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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

73 Escherichia coli O157:H7 causes diarrhoea, haemorrhagic

74 Escherichia coli O157:H7 causes food and waterborne ente

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

76 Escherichia coli O157:H7 causes severe enteritis and hem

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

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

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

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

81 0, and 20 muM) on Listeria monocytogenes and Escherichia coli O157:H7 cultivated in tryptic soy broth

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

100 94, 21 cases (19 primary and 2 secondary) of Escherichia coli O157:H7 infection were identified in th

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

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

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

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

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

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

107 Escherichia coli O157:H7 infections have traditionally b

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

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

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

111 Escherichia coli O157:H7 is a foodborne pathogen disting

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

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

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

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

116 Escherichia coli O157:H7 is a notorious foodborne pathog

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

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

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

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

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

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

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

124 Escherichia coli O157:H7 is an increasingly common cause

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

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

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

128 Escherichia coli O157:H7 is increasingly recognized as a

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

159 Escherichia coli O157:H7 survives in diverse environment

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

239 2009 outbreak of Shiga-like toxin-producing Escherichia coli O157 infection associated with a pettin

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

241 Escherichia coli O157 infections are the cause of sporad

242 Quantification of Escherichia coli O157 is also desirable.

243 Escherichia coli O157 is an uncommon but serious cause o

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

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

246 Escherichia coli O157 is the most common STEC, although

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

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

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

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

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

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

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

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

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

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

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

258 Escherichia coli O157 was first identified as a human pa

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

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