ライフサイエンスコーパス: enterocolitica

1 ontyphoidal Salmonella species, and Yersinia enterocolitica.

2 adA) is a major virulence factor of Yersinia enterocolitica.

3 e membrane topologies of PspB and PspC in Y. enterocolitica.

4 wing either i.p. or i.v. inoculation with Y. enterocolitica.

5 extensively in Escherichia coli and Yersinia enterocolitica.

6 tive immunity against Gram-negative Yersinia enterocolitica.

7 against the Gram-negative bacterium Yersinia enterocolitica.

8 riaceae, such as the enteropathogen Yersinia enterocolitica.

9 type III secretion system (T3SS) of Yersinia enterocolitica.

10 tive signal transduction pathway in Yersinia enterocolitica.

11 An aspirate from the axillary mass grew Y. enterocolitica.

12 es using the gastroenteric pathogen Yersinia enterocolitica.

13 ted with the AHL-producing pathogen Yersinia enterocolitica.

14 AHLs to mimic a constant interaction with Y. enterocolitica.

15 in naive macrophages infected with Yersinia enterocolitica.

16 n of FtsQ from Escherichia coli and Yersinia enterocolitica.

17 nes in response to S. typhimurium but not Y. enterocolitica.

18 response to prolonged secretin stress in Y. enterocolitica.

19 s susceptible to the enteropathogen Yersinia enterocolitica.

20 transmission for the enteropathogen Yersinia enterocolitica.

21 o alleviate transcriptional repression in Y. enterocolitica.

22 N-acylhomoserine lactone (AHL) profile of Y. enterocolitica.

23 y and specifically to the inv promoter of Y. enterocolitica.

24 ric lymph nodes after oral infection with Y. enterocolitica.

25 tive regulators of psp gene expression in Y. enterocolitica.

26 intestinal lymphatic tissue infected with Y. enterocolitica.

27 for the existence of three subspecies of Y. enterocolitica.

28 s, Yersinia pseudotuberculosis, and Yersinia enterocolitica.

29 se (LD(50)) following oral infection with Y. enterocolitica.

30 o intravenous (i.v.) infection with Yersinia enterocolitica.

31 role of the Ysps during the life cycle of Y. enterocolitica.

32 es, Yersinia pseudotuberculosis and Yersinia enterocolitica.

33 ssed by Yersinia pestis, but not by Yersinia enterocolitica.

34 compared to those infected with wild-type Y. enterocolitica.

35 ric infection by the proteobacteria Yersinia enterocolitica.

36 mg/L respectively) were observed against Y. enterocolitica.

37 ellin of Salmonella Typhimurium and Yersinia enterocolitica.

38 lague, Yersinia pseudotuberculosis, Yersinia enterocolitica.

39 y informative typing scheme available for Y. enterocolitica.

40 to reverse the uptake blockade imposed by Y. enterocolitica.

41 istant to orogastric infection with Yersinia enterocolitica.

42 spontaneously arising pathogenic Ab with Y. enterocolitica.

43 coccus aureus, Escherichia coli and Yersinia enterocolitica.

44 OmpC, and OmpF confirming reactivity with Y. enterocolitica.

45 thogenesis, including the bacterium Yersinia enterocolitica.

46 illus cereus, Escherichia coli, and Yersinia enterocolitica.

47 teins at their endogenous levels in Yersinia enterocolitica.

48 dA, which is the primary C4BP receptor of Y. enterocolitica.

49 omonas sp. (23.8%) by FilmArray and Yersinia enterocolitica (48.1%) by the Luminex assay.

50 t in all 47 low-pathogenicity strains and Y. enterocolitica 8081 but absent from all nonpathogenic 1A

51 (99.4 to 99.8), and 0.96 (0.93 to 0.99); Y. enterocolitica, 99.0% (94.8 to 99.8), 99.9% (99.8 to 99.

52 In Y. enterocolitica, a rovA mutant is attenuated for virulenc

53 obacter jejuni), Shigella flexneri, Yersinia enterocolitica, adenovirus, and Strongyloides fulleborni

54 t that EmaA is an orthologue of the Yersinia enterocolitica adhesin YadA.

55 limatization of the psychrotolerant Yersinia enterocolitica after a cold shock from 30 degrees C to 1

56 , we engineered EHEC to express the Yersinia enterocolitica AHL synthase gene yenI, which constitutiv

57 We find that IECs infected with Yersinia enterocolitica, an enteric pathogen, use beta1 integrins

58 Yersinia enterocolitica, an important cause of human gastroenteri

59 gellar type III secretion system of Yersinia enterocolitica and a phospholipase reporter (yplA).

60 ive clearance of the ileal pathogen Yersinia enterocolitica and an elevated inflammatory cytokine res

61 PspC destabilization is conserved between Y. enterocolitica and E. coli.

62 fore, we investigated the role of ArcB in Y. enterocolitica and E. coli.

63 sis while negatively regulated by YmoA in Y. enterocolitica and H-NS in Y. pseudotuberculosis.

64 e translocator domains of YadA from Yersinia enterocolitica and Hia from Haemophilus influenzae.

65 antipathogenic effects in the gut against Y. enterocolitica and highlight the need to investigate the

66 l)-l-homoserine lactone (3-oxo-C6-HSL) in Y. enterocolitica and inhibit QS-associated biofilm maturat

67 secretes (Yops), prevents phagocytosis of Y. enterocolitica and is required for disease processes in

68 e Yop secretion protein (Ysc) M2 of Yersinia enterocolitica and LcrQ of Y. pestis, formerly described

69 higella spp., Campylobacter spp. or Yersinia enterocolitica and matched each with up to 4 unexposed s

70 Yersinia enterocolitica and related bacteria with a defective Psp

71 The in situ structures of the Y. enterocolitica and S. flexneri injectisomes had similar

72 Escherichia coli, Yersinia enterocolitica and Salmonella enterica serovar Typhimuri

73 response required for virulence in Yersinia enterocolitica and Salmonella enterica.

74 irst three-dimensional structure of Yersinia enterocolitica and Shigella flexneri injectisomes in sit

75 cylhomoserine lactones (AHLs) produced by Y. enterocolitica and upregulates the expression of an inva

76 ttle overlap between the RovA regulons of Y. enterocolitica and Y. pestis despite the fact that RovA

77 actors Vn and C4BP, and Ail homologs from Y. enterocolitica and Y. pseudotuberculosis recruit factor

78 ediates the transcription of inv in Yersinia enterocolitica and Y. pseudotuberculosis.

79 erved mechanism of inv regulation between Y. enterocolitica and Y. pseudotuberculosis.

80 are conserved in Yersinia, divergence of Y. enterocolitica and Y. pseudotuberculosis/Y. pestis durin

81 ences between Yersinia enterocolitica subsp. enterocolitica and Yersinia enterocolitica subsp. palear

82 h is positively regulated by RovA in both Y. enterocolitica and Yersinia pseudotuberculosis while neg

83 jor adhesion and invasion factor in Yersinia enterocolitica and Yersinia pseudotuberculosis.

84 nce method was 1.2% ETEC, 0.1% Vibrio, 0% Y. enterocolitica, and 0% P. shigelloides Compared to the r

85 identified the Salmonella species, Yersinia enterocolitica, and Campylobacter species but failed to

86 mon food pathogens, including E. coli and Y. enterocolitica, and could even detect Salmonella spp. fr

87 ethods for the detection of ETEC, Vibrio, Y. enterocolitica, and P. shigelloides in stool specimens f

88 10-fold higher than that of the wild-type Y. enterocolitica, and there are significant inflammatory r

89 , E. coli O157:H7, Vibrio cholerae, Yersinia enterocolitica, and toxigenic Clostridium difficile), pa

90 he pathogenic Yersiniae (Yersinia pestis, Y. enterocolitica, and Y. pseudotuberculosis).

91 this study we show that PspB and PspC of Y. enterocolitica are dual function proteins, acting both a

92 ar Typhimurium (S. typhimurium) and Yersinia enterocolitica are enteric pathogens capable of colonizi

93 spectroscopy, we show that in live Yersinia enterocolitica bacteria these soluble proteins form comp

94 We also show that RovA and H-NS from Y. enterocolitica bind to a similar region of the inv promo

95 Y. enterocolitica biovar 1B additionally has a distinct chr

96 Yersinia enterocolitica biovar 1B contains two type III secretion

97 Yersinia enterocolitica biovar 1B employs two type three secretio

98 Yersinia enterocolitica biovar 1B maintains three distinct type I

99 Full virulence of Yersinia enterocolitica Biovar 1B requires two distinct and dista

100 rally dynamic gene expression patterns of Y. enterocolitica biovar 1B through the course of an in vit

101 opened with the discovery of the Ysps of Y. enterocolitica Biovar 1B, which are translocated into ho

102 FtsH destabilizes PspC in Y. enterocolitica, but coproduction of PspC with its bindin

103 when YspP was constitutively expressed in Y. enterocolitica bv.

104 ances gastrointestinal infection by Yersinia enterocolitica bv. 1B.

105 dritic cells, and a yopP mutant of a live Y. enterocolitica carrier vaccine elicited effective primin

106 Yersinia enterocolitica causes a severe enteric infection in infa

107 Infection with Yersinia enterocolitica causes acute diarrhea in early childhood.

108 Yersinia enterocolitica causes an estimated 116,716 illnesses ann

109 Yersinia enterocolitica causes human gastroenteritis, and many is

110 After Y. enterocolitica challenge, YopB/LcrV+dmLT-vaccinated mice

111 es to protect against an otherwise lethal Y. enterocolitica challenge.

112 ytxAB genes are not closely linked in the Y. enterocolitica chromosome, and whereas ytxR is present i

113 curring in response to S. typhimurium and Y. enterocolitica colonization of PP using Affymetrix GeneC

114 ate a diverse collection of 94 strains of Y. enterocolitica consisting of 35 human, 35 pig, 15 sheep,

115 These results reveal facets of how Y. enterocolitica controls the function of the Ysa TTS syst

116 The enteropathogenic bacterium Yersinia enterocolitica deactivates TLR-induced signaling pathway

117 coccus aureus, Escherichia coli and Yersinia enterocolitica--demonstrated that the zone of inhibition

118 n that a number of RovA-regulated loci in Y. enterocolitica do not have orthologues in Y. pestis and

119 few intestinal pathogens, including Yersinia enterocolitica, do produce acyl-HSLs, and Salmonella can

120 Further analysis revealed that Y. enterocolitica does not cluster according to source (hos

121 These findings add a new aspect of how Y. enterocolitica effectively evades the host complement sy

122 retion system of the human pathogen Yersinia enterocolitica enabled efficient identification of secre

123 irus, rotavirus A, Vibrio cholerae, Yersinia enterocolitica, Entamoeba histolytica, Cryptosporidium s

124 spp., Vibrio spp., Vibrio cholerae, Yersinia enterocolitica, enteroaggregative E. coli, enteropathoge

125 tool specimens for the detection of Yersinia enterocolitica, enterotoxigenic Escherichia coli (ETEC),

126 After i.p. inoculation with Y. enterocolitica, fibrinogen-deficient mice display impair

127 However, Y. enterocolitica had no effect on S. Typhimurium uptake by

128 udotuberculosis and Y. pestis and YopP in Y. enterocolitica has been shown to regulate host immune re

129 Yersinia enterocolitica has three type three secretion systems, t

130 in the genomes of E. coli O157:H7, Yersinia enterocolitica, Helicobacter pylori, and Vibrio cholerae

131 a does detect the AHL production of Yersinia enterocolitica in mouse Peyer's patches.

132 al the complete set of genes expressed by Y. enterocolitica in response to infection and provide the

133 Even though Y. enterocolitica induces a robust inflammatory response du

134 ro FTY720 treatment downregulated CCR7 on Y. enterocolitica-infected bone marrow-derived DCs and puri

135 NF-Y increases Yop translocation in Yersinia enterocolitica-infected cells up to 5-fold.

136 Fingolimod (FTY720) treatment of Y. enterocolitica-infected mice reduced the CD11b(-) subset

137 D103(+)CD11b(+)) were found in the RLN of Y. enterocolitica-infected TNFRp55(-/-) mice.

138 On day 14 after Y. enterocolitica infection (arthritis onset), we found tha

139 During Yersinia enterocolitica infection CD4+ cells are the source of de

140 inflammatory cytokines in the control of Y. enterocolitica infection in IL-6(-/-) mice was undertake

141 ribed here compare oral S. typhimurium or Y. enterocolitica infection in stromelysin-1 (MMP-3)-defici

142 A striking feature of the pathology of a Y. enterocolitica infection is inflammation.

143 rant acute inflammatory response to Yersinia enterocolitica infection leads to long-lasting shifts in

144 One role of IL-6 during a Y. enterocolitica infection may be the downmodulation of th

145 Y. enterocolitica infection promoted the development of ant

146 Establishment of S2 cells as a model for Y. enterocolitica infection provides a versatile tool to el

147 of 7-day-old and adult mice to orogastric Y. enterocolitica infection were assessed in 50% lethal dos

148 nt secretion of IL-8 in response to Yersinia enterocolitica infection were dependent on extracellular

149 (1) receptor is important for controlling Y. enterocolitica infection within the Peyer's patches and

150 -6 plays an anti-inflammatory role during Y. enterocolitica infection, and in other systems IL-6 has

151 LT achieved 60% protection against lethal Y. enterocolitica infection, and vaccine efficacy increased

152 g protective roles for CD4 T cells during Y. enterocolitica infection, vaccinating mice with a 16-ami

153 y to activate innate immunity after Yersinia enterocolitica infection.

154 ion of gut inflammation characteristic of Y. enterocolitica infection.

155 for protection of neonates during primary Y. enterocolitica infection.

156 significantly up-regulated in response to Y. enterocolitica infection.

157 intestinal inflammation in response to a Y. enterocolitica infection.

158 l model for studying the host response to Y. enterocolitica infection.

159 stics previously described following i.v. Y. enterocolitica infection.

160 ory role of this endogenous lectin during Y. enterocolitica infection.

161 exhibited higher expression of CCR7 after Y. enterocolitica infection.

162 Y. enterocolitica infections in FoodNet sites have signific

163 From 1996 through 2009, 2085 Y. enterocolitica infections were reported to FoodNet.

164 ive surveillance for laboratory-confirmed Y. enterocolitica infections, defined as the isolation of Y

165 These data suggest that Y. enterocolitica inhibits intracellular pre-IL-1alpha sign

166 SA (via an IC intermediate) as does Yersinia enterocolitica Irp9.

167 Yersinia enterocolitica is a food-borne pathogen that preferentia

168 Yersinia enterocolitica is a gram-negative enteric pathogen respo

169 hanisms in which the enteropathogen Yersinia enterocolitica is able to disseminate from the lumen of

170 Yersinia enterocolitica is able to efficiently invade Peyer's pat

171 Yersinia enterocolitica is an enteric pathogen capable of causing

172 Yersinia enterocolitica is an enteropathogenic bacterium that cau

173 We show here that Y. enterocolitica is capable of infecting S2 cells and repl

174 The salicylate synthase, Irp9, from Yersinia enterocolitica is involved in the biosynthesis of the si

175 However, because Y. enterocolitica is typically a food-borne pathogen, the o

176 Yersinia enterocolitica is typically considered an extracellular

177 Escherichia coli (EHEC) isolates, 2 Yersinia enterocolitica isolates, 2 Campylobacter species, and 23

178 Y. enterocolitica lacking the virulence plasmid failed to i

179 as prevented when mice were infected with Y. enterocolitica lacking YopP or YopH, two critical effect

180 neonatal mice with low doses of virulent Y. enterocolitica leads to vigorous intestinal and systemic

181 ified a new positive regulator of rovA in Y. enterocolitica, LeuO.

182 oan (Toxoplasma gondii), bacterial (Yersinia enterocolitica, Listeria monocytogenes, and Mycobacteriu

183 The Yersinia enterocolitica LuxI homologue YenI directs the synthesis

184 Pathogenic biovars of Yersinia enterocolitica maintain the well-studied plasmid-encoded

185 Y. enterocolitica mutants lacking either the Ysa or Ysc T3S

186 4, 8%), norovirus (n = 14, 8%), and Yersinia enterocolitica (n = 7, 4%).

187 =14, 8%), norovirus (n=14, 8%), and Yersinia enterocolitica (n=7, 4%).

188 osa and joints in a murine model of Yersinia enterocolitica O:3-induced reactive arthritis (ReA) in T

189 on-ready tetrasaccharide of O-PS of Yersinia enterocolitica O:50 strain 3229 and the trisaccharide of

190 s KIM D27 LcrV (LcrV(D27)) bind LcrV from Y. enterocolitica O:9 strain W22703 (LcrV(W22703)) or O:8 s

191 no effect on extracellular nonsiderophilic Y enterocolitica O8 or Staphylococcus aureus Hepcidin anal

192 derophilic extracellular pathogens (Yersinia enterocolitica O9) by controlling non-transferrin-bound

193 Mutating all CSC-boxes in Y. enterocolitica of a plasmid bound cspA1/A2 dramatically

194 t interactions between S. Typhimurium and Y. enterocolitica or that the SdiA regulon members do not f

195 a infections, defined as the isolation of Y. enterocolitica or unspeciated Yersinia from a human clin

196 modest (10-30%) protection against lethal Y. enterocolitica oral infection.

197 Y. enterocolitica organisms were more virulent in the IL-6(

198 a regulatory role for this lectin during Y. enterocolitica pathogenesis, mice lacking Gal-1 showed i

199 ressed in mucosal tissues, contributes to Y. enterocolitica pathogenicity by undermining protective a

200 2 recombined with a close relative of the Y. enterocolitica phage phiYeO3-12 to yield progeny phages,

201 The Yersinia enterocolitica phage shock protein (Psp) stress response

202 The Yersinia enterocolitica phage shock protein (Psp) system is induc

203 The Yersinia enterocolitica phage-shock-protein (Psp) stress response

204 e early precursor B cells are expanded by Y. enterocolitica porins to undergo somatic hypermutation t

205 ngle factor mediating serum resistance of Y. enterocolitica, presumably by binding C4b binding protei

206 (A) modified with C16:0 predominated, and Y. enterocolitica produced a unique tetra-acylated lipid A.

207 The mammalian enteropathogen Yersinia enterocolitica produces two main N-acylhomoserine lacton

208 -NS and RovA bind is not conserved in the Y. enterocolitica promoter.

209 rall, these studies support the idea that Y. enterocolitica promotes the development of highly inflam

210 ologues but is not conserved in the Yersinia enterocolitica protein.

211 The role of microbial Ags was tested with Y. enterocolitica proteins.

212 The Y. enterocolitica psp locus is made up of two divergently t

213 Yersinia enterocolitica psp mutants cannot grow when the secretin

214 ore, PspG is the missing component of the Y. enterocolitica Psp regulon that was previously predicted

215 e proteins involved in inducing the Yersinia enterocolitica Psp stress response.

216 tudy addressed these issues for the Yersinia enterocolitica Psp system.

217 We also compared induction of the Y. enterocolitica Psp, RpoE, and Cpx responses.

218 Previously, we reported that Y. enterocolitica PspB functions to positively control the

219 dence that it is the C-terminal domain of Y. enterocolitica PspC (PspC(CT)) that interacts directly w

220 The Y. enterocolitica pspG gene was identified because its prom

221 In adult mice, Y. enterocolitica rapidly disseminated to the spleen and li

222 Yersinia enterocolitica rarely causes extraintestinal disease.

223 Enteric pathogens such as Yersinia enterocolitica readily colonize and induce disease withi

224 dent and distantly related TTS systems of Y. enterocolitica recognize protein substrates by a similar

225 Y. enterocolitica reduces S. Typhimurium invasion of HeLa a

226 ion with the model enteric pathogen Yersinia enterocolitica reduces the mean time to death by 1 day (

227 The YenR and YenI proteins of Yersinia enterocolitica resemble the quorum sensing proteins LuxR

228 ogenous chromosomally encoded proteins in Y. enterocolitica revealed discrete complexes corresponding

229 Analysis of the core gene set for Y. enterocolitica revealed that 20.8% of the genes were sha

230 protein reporters, we determined that the Y. enterocolitica rovA (rovA(Yent)) promoter is weaker than

231 A Y. enterocolitica rovA mutant has a significant decrease in

232 In Yersinia pseudotuberculosis and Yersinia enterocolitica, RovA regulates expression of the invasio

233 Furthermore, in Y. enterocolitica RovM only in the presence of Hfq affected

234 raphy to solve the structure of the Yersinia enterocolitica RsmA homologue.

235 he rfaH genes from Vibrio cholerae, Yersinia enterocolitica, S. enterica serovar Typhimurium, and Kle

236 in the physiology and virulence of Yersinia enterocolitica serotype O:3.

237 ches of mice infected orogastrically with Y. enterocolitica serotype O:8 compared with noninfected ho

238 the lipopolysaccharide O-antigen of Yersinia enterocolitica serovars O:5/O:5,27.

239 Sequence analysis of the JB580v strain of Y. enterocolitica shows that, due to a premature stop codon

240 pestis) was obtained with 1 (of 10) Yersinia enterocolitica strains and 2 (of 10) Yersinia pseudotube

241 cannot block type III injection by Yersinia enterocolitica strains and suggested that lcrV polymorph

242 Infection of eukaryotic cells with Y. enterocolitica strains expressing a Ysp-CyaA chimeric pr

243 The highly pathogenic Yersinia enterocolitica strains have a chromosomally encoded type

244 unable to block the type III injection of Y. enterocolitica strains, expression of lcrV(W22703) or lc

245 ise unable to block type III injection by Y. enterocolitica strains.

246 tained using two different high-virulence Y. enterocolitica strains.

247 ss, the ytxAB genes are conserved in many Y. enterocolitica strains.

248 ia species, and differences between Yersinia enterocolitica subsp. enterocolitica and Yersinia entero

249 ocolitica subsp. enterocolitica and Yersinia enterocolitica subsp. palearctica.

250 m is primarily an intracellular pathogen, Y. enterocolitica survives primarily extracellularly.

251 t the RovA regulon may be dispensable for Y. enterocolitica systemic disease and inflammatory respons

252 s maltophilia, Vibrio cholerae, and Yersinia enterocolitica T2S-expressing plant pathogens include Di

253 d to the N-terminal fragment of the Yersinia enterocolitica T3S substrate YopE, are effectively deliv

254 slocation of TARP by a heterologous Yersinia enterocolitica T3SS.

255 Y. enterocolitica tends to persist in soil for long periods

256 ction, C57BL/6 mice are more resistant to Y. enterocolitica than are BALB/c mice.

257 rough mice infected with a yenI mutant of Y. enterocolitica that cannot synthesize AHLs.

258 nic Yersinia pseudotuberculosis and Yersinia enterocolitica) that mediate a low-calcium response.

259 CSC-box into a plasmid-bound lacZ gene in Y. enterocolitica, the mRNA of this construct was cleaved w

260 the Ysa TTS system impacts the ability of Y. enterocolitica to colonize gastrointestinal tissues.

261 In this study, we tested the ability of Y. enterocolitica to modulate intracellular IL-1alpha-depen

262 important human-pathogenic species Yersinia enterocolitica to whole-genome resolution levels.

263 Yersinia enterocolitica transports YscM1 and YscM2 via the type I

264 Yersinia enterocolitica type III secretion machines transport Yop

265 To subvert the host's immune response, Y. enterocolitica uses a type III secretion system consisti

266 Yersinia enterocolitica uses type III secretion to transport Yop

267 en linked to robust phenotypes, including Y. enterocolitica virulence.

268 otein (Psp) system is essential for Yersinia enterocolitica virulence.

269 yopR variants of Yersinia enterocolitica W22703 displayed a reduced ability to inj

270 screened transposon insertion mutants of Y. enterocolitica W22703 for defects in type III secretion

271 n against lethal oral infections by Yersinia enterocolitica WA and Y. pseudotuberculosis PB1+.

272 Y. enterocolitica was also able to inhibit the invasion of

273 s cereus was the most sensitive and Yersinia enterocolitica was found to be the most resistant.

274 Y. enterocolitica was present within the murine mucosa of b

275 he bacteria to colonize neonatal tissues; Y. enterocolitica was readily detectable in the intestine a

276 -coil adhesin homologous to YadA of Yersinia enterocolitica, was hypothesized to mediate the interact

277 ical properties of YscN and YscL of Yersinia enterocolitica, we have characterized them as the ATPase

278 to host cell uptake of S. Typhimurium and Y. enterocolitica, we investigated how each pathogen influe

279 Using Yersinia enterocolitica, we show that oral infection promotes T(H

280 responses elicited in neonates exposed to Y. enterocolitica were associated with long-term protection

281 val of MMP-3-deficient mice infected with Y. enterocolitica when compared with littermate controls.

282 a Gram-negative bacterial pathogen, Yersinia enterocolitica, when subjected to low temperature and se

283 coli, Salmonella enterica and also Yersinia enterocolitica, where it is essential for virulence.

284 yopP-deficient strain than with wild-type Y. enterocolitica, whereas only modest increases occurred i

285 osed of ~22 copies of SctQ (YscQ in Yersinia enterocolitica), which require the presence of YscQC, th

286 a marcescens, Escherichia coli, and Yersinia enterocolitica, which have some similarities in their MA

287 mon to three pathogenic Yersinia species: Y. enterocolitica, Y. pseudotuberculosis, and Y. pestis.

288 ilus influenzae Hia adhesin and the Yersinia enterocolitica YadA adhesin.

289 g model of factor H to YadA and show that Y. enterocolitica YadA recruits C3b and iC3b directly, with

290 rsinia pseudotuberculosis (Ypt) and Yersinia enterocolitica (Ye), as well as the causative agent of p

291 In a Y. enterocolitica yenI mutant, swimming motility is tempora

292 ivity, we have characterized the OGL from Y. enterocolitica, YeOGL, on oligogalacturonides and determ

293 The type III secretion signal of Yersinia enterocolitica YopN was mapped using a gene fusion appro

294 We report the MgADP structure of Yersinia enterocolitica YopO in complex with actin, which reveals

295 The Yersinia enterocolitica ysa T3SS is activated in response to NaCl

296 The Yersinia enterocolitica Ysa T3SS is such a system, where the appa

297 Using a genetic approach, a collection of Y. enterocolitica Ysa TTS mutants was generated by mutagene

298 osttranscriptional gene regulation, Yersinia enterocolitica yscM1 and yscM2 as well as Yersinia pesti

299 regulator that controls expression of the Y. enterocolitica ytxAB genes.

300 The Yersinia enterocolitica YtxR protein is a LysR-type transcription