ライフサイエンスコーパス: elicitor

1 veral pathogen-associated molecules (general elicitors).

2 served after treatment with each the abiotic elicitor.

3 es, respectively, in response to wall glucan elicitor.

4 e clavulanic acid (Clav), is the most common elicitor.

5 es of H. calycinum after the addition of the elicitor.

6 calcium signalling in response to cryptogein elicitor.

7 nzofuran-3-one) as a major response to yeast elicitor.

8 and cell death responses to cell wall glucan elicitor.

9 zae pv. oryzae strains producing the AvrXa21 elicitor.

10 -OH-C10:0] representing the strongest immune elicitor.

11 the biosynthetic pathways switched on by the elicitor.

12 d in OcXII RNAi plants subjected to a fungal elicitor.

13 revention measures offered varied across the elicitors.

14 f prenylated stilbenoids upon treatment with elicitors.

15 e exogenous application of chemical inducers/elicitors.

16 oids, respectively, in response to microbial elicitors.

17 ng silent gene clusters using small molecule elicitors.

18 dants, which can be improved in plants using elicitors.

19 hich its expression was induced by microbial elicitors.

20 arkably little about the diversity of immune elicitors.

21 bon-based defence production and response to elicitors.

22 edlings were observed between MeJA and other elicitors.

23 patterns seen in the few well-characterized elicitors.

24 the response to other non-bacterial defense elicitors.

25 enous peptide elicitors and pathogen-derived elicitors.

26 rk that decreases gut permeability to immune elicitors.

27 al movement responses to bacteria and biotic elicitors.

28 nd facilitates the identification of defense elicitors.

29 of the response to the application of these elicitors.

30 lence, respectively, identified candidate OG elicitors.

31 onas oryzae pv. oryzae) and several chemical elicitors.

32 activated when plant NLRs recognize non-self elicitors.

33 roven their potential as plant immune-system elicitors.

34 t-insect interactions by triggering salivary elicitors.

35 e structurally distinct from natural defense elicitors.

36 ugh the manipulation of growth conditions by elicitors.

37 e structurally distinct from natural defense elicitors.

38 The P. sojae cell wall glucan elicitor, a potent elicitor of 5-deoxyisoflavonoids, tri

39 Most studies indicate that microbial elicitors activate the PO cascade, which results in proc

40 ration of tomato roots or leaves with MBI600 elicitors activated JA/ET signaling at the expense of SA

41 ellin and elongation factor EF-Tu (and their elicitor-active epitopes flg22 and elf18), respectively.

42 P1 RECEPTOR1 (PEPR1) and PEPR2 recognize the elicitor-active Pep epitopes conserved in Arabidopsis EL

43 (Arabidopsis thaliana), the receptor for the elicitor-active peptide epitope of bacterial flagellin,

44 remain unknown, the unpredictable nature of elicitor activity between plant species supports the exi

45 Vu-In(DeltaV); +ICDINGVCVDV-) retaining full elicitor activity was found to accumulate in VBC OS.

46 o investigate the phylogenic distribution of elicitor activity, we tested representatives from three

47 trypsin cleavage site rapidly lost OS-based elicitor activity.

48 i [corrected] plants treated with the fungal elicitor alamethicin, showing that they are also formed

49 etic pathways that are inducible by a fungal elicitor, alamethicin.

50 Moreover, the application of the yeast elicitor also enhanced grape stilbene content.

51 The application of the tested elicitor also influenced the chemical composition of bas

52 that may function as a receptor for the egg elicitor and other genes implicated in early plant defen

53 to fractions DP4-DP12, which were tested for elicitor and priming activities in rice cells.

54 ) receptors to recognize and parse microbial elicitors and drive intracellular signaling to limit or

55 xpression of AtLYK3 is strongly repressed by elicitors and fungal infection and is induced by the hor

56 Many strains produce elicitors and induce resistance in plants through coloni

57 ore oral secretions and fatty acid conjugate elicitors and is accompanied by a rapid transcriptional

58 mers may be similarly biologically active as elicitors and may help to reinforce the perception of da

59 that is typical of other endogenous peptide elicitors and pathogen-derived elicitors.

60 tion proposes a new approach for identifying elicitors and pathogenic factors.

61 reactive oxygen species (ROS) in response to elicitors and pathogens.

62 s, and responded to a wide range of pathogen elicitors and phytohormones.

63 Proteomic analysis of ECB salivary elicitors and plant receptors/signaling mechanisms invol

64 ulates the expression of genes responding to elicitors and plays an important role in pathogen defenc

65 dase activity in the presence of a number of elicitors and retains structural and functional integrit

66 stomatal movement only in response to biotic elicitors and support a model in which TARK1 regulates s

67 wild and cultivated hosts of CPB by chemical elicitors and their symbiotic bacteria.

68 scorch is caused by fungal pathogen-derived elicitors and toxins.

69 and allows a comparison of symptom patterns, elicitors and treatment habits between referral centres

70 Occurrence, elicitors and treatment of severe allergic reactions are

71 the oxidative burst in response to a fungal elicitor, and cause enhanced susceptibility to a broad r

72 re strongly affected by concentration of the elicitor, and time and intervals of its application.

73 e overcome by salient environmental response elicitors, and extends this notion by showing that D1 re

74 Elicitor application constitutes an interesting field of

75 lity of lettuce caused by different chemical elicitors: arachidonic acid (AA), jasmonic acid (JA), an

76 Synthetic elicitors are drug-like compounds that are structurally

77 Synthetic elicitors are drug-like compounds that induce plant immu

78 in planta PR gene expression and release of elicitors are the result of ectopic expression in xylem

79 usters, but also reveal that the majority of elicitors are themselves antibiotics, most in common cli

80 Therefore, such an elicitor as ChL can enhance the accumulation of valuable

81 s); however, precisely defined receptors and elicitors associated with herbivore recognition remain e

82 The effect of elicitors associated with host defence on betacyanin acc

83 All elicitors at medium and high concentrations reduced the

84 tudy, we used representative danger signals (elicitors) belonging to the classes of the damage- and p

85 ld be induced by application of the chemical elicitor beta-amino butyric acid, the non-pathogenic bac

86 In rice (Oryza sativa), the chitin elicitor binding protein (CEBiP) recognizes chitin oligo

87 e LysM-containing protein, CEBiP (for chitin elicitor-binding protein), was shown to be involved in c

88 athway gene transcripts in response to yeast elicitor, but not MJ, and differential induction by the

89 Sucrose, identified as the most effective elicitor by principal component analysis, induced a sign

90 f Eschscholzia californica react to a fungal elicitor by the overproduction of antimicrobial benzophe

91 y to insects may involve early perception of elicitors by cell surface-localized PRRs, leading to sub

92 Cda1 to 3) or released from the cell wall as elicitors by human chitinases, thus making the fungus le

93 We then validated selected candidate elicitors by showing that they induce Arabidopsis thalia

94 we partially purified a novel proteinaceous elicitor called sclerotinia culture filtrate elicitor1 (

95 (PTI), which is triggered by recognition of elicitors called microbe-associated molecular patterns (

96 mmunity (PTI) is triggered by recognition of elicitors called microbe-associated molecular patterns (

97 potential microbial pathogens by recognizing elicitors called PAMPs.

98 refore, we hypothesized that novel bacterial elicitors can be identified through these opposing force

99 sistance and non-host responses or following elicitor challenges.

100 shown to be induced by the fungal cell wall elicitor chitin.

101 al and guard cells in response to the fungal elicitor chitin.

102 ayed defects in immune priming by the fungal elicitor, chitin.

103 families examined responded to at least one elicitor class with significant increases in E and JA pr

104 tested representatives from three different elicitor classes on the time course of defense-related p

105 Some of the elicitor concentrations used also caused an increase in

106 In 13 patients (10.5%), no elicitor could be identified.

107 Therefore, treatment with elicitors could be a useful tool for improving the healt

108 bility is that immune priming with microbial elicitors could stimulate immune protection against subs

109 The fungal elicitor cryptogein triggers a light-dependent hypersens

110 s syringae pv. tomato DC3000 and the general elicitor cryptogein-induced cell death.

111 sis thaliana, AtSERK3/BAK1 rapidly enters an elicitor-dependent complex with FLAGELLIN SENSING 2 (FLS

112 ferent elicitors produced concentration- and elicitor-dependent specific changes in the content of al

113 ave been identified as peptides, but peptide elicitors derived from the plant itself that activate de

114 mpose strong positive selective pressure for elicitor diversification to avoid host recognition.

115 nt model for studying the action of numerous elicitors, E and JA exist as highly conserved and readil

116 on by anthocyanins was stimulated by abiotic elicitors, except for JA-sample.

117 0muM), JA (250muM) and MET (10mM) before the elicitor exogenous treatment.

118 atory inhibition, sugar supplementation, and elicitor exposure revealed a remarkable degree of plasti

119 racellular H(2) O(2) dynamics in response to elicitor exposure reveals the late and prolonged impact

120 e activation with Arabidopsis upon bacterial elicitor flagellin perception.

121 Arabidopsis cells treated with the bacterial elicitor flagellin.

122 ct stomatal closure induced by the bacterial elicitor flg22.

123 Furthermore, the elicitor food (adjusted OR = 0.29; 95% CI, 0.21-0.41, P

124 PS A1 motif was included to act as an MHCII elicitor for a T-cell-dependent immune response with inc

125 es are specific and activated in plants when elicitors, frequently found in the herbivores' oral secr

126 f Harosoy 63 upon treatment with wall glucan elicitor from P. sojae and identified two homologous R2R

127 In rowan cell cultures treated with elicitor from the scab fungus, transient increases in th

128 ed by the perception of herbivore associated elicitors (HAE) that includes transient accumulations of

129 The hypersensitive response elicitor harpin (HrpN) of soft rot pathogen Erwinia chry

130 Some plant pathogen-derived elicitors have been identified as peptides, but peptide

131 Caeliferins are nonlepidopteran elicitors identified in insect herbivores.

132 The presence of an elicitor in S. sclerotiorum evoking MAMP-triggered immun

133 e hypothesis with the recognition of general elicitors in a single model.

134 The application of elicitors in bean seed during sprouting enhances their n

135 ioassay methods to determine the role of ECB elicitors in modulating defenses in both tomato and maiz

136 Cow's milk and hen's egg were prevalent elicitors in the first 2 years, hazelnut and cashew in p

137 IR-NB-ARC portion is sufficient to induce an elicitor-independent cell death.

138 induced by certain phytohormones and fungal elicitors, indicating the involvement of a complex trans

139 Aphid-derived elicitors induce expression of PHYTOALEXIN DEFICIENT3 (P

140 In contrast, both elicitors induced genes encoding enzymes for conversion

141 00 and flg22 (a bacterial flagellin peptide) elicitors induced, in a similar manner, biotic and abiot

142 fferential tissue-specific and infection- or elicitor-induced expression, but not always in parallel

143 Notably, ANPs are also required for both the elicitor-induced oxidative burst and the transduction of

144 oncentration and to the amplification of the elicitor-induced oxidative burst.

145 te the genetic and biochemical regulation of elicitor-induced p-coumaraldehyde accumulation in plants

146 Elicitor-induced plant volatiles can function as attract

147 Plant derived elicitors/inducers of resistance are natural compounds t

148 show that treatment with the bacterial flg22 elicitor induces CAMTA3 phosphorylation, which is accomp

149 Treatment with herbivore or jasmonate elicitors induces emission of (E)-alpha-bergamotene in w

150 ouble knockdown of CYP76M7 and -8 suppresses elicitor inducible phytocassane production, indicating a

151 uced by non-host flagellins and the oomycete elicitor INF1.

152 that the EcNHX1 antiporter functions in the elicitor-initiated expression of alkaloid biosynthetic g

153 the activation of defenses by converting an elicitor into an antagonist effector and identify an ami

154 tection in maize and that the functional Sm1 elicitor is required for this activity.

155 information on the nature of egg-associated elicitors is scarce.

156 The present study indicates that age, the elicitor itself and the presence of atopic diseases have

157 essing the mechanism of induction by the two elicitors led to the identification of a pathway-specifi

158 terns (DAMPs) was proposed to describe plant elicitors like oligogalacturonides (OGs), which can be d

159 terial pathogen-associated molecular pattern elicitor lipopolysaccharide activates a CNGC Ca(2+) curr

160 Elicitor-mediated folate enhancement also imparted reduc

161 BAK1 is required for GPA elicitor-mediated induction of reactive oxygen species a

162 ulated herbivory with the well-known defense elicitor methyl jasmonate (MeJA) to young leaves of Arab

163 e was to optimize the treatment doses of the elicitors: methyl jasmonate (MeJA), jasmonic acid (JA) a

164 present experiment, chitosan was used as an elicitor molecule to improve the phytochemical content o

165 luated the role of European corn borer (ECB) elicitors (molecules secreted by herbivores) that either

166 matched anaphylaxis cases triggered by other elicitors (non-VIA cases [n = 3,605]).

167 d inhibition of seedling growth by the flg22 elicitor occurred normally in the Y610F-directed mutant.

168 P. sojae cell wall glucan elicitor, a potent elicitor of 5-deoxyisoflavonoids, triggered a cell death

169 omyces ghanaensis identified amygdalin as an elicitor of a novel non-ribosomal peptide, which we term

170 agweed (Ambrosia artemisiifolia) is a strong elicitor of allergic airway inflammation with worldwide

171 most important allergen sources and a major elicitor of allergic asthma.

172 hylaxis Registry confirmed food as the major elicitor of anaphylaxis in children, specifically hen's

173 show here that the response to flagellin, an elicitor of basal resistance, is unaltered in srfr1-1.

174 lthough the amino acid glutamine is a potent elicitor of GLP-1 secretion, the responsible mechanism r

175 ight the role of prior beliefs as a critical elicitor of hallucinations.

176 PKCdeltaI is an important elicitor of inflammation and apoptosis in adipocytes.

177 of Gram-negative peptidoglycan, is a potent elicitor of innate immune responses in Drosophila.

178 Acute ozone is a model abiotic elicitor of oxidative stress and a useful tool for under

179 s chronically exposed to methamphetamine, an elicitor of paranoia in humans.

180 lg22 flagellin peptide, a well-characterized elicitor of plant basal immunity, did not induce closure

181 nase (Eix) of Trichoderma viride is a potent elicitor of plant defense responses in specific cultivar

182 outria sachalinensis, RS) extract is a known elicitor of plant defenses but its mode of action remain

183 treated with methyl jasmonate, a well-known elicitor of plant specialized metabolism.

184 ate (MeJA) treatment, which is considered an elicitor of secondary metabolites, and identified 388 ca

185 Fish is a frequent elicitor of severe IgE-mediated allergic reactions.

186 itively establishes TCT as the long-distance elicitor of systemic immune responses to intestinal bact

187 In the multivariate analysis, the elicitor of the reaction, age of the patient, mastocytos

188 osophila antibacterial response, is also the elicitor of this behavioral change.

189 ed that subtle reciprocal cues remain potent elicitors of altruism, whereas a fourth study with presc

190 Elicitors of anaphylactic reactions are any sources of p

191 mologous in structure and described as major elicitors of anaphylactic reactions to peanut (allergens

192 Fish is one of the most common elicitors of food-allergic reactions worldwide.

193 The elicitors of immune responses in the nematode Caenorhabd

194 Administration of LPS or CpG, known elicitors of innate immune defense, reduced the loads of

195 gh-dose drugs, were most often identified as elicitors of MDH, especially at the first DHR, followed

196 g triggered by cryptogein and flagellin, two elicitors of plant defense reactions.

197 primary contributions involved race-specific elicitors of plant defenses and bacterial pectic enzymes

198 adds a category of insect herbivore-produced elicitors of plant responses, providing further evidence

199 charge-heterogeneous pectic oligosaccharide elicitors of PR gene expression.

200 ot MJ, and differential induction by the two elicitors of sets of genes encoding transcription factor

201 ur data show that food products are frequent elicitors of severe allergic reactions in the general po

202 pproach ("HiTES") to discover small molecule elicitors of silent biosynthetic gene clusters.

203 antibiotics, RCM and clindamycin, are common elicitors of subsequent DHR in patients with MDH.

204 as treatment with heat, chemicals, or virus elicitors of UPR.

205 effect of the application of three different elicitors on both grape and wine phenolic content.

206 the effects of benzothiadiazole and chitosan elicitors on content of sterols in grapes and their leve

207 However, research about the effect of elicitors on grape amino acid content is scarce.

208 he effect of preharvest application of these elicitors on the composition and structure of the skin c

209 phytoalexin medicarpin in response to yeast elicitor or methyl jasmonate (MJ), accompanied by decrea

210 ither directly by perception of pest-derived elicitors or indirectly through resistance protein recog

211 pathogen secretory proteins are known to be elicitors or pathogenic factors,which play an important

212 mediated by the tobacco mosaic virus defense elicitor p50.

213 f active fragments from a general resistance elicitor (pathogen-associated molecular pattern) is nece

214 that a member of the maize (Zea mays) plant elicitor peptide (Pep) family, ZmPep3, regulates respons

215 gene, which encodes the precursor protein of elicitor peptide 1 (AtPep1).

216 s MPK3 and MPK6 in response to the flagellin elicitor peptide flg22.

217 active Pep epitopes conserved in Arabidopsis ELICITOR PEPTIDE PRECURSORs (PROPEPs).

218 Glutamate, ATP, Arabidopsis PLANT ELICITOR PEPTIDE, and glutathione disulfide (GSSG) treat

219 The Arabidopsis thaliana endogenous elicitor peptides (AtPeps) are released into the apoplas

220 work focuses on the Arabidopsis DAMPs plant elicitor peptides (Peps) and their receptors, PEPR1 and

221 Plant elicitor peptides (Peps) are conserved regulators of def

222 Endogenous plant elicitor peptides (Peps) can act to facilitate immune si

223 These immunogenic elicitor peptides are embedded in the flagellin polymer

224 ple plant receptors of fungal-derived chitin elicitors, phosphorylation of membrane-associated signal

225 Elicitors present in herbivore oral secretions are belie

226 The exposure to different elicitors produced concentration- and elicitor-dependent

227 ion and characterization of an extracellular elicitor protein, designated AsES, produced by an avirul

228 with these, receptor kinases such as chitin elicitor receptor kinase (HvCERK1) and protein kinases s

229 Rice receptor kinase CHITIN ELICITOR RECEPTOR KINASE 1 (CERK1) and alpha/beta-fold h

230 aling mediated by the chitin receptor CHITIN ELICITOR RECEPTOR KINASE 1 (CERK1).

231 NG2 (FLS2), EF-TU RECEPTOR (EFR), and CHITIN ELICITOR RECEPTOR KINASE1 (CERK1) recognize microbe-asso

232 ucing the formation of a complex with CHITIN ELICITOR RECEPTOR KINASE1 (CERK1).

233 ive putative LYKs; among them, AtLYK1/CHITIN ELICITOR RECEPTOR KINASE1 is required for response to ch

234 LysM-containing receptor-like kinase1/chitin elicitor receptor kinase1) was shown to be essential for

235 er, little is known about the specificity of elicitor recognition in plants.

236 metabolite analysis revealed its role as an elicitor recognition receptor that triggered downstream

237 this activity can lead to multiple rounds of elicitor recognition, providing a means of signal amplif

238 Interferon elicitors recruited the transcription factor IRF3 to the

239 otein in N. attenuata (NaHER1; for herbivore elicitor regulated) and show that it is an indispensable

240 of Nicotiana benthamiana promotes hydrolytic elicitor release and acts in immunity against pathogenic

241 Furthermore, silencing of the elicitor-releasing endoglucanase (PR-2) led to a loss of

242 anisms involved in recognizing different ECB elicitors remains to be determined.

243 transferase, linalool synthase, peroxidases, elicitor responsive proteins, linamarase, nerolidol lina

244 o synthetic promoters 4D and 2S2D harbouring elicitor-responsive cis-elements.

245 Many of the elicitor-responsive cis-sequences also drive reporter ge

246 significantly increases the number of known elicitor-responsive cis-sequences and demonstrates the s

247 with an internal transformation control, 25 elicitor-responsive cis-sequences from 10 different moti

248 ioinformatics and synthetic promoters, novel elicitor-responsive cis-sequences were discovered in pro

249 e and adjacent nucleotides are essential for elicitor-responsive gene expression in a parsley protopl

250 In both plants, an elicitor-responsive phospholipase A2 (PLA2) at the plasm

251 Strongly elicitor-responsive phosphorylation sites may reflect di

252 xpression of WsMYC2 in response to exogenous elicitors resulted in enhanced withanolides production.

253 n of a plant NB-LRR protein with its cognate elicitor results in an antiviral response that inhibits

254 The detection of microbial elicitors results in the up-regulation of defense-relate

255 A screen for putative IL-10 elicitors revealed that IL-2, IL-4, IL-27, IL-10, and ne

256 The data presented suggest that the elicitor's aggregation may control the Trichoderma-plant

257 ity assays are combined with high-throughput elicitor screening (HiTES) to access cryptic, bioactive

258 we report the combination of high-throughput elicitor screening (HiTES) with matrix-assisted laser de

259 r kinase CERK1, which is critical for chitin elicitor signaling and resistance to fungal pathogens, p

260 cretes the highly effective hydrophobin-like elicitor Sm1 that induces systemic disease resistance in

261 some similarities to responses to well-known elicitors such as chitooligomers and OGs.

262 ion, with different concentrations of biotic elicitors such as chitosan and jasmonic acid also signif

263 to increase their levels include the use of elicitors such as methyl jasmonate (MeJ) and benzothiadi

264 Hormonal elicitors, such as jasmonates, trigger a complex signali

265 r work demonstrates the feasibility of using elicitors, such as plant stress hormones, by priming and

266 of damage by perceiving herbivore-associated elicitors, such as the fatty acid-amino acid conjugates

267 ed the influence of treatment with different elicitors (sucrose, mannitol, NaCl, 1-aminocyclopropane-

268 omal lipopeptides such as the plant immunity elicitor surfactin or the highly fungitoxic iturins and

269 terize severe allergic reactions in terms of elicitors, symptoms, emergency treatment, and long-term

270 -regulation of Sm1, the Trichoderma-secreted elicitor that systemically activates the defense mechani

271 ning, we previously identified 114 synthetic elicitors that activate expression of the pathogen-respo

272 ning, we previously identified 114 synthetic elicitors that activate the expression of a pathogen-res

273 ghput screening system for synthetic defense elicitors that can be used to trigger defined subsets of

274 phytopathogens and identifying 56 candidate elicitors that have an excess of positively selected res

275 In response to a pathogen elicitor, the activity of NADKc, which is associated wit

276 thaliana) roots challenged with two immunity elicitors, the bacterial flagellin-derived flg22 and the

277 Upon recognition of pathogen-derived elicitors, these NB-LRR proteins are thought to initiate

278 allergists reveal a different rank order of elicitors, this study suggests that food-allergic adult

279 upon environmental stress may function as an elicitor to activate plant defense responses.

280 ttention has been paid to the application of elicitors to vineyard.

281 ne that had been exposed to bacterial immune elicitors, to live E. coli infections or to no challenge

282 m expression where the hydraulic failure and elicitor/toxin hypotheses are not necessarily mutually e

283 d to assess experimental wines obtained from elicitor-treated grapes.

284 lyses to discover prenyltransferase genes in elicitor-treated peanut hairy root cultures.

285 The biotic elicitor treatment could thus prove to be an important s

286 after pathogen-associated molecular pattern elicitor treatment, as well as enhanced resistance to bo

287 signaling platform formation in response to elicitor treatment.

288 phytoalexin, hyperxanthone E, in response to elicitor treatment.

289 iple mutants show that ANPs are required for elicitor-triggered defense responses and protection agai

290 dependent efflux of vacuolar protons and (2) elicitor-triggered overproduction of alkaloids.

291 s we challenged aphids with bacterial immune elicitors twenty-four hours prior to live bacterial path

292 s content was significantly increased by all elicitors used in this study; however, no increase was o

293 The most common elicitor was drugs (41.1%) followed by venom (27.4%) and

294 In short, both the elicitors were able to increase the shelf life of fruits

295 The most common elicitors were food products (32.2%), drugs (29.2%) and

296 y fatty acid from grasshoppers, was the only elicitor with demonstrable activity in Arabidopsis thali

297 revealed similar concentrations of the three elicitors with 80% of the potential inceptin-related pep

298 Symptom patterns differed by elicitor, with the skin being affected most often (84.1%

299 we found that, in addition to PA, the fungal elicitor xylanase activated PDK1, suggesting that PDK1 h

300 cell suspension cultures responding to yeast elicitor (YE) or methyl jasmonate (MeJA).