ライフサイエンスコーパス: solanacearum

1 seudomonas syringae and PopP2 from Ralstonia solanacearum.

2 in another P. syringae strain and Ralstonia solanacearum.

3 ulation of flagellum-mediated motility in R. solanacearum.

4 (bp) genes, as well as their orthologs in R. solanacearum.

5 ytopathogenic Xanthomonas spp. and Ralstonia solanacearum.

6 tii, as well as the plant pathogen Ralstonia solanacearum.

7 ulence genes in the plant pathogen Ralstonia solanacearum.

8 unknown function, and 13% were unique to R. solanacearum.

9 nas campestris pv. vesicatoria and Ralstonia solanacearum.

10 ve as sole carbon or nitrogen sources for R. solanacearum.

11 ty was with Ralstonia eutropha and Ralstonia solanacearum.

12 or (VEF) produced by wild-type strains of R. solanacearum.

13 h includes R. eutropha, R. pickettii, and R. solanacearum.

14 operon is the major virulence factor for R. solanacearum.

15 es virulence gene expression in wild-type R. solanacearum.

16 ributes substantially to the virulence of R. solanacearum.

17 oA) and/or substrate Resistance to Ralstonia solanacearum 1 (RRS1-R)WRKY.

18 Ralstonia (Pseudomonas) solanacearum, a phytopathogenic bacterium that appears t

19 ntly showed that, in Ralstonia (Pseudomonas) solanacearum, a phytopathogenic bacterium, acyl-HSL prod

20 Expression of virulence genes in Ralstonia solanacearum, a phytopathogenic bacterium, is controlled

21 Ralstonia solanacearum, a soilborne plant pathogen of considerable

22 Ralstonia solanacearum, a widely distributed and economically impo

23 Cloned R. solanacearum aer1 and aer2 genes restored aerotaxis to a

24 red for a wild-type level of virulence in R. solanacearum although its individual role in wilt diseas

25 hogens, Phytophthora infestans and Ralstonia solanacearum, among others, are considered.

26 Ralstonia solanacearum, an economically important plant pathogen,

27 omonas syringae, Xanthomonas spp., Ralstonia solanacearum and Erwinia species.

28 stinct from those of Ralstonia (Pseudomonas) solanacearum and Xanthomonas campestris.

29 vity in plant-pathogenic bacteria (Ralstonia solanacearum) and fungi (Cochliobolus heterostrophus) re

30 dule, a fucose-binding lectin from Ralstonia solanacearum, and human norovirus VA387 P particle (24-m

31 domonas viridiflava, Ralstonia (Pseudomonas) solanacearum, and Xanthomonas campestris.

32 K60 generally resembles R. solanacearum CFBP2957, a Caribbean tomato isolate, but h

33 ly-related bacteria 'Candidatus Liberibacter solanacearum' (CLso), associated with vegetative disorde

34 e of ipx genes suggests that in its host, R. solanacearum confronts and overcomes a stressful and nut

35 In the phytopathogen Ralstonia (Pseudomonas) solanacearum, control of many virulence genes is partly

36 ting that the main location in tomato for R. solanacearum during pathogenesis is iron replete.

37 The identification of the R. solanacearum enzyme enables us to propose that the ances

38 aracterized, and mutated two genes in the R. solanacearum flagellar biosynthetic pathway.

39 The predicted R. solanacearum FliM closely resembled motor switch protein

40 Ralstonia solanacearum forms biofilm in vitro, but it was not know

41 py revealed that during tomato infection, R. solanacearum forms biofilm-like masses in xylem vessels.

42 dge, this is the first demonstration that R. solanacearum forms biofilms in plant xylem vessels, and

43 d no clues as to the role of acyl-HSLs in R. solanacearum gene regulation.

44 The R. solanacearum genome encodes two putative aerotaxis trans

45 a cenocepacia J2315 genome and the Ralstonia solanacearum genome.

46 accelerated wilt symptom development and R. solanacearum growth and systemic spread.

47 The phytopathogen Ralstonia solanacearum has over 5000 genes, many of which probably

48 n resistance to the plant pathogen Ralstonia solanacearum in microcosms and in tomato plant rhizosphe

49 tor produced by the plant pathogen Ralstonia solanacearum, in complex with inositol hexaphosphate (In

50 oduction, whereas inactivation of phcA in R. solanacearum increases siderophore production.

51 rum, was enriched 76-fold to 37 microM in R. solanacearum-infected sap.

52 ics identified 22 metabolites enriched in R. solanacearum-infected sap.

53 Ralstonia solanacearum is a major phytopathogen that attacks many

54 Ralstonia (Pseudomonas) solanacearum is a soil-borne phytopathogen that causes a

55 Ralstonia solanacearum is a soil-borne plant pathogen that causes

56 Ralstonia solanacearum is a soil-borne vascular pathogen that colo

57 Ralstonia solanacearum is a soilborne pathogen that causes bacteri

58 Ralstonia solanacearum is a widespread and destructive plant patho

59 Expression of virulence factors in Ralstonia solanacearum is controlled by a complex regulatory netwo

60 vessels of infected plants, we found that R. solanacearum is essentially nonmotile in planta, althoug

61 cyl-HSL-dependent autoinduction system in R. solanacearum is part of a more complex autoregulatory hi

62 Ralstonia solanacearum is the causal agent of bacterial wilt of ma

63 one of the exo-PGs, pehB, was cloned from R. solanacearum K60.

64 ormed by oligomerization as in the Ralstonia solanacearum lectin and not by sequential domains like t

65 We found that R. solanacearum manipulates its host to increase nutrients

66 An R. solanacearum mutant lacking the pathogen's two extracell

67 an extracellular factor that complements R. solanacearum mutants deficient in production of the 3-OH

68 Two site-directed R. solanacearum mutants lacking either CheA or CheW, which

69 To locate and infect host plant roots R. solanacearum needs taxis, the ability to move toward mor

70 llids infected with "Candidatus Liberibacter solanacearum" or to uninfected psyllids.

71 ligenes eutrophus) that fully complements R. solanacearum phcA mutants.

72 type rescued DeltaspeC growth, indicating R. solanacearum produced and exported putrescine to xylem s

73 phy, and mass spectroscopy indicated that R. solanacearum produces staphyloferrin B rather than schiz

74 oea stewartii, Erwinia carotovora, Ralstonia solanacearum, Pseudomonas syringae, Pseudomonas aerugino

75 phores present in culture supernatants of R. solanacearum, R. metallidurans, and Bacillus megaterium

76 Mutation of rpoS(Rso) in R. solanacearum reduced survival during starvation and low

77 of the phytopathogen Ralstonia (Pseudomonas) solanacearum, requires the products of at least seven re

78 R. solanacearum RpoS (RpoS(Rso)) was demonstrated to functi

79 he gene encoding the catalytic subunit of R. solanacearum's sole assimilatory nitrate reductase, did

80 in recent years led to the concept of an R. solanacearum species complex.

81 haracterize a gene (RsU4kpxs) from Ralstonia solanacearum str.

82 As reported previously for Ralstonia solanacearum strain GMI1000, wild-type strains AW1 and K

83 (IVET), we screened a library of 133 200 R. solanacearum strain K60 promoter fusions and isolated ap

84 While Phc is present in most R. solanacearum strains, it is apparently absent from other

85 R. solanacearum synthesized putrescine via a SpeC ornithine

86 olog of HrpB, the master regulator of the R. solanacearum T3SS (T3SS(rso)) and its secreted effectors

87 Therefore, in R. solanacearum the acyl-HSL-dependent autoinduction system

88 Liberibacter solanacearum," the bacterium associated with potato zebr

89 Ralstonia solanacearum thrives in plant xylem vessels and causes b

90 syringae and the vascular pathogen Ralstonia solanacearum Thus, the GFP strand system can be broadly

91 ntributes significantly to the ability of R. solanacearum to locate and effectively interact with its

92 a naturally acyl-HSL-defective strain of R. solanacearum to produce acyl-HSLs.

93 plants against the plant pathogen Ralstonia solanacearum under greenhouse conditions.

94 uggest that nitrate assimilation promotes R. solanacearum virulence by enhancing root attachment, the

95 nvestigate the role of these acyl-HSLs in R. solanacearum virulence gene expression, transposon mutan

96 on of many ipx genes was subject to known R. solanacearum virulence regulators.

97 not a sole carbon or nitrogen source for R. solanacearum, was enriched 76-fold to 37 microM in R. so

98 the growth of a bacterial invader, Ralstonia solanacearum, when introduced into communities comprised

99 tively activates motility, in contrast to R. solanacearum where it represses motility.

100 Ralstonia solanacearum, which causes bacterial wilt disease of man

101 The chromosomal pehB genes in R. solanacearum wild-type strain K60 and in an endo-PG PehA

102 ovora, Pectobacterium carotovorum, Ralstonia solanacearum, Xanthomonas campestris, Xanthomonas oryzae