
108 were positive for Shigella sonnei (n = 66), enterotoxigenic Escherichia coli (ETEC) (n = 31) or nega
109 ubstrates: heat-labile enterotoxin (LT) from enterotoxigenic Escherichia coli (ETEC) and cholera toxi
110 This study was designed to determine if enterotoxigenic Escherichia coli (ETEC) and enteroaggreg
113 dity, and childhood stunting attributable to enterotoxigenic Escherichia coli (ETEC) and shigella inf
118 CS1 is the prototype of a class of pili of enterotoxigenic Escherichia coli (ETEC) associated with
124 ation factor antigen I (CFA/I), archetype of enterotoxigenic Escherichia coli (ETEC) Class 5 fimbriae
131 fic activity against colonization factors of enterotoxigenic Escherichia coli (ETEC) could provide pa
133 ity of a recombinant subunit vaccine against enterotoxigenic Escherichia coli (ETEC) delivered by TCI
134 ype of eight genetically related fimbriae of enterotoxigenic Escherichia coli (ETEC) designated class
137 of an animal model that closely approximates enterotoxigenic Escherichia coli (ETEC) disease in human
138 id vectors, we designed SC608 to express the enterotoxigenic Escherichia coli (ETEC) fimbrial subunit
141 nd heat-labile (LT) enterotoxins produced by enterotoxigenic Escherichia coli (ETEC) have been docume
144 n (LT) provides a colonization advantage for enterotoxigenic Escherichia coli (ETEC) in vivo, we hypo
164 oral vaccine against both Shigella spp. and enterotoxigenic Escherichia coli (ETEC) is being develop
170 antigen expressed in nearly 20% of clinical enterotoxigenic Escherichia coli (ETEC) isolates, is com
171 with clinical and epidemiologic features of enterotoxigenic Escherichia coli (ETEC) occurred among p
172 safety and immunogenicity of an oral, killed enterotoxigenic Escherichia coli (ETEC) plus cholera tox
178 coded on an apparent pathogenicity island of enterotoxigenic Escherichia coli (ETEC) strain H10407, m
187 mber of serologically distinct pili found in enterotoxigenic Escherichia coli (ETEC) strains associat
189 B/c mice by intranasal (i.n.) inoculation of enterotoxigenic Escherichia coli (ETEC) strains H10407 (
195 olonize the small intestine is essential for enterotoxigenic Escherichia coli (ETEC) to cause diarrhe
197 specific polymerase chain reaction (PCR) for enterotoxigenic Escherichia coli (ETEC) toxins after cha
199 terotoxin (LT) is retained on the surface of enterotoxigenic Escherichia coli (ETEC) via an interacti
200 er membrane protein NlpA is repressed by the enterotoxigenic Escherichia coli (ETEC) virulence regula
201 uster of the CS18 (PCFO20) fimbriae of human enterotoxigenic Escherichia coli (ETEC) was found to inc
204 for many Gram-negative pathogens, including enterotoxigenic Escherichia coli (ETEC), a major cause o
206 stinal colonization and diarrheal disease by enterotoxigenic Escherichia coli (ETEC), an E. coli path
209 olunteer challenges with Vibrio cholerae O1, enterotoxigenic Escherichia coli (ETEC), enteropathogeni
211 rototype hybrid vaccine against Shigella and enterotoxigenic Escherichia coli (ETEC), the genes encod
212 ing challenge in developing vaccines against enterotoxigenic Escherichia coli (ETEC), the most common
213 or the detection of Yersinia enterocolitica, enterotoxigenic Escherichia coli (ETEC), Vibrio, and Ple
221 cter jejuni, Salmonella spp., Shigella spp., enterotoxigenic Escherichia coli [ETEC], Shiga toxin-pro
222 ization factor antigen I fimbriae (CFA/I) of enterotoxigenic Escherichia coli and is thought to be es
224 n (nCT) and the heat-labile toxin 1 (nLT) of enterotoxigenic Escherichia coli are AB5-type enterotoxi
225 olerae and heat-labile enterotoxin (LT) from enterotoxigenic Escherichia coli are notorious for their
229 ted from infection with the enteric pathogen enterotoxigenic Escherichia coli by maternal natural IgG
231 i-inflammatory Salmonella vaccine expressing enterotoxigenic Escherichia coli colonization factor Ag
235 e with the heat-labile enterotoxin (LT) from enterotoxigenic Escherichia coli elicited the spectrum o
236 were due to rotavirus, Cryptosporidium spp, enterotoxigenic Escherichia coli encoding heat-stable to
238 s) were fused to a rotavirus enterotoxin and enterotoxigenic Escherichia coli fimbrial antigen genes
239 otein was used to isolate DNA fragments from enterotoxigenic Escherichia coli genomic DNA that carry
241 sed Organ-Chips (Intestine-Chips) exposed to enterotoxigenic Escherichia coli heat-stable enterotoxin
244 , and an inverse relationship exists between enterotoxigenic Escherichia coli infections producing th
246 The tip adhesin FasG of the 987P fimbriae of enterotoxigenic Escherichia coli mediates two distinct a
247 igs infected with hemolytic F4(+) strains of enterotoxigenic Escherichia coli often develop septicemi
249 four pathogens: rotavirus, Cryptosporidium, enterotoxigenic Escherichia coli producing heat-stable t
250 g colonization factor antigen I (CFA/I) from enterotoxigenic Escherichia coli results in the rapid on
252 CS1 pili are important virulence factors of enterotoxigenic Escherichia coli strains associated with
254 serologically distinct pili associated with enterotoxigenic Escherichia coli that cause diarrhoea in
257 here is no evidence that Rns, a regulator of enterotoxigenic Escherichia coli virulence genes, respon
260 lobacter, Salmonella, and Vibrio species and enterotoxigenic Escherichia coli), only 24% were suscept
261 Although FoodNet surveillance does not cover enterotoxigenic Escherichia coli, a common travel-associ
262 , particularly for noroviruses, rotaviruses, enterotoxigenic Escherichia coli, and Campylobacter jeju
263 itive stool samples also tested positive for enterotoxigenic Escherichia coli, indicating that dual i
266 enteric pathogens include Ascaris, Giardia, enterotoxigenic Escherichia coli, Shigella, and Campylob
267 detection rates >20% were found for each of enterotoxigenic Escherichia coli, Shigella, Campylobacte
268 Entamoeba histolytica, Salmonella enterica, enterotoxigenic Escherichia coli, Vibrio cholerae, Campy
269 ain, which degrades enterocyte receptors for enterotoxigenic Escherichia coli, was shown in an experi
276 f HRV against acute diarrhea associated with enterotoxigenic Escherichia coli; it was 4.0% (95% CI, -
278 gella spp., Yersinia spp., Citrobacter spp., enterotoxigenic (ETEC) and enteroaggregative E. coli (EA
280 Escherichia coli O148 is a nonencapsulated enterotoxigenic (ETEC) Gram negative bacterium that can
281 mannose-sensitive hemagglutinin (MSHA), and enterotoxigenic hemolysin (HlyA); C-II encodes a variant
283 gene sequences were detected in eight known enterotoxigenic human isolates and nine enterotoxigenic
285 ) concentration observed during infection by enterotoxigenic organisms retards the intestinal repair
286 gs of the stbDE genes were identified on the enterotoxigenic plasmid P307 from Escherichia coli and o
289 could be used to look at the epidemiology of enterotoxigenic strains of B. fragilis in clinical infec
292 secretory diarrhea induced by infection with enterotoxigenic strains of Escherichia coli involves bin
294 The FasG subunit of the 987P fimbriae of enterotoxigenic strains of Escherichia coli was previous
297 the pathogenicity islet from two additional enterotoxigenic strains, along with PCR analysis of 20 a
298 ns, along with PCR analysis of 20 additional enterotoxigenic strains, revealed that the islet is inse
299 a duplex PCR assay that can rapidly genotype enterotoxigenic type A isolates (i.e., determine whether
300 Previous studies have determined that the enterotoxigenic type A isolates causing both non-food-bo