ライフサイエンスコーパス: pv.

1 with stage I ADC in both the NLST (n = 123, pv = 0.0089) and SPORE (n = 68, pv = 0.032) cohorts.

2 for both the NLST (Hazard Ratio (HR) = 2.20, pv = 0.01) and the SPORE cohorts (HR = 2.15 and pv = 0.0

3 ST (n = 123, pv = 0.0089) and SPORE (n = 68, pv = 0.032) cohorts.

4 e focal adhesion protein alpha-parvin (alpha-pv) is essential for vascular development.

5 In the absence of alpha-pv, blood vessels display impaired VE-cadherin junction

6 = 0.01) and the SPORE cohorts (HR = 2.15 and pv = 0.044), respectively, after adjusting for key clini

7 Xanthomonas oryzae pathovar (pv.) oryzae and pv. oryzicola produce numerous transcription activator-l

8 eudomonas syringae pathovar (pv.) tomato and pv. maculicola were made by insertion of the luxCDABE op

9 gens Xanthomonas oryzae pv. oryzae (Xoo) and pv. oryzicola (Xoc) encode numerous secreted transcripti

10 nome of citrus canker pathogen X. axonopodis pv. citri 306.

11 odis pv. citrumelo to those of X. axonopodis pv. citri and X. campestris pv. vesicatoria provides val

12 . axonopodis pv. citrumelo and X. axonopodis pv. citri.

13 on citrus compared to that of X. axonopodis pv. citri.

14 y genes, which were present in X. axonopodis pv. citri.

15 t range as compared to that of X. axonopodis pv. citri.

16 pv. citrumelo while present in X. axonopodis pv. citri.

17 X. axonopodis pv. citrumelo also lacks various genes, such as syrE1, s

18 ith the distinct virulences of X. axonopodis pv. citrumelo and X. axonopodis pv. citri.

19 a complete genome sequence of X. axonopodis pv. citrumelo strain F1, 4.9 Mb in size.

20 identified unique effectors in X. axonopodis pv. citrumelo that may be related to the different host

21 We also compared X. axonopodis pv. citrumelo to the genome of citrus canker pathogen X.

22 he complete genome sequence of X. axonopodis pv. citrumelo to those of X. axonopodis pv. citri and X.

23 pAI, and hrpW were absent from X. axonopodis pv. citrumelo while present in X. axonopodis pv. citri.

24 anker (CBC) caused by Xanthomonas axonopodis pv. citri (Xac) was first documented in India and Java i

25 The protein Clp from Xanthomonas axonopodis pv. citri regulates pathogenesis and is a member of the

26 Xanthomonas axonopodis pv. citrumelo is a citrus pathogen causing citrus bacter

27 ght (CBB), incited by Xanthomonas axonopodis pv. manihotis (Xam), is the most important bacterial dis

28 aused by the pathogen Xanthomonas axonopodis pv. manihotis (Xam).

29 Mb genome sequence of Xanthomonas axonopodis pv. punicae strain LMG 859, the causal agent of bacteria

30 v library were conjugated into X. campestris pv. campestris (Xcc) and exconjugants were scored for an

31 f N-glycopeptide processing by X. campestris pv. campestris.

32 tomato bacterial spot pathogen X. campestris pv. vesicatoria 85-10, with a completely different host

33 of X. axonopodis pv. citri and X. campestris pv. vesicatoria provides valuable insights into the mech

34 to B. cinerea infection and to X. campestris pv. vesicatoria, correlated with cuticle permeability an

35 rols the virulence of Xanthomonas campestris pv. campestris (Xcc) to plants.

36 In Xanthomonas campestris pv. campestris (Xcc), the proteins encoded by the rpf (r

37 a Abra43 (Abra43) and Xanthomonas campestris pv. campestris 8004 (Xcc8004), on the structure and func

38 Xanthomonas campestris pv. campestris can express AvrXa21 activity if raxST, en

39 family encoded by the Xanthomonas campestris pv. campestris str. ATCC 33913 genome (GI:21233491).

40 Xanthomonas campestris pv. campestris, the causal agent of black rot disease of

41 lt disease, caused by Xanthomonas campestris pv. musacearum (Xcm), is a major threat to banana produc

42 e-genome sequences of Xanthomonas campestris pv. raphani strain 756C and X. oryzae pv. oryzicola stra

43 confers resistance to Xanthomonas campestris pv. vesicatoria (Xcv) pathogenic strains which contain t

44 g bacterial pathogen, Xanthomonas campestris pv. vesicatoria (Xcv).

45 he non-host pathogen, Xanthomonas campestris pv. vesicatoria (Xcv).

46 ecreted effector from Xanthomonas campestris pv. vesicatoria, is a desumoylating enzyme with strict s

47 nslocator, HrpF, from Xanthomonas campestris pv. vesicatoria.

48 ic bacterial pathogen Xanthomonas campestris pv. vesicatoria.

49 Pseudomonas aeruginosa PAO1 K648 (pvd-, pch-) exhibited greater promiscuity than that of E

50 pic mechanism of thermal transport in MgSiO3 pv, and provide reference data for understanding heat co

51 Although X. o. pv. oryzicola does not cause disease on maize, we identi

52 esults support the hypothesis that X. oryzae pv. oryzae commandeers the regulation of otherwise devel

53 ive resistance to PthXo2-dependent X. oryzae pv. oryzae due to promoter variations of OsSWEET13 in ja

54 esults corroborate a model whereby X. oryzae pv. oryzae enhances the release of sucrose from host cel

55 These results suggest that the X. oryzae pv. oryzae PhoPQ TCS functions in virulence and in the p

56 X. oryzae pv. oryzae requires a regulatory two-component system (T

57 X. oryzae pv. oryzae therefore modulates the expression of multipl

58 ain and found it to be impaired in X. oryzae pv. oryzae virulence and no longer able to activate the

59 that PhoP controls a key aspect of X. oryzae pv. oryzae virulence through regulation of hrpG.

60 ependent disease susceptibility to X. oryzae pv. oryzae.

61 WEET13 induction by 42 isolates of X. oryzae pv. oryzae.

62 estris pv. raphani strain 756C and X. oryzae pv. oryzicola strain BLS256, pathogens that infect the m

63 he strains in the African clade of X. oryzae pv. oryzicola, representing the first dominant resistanc

64 m and mesophyll pathogens Xanthomonas oryzae pv. oryzae (Xoo) and pv. oryzicola (Xoc) encode numerous

65 hway of the rice pathogen Xanthomonas oryzae pv. oryzae (Xoo) in a semi-isolated environment represen

66 The biotrophic pathogen Xanthomonas oryzae pv. oryzae (Xoo) produces a sulfated peptide named RaxX,

67 ce to a broad spectrum of Xanthomonas oryzae pv. oryzae (Xoo) races that cause bacterial blight disea

68 bacterial blight pathogen Xanthomonas oryzae pv. oryzae (Xoo) that deliver the TAL effector AvrXa27.

69 livered by the pathogenic Xanthomonas oryzae pv. oryzae (Xoo), in revealing the new function of two p

70 The pathogen, Xanthomonas oryzae pv. oryzae (Xoo), secretes one or more of six known tran

71 ceptor confer immunity to Xanthomonas oryzae pv. oryzae (Xoo), the causal agent of bacterial leaf bli

72 n by pathogenic bacterium Xanthomonas oryzae pv. oryzae (Xoo), which causes a vascular disease in ric

73 (Oryza sativa) caused by Xanthomonas oryzae pv. oryzae (Xoo).

74 cterial blight, caused by Xanthomonas oryzae pv. oryzae (Xoo).

75 ed with pathogens such as Xanthomonas oryzae pv. oryzae (Xoo).

76 strains of the bacterium Xanthomonas oryzae pv. oryzae (Xoo).

77 nity X (RaxX) produced by Xanthomonas oryzae pv. oryzae (Xoo).

78 onfers resistance against Xanthomonas oryzae pv. oryzae (Xoo).

79 o the bacterial pathogen, Xanthomonas oryzae pv. oryzae (Xoo).

80 blight diseases caused by Xanthomonas oryzae pv. oryzae (Xoo).

81 acterial blight caused by Xanthomonas oryzae pv. oryzae (Xoo).

82 acterial blight caused by Xanthomonas oryzae pv. oryzae (Xoo).

83 Xanthomonas oryzae pv. oryzae causes bacterial blight of rice (Oryza sativa

84 xtraordinary diversity of Xanthomonas oryzae pv. oryzae genotypes and races that have been isolated f

85 ing disease by strains of Xanthomonas oryzae pv. oryzae is dependent on major transcription activatio

86 the sulfated form of the Xanthomonas oryzae pv. oryzae secreted protein Ax21.

87 levated upon infection by Xanthomonas oryzae pv. oryzae strain PXO99(A) and depends on the type III e

88 Xanthomonas oryzae pv. oryzae strain PXO99(A) induces the expression of the

89 21, confers resistance to Xanthomonas oryzae pv. oryzae strains producing the AvrXa21 elicitor.

90 21, confers resistance to Xanthomonas oryzae pv. oryzae strains producing the type one system-secrete

91 ative bacterial pathogen, Xanthomonas oryzae pv. oryzae upon recognition of a small protein, Ax21, th

92 , Rhizoctonia solani, and Xanthomonas oryzae pv. oryzae) and several chemical elicitors.

93 ae) and bacterial blight (Xanthomonas oryzae pv. oryzae).

94 tibility to M. oryzae and Xanthomonas oryzae pv. oryzae, hemibiotrophic pathogens, but enhanced resis

95 Gram-negative bacterium, Xanthomonas oryzae pv. oryzae, is a tyrosine sulfotransferase.

96 the gamma-proteobacterium Xanthomonas oryzae pv. oryzae, which utilizes a group of type III TAL (tran

97 nd rapid evolution within Xanthomonas oryzae pv. oryzae.

98 ns Magnaporthe oryzae and Xanthomonas oryzae pv. oryzae.

99 er infection of bacterium Xanthomonas oryzae pv. oryzae.

100 Gram-negative bacterium, Xanthomonas oryzae pv. oryzae; NH1, the rice ortholog of NPR1, a key regula

101 rial leaf streak pathogen Xanthomonas oryzae pv. oryzicola (Xoc) contains a homologous operon.

102 e rice bacterial pathogen Xanthomonas oryzae pv. oryzicola (Xoc) has been demonstrated to contain a b

103 rial leaf streak pathogen Xanthomonas oryzae pv. oryzicola (Xoc).

104 Xanthomonas oryzae pv. oryzicola causes bacterial leaf streak of rice.

105 native TAL effector from Xanthomonas oryzae pv. oryzicola drives expression of a target with an EBE

106 cognizes a rice pathogen, Xanthomonas oryzae pv. oryzicola, which causes bacterial streak disease.

107 ive flg22(Xo) peptides of Xanthomonas oryzae pvs. oryzae (Xoo) and oryzicola (Xoc).

108 rice pathogens Xanthomonas oryzae pathovar (pv.) oryzae and pv. oryzicola produce numerous transcrip

109 ana pathogens Pseudomonas syringae pathovar (pv.) tomato and pv. maculicola were made by insertion of

110 mal conductivity kappa of MgSiO3 perovskite (pv) by ab initio lattice dynamics calculations combined

111 their control proteins HrpV and HrpG from Ps pv. tomato DC3000 in vitro establish that HrpRS forms a

112 eath in N. benthamiana inoculated with P. s. pv. tabaci was also reduced.

113 ene production and increases growth of P. s. pv. tomato and severity of speck disease on susceptible

114 st response to the large collection of P. s. pv. tomato strains that express different combinations o

115 the host Pto kinase, which recognizes P. s. pv. tomato strains that express the effector AvrPto.

116 Pto and for elicitation of immunity to P. s. pv. tomato.

117 ing Pto/Prf-dependent immunity against P. s. pv. tomato.

118 n both the olive tree pathogen P. savastanoi pv. savastanoi and the human opportunistic pathogen Pseu

119 Deletion of the dgcP gene in P. savastanoi pv. savastanoi NCPPB 3335 and P. aeruginosa PAK reduced

120 aused by the bacteria Pseudomonas savastanoi pv. savastanoi (Psv) on the epiphytic and endophytic fun

121 e olive tree pathogen Pseudomonas savastanoi pv. savastanoi is dependent on the integrity of its GGDE

122 ity to infection by host pathogen P syringae pv. tomato DC3000.

123 Both Sanger sequencing of 50 P. syringae pv. atrofaciens mutant clones for each genotype and popu

124 mutations allowing infection of P. syringae pv. atrofaciens.

125 sistance against virulent Pst or P. syringae pv. maculicola (Psm) pathogens.

126 phaseolicola, and pPMA4326A from P. syringae pv. maculicola encoded a type IVA T4SS (VirB-VirD4 conju

127 owth of the universally virulent P. syringae pv. maculicola ES4326 among more than 100 Arabidopsis ec

128 udomonas syringae pv. tomato and P. syringae pv. maculicola.

129 udomonas syringae pv. tomato and P. syringae pv. maculicola.

130 P. syringae pv. syringae 61 and P. syringae pv. phaseolicola 1448A restored HR elicitation and patho

131 report on the genome sequence of P. syringae pv. phaseolicola isolate 1448A, which encodes 5,353 open

132 syringae pv. tomato, and 19 from P. syringae pv. phaseolicola race 6.

133 ngae pv. syringae, pPh1448B from P. syringae pv. phaseolicola, and pPMA4326A from P. syringae pv. mac

134 delivered by the RW60 strain of P. syringae pv. phaseolicola.

135 e of the sequenced bean pathogen P. syringae pv. syringae (Psy) B728a using bioinformatics.

136 P. syringae pathovars, hrpP from P. syringae pv. syringae 61 and P. syringae pv. phaseolicola 1448A r

137 g a plasmid-encoded T3SS and the P. syringae pv. syringae 61 effector gene hopA1 increased in planta

138 ied in the functional cluster of P. syringae pv. syringae 61 hrp genes cloned in cosmid pHIR11.

139 usceptible to non-host pathogens P. syringae pv. syringae and P. syringae pv. tabaci.

140 Here we characterize a gene in P. syringae pv. syringae B728a and P. syringae pv. tomato DC3000, te

141 e supporting the hypothesis that P. syringae pv. syringae B728a produces both of these siderophores.

142 contributions of 4,296 genes in P. syringae pv. syringae B728a were determined by genome-wide fitnes

143 losely related pathogenic strain P. syringae pv. syringae B728a, but none were detected.

144 only siderophores synthesized by P. syringae pv. syringae B728a.

145 welve PFPs along with pPSR1 from P. syringae pv. syringae, pPh1448B from P. syringae pv. phaseolicola

146 in (MBP) in Escherichia coli and P. syringae pv. syringae.

147 ana did not confer resistance to P. syringae pv. tabaci (Pta) expressing avrPto or avrPtoB, but recog

148 lenge infections with DC3000 and P. syringae pv. tabaci 11528, respectively.

149 fect was suppressed by wild-type P. syringae pv. tabaci and P. fluorescens heterologously expressing

150 cens, a TTSS-deficient mutant of P. syringae pv. tabaci, or flg22 (a flagellin-derived peptide elicit

151 ens P. syringae pv. syringae and P. syringae pv. tabaci.

152 AD(P) leaking into the ECC after P. syringae pv. tobacco DC3000/avrRpt2 infection is sufficient for i

153 y related to the tomato pathogen P. syringae pv. tomato (Pto), including strains isolated from snowpa

154 ficantly when co-inoculated with P. syringae pv. tomato but not when co-inoculated with a type III se

155 ned and is compared with that of P. syringae pv. tomato DC3000 (Pst DC3000).

156 not prevent the HR activated by P. syringae pv. tomato DC3000 + avrB, avrRpm1, avrRps4 or avrRpt2, b

157 and related T3SS substrates for P. syringae pv. tomato DC3000 and three other sequenced strains.

158 The P. syringae pv. tomato DC3000 effector HopF2 suppresses Arabidopsis

159 d to test the ability of several P. syringae pv. tomato DC3000 effectors for their ability to suppres

160 ated with the Hrp T3SS system in P. syringae pv. tomato DC3000 have predicted lytic transglycosylase

161 The P. syringae pv. tomato DC3000 HopK1 type-III effector was known to s

162 P. syringae pv. tomato DC3000 HrpP has a C-terminal, putative T3SS s

163 variance of basal resistance to P. syringae pv. tomato DC3000 in the Col-0 x Fl-1 F(2) population.

164 Analyses of P. syringae pv. tomato DC3000 mutants indicated that both type III s

165 the loss of swarming motility of P. syringae pv. tomato DC3000 on medium containing a low percentage

166 slocated into plant cells by the P. syringae pv. tomato DC3000 TTSS.

167 repertoire of the model pathogen P. syringae pv. tomato DC3000 were deleted to produce polymutant DC3

168 ogenetically divergent pathovar, P. syringae pv. tomato DC3000, revealed a strong degree of conservat

169 syringae pv. syringae B728a and P. syringae pv. tomato DC3000, termed phcA, that has homology to a f

170 e when challenge inoculated with P. syringae pv. tomato DC3000.

171 frames (ORFs) within the EEL of P. syringae pv. tomato DC3000.

172 1-1, hopS1, and hopS2 operons in P. syringae pv. tomato DC3000; these operons encode three homologous

173 with pDC3000A and pDC3000B from P. syringae pv. tomato encoded a type IVB T4SS (tra system).

174 a virulence protein by promoting P. syringae pv. tomato growth and enhancing symptoms associated with

175 The P. syringae pv. tomato OpuC transporter had a high affinity for glyc

176 The P. syringae pv. tomato OpuC transporter was more closely related to

177 IAA levels during infection with P. syringae pv. tomato strain DC3000 (PstDC3000).

178 ine family transporter (BCCT) in P. syringae pv. tomato strain DC3000 that mediates the transport of

179 In this study, we found that P. syringae pv. tomato strain DC3000 was distinct from most bacteria

180 hat were susceptible to virulent P. syringae pv. tomato strain DC3000, but resistant to DC3000 expres

181 efined 29 type III proteins from P. syringae pv. tomato, and 19 from P. syringae pv. phaseolicola rac

182 itica and the bacterial pathogen P. syringae pv. tomato.

183 The introduction of Pseudomonas syringae pv. actinidiae (Psa) severely damaged the New Zealand ki

184 ants) on the novel host Pseudomonas syringae pv. atrofaciens.

185 The Pseudomonas syringae pv. glycinea effector protein AvrB induces resistance re

186 the bacterial pathogen Pseudomonas syringae pv. maculicola (Pma) ES4326 and activation of SA synthes

187 nced resistance to both Pseudomonas syringae pv. maculicola (Psm) ES4326 and Hyaloperonospora parasit

188 se against the pathogen Pseudomonas syringae pv. maculicola ES4326 (Pma ES4326).

189 the bacterial pathogen Pseudomonas syringae pv. maculicola ES4326.

190 s locally infected with Pseudomonas syringae pv. maculicola Whole transcriptome shotgun sequencing an

191 the bacterial pathogen Pseudomonas syringae pv. maculicola.

192 real bacterial pathogen Pseudomonas syringae pv. oryzae, transgenic EFR wheat lines had reduced lesio

193 from the bean pathogen Pseudomonas syringae pv. phaseolicola (Pph) is driven by exposure to the stre

194 subsp. citri (Xcc) and Pseudomonas syringae pv. phaseolicola (Psp) NPS3121.

195 with the bean pathogen Pseudomonas syringae pv. phaseolicola illustrate how exposure to resistance m

196 opsis is a non-host for Pseudomonas syringae pv. phaseolicola NPS3121 (Pph), a bacterial pathogen of

197 rming enzyme (EFE) from Pseudomonas syringae pv. phaseolicola PK2 is a member of the mononuclear nonh

198 with the plant pathogen Pseudomonas syringae pv. phaseolicola where isolates that have lost the genom

199 Pseudomonas syringae pv. phaseolicola, a gram-negative bacterial plant pathog

200 A Pseudomonas syringae pv. pisi effector protein, AvrRPS4, triggers RPS4-depend

201 n effector protein from Pseudomonas syringae pv. pisi, triggers RPS4-dependent immunity in resistant

202 ete hrp/hrc region from Pseudomonas syringae pv. syringae 61 into the genome of the soil bacterium Ps

203 ated as a phytotoxin by Pseudomonas syringae pv. syringae B301D contains a 4-Cl-L-Thr-9 moiety where

204 ete genomic sequence of Pseudomonas syringae pv. syringae B728a (Pss B728a) has been determined and i

205 p)ppGpp on virulence of Pseudomonas syringae pv. syringae B728a (PssB728a) was investigated.

206 Pseudomonas syringae pv. syringae B728a is a resident on leaves of common bea

207 Pseudomonas syringae pv. syringae B728a is known to produce the siderophore p

208 its of syringafactin by Pseudomonas syringae pv. syringae B728a on leaves.

209 transcript profiles of Pseudomonas syringae pv. syringae B728a support a model in which leaf surface

210 surfactant produced by Pseudomonas syringae pv. syringae B728a that was not detected by traditional

211 nas aeruginosa PAO1 and Pseudomonas syringae pv. syringae B728a.

212 Pseudomonas syringae pv. syringae cell densities fluctuate regularly during h

213 in and syringopeptin by Pseudomonas syringae pv. syringae is controlled by the regulatory genes salA

214 yrB2 from the bacterium Pseudomonas syringae pv. syringae.

215 (syp) genomic island of Pseudomonas syringae pv. syringae.

216 lowing inoculation with Pseudomonas syringae pv. tabaci carrying avrPto, aconitase-silenced N. bentha

217 plants infiltrated with Pseudomonas syringae pv. tabaci expressing AvrPto or HopQ1-1.

218 obacco mosaic virus and Pseudomonas syringae pv. tabaci.

219 mplement recognition of Pseudomonas syringae pv. tomato (Pst) bacteria expressing either avrPto or av

220 (COR) toxin produced by Pseudomonas syringae pv. tomato (Pst) DC3000 functions to overcome plant immu

221 ility of Arabidopsis to Pseudomonas syringae pv. tomato (Pst) DC3000 independently of the phyB/PIF th

222 the bacterial pathogen Pseudomonas syringae pv. tomato (Pst) DC3000, including increased disease res

223 is hyper-susceptible to Pseudomonas syringae pv. tomato (Pst) DC3000, while Arabidopsis lines overexp

224 nit of the Hrp pilus in Pseudomonas syringae pv. tomato (Pst) DC3000.

225 triggered resistance to Pseudomonas syringae pv. tomato (Pst) DC3000.

226 phic bacterial pathogen Pseudomonas syringae pv. tomato (Pst) DC3000.

227 lent bacterial pathogen Pseudomonas syringae pv. tomato (Pst) DC3000/avrRpt2, and renders plants susc

228 Pseudomonas syringae pv. tomato (Pst) delivers effector proteins into the pla

229 the bacterial pathogen Pseudomonas syringae pv. tomato (Pst) in the cultivated tomato, Lycopersicon

230 retion system (TTSS) of Pseudomonas syringae pv. tomato (Pst) injects into the plant cell effector pr

231 The bacterial pathogen Pseudomonas syringae pv. tomato (Pst) strain DC3000 infects tomato and Arabid

232 the bacterial pathogen Pseudomonas syringae pv. tomato (Pst), contains two MAMPs, flg22 and flgII-28

233 ermine immunity against Pseudomonas syringae pv. tomato (Pst).

234 the bacterial pathogen Pseudomonas syringae pv. tomato (Pst).

235 n of bacterial pathogen Pseudomonas syringae pv. tomato (Pst).

236 including the bacterium Pseudomonas syringae pv. tomato (Pst).

237 lent bacterial pathogen Pseudomonas syringae pv. tomato (Pto) DC3000.

238 * Pseudomonas syringae pv. tomato (Pto) T1 is pathogenic in tomato (Solanum lyc

239 the bacterial pathogens Pseudomonas syringae pv. tomato and P. syringae pv. maculicola.

240 COR-producing pathogens Pseudomonas syringae pv. tomato and P. syringae pv. maculicola.

241 acterial plant pathogen Pseudomonas syringae pv. tomato DC3000 (DC3000) causes disease in Arabidopsis

242 The plant pathogen Pseudomonas syringae pv. tomato DC3000 (DC3000) is found in a wide variety of

243 role of siderophores in Pseudomonas syringae pv. tomato DC3000 (DC3000) virulence in tomato.

244 sigma factor encoded by Pseudomonas syringae pv. tomato DC3000 (DC3000), a plant pathogen that is lik

245 on after infection with Pseudomonas syringae pv. tomato DC3000 (Pst DC3000), demonstrating that the t

246 st avirulent strains of Pseudomonas syringae pv. tomato DC3000 (Pst) carrying AvrRpt2, AvrB, or AvrPp

247 Pseudomonas syringae pv. tomato DC3000 (Pst) is a virulent pathogen that caus

248 g22 or inoculation with Pseudomonas syringae pv. tomato DC3000 (PstDC3000) hrcC mutant, which is defi

249 resistance to virulent Pseudomonas syringae pv. tomato DC3000 (PstDC3000).

250 lecular function of the Pseudomonas syringae pv. tomato DC3000 (Pto) effector HopQ1.

251 the biotrophic bacteria Pseudomonas syringae pv. tomato DC3000 and for susceptibility to the necrotro

252 purified 6x His-HrpW of Pseudomonas syringae pv. tomato DC3000 and human transferrin.

253 stance to the bacterium Pseudomonas syringae pv. tomato DC3000 and the fungal pathogen Botrytis ciner

254 ll as non-host pathogen Pseudomonas syringae pv. tomato DC3000 and the general elicitor cryptogein-in

255 the virulent bacterium Pseudomonas syringae pv. tomato DC3000 and the necrotrophic fungus Botrytis c

256 to "mine" the genome of Pseudomonas syringae pv. tomato DC3000 for the metabolic potential to biosynt

257 Pseudomonas syringae pv. tomato DC3000 is a bacterial pathogen of Arabidopsis

258 fection with pathogenic Pseudomonas syringae pv. tomato DC3000 lacking hopQ1-1 [PtoDC3000(DeltahQ)] w

259 The bacterial pathogen Pseudomonas syringae pv. tomato DC3000 must detoxify plant-produced hydrogen

260 odel plant pathosystem, Pseudomonas syringae pv. tomato DC3000 on tomato and Arabidopsis thaliana hos

261 ut not to the bacterium Pseudomonas syringae pv. tomato DC3000 or to the oomycete Hyaloperonospora ar

262 signalling, for example Pseudomonas syringae pv. tomato DC3000 produces coronatine (COR), a jasmonic

263 Pseudomonas syringae pv. tomato DC3000 produces the phytotoxin coronatine, a

264 how the plant pathogen Pseudomonas syringae pv. tomato DC3000 responds to iron limitation and have f

265 The bacterial pathogen Pseudomonas syringae pv. tomato DC3000 suppresses the two-tiered plant innate

266 The Pseudomonas syringae pv. tomato DC3000 type III secretion system (TTSS) is re

267 nse, the plant pathogen Pseudomonas syringae pv. tomato DC3000 uses the virulence factor coronatine t

268 Pseudomonas syringae pv. tomato DC3000 was previously reported to produce two

269 athogen of A. thaliana (Pseudomonas syringae pv. tomato DC3000) using a proteomic approach.

270 ne were challenged with Pseudomonas syringae pv. tomato DC3000, which is a bacterial pathogen of bras

271 y the virulent pathogen Pseudomonas syringae pv. tomato DC3000.

272 ocin, syringacin M from Pseudomonas syringae pv. tomato DC3000.

273 the bacterial pathogen Pseudomonas syringae pv. tomato DC3000.

274 speck disease caused by Pseudomonas syringae pv. tomato expressing avrPto or avrPtoB.

275 esistance to strains of Pseudomonas syringae pv. tomato expressing AvrRpt2 and Ralstonia pseudosolana

276 in tomato to strains of Pseudomonas syringae pv. tomato expressing the (a)virulence proteins AvrPto o

277 eraction of tomato with Pseudomonas syringae pv. tomato is an established model system for understand

278 ersicum), resistance to Pseudomonas syringae pv. tomato is elicited by the interaction of the host Pt

279 tor protein AvrPto from Pseudomonas syringae pv. tomato is secreted into plant cells where it promote

280 nomical relevant tomato-Pseudomonas syringae pv. tomato pathosystem is widely used to explore and und

281 The Pseudomonas syringae pv. tomato protein AvrPtoB is translocated into plant ce

282 for the plant pathogen Pseudomonas syringae pv. tomato str. DC3000.

283 ity to the hemibiotroph Pseudomonas syringae pv. tomato strain DC3000 (Pto DC3000) was attenuated in

284 cted a mutant screen of Pseudomonas syringae pv. tomato strain DC3000 to identify genes that contribu

285 se has been cloned from Pseudomonas syringae pv. tomato strain DC3000, Pseudomonas putida KT2440, and

286 genic bacteria, such as Pseudomonas syringae pv. tomato strain DC3000, the causative agent of tomato

287 the bacterial pathogen Pseudomonas syringae pv. tomato strain DC3000.

288 on inoculation with the Pseudomonas syringae pv. tomato strain DC3000.

289 ses upon recognition of Pseudomonas syringae pv. tomato strains expressing the AvrPto or AvrPtoB prot

290 d nonhost resistance to Pseudomonas syringae pv. tomato T1.

291 d by the plant pathogen Pseudomonas syringae pv. tomato, has a carboxy-terminal domain that is an E3

292 enhanced resistance to Pseudomonas syringae pv. tomato, which is consistent with a previous study sh

293 t pathogenic bacterium, Pseudomonas syringae pv. tomato.

294 r AvrPtoB (HopAB2) from Pseudomonas syringae pv. tomato.

295 nd avirulent strains of Pseudomonas syringae pv. tomato.

296 in tomato is caused by Pseudomonas syringae pv. tomato.

297 and, for the first time, Pseudomonas syringe pv. actinidiae.

298 t the bacterial pathogen Pseudomonas syringe pv. tomato (Pst) DC3000 in the salicylic acid (SA)- and

299 t the wheat pathogen Xanthomonas translucens pv. undulosa elevates expression of the host gene encodi

300 resistance to the pathogen Xanthomonasoryzae pv. oryzae (Xoo), suggesting the presence of a related d