ライフサイエンスコーパス: Escherichia coli O157

1 Multiplex analysis of 191-bp amplicons from Escherichia coli O157 and 256-bp amplicons from E. coli

2 Two model bacteria, Escherichia coli O157 and Salmonella typhimurium, were c

3 hree commercial latex reagents for detecting Escherichia coli O157 antigen (Oxoid Diagnostic Reagents

4 of Citrobacter sedlakii which expresses the Escherichia coli O157 antigen is described.

5 jor reservoir host for the zoonotic pathogen Escherichia coli O157, are known to exhibit a high degre

6 Infection with Escherichia coli O157 causes an estimated 70 000 diarrhe

7 Escherichia coli O157 causes severe enteritis and the ex

8 la, Campylobacter, Giardia, Cryptosporidium, Escherichia coli O157, enterotoxigenic E. coli (ETEC), a

9 ity into an agent-based simulation model for Escherichia coli O157 environmental transmission in catt

10 key agar (SMAC) culture for the detection of Escherichia coli O157 from stool specimens.

11 While the differential association of Escherichia coli O157 genotypes with animal and human ho

12 An atypical, Stx2-producing, pathogenic Escherichia coli O157:H(-) strain has been isolated with

13 A virulent European Escherichia coli O157:H- isolate is nonmotile due to a 1

14 used by infection with Shiga-toxin-producing Escherichia coli (O157:H7).

15 Escherichia coli O157:H7 (E. coli O157:H7) emerges as a

16 or for the detection of the food contaminant Escherichia coli O157:H7 (E. coli O157:H7) in complex fo

17 antibody-free, and aptamer-free detection of Escherichia coli O157:H7 (E. coli O157:H7) in water samp

18 as used for the detection of food pathogenic Escherichia coli O157:H7 (E.coli O157:H7), a dangerous s

19 Outbreaks of Escherichia coli O157:H7 (ECO157) in romaine lettuce rem

20 Surviving predation is a fitness trait of Escherichia coli O157:H7 (EcO157) that provides ample ti

21 Enterohemorrhagic Escherichia coli O157:H7 (EHEC O157) is an important cau

22 Enterohemorrhagic Escherichia coli O157:H7 (EHEC) causes bloody diarrhea a

23 Enterohemorrhagic Escherichia coli O157:H7 (EHEC) is a foodborne pathogen

24 Here, we demonstrate that enterohemorrhagic Escherichia coli O157:H7 (EHEC) regulates virulence via

25 roduct of the eaeA gene in enterohemorrhagic Escherichia coli O157:H7 (EHEC), is required for intimat

26 h predicted a duplicated type I locus within Escherichia coli O157:H7 (EHEC), which we have named the

27 teric pathogens, including enterohemorrhagic Escherichia coli O157:H7 (EHEC).

28 Shiga toxin-producing Escherichia coli O157:H7 (O157) can cause mild to severe

29 The locus of enterocyte effacement (LEE) of Escherichia coli O157:H7 (O157) encodes a type III secre

30 l models, we directly identified immunogenic Escherichia coli O157:H7 (O157) proteins expressed eithe

31 Escherichia coli O157:H7 (O157) strains are commonly typ

32 Escherichia coli O157:H7 (O157) strains demonstrate vari

33 orphic amplified typing sequences (PATS) for Escherichia coli O157:H7 (O157) was previously based on

34 Shiga-toxin producing Escherichia coli O157:H7 (O157)-based vaccines can provi

35 Infections by Shiga toxin-producing Escherichia coli O157:H7 (STEC O157) are the predominant

36 In the 1980s, Shiga toxin (Stx)-producing Escherichia coli O157:H7 (STEC) was identified as a caus

37 The effects of Escherichia coli O157:H7 (strains E30480 and PM601) and

38 lerae O1 (the causative agent of cholera) or Escherichia coli O157:H7 (the leading cause of food-born

39 etect Shiga-like toxin gene II (SLT-II) from Escherichia coli O157:H7 after asymmetric, capillary, PC

40 nvestigation of four cases of infection with Escherichia coli O157:H7 among laboratorians from differ

41 ic region between the mutS and rpoS genes of Escherichia coli O157:H7 and closely related strains rep

42 ods with samples from children infected with Escherichia coli O157:H7 and correlated the antigen dete

43 Enterohemorrhagic Escherichia coli O157:H7 and enteropathogenic E. coli ca

44 The isolation and characterization of Escherichia coli O157:H7 and non-O157 Shiga toxin-produc

45 Six protein biomarkers from two strains of Escherichia coli O157:H7 and one non-O157:H7, nonpathoge

46 The mechanisms underlying the adherence of Escherichia coli O157:H7 and other enterohemorrhagic E.

47 rial strain identification for the typing of Escherichia coli O157:H7 and other gram-negative organis

48 ins (Stx) are critical virulence factors for Escherichia coli O157:H7 and other serotypes of enterohe

49 Escherichia coli O157:H7 and other Shiga toxin (Stx)-pro

50 Escherichia coli O157:H7 and other Shiga toxin-producing

51 en implicated as a major virulence factor of Escherichia coli O157:H7 and other Shiga toxin-producing

52 e important contributors to the virulence of Escherichia coli O157:H7 and other Stx-producing E. coli

53 e of commensal flora reduced colonization of Escherichia coli O157:H7 and production of Shiga toxin (

54 AMP magainin I as a recognition element for Escherichia coli O157:H7 and Salmonella typhimurium dete

55 In Escherichia coli O157:H7 and Salmonella, QseC has been p

56 fection of humans with Shiga toxin-producing Escherichia coli O157:H7 and Shigella dysenteriae 1 is s

57 o examine the impact of pathogenic bacteria, Escherichia coli O157:H7 and three different Salmonella

58 as fabricated by covalently grafting an anti-Escherichia coli O157:H7 antibody onto SAM-modified gold

59 n with gastrointestinal infections caused by Escherichia coli O157:H7 are at risk for the hemolytic-u

60 Shiga toxin (Stx)-producing Escherichia coli O157:H7 are the most common cause of he

61 mmunofilter captured the targeted pathogens, Escherichia coli O157:H7 as an example for bacteria and

62 he few adhesive factors of enterohemorrhagic Escherichia coli O157:H7 associated with colonization of

63 In this study, we used the Escherichia coli O157:H7 autotransporter EspP as a model

64 eine residues in the passenger domain of the Escherichia coli O157:H7 autotransporter EspP at differe

65 mall linker into the passenger domain of the Escherichia coli O157:H7 autotransporter EspP effectivel

66 he C terminus of the passenger domain of the Escherichia coli O157:H7 autotransporter EspP have been

67 ient to promote the complete assembly of the Escherichia coli O157:H7 autotransporter EspP in vitro.

68 ere we show that the passenger domain of the Escherichia coli O157:H7 autotransporter EspP is release

69 ent secretion of the passenger domain of the Escherichia coli O157:H7 autotransporter EspP requires t

70 se toxin CyaA fused to the C terminus of the Escherichia coli O157:H7 autotransporter EspP to test th

71 emerged from an analysis of mutations in the Escherichia coli O157:H7 autotransporter EspP.

72 f an enclosed loop in the beta domain of the Escherichia coli O157:H7 autotransporter EspP.

73 complex interact with the beta domain of the Escherichia coli O157:H7 autotransporter extracellular s

74 a significantly enhanced the sensitivity for Escherichia coli O157:H7 bacteria detection.

75 developed for highly sensitive detection of Escherichia coli O157:H7 bacteria.

76 Four tailspike proteins (TSP1-4) of Escherichia coli O157:H7 bacteriophage CBA120 enable inf

77 The Escherichia coli O157:H7 bacteriophage CBA120 genome enc

78 The genome of Escherichia coli O157:H7 bacteriophage vB_EcoM_CBA120 en

79 sensor chips were developed for detection of Escherichia coli O157:H7 based on the surface immobiliza

80 d toxin homologous to a predicted toxin from Escherichia coli O157:H7 but had apparently lost the try

81 or/bioreactor was developed for detection of Escherichia coli O157:H7 by chemically immobilizing anti

82 Infection with Escherichia coli O157:H7 can lead to hemolytic uremic sy

83 Human infections with Escherichia coli O157:H7 cause hemorrhagic colitis that

84 ated to an outbreak of Shiga toxin-producing Escherichia coli O157:H7 caused by the consumption of ra

85 Escherichia coli O157:H7 causes diarrhoea, haemorrhagic

86 Escherichia coli O157:H7 causes food and waterborne ente

87 The human pathogen Escherichia coli O157:H7 causes hemorrhagic colitis and

88 Escherichia coli O157:H7 causes severe enteritis and hem

89 Escherichia coli O157:H7 causes Shiga toxin (Stx)-mediat

90 udied interactions of antibodies with single Escherichia coli O157:H7 cells and demonstrated a capabi

91 ed by lateral flow strip detection of viable Escherichia coli O157:H7 cells by detecting the RNA of t

92 ric sensor (LAPS) for the rapid detection of Escherichia coli O157:H7 cells in buffered saline.

93 nce of the sensor was evaluated by capturing Escherichia coli O157:H7 cells on the antibody-stamped l

94 differentiate 10(3) and 10(6) CFU/uL initial Escherichia coli O157:H7 concentrations compared to NTC

95 0, and 20 muM) on Listeria monocytogenes and Escherichia coli O157:H7 cultivated in tryptic soy broth

96 ng approach carried out in a single step for Escherichia coli O157:H7 detection.

97 question, we separated the production of an Escherichia coli O157:H7 exoprotein (OtpA) and its trans

98 effector protein Tir from enterohemorrhagic Escherichia coli O157:H7 expressed in epithelial cells i

99 The rapid emergence of Escherichia coli O157:H7 from an unknown strain in 1982

100 irms on-chip detection and identification of Escherichia coli O157:H7 from colony isolates in a color

101 ivity ( approximately 95%) in isolating live Escherichia coli O157:H7 from cultures containing 1000 E

102 Escherichia coli O157:H7 has been shown to express heme

103 Recent outbreaks of disease caused by Escherichia coli O157:H7 have focused much attention on

104 The food-borne pathogen Escherichia coli O157:H7 impacts the transcription of a

105 Persistence of Escherichia coli O157:H7 in 32 (16 organically managed a

106 r of protocols for the cultural detection of Escherichia coli O157:H7 in clinical fecal specimens hav

107 aditional fecal culture for the detection of Escherichia coli O157:H7 in experimentally infected and

108 ay for rapid detection and quantification of Escherichia coli O157:H7 in meat and water samples based

109 n of the O-antigen biosynthesis cluster from Escherichia coli O157:H7 in strain 1244 resulted in the

110 ous detection of Salmonella, Legionella, and Escherichia coli O157:H7 in tap water and wastewater.

111 ources that support the growth of pathogenic Escherichia coli O157:H7 in the mammalian intestine have

112 The largest reported outbreak of waterborne Escherichia coli O157:H7 in the United States occurred i

113 Limits of detection of Escherichia coli O157:H7 in undiluted milk were determin

114 In addition to causing diarrhea, Escherichia coli O157:H7 infection can lead to hemolytic

115 The use of antibiotics for treatment of Escherichia coli O157:H7 infection has become controvers

116 94, 21 cases (19 primary and 2 secondary) of Escherichia coli O157:H7 infection were identified in th

117 Risk factors for Escherichia coli O157:H7 infection were investigated in

118 ncluding the need for vigilance in detecting Escherichia coli O157:H7 infection.

119 mic syndrome is a thrombotic complication of Escherichia coli O157:H7 infection.

120 ts were identified with laboratory-confirmed Escherichia coli O157:H7 infection; 52 residents had blo

121 In a recent cluster of Escherichia coli O157:H7 infections attributed to salad

122 Outbreaks of Escherichia coli O157:H7 infections have involved direct

123 Escherichia coli O157:H7 infections have traditionally b

124 A protracted outbreak of Escherichia coli O157:H7 infections was caused by consum

125 loping hemolytic uremic syndrome (HUS) after Escherichia coli O157:H7 infections.

126 Escherichia coli O157:H7 is a commensal organism in catt

127 Escherichia coli O157:H7 is a foodborne pathogen disting

128 ultilocus-genotyping methods have shown that Escherichia coli O157:H7 is a geographically disseminate

129 Escherichia coli O157:H7 is a leading cause of diarrhea

130 Escherichia coli O157:H7 is a major cause of food-borne

131 Escherichia coli O157:H7 is a major cause of foodborne i

132 Escherichia coli O157:H7 is a notorious foodborne pathog

133 Escherichia coli O157:H7 is a Shiga toxin-producing E. c

134 Escherichia coli O157:H7 is a source of foodborne illnes

135 Long polar fimbriae 1 (Lpf1) of Escherichia coli O157:H7 is a tightly regulated adhesin,

136 The bacterium Escherichia coli O157:H7 is a worldwide threat to public

137 Escherichia coli O157:H7 is a zoonotic pathogen that can

138 Escherichia coli O157:H7 is an important food-borne path

139 Escherichia coli O157:H7 is an important pathogen of hum

140 Escherichia coli O157:H7 is an increasingly common cause

141 magnetoelastic immunosensor for detection of Escherichia coli O157:H7 is described, based on immobili

142 A hemolytic determinant of enterohemorrhagic Escherichia coli O157:H7 is encoded on a 90-kbp plasmid

143 a toxin 2 (Stx2) from the foodborne pathogen Escherichia coli O157:H7 is encoded on a temperate bacte

144 Escherichia coli O157:H7 is increasingly recognized as a

145 Rapid detection of the foodborne pathogen Escherichia coli O157:H7 is of vital importance for publ

146 Consumption of food contaminated with Escherichia coli O157:H7 is one of the major concerns in

147 Escherichia coli O157:H7 is one of the most notorious fo

148 Enterohemorrhagic Escherichia coli O157:H7 is responsible for many outbrea

149 Escherichia coli O157:H7 is the leading cause of hemolyt

150 Pulsed-field gel electrophoresis of Escherichia coli O157:H7 isolates (n = 228) from 122 hea

151 Antibodies to Campylobacter jejuni and Escherichia coli O157:H7 lipopolysaccharide (O157 LPS) i

152 recommended that all stools be cultured for Escherichia coli O157:H7 on selective medium as well as

153 netic nanoparticles functionalized with anti-Escherichia coli O157:H7 or anti-Salmonella typhimurium

154 estimate the frequency of enterohemorrhagic Escherichia coli O157:H7 or O157:nonmotile (EHEC O157) i

155 ic uremic syndrome after oral infection with Escherichia coli O157:H7 or other Shiga toxin--producing

156 In 2006, a deadly Escherichia coli O157:H7 outbreak in bagged spinach was

157 ubtyping method for detecting and evaluating Escherichia coli O157:H7 outbreaks.

158 Shiga toxin-producing Escherichia coli O157:H7 primarily resides in cattle asy

159 ss outbreaks resulting from contamination of Escherichia coli O157:H7 remain a serious concern in foo

160 R from Mu-like prophage sequences present in Escherichia coli O157:H7 Sakai, Haemophilus influenzae R

161 say to detect single cells of the pathogenic Escherichia coli O157:H7 serotype.

162 ment (LEE) from EDL933, an enterohemorrhagic Escherichia coli O157:H7 serovar originally isolated fro

163 Escherichia coli O157:H7 Shiga toxin 2 (Stx2), one of th

164 Comparison of two strains of Escherichia coli O157:H7 shows a preponderance of indels

165 ve constructed NheI and XhoI optical maps of Escherichia coli O157:H7 solely from genomic DNA molecul

166 NanoGene assay for detecting and quantifying Escherichia coli O157:H7 specific eaeA gene.

167 In Escherichia coli O157:H7 strain ATCC 43895, a guanine-to

168 Recent genomic analyses of Escherichia coli O157:H7 strain EDL933 revealed two loci

169 described in the annotation of the genome of Escherichia coli O157:H7 strain EDL933.

170 we identified the iron-transport systems of Escherichia coli O157:H7 strain EDL933.

171 Promoter alterations in the csgD gene of Escherichia coli O157:H7 strains ATCC 43894 and ATCC 438

172 nd naturally occurring, potentially virulent Escherichia coli O157:H7 strains in sheep.

173 The rapid and accurate identification of Escherichia coli O157:H7 strains is central to reducing

174 An Escherichia coli O157:H7 subtyping method based on PCR a

175 Escherichia coli O157:H7 survives in diverse environment

176 onocytogenes, but was less effective against Escherichia coli O157:H7 than free LAE, which was correl

177 entified StcE, a metalloprotease secreted by Escherichia coli O157:H7 that cleaves the serpin C1 este

178 quired genomic regions of enterohaemorrhagic Escherichia coli O157:H7 that regulate expression of the

179 and duration of fecal shedding of wild-type Escherichia coli O157:H7 to that of an isogenic intimin

180 Enterohemorrhagic Escherichia coli O157:H7 translocates 2 effectors to tri

181 Here we identify the enterohaemorrhagic Escherichia coli O157:H7 type III effector EspG as a reg

182 microbalance for the detection of pathogenic Escherichia coli O157:H7 using TCEP-reduced antibody wit

183 eal-time PCR assay to detect the presence of Escherichia coli O157:H7 using these fluorogenic reporte

184 Efficient photocatalytic disinfection of Escherichia coli O157:H7 was achieved by using a C70 mod

185 demonstrated in a model experiment in which Escherichia coli O157:H7 was detected at concentrations

186 Outer membrane permeability of Escherichia coli O157:H7 was determined by an in vivo ki

187 mpedance immunosensor for rapid detection of Escherichia coli O157:H7 was developed by immobilizing a

188 a enrichment and detection system for viable Escherichia coli O157:H7 was developed using a piezoelec

189 al immunosensor for the common food pathogen Escherichia coli O157:H7 was developed.

190 polar fimbriae to intestinal colonization by Escherichia coli O157:H7 was evaluated in sheep, convent

191 An outbreak of Escherichia coli O157:H7 was identified in Oregon throug

192 Escherichia coli O157:H7 was isolated from 118 (0.39%) o

193 Escherichia coli O157:H7 was more likely to be isolated

194 e (PG) in the presence of UV-A light against Escherichia coli O157:H7 were investigated.

195 Bacteria inhibitory to Escherichia coli O157:H7 were isolated from cattle and e

196 a toxin (Stx)-producing, food-borne pathogen Escherichia coli O157:H7 will develop a life-threatening

197 l RNA samples, the assay truly discriminated Escherichia coli O157:H7's 16s rRNA from closely related

198 Whole bacteria (Escherichia coli O157:H7) were assayed in buffer as well

199 genes) than from the gram-negative organism (Escherichia coli O157:H7), preventing unbiased detection

200 lucose) or detection of pathogenic bacteria (Escherichia coli O157:H7).

201 egative microbes (Salmonella enteritidis and Escherichia coli O157:H7).

202 Escherichia coli O157:H7, a major Shiga toxin-producing

203 Evolutionary analysis of Escherichia coli O157:H7, a pathogen that has emerged as

204 Escherichia coli O157:H7, a toxin-producing food and wat

205 erization of an effector protein (NleL) from Escherichia coli O157:H7, a widespread pathogen causing

206 Enterohemorrhagic Escherichia coli O157:H7, a world-wide human food-borne

207 tensively to investigate the epidemiology of Escherichia coli O157:H7, although it has not been evalu

208 cterium in the order: Enterococcus faecalis, Escherichia coli O157:H7, and Escherichia coli D21f2.

209 ts, with an emphasis on Salmonella enterica, Escherichia coli O157:H7, and Listeria monocytogenes.

210 ve bacteria, including Campylobacter jejuni, Escherichia coli O157:H7, and multidrug resistant Klebsi

211 pXO1 from Bacillus anthracis, and pO157 from Escherichia coli O157:H7, as well as the broad host rang

212 versity and survival of the invading species Escherichia coli O157:H7, assessed by using the marked d

213 to the strong interaction between AuNPs and Escherichia coli O157:H7, AuNPs attached to the surface

214 e technique for rapid detection of low-level Escherichia coli O157:H7, Bacillus subtilis var. niger s

215 To better define the bovine reservoir of Escherichia coli O157:H7, cattle were tested monthly by

216 analyses of previously sequenced strains of Escherichia coli O157:H7, EDL933 and Sakai, localized th

217 r flagellar filaments from enterohemorrhagic Escherichia coli O157:H7, enteropathogenic E. coli O127:

218 The food-borne pathogen, Escherichia coli O157:H7, has been associated with gastr

219 ca serotype Enteritidis (S. enteritidis) and Escherichia coli O157:H7, has generated increasing inter

220 cluding tests for a drugs of abuse panel and Escherichia coli O157:H7, have been developed.

221 E) was used to compare Wisconsin isolates of Escherichia coli O157:H7, including 39 isolates from a 1

222 llowing infection by the intestinal pathogen Escherichia coli O157:H7, is due to the ability of the p

223 Gnotobiotic piglets inoculated with Escherichia coli O157:H7, its luxS mutant derivative, or

224 ht emitting diodes (LEDs) against pathogenic Escherichia coli O157:H7, Listeria monocytogenes, Pseudo

225 ates of the recently emerged clonal pathogen Escherichia coli O157:H7, making them a very useful mole

226 spersion of pathogens (Campylobacter jejuni, Escherichia coli O157:H7, non-O157 E. coli, Listeria mon

227 uenced evolutionarily instructive pathogenic Escherichia coli O157:H7, O157:H(-), and O55:H7.

228 We sought Aeromonas, Campylobacter, Escherichia coli O157:H7, Pleisiomonas shigelloides, Sal

229 effacing (A/E) bacterial pathogens, such as Escherichia coli O157:H7, pose a serious threat to publi

230 inst Staphylococcus aureus, Bacillus cereus, Escherichia coli O157:H7, Pseudomonas aeruginosa and Sal

231 -MNP induced strong dose-dependent bacteria (Escherichia coli O157:H7, Salmonella enterica serovar Ty

232 against common foodborne pathogens including Escherichia coli O157:H7, Salmonella enteritidis, Salmon

233 (LOD) was <5 CFU/mL of the tested pathogens (Escherichia coli O157:H7, Salmonella typhimurium, and Li

234 osis, the 5' 350 bp of the 16S rRNA genes of Escherichia coli O157:H7, Salmonella typhimurium, Salmon

235 isolates of food-borne pathogens (currently Escherichia coli O157:H7, Salmonella, Shigella, and List

236 Recently, in Escherichia coli O157:H7, the catecholamines adrenaline

237 Intimin is the primary adhesin of Escherichia coli O157:H7, the most common infectious cau

238 lly identify a variety of bacterium, such as Escherichia coli O157:H7, through antibody-antigen inter

239 olorimetric immunoassay for the detection of Escherichia coli O157:H7, using antibody-directed liposo

240 swab samples cultured in our laboratory for Escherichia coli O157:H7, we frequently isolated E. coli

241 In the enteric pathogen Escherichia coli O157:H7, which causes hemorrhagic colit

242 that of a recently identified stcE gene from Escherichia coli O157:H7, which encoded a protein (StcE)

243 network is important for the pathogenesis of Escherichia coli O157:H7, which has captured many virule

244 nts, specifically pathogenic species such as Escherichia coli O157:H7, which is a highly infectious a

245 gen is an essential part of the detection of Escherichia coli O157:H7, which is recognized as a major

246 Escherichia coli O157:H7-associated hemolytic-uremic syn

247 aT2 toxin from a toxin-antitoxin system from Escherichia coli O157:H7.

248 onent parDE-like toxin-antitoxin module from Escherichia coli O157:H7.

249 EspP, a prototype SPATE protein produced by Escherichia coli O157:H7.

250 -negative bacteria as Vibrio cholerae O1 and Escherichia coli O157:H7.

251 tion of virulence genes in enterohemorrhagic Escherichia coli O157:H7.

252 p mutants and the human pathogenic bacterium Escherichia coli O157:H7.

253 ozoan; Norwalk-like virus; and the bacterium Escherichia coli O157:H7.

254 lity enhancement and immunoimmobilization of Escherichia coli O157:H7.

255 borne pathogens, Listeria monocytogenes and Escherichia coli O157:H7.

256 five genetically distinct patient strains of Escherichia coli O157:H7.

257 emic syndrome, risk factor, antibiotics, and Escherichia coli O157:H7.

258 was nearly identical to an int gene found in Escherichia coli O157:H7.

259 platform was developed for the detection of Escherichia coli O157:H7.

260 nterica subsp. enterica serovar Bareilly and Escherichia coli O157:H7.

261 amin D and challenged with enterohemorrhagic Escherichia coli O157:H7.

262 ks of foodborne illness caused by strains of Escherichia coli O157:H7.

263 toxin type 2 (Stx2), produced by pathogenic Escherichia coli O157:H7.

264 2009 outbreak of Shiga-like toxin-producing Escherichia coli O157 infection associated with a pettin

265 obacter infection, 2.7 {CI, 1.5-4.8}; OR for Escherichia coli O157 infection, 7.4 {CI, 2.1-26.1}]).

266 Escherichia coli O157 infections are the cause of sporad

267 Quantification of Escherichia coli O157 is also desirable.

268 Escherichia coli O157 is an uncommon but serious cause o

269 Detailed laboratory characterization of Escherichia coli O157 is essential to inform epidemiolog

270 Escherichia coli O157 is the major cause of diarrhea-ass

271 Escherichia coli O157 is the most common STEC, although

272 erformed pulsed-field gel electrophoresis on Escherichia coli O157 isolates (n = 318) from 199 health

273 nd ribotyping, were used to characterize 207 Escherichia coli O157 isolates from food animals, foods

274 addition of the target ligand (in this case Escherichia coli O157) leads to the formation of a nanop

275 mate different species of pathogens, such as Escherichia coli O157, Listeria innocua, Staphylococcus

276 fection with nonmotile Shiga toxin-producing Escherichia coli O157 occurred.

277 ria, specifically Campylobacter, Salmonella, Escherichia coli O157, or Shigella (REI-B).

278 l enteropathogens: Aeromonas, Campylobacter, Escherichia coli O157, other Shiga toxin-producing E. co

279 Patients (n=186) infected during the Escherichia coli O157 outbreak in Scotland in 1996 were

280 tic thrombocytopenic purpura (TTP) during an Escherichia coli O157 outbreak occurred in 1996 in centr

281 or 0/2 Campylobacter-positive specimens, 0/4 Escherichia coli O157-positive specimens, 0/9 Salmonella

282 nal pathogens, such as Shiga toxin-producing Escherichia coli O157 (STEC O157), is key to rapidly ide

283 Secreted proteins of verotoxigenic Escherichia coli O157 strains include components of a tr

284 Citrobacter rodentium and Escherichia coli O157 triggered similar Th17 responses,

285 ks of vero cytotoxin (shiga toxin) producing Escherichia coli O157 (VTEC O157) infection have stimula

286 Escherichia coli O157 was first identified as a human pa

287 One such global pathogen is Escherichia coli O157, which causes a serious and someti

288 ransmission of a microparasite, in this case Escherichia coli O157, within a multigroup system, namel