1 usarium species are among the most important
phytopathogenic and toxigenic fungi.
2 Ocatin inhibits the growth of several
phytopathogenic bacteria (Agrobacterium tumefaciens, Agr
3 induced in leaves after being challenged by
phytopathogenic bacteria also has BEBT activity, whereas
4 Plasmids are common residents of
phytopathogenic bacteria and contribute significantly to
5 s of enhanced susceptibility to a variety of
phytopathogenic bacteria and to the obligate biotrophic
6 romoting type III secretion system (T3SS) in
phytopathogenic bacteria are induced at the start of inf
7 Most plasmids characterized in
phytopathogenic bacteria are self-transmissible and poss
8 it is beginning to provide insights into how
phytopathogenic bacteria cause disease on their hosts.
9 Phytopathogenic bacteria deliver effectors of disease in
10 To overcome such immunity,
phytopathogenic bacteria deliver virulence molecules cal
11 To prevent this response,
phytopathogenic bacteria deploy a repertoire of effector
12 y been considered as substrates exploited by
phytopathogenic bacteria during plant infection.
13 toire of molecules putatively metabolized by
phytopathogenic bacteria during their life cycle.
14 in studying the etiology and epidemiology of
phytopathogenic bacteria from epidemics, as was done in
15 This review describes how
phytopathogenic bacteria have incorporated QS mechanisms
16 the most important groups of genes found in
phytopathogenic bacteria in relationship to pathogenicit
17 Avr-proteins of
phytopathogenic bacteria include type III effector prote
18 pathway has revealed new mechanisms by which
phytopathogenic bacteria infect plants.
19 Many
phytopathogenic bacteria inject virulence effector prote
20 However, its function in
phytopathogenic bacteria is not yet understood.
21 Phytopathogenic bacteria possess a large number of genes
22 e applied this method to two isolates of the
phytopathogenic bacteria Pseudomonas syringae.
23 Xanthomonas spp. are
phytopathogenic bacteria that can cause disease on a wid
24 retion system (T3SS) substrates found in all
phytopathogenic bacteria that utilize a T3SS.
25 hrp genes control the ability of
phytopathogenic bacteria to cause disease and to elicit
26 of mosaic and ever-changing plasmids allows
phytopathogenic bacteria to maintain a dynamic, flexible
27 Gram-negative
phytopathogenic bacteria translocate effector proteins i
28 Many
phytopathogenic bacteria use a type III secretion system
29 alicylic acid (SA), methyl jasmonate (MeJA),
phytopathogenic bacteria, and flagellin.
30 This reveals that, similar to effectors of
phytopathogenic bacteria, recognition of filamentous pat
31 Gram-negative
phytopathogenic bacteria, such as Pseudomonas syringae,
32 eports linking actin with resistance against
phytopathogenic bacteria.
33 eas homologs for the rest are found in other
phytopathogenic bacteria.
34 namically and discriminately to infection by
phytopathogenic bacteria.
35 d reveal a commonality between symbiotic and
phytopathogenic bacteria.
36 cess related to the PCD pathway activated by
phytopathogenic bacteria.
37 In addition, the
phytopathogenic bacterial plasmid "mobilome" includes in
38 omonas syringae pv. syringae (Pss) and other
phytopathogenic bacterial species.
39 of exopolysaccharide (EPS) synthesis in the
phytopathogenic bacterium Pantoea stewartii ssp. stewart
40 The
phytopathogenic bacterium Pantoea stewartii subsp. stewa
41 The
phytopathogenic bacterium Pseudomonas syringae can suppr
42 or-gene disease resistance to strains of the
phytopathogenic bacterium Pseudomonas syringae carrying
43 sis thaliana) following inoculation with the
phytopathogenic bacterium Pseudomonas syringae pv tomato
44 dependent responses when challenged with the
phytopathogenic bacterium Pseudomonas syringae.
45 vation of EFR and downstream immunity to the
phytopathogenic bacterium Pseudomonas syringae.
46 the phytotoxin coronatine synthesized by the
phytopathogenic bacterium Pseudomonas syringae.
47 Ralstonia (Pseudomonas) solanacearum, a
phytopathogenic bacterium that appears to autoregulate i
48 Agrobacterium tumefaciens is a
phytopathogenic bacterium that induces the 'crown gall'
49 hydathode infection by the adapted vascular
phytopathogenic bacterium Xanthomonas campestris pv camp
50 Xp10 is a lytic bacteriophage of the
phytopathogenic bacterium Xanthomonas oryzae.
51 , in Ralstonia (Pseudomonas) solanacearum, a
phytopathogenic bacterium, acyl-HSL production requires
52 virulence genes in Ralstonia solanacearum, a
phytopathogenic bacterium, is controlled by a complex re
53 mplete and two draft genome sequences of the
phytopathogenic bacterium, Xylella fastidiosa, which cau
54 s an important virulence determinant of this
phytopathogenic bacterium.
55 ological systems: i) synthetic dsDNA and two
phytopathogenic diseases, ii) the severe CB-form of Citr
56 sly shown that they promote infection by the
phytopathogenic enterobacteria Dickeya dadantii and Erwi
57 A-binding protein referred to as CsrA or, in
phytopathogenic Erwinia species, RsmA (repressor of stat
58 n-activated protein kinase (FsMAPK) from the
phytopathogenic filamentous fungus F. solani f. sp. pisi
59 ve a putative or experimentally demonstrable
phytopathogenic function.
60 idae are believed to occur commonly in their
phytopathogenic fungal and plant hosts.
61 ssociated with a debilitating disease of its
phytopathogenic fungal host.
62 iseases and/or reduce the virulence of their
phytopathogenic fungal hosts.
63 It highlights what is known about the
phytopathogenic fungal wall and what needs to be discove
64 owledge of the functions of MAPK cascades in
phytopathogenic fungi and highlight the central role pla
65 During interaction between
phytopathogenic fungi and plants, fungal MAPKs help to p
66 The idea that
phytopathogenic fungi associated with tree-killing bark
67 exhibit antifungal activity against numerous
phytopathogenic fungi at physiologically relevant concen
68 function analyses of two homologues from the
phytopathogenic fungi Colletotrichum graminicola and C.
69 Phytopathogenic fungi encounter toxic environments durin
70 Phytopathogenic fungi have evolved an amazing diversity
71 Germinating conidia of many
phytopathogenic fungi must differentiate into an infecti
72 The germinating conidia of many
phytopathogenic fungi on hosts must differentiate into a
73 Many
phytopathogenic fungi use infection structures (IFSs, i.
74 there is growing evidence that at least some
phytopathogenic fungi use mannitol to suppress ROS-media
75 h their total antagonistic potential against
phytopathogenic fungi was not reduced.
76 inants, to serve as bacterial antagonists to
phytopathogenic fungi, and to secrete the highly useful
77 Finally, two of the most widespread
phytopathogenic fungi, Fusarium oxysporum and Botrytis c
78 Oxalic acid is a virulence factor of several
phytopathogenic fungi, including Sclerotinia sclerotioru
79 Tentoxin, produced by
phytopathogenic fungi, selectively affects the function
80 nctions in a variety of organisms, including
phytopathogenic fungi.
81 ession of CWDE genes in both saprophytic and
phytopathogenic fungi.
82 ding canola with resistance against multiple
phytopathogenic fungi.
83 that is implicated in plant defense against
phytopathogenic fungi.
84 n structure (appressorium) formation in many
phytopathogenic fungi.
85 of mannitol production and secretion in the
phytopathogenic fungus Alternaria alternata in the prese
86 re we show that RNAi can be expressed in the
phytopathogenic fungus Colletotrichum acutatum (strain C
87 Ustilago maydis is a
phytopathogenic fungus exhibiting extreme resistance to
88 oxins, the endoplasmic reticulum (ER) of the
phytopathogenic fungus Fusarium graminearum is reorganiz
89 Macrophomate synthase (MPS) of the
phytopathogenic fungus Macrophoma commelinae catalyzes t
90 he extracellular or secreted enzyme from the
phytopathogenic fungus Magnaporthe grisea.
91 verse propagules, such as teliospores of the
phytopathogenic fungus Ustilago maydis and spores of the
92 s and resistance to Ceratocystis polonica, a
phytopathogenic fungus vectored by the spruce bark beetl
93 e required for plant infection in this model
phytopathogenic fungus.
94 The circular single-stranded DNA of
phytopathogenic geminiviruses is propagated by three mod
95 on this first functional reconstruction of a
phytopathogenic microbe, we spotlight an unusual respira
96 roducts that attract insects, defend against
phytopathogenic microbes and combat human diseases.
97 idopsis plants can respond to VCs emitted by
phytopathogenic microorganisms by triggering pPGI-indepe
98 Plant resistance to
phytopathogenic microorganisms mainly relies on the acti
99 teorin, and inhibition of Pythium ultimum, a
phytopathogenic oomycete sensitive to pyoluteorin.
100 Phytopathogenic oomycetes cause some of the most devasta
101 es revealed they all have orthologs in other
phytopathogenic or symbiotic bacteria, and are involved
102 Plant resistance to disease caused by
phytopathogenic organisms is often triggered by the abil
103 onB-dependent receptor, which is utilized by
phytopathogenic Pectobacterium spp. to obtain iron from
104 thogenicity, we were unable to demonstrate a
phytopathogenic phenotype for B. thailandensis in three
105 While the organism's
phytopathogenic potential has been well documented, it h
106 ce of A. thaliana to infection with virulent
phytopathogenic Pseudomonas syringae strains.
107 ytotoxin synthesized by several pathovars of
phytopathogenic Pseudomonas syringae.
108 TTSS pathway targeting signals suggest that
phytopathogenic Pseudomonas, Xanthomonas, and Ralstonia
109 Dimorphic pathogens such as the
phytopathogenic smut fungi, Ustilago maydis and Microbot
110 In addition, many economically important
phytopathogenic species are nested within this complex.
111 The genus Verticillium encompasses
phytopathogenic species that cause vascular wilts of pla
112 in the overall levels of gene duplication in
phytopathogenic species versus non-pathogenic relatives
113 cluster is widespread within biocontrol and
phytopathogenic strains of the enterobacteria, Serratia
114 (HGT) has played a role in the evolution of
phytopathogenic traits in fungi and oomycetes.
115 uction of plant defense-related responses by
phytopathogenic xanthomonads in leaves of pepper (Capsic
116 TAL effectors delivered by
phytopathogenic Xanthomonas species are DNA-sequence-spe
117 a spp. and is very similar to T3SSs found in
phytopathogenic Xanthomonas spp. and Ralstonia solanacea