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1 m, the causal agent of wheat and barley head blight.
2 ae (Xoo), the causal agent of bacterial leaf blight.
3 um graminearum, a causal agent of wheat head blight.
4 ffective against specific races of bacterial blight.
5 he cause of Stewart's vascular wilt and fire blight.
6 a, including the causal agent of potato late blight.
7 ria parasitica, the causal agent of chestnut blight.
8 e R1 resistance (R) gene against potato late blight.
9 s-like microbes and the cause of potato late blight.
10 re of the variation, up to 37.2% for foliage blight.
11 maturity, height, tuber blight, and foliage blight.
12 , a Gram-negative bacterium that causes rice blight.
13 hogen responsible for the plant disease fire blight.
14 ophthora infestans, the causal agent of late blight.
15 a4) at two field sites endemic for bacterial blight.
16 yphonectria parasitica, incitant of chestnut blight.
17 on in the phloem is characteristic of citrus blight.
18 ts that altered tissue structure accompanies blight.
19 ) offers a promising solution to manage late blight.
20 d signaling networks triggered by Alternaria blight.
21 nt lines that are most likely to resist rice blight.
22 fers persistent resistance to rice bacterial blight.
23 t wheat (T. aestivum) disease, Fusarium head blight.
25 Malus domestica) cultivars resistant to fire blight, a devastating bacterial disease caused by Erwini
26 pathogen Erwinia amylovora that causes fire blight, a devastating disease of apple and pear, have be
27 or Jagger is the causal agent of Sclerotinia blight, a highly destructive disease of peanut (Arachis
28 g population for resistance to northern leaf blight, a maize disease of global economic importance.
30 one, is now besieged by an aggressive foliar blight active over a broad temperature range when there
31 tein (ZBP) from phloem tissue of healthy and blight-affected citrus (Citrus sinensis [L.] Osbeck on C
36 phytopathogen Erwinia amylovora causes fire blight, an invasive disease that threatens a wide range
37 to enhance resistance to both southern leaf blight and anthracnose stalk rot caused by Cochliobolis
39 ne provides protection against a lethal leaf blight and ear mold disease caused by Cochliobolus carbo
40 aturity, short plants, and susceptibility to blight and explained 54.7, 26.5, 26.3, and 17.5% of the
42 tions for HsvA as a virulence factor in fire blight and may also provide a basis for strategies to co
43 enes that co-localize with QTL for bacterial blight and sheath blight disease resistance on rice chro
45 the function of GhSWEETs in cotton bacterial blight and the promise of disrupting the TALE-binding si
48 zae pv oryzae, the causal agent of bacterial blight, and the recessive allele is defeated by strains
49 resistance to anthracnose and Phomopsis stem blight; and, (iii) define regions of synteny between the
50 ual worldwide potato crop losses due to late blight are conservatively estimated at $6.7 billion.
51 spot, northern leaf blight and southern leaf blight are three of the most destructive foliar diseases
52 Golden Delicious were infected with the fire blight bacterium, highest MdB4H transcript levels were o
56 Z-3-HAC protects wheat against Fusarium head blight by priming for enhanced JA-dependent defenses dur
61 ly broad spectrum of resistance to bacterial blight caused by Xanthomonas oryzae pv. oryzae (Xoo).
62 ly broad spectrum of resistance to bacterial blight caused by Xanthomonas oryzae pv. oryzae (Xoo).
72 re the most effective solution for bacterial blight, caused by Xanthomonas oryzae pv. oryzae (Xoo).
74 saic disease (CMD) and the cassava bacterial blight (CBB), and MECU72, resistant to cassava white fly
78 ant pathogen and causative agent of chestnut blight, contains three G alpha, one G beta, one G gamma
79 ution of redox-mediated pathways, Alternaria blight continues to infect crops in the Brassicaceae fam
80 ctions between host and pathogen during fire blight development and for the identification of resista
83 the plant pathogen and causal agent of fire blight disease Erwinia amylovora has not been studied pr
84 nia amylovora, the cause of devastating fire blight disease in apple and pear, have shown that HsvA,
86 winia amylovora, the causative agent of fire blight disease of apple and pear trees, causes disease o
87 ing plant pathogen causing necrotrophic fire blight disease of apple, pear, and other rosaceous plant
89 ophthora infestans, the causal agent of late blight disease of potato (Solanum tuberosum), depends on
91 kinase XA21 confers resistance to bacterial blight disease of rice (Oryza sativa) caused by Xanthomo
93 infestans, the agent of the devastating late blight disease of tomato (Lycopersicon esculentum) and p
95 ne race 6 (PR6) is unable to cause bacterial blight disease on rice lines containing the rice resista
97 ction in Germany is highly resistant to fire blight disease, incited by different strains of the caus
98 ce (RNAi)-mediated resistance against sheath blight disease, we identified genes encoding proteins an
99 omato crops have fallen owing to potato late blight disease, which is caused by Phytophthora infestan
109 nced resistant to most devastating bacterial blight diseases caused by Xanthomonas oryzae pv. oryzae
110 gens (causal agents of rice blast and sheath blight diseases) revealed that as more chr 8 OsGLP genes
116 stant genotype CI89831 against Fusarium head blight (FHB) based on metabolo-transcriptomics approach.
117 stant genotype CI89831 against Fusarium head blight (FHB) based on metabolo-transcriptomics approach.
119 The devastating effect of Fusarium head blight (FHB) caused by Fusarium graminearum has led to s
129 Breeding for resistance to Fusarium head blight (FHB) relies strongly on a limited number of larg
136 ecimated by the introduction of the chestnut blight fungus (Cryphonectria parasitica) in the early 20
137 s isolated from strain NB631 of the chestnut blight fungus (Cryphonectria parasitica), a model filame
138 induced in a virulent strain of the chestnut blight fungus Cryphonectria parasitica (Murr.) Barr.
140 y (vic)] loci were disrupted in the chestnut blight fungus Cryphonectria parasitica using an adapted
141 e of two dicer genes, dcl-2, of the chestnut blight fungus Cryphonectria parasitica was recently show
142 attenuation (hypovirulence) of the chestnut blight fungus Cryphonectria parasitica were used to cons
145 attenuation (hypovirulence) of the chestnut blight fungus Cryphonectria parasitica, could serve as g
146 , and CHV-1/EP721, which infect the chestnut blight fungus Cryphonectria parasitica, differ in their
147 attenuation (hypovirulence) of the chestnut blight fungus Cryphonectria parasitica, encodes two papa
148 g antiviral defense response in the chestnut blight fungus Cryphonectria parasitica, is inducible upo
149 orulation by the infected host, the chestnut blight fungus Cryphonectria parasitica, while being disp
157 uation) observed for strains of the chestnut blight fungus, Cryphonectria parasitica, harboring membe
159 eport that DI RNA production in the chestnut blight fungus, Cryphonectria parasitica, persistently in
160 terized of a number of genes in the chestnut blight fungus, Cryphonectria parasitica, that are repres
161 al transcriptional responses of the chestnut blight fungus, Cryphonectria parasitica, to infection by
162 pMV1) from U.S. strain NB631 of the chestnut blight fungus, Cryphonectria parasitica, was the first v
163 ype, such as the hypoviruses of the chestnut-blight fungus, have been studied for their potential as
164 ne in Cryphonectria parasitica, the chestnut blight fungus, reduces the ability of the fungus to form
166 , causal agent of the tomato and potato late blight, generates important economic and environmental l
167 mportant foliar maize diseases-southern leaf blight, gray leaf spot and northern leaf blight-has been
168 ns causing necrotic symptoms such as blossom blights (group 1), and specialist flower pathogens which
170 19th century from plants infected with late blight has shown that the potato famines of the 1840s we
172 ns (Rpi) genes effective against potato late blight have been cloned, few have been cloned against ot
174 tive trait loci (QTL) for resistance to late blight, height, and maturity was performed on a tetraplo
183 agnostic kit to enable analysis of bacterial blight in the field and identification of suitable resis
185 rgely used in food industry against mold and blight in vegetables and fruits during transportation an
187 that the average global risk of potato late blight increases initially, when compared with historic
188 oding MdBIS1 to MdBIS4 were cloned from fire-blight-infected shoots of apple 'Holsteiner Cox,' hetero
189 thora infestans (causal agent of potato late blight) inoculum and the subsequent risk of infection.
192 pression of the blossom-blight phase of fire blight is a key point in the management of this destruct
194 ophthora infestans, the cause of potato late blight, is infamous for having triggered the Irish Great
196 naria linariae or Alternaria solani and leaf blight (LB) caused by A. alternata are economically impo
199 stics enables much greater precision in late blight management to produce recommendations that are si
200 mmercial potato varieties are susceptible to blight, many wild potato relatives show variation for re
201 hods with conventional management of blossom blight may be achievable by increasing the diversity of
203 titative disease resistance to northern leaf blight (NLB) and secondarily for common rust resistance
206 but its effects on controlling phytophthora blight of container-grown peppers have less been explore
210 ungus Cochliobolus victoriae causes Victoria blight of oats (Avena sativa) and is pathogenic due to i
211 olus victoriae, the causal agent of victoria blight of oats, has been demonstrated to bind to the mit
213 or Phytophthora infestans, which causes late blight of potato, and Phytophthora sojae, which affects
214 ve resistance to the rice blast fungus, late blight of potato, gray leaf spot of maize, bacterial wil
215 nthomonas oryzae pv. oryzae causes bacterial blight of rice (Oryza sativa L.), a major disease that c
216 istance gene xa5,for resistance to bacterial blight of rice (Oryza sativa), is dependent on the effec
217 Burkholderia glumae causes bacterial panicle blight of rice and produces major virulence factors, inc
221 e plant disease called scab or Fusarium head blight of wheat and barley has reached epidemic proporti
224 arum and related species cause Fusarium head blight on cultivated grasses, such as wheat and barley.
226 ls from the regressions of foliage and tuber blight on maturity were analyzed, there was no significa
227 m causes the important disease Fusarium head blight on various species of cereals, leading to contami
228 dverse events (iodine group: abortion, n=20; blighted ovum, and n=2; intrauterine death, n=2; placebo
229 e death, n=2; placebo group: abortion, n=22; blighted ovum, n=1; intrauterine death, n=2; early neona
232 ein is critical to the virulence of the fire blight pathogen Erwinia amylovora in host plants like ap
234 center of origin not only of the potato late blight pathogen P. infestans, but also of several relate
238 ants which, as shown for the infamous potato blight pathogen Phytophthora infestans, make up < 1% of
240 nfers resistance to strains of the bacterial blight pathogen Xanthomonas oryzae pv. oryzae (Xoo) that
245 ique to the incompatible interaction of late-blight pathogen, thereby providing a foundation for furt
246 QTLs that confer resistance to the bacterial blight pathogen, Xanthomonas campestris pv. malvacearum
252 mylovora, the bacterium responsible for fire blight, relies on a type III secretion system and a sing
254 ly, pre-treatment with auxin enhanced sheath blight resistance by affecting endogenous auxin homeosta
256 e presence of the Solanum bulbocastanum late blight resistance genes Rpi-blb1 and Rpi-blb2, thereby e
259 'Idared', the locus (Mfu10) controlling fire blight resistance mapped on linkage group 10 (LG10) and
262 ess tolerance, photosynthetic activity, fire blight resistance, and other differences conferred by th
263 resistance, low alkaloids and Phomopsis stem blight resistance, highlighting different genetic contro
272 DNA library from leaf tissue of the blister blight-resistant tea cultivar TRI2043 and functionally c
275 capsici Leonian, the causal agent of foliar blight, root rot, fruit rot and crown rot syndromes in s
276 ed knowledge about genetic diversity in fire blight S genes in diverse apple accessions and identifie
282 environments for resistance to southern leaf blight (SLB) disease caused by Cochliobolus heterostroph
284 M and DIPM gene families with a role in fire blight susceptibility (S genes) can help achieve sustain
285 rgeting the promoter region of the bacterial blight susceptibility genes, OsSWEET14 and OsSWEET11, we
287 ignificant associations (p < 0.05) with fire blight susceptibility traits, while two of these SNPs sh
288 develop apple cultivars with decreased fire blight susceptibility via marker-assisted breeding or bi
290 essary to restrict pathogen growth and early blight symptom development in both potato foliage and tu
292 obal effect of climate change on potato late blight, the disease that caused the Irish potato famine
293 oomycete Phytophthora infestans causes late blight, the potato disease that precipitated the Irish f
294 in wheat grains susceptible to fusarium head blight treated with fungicides, and to evaluate the rela
298 sed methods to investigate cassava bacterial blight, which is caused by the pathogen Xanthomonas axon
299 urrent climatic conditions, the risk of late blight will increase in Scotland during the first half o