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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,
5 A multiplex PCR was developed to identify enterotoxigenic, attaching and effacing, and Shiga toxin
6 the entire B. fragilis toxin gene (bft) from enterotoxigenic B. fragilis (ETBF) 86-5443-2-2 is report
7 des fragilis pathogenicity island (BfPAI) in enterotoxigenic B. fragilis (ETBF) strain 86-5443-2-2 an
9 and sensitive assay can be used to identify enterotoxigenic B. fragilis and may be used clinically t
11 fragilis associated with diarrheal disease (enterotoxigenic B. fragilis) produce a 20-kDa zinc-depen
12 associated with diarrhea in children (termed enterotoxigenic B. fragilis, or ETBF) produce a heat-lab
15 n cancer-spared regions is the prevalence of enterotoxigenic bacteria associated with diarrheal disea
16 Infectious diarrhea caused by viruses plus enterotoxigenic bacteria is often more severe than diarr
22 t of gastrointestinal disease, the bacterium enterotoxigenic Bacteroides fragilis (ETBF) is a signifi
28 ed enteric pathogens, Arcobacter species and enterotoxigenic Bacteroides fragilis (ETBF), in 201 U.S.
29 p) (c+/-) mice with the human gut bacterium, enterotoxigenic Bacteroides fragilis (ETBF), to investig
35 rigenesis-including Fusobacterium nucleatum, enterotoxigenic Bacteroides fragilis, and colibactin-pro
36 ssage in the transformants and the naturally enterotoxigenic C. perfringens NCTC 8239 were similar an
37 ingens type A food poisoning, is produced by enterotoxigenic C. perfringens type A isolates when thes
41 teropathogenic Escherichia coli, heat-stable enterotoxigenic E coli, rotavirus, Shigella spp and ente
42 egorized as enteropathogenic E. coli (1.8%), enterotoxigenic E. coli (2.4%), enteroinvasive E. coli (
44 li (EHEC), enteroinvasive E. coli (EIEC) and enterotoxigenic E. coli (ETEC) are major causes of food
45 nteroaggregative Escherichia coli (EAEC) and enterotoxigenic E. coli (ETEC) infection was studied amo
47 rt LT-IIc, a new type II HLT encoded from an enterotoxigenic E. coli (ETEC) strain isolated from an a
48 For comparison, we also sequenced a human enterotoxigenic E. coli (ETEC) strain of the same ST23 s
50 , enteroaggregative Escherichia coli (EAEC), enterotoxigenic E. coli (ETEC), enteropathogenic E. coli
51 or enteropathogenic Escherichia coli (EPEC), enterotoxigenic E. coli (ETEC), Shiga toxin-producing E.
52 tity to proteins of the type IV COF pilus of enterotoxigenic E. coli (ETEC), the toxin co-regulated p
56 including enteroaggregative E. coli [EAEC], enterotoxigenic E. coli [ETEC], enteropathogenic E. coli
57 rrheogenic E. coli, 4 of 43 sauces contained enterotoxigenic E. coli and 14 of 32 contained enteroagg
58 ing those encoding the CS2 and CFA/I pili of enterotoxigenic E. coli and the global regulator virB of
60 ive, attenuated Salmonella vector-expressing enterotoxigenic E. coli fimbriae, colonization factor Ag
62 high morbidity and mortality associated with enterotoxigenic E. coli infection, little is known of th
65 monstrate by multilocus sequence typing that enterotoxigenic E. coli isolates are present in all phyl
67 TI89, enterohemorrhagic E. coli O157:H7, and enterotoxigenic E. coli O78:H11, compared to the parent
68 previously associated with the virulence of enterotoxigenic E. coli revealed that they were not abun
71 ion of the cmlA gene among diverse hemolytic enterotoxigenic E. coli strains demonstrates its broad d
72 to protect against human diarrhea caused by enterotoxigenic E. coli strains that have serologically
73 hemolysin would reduce the ability of F4(+) enterotoxigenic E. coli to cause septicemia in swine fol
74 hought to be essential for the attachment of enterotoxigenic E. coli to the human small intestine ear
77 (STb) in neonatal porcine diarrhea caused by enterotoxigenic E. coli was examined by comparing adhere
78 ization factor antigen I (CFA/I) fimbriae of enterotoxigenic E. coli was proposed to proceed via the
79 at the results obtained here for CS1 pili in enterotoxigenic E. coli will help develop an understandi
80 herichia coli, enteropathogenic E. coli, and enterotoxigenic E. coli), 137 (94.5%) follow-up tests an
81 . coli (EHEC), 41% of 227 EAggEC, 41% of 149 enterotoxigenic E. coli, 22% of 65 enteropathogenic E. c
82 ), a doughnut-shaped oligomeric protein from enterotoxigenic E. coli, activates the TLR2/TLR1 heterod
83 thogenic E. coli, enterohemorrhagic E. coli, enterotoxigenic E. coli, and uropathogenic E. coli, in d
84 eroaggregative E. coli, stIa/stIb and lt for enterotoxigenic E. coli, eaeA for enteropathogenic E. co
85 que features of three unsequenced pathovars, enterotoxigenic E. coli, enteropathogenic E. coli, and e
86 trate that EtpA, a TPS exoprotein adhesin of enterotoxigenic E. coli, mimics and interacts with highl
87 h enteroaggregative Escherichia coli (EAEC), enterotoxigenic E. coli, or Salmonella or Shigella speci
88 gregative E. coli, enteropathogenic E. coli, enterotoxigenic E. coli, Shiga-like toxin-producing E. c
93 Heat-stable enterotoxin (STa), elaborated by enterotoxigenic Echerichia coli, is a worldwide cause of
94 and pathophysiology plus new mechanisms for enterotoxigenic, enteroadherent, enterohemorrhagic, and
95 ultiplex polymerase chain reaction assay for enterotoxigenic, enteroaggregative, and enteropathogenic
96 ly, including Hly- EAggEC strains as well as enterotoxigenic, enteropathogenic, and enterohemorrhagic
97 es screened, as well as lower proportions of enterotoxigenic, enteropathogenic, enterohemorrhagic, an
98 were positive for Shigella sonnei (n = 66), enterotoxigenic Escherichia coli (ETEC) (n = 31) or nega
99 ubstrates: heat-labile enterotoxin (LT) from enterotoxigenic Escherichia coli (ETEC) and cholera toxi
100 This study was designed to determine if enterotoxigenic Escherichia coli (ETEC) and enteroaggreg
103 neri 2a strain CVD 1203 as a live vector for enterotoxigenic Escherichia coli (ETEC) antigens is repo
106 CS1 is the prototype of a class of pili of enterotoxigenic Escherichia coli (ETEC) associated with
111 ation factor antigen I (CFA/I), archetype of enterotoxigenic Escherichia coli (ETEC) Class 5 fimbriae
117 fic activity against colonization factors of enterotoxigenic Escherichia coli (ETEC) could provide pa
119 ity of a recombinant subunit vaccine against enterotoxigenic Escherichia coli (ETEC) delivered by TCI
120 ype of eight genetically related fimbriae of enterotoxigenic Escherichia coli (ETEC) designated class
123 id vectors, we designed SC608 to express the enterotoxigenic Escherichia coli (ETEC) fimbrial subunit
126 nd heat-labile (LT) enterotoxins produced by enterotoxigenic Escherichia coli (ETEC) have been docume
129 n (LT) provides a colonization advantage for enterotoxigenic Escherichia coli (ETEC) in vivo, we hypo
148 oral vaccine against both Shigella spp. and enterotoxigenic Escherichia coli (ETEC) is being develop
154 with clinical and epidemiologic features of enterotoxigenic Escherichia coli (ETEC) occurred among p
155 safety and immunogenicity of an oral, killed enterotoxigenic Escherichia coli (ETEC) plus cholera tox
162 coded on an apparent pathogenicity island of enterotoxigenic Escherichia coli (ETEC) strain H10407, m
171 mber of serologically distinct pili found in enterotoxigenic Escherichia coli (ETEC) strains associat
173 B/c mice by intranasal (i.n.) inoculation of enterotoxigenic Escherichia coli (ETEC) strains H10407 (
179 olonize the small intestine is essential for enterotoxigenic Escherichia coli (ETEC) to cause diarrhe
181 specific polymerase chain reaction (PCR) for enterotoxigenic Escherichia coli (ETEC) toxins after cha
182 terotoxin (LT) is retained on the surface of enterotoxigenic Escherichia coli (ETEC) via an interacti
183 er membrane protein NlpA is repressed by the enterotoxigenic Escherichia coli (ETEC) virulence regula
184 uster of the CS18 (PCFO20) fimbriae of human enterotoxigenic Escherichia coli (ETEC) was found to inc
187 for many Gram-negative pathogens, including enterotoxigenic Escherichia coli (ETEC), a major cause o
189 stinal colonization and diarrheal disease by enterotoxigenic Escherichia coli (ETEC), an E. coli path
192 olunteer challenges with Vibrio cholerae O1, enterotoxigenic Escherichia coli (ETEC), enteropathogeni
194 rototype hybrid vaccine against Shigella and enterotoxigenic Escherichia coli (ETEC), the genes encod
195 ing challenge in developing vaccines against enterotoxigenic Escherichia coli (ETEC), the most common
196 or the detection of Yersinia enterocolitica, enterotoxigenic Escherichia coli (ETEC), Vibrio, and Ple
203 cter jejuni, Salmonella spp., Shigella spp., enterotoxigenic Escherichia coli [ETEC], Shiga toxin-pro
205 ization factor antigen I fimbriae (CFA/I) of enterotoxigenic Escherichia coli and is thought to be es
207 n (nCT) and the heat-labile toxin 1 (nLT) of enterotoxigenic Escherichia coli are AB5-type enterotoxi
211 i-inflammatory Salmonella vaccine expressing enterotoxigenic Escherichia coli colonization factor Ag
216 e with the heat-labile enterotoxin (LT) from enterotoxigenic Escherichia coli elicited the spectrum o
218 s) were fused to a rotavirus enterotoxin and enterotoxigenic Escherichia coli fimbrial antigen genes
219 otein was used to isolate DNA fragments from enterotoxigenic Escherichia coli genomic DNA that carry
223 , and an inverse relationship exists between enterotoxigenic Escherichia coli infections producing th
225 The tip adhesin FasG of the 987P fimbriae of enterotoxigenic Escherichia coli mediates two distinct a
226 igs infected with hemolytic F4(+) strains of enterotoxigenic Escherichia coli often develop septicemi
228 four pathogens: rotavirus, Cryptosporidium, enterotoxigenic Escherichia coli producing heat-stable t
229 g colonization factor antigen I (CFA/I) from enterotoxigenic Escherichia coli results in the rapid on
231 CS1 pili are important virulence factors of enterotoxigenic Escherichia coli strains associated with
233 serologically distinct pili associated with enterotoxigenic Escherichia coli that cause diarrhoea in
236 here is no evidence that Rns, a regulator of enterotoxigenic Escherichia coli virulence genes, respon
239 ercooked scallops (three outbreaks caused by enterotoxigenic Escherichia coli), eggs (two outbreaks c
240 lobacter, Salmonella, and Vibrio species and enterotoxigenic Escherichia coli), only 24% were suscept
241 Although FoodNet surveillance does not cover enterotoxigenic Escherichia coli, a common travel-associ
242 itive stool samples also tested positive for enterotoxigenic Escherichia coli, indicating that dual i
243 Heat-labile enterotoxin (LT), produced by enterotoxigenic Escherichia coli, is a close relative of
246 enteric pathogens include Ascaris, Giardia, enterotoxigenic Escherichia coli, Shigella, and Campylob
247 detection rates >20% were found for each of enterotoxigenic Escherichia coli, Shigella, Campylobacte
248 ain, which degrades enterocyte receptors for enterotoxigenic Escherichia coli, was shown in an experi
255 f HRV against acute diarrhea associated with enterotoxigenic Escherichia coli; it was 4.0% (95% CI, -
256 gella spp., Yersinia spp., Citrobacter spp., enterotoxigenic (ETEC) and enteroaggregative E. coli (EA
258 Escherichia coli O148 is a nonencapsulated enterotoxigenic (ETEC) Gram negative bacterium that can
259 mannose-sensitive hemagglutinin (MSHA), and enterotoxigenic hemolysin (HlyA); C-II encodes a variant
261 gene sequences were detected in eight known enterotoxigenic human isolates and nine enterotoxigenic
264 ) concentration observed during infection by enterotoxigenic organisms retards the intestinal repair
265 gs of the stbDE genes were identified on the enterotoxigenic plasmid P307 from Escherichia coli and o
268 could be used to look at the epidemiology of enterotoxigenic strains of B. fragilis in clinical infec
271 secretory diarrhea induced by infection with enterotoxigenic strains of Escherichia coli involves bin
273 The FasG subunit of the 987P fimbriae of enterotoxigenic strains of Escherichia coli was previous
276 the pathogenicity islet from two additional enterotoxigenic strains, along with PCR analysis of 20 a
277 ns, along with PCR analysis of 20 additional enterotoxigenic strains, revealed that the islet is inse
278 a duplex PCR assay that can rapidly genotype enterotoxigenic type A isolates (i.e., determine whether
279 Previous studies have determined that the enterotoxigenic type A isolates causing both non-food-bo
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