ライフサイエンスコーパス: Yersinia pestis

1 trophic European Black Death/bubonic plague (Yersinia pestis).

2 formational stability of the chaperone LcrH (Yersinia pestis).

3 om the genome of the closely related species Yersinia pestis.

4 oding putative c-di-GMP metabolic enzymes in Yersinia pestis.

5 -encoded type III secretion system (T3SS) of Yersinia pestis.

6 tes, obesity, and infection by the bacterium Yersinia pestis.

7 rulence protein YopM of the plague bacterium Yersinia pestis.

8 in human history, is caused by the bacterium Yersinia pestis.

9 ics against the potential bioterrorism agent Yersinia pestis.

10 nto eukaryotic cells by the plague bacterium Yersinia pestis.

11 tions, is transmitted by fleas infected with Yersinia pestis.

12 re resistant to several pathogens, including Yersinia pestis.

13 nctioning in Yersinia pseudotuberculosis and Yersinia pestis.

14 hilum, and five (2.7%) were seropositive for Yersinia pestis.

15 Salmonella spp., Yersinia enterocolitica and Yersinia pestis.

16 the phosphatase YopH, a bacterial toxin from Yersinia pestis.

17 cterial pathogens Listeria monocytogenes and Yersinia pestis.

18 responses that occur following inhalation of Yersinia pestis.

19 ts from pulmonary infection by the bacterium Yersinia pestis.

20 ncient plague strains are basal to all known Yersinia pestis.

21 genome sequences, of which the majority are Yersinia pestis.

22 ue is a deadly respiratory disease caused by Yersinia pestis.

23 ement for Hfq in the closely related species Yersinia pestis.

24 Yersinia pestis, a Gram-negative bacterium that causes b

25 Plague is initiated by Yersinia pestis, a highly virulent bacterial pathogen.

26 Here we studied the interaction between the Yersinia pestis ABC heme importer (HmuUV) and its partne

27 The Yersinia pestis adhesin molecule Ail interacts with the

28 Yersinia pestis adopts a unique life stage in the digest

29 he consequence of a singular introduction of Yersinia pestis, after which the disease established its

30 oximately 150 in silico DNA fingerprints for Yersinia pestis and 250 fingerprints for Francisella tul

31 specially potential bioterrorism agents like Yersinia pestis and Bacillus anthracis which feature on

32 of the same species, including 5 strains of Yersinia pestis and Bacillus anthracis.

33 the strictly conserved glycine to serine in Yersinia pestis and Escherichia coli topoisomerase I res

34 Characterization of these mutants of Yersinia pestis and Escherichia coli topoisomerase I sho

35 ly or intratracheally with the F1 antigen of Yersinia pestis and flagellin exhibited dramatic increas

36 tant of 20 nM between EGFP-labeled LcrV from Yersinia pestis and its cognate membrane-bound protein Y

37 Yersinia pestis and many other Gram-negative pathogenic

38 shared approximately 70-kb plasmids (pCD in Yersinia pestis and pYV in enteropathogenic Yersinia pse

39 he cell surface of both Escherichia coli and Yersinia pestis and show that a subset of these proteins

40 o systemic infection with the KIM5 strain of Yersinia pestis and that B10.T(6R) mice become susceptib

41 tant to pigmentation locus-negative (pgm(-)) Yersinia pestis and that this phenotype maps to a 30-cen

42 s both the protective F1 capsular antigen of Yersinia pestis and the LcrV protein required for secret

43 e identification of new virulence factors in Yersinia pestis and understanding their molecular mechan

44 We report that biofilms produced by Yersinia pestis and Y. pseudotuberculosis, which bind th

45 owed differences in virulence genes found in Yersinia pestis and Yersinia pseudotuberculosis compared

46 nt of YopJ-dependent cytotoxicity induced by Yersinia pestis and Yersinia pseudotuberculosis paradoxi

47 ages were infected with a panel of different Yersinia pestis and Yersinia pseudotuberculosis strains

48 transcription factor, regulates virulence in Yersinia pestis and Yersinia pseudotuberculosis.

49 Flea-borne zoonoses such as plague (Yersinia pestis) and murine typhus (Rickettsia typhi) ca

50 flammatory response induced by other lethal (Yersinia pestis) and non-lethal (Legionella pneumophila,

51 a and Salmonella enterica serovar Typhi, and Yersinia pestis), and 3 protozoa (Leishmania spp., Plasm

52 athogenicity island, originally described in Yersinia pestis, and encodes proteins with apparent homo

53 Pseudomonas aeruginosa, Salmonella enterica, Yersinia pestis, and Enterococcus faecalis, indicating t

54 rofloxacin resistance in Bacillus anthracis, Yersinia pestis, and Francisella tularensis.

55 een host-pathogen interactions of B. mallei, Yersinia pestis, and Salmonella enterica.

56 des genes from pathogens such as Salmonella, Yersinia pestis, and the virulent Francisella tularensis

57 The reaction mechanism of Yersinia pestis arginine decarboxylase has been investig

58 ut a potential use of the causative bacteria Yersinia pestis as an agent of biological warfare have h

59 gens, including the plague causing bacterium Yersinia pestis, avoid activating this pathway to enhanc

60 ion of either Yersinia pseudotuberculosis or Yersinia pestis bacteria express the small RNAs YSR35 or

61 molecule cyclic diguanylate is essential for Yersinia pestis biofilm formation that is important for

62 itted by fleas whose feeding is blocked by a Yersinia pestis biofilm in the digestive tract.

63 and type of medium peptides associated with Yersinia pestis biomass and improve the quality of prote

64 a) in a 19th century intestinal specimen and Yersinia pestis ("Black Death" plague) in a medieval too

65 Several gram-negative pathogens, including Yersinia pestis, Burkholderia cepacia, and Acinetobacter

66 ity pathogens, including Bacillus anthracis, Yersinia pestis, Burkholderia mallei, Francisella tulare

67 Misidentification of Yersinia pestis by automated identification systems cont

68 for the type III secretion system (T3SS) in Yersinia pestis by interaction with the negative regulat

69 nto a constitutively active IpaH enzyme from Yersinia pestis by introduction of single site substitut

70 trument's response to Bacillus anthracis and Yersinia pestis by spiking the liquid sample stream with

71 es the invasiveness of the plague bacterium, Yersinia pestis, by activating plasminogen to plasmin to

72 The plague bacillus Yersinia pestis can achieve transmission by biofilm bloc

73 To test whether the protective Ags to Yersinia pestis can be orally delivered, the Y. pestis c

74 Surprisingly, Yersinia pestis can promote PhoP-dependent modification

75 ine against plague currently consists of the Yersinia pestis capsular antigen F1 and the type 3 secre

76 The Gram-negative bacteria Yersinia pestis, causative agent of plague, is extremely

77 The 14th-18th century pandemic of Yersinia pestis caused devastating disease outbreaks in

78 Yersinia pestis causes bubonic plague, a fulminant disea

79 Yersinia pestis causes bubonic plague, characterized by

80 Yersinia pestis causes bubonic, pneumonic, and septicemi

81 The Gram-negative bacterium Yersinia pestis causes plague, a rapidly progressing and

82 Pulmonary infection by Yersinia pestis causes pneumonic plague, a necrotic bron

83 Pulmonary infection by Yersinia pestis causes pneumonic plague, a rapidly progr

84 The Gram-negative bacterium Yersinia pestis causes pneumonic plague, an acutely leth

85 Pulmonary infection with the bacterium Yersinia pestis causes pneumonic plague, an often-fatal

86 Yersinia pestis causes primary pneumonic plague in many

87 Yersinia pestis causes the fatal respiratory disease pne

88 The aerosol form of the bacterium Yersinia pestis causes the pneumonic plague, a rapidly f

89 tructures of three active-site complexes for Yersinia pestis class IV AC (AC-IV)-two with substrate a

90 aled dose of 1.02 x 10(6) CFU of aerosolized Yersinia pestis CO92 (50% lethal dose, 6.8 x 10(4) CFU).

91 Yersinia pestis CO92 has 12 open reading frames encoding

92 Braun lipoprotein (Lpp) and MsbB attenuated Yersinia pestis CO92 in mouse and rat models of bubonic

93 sal instillation of a fully virulent strain, Yersinia pestis CO92, guinea pigs developed lethal lung

94 mples from mice experimentally infected with Yersinia pestis CO92.

95 Vaccination with live attenuated Yersinia pestis confers protection against pneumonic pla

96 The pH 6 antigen (Psa) of Yersinia pestis consists of fimbriae that bind to two re

97 The pH 6 antigen (Psa) of Yersinia pestis consists of fimbriae with adhesive prope

98 ella enterica serovar Typhimurium) and HmsT (Yersinia pestis) contain GGDEF domains and are required

99 Analysis of a Yersinia pestis Delta caf1A mutant demonstrated that the

100 A Yersinia pestis-derived fusion protein (F1-V) has shown

101 l infection of BALB/c mice with nonpigmented Yersinia pestis does not result in pneumonic plague.

102 ts the most severe form of disease caused by Yersinia pestis due to its ease of transmission, rapid p

103 ylase (KdoO) from Burkholderia ambifaria and Yersinia pestis, encoded by the bamb_0774 (BakdoO) and t

104 iosynthesis from Mycobacterium tuberculosis, Yersinia pestis, Escherichia coli, Vibrio cholerae, Baci

105 Yersinia pestis evolved from Y. pseudotuberculosis to be

106 In American grasslands, plague, caused by Yersinia pestis, exemplifies this quiescent-outbreak pat

107 0 degrees C), the causative agent of plague, Yersinia pestis, expresses a profile of genes distinct f

108 of mice with a recombinant fusion protein of Yersinia pestis F1 and LcrV Ags (F1-V) together with EdT

109 plant-made plague vaccine, we expressed the Yersinia pestis F1-V antigen fusion protein in tomato.

110 vaccine, we expressed our model antigen, the Yersinia pestis F1-V antigen fusion protein, with and wi

111 pture-based immunochromatographic dipsticks, Yersinia Pestis (F1) Smart II and Plague BioThreat Alert

112 ewanella oneidensis, Salmonella typhimurium, Yersinia pestis) for training and validation within and

113 s, Bacteroides fragilis, Bacillus anthracis, Yersinia pestis, Francisella tularensis, and Brucella ab

114 aromyces cerevisiae, Pseudomonas aeruginosa, Yersinia pestis, Francisella tularensis, Bacillus anthra

115 uences were designed for Bacillus anthracis, Yersinia pestis, Francisella tularensis, Brucella melite

116 acids from BT organisms (Bacillus anthracis, Yersinia pestis, Francisella tularensis, Brucella spp.,

117 -six distinct strains of Bacillus anthracis, Yersinia pestis, Francisella tularensis, Burkholderia ma

118 C57BL/6 mice infected with attenuated Yersinia pestis generate a dominant H2-Kb-restricted CD8

119 entional autotransporters are present in the Yersinia pestis genome, but only one, YapE, is conserved

120 Yersinia pestis has acquired a variety of complex strate

121 Yersinia pestis has caused at least three human plague p

122 ated human pathogens Salmonella enterica and Yersinia pestis has entailed functional changes in the P

123 While Yersinia pestis has multiple iron transporters, the yers

124 The causative bacterium, Yersinia pestis, has the potential to be exploited as a

125 Because Yersinia pestis HasA (HasA(yp)) presents a Gln at positi

126 utic strategies that prevent infections with Yersinia pestis have been sought for over a century.

127 o conditionally virulent Deltapgm strains of Yersinia pestis; however, fully virulent Y. pestis is no

128 ere, we report the oldest direct evidence of Yersinia pestis identified by ancient DNA in human teeth

129 tudies (influenza A in lesser snow geese and Yersinia pestis in coyotes), we argue that with careful

130 ery that regulates the entry and survival of Yersinia pestis in host macrophages is poorly understood

131 activator PhoP is important for survival of Yersinia pestis in macrophage phagosomes.

132 Growth restriction of Yersinia pestis in the absence of calcium (low-calcium r

133 ated with iron(III)-yersiniabactin import in Yersinia pestis In this study, we compared the impact of

134 responses of C57BL/6 and SEG MPs exposed to Yersinia pestis in vitro were examined.

135 Pneumonic plague resulting from Yersinia pestis induces swiftly lethal sepsis and is a m

136 ns cause host cell death upon infection, and Yersinia pestis, infamous for its role in large pandemic

137 HMBPP/IL-2 administration after inhalational Yersinia pestis infection induced marked expansion of Vg

138 A hallmark of Yersinia pestis infection is a delayed inflammatory resp

139 te to one of the most documented symptoms of Yersinia pestis infection, extensive bleeding.

140 n lymph nodes (LNs), or buboes, characterize Yersinia pestis infection, yet how they form and functio

141 ns, particularly the N terminus of YscF from Yersinia pestis, influences host immune responses.

142 Cell contact by the plague bacterium Yersinia pestis initiates the injection of several virul

143 Here we show that in Yersinia pestis, irp2, a gene encoding the synthetase (H

144 Yersinia pestis is a Gram-negative bacterium that is the

145 Yersinia pestis is a highly pathogenic Gram-negative org

146 LcrV of Yersinia pestis is a major protective antigen proposed f

147 The V antigen (LcrV) of the plague bacterium Yersinia pestis is a potent protective antigen that is u

148 Yersinia pestis is a tier 1 agent due to its contagious

149 Yersinia pestis is able to survive and replicate within

150 Yersinia pestis is an arthropod-borne bacterial pathogen

151 Yersinia pestis is an important human pathogen that is m

152 The plasminogen activator (Pla) of Yersinia pestis is an omptin family member that is very

153 Transmission of Yersinia pestis is greatly enhanced after it forms a bac

154 The pathogenicity of the plague agent Yersinia pestis is largely due to the injection of effec

155 Yersinia pestis is perhaps the most feared infectious ag

156 This frenzied inflammatory response to Yersinia pestis is poorly understood.

157 Yersinia pestis is the causative agent of bubonic and pn

158 Yersinia pestis is the causative agent of plague, a dise

159 Yersinia pestis is the causative agent of plague.

160 Yersinia pestis is the etiologic agent of bubonic and pn

161 The bacteria Yersinia pestis is the etiological agent of plague and h

162 Yersinia pestis is the etiological agent of the plague.

163 Yersinia pestis is transmitted by fleas and causes bubon

164 The plague bacillus Yersinia pestis is unique among the pathogenic Enterobac

165 Plague (caused by the bacterium Yersinia pestis) is a zoonotic reemerging infectious dis

166 ds that the causative agent of this disease, Yersinia pestis, is able to survive and multiply in both

167 lague, caused by the Gram-negative bacterium Yersinia pestis, is favored by a robust early innate imm

168 YopM, a protein toxin of Yersinia pestis, is necessary for virulence in a mouse m

169 ce, also been identified in a drug-resistant Yersinia pestis isolate (IP275) from Madagascar.

170 Yersinia pestis KIM D27 mutants lacking yopR were defect

171 tion of putative transmembrane proteins from Yersinia pestis KIM D27 with the combined PF2D and gel e

172 s from cultures of two attenuated strains of Yersinia pestis [KIM D27 (pgm-) and KIM D1 (lcr-)] grown

173 genomic DNA near IL-10 confers resistance to Yersinia pestis KIM5 and contributes to the observed res

174 Two mutant strains of Yersinia pestis KIM5+, a Deltacrp mutant and a mutant wi

175 ive TnphoA mutant library was constructed in Yersinia pestis KIM6 to identify surface proteins involv

176 ing the human pathogens Burkholderia mallei, Yersinia pestis, Klebsiella pneumoniae, Legionella longb

177 Since possible exposure to plague is via Yersinia pestis-laden aerosols that results in pneumonic

178 We report that Yersinia pestis LcrF binds to and activates transcriptio

179 ia enterocolitica yscM1 and yscM2 as well as Yersinia pestis lcrQ, relieve the YopE-DHFR-imposed bloc

180 d monoclonal antibodies with specificity for Yersinia pestis LcrV and F1 antigens protected mice in a

181 nst His-tagged influenza hemagglutinin 5 and Yersinia pestis LcrV antigens.

182 In contrast to Yersinia pestis LcrV, the recombinant V10 (rV10) variant

183 We find the origins of the Yersinia pestis lineage to be at least two times older t

184 Two MarA-like proteins have been found in Yersinia pestis: MarA47 and MarA48.

185 g peptides but not peptides from a disparate Yersinia pestis microbe.

186 cessfully produce disease, the causal agent (Yersinia pestis) must rapidly sense and respond to rapid

187 biothreat agents such as Bacillus anthracis, Yersinia pestis, or Burkholderia pseudomallei Convention

188 We solved the crystal structures of a Yersinia pestis outer membrane transporter called FyuA a

189 high mortality, but the mechanisms by which Yersinia pestis overwhelms the lungs are largely unknown

190 n are broadly used in many fields, including Yersinia pestis pathogenesis.

191 total of ca. 36 kb of DNA from the ca. 70-kb Yersinia pestis pCD1 virulence plasmid were constructed

192 Attenuated Yersinia pestis pgm strains, such as KIM5, lack the side

193 Nonpigmented Yersinia pestis (pgm) strains are defective in scavengin

194 lly attenuated, pigmentation (Pgm)-deficient Yersinia pestis primes T cells that protect mice against

195 rate chain to the 2' position of lipid A, in Yersinia pestis produced bisphosphoryl hexa-acylated lip

196 Inhaled Yersinia pestis produces a severe primary pneumonia know

197 Yersinia pestis produces and secretes a toxin named pest

198 ymerization of a single protein, e.g., YscF (Yersinia pestis), PscF (Pseudomonas aeruginosa), PrgI (S

199 n model of pneumonic plague, it appears that Yersinia pestis quickly creates a localized, dominant an

200 Pneumonic plague, caused by inhalation of Yersinia pestis, represents a major bioterrorism threat

201 To establish a successful infection, Yersinia pestis requires the delivery of cytotoxic Yops

202 Pathogens such as Yersinia pestis resist destruction by the innate immune

203 Inhalation of the bacterium Yersinia pestis results in primary pneumonic plague.

204 The etiologic agent of bubonic plague, Yersinia pestis, senses self-produced, secreted chemical

205 hat the base pairing function of E. coli and Yersinia pestis SgrS homologs is critical for rescue fro

206 atants of the recombinant YspI and wild-type Yersinia pestis showed similar profiles of AHLs.

207 e LDC activity of a DABA DC homologue from a Yersinia pestis siderophore biosynthetic pathway.

208 In Yersinia pestis, single mutations in either yfe or feo r

209 We report the crystal structure of Yersinia pestis SspA, which is 83% identical to E. coli

210 to approximately 100 50% effective doses of Yersinia pestis strain CO92 and necropsied at 24-h inter

211 In all Yersinia pestis strains examined, the adhesin/invasin ya

212 lague, we have sequenced the genomes of four Yersinia pestis strains isolated from the zoonotic roden

213 Yersinia pestis survives and replicates in phagosomes of

214 malian body temperature, the plague bacillus Yersinia pestis synthesizes lipopolysaccharide (LPS)-lip

215 roinflammatory responses through TLRs by the Yersinia pestis T3S needle protein, YscF, the Salmonella

216 tag to measure the injection of Yops by the Yersinia pestis T3SS.

217 f the enzootic maintenance of the bacterium (Yersinia pestis) that causes plague and the sporadic epi

218 In Yersinia pestis the autotransporter YapE has adhesive pr

219 Yersinia pestis (the plague bacillus) and its ancestor,

220 nse is a prominent feature of infection with Yersinia pestis, the agent of bubonic and pneumonic plag

221 Yersinia pestis, the agent of bubonic plague, evolved fr

222 r gene products are functional receptors for Yersinia pestis, the agent of plague, as shown by overex

223 Yersinia pestis, the agent of plague, is usually transmi

224 Yersinia pestis, the bacterial agent of plague, forms a

225 The arthropod-borne transmission route of Yersinia pestis, the bacterial agent of plague, is a rec

226 Yersinia pestis, the bacterial agent of plague, secretes

227 Yersinia pestis, the causative agent of bubonic and pneu

228 ly, there is no FDA-approved vaccine against Yersinia pestis, the causative agent of bubonic and pneu

229 Yersinia pestis, the causative agent of plague, autoaggr

230 Yersinia pestis, the causative agent of plague, binds ho

231 Yersinia pestis, the causative agent of plague, evades h

232 Yersinia pestis, the causative agent of plague, evolved

233 Yersinia pestis, the causative agent of plague, expresse

234 Yersinia pestis, the causative agent of plague, expresse

235 hat distinguish DNA amplicons generated from Yersinia pestis, the causative agent of plague, from the

236 Yersinia pestis, the causative agent of plague, has been

237 Yersinia pestis, the causative agent of plague, is a fac

238 Yersinia pestis, the causative agent of plague, is able

239 Yersinia pestis, the causative agent of plague, is capab

240 Yersinia pestis, the causative agent of plague, is one o

241 Yersinia pestis, the causative agent of plague, is uniqu

242 Yersinia pestis, the causative agent of plague, must sur

243 For transmission to new hosts, Yersinia pestis, the causative agent of plague, replicat

244 Yersinia pestis, the causative agent of plague, secretes

245 Yersinia pestis, the causative agent of plague, showed a

246 Yersinia pestis, the causative agent of plague, uses a t

247 Yersinia pestis, the causative agent of plague, utilizes

248 Yersinia pestis, the causative agent of plague, utilizes

249 -ssrA genes are required for pathogenesis of Yersinia pestis, the causative agent of plague.

250 ink between polyamines and biofilm levels in Yersinia pestis, the causative agent of plague.

251 nd F1-V, a candidate recombinant antigen for Yersinia pestis, the causative agent of plague.

252 m (T3SS) is essential in the pathogenesis of Yersinia pestis, the causative agent of plague.

253 f essential gene prediction in the bacterium Yersinia pestis, the causative agent of plague.

254 mical characterization of the AI-2 system in Yersinia pestis, the causative agent of plague.

255 Yersinia pestis, the cause of bubonic plague, blocks fee

256 Yersinia pestis, the cause of the disease plague, forms

257 In Yersinia pestis, the cytosolic LcrG protein and a cytoso

258 Yersinia pestis, the etiologic agent of plague, has only

259 Yersinia pestis, the etiologic agent of plague, has shap

260 Yersinia pestis, the etiologic agent of plague, is a bac

261 9 (TLR9) agonist, confers protection against Yersinia pestis, the etiologic agent of plague.

262 Dissemination of Yersinia pestis, the etiological agent of plague, by blo

263 Yersinia pestis, the highly virulent agent of plague, is

264 in the delivery of cytotoxic Yop proteins by Yersinia pestis, the mechanism has not been defined.

265 Little is known about Zn homeostasis in Yersinia pestis, the plague bacillus.

266 festation of disease caused by the bacterium Yersinia pestis, there is surprisingly little informatio

267 The ability of Yersinia pestis to forestall the mammalian innate immune

268 edium- to high-copy-number plasmid clones of Yersinia pestis topoisomerase I (YpTOP) with Asp-to-Asn

269 hionine residue with arginine in recombinant Yersinia pestis topoisomerase I (YTOP) was the only subs

270 We isolated a mutant of recombinant Yersinia pestis topoisomerase I that forms a stabilized

271 Mutants of recombinant Yersinia pestis topoisomerase I with hydrophobic substit

272 mal system for interrogating such couplings: Yersinia pestis transmission exerts intense selective pr

273 LcrV-specific antibodies block Yersinia pestis type III injection of Yop effectors into

274 During infection, Yersinia pestis uses its F1 capsule to enhance survival

275 n, the serine/threonine kinase YopO (YpkA in Yersinia pestis), uses monomeric actin as bait to recrui

276 ulation tests for Francisella tularensis and Yersinia pestis, using a well-established hybridization

277 The plague-causing bacterium Yersinia pestis utilizes a type III secretion system to

278 ia, including enzymes from pathogens such as Yersinia pestis, Vibrio cholera and Salmonella sp.

279 the possible role of Na(+)/H(+) antiport in Yersinia pestis virulence and found that Y. pestis strai

280 To validate these vector attributes, the Yersinia pestis virulence antigen LcrV was used to devel

281 es that demonstrated a role played by Lpp in Yersinia pestis virulence in mouse models of bubonic and

282 ro, His-tagged recombinant LcrV (rLcrV) from Yersinia pestis was cloned and expressed in Escherichia

283 for antimicrobial susceptibility testing of Yersinia pestis was evaluated in comparison with broth m

284 tion of the highly virulent plague bacterium Yersinia pestis was the acquisition of plasmid pPCP1, wh

285 end, immunity to LcrV, a protective Ag from Yersinia pestis, was tested in young and old baboons.

286 and genome evolution of the plague bacterium Yersinia pestis, we have sequenced the deep-rooted strai

287 atory mice are usually highly susceptible to Yersinia pestis, we recently identified a mouse strain (

288 .3, raised to the LcrV virulence factor from Yersinia pestis were characterised for their Fab affinit

289 that includes serious pathogens such as the Yersinia pestis, which causes plague, Yersinia pseudotub

290 the involvement of RovA in the virulence of Yersinia pestis, which naturally lacks a functional inv

291 Intentional release of Yersinia pestis will likely be propagated by aerosol exp

292 ent resistance) in the pathogenic Yersiniae (Yersinia pestis, Y. enterocolitica, and Y. pseudotubercu

293 Yersinia pestis YapV is homologous to Shigella flexneri

294 of Vibrio cholerae vibriobactin and HMWP2 of Yersinia pestis yersiniabactin assembly lines were evolv

295 two inorganic iron ABC transport systems of Yersinia pestis, Yfe and Yfu, have been characterized.

296 investigated recognition of target genes by Yersinia pestis YopD.

297 eins, the Shigella flexneri OspF protein and Yersinia pestis YopH protein, to rewire kinase-mediated

298 We evaluated the role of Yersinia pestis YopJ in a rat model of bubonic plague fo

299 e of the class IV adenylyl cyclase (AC) from Yersinia pestis (Yp) is reported at 1.9 A resolution.

300 HSL synthases: Burkholderia mallei BmaI1 and Yersinia pestis YspI.