ライフサイエンスコーパス: mildew

1 rasitica (P.p.) races Emoy2 and Emwa1 (downy mildew).

2 stresses (watermelon mosaic virus and downy mildew).

3 asal and RPW8-mediated resistance to powdery mildew.

4 confer broad-spectrum resistance to powdery mildew.

5 in penetration success by the barley powdery mildew.

6 to NHR in Arabidopsis against wheat powdery mildew.

7 rimary foliar diseases, Botrytis and powdery mildew.

8 ild type in response to infection by powdery mildew.

9 siphe cichoracearum, causal agent of powdery mildew.

10 he corresponding avirulence genes in powdery mildew.

11 ng and extent of outbreaks of cucurbit downy mildew.

12 h levels of quantitative resistance to downy mildew.

13 s upon inoculation with a nonadapted powdery mildew.

14 interactions between Arabidopsis and powdery mildew.

15 R1, and fully enhanced resistance to powdery mildew.

16 re-invasive immune responses against powdery mildews.

17 exhibit biological activity against powdery mildews.

18 putative chromatin regulator Enhanced Downy Mildew 2 (EDM2) as a cellular antisilencing factor and r

19 We identified EDM2 (enhanced downy mildew 2) in a genetic screen for RPP7 suppressors.

20 a forward genetic screen with barley powdery mildew and consequently characterized it by pathogen ass

21 uding enhanced disease resistance to powdery mildew and enhanced ethylene-induced senescence; thus, t

22 silenced plants were more resistant to downy mildew and Soybean mosaic virus compared with vector con

23 Powdery mildews and other obligate biotrophic pathogens are high

24 eronospora parasitica (causal agent of downy mildew), and encodes an NBS-LRR type R protein with a pu

25 es, those living in houses with pets, pests, mildew, and water damage, those whose parents had asthma

26 Powdery mildews are phytopathogens whose growth and reproduction

27 The perception of downy mildew avirulence (Arabidopsis thaliana Recognized [ATR]

28 By contrast, the nonhost barley powdery mildew Blumeria graminis f. sp. hordei (Bgh) typically f

29 penetration resistance to the barley powdery mildew Blumeria graminis f. sp. hordei.

30 nfection studies with the nonadapted powdery mildew Blumeria graminis f. sp. hordei.

31 mportant race-specific resistance to powdery mildew (Blumeria graminis).

32 Barley powdery mildew, Blumeria graminis f. sp. hordei (Bgh), is an obl

33 enetration resistance against barley powdery mildew, Blumeria graminis f. sp. hordei, and we isolated

34 resent the genome analysis of barley powdery mildew, Blumeria graminis f.sp. hordei (Blumeria), as we

35 ex, presence of water damage or visible mold/mildew, born in winter, breastfeeding, and being exposed

36 ight function in basal resistance to powdery mildew by influencing microtubule organization.

37 dozyma flocculosa for the control of powdery mildew by two Canadian research programs is presented.

38 escribe two barley (Hordeum vulgare) powdery mildew candidate secreted effector proteins, CSEP0105 an

39 des Dm3 which determines resistance to downy mildew caused by the oomycete Bremia lactucae carrying t

40 ly elusive 5' sequence of the barley powdery mildew chitin synthase gene, BgChs2, which includes a my

41 not associated with the collapse of powdery mildew colonies.

42 O2, MLO6 and MLO12 not only restrict powdery mildew colonization, but also affect interactions with a

43 ivation, and reduced susceptibility to downy mildew disease (Hyaloperonospora arabidopsidis).

44 associated with defense responses to powdery mildew disease but function in different signaling pathw

45 ar leafy vegetable, are susceptible to downy mildew disease caused by Bremia lactucae.

46 ment provided primed defence against powdery mildew disease caused by the biotrophic fungal pathogen,

47 of Arabidopsis confers resistance to powdery mildew disease caused by the fungus Erysiphe cichoracear

48 ide a novel strategy for controlling powdery mildew disease in crops.

49 lex inheritance of resistance to the powdery mildew disease in the model plant Arabidopsis thaliana,

50 study suggests that the Arabidopsis powdery mildew disease will be a suitable model system in which

51 f. sp. hordei (Bgh), casual agent of powdery mildew disease.

52 sp hordei (Bgh), the causal agent of powdery mildew disease.

53 p. hordei (Bgh), the causal agent of powdery mildew disease.

54 f ABA signaling affects the outcome of downy mildew disease.

55 p. hordei (Bgh), the causal agent of powdery mildew disease.

56 Powdery mildew diseases are economically important diseases, cau

57 and accession Ms-0 was resistant, to powdery mildew diseases caused by Erysiphe cruciferarum UEA1 and

58 hogens Golovinomyces spp. that cause powdery mildew diseases on multiple plant species.

59 vinomyces spp., the causal agents of powdery mildew diseases on multiple plant species.

60 al species of the oomycetes that cause downy mildew diseases.

61 model system in which to investigate powdery mildew diseases.

62 ntal changes in our understanding of powdery mildews (Erysiphales).

63 rabidopsis thaliana is a host to the powdery mildew Erysiphe cichoracearum and nonhost to Blumeria gr

64 Attack by the host powdery mildew Erysiphe cichoracearum usually results in success

65 o the nonadapted pea (Pisum sativum) powdery mildew Erysiphe pisi However, PLC2-silenced plants displ

66 phenotype, conferring resistance to powdery mildew (Erysiphe cichoracearum) and enhancing ethylene-i

67 enhanced sensitivity to the pathogen powdery mildew (Erysiphe cruciferarum) and fails to induce SA bi

68 itional inappropriate biotrophs, pea powdery mildew (Erysiphe pisi) and potato late blight (Phytophth

69 ose inoculated with a virulent, host powdery mildew, Erysiphe cichoracearum.

70 Barley powdery mildew, Erysiphe graminis f.sp. hordei, is an obligate b

71 I 1.14-2.04, and work environments with mold/mildew exposures [environments with possible exposures t

72 enic tomato variety resistant to the powdery mildew fungal pathogen using the CRISPR/Cas9 technology.

73 Powdery mildew fungal pathogens penetrate the plant cell wall an

74 naling in nonhost resistance against powdery mildew fungi and put PLDdelta forward as the main isofor

75 ial and quality, the three rusts and powdery mildew fungi have historically caused major crop losses

76 ich spores of adapted and nonadapted powdery mildew fungi showed reduced germination.

77 herwise virulent obligate biotrophic powdery mildew fungi such as Golovinomyces orontii.

78 s for viruses and for rust, smut and powdery mildew fungi that infect 473 plant species naturalized t

79 Penetration resistance to powdery mildew fungi, conferred by localized cell wall appositio

80 n of PEN3-GFP after inoculation with powdery mildew fungi.

81 otype against adapted and nonadapted powdery mildew fungi.

82 of defense components in response to powdery mildew fungi.

83 vasive immunity against a nonadapted powdery mildew fungus (Blumeria graminis f.

84 ed resistance against the biotrophic powdery mildew fungus (Blumeria graminis f.sp. hordei), while MO

85 a wide spectrum of resistance to the powdery mildew fungus (PM), Erysiphe necator (Schw.) Burr., but

86 on formation due to infection by the powdery mildew fungus Blumeria f. sp. tritici.

87 NHR in Arabidopsis against the wheat powdery mildew fungus Blumeria graminis f. sp. tritici (Bgt).

88 Arabidopsis thaliana) and the barley powdery mildew fungus Blumeria graminis f.sp. hordei (Bgh) was i

89 nteraction of barley with the barley powdery mildew fungus Blumeria graminis f.sp. hordei.

90 o enhance resistance of wheat to the powdery mildew fungus Blumeria graminis f.sp. tritici, a novel e

91 conferring resistance to the oomycete downy mildew fungus Bremia lactucae map to the major resistanc

92 responses to a host-adapted virulent powdery mildew fungus but were impaired in preinvasive defenses

93 Our findings imply that the mildew fungus has a repertoire of AVR genes, which may f

94 ntify AVR(a10) and AVR(k1) of barley powdery mildew fungus, Blumeria graminis f sp hordei (Bgh), and

95 bidopsis thaliana against the barley powdery mildew fungus, Blumeria graminis f. sp. hordei.

96 two MAP kinase genes from the barley powdery mildew fungus, Blumeria graminis.

97 tance against another nonadapted pea powdery mildew fungus, Erysiphe pisi.

98 also mediates defense to an adapted powdery mildew fungus, thus regulating a durable type of defense

99 ating Arabidopsis infection with the powdery mildew fungus, we find that the Arabidopsis atypical E2F

100 all known isolates of the widespread powdery mildew fungus.

101 at are homologous with gEgh16 of the powdery mildew fungus.

102 fector-induced HR in response to the powdery mildew fungus.

103 fector-induced HR in response to the powdery mildew fungus.

104 t cell inaccessible for the invading powdery mildew fungus.

105 ed 'step down' PCR to attain the full length mildew genomic clones.

106 netration resistance to the virulent powdery mildew Golovinomyces cichoracearum due to enhanced callo

107 h post inoculation with the virulent powdery mildew Golovinomyces cichoracearum.

108 enhanced resistance to infection by powdery mildew (Golovinomyces cichoracearum).

109 We evaluated the effects of grape powdery mildew (GPM) as supplemental food, and habitat structura

110 The host-adapted powdery mildew had a reduced reproductive fitness on rop6(DN) pl

111 The resurgence of cucurbit downy mildew has dramatically influenced production of cucurbi

112 hronized with a higher expression of powdery mildew haustorial effectors, a sharp decline in the phot

113 he 3221 mutant exhibited resistance to downy mildew (Hyaloperonospora arabidopsidis) and green peach

114 ts deficient in resistance to barley powdery mildew identified PENETRATION3 (PEN3).

115 in R-gene-mediated resistance against downy mildew in Arabidopsis and their regulatory control by th

116 s SA-dependent basal defense against powdery mildew in Arabidopsis.

117 A recent outbreak of sorghum downy mildew in Texas has led to the discovery of both metalax

118 confers resistance to Bremia lactucae (downy mildew) in 1033 accessions of Lactuca serriola (prickly

119 ertion allele in DRP1E did not cause powdery mildew-induced lesions, suggesting that this phenotype i

120 protected wheat systemically against powdery mildew infection by affecting multiple steps in the life

121 rsensitive response (HR) to restrict powdery mildew infection via the salicylic acid-dependent signal

122 ransgenic lines during both types of powdery mildew infection, and neither the salicylic acid-depende

123 ) gene confer enhanced resistance to powdery mildew infection, enhanced senescence, and enhanced prog

124 illa formation in the epidermis upon powdery mildew infection.

125 d in development and associated with powdery mildew infection.

126 made Arabidopsis hypersusceptible to powdery mildew infection.

127 which do not effectively block host powdery mildew infections.

128 ays played a role in blocking barley powdery mildew infections.

129 penetration by Bgh during the barley-powdery mildew interaction but is independent of gene-for-gene r

130 ude that edr1-mediated resistance to powdery mildew is mediated, in part, by enhanced ABA signaling.

131 ergent alleles of ATR1NdWsB from eight downy mildew isolates and demonstrate that the ATR1NdWsB allel

132 aize, sugarcane, pearl millet and rose downy mildew isolates.

133 Powdery mildews may already be responding to climate change, sug

134 e logistic regression to investigate whether mildew/musty odour and increased concentrations of Alter

135 Reporting of a mildew/musty odour was associated with increased risk of

136 Exposure to a mildew/musty odour, as a proxy for exposure to fungus, w

137 Powdery mildews, obligate biotrophic fungal parasites on a wide

138 f Hyaloperonospora arabidopsidis (Hpa, downy mildew of Arabidopsis) contains at least 134 candidate R

139 Powdery mildew of barley, caused by Erysiphe graminis f. sp. hor

140 errations and altered sensitivity to powdery mildews of rop6(DN) plants result from perturbations tha

141 been well demonstrated for rusts and powdery mildews of small grain crops.

142 l as from 5 related species that cause downy mildew on other hosts, the number of different bands det

143 92 in response to inoculation with the downy mildew oomycete pathogen Sclerospora graminicola.

144 iated enhanced disease resistance to powdery mildew or spontaneous lesions, indicating that these phe

145 te to pearl millet defense against the downy mildew pathogen by activating the expression of defense

146 d enhanced disease resistance to the powdery mildew pathogen Erysiphe cichoracearum and identified th

147 resistance (edr2) to the biotrophic powdery mildew pathogen Erysiphe cichoracearum.

148 not support the normal growth of the powdery mildew pathogen Erysiphe cichoracearum.

149 The biotrophic downy mildew pathogen Hyaloperonospora arabidopsidis encodes 1

150 ired for successful infection with the downy mildew pathogen Hyaloperonospora arabidopsidis.

151 We study the oomycete downy mildew pathogen of Arabidopsis, Hyaloperonospora arabido

152 Hyaloperonospora arabidopsidis, a downy mildew pathogen of the model plant Arabidopsis, has been

153 Interactions between barley and the powdery mildew pathogen, Blumeria graminis f. sp. hordei, (Bgh)

154 do not support normal growth of the powdery mildew pathogen, Erysiphe cichoracearum.

155 resistance to a wild isolate of the powdery mildew pathogen, Erysiphe cichoracearum.

156 a (gl1), which is susceptible to the powdery mildew pathogen, were performed.

157 olumbia-0 (Col-0) virulent isolates of downy mildew pathogen.

158 pe plants inoculated with a virulent powdery mildew pathogen.

159 ce, resulting in reduced growth of a powdery mildew pathogen.

160 Blumeria graminis f. sp hordei, the powdery mildew pathogenic on barley (Hordeum vulgare).

161 comparison with the analysis of two powdery mildews pathogenic on dicotyledonous plants.

162 solving among phylogenetically related downy mildew pathogens dramatically point out the need for sim

163 confers broad-spectrum resistance to powdery mildew pathogens.

164 ing to incursions of new or reemerging downy mildew pathogens.

165 ntrol resistance to a broad range of powdery mildew pathogens.

166 fers AtSgt1b-independent resistance to downy mildew (Peronospora parasitica) isolate Hiks1.

167 wth and reproduction of the virulent powdery mildew (PM) Golovinomyces orontii on Arabidopsis (Arabid

168 exhibited altered expression at the powdery mildew (PM) infection site, with subsets of these playin

169 Tissue colonization by grape powdery mildew (PM) pathogen Erysiphe necator (Schw.) Burr trigg

170 Wheat powdery mildew (PM), caused by Blumeria graminis f.

171 ntified and mapped three independent powdery mildew quantitative disease resistance loci, which act a

172 e MAP kinases AtMPK6 and AtMPK3, the powdery mildew R proteins RPW8.1 and RPW8.2, EDS1 and PR protein

173 inoculations with non-host and host powdery mildews relative to non-inoculated control plants accoun

174 tivar C.I. 16151 (harboring the Mla6 powdery mildew resistance allele) and its fast neutron-derived B

175 S5, NPR1 and SGT1b for activation of powdery mildew resistance and HR.

176 tive regulation on HR cell death and powdery mildew resistance by limiting the transcriptional amplif

177 barley (Hordeum vulgare), the Mla13 powdery mildew resistance gene confers Rar1-dependent, AvrMla13-

178 -mediated resistance to TMV and some powdery mildew resistance genes in barley provide the first exam

179 In cereals, several mildew resistance genes occur as large allelic series; f

180 r to that conferred by "late-acting" powdery mildew resistance genes of wheat and barley.

181 that RPW8.2 from A. lyrata conferred powdery mildew resistance in A. thaliana, suggesting that RPW8.2

182 om Ethiopian landraces and nowadays controls mildew resistance in the majority of cultivated European

183 Barley (Hordeum vulgare L.) Mildew resistance locus a (Mla) confers allele-specific

184 * Barley (Hordeum vulgare L.) Mildew resistance locus a (Mla) confers allele-specific

185 l resistance and effector-triggered, powdery mildew resistance locus A12-mediated resistance against

186 abidopsis thaliana), NORTIA, a member of the MILDEW RESISTANCE LOCUS O (MLO) family of proteins, play

187 enes encoding protein homologs of the barley mildew resistance locus o (MLO) protein biochemically sh

188 netically related Arabidopsis thaliana genes MILDEW RESISTANCE LOCUS O 4 (MLO4) and MLO11, encoding h

189 of the Mla locus can dictate similar powdery mildew resistance phenotypes yet still require distinct

190 bidopsis thaliana) RLPs, including the downy mildew resistance protein RPP27.

191 Here, we report that the broad-spectrum mildew resistance protein RPW8.2 from Arabidopsis thalia

192 t region from the orthologous barley powdery mildew resistance protein, MLA10, but is similar to the

193 essions Wa-1, Kas-1, Stw-0 and Su-0, powdery mildew resistance was encoded by a semi-dominant allele.

194 oria is key for RPW8-mediated broad-spectrum mildew resistance.

195 screened for spontaneous mutations in downy mildew resistance.

196 eral R genes that confer bacterial and downy mildew resistance.

197 barley cv Morex that spans the Mla (powdery mildew) resistance locus.

198 nations of host resistance genes, designated Mildew-resistance locus (Ml), and cognate pathogen aviru

199 eage, and are homologs of the barley powdery mildew-resistance protein MLA10.

200 Mapping studies revealed that powdery mildew resistances in Kas-1, Wa-1, Te-0, Su-0 and Stw-0

201 indicated that four loci, designated powdery mildew resistant 1-4 (pmr1-4), are defined by this colle

202 Surprisingly, here we found that powdery mildew resistant 4 (pmr4), a mutant lacking pathogen-ind

203 ection phenotypes of two independent powdery mildew-resistant triple mutant lines with a range of mic

204 genic Arabidopsis lines that express POWDERY MILDEW RESISTANT4 (PMR4), which encodes a stress-induced

205 We also show here that DOWNY MILDEW RESISTANT6 (AtDMR6), the Arabidopsis homologous e

206 root rot (Rps1, Rps2, and Rps3), and powdery mildew (rmd).

207 Resistance to powdery mildew (Rmd-c), Phytophthora stem and root rot (Rps2), a

208 endered Arabidopsis resistant to the powdery mildew species Erysiphe cichoracearum and Erysiphe oront

209 Powdery mildew species Oidium neolycopersici (On) can cause seri

210 o E. orontii, a very closely related powdery mildew, suggesting that a very specific resistance mecha

211 10) define a core set conserved in all three mildews, suggesting that most effectors represent specie

212 susceptible to the fungal pathogen, powdery mildew, than wild type as measured by conidiophore produ

213 pairs studied in detail using DNA from downy mildews that attack maize (P. maydis & P. philippinensis

214 ant surfaces among distantly related powdery mildews that is based on KCS6-derived wax components.

215 For plant pathogenic fungi, such as powdery mildews, that survive only on a limited number of host p

216 gen but rather a biocontrol agent of powdery mildews; this relationship makes it unique for the study

217 inoculated with the non-host barley powdery mildew to those inoculated with a virulent, host powdery

218 ommon parasite Peronospora parasitica (downy mildew) to study the evolution of resistance specificity

219 h and enhanced disease resistance to powdery mildew via the SA-dependent signaling pathway.

220 ell death and enhanced resistance to powdery mildew via the salicylic acid-dependent signaling pathwa

221 rolling for age, ethnicity, medication, mold/mildew, water leaks, and season of sampling.

222 of three Phytophthora species and one downy mildew were identified and could serve as useful phyloge