ライフサイエンスコーパス: phytopathogen

1 studies, and quarantine of this devastating phytopathogen.

2 ase caused by this organism beyond that of a phytopathogen.

3 otes resistance against bacterial and fungal phytopathogens.

4 high broad-spectrum activity against fungal phytopathogens.

5 o affect interactions with a number of other phytopathogens.

6 o protect susceptible crops against multiple phytopathogens.

7 icient to transition beneficial symbionts to phytopathogens.

8 al resource for protection of plants against phytopathogens.

9 of surface proteins of CTV and X. fastidiosa phytopathogens.

10 ific pool of InsP6 regulates defence against phytopathogens.

11 is often the structure first encountered by phytopathogens.

12 uld have an influence on plant resistance to phytopathogens.

13 on to plant species against given species of phytopathogens.

14 confer resistance against a wide variety of phytopathogens.

15 id oxidation pathway in two important fungal phytopathogens.

16 are prevalent between plants and specialized phytopathogens.

17 nsights into the potential pathways that the phytopathogen A. alternata copes with oxidative stress.

18 nia sclerotiorum is a filamentous ascomycete phytopathogen able to infect an extremely wide range of

19 Export of oncogenic T-DNA from the phytopathogen Agrobacterium tumefaciens is mediated by t

20 nts of the VirB/D4 conjugation system of the phytopathogen Agrobacterium tumefaciens.

21 ay to growth, motility, and virulence of the phytopathogen Agrobacterium tumefaciens.

22 now fourteen completed genomes of bacterial phytopathogens, all of which have been generated in the

23 critical role in determining avirulence of a phytopathogen and reveal a commonality between symbiotic

24 e critical strategies employed by biotrophic phytopathogens and hemibiotrophs whose infection mechani

25 is by examining the genomes of six bacterial phytopathogens and identifying 56 candidate elicitors th

26 These pectins are also attacked by PMEs from phytopathogens and phytophagous insects.

27 ional conservation in filamentous ascomycete phytopathogens and saprobes.

28 ee of susceptibility to a panel of bacterial phytopathogens and the ability to activate pathogenesis-

29 ta, we estimated that bacterial effectors of phytopathogens are highly enriched in long-disordered re

30 ot known whether other type III effectors of phytopathogens behave similarly.

31 quired for basal immunity against the fungal phytopathogen Botrytis cinerea.

32 acco conferred protection against the fungal phytopathogen Botrytis cinerea.

33 inducible promoter are more resistant to the phytopathogens Botrytis cinerea, Pectobacterium carotovo

34 plant pathogen Ustilago maydis yet is not a phytopathogen but rather a biocontrol agent of powdery m

35 45 treated with either ozone or an avirulent phytopathogen, but was not detected in NE-388.

36 Phytopathogens can influence or manipulate insect behavi

37 Phytopathogens can manipulate plant hormone signaling to

38 in the unique Ras gene (DARas) of the fungal phytopathogen Colletotrichum trifolii displays a nutrien

39 Phytopathogens coordinate multifaceted life histories an

40 Phytopathogens deliver effector proteins inside host pla

41 communication underlying the basis for this phytopathogen-dependent biocontrol is still unknown.

42 seed novel directions for the advancement of phytopathogen-dependent biocontrol, including the genera

43 We identified and localized four phytopathogen-dependent secondary metabolites, including

44 potential to regulate c-di-GMP levels in the phytopathogen Dickeya dadantii 3937.

45 relative assay targeting 445 proteins of the phytopathogen Dickeya dadantii during plant infection.

46 ovel protein targeting system in the enteric phytopathogen, Dickeya dadantii.

47 to the group I hrp clusters found in certain phytopathogens (e.g., P. syringae and Erwinia amylovora)

48 Bacterial phytopathogens employ a type III secretion system to del

49 computational approach, we identified seven phytopathogen-enriched protein families putatively secre

50 The enterobacterial phytopathogen Erwinia amylovora causes fire blight, an i

51 s of virulence determinants in the bacterial phytopathogen Erwinia amylovora, the cause of devastatin

52 In the Gram-negative phytopathogen, Erwinia carotovora ssp. atroseptica (Eca)

53 and exoenzyme virulence determinants in the phytopathogen, Erwinia carotovora subspecies carotovora.

54 Strain GS101 of the bacterial phytopathogen, Erwinia carotovora, makes the simple beta

55 Filamentous phytopathogens form sophisticated intracellular feeding

56 ative rod in the family Comamonadaceae and a phytopathogen found in the environment.

57 efficiently induced defense reactions to the phytopathogens H. parasitica and Pseudomonas syringae.

58 Phytopathogens have developed elaborate mechanisms to at

59 Phytopathogens have mastered the ability to evade plant

60 Some phytopathogens have transcriptionally active prophage ge

61 ly of proteins that are induced by different phytopathogens in many plants and share significant sequ

62 mentally regulated defense mechanism against phytopathogens in the maturing fruit.

63 idopsis thaliana is a host for many types of phytopathogens including bacteria, fungi, viruses and ne

64 s an attenuated level of ozone-, wound-, and phytopathogen-induced defense gene expression.

65 Differentiation of fungal conidia of phytopathogens into the infection structure, appressoriu

66 diseases of cocoa trees is caused by fungal phytopathogen Moniliophthora roreri.

67 Both Pseudomonas aeruginosa and the phytopathogen P. syringae produce the exopolysaccharide

68 Pseudomonas aeruginosa and the phytopathogen P. syringae produce the exopolysaccharide

69 The phytopathogen Pectobacterium atrosepticum SCRI1043 (Pba1

70 d 2 (HAI2), present in the chromosome of the phytopathogen Pectobacterium atrosepticum SCRI1043, was

71 In the economically important phytopathogen, Pectobacterium atrosepticum, expression o

72 e AvrRpt2-like homologs can be found in some phytopathogens, plant-associated and soil bacteria.

73 und that volatile emissions from this fungal phytopathogen promote growth, photosynthesis, and the ac

74 onfer resistance to strains of the bacterial phytopathogen Pseudomonas syringae carrying the avirulen

75 The phytopathogen Pseudomonas syringae competes with other e

76 eport that virulent strains of the bacterial phytopathogen Pseudomonas syringae induce systemic susce

77 A and glnF) gene encoding sigma(54) from the phytopathogen Pseudomonas syringae pv. maculicola strain

78 for the hrpZ, hrpL, and hrpS genes from the phytopathogen Pseudomonas syringae pv. maculicola strain

79 hrp and hrc genes in the hrpC operon of the phytopathogen Pseudomonas syringae pv. syringae 61 have

80 opZ1a is an acetyltransferase carried by the phytopathogen Pseudomonas syringae that elicits effector

81 lling pathways are utilized by the bacterial phytopathogen Pseudomonas syringae to promote pathogenes

82 ess in identifying effectors was made in the phytopathogen Pseudomonas syringae using a novel genetic

83 Whole-cell bacterial bioreporters of the phytopathogen Pseudomonas syringae were constructed that

84 opsis thaliana, the hemibiotrophic bacterial phytopathogen Pseudomonas syringae, and herbivorous larv

85 rential screen of plants challenged with the phytopathogen Pseudomonas syringae.

86 In the phytopathogen Ralstonia (Pseudomonas) solanacearum, cont

87 an exopolysaccharide virulence factor of the phytopathogen Ralstonia (Pseudomonas) solanacearum, requ

88 The phytopathogen Ralstonia solanacearum has over 5000 genes

89 ar mechanisms of effector delivery by fungal phytopathogens remain elusive.

90 ge organism Zygosaccharomyces bailii and the phytopathogens Rhizoctonia solani and Zymoseptoria triti

91 acterized a CP (SsCP1) from the necrotrophic phytopathogen Sclerotinia sclerotiorum.

92 Fungal phytopathogens showed globally altered patterns of gene

93 omic DNA segment, previously cloned from the phytopathogen Spiroplasma citri BR3-3X, contained severa

94 Ralstonia solanacearum is a major phytopathogen that attacks many crops and other plants o

95 a (Pseudomonas) solanacearum is a soil-borne phytopathogen that causes a wilting disease of many impo

96 Agrobacterium tumefaciens is a soil phytopathogen that elicits neoplastic growths on the hos

97 a focus on identifying proteins enriched in phytopathogens that could explain the lifestyle and the

98 Arabidopsis and is related to other oomycete phytopathogens that include several species of Phytophth

99 hytoplasmas are insect-transmitted bacterial phytopathogens that secrete virulence effectors and indu

100 d important virulence determinants of fungal phytopathogens, the lack of suitable screening strategie

101 Despite the importance of this class of phytopathogen, there have been no estimates of the rate

102 the adaptations of this widespread bacterial phytopathogen to distinct habitats within its host.

103 iens are crucial in the ability of this soil phytopathogen to infect susceptible host plants.

104 l regulation of four distantly related model phytopathogens to evaluate large-scale events and mechan

105 nd/or virulence gene products exit bacterial phytopathogens via Hrp pathways.

106 Activity of the CPS and KS found in this phytopathogen was verified - that is, Xoc is capable of

107 Owing to the public importance of this phytopathogen we embarked on a comparative analysis of t

108 terium atrosepticum (Pca) is a Gram-negative phytopathogen which causes disease by secreting plant ce

109 Dickeya dadantii is a globally dispersed phytopathogen which causes diseases on a wide range of h

110 Powdery mildews are phytopathogens whose growth and reproduction are entirel