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1 y also serve a protective function against a phytopathogen.
2  studies, and quarantine of this devastating phytopathogen.
3 ase caused by this organism beyond that of a phytopathogen.
4 xicity, being a candidate for the control of phytopathogens.
5 id oxidation pathway in two important fungal phytopathogens.
6 are prevalent between plants and specialized phytopathogens.
7 xhibit increased susceptibility to different phytopathogens.
8 ructural phylogenomic studies across diverse phytopathogens.
9  to understand their evolution across fungal phytopathogens.
10 es to mitigate risks from diseases caused by phytopathogens.
11 ve element for plants during infections with phytopathogens.
12 ns (NLPs) are MAMPs found in a wide range of phytopathogens.
13 f Bacillus spp. as biocontrol agents against phytopathogens.
14 o affect interactions with a number of other phytopathogens.
15 icient to transition beneficial symbionts to phytopathogens.
16 at enable rapid evolution of both plants and phytopathogens.
17 uld have an influence on plant resistance to phytopathogens.
18 otes resistance against bacterial and fungal phytopathogens.
19  high broad-spectrum activity against fungal phytopathogens.
20 o protect susceptible crops against multiple phytopathogens.
21 al resource for protection of plants against phytopathogens.
22 of surface proteins of CTV and X. fastidiosa phytopathogens.
23 des with a MIC dosage of 0.1% (v/v) for both phytopathogens.
24 ific pool of InsP6 regulates defence against phytopathogens.
25  is often the structure first encountered by phytopathogens.
26  and OxB was required for protection against phytopathogens.
27 on to plant species against given species of phytopathogens.
28  confer resistance against a wide variety of phytopathogens.
29 nsights into the potential pathways that the phytopathogen A. alternata copes with oxidative stress.
30  of Sclerotinia sclerotiorum, a necrotrophic phytopathogen, a secreted protein named SsPEIE1 (Sclerot
31 nia sclerotiorum is a filamentous ascomycete phytopathogen able to infect an extremely wide range of
32 h predicts tight co-clustering with putative phytopathogens across hosts.
33           Export of oncogenic T-DNA from the phytopathogen Agrobacterium tumefaciens is mediated by t
34 nts of the VirB/D4 conjugation system of the phytopathogen Agrobacterium tumefaciens.
35 ay to growth, motility, and virulence of the phytopathogen Agrobacterium tumefaciens.
36  now fourteen completed genomes of bacterial phytopathogens, all of which have been generated in the
37 m tumefaciens, a previously known generalist phytopathogen, also increased with alfalfa-fescue plant
38 critical role in determining avirulence of a phytopathogen and reveal a commonality between symbiotic
39 nal Enterobacteriaceae species, encompassing phytopathogens and environmental isolates.
40 e critical strategies employed by biotrophic phytopathogens and hemibiotrophs whose infection mechani
41 is by examining the genomes of six bacterial phytopathogens and identifying 56 candidate elicitors th
42 These pectins are also attacked by PMEs from phytopathogens and phytophagous insects.
43 ional conservation in filamentous ascomycete phytopathogens and saprobes.
44 ee of susceptibility to a panel of bacterial phytopathogens and the ability to activate pathogenesis-
45 s detailing the reprogramming of plant AS by phytopathogens and the functional implications on diseas
46  known that the CW acts as a barrier against phytopathogens and undergoes modifications to limit thei
47 te to the development of antifungals against phytopathogens and, with the afc gene cluster being cons
48 ta, we estimated that bacterial effectors of phytopathogens are highly enriched in long-disordered re
49               Thanks to this capacity, these phytopathogens became a powerful and indispensable tool
50 ot known whether other type III effectors of phytopathogens behave similarly.
51 ssociated bacteria, including many important phytopathogens belonging to the genera Brenneria, Dickey
52 y, we show that donor plants infected by the phytopathogen Botrytis cinerea transfer jasmonic acid vi
53 in the mycoparasitic interaction against the phytopathogen Botrytis cinerea.
54 quired for basal immunity against the fungal phytopathogen Botrytis cinerea.
55 acco conferred protection against the fungal phytopathogen Botrytis cinerea.
56 inducible promoter are more resistant to the phytopathogens Botrytis cinerea, Pectobacterium carotovo
57  plant pathogen Ustilago maydis yet is not a phytopathogen but rather a biocontrol agent of powdery m
58 45 treated with either ozone or an avirulent phytopathogen, but was not detected in NE-388.
59 ant PGIPs not only confer resistance against phytopathogens, but may also aid in defense against herb
60 play a crucial role in plant defense against phytopathogens by inhibiting microbial polygalacturonase
61 dicts that the confrontation of plant with a phytopathogen can lead to the recruitment and accumulati
62                                              Phytopathogens can influence or manipulate insect behavi
63                                              Phytopathogens can manipulate plant hormone signaling to
64                                       Fungal phytopathogens can suppress plant immune mechanisms in o
65 syllid, which carries the putative bacterial phytopathogen, Candidatus Liberibacter asiaticus (CLas).
66 e bacterium Ralstonia solanacearum, a global phytopathogen capable of infecting various crops(6,7).
67                                              Phytopathogens cause plant diseases that threaten food s
68 in the unique Ras gene (DARas) of the fungal phytopathogen Colletotrichum trifolii displays a nutrien
69                                              Phytopathogens coordinate multifaceted life histories an
70                                              Phytopathogens deliver effector proteins inside host pla
71  communication underlying the basis for this phytopathogen-dependent biocontrol is still unknown.
72 seed novel directions for the advancement of phytopathogen-dependent biocontrol, including the genera
73             We identified and localized four phytopathogen-dependent secondary metabolites, including
74 potential to regulate c-di-GMP levels in the phytopathogen Dickeya dadantii 3937.
75 relative assay targeting 445 proteins of the phytopathogen Dickeya dadantii during plant infection.
76 plays a crucial role in the virulence of the phytopathogen Dickeya dadantii.
77 ovel protein targeting system in the enteric phytopathogen, Dickeya dadantii.
78                                 Importantly, phytopathogen diversity will increase largely in forest
79 to the group I hrp clusters found in certain phytopathogens (e.g., P. syringae and Erwinia amylovora)
80                                    Bacterial phytopathogens employ a type III secretion system to del
81  computational approach, we identified seven phytopathogen-enriched protein families putatively secre
82                          The enterobacterial phytopathogen Erwinia amylovora causes fire blight, an i
83         Fire blight, caused by the bacterial phytopathogen Erwinia amylovora, is an economically impo
84 s of virulence determinants in the bacterial phytopathogen Erwinia amylovora, the cause of devastatin
85                         In the Gram-negative phytopathogen, Erwinia carotovora ssp. atroseptica (Eca)
86  and exoenzyme virulence determinants in the phytopathogen, Erwinia carotovora subspecies carotovora.
87                Strain GS101 of the bacterial phytopathogen, Erwinia carotovora, makes the simple beta
88                                  Filamentous phytopathogens form sophisticated intracellular feeding
89 ative rod in the family Comamonadaceae and a phytopathogen found in the environment.
90  were systematically characterized using the phytopathogen Fusarium graminearum as the model species,
91 nd its antifungal activity against the melon phytopathogen Fusarium jinanense.
92 efficiently induced defense reactions to the phytopathogens H. parasitica and Pseudomonas syringae.
93                                              Phytopathogens have developed elaborate mechanisms to at
94                                              Phytopathogens have mastered the ability to evade plant
95                                         Some phytopathogens have transcriptionally active prophage ge
96 l insight into the role of putrescine during phytopathogen-host interactions and broaden our knowledg
97 pathogens are an important aspect of complex phytopathogen-host interactions and can be crucial for v
98 ly of proteins that are induced by different phytopathogens in many plants and share significant sequ
99 mentally regulated defense mechanism against phytopathogens in the maturing fruit.
100 findings reveal a defensive strategy against phytopathogens in the phyllosphere, highlighting the pot
101 idopsis thaliana is a host for many types of phytopathogens including bacteria, fungi, viruses and ne
102 uces a new perspective for understanding how phytopathogen-induced alterations in host AS cause disea
103 s an attenuated level of ozone-, wound-, and phytopathogen-induced defense gene expression.
104         Differentiation of fungal conidia of phytopathogens into the infection structure, appressoriu
105 ot permeability constitutes a bottleneck for phytopathogen invasion and genetic diversity.
106                                    Bacterial phytopathogens living on the surface or within plant tis
107  diseases of cocoa trees is caused by fungal phytopathogen Moniliophthora roreri.
108                                              Phytopathogens often secrete effectors to enhance their
109          Both Pseudomonas aeruginosa and the phytopathogen P. syringae produce the exopolysaccharide
110               Pseudomonas aeruginosa and the phytopathogen P. syringae produce the exopolysaccharide
111 ns (B. cereus, L. monocytogenes, S. aureus), phytopathogens (P. carotovorum), and bacterial starter c
112                                          The phytopathogen Pectobacterium atrosepticum SCRI1043 (Pba1
113 d 2 (HAI2), present in the chromosome of the phytopathogen Pectobacterium atrosepticum SCRI1043, was
114 e, we identify the PacF chemoreceptor in the phytopathogen Pectobacterium atrosepticum that recognize
115  We identify the chemoreceptor PacP from the phytopathogen Pectobacterium atrosepticum, which exclusi
116                In the economically important phytopathogen, Pectobacterium atrosepticum, expression o
117 e AvrRpt2-like homologs can be found in some phytopathogens, plant-associated and soil bacteria.
118 oots and xylem inoculation) and quantify the phytopathogen population dynamics during invasion.
119 could be considered a genetic bottleneck for phytopathogen populations.
120 und that volatile emissions from this fungal phytopathogen promote growth, photosynthesis, and the ac
121 onfer resistance to strains of the bacterial phytopathogen Pseudomonas syringae carrying the avirulen
122                                          The phytopathogen Pseudomonas syringae competes with other e
123 eport that virulent strains of the bacterial phytopathogen Pseudomonas syringae induce systemic susce
124                                          The phytopathogen Pseudomonas syringae pv. actinidiae (Psa)
125 A and glnF) gene encoding sigma(54) from the phytopathogen Pseudomonas syringae pv. maculicola strain
126  for the hrpZ, hrpL, and hrpS genes from the phytopathogen Pseudomonas syringae pv. maculicola strain
127  hrp and hrc genes in the hrpC operon of the phytopathogen Pseudomonas syringae pv. syringae 61 have
128    To avoid recognition, the bacterial model phytopathogen Pseudomonas syringae pv. tomato DC3000 pro
129 opZ1a is an acetyltransferase carried by the phytopathogen Pseudomonas syringae that elicits effector
130 lling pathways are utilized by the bacterial phytopathogen Pseudomonas syringae to promote pathogenes
131 ess in identifying effectors was made in the phytopathogen Pseudomonas syringae using a novel genetic
132     Whole-cell bacterial bioreporters of the phytopathogen Pseudomonas syringae were constructed that
133 opsis thaliana, the hemibiotrophic bacterial phytopathogen Pseudomonas syringae, and herbivorous larv
134 rential screen of plants challenged with the phytopathogen Pseudomonas syringae.
135                                       In the phytopathogen Ralstonia (Pseudomonas) solanacearum, cont
136 an exopolysaccharide virulence factor of the phytopathogen Ralstonia (Pseudomonas) solanacearum, requ
137                                          The phytopathogen Ralstonia solanacearum has over 5000 genes
138 n IsoF can protect tomato plants against the phytopathogen Ralstonia solanacearum in a T4BSS-dependen
139 ect vector and its interaction with the CLas phytopathogen remain unclear.
140 ar mechanisms of effector delivery by fungal phytopathogens remain elusive.
141 ge organism Zygosaccharomyces bailii and the phytopathogens Rhizoctonia solani and Zymoseptoria triti
142     Gram-positive bacteria like Bacillus and phytopathogen Rhodococcus fascians showed inhibited grow
143 gram-positive bacteria Bacillus subtilis and phytopathogen Rhodococcus fascians.
144 acterized a CP (SsCP1) from the necrotrophic phytopathogen Sclerotinia sclerotiorum.
145                                              Phytopathogens secrete effector molecules to manipulate
146                                              Phytopathogens secrete effectors to suppress plant defen
147 ng spheres that, when released by plants and phytopathogens, shape the outcome of the interaction, i.
148                                       Fungal phytopathogens showed globally altered patterns of gene
149 eins from 14 agriculturally important fungal phytopathogens, six non-pathogenic fungi and one oomycet
150 omic DNA segment, previously cloned from the phytopathogen Spiroplasma citri BR3-3X, contained severa
151  2,4-DTBP showed activity against other rice phytopathogens, such as Fusarium fujikuroi.
152            Ralstonia solanacearum is a major phytopathogen that attacks many crops and other plants o
153 a (Pseudomonas) solanacearum is a soil-borne phytopathogen that causes a wilting disease of many impo
154          Agrobacterium tumefaciens is a soil phytopathogen that elicits neoplastic growths on the hos
155  the leaves of Indian Hawthorn (HAL) against phytopathogens that are known to harm maize crops, Fusar
156  a focus on identifying proteins enriched in phytopathogens that could explain the lifestyle and the
157                         Citrus hosts various phytopathogens that have impacted productivity, includin
158 Arabidopsis and is related to other oomycete phytopathogens that include several species of Phytophth
159 lar wilt fungi are a group of hemibiotrophic phytopathogens that infect diverse crop plants.
160 hytoplasmas are insect-transmitted bacterial phytopathogens that secrete virulence effectors and indu
161 d important virulence determinants of fungal phytopathogens, the lack of suitable screening strategie
162      Despite the importance of this class of phytopathogen, there have been no estimates of the rate
163 s a significant impact on the ability of the phytopathogen to compete with other bacterial species in
164 the adaptations of this widespread bacterial phytopathogen to distinct habitats within its host.
165 iens are crucial in the ability of this soil phytopathogen to infect susceptible host plants.
166 l regulation of four distantly related model phytopathogens to evaluate large-scale events and mechan
167 ceptors in regulating plant immunity and how phytopathogens use effector proteins to target key compo
168                               Many bacterial phytopathogens use type III effector (T3E) proteins to i
169 -dimensional (3D) genome organization of the phytopathogen Verticillium dahliae, known to possess dis
170 nd/or virulence gene products exit bacterial phytopathogens via Hrp pathways.
171     Activity of the CPS and KS found in this phytopathogen was verified - that is, Xoc is capable of
172       Owing to the public importance of this phytopathogen we embarked on a comparative analysis of t
173 terium atrosepticum (Pca) is a Gram-negative phytopathogen which causes disease by secreting plant ce
174     Dickeya dadantii is a globally dispersed phytopathogen which causes diseases on a wide range of h
175                          Powdery mildews are phytopathogens whose growth and reproduction are entirel
176 ided analysis to more evolutionarily distant phytopathogens with similar lifestyles, we used AlphaFol
177  2.2-A crystal structure of apo Zur from the phytopathogen Xanthomonas campestris pv. campestris (XcZ

 
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