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1 very similar in the motifs of Plasmodium and Phytophthora.
2 ong to a large and complex protein family in Phytophthora.
3 s negative regulators of plant resistance to Phytophthora.
4 ic diseases but have not yet been studied in Phytophthora.
5 contains one-third fewer of these genes than Phytophthora.
7 tetrapetalum from Ecuador was identified as Phytophthora andina and evolved from a common ancestor o
9 eteroploid-interspecific hybrids involving a Phytophthora cambivora-like species and an unknown taxon
10 tor domains from two oomycete RXLR proteins, Phytophthora capsici AVR3a11 and Phytophthora infestans
12 usly shown to effect premature encystment of Phytophthora capsici zoospores, were fused to maize cyto
14 n the range of the generalist plant pathogen Phytophthora cinnamomi (Pc): through changing winter soi
15 ns, and Pseudomonas aureofaciens) and fungi (Phytophthora cinnamomi, Fusarium oxysporum, Rhizoctonia
16 suggests that a diverse, trophically complex Phytophthora community is important in many forests.
19 ed in the late 1980s as abundant proteins in Phytophthora culture filtrates that have the capacity to
20 actors in the environmental component of the Phytophthora disease triangle and of communal infection
23 canopies of trees are now being explored for Phytophthora diversity, and a new appreciation for the e
27 ae such as diatoms, and the presence of many Phytophthora genes of probable phototroph origin support
31 rmone alpha 1 of the virulent plant pathogen Phytophthora has been synthesized in 12 steps and 28 % o
32 esis provided all eight diastereomers of the phytophthora hormone alpha1 with the R configuration at
33 gene confers significant protection against Phytophthora in alfalfa, possibly via indirect effects o
34 ytopathogens that include several species of Phytophthora, including the causal agent of potato late
37 uture connectivity of crop distributions for Phytophthora infestans (causal agent of potato late blig
39 ctor Pi04089 from the potato blight pathogen Phytophthora infestans accumulates in the host nucleus a
41 ds new light on the biology and evolution of Phytophthora infestans and other related Phytophthora pa
42 the project, several investigators prepared Phytophthora infestans and Phytophthora sojae EST and Ph
44 because effector proteins from the oomycete Phytophthora infestans and virulence determinants from t
45 roteins from Hyaloperonospora parasitica and Phytophthora infestans are detected in the plant host cy
52 tments only when coexpressed with recognized Phytophthora infestans effector form AVR3a(KI) and not u
53 silencing (VIGS) and transient expression of Phytophthora infestans effectors PiAVR3a and PexRD2 were
54 ort here the characterization of a gene from Phytophthora infestans encoding a deduced amino acid (aa
55 peline to the three ancient and seven modern Phytophthora infestans genomes as described here takes 5
58 New tools have revealed that migrations of Phytophthora infestans have been a dominant feature of t
59 Filamentous pathogens such as the oomycete Phytophthora infestans infect plants by developing speci
62 Effector AVR3a from potato blight pathogen Phytophthora infestans is translocated into host cells a
64 function in regulating transcription of the Phytophthora infestans piypt1 gene, a gene that encodes
69 a different pathogen of tomato, the oomycete Phytophthora infestans that is distantly related to fung
70 ted protein from the hemibiotrophic oomycete Phytophthora infestans that is specifically expressed at
71 fector Pi04314 enhances leaf colonization by Phytophthora infestans via activity in the host nucleus
72 ation of the diploid oomycete plant pathogen Phytophthora infestans with antisense, sense, and promot
75 ospores are critical in the disease cycle of Phytophthora infestans, a member of the oomycete group o
76 ctors from the Irish potato famine pathogen, Phytophthora infestans, and its sister species, Phytopht
77 fector from the Irish potato famine pathogen Phytophthora infestans, binds host autophagy protein ATG
78 were triggered by a single clonal lineage of Phytophthora infestans, called HERB-1, which persisted f
80 es, such as the Irish potato famine pathogen Phytophthora infestans, deliver RXLR effector proteins t
81 lineage of the Irish potato famine organism Phytophthora infestans, evolve by host jumps followed by
82 light, caused by the oomycete plant pathogen Phytophthora infestans, is a devastating disease of pota
83 sed by the destructive Irish famine pathogen Phytophthora infestans, is a major threat to global food
85 Late blight, caused by the oomycete pathogen Phytophthora infestans, is the most devastating potato d
87 nd tomato (Lycopersicon esculentum) pathogen Phytophthora infestans, secrete a diverse family of seri
89 iana to successfully prevent colonization by Phytophthora infestans, the causal agent of late blight
90 with either virulent or avirulent strains of Phytophthora infestans, the causal agent of late blight.
92 l development in the heterothallic oomycete, Phytophthora infestans, were identified by suppression s
93 ene expression and functional assay data for Phytophthora infestans, which causes late blight of pota
94 after inoculation with spore suspensions of Phytophthora infestans, which is the cause of late bligh
106 n the defense against Rhizoctonia solani and Phytophthora medicaginis, with the latter interaction li
107 either treated with an elicitor derived from Phytophthora megasperma or infected with Pseudomonas syr
109 tophthora infestans, and its sister species, Phytophthora mirabilis, which is responsible for infecti
112 AdVPE exhibited enhanced resistance against Phytophthora parasitica var. nicotianae, Alternaria alte
114 irus, tobacco etch virus, black shank fungus Phytophthora parasitica, and wild fire bacterium Pseudom
116 orphisms of total DNA that a new, aggressive Phytophthora pathogen of alder trees in Europe comprises
124 d Ustilaginales, including necrosis-inducing-Phytophthora-protein- and Lysin-motif- containing protei
125 mating-induced genes resembled two types of Phytophthora proteins previously shown to elicit plant d
126 TP binding cassette (ABC) superfamily in the Phytophthora ramorum and P. sojae genomes has identified
127 ed proteome of the sudden oak death parasite Phytophthora ramorum has been acquired from fungi by HGT
129 omycete plant pathogens, Phytophthora sojae, Phytophthora ramorum, and Hyaloperonospora parasitica, t
132 ath in California coastal forests, caused by Phytophthora ramorum, in communities dominated by bay la
133 ether and how the sudden oak death pathogen, Phytophthora ramorum, survived the wildfires, we complet
134 or slow invasion by such organisms, and use Phytophthora ramorum, the cause of sudden oak death, to
135 osts along a gradient of mortality caused by Phytophthora ramorum, the cause of sudden oak death.
136 s lacked orthologs in Phytophthora sojae and Phytophthora ramorum, were relatively fast-evolving with
140 nvestigate the possible mechanism of gain of Phytophthora resistance in M1, the novel race specificit
142 or resistance to potyviruses (Rsv1 and Rpv), Phytophthora root rot (Rps1, Rps2, and Rps3), and powder
143 me sequence, was derived from backcrossing a Phytophthora root rot resistance locus from the donor pa
144 old occurs in approximately 44% of annotated Phytophthora RXLR effectors, both as a single domain and
145 ces plant susceptibility to both a virus and Phytophthora, showing that some eukaryotic pathogens hav
146 tor PsAvh23 produced by the soybean pathogen Phytophthora sojae acts as a modulator of histone acetyl
147 he epiC1 and epiC2 genes lacked orthologs in Phytophthora sojae and Phytophthora ramorum, were relati
149 -0 is nonhost to the oomycete plant pathogen Phytophthora sojae and the fungal plant pathogen Fusariu
150 ave been determined for the soybean pathogen Phytophthora sojae and the sudden oak death pathogen Phy
151 ora infestans and Phytophthora sojae EST and Phytophthora sojae BAC libraries and sent them to anothe
153 es and three homologous proteins specific to Phytophthora sojae effectors were also identified, which
154 tigators prepared Phytophthora infestans and Phytophthora sojae EST and Phytophthora sojae BAC librar
155 ict soybean plant resistance to the pathogen Phytophthora sojae from training sets including phenotyp
156 nce of soybean against the oomycete pathogen Phytophthora sojae is conferred by a series of Rps genes
157 f soybean tissues with the oomycete pathogen Phytophthora sojae or the bacterial pathogen Pseudomonas
158 o effectors from the oomycete plant pathogen Phytophthora sojae suppress RNA silencing in plants by i
159 Here we report that the soybean pathogen Phytophthora sojae uses an essential effector PsAvh262 t
160 ently found that the oomycete plant pathogen Phytophthora sojae uses nuclear localization signals (NL
161 Moreover, if the wall glucan elicitor from Phytophthora sojae was present during lactofen treatment
163 ns (GIPs), that are secreted by the oomycete Phytophthora sojae, a pathogen of soybean, and that spec
165 rt here that in particular hybrid strains of Phytophthora sojae, an oomycete pathogen of soybean, hig
166 irulent Pseudomonas syringae pv glycinea and Phytophthora sojae, but some of the mutants developed si
167 Soybean mosaic virus, Pseudomonas syringae, Phytophthora sojae, Phakopsora pachyrhizi, and Heteroder
168 sequences of three oomycete plant pathogens, Phytophthora sojae, Phytophthora ramorum, and Hyaloperon
169 soybean defense in response to infection by Phytophthora sojae, the second most destructive pathogen
172 zation of the Arabidopsis nonhost resistance Phytophthora sojae-susceptible gene locus, PSS1 In this
181 ed to other oomycete plant pathogens such as Phytophthora species and are ubiquitous in their geograp
182 are lacking in the genome sequences of three Phytophthora species and one downy mildew were identifie
185 We close with the hypothesis that these Phytophthora species evolved sympatrically from one ance
187 en P. infestans, but also of several related Phytophthora species including P. mirabilis, P. ipomoeae
188 of effectors identified in plant pathogenic Phytophthora species possess N-terminal motifs (RXLR-dEE
190 al providers that promote plant infection by Phytophthora species, advancing our understanding of bio
192 oding PsXEG1 and PsXLP1 is conserved in many Phytophthora species, and the P. parasitica orthologs Pp
193 ecognition of elicitin proteins from several Phytophthora species, including four diverse elicitins f
194 mparison to the predicted proteomes of three Phytophthora species, suggesting a broad representation
195 ison with genomes of related, hemibiotrophic Phytophthora species, the Hpa genome exhibits dramatic r
200 olonization of rhododendron leaf discs by 12 Phytophthora species/isolates was significantly enhanced
203 ; however, in only two cases, both involving Phytophthora spp., did genes at corresponding positions
206 secreted cell death-inducing effectors from Phytophthora that are expressed during the necrotrophic
208 d implications in environmental transport of Phytophthora zoospores in natural soils as well as in co
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