ライフサイエンスコーパス: enterocolitica

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

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

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

4 extensively in Escherichia coli and Yersinia enterocolitica.

5 tive immunity against Gram-negative Yersinia enterocolitica.

6 against the Gram-negative bacterium Yersinia enterocolitica.

7 riaceae, such as the enteropathogen Yersinia enterocolitica.

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

9 tive signal transduction pathway in Yersinia enterocolitica.

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

11 es using the gastroenteric pathogen Yersinia enterocolitica.

12 ted with the AHL-producing pathogen Yersinia enterocolitica.

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

14 in naive macrophages infected with Yersinia enterocolitica.

15 n of FtsQ from Escherichia coli and Yersinia enterocolitica.

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

17 response to prolonged secretin stress in Y. enterocolitica.

18 s susceptible to the enteropathogen Yersinia enterocolitica.

19 ric infection by the proteobacteria 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 ellin of Salmonella Typhimurium and Yersinia enterocolitica.

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

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

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

33 lague, Yersinia pseudotuberculosis, Yersinia enterocolitica.

34 es, Yersinia pseudotuberculosis and Yersinia enterocolitica.

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

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

37 h is the primary invasion factor of Yersinia enterocolitica.

38 y informative typing scheme available for Y. enterocolitica.

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

40 istant to orogastric infection with Yersinia enterocolitica.

41 spontaneously arising pathogenic Ab with Y. enterocolitica.

42 coccus aureus, Escherichia coli and Yersinia enterocolitica.

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

44 thogenesis, including the bacterium Yersinia enterocolitica.

45 illus cereus, Escherichia coli, and Yersinia enterocolitica.

46 teins at their endogenous levels in Yersinia enterocolitica.

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

48 ontyphoidal Salmonella species, and Yersinia 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 ediates the transcription of inv in Yersinia enterocolitica and Y. pseudotuberculosis.

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

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

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

81 li, Shigella spp., Salmonella spp., Yersinia enterocolitica and Yersinia pestis.

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 Infection with Yersinia enterocolitica causes acute diarrhea in early childhood.

107 Yersinia enterocolitica causes an estimated 116,716 illnesses ann

108 Yersinia enterocolitica causes human gastroenteritis, and many is

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

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

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

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

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

114 itial examination of the effectiveness of Y. enterocolitica cya and crp mutants to stimulate protecti

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

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

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

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

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

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

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

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

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

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

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

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

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

128 Yersinia enterocolitica has three type three secretion systems, t

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

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

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

132 on of Ysps with Yop effectors secreted by Y. enterocolitica indicated that YspG, YspH, and YspJ have

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

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

135 Examination of Y. enterocolitica-infected J774A.1 macrophages revealed tha

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

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

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

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

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

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

142 Y. enterocolitica infection promoted the development of ant

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

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

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

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

147 -6 plays an anti-inflammatory role during Y. enterocolitica infection, and in other systems IL-6 has

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

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

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

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

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

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

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

155 y to activate innate immunity after Yersinia enterocolitica infection.

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

157 Y. enterocolitica infections in FoodNet sites have signific

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

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

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

161 of targeting YopP and that they influence Y. enterocolitica interactions with macrophages.

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

163 Yersinia enterocolitica is a food-borne pathogen that preferentia

164 Yersinia enterocolitica is a gram-negative enteric pathogen respo

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

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

167 Yersinia enterocolitica is an enteric pathogen capable of causing

168 Yersinia enterocolitica is an enteropathogenic bacterium that cau

169 Yersinia enterocolitica is an invasive enteric pathogen that caus

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

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

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

173 Yersinia enterocolitica is typically considered an extracellular

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

175 Y. enterocolitica lacking the virulence plasmid failed to i

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

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

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

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

180 The Yersinia enterocolitica LuxI homologue YenI directs the synthesis

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

182 Yersinia enterocolitica maintains three different pathways for ty

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

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

185 Yersinia enterocolitica O:8 has two contact-dependent type III se

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

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

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

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

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

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

192 Yersinia enterocolitica organisms secrete Yop proteins via the ty

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

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

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

196 2 recombined with a close relative of the Y. enterocolitica phage phiYeO3-12 to yield progeny phages,

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

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

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

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

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

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

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

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

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

206 in Yersinia pseudotuberculosis and Yersinia enterocolitica prompted the model in which LcrQ negative

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

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

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

210 Yersinia enterocolitica psp mutants cannot grow when the secretin

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

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

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

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

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

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

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

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

219 Yersinia enterocolitica rarely causes extraintestinal disease.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

245 ocolitica subsp. enterocolitica and Yersinia enterocolitica subsp. palearctica.

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

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

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

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

250 slocation of TARP by a heterologous Yersinia enterocolitica T3SS.

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

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

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

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

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

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

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

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

259 Yersinia enterocolitica transports YscM1 and YscM2 via the type I

260 Yersinia enterocolitica type III secretion machines transport Yop

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

262 Yersinia enterocolitica uses type III secretion to transport Yop

263 that the Ysa and Ysc TTSSs contribute to Y. enterocolitica virulence by exporting both unique and co

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

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

266 AMP-CRP regulatory system is required for Y. enterocolitica virulence.

267 lipase YplA, which has been implicated in Y. enterocolitica virulence.

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

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

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

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

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

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

274 outer membrane adhesin/invasin from Yersinia enterocolitica, was detected in purified outer membrane

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

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

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

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

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

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

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

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

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

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

285 ons were isolated in cya and crp of Yersinia enterocolitica, which encode adenylate cyclase and the c

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

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

292 gatively regulate the expression of Yersinia enterocolitica yop genes.

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