ライフサイエンスコーパス: enteropathogenic

1 s induced by the IMD-Relish response to both enteropathogenic and commensal bacteria.

2 hown to be manipulated during infection with enteropathogenic and enterohaemorrhagic Escherichia coli

3 n infections with the attaching and effacing enteropathogenic and enterohaemorrhagic Escherichia coli

4 In enteropathogenic and enterohaemorrhagic Escherichia coli

5 During the course of infection, enteropathogenic and enterohaemorrhagic Escherichia coli

6 Enteropathogenic and enterohaemorrhagic Escherichia coli

7 uman and animal enteric pathogens, including enteropathogenic and enterohaemorrhagic Escherichia coli

8 Enteropathogenic and enterohaemorrhagic Escherichia coli

9 secreted by the type III secretion system of enteropathogenic and enterohemorrhagic Escherichia coli

10 The human pathogens enteropathogenic and enterohemorrhagic Escherichia coli

11 In common with enteropathogenic and enterohemorrhagic Escherichia coli

12 lasia and colitis and is used as a model for enteropathogenic and enterohemorrhagic Escherichia coli

13 Enteropathogenic and enterohemorrhagic Escherichia coli

14 ression of the type III secretion systems of enteropathogenic and enterohemorrhagic Escherichia coli

15 Enteropathogenic and enterohemorrhagic Escherichia coli

16 lence of the closely related human pathogens enteropathogenic and enterohemorrhagic Escherichia coli

17 oC SboC and SeoC are homologues of EspJ from enteropathogenic and enterohemorrhagic Escherichia coli

18 hing and effacing mouse pathogen that models enteropathogenic and enterohemorrhagic Escherichia coli

19 rocyte effacement-encoded regulator (Ler) of enteropathogenic and enterohemorrhagic Escherichia coli

20 However, the TTSS of enteropathogenic and enterohemorrhagic Escherichia coli,

21 ses resembling those of humans infected with enteropathogenic and enterohemorrhagic Escherichia coli.

22 cus of enterocyte effacement (LEE), a PAI of enteropathogenic and enterohemorrhagic Escherichia coli.

23 e occasions within the different lineages of enteropathogenic and enterohemorrhagic Escherichia coli.

24 ntium is a natural mouse pathogen related to enteropathogenic and enterohemorrhagic Escherichia coli.

25 Our data suggest that enteropathogenic and VT-expressing E. coli O26 strains r

26 e investigated the effects of nonpathogenic, enteropathogenic, and probiotic bacteria on the dynamics

27 sing chaperone HdeA promotes the survival of enteropathogenic bacteria during transit through the har

28 centrally important in adaptive immunity to enteropathogenic bacteria, viruses, and toxins.

29 P are less prevalent and are mainly found in enteropathogenic bacteria, where they play key roles in

30 We find that enteropathogenic bacteria-secreted particles (ET-BSPs) s

31 rough IL-22, and it promoted protection from enteropathogenic bacteria.

32 also affect susceptibility to infections by enteropathogenic bacteria.

33 Efficient host protection against enteropathogenic bacterial infection is characterized by

34 IL-1 superfamily members, yet their role in enteropathogenic bacterial infection remains poorly defi

35 ive immunity leading to host defense against enteropathogenic bacterial infection.

36 Enteropathogenic bacterial infections are a global healt

37 t successful establishment in the gut by the enteropathogenic bacterium Salmonella enterica serovar T

38 Yersinia enterocolitica is an enteropathogenic bacterium that causes gastrointestinal

39 The enteropathogenic bacterium Yersinia enterocolitica deact

40 and histological data characterizing a novel enteropathogenic BEC strain, NB, detected in fecal speci

41 The assay identifies enteropathogenic campylobacters to the species level on

42 ater secretion, antibiotic prescription, and enteropathogenic colonization, each of which involves an

43 Porcine epidemic diarrhea virus (PEDV) is an enteropathogenic coronavirus causing lethal watery diarr

44 irus (TGEV) are economically important swine enteropathogenic coronaviruses.

45 hazard ratio [HR] 1.9; 0.99-3.5) and typical enteropathogenic E coli (HR 2.6; 1.6-4.1) in infants age

46 bowel diseases (such as enteroaggregative or enteropathogenic E coli or Salmonella).

47 Shigella, ST-ETEC, Cryptosporidium, typical enteropathogenic E coli) can substantially reduce the bu

48 leal bacteria (P = .03) when challenged with enteropathogenic E coli, and were protected from immune

49 that cause significant human disease are the enteropathogenic E. coli (EPEC) and enterotoxigenic E. c

50 compared these TIR interactions in EHEC and enteropathogenic E. coli (EPEC) and found that five inte

51 Detailed analysis of the H-NST proteins from enteropathogenic E. coli (EPEC) and uropathogenic E. col

52 Enterotoxigenic Escherichia coli (ETEC) and enteropathogenic E. coli (EPEC) are common causes of dia

53 nterohemorrhagic Escherichia coli (EHEC) and enteropathogenic E. coli (EPEC) are enteric bacterial pa

54 beled Shiga toxin-producing E. coli; whereas enteropathogenic E. coli (EPEC) are LEE+ and often carry

55 (Stx)-producing Escherichia coli (STEC) and enteropathogenic E. coli (EPEC) are the major foodborne

56 Several microbial pathogens including enteropathogenic E. coli (EPEC) exploit mammalian tyrosi

57 Enteropathogenic E. coli (EPEC) is a human pathogen that

58 Enteropathogenic E. coli (EPEC) is a major cause of infa

59 Diarrhoeal disease caused by enteropathogenic E. coli (EPEC) is dependent on a delive

60 EC O157:H7 serotype arose from its ancestor, enteropathogenic E. coli (EPEC) O55:H7 (sorbitol ferment

61 ely, new isolates continue to be mistyped as enteropathogenic E. coli (EPEC) or enterohemorrhagic E.

62 C001 is present and conserved in EHEC and in enteropathogenic E. coli (EPEC) strains.

63 menal bacteria, (3) prevent the adherence of enteropathogenic E. coli (EPEC) to epithelial monolayers

64 detect the role of phenotypic variability in enteropathogenic E. coli (EPEC), an important human path

65 s enterohemorrhagic Escherichia coli (EHEC), enteropathogenic E. coli (EPEC), and Citrobacter rodenti

66 Pathogenic Escherichia coli, including enteropathogenic E. coli (EPEC), enterohaemorrhagic E. c

67 er enterohemorrhagic E. coli (EHEC), typical enteropathogenic E. coli (EPEC), or atypical EPEC, depen

68 coli (EAEC), enterotoxigenic E. coli (ETEC), enteropathogenic E. coli (EPEC), Shigella spp., Campylob

69 terohaemorrhagic Escherichia coli (EHEC) and enteropathogenic E. coli (EPEC).

70 nterohemorrhagic Escherichia coli (EHEC) and enteropathogenic E. coli (EPEC).

71 15:H-) and compared it with those from human enteropathogenic E. coli (EPEC, O127:H6) and enterohemor

72 i (in 21.2% and 8.5%, respectively), typical enteropathogenic E. coli (in 18.0% and 8.3%, respectivel

73 An almost identical gene in enteropathogenic E. coli (lifA) mediates the inhibition

74 on was found between norovirus GII + typical enteropathogenic E. coli (OR = 0.09, 95% CI: 0.01, 0.95)

75 osubstrate, also significantly decreased the enteropathogenic E. coli -associated decrease in transep

76 a diverse array of clonal groups, including enteropathogenic E. coli 2 (EPEC 2), enterohemorrhagic E

77 coli [EAEC], enterotoxigenic E. coli [ETEC], enteropathogenic E. coli [EPEC], and Shiga-toxigenic E.

78 athotypes (enteroaggregative E. coli [EAEC], enteropathogenic E. coli [EPEC], enterotoxigenic E. coli

79 ntial regulation of protein kinase C-zeta by enteropathogenic E. coli and enterohemorrhagic E. coli m

80 tion of tight junctions after infection with enteropathogenic E. coli and enterohemorrhagic E. coli.

81 and lt for enterotoxigenic E. coli, eaeA for enteropathogenic E. coli and Shiga toxin-producing E. co

82 In addition, several enteropathogenic E. coli and Shigella effectors were fou

83 ithelial tight junctions, but the effects of enteropathogenic E. coli are more profound than those of

84 mucus-associated bacteria and resistance to enteropathogenic E. coli colonization.

85 and probably contributes to the survival of enteropathogenic E. coli during the intestinal inflammat

86 activated luxS in three E. coli backgrounds: enteropathogenic E. coli E2348-69, and enterohaemorrhagi

87 found that uropathogenic E. coli CFT073 and enteropathogenic E. coli E2348/69 occupy intestinal nich

88 n of modified filaments when expressed in an enteropathogenic E. coli espA mutant.

89 Enteropathogenic E. coli establish close contact with ho

90 fall into any of the four classical EHEC and enteropathogenic E. coli groups but instead was closely

91 ar colitis in mice and serves as a model for enteropathogenic E. coli infection in humans.

92 transepithelial electrical resistance after enteropathogenic E. coli infection.

93 in the suppression of IL-8 secretion during enteropathogenic E. coli infection.

94 coordinated response to enterotoxigenic and enteropathogenic E. coli infections.

95 The TTSS of enteropathogenic E. coli is unique in that one of the tr

96 We constructed a tightly inducible clone of enteropathogenic E. coli O127:H6 lifA for affinity purif

97 Two of these rabbits harbored enteropathogenic E. coli O145:H(-), and 1 rabbit was coi

98 g the O157:H7 serotype and are found in some enteropathogenic E. coli O55:H7 strains but are absent f

99 intestinal epithelial monolayers infected by enteropathogenic E. coli or enterohemorrhagic E. coli we

100 stal structure of the intimin-Tir complex of enteropathogenic E. coli predicts that each of these fou

101 ivatives, which are common in other EHEC and enteropathogenic E. coli serotypes.

102 esolution crystal structures of Gmm from the enteropathogenic E. coli strain O128: the structure of t

103 ypical virulence factors commonly carried by enteropathogenic E. coli strains.

104 employed two proteins, intimin and tir, from enteropathogenic E. coli that are critical to the bacter

105 equenced pathovars, enterotoxigenic E. coli, enteropathogenic E. coli, and enteroaggregative E. coli.

106 fficile, enteroaggregative Escherichia coli, enteropathogenic E. coli, and enterotoxigenic E. coli),

107 O1, enterotoxigenic Escherichia coli (ETEC), enteropathogenic E. coli, Campylobacter jejuni, and Giar

108 ral pathogenic strains of E. coli, including enteropathogenic E. coli, enterohemorrhagic E. coli, ent

109 a enterocolitica, enteroaggregative E. coli, enteropathogenic E. coli, enterotoxigenic E. coli, Shiga

110 c from EAEC and Shigella flexneri, EspC from enteropathogenic E. coli, EspP from enterohemorrhagic E.

111 aggregative Escherichia coli, Campylobacter, enteropathogenic E. coli, rotavirus, and Entamoeba histo

112 ichia coli, particularly enterotoxigenic and enteropathogenic E. coli, rotavirus, Giardia lamblia, an

113 In contrast to enteropathogenic E. coli, the level of protein kinase C-

114 for enterotoxigenic, enteroaggregative, and enteropathogenic E. coli.

115 ogens enterohemorrhagic Escherichia coli and enteropathogenic E. coli.

116 athogens including Salmonella, Shigella, and enteropathogenic E. coli.

117 ecretion than eae- and espB-positive STEC or enteropathogenic E. coli.

118 a T3SS-associated PG-lytic enzyme, EtgA from enteropathogenic E. coli.

119 ded enterotoxigenic Escherichia coli (ETEC), enteropathogenic E.coli (EPEC), Listeria monocytogenes,

120 three CPE-positive type C EN strains caused enteropathogenic effects in rabbit small intestinal loop

121 ing that both CPB and CPE are needed for the enteropathogenic effects of CN3758 MDS lysate supernatan

122 The enteropathogenic effects of CPE result from formation of

123 nsequently, CPE and CPB contributions to the enteropathogenic effects of MDS lysate supernatants of C

124 t or reversing the cpb mutation restored the enteropathogenic effects of MDS lysate supernatants.

125 f either purified toxin independently caused enteropathogenic effects.

126 ell as lower proportions of enterotoxigenic, enteropathogenic, enterohemorrhagic, and commensal E. co

127 The hallmark of enteropathogenic (EPEC) and enterohaemorrhagic (EHEC) Es

128 Like many Gram-negative pathogens, enteropathogenic (EPEC) and enterohaemorrhagic Escherich

129 Atypical enteropathogenic Escherichia coli (aEPEC) is an umbrella

130 Some mice were gavaged with enteropathogenic Escherichia coli (E2348/69) to induce i

131 The human pathogens enterohemorrhagic and enteropathogenic Escherichia coli (EHEC and EPEC), as we

132 ith SadA from Salmonella enterica, EhaG from enteropathogenic Escherichia coli (EHEC), and UpaG from

133 eotide sequence was determined for pMAR7, an enteropathogenic Escherichia coli (EPEC) adherence facto

134 of attaching and effacing pathogens such as enteropathogenic Escherichia coli (EPEC) and Citrobacter

135 Enteropathogenic Escherichia coli (EPEC) and enterohaemo

136 It had been suggested that the flagella of enteropathogenic Escherichia coli (EPEC) and enterohemor

137 Enteropathogenic Escherichia coli (EPEC) and enterohemor

138 Enteropathogenic Escherichia coli (EPEC) and enterohemor

139 Enteropathogenic Escherichia coli (EPEC) and enterohemor

140 Enteropathogenic Escherichia coli (EPEC) and enterohemor

141 The enteric pathogens enteropathogenic Escherichia coli (EPEC) and enterohemor

142 on of several important virulence factors in enteropathogenic Escherichia coli (EPEC) and reduced EPE

143 ues and fluids in response to infection with enteropathogenic Escherichia coli (EPEC) and Shiga-toxig

144 Enteropathogenic Escherichia coli (EPEC) and Shigella fl

145 The human pathogens enteropathogenic Escherichia coli (EPEC) and vaccinia vi

146 In many parts of the world, enteropathogenic Escherichia coli (EPEC) are a leading c

147 Enteropathogenic Escherichia coli (EPEC) are deadly cont

148 Enteropathogenic Escherichia coli (EPEC) are diarrhoeage

149 The type IV bundle-forming pili (BFP) of enteropathogenic Escherichia coli (EPEC) are required fo

150 ude two hydrophobic proteins, represented in enteropathogenic Escherichia coli (EPEC) by EspB and Esp

151 Enteropathogenic Escherichia coli (EPEC) cause intestina

152 This study found that enteropathogenic Escherichia coli (EPEC) caused acute co

153 Noninvasive enteropathogenic Escherichia coli (EPEC) colonize the gu

154 Enteropathogenic Escherichia coli (EPEC) continues to be

155 Enteropathogenic Escherichia coli (EPEC) disrupts the st

156 The genome of enteropathogenic Escherichia coli (EPEC) encodes a globa

157 lifA, for lymphocyte inhibitory factor A) in enteropathogenic Escherichia coli (EPEC) encoding a prot

158 The attaching and effacing (A/E) pathogen enteropathogenic Escherichia coli (EPEC) forms character

159 Using the enteropathogenic Escherichia coli (EPEC) genome sequence

160 The type III secretion system (TTSS) of enteropathogenic Escherichia coli (EPEC) has been associ

161 yte effacement (LEE) pathogenicity island of enteropathogenic Escherichia coli (EPEC) has not been de

162 The hallmarks of enteropathogenic Escherichia coli (EPEC) infection are f

163 The hallmark of enteropathogenic Escherichia coli (EPEC) infection is th

164 The hallmark of enteropathogenic Escherichia coli (EPEC) infection is th

165 Enteropathogenic Escherichia coli (EPEC) infection trigg

166 Enteropathogenic Escherichia coli (EPEC) infections are

167 Enteropathogenic Escherichia coli (EPEC) inhibits inflam

168 During infection, enteropathogenic Escherichia coli (EPEC) injects effecto

169 In children, typical enteropathogenic Escherichia coli (EPEC) is a common cau

170 Enteropathogenic Escherichia coli (EPEC) is a food-borne

171 Enteropathogenic Escherichia coli (EPEC) is a leading ca

172 Enteropathogenic Escherichia coli (EPEC) is a leading ca

173 Enteropathogenic Escherichia coli (EPEC) is a major bact

174 Enteropathogenic Escherichia coli (EPEC) is a major caus

175 Enteropathogenic Escherichia coli (EPEC) is a major caus

176 Enteropathogenic Escherichia coli (EPEC) is a major caus

177 The bundle-forming pilus (BFP) of enteropathogenic Escherichia coli (EPEC) is a prototypic

178 Enteropathogenic Escherichia coli (EPEC) is an extracell

179 The bundle-forming pilus (BFP) of enteropathogenic Escherichia coli (EPEC) is an important

180 Enteropathogenic Escherichia coli (EPEC) is an important

181 Enteropathogenic Escherichia coli (EPEC) is an important

182 Enteropathogenic Escherichia coli (EPEC) is an important

183 Enteropathogenic Escherichia coli (EPEC) is an important

184 The plasmid-encoded Per regulatory locus of enteropathogenic Escherichia coli (EPEC) is generally co

185 Virulence gene expression in enteropathogenic Escherichia coli (EPEC) is governed by

186 diarrhea induced by the food-borne pathogen enteropathogenic Escherichia coli (EPEC) is not known.

187 The diarrheagenic pathogen enteropathogenic Escherichia coli (EPEC) is responsible

188 Enteropathogenic Escherichia coli (EPEC) is the most imp

189 Enteropathogenic Escherichia coli (EPEC) is the single m

190 rial pathogens like Salmonella, Shigella and enteropathogenic Escherichia coli (EPEC) is the transloc

191 initial steps in biofilm development, and in enteropathogenic Escherichia coli (EPEC) it is mediated

192 The diarrheagenic pathogen enteropathogenic Escherichia coli (EPEC) limits the deat

193 The enteropathogenic Escherichia coli (EPEC) locus of entero

194 Although the bundle-forming pilus (BFP) of enteropathogenic Escherichia coli (EPEC) mediates microc

195 ttens that were presumptively diagnosed with enteropathogenic Escherichia coli (EPEC) on the basis of

196 Enteropathogenic Escherichia coli (EPEC) primarily infec

197 Enteropathogenic Escherichia coli (EPEC) produces a lesi

198 Enteropathogenic Escherichia coli (EPEC) produces the bu

199 Map is an enteropathogenic Escherichia coli (EPEC) protein that is

200 Production of type IV bundle-forming pili by enteropathogenic Escherichia coli (EPEC) requires BfpB,

201 tion of type IV bundle-forming pili (BFP) by enteropathogenic Escherichia coli (EPEC) requires the pr

202 The presence of the enteropathogenic Escherichia coli (EPEC) serotype is of

203 Among the enteric pathogens, enteropathogenic Escherichia coli (EPEC) stands out as s

204 Enteropathogenic Escherichia coli (EPEC) stimulates tyro

205 and virulence-associated -components in the enteropathogenic Escherichia coli (EPEC) strain E2348/69

206 gative transfer system identified in O119:H2 enteropathogenic Escherichia coli (EPEC) strain MB80 by

207 Enteropathogenic Escherichia coli (EPEC) strains continu

208 Enteropathogenic Escherichia coli (EPEC) strains that ca

209 n, CesT, serves a chaperone function for the enteropathogenic Escherichia coli (EPEC) translocated in

210 Enteropathogenic Escherichia coli (EPEC) translocates ef

211 Here, we demonstrate that the enteropathogenic Escherichia coli (EPEC) type III effect

212 Clustering of the enteropathogenic Escherichia coli (EPEC) type III secret

213 Enteropathogenic Escherichia coli (EPEC) use a type III

214 Enteropathogenic Escherichia coli (EPEC) uses a type III

215 Here, we report that the bacterial pathogen enteropathogenic Escherichia coli (EPEC) uses the type I

216 Outer membrane intimin directs attachment of enteropathogenic Escherichia coli (EPEC) via its Tir rec

217 Enteropathogenic Escherichia coli (EPEC) virulence is co

218 to inhibit attachment of microcolony-forming enteropathogenic Escherichia coli (EPEC) was investigate

219 Enteropathogenic Escherichia coli (EPEC) was recognized

220 Enteropathogenic Escherichia coli (EPEC), a major cause

221 Enteropathogenic Escherichia coli (EPEC), an important c

222 The mechanisms by which enteropathogenic Escherichia coli (EPEC), an important c

223 EspG, a secreted effector of enteropathogenic Escherichia coli (EPEC), as well as its

224 The human intestinal pathogen, enteropathogenic Escherichia coli (EPEC), causes diarrho

225 The PerC protein of enteropathogenic Escherichia coli (EPEC), encoded by the

226 ns and actin polymerization, the hallmark of enteropathogenic Escherichia coli (EPEC), enterohemorrha

227 es, collected semimonthly, were screened for enteropathogenic Escherichia coli (EPEC), enterotoxigeni

228 Enteropathogenic Escherichia coli (EPEC), like many othe

229 processes as well as actin-based motility of enteropathogenic Escherichia coli (EPEC), vaccinia, and

230 e factor in two groups of enteric pathogens: enteropathogenic Escherichia coli (EPEC), which is a maj

231 ere infected with the attaching and effacing enteropathogenic Escherichia coli (EPEC).

232 roteins responsible for the pathogenicity of enteropathogenic Escherichia coli (EPEC).

233 acing lesion formation during infection with enteropathogenic Escherichia coli (EPEC).

234 nt in the pathogenesis of diarrhea caused by enteropathogenic Escherichia coli (EPEC).

235 acter rodentium infection, a mouse model for enteropathogenic Escherichia coli (EPEC).

236 mmon organisms detected by the GI panel were enteropathogenic Escherichia coli (EPEC, n = 21), norovi

237 eal pathogens in the post-GI PCR cohort were enteropathogenic Escherichia coli (n = 14, 8%), noroviru

238 eal pathogens in the post-GI PCR cohort were enteropathogenic Escherichia coli (n=14, 8%), norovirus

239 -to-severe diarrhoea associated with typical enteropathogenic Escherichia coli among children aged 6-

240 nding cis-complemented derivatives of rabbit enteropathogenic Escherichia coli and compared their abi

241 derstanding of the molecular pathogenesis of enteropathogenic Escherichia coli and enterohemorrhagic

242 Enteropathogenic Escherichia coli and enterohemorrhagic

243 related clinically important human pathogens enteropathogenic Escherichia coli and enterohemorrhagic

244 Enteropathogenic Escherichia coli and enterohemorrhagic

245 n secretion and translocation from wild-type enteropathogenic Escherichia coli and hypersecretion fro

246 In ex vivo models of enteropathogenic Escherichia coli and Shigella flexneri

247 Enterohemorrhagic and enteropathogenic Escherichia coli are among the most imp

248 Using the bundle-forming pilus (BFP) of enteropathogenic Escherichia coli as a model Tfp system,

249 angstrom resolution cryo-EM structure of the enteropathogenic Escherichia coli ATPase EscN in complex

250 We purified the PulE homologue BfpD of the enteropathogenic Escherichia coli bundle-forming pilus (

251 The enteropathogenic Escherichia coli bundle-forming pilus i

252 gens such as Yersinia pseudotuberculosis and enteropathogenic Escherichia coli disarm host cells by i

253 rt the 1.9 A resolution crystal structure of enteropathogenic Escherichia coli GfcC, a periplasmic pr

254 Using synthetic derivatives of the enteropathogenic Escherichia coli guanine-nucleotide exc

255 cted with Citrobacter rodentium, a model for enteropathogenic Escherichia coli infection in humans, t

256 acter rodentium infection, a mouse model for enteropathogenic Escherichia coli infection, Hvem-/- mic

257 secretion system effector protein NleE from enteropathogenic Escherichia coli plays a key role in th

258 orum sensing to TTS in enterohemorrhagic and enteropathogenic Escherichia coli show that quorum sensi

259 entium uses virulence factors similar to the enteropathogenic Escherichia coli to produce attaching a

260 The Gram-negative bacterium enteropathogenic Escherichia coli uses a syringe-like ty

261 Enteropathogenic Escherichia coli utilise a filamentous

262 zyme in the interaction between the host and enteropathogenic Escherichia coli(EPEC) and Shiga-toxige

263 Enteropathogenic Escherichia coli(EPEC) requires the tna

264 cellular (S. Typhimurium) and extracellular (enteropathogenic Escherichia coli) enteric pathogens, vi

265 perone-delivered to the translocase, EscV in enteropathogenic Escherichia coli, and cross it in stric

266 bacter rodentium is the rodent equivalent of enteropathogenic Escherichia coli, and it causes colitis

267 The outer membrane adhesins of enteropathogenic Escherichia coli, Citrobacter rodentium

268 Enteropathogenic Escherichia coli, enterohemorrhagic E.

269 Enteropathogenic Escherichia coli, enterohemorrhagic E.

270 n 24 months with MSD, infection with typical enteropathogenic Escherichia coli, enterotoxigenic E col

271 and Campylobacter coli, Cryptosporidium spp, enteropathogenic Escherichia coli, heat-stable enterotox

272 rodentium, a murine model pathogen for human enteropathogenic Escherichia coli, predominantly coloniz

273 how that important other pathogens including enteropathogenic Escherichia coli, Shigella flexneri, an

274 rmation of attaching and effacing lesions by enteropathogenic Escherichia coli.

275 uptake as well as Cdc42-dependent uptake of enteropathogenic Escherichia coli.

276 shigella, salmonella, Yersinia species, and enteropathogenic Escherichia coli.

277 he attachment and effacement associated with enteropathogenic Escherichia coli.

278 osure of calpastatin-overexpressing cells to enteropathogenic Escherichia coli.

279 causes disease similar to the human pathogen enteropathogenic Escherichia coli.

280 d that extrinsic stress signals generated by enteropathogenic infection are epistatic to the hypoplas

281 s, many of which are remnants of a redundant enteropathogenic lifestyle.

282 Enteropathogenic Salmonella induced a classical proinfla

283 in, the major proinflammatory determinant of enteropathogenic Salmonella, which was found to be glyco

284 nd is a major proinflammatory determinant of enteropathogenic Salmonella.

285 ce factor-depleted E. coli C600 strains with enteropathogenic Shiga-toxin negative E. coli O26:H11, a

286 eagenic Escherichia coli (enteroaggretative, enteropathogenic), Shigella, and Campylobacter were the

287 the plague bacillus Yersinia pestis and two enteropathogenic species, Yersinia pseudotuberculosis an

288 For the human enteropathogenic strain F4969, it was then determined th

289 not clear why these avian coronaviruses are enteropathogenic, whereas other closely related avian co

290 ed to mount a robust immune response against enteropathogenic Y. pseudotuberculosis by promoting Th17

291 es) do not display altered susceptibility to enteropathogenic Yersinia compared to wild-type mice.

292 milar in TLR2(+/+) and TLR2(-/-) mice during enteropathogenic Yersinia infection.

293 plasmids (pCD in Yersinia pestis and pYV in enteropathogenic Yersinia pseudotuberculosis and Yersini

294 Enteropathogenic Yersinia species encode invasin, which

295 es have demonstrated that TTSS expression in enteropathogenic Yersinia spp. also inhibits the respira

296 oonotic pathogen hepatitis E virus (HEV) and enteropathogenic Yersinia spp. were analyzed in parallel

297 support nuclear localization of YopM from an enteropathogenic Yersinia strain.

298 s to, or the in vivo growth and survival of, enteropathogenic Yersinia.

299 yzed the susceptibility of TLR2(-/-) mice to enteropathogenic Yersinia.

300 Bacteriostasis of Y. pestis (but not enteropathogenic yersiniae) was abrupt in Ca(2+)-deficie