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1 g colonization factor antigen I (CFA/I) from enterotoxigenic Escherichia coli.
2 s an important virulence factor expressed by enterotoxigenic Escherichia coli.
3 cally secreted onto the surface of wild type enterotoxigenic Escherichia coli.
4 essing colonization factor Ag I (CFA/I) from enterotoxigenic Escherichia coli.
5 detoxified form of the heat-labile toxin of enterotoxigenic Escherichia coli.
6 ppendages found on the surface of strains of enterotoxigenic Escherichia coli.
7 Although FoodNet surveillance does not cover enterotoxigenic Escherichia coli, a common travel-associ
9 ization factor antigen I fimbriae (CFA/I) of enterotoxigenic Escherichia coli and is thought to be es
11 n (nCT) and the heat-labile toxin 1 (nLT) of enterotoxigenic Escherichia coli are AB5-type enterotoxi
16 i-inflammatory Salmonella vaccine expressing enterotoxigenic Escherichia coli colonization factor Ag
19 ercooked scallops (three outbreaks caused by enterotoxigenic Escherichia coli), eggs (two outbreaks c
21 e with the heat-labile enterotoxin (LT) from enterotoxigenic Escherichia coli elicited the spectrum o
22 were positive for Shigella sonnei (n = 66), enterotoxigenic Escherichia coli (ETEC) (n = 31) or nega
23 ubstrates: heat-labile enterotoxin (LT) from enterotoxigenic Escherichia coli (ETEC) and cholera toxi
27 neri 2a strain CVD 1203 as a live vector for enterotoxigenic Escherichia coli (ETEC) antigens is repo
30 CS1 is the prototype of a class of pili of enterotoxigenic Escherichia coli (ETEC) associated with
35 ation factor antigen I (CFA/I), archetype of enterotoxigenic Escherichia coli (ETEC) Class 5 fimbriae
41 fic activity against colonization factors of enterotoxigenic Escherichia coli (ETEC) could provide pa
43 ity of a recombinant subunit vaccine against enterotoxigenic Escherichia coli (ETEC) delivered by TCI
44 ype of eight genetically related fimbriae of enterotoxigenic Escherichia coli (ETEC) designated class
47 id vectors, we designed SC608 to express the enterotoxigenic Escherichia coli (ETEC) fimbrial subunit
50 nd heat-labile (LT) enterotoxins produced by enterotoxigenic Escherichia coli (ETEC) have been docume
53 n (LT) provides a colonization advantage for enterotoxigenic Escherichia coli (ETEC) in vivo, we hypo
72 oral vaccine against both Shigella spp. and enterotoxigenic Escherichia coli (ETEC) is being develop
78 with clinical and epidemiologic features of enterotoxigenic Escherichia coli (ETEC) occurred among p
79 safety and immunogenicity of an oral, killed enterotoxigenic Escherichia coli (ETEC) plus cholera tox
86 coded on an apparent pathogenicity island of enterotoxigenic Escherichia coli (ETEC) strain H10407, m
95 mber of serologically distinct pili found in enterotoxigenic Escherichia coli (ETEC) strains associat
97 B/c mice by intranasal (i.n.) inoculation of enterotoxigenic Escherichia coli (ETEC) strains H10407 (
103 olonize the small intestine is essential for enterotoxigenic Escherichia coli (ETEC) to cause diarrhe
105 specific polymerase chain reaction (PCR) for enterotoxigenic Escherichia coli (ETEC) toxins after cha
106 terotoxin (LT) is retained on the surface of enterotoxigenic Escherichia coli (ETEC) via an interacti
107 er membrane protein NlpA is repressed by the enterotoxigenic Escherichia coli (ETEC) virulence regula
108 uster of the CS18 (PCFO20) fimbriae of human enterotoxigenic Escherichia coli (ETEC) was found to inc
112 for many Gram-negative pathogens, including enterotoxigenic Escherichia coli (ETEC), a major cause o
113 stinal colonization and diarrheal disease by enterotoxigenic Escherichia coli (ETEC), an E. coli path
116 olunteer challenges with Vibrio cholerae O1, enterotoxigenic Escherichia coli (ETEC), enteropathogeni
118 rototype hybrid vaccine against Shigella and enterotoxigenic Escherichia coli (ETEC), the genes encod
119 ing challenge in developing vaccines against enterotoxigenic Escherichia coli (ETEC), the most common
120 or the detection of Yersinia enterocolitica, enterotoxigenic Escherichia coli (ETEC), Vibrio, and Ple
126 cter jejuni, Salmonella spp., Shigella spp., enterotoxigenic Escherichia coli [ETEC], Shiga toxin-pro
129 s) were fused to a rotavirus enterotoxin and enterotoxigenic Escherichia coli fimbrial antigen genes
130 otein was used to isolate DNA fragments from enterotoxigenic Escherichia coli genomic DNA that carry
133 itive stool samples also tested positive for enterotoxigenic Escherichia coli, indicating that dual i
135 , and an inverse relationship exists between enterotoxigenic Escherichia coli infections producing th
137 Heat-labile enterotoxin (LT), produced by enterotoxigenic Escherichia coli, is a close relative of
139 f HRV against acute diarrhea associated with enterotoxigenic Escherichia coli; it was 4.0% (95% CI, -
141 The tip adhesin FasG of the 987P fimbriae of enterotoxigenic Escherichia coli mediates two distinct a
142 igs infected with hemolytic F4(+) strains of enterotoxigenic Escherichia coli often develop septicemi
143 lobacter, Salmonella, and Vibrio species and enterotoxigenic Escherichia coli), only 24% were suscept
145 four pathogens: rotavirus, Cryptosporidium, enterotoxigenic Escherichia coli producing heat-stable t
147 g colonization factor antigen I (CFA/I) from enterotoxigenic Escherichia coli results in the rapid on
148 enteric pathogens include Ascaris, Giardia, enterotoxigenic Escherichia coli, Shigella, and Campylob
149 detection rates >20% were found for each of enterotoxigenic Escherichia coli, Shigella, Campylobacte
151 CS1 pili are important virulence factors of enterotoxigenic Escherichia coli strains associated with
153 serologically distinct pili associated with enterotoxigenic Escherichia coli that cause diarrhoea in
156 here is no evidence that Rns, a regulator of enterotoxigenic Escherichia coli virulence genes, respon
157 ain, which degrades enterocyte receptors for enterotoxigenic Escherichia coli, was shown in an experi
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