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1 esent in the lipopolysaccharide of Ralstonia solanacearum.
2 ty was with Ralstonia eutropha and Ralstonia solanacearum.
3 or (VEF) produced by wild-type strains of R. solanacearum.
4 h includes R. eutropha, R. pickettii, and R. solanacearum.
5  operon is the major virulence factor for R. solanacearum.
6 es virulence gene expression in wild-type R. solanacearum.
7 ributes substantially to the virulence of R. solanacearum.
8 ts efficacy and biosafety profile against R. solanacearum.
9 e effector from the plant pathogen Ralstonia solanacearum.
10 ial species that were antagonistic toward R. solanacearum.
11  by the plant-pathogenic bacterium Ralstonia solanacearum.
12 ibits bacterial niche competitors but not R. solanacearum.
13 ve as sole carbon or nitrogen sources for R. solanacearum.
14 seudomonas syringae and PopP2 from Ralstonia solanacearum.
15  in another P. syringae strain and Ralstonia solanacearum.
16 ulation of flagellum-mediated motility in R. solanacearum.
17 (bp) genes, as well as their orthologs in R. solanacearum.
18 ytopathogenic Xanthomonas spp. and Ralstonia solanacearum.
19 tii, as well as the plant pathogen Ralstonia solanacearum.
20 ulence genes in the plant pathogen Ralstonia solanacearum.
21  unknown function, and 13% were unique to R. solanacearum.
22 nas campestris pv. vesicatoria and Ralstonia solanacearum.
23 liana (Arabidopsis), Resistance to Ralstonia solanacearum 1 (RRS1-R) and Resistance to Pseudomonas sy
24 oA) and/or substrate Resistance to Ralstonia solanacearum 1 (RRS1-R)WRKY.
25                                           L. solanacearum' 16S ribosomal RNA, 50S ribosomal proteins
26  Our findings suggest that Brg11 may give R. solanacearum a competitive advantage and uncover a role
27 ineages, to suppress the bacterium Ralstonia solanacearum, a global phytopathogen capable of infectin
28                      Ralstonia (Pseudomonas) solanacearum, a phytopathogenic bacterium that appears t
29 ntly showed that, in Ralstonia (Pseudomonas) solanacearum, a phytopathogenic bacterium, acyl-HSL prod
30   Expression of virulence genes in Ralstonia solanacearum, a phytopathogenic bacterium, is controlled
31 tomato (Solanum lycopersicum) with Ralstonia solanacearum, a soilborne pathogen that causes bacterial
32                                    Ralstonia solanacearum, a soilborne plant pathogen of considerable
33                                    Ralstonia solanacearum, a widely distributed and economically impo
34                                    Cloned R. solanacearum aer1 and aer2 genes restored aerotaxis to a
35 red for a wild-type level of virulence in R. solanacearum although its individual role in wilt diseas
36 hogens, Phytophthora infestans and Ralstonia solanacearum, among others, are considered.
37                                    Ralstonia solanacearum, an economically important plant pathogen,
38 omonas syringae, Xanthomonas spp., Ralstonia solanacearum and Erwinia species.
39  80 mug/ml for X. citri to 600 mug/ml for R. solanacearum and X. euvesicatoria.
40 stinct from those of Ralstonia (Pseudomonas) solanacearum and Xanthomonas campestris.
41                                 Liberibacter solanacearum" and the potato psyllid at the gut interfac
42                                 Liberibacter solanacearum" and the potato psyllid, which is crucial t
43 vity in plant-pathogenic bacteria (Ralstonia solanacearum) and fungi (Cochliobolus heterostrophus) re
44 dule, a fucose-binding lectin from Ralstonia solanacearum, and human norovirus VA387 P particle (24-m
45 domonas viridiflava, Ralstonia (Pseudomonas) solanacearum, and Xanthomonas campestris.
46 ering from wilt disease (caused by Ralstonia solanacearum) as source for potential prebiotic metaboli
47 ss the soil-borne, phytopathogenic Ralstonia solanacearum bacterium.
48 ercomonas sp.) affect the pathogen Ralstonia solanacearum, both on individual beneficial bacteria and
49  bacteria (not positively correlated with R. solanacearum) but not efficiently used by the pathogen i
50     plantarum ZPZ inhibited the growth of R. solanacearum by 72.46 +/- 14.42% based on OD(600) measur
51                                           L. solanacearum' by polymerase chain reaction.
52                   K60 generally resembles R. solanacearum CFBP2957, a Caribbean tomato isolate, but h
53                                 Liberibacter solanacearum" (CLso) pathosystem was investigated to dis
54 ly-related bacteria 'Candidatus Liberibacter solanacearum' (CLso), associated with vegetative disorde
55 ologs from Brucella abortus and Liberobacter solanacearum complement the RF auxotrophy of the Sm1021D
56 e of ipx genes suggests that in its host, R. solanacearum confronts and overcomes a stressful and nut
57 In the phytopathogen Ralstonia (Pseudomonas) solanacearum, control of many virulence genes is partly
58 ting that the main location in tomato for R. solanacearum during pathogenesis is iron replete.
59 d L-phenylalaninamide were tested against R. solanacearum, E. coli, Staphylococcus sp. and B. subtili
60                 The identification of the R. solanacearum enzyme enables us to propose that the ances
61 aracterized, and mutated two genes in the R. solanacearum flagellar biosynthetic pathway.
62                             The predicted R. solanacearum FliM closely resembled motor switch protein
63                                    Ralstonia solanacearum forms biofilm in vitro, but it was not know
64 py revealed that during tomato infection, R. solanacearum forms biofilm-like masses in xylem vessels.
65 dge, this is the first demonstration that R. solanacearum forms biofilms in plant xylem vessels, and
66 d no clues as to the role of acyl-HSLs in R. solanacearum gene regulation.
67                                       The R. solanacearum genome encodes two putative aerotaxis trans
68 a cenocepacia J2315 genome and the Ralstonia solanacearum genome.
69  accelerated wilt symptom development and R. solanacearum growth and systemic spread.
70                                 Liberibacter solanacearum" haplotype.
71 proteins encoded by 'Candidatus Liberibacter solanacearum' haplotype B, CKC_05770 and CKC_00930, whic
72                                           L. solanacearum' haplotype F was not detected in this study
73                                 Liberibacter solanacearum" haplotypes, LsoA and LsoB.
74                  The phytopathogen Ralstonia solanacearum has over 5000 genes, many of which probably
75 s of the bacterium, 'Candidatus Liberibacter solanacearum', have been identified worldwide, several o
76 o plants against the phytopathogen Ralstonia solanacearum in a T4BSS-dependent manner, suggesting tha
77 n resistance to the plant pathogen Ralstonia solanacearum in microcosms and in tomato plant rhizosphe
78                                 Liberibacter solanacearum" in the gut of adult psyllids.
79 tor produced by the plant pathogen Ralstonia solanacearum, in complex with inositol hexaphosphate (In
80 oduction, whereas inactivation of phcA in R. solanacearum increases siderophore production.
81 ics identified 22 metabolites enriched in R. solanacearum-infected sap.
82 rum, was enriched 76-fold to 37 microM in R. solanacearum-infected sap.
83 of different phage combinations on Ralstonia solanacearum infection in tomato.
84                                 Liberibacter solanacearum" infection.
85                                    Ralstonia solanacearum is a major phytopathogen that attacks many
86                      Ralstonia (Pseudomonas) solanacearum is a soil-borne phytopathogen that causes a
87                                    Ralstonia solanacearum is a soil-borne plant pathogen that causes
88                                    Ralstonia solanacearum is a soil-borne vascular pathogen that colo
89                                    Ralstonia solanacearum is a soilborne pathogen that causes bacteri
90                                    Ralstonia solanacearum is a widespread and destructive plant patho
91 Expression of virulence factors in Ralstonia solanacearum is controlled by a complex regulatory netwo
92 vessels of infected plants, we found that R. solanacearum is essentially nonmotile in planta, althoug
93 cyl-HSL-dependent autoinduction system in R. solanacearum is part of a more complex autoregulatory hi
94                                    Ralstonia solanacearum is the causal agent of bacterial wilt of ma
95                     "Candidatus Liberibacter solanacearum" is a pathogen transmitted by the potato ps
96 one of the exo-PGs, pehB, was cloned from R. solanacearum K60.
97 ormed by oligomerization as in the Ralstonia solanacearum lectin and not by sequential domains like t
98 em-limited bacterium Candidatus Liberibacter solanacearum (Lso), the causative agent of economically
99  is associated with "Candidatus Liberibacter solanacearum" (Lso), which is transmitted by the tomato/
100                     'Candidatus Liberibacter solanacearum' (Lso) is a pathogen of solanaceous crops.
101 m limited bacterium 'Candidatus Liberibacter solanacearum' (Lso) is associated with disease in Solana
102                             We found that R. solanacearum manipulates its host to increase nutrients
103                                        An R. solanacearum mutant lacking the pathogen's two extracell
104  an extracellular factor that complements R. solanacearum mutants deficient in production of the 3-OH
105                         Two site-directed R. solanacearum mutants lacking either CheA or CheW, which
106     To locate and infect host plant roots R. solanacearum needs taxis, the ability to move toward mor
107 tal variability, the biocontrol of Ralstonia solanacearum, one of the most destructive plant pathogen
108 bition zones were produced against Ralstonia solanacearum only when grown in the presence of the indi
109 llids infected with "Candidatus Liberibacter solanacearum" or to uninfected psyllids.
110 fectors, named RipI, is required for full R. solanacearum pathogenicity.
111 ligenes eutrophus) that fully complements R. solanacearum phcA mutants.
112                                 Liberibacter solanacearum" present in the psyllid gut.
113 type rescued DeltaspeC growth, indicating R. solanacearum produced and exported putrescine to xylem s
114 phy, and mass spectroscopy indicated that R. solanacearum produces staphyloferrin B rather than schiz
115           Further, tri-cultures of Ralstonia solanacearum, Pseudomonas aeruginosa, and Aspergillus fl
116 oea stewartii, Erwinia carotovora, Ralstonia solanacearum, Pseudomonas syringae, Pseudomonas aerugino
117 phores present in culture supernatants of R. solanacearum, R. metallidurans, and Bacillus megaterium
118                  Mutation of rpoS(Rso) in R. solanacearum reduced survival during starvation and low
119 of the phytopathogen Ralstonia (Pseudomonas) solanacearum, requires the products of at least seven re
120                                           R. solanacearum RpoS (RpoS(Rso)) was demonstrated to functi
121 he gene encoding the catalytic subunit of R. solanacearum's sole assimilatory nitrate reductase, did
122            The soil-borne pathogen Ralstonia solanacearum (Smith), the causal agent of bacterial wilt
123  in recent years led to the concept of an R. solanacearum species complex.
124 haracterize a gene (RsU4kpxs) from Ralstonia solanacearum str.
125         As reported previously for Ralstonia solanacearum strain GMI1000, wild-type strains AW1 and K
126  (IVET), we screened a library of 133 200 R. solanacearum strain K60 promoter fusions and isolated ap
127              While Phc is present in most R. solanacearum strains, it is apparently absent from other
128 isogenic and individually barcoded Ralstonia solanacearum strains.
129                                           R. solanacearum synthesized putrescine via a SpeC ornithine
130 olog of HrpB, the master regulator of the R. solanacearum T3SS (T3SS(rso)) and its secreted effectors
131 fector from the bacterial pathogen Ralstonia solanacearum, targets the plant E3 ubiquitin ligase PUB4
132                             Therefore, in R. solanacearum the acyl-HSL-dependent autoinduction system
133                                 Liberibacter solanacearum": the apoptosis-inducing factor AIF3 was do
134                                 Liberibacter solanacearum," the bacterium associated with potato zebr
135                                    Ralstonia solanacearum thrives in plant xylem vessels and causes b
136 e against Pseudomonas syringae and Ralstonia solanacearum through activation of elicitor-mediated def
137 syringae and the vascular pathogen Ralstonia solanacearum Thus, the GFP strand system can be broadly
138 ntributes significantly to the ability of R. solanacearum to locate and effectively interact with its
139  a naturally acyl-HSL-defective strain of R. solanacearum to produce acyl-HSLs.
140  plants against the plant pathogen Ralstonia solanacearum under greenhouse conditions.
141 ted by the bacterial wilt pathogen Ralstonia solanacearum, undergoes phosphorylation at specific resi
142 etween noroVLPs and a lectin (from Ralstonia solanacearum) upon binding to these GSLs.
143 s syringae pv. pisi and PopP2 from Ralstonia solanacearum via an integrated WRKY domain in RRS1-R.
144 uggest that nitrate assimilation promotes R. solanacearum virulence by enhancing root attachment, the
145 nvestigate the role of these acyl-HSLs in R. solanacearum virulence gene expression, transposon mutan
146 on of many ipx genes was subject to known R. solanacearum virulence regulators.
147  not a sole carbon or nitrogen source for R. solanacearum, was enriched 76-fold to 37 microM in R. so
148 the growth of a bacterial invader, Ralstonia solanacearum, when introduced into communities comprised
149 tively activates motility, in contrast to R. solanacearum where it represses motility.
150                                    Ralstonia solanacearum, which causes bacterial wilt disease of man
151                                           L. solanacearum, which is associated with psyllid yellows d
152             The chromosomal pehB genes in R. solanacearum wild-type strain K60 and in an endo-PG PehA
153 ovora, Pectobacterium carotovorum, Ralstonia solanacearum, Xanthomonas campestris, Xanthomonas oryzae
154            Rhizobium radiobacter), Ralstonia solanacearum, Xanthomonas citri subsp. citri (X. citri),

 
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