ライフサイエンスコーパス: blight

1 he cause of Stewart's vascular wilt and fire blight.

2 a, including the causal agent of potato late blight.

3 ria parasitica, the causal agent of chestnut blight.

4 e R1 resistance (R) gene against potato late blight.

5 s-like microbes and the cause of potato late blight.

6 re of the variation, up to 37.2% for foliage blight.

7 maturity, height, tuber blight, and foliage blight.

8 fers persistent resistance to rice bacterial blight.

9 , a Gram-negative bacterium that causes rice blight.

10 hogen responsible for the plant disease fire blight.

11 ophthora infestans, the causal agent of late blight.

12 a4) at two field sites endemic for bacterial blight.

13 yphonectria parasitica, incitant of chestnut blight.

14 on in the phloem is characteristic of citrus blight.

15 ts that altered tissue structure accompanies blight.

16 t wheat (T. aestivum) disease, Fusarium head blight.

17 m, the causal agent of wheat and barley head blight.

18 ae (Xoo), the causal agent of bacterial leaf blight.

19 ffective against specific races of bacterial blight.

20 In citrus blight, a decline disorder of unknown etiology, the tree

21 pathogen Erwinia amylovora that causes fire blight, a devastating disease of apple and pear, have be

22 or Jagger is the causal agent of Sclerotinia blight, a highly destructive disease of peanut (Arachis

23 g population for resistance to northern leaf blight, a maize disease of global economic importance.

24 oomycete Phytophthora infestans causes late blight, a ravaging disease of potato and tomato.

25 tein (ZBP) from phloem tissue of healthy and blight-affected citrus (Citrus sinensis [L.] Osbeck on C

26 e in response to wounding or other stress of blight-affected citrus.

27 phytopathogen Erwinia amylovora causes fire blight, an invasive disease that threatens a wide range

28 to enhance resistance to both southern leaf blight and anthracnose stalk rot caused by Cochliobolis

29 asis of resistance in rice to bacterial leaf blight and blast.

30 ne provides protection against a lethal leaf blight and ear mold disease caused by Cochliobolus carbo

31 aturity, short plants, and susceptibility to blight and explained 54.7, 26.5, 26.3, and 17.5% of the

32 uantitative resistance to both southern leaf blight and gray leaf spot.

33 tions for HsvA as a virulence factor in fire blight and may also provide a basis for strategies to co

34 enes that co-localize with QTL for bacterial blight and sheath blight disease resistance on rice chro

35 of the variation for maturity, height, tuber blight, and foliage blight.

36 inct rice diseases, bacterial blight, sheath blight, and rice blast.

37 zae pv oryzae, the causal agent of bacterial blight, and the recessive allele is defeated by strains

38 resistance to anthracnose and Phomopsis stem blight; and, (iii) define regions of synteny between the

39 ual worldwide potato crop losses due to late blight are conservatively estimated at $6.7 billion.

40 Golden Delicious were infected with the fire blight bacterium, highest MdB4H transcript levels were o

41 Rice bacterial blight (BB) is a devastating rice disease.

42 ovide a basis for strategies to control fire blight by inhibiting HsvA activity.

43 Z-3-HAC protects wheat against Fusarium head blight by priming for enhanced JA-dependent defenses dur

44 Fusarium head blight caused by Fusarium graminearum is one of the most

45 Head blight caused by Fusarium graminearum threatens world-wi

46 Biological control of chestnut blight caused by the filamentous ascomycete Cryphonectri

47 ly broad spectrum of resistance to bacterial blight caused by Xanthomonas oryzae pv. oryzae (Xoo).

48 ly broad spectrum of resistance to bacterial blight caused by Xanthomonas oryzae pv. oryzae (Xoo).

49 Fire blight, caused by the bacterium Erwinia amylovora, is a

50 Potato late blight, caused by the destructive Irish famine pathogen

51 Late blight, caused by the oomycete pathogen Phytophthora inf

52 Late blight, caused by the oomycete plant pathogen Phytophtho

53 A protein associated with citrus blight (CB), a disease of unknown cause, was partially c

54 saic disease (CMD) and the cassava bacterial blight (CBB), and MECU72, resistant to cassava white fly

55 a Mosaic Disease (CMD) and Cassava Bacterial Blight (CBB), drought, and acid soils.

56 Cassava bacterial blight (CBB), incited by Xanthomonas axonopodis pv. mani

57 ant pathogen and causative agent of chestnut blight, contains three G alpha, one G beta, one G gamma

58 ctions between host and pathogen during fire blight development and for the identification of resista

59 d it sheds new light on the mechanism of the blight disease caused by M. oryzae.

60 the plant pathogen and causal agent of fire blight disease Erwinia amylovora has not been studied pr

61 nia amylovora, the cause of devastating fire blight disease in apple and pear, have shown that HsvA,

62 LMG 859, the causal agent of bacterial leaf blight disease in pomegranate.

63 ing plant pathogen causing necrotrophic fire blight disease of apple, pear, and other rosaceous plant

64 two fungal species causing a newly emergent blight disease of boxwood.

65 ophthora infestans, the causal agent of late blight disease of potato (Solanum tuberosum), depends on

66 hthora infestans, which is the cause of late blight disease of potato.

67 kinase XA21 confers resistance to bacterial blight disease of rice (Oryza sativa) caused by Xanthomo

68 infestans, the agent of the devastating late blight disease of tomato (Lycopersicon esculentum) and p

69 sarium graminearum and F. culmorum cause ear blight disease on cereal crops worldwide.

70 ne race 6 (PR6) is unable to cause bacterial blight disease on rice lines containing the rice resista

71 ize with QTL for bacterial blight and sheath blight disease resistance on rice chromosome 2.

72 omato crops have fallen owing to potato late blight disease, which is caused by Phytophthora infestan

73 cific races of the causal agent of bacterial blight disease, Xanthomonas oryzae pv oryzae.

74 specific function in facilitating bacterial blight disease.

75 Erwinia amylovora, the causal agent of fire blight disease.

76 the filamentous fungus that causes chestnut blight disease.

77 vented the fungus from causing Fusarium head blight disease.

78 ing holoenzymes with Pi04314 to promote late blight disease.

79 pv. oryzae (Xoo) races that cause bacterial blight disease.

80 nced resistant to most devastating bacterial blight diseases caused by Xanthomonas oryzae pv. oryzae

81 gens (causal agents of rice blast and sheath blight diseases) revealed that as more chr 8 OsGLP genes

82 Solanum lycopersicum L.) yield causing early blight (EB) disease in tropical environment.

83 Any factor reducing the rate of chestnut blight epidemics enhances hypovirus invasion.

84 stant genotype CI89831 against Fusarium head blight (FHB) based on metabolo-transcriptomics approach.

85 stant genotype CI89831 against Fusarium head blight (FHB) based on metabolo-transcriptomics approach.

86 The devastating effect of Fusarium head blight (FHB) caused by Fusarium graminearum has led to s

87 Fusarium head blight (FHB) caused by Fusarium graminearum is a devasta

88 Fusarium head blight (FHB) is a cereal disease caused by Fusarium gram

89 Fusarium head blight (FHB) is a devastating disease of wheat and barle

90 Fusarium head blight (FHB) is a plant disease with serious economic an

91 Fusarium head blight (FHB) management is a great challenge in barley a

92 Fusarium head blight (FHB), caused by Fusarium graminearum, is a devas

93 tivating disease resistance against the late blight fungal pathogen Phytophthora infestans.

94 induced in a virulent strain of the chestnut blight fungus Cryphonectria parasitica (Murr.) Barr.

95 Hypovirus infection of the chestnut blight fungus Cryphonectria parasitica results in a spec

96 y (vic)] loci were disrupted in the chestnut blight fungus Cryphonectria parasitica using an adapted

97 e of two dicer genes, dcl-2, of the chestnut blight fungus Cryphonectria parasitica was recently show

98 attenuation (hypovirulence) of the chestnut blight fungus Cryphonectria parasitica were used to cons

99 Infection of the chestnut blight fungus Cryphonectria parasitica with Cryphonectri

100 Persistent infection of the chestnut blight fungus Cryphonectria parasitica with the prototyp

101 attenuation (hypovirulence) of the chestnut blight fungus Cryphonectria parasitica, could serve as g

102 , and CHV-1/EP721, which infect the chestnut blight fungus Cryphonectria parasitica, differ in their

103 attenuation (hypovirulence) of the chestnut blight fungus Cryphonectria parasitica, encodes two papa

104 g antiviral defense response in the chestnut blight fungus Cryphonectria parasitica, is inducible upo

105 orulation by the infected host, the chestnut blight fungus Cryphonectria parasitica, while being disp

106 tions on mycovirus infection of the chestnut blight fungus Cryphonectria parasitica.

107 ses, including pathogenesis, in the chestnut blight fungus Cryphonectria parasitica.

108 ed virulence (hypovirulence) of the chestnut blight fungus Cryphonectria parasitica.

109 e incompatibility (vic) loci of the chestnut blight fungus Cryphonectria parasitica.

110 tor present in the lipids of the potato late blight fungus Phytophthora infestans.

111 The rice seedling blight fungus Rhizopus microsporus and its endosymbiont

112 uation) observed for strains of the chestnut blight fungus, Cryphonectria parasitica, harboring membe

113 Most hypovirulence in the chestnut blight fungus, Cryphonectria parasitica, is associated w

114 eport that DI RNA production in the chestnut blight fungus, Cryphonectria parasitica, persistently in

115 terized of a number of genes in the chestnut blight fungus, Cryphonectria parasitica, that are repres

116 al transcriptional responses of the chestnut blight fungus, Cryphonectria parasitica, to infection by

117 ype, such as the hypoviruses of the chestnut-blight fungus, have been studied for their potential as

118 ne in Cryphonectria parasitica, the chestnut blight fungus, reduces the ability of the fungus to form

119 by the causal fungal agent of Fusarium head blight, Fusarium graminearum.

120 , causal agent of the tomato and potato late blight, generates important economic and environmental l

121 mportant foliar maize diseases-southern leaf blight, gray leaf spot and northern leaf blight-has been

122 ns causing necrotic symptoms such as blossom blights (group 1), and specialist flower pathogens which

123 19th century from plants infected with late blight has shown that the potato famines of the 1840s we

124 eaf blight, gray leaf spot and northern leaf blight-has been identified on maize chromosome 9.

125 living fungal cells and cause rice seedling blight have been identified.

126 tive trait loci (QTL) for resistance to late blight, height, and maturity was performed on a tetraplo

127 Confidence in this approach is blighted however by lamentable inconsistency in publishe

128 olecular basis of resistance to Fusarium ear blight in cereal species is poorly understood.

129 It promotes the development of halo blight in common bean (Phaseolus vulgaris).

130 an confer enhanced resistance to Sclerotinia blight in peanut.

131 dependent R gene for resistance to bacterial blight in rice (Oryza sativa).

132 d recessive forms of resistance to bacterial blight in rice.

133 erring race-specific resistance to bacterial blight in rice.

134 Control of late blight in the United States and other developed countrie

135 rgely used in food industry against mold and blight in vegetables and fruits during transportation an

136 that the average global risk of potato late blight increases initially, when compared with historic

137 oding MdBIS1 to MdBIS4 were cloned from fire-blight-infected shoots of apple 'Holsteiner Cox,' hetero

138 thora infestans (causal agent of potato late blight) inoculum and the subsequent risk of infection.

139 Fire blight is a devastating disease of rosaceous plants caus

140 pression of the blossom-blight phase of fire blight is a key point in the management of this destruct

141 ophthora infestans, the cause of potato late blight, is infamous for having triggered the Irish Great

142 oil fungus, Pythium irregulare, was found to blight jar1-1.

143 Fusarium head blight, leaf spotting diseases, and, more recently, whea

144 ive strategy from both an agronomic and late blight management perspective.

145 stics enables much greater precision in late blight management to produce recommendations that are si

146 mmercial potato varieties are susceptible to blight, many wild potato relatives show variation for re

147 hods with conventional management of blossom blight may be achievable by increasing the diversity of

148 Northern corn leaf blight (NCLB) caused by the hemibiotrophic fungus Exsero

149 titative disease resistance to northern leaf blight (NLB) and secondarily for common rust resistance

150 Victoria blight of Avena sativa (oat) is caused by the fungus Coc

151 plant pathogen, is the causal agent of halo blight of bean.

152 alvacearum (Xcm) are essential for bacterial blight of cotton (BBC).

153 an important plant pathogen that causes head blight of major cereal crops.

154 ungus Cochliobolus victoriae causes Victoria blight of oats (Avena sativa) and is pathogenic due to i

155 olus victoriae, the causal agent of victoria blight of oats, has been demonstrated to bind to the mit

156 olus victoriae, the causal agent of victoria blight of oats.

157 or Phytophthora infestans, which causes late blight of potato, and Phytophthora sojae, which affects

158 ve resistance to the rice blast fungus, late blight of potato, gray leaf spot of maize, bacterial wil

159 nthomonas oryzae pv. oryzae causes bacterial blight of rice (Oryza sativa L.), a major disease that c

160 istance gene xa5,for resistance to bacterial blight of rice (Oryza sativa), is dependent on the effec

161 Burkholderia glumae causes bacterial panicle blight of rice and produces major virulence factors, inc

162 Bacterial blight of rice is caused by the gamma-proteobacterium Xa

163 n increased host susceptibility to bacterial blight of rice.

164 e plant disease called scab or Fusarium head blight of wheat and barley has reached epidemic proporti

165 devastating and economically important head blight of wheat and related species.

166 13.6% of the variation for foliage and tuber blight on an additive model.

167 arum and related species cause Fusarium head blight on cultivated grasses, such as wheat and barley.

168 eafood-borne gastroenteritis worldwide and a blight on global aquaculture.

169 ls from the regressions of foliage and tuber blight on maturity were analyzed, there was no significa

170 m causes the important disease Fusarium head blight on various species of cereals, leading to contami

171 dverse events (iodine group: abortion, n=20; blighted ovum, and n=2; intrauterine death, n=2; placebo

172 e death, n=2; placebo group: abortion, n=22; blighted ovum, n=1; intrauterine death, n=2; early neona

173 issues, and tissues challenged with the late-blight pathogen (Phytophthora infestans).

174 f genetic diversity for both the potato late blight pathogen and for tuber-bearing Solanum spp.

175 ein is critical to the virulence of the fire blight pathogen Erwinia amylovora in host plants like ap

176 irulence regulator in the Gram-negative fire blight pathogen Erwinia amylovora.

177 center of origin not only of the potato late blight pathogen P. infestans, but also of several relate

178 RXLR effector Pi04089 from the potato blight pathogen Phytophthora infestans accumulates in th

179 Effector AVR3a from potato blight pathogen Phytophthora infestans is translocated i

180 The potato blight pathogen Phytophthora infestans secretes effector

181 o-segregate with resistance towards the late blight pathogen Phytophthora infestans.

182 nfers resistance to strains of the bacterial blight pathogen Xanthomonas oryzae pv. oryzae (Xoo) that

183 The haploid, ascomycete chestnut blight pathogen, Cryphonectria parasitica, has previousl

184 script levels were also affected by the late blight pathogen, Phytophthora infestans.

185 The bean halo blight pathogen, Pseudomonas syringae pv. phaseolicola (

186 ique to the incompatible interaction of late-blight pathogen, thereby providing a foundation for furt

187 QTLs that confer resistance to the bacterial blight pathogen, Xanthomonas campestris pv. malvacearum

188 Adaptation of the bacterial blight pathogen, Xanthomonas oryzae pv. oryzae (Xoo), to

189 oryzae pv. oryzae (Xoo), the rice bacterial blight pathogen.

190 Suppression of the blossom-blight phase of fire blight is a key point in the manage

191 wdery mildew (Erysiphe pisi) and potato late blight (Phytophthora infestans).

192 mylovora, the bacterium responsible for fire blight, relies on a type III secretion system and a sing

193 All late blight resistance genes identified to date belong to the

194 e presence of the Solanum bulbocastanum late blight resistance genes Rpi-blb1 and Rpi-blb2, thereby e

195 A major gene for blight resistance in Stirling was also mapped to LGXI.

196 rtance, scientists have aggressively pursued blight resistance through various approaches.

197 ess tolerance, photosynthetic activity, fire blight resistance, and other differences conferred by th

198 resistance, low alkaloids and Phomopsis stem blight resistance, highlighting different genetic contro

199 bean cultivars carrying the R1 gene for halo-blight resistance, such as Red Mexican.

200 -alkaloids and phenylpropanoids during early blight resistance.

201 programs intended to obtained Fusarium head blight resistance.

202 ese four genes displayed broad spectrum late blight resistance.

203 ckcrossing, and generated a nearly isogenic, blight-resistant 9311/Xa21 rice.

204 provides a new resource for developing late blight-resistant potato varieties.

205 DNA library from leaf tissue of the blister blight-resistant tea cultivar TRI2043 and functionally c

206 ly used in China for controlling rice sheath blight, Rhizoctonia solani.

207 South American leaf blight (SALB) of rubber has been the main constraint to

208 The disease Fusarium head blight (scab) causes severe problems for farmers and for

209 primary etiological agents of Fusarium head blight (scab) of wheat and barley.

210 y to three distinct rice diseases, bacterial blight, sheath blight, and rice blast.

211 environments for resistance to southern leaf blight (SLB) disease caused by Cochliobolus heterostroph

212 as evaluated for resistance to southern leaf blight (SLB) disease.

213 rgeting the promoter region of the bacterial blight susceptibility genes, OsSWEET14 and OsSWEET11, we

214 ootstock is dwarfing and does not alter fire blight susceptibility of the scion.

215 is a host susceptibility gene for bacterial blight targeted by the type III effector PthXo1.

216 obal effect of climate change on potato late blight, the disease that caused the Irish potato famine

217 oomycete Phytophthora infestans causes late blight, the potato disease that precipitated the Irish f

218 in wheat grains susceptible to fusarium head blight treated with fungicides, and to evaluate the rela

219 Hypovirulence has controlled chestnut blight well in some locations in Europe and in Michigan

220 Head blight, which is caused by mycotoxin-producing fungi of

221 sed methods to investigate cassava bacterial blight, which is caused by the pathogen Xanthomonas axon

222 urrent climatic conditions, the risk of late blight will increase in Scotland during the first half o

223 ice blast (Magnaporthe oryzae) and bacterial blight (Xanthomonas oryzae pv. oryzae).