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To better understand the role of these compounds during the early steps of the alfalfa-Sinorhizobium meliloti symbiosis and the regulation of their production we have isolated nod gene inducers from alfalfa roots. All the compounds that we identified in this study as nod gene inducers in the root are flavonoids, indicating that other compounds with nod gene activator capacity may have little contribution, if any, to nod gene activation. Most of the intermediates of the flavonoid pathway were found in Medicago sativa roots and nodules, but only end products of the flavonoid pathway were identified in the root exudate. We have also studied flavonoid production in different parts of the root and found that it is developmentally regulated during root growth. Finally, we have shown that coumestrol and medicarpin, present in the exudates and previously described as phytoalexins, possess nod gene repressing activity, indicating that the in vivo nod gene inducing activity of the root exudate results from positive as well as negative controls of nod gene expression by the flavonoids.\u003C\u002Fjats:p>",{"EN":578},"Production of\u003Ci>Sinorhizobium meliloti nod\u003C\u002Fi>Gene Activator and Repressor Flavonoids from\u003Ci>Medicago sativa\u003C\u002Fi>Roots",{"VOID":580},"10.1094\u002Fmpmi.1998.11.8.784",[143],"https:\u002F\u002Fapsjournals.apsnet.org\u002Fdoi\u002F10.1094\u002FMPMI.1998.11.8.784",[584,593,602,611,622,631],{"id":585,"sortIndex":162,"researcher":24,"roles":586,"affiliations":587,"properties":588},"5fdb2b6e-bd11-4b5e-abcb-af9f5c9a10c0",[],[],{"openalex":589,"title":591},{"VOID":590},"A5057394694",{"EN":592},"Pierre Henri Clergeot",{"id":594,"sortIndex":209,"researcher":24,"roles":595,"affiliations":596,"properties":597},"b5c751fe-6e77-4916-92ca-7c2a5080127a",[],[],{"openalex":598,"title":600},{"VOID":599},"A5074695418",{"EN":601},"H.‐P. 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We used the model legume Medicago truncatula Gaert. (barrel medic) to elucidate host resistance to aphids and identified a single dominant gene which confers resistance to Acyrthosiphon kondoi Shinji (bluegreen aphid). To understand how this gene conditions resistance to bluegreen aphid, transcription profiling of 23 defense-related genes representing various signaling pathways was undertaken using a pair of near-isogenic lines that are susceptible or resistant to bluegreen aphid. All salicylic acid- and ethylene-responsive genes tested were induced by blue-green aphid in resistant and susceptible plants, although there were some differences in the magnitude and kinetics of the induction. In contrast, 10 of 13 genes associated with the octadecanoid pathway were induced exclusively in the resistant plants following bluegreen aphid infestation. These results are in contrast to plant-pathogen interactions where similar sets of defense genes typically are induced in compatible interactions, but to a lesser degree and later than in incompatible interactions. Treatment of susceptible plants with methyl jasmonate reduced bluegreen aphid infestation but not to the same levels as the resistant line. Together, these results strongly suggest that the octa-decanoid pathway is important for this naturally derived aphid resistance trait. \u003C\u002Fjats:p>",{"EN":922},"Involvement of the Octadecanoid Pathway in Bluegreen Aphid Resistance in \u003Ci>Medicago truncatula\u003C\u002Fi>",{"VOID":924},"17249425",{"VOID":926},"10.1094\u002Fmpmi-20-0082",[143],"https:\u002F\u002Fapsjournals.apsnet.org\u002Fdoi\u002F10.1094\u002FMPMI-20-0082",[930,952,963,974,991,1013],{"id":931,"sortIndex":148,"researcher":24,"roles":932,"affiliations":933,"properties":945},"352d4307-e3e7-420e-8e54-dee83747ec74",[],[934],{"id":935,"sortIndex":25,"affiliation":936,"properties":24},"2a3ca0f0-28db-4b0c-832b-045f59bb7403",{"id":937,"createTime":938,"updateTime":939,"relativeEntities":940,"slug":941,"properties":942,"entityType":61,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"547e306e-f2be-4480-a1cc-26a05ca43125","2024-09-27T23:28:38.140+00:00","2024-10-16T07:41:10.995+00:00",[],"The-UWA-Institute-of-Agriculture",{"title":943},{"EN":944},"The UWA Institute of Agriculture",{"openalex":946,"orcid":948,"title":950},{"VOID":947},"A5048970587",{"VOID":949},"https:\u002F\u002Forcid.org\u002F0000-0002-2777-7448",{"EN":951},"Karam B. 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L., 2000, J. Plant Growth Regul., 19, 195, 10.1007\u002Fs003440000026",{"doi":1272},"10.1007\u002Fs003440000026",{"id":24,"text":1274,"url":24,"identifiers":1275},"10.1111\u002Fj.1672-9609.2005.00002.x",{"doi":1274},{"id":24,"text":1277,"url":24,"identifiers":1278},"10.1104\u002Fpp.103.028324",{"doi":1277},{"id":1280,"createTime":1281,"updateTime":1281,"relativeEntities":1282,"slug":1283,"properties":1284,"entityType":140,"verifyStatus":1298,"verifyTime":1299,"verifyNote":1300,"syncStatus":23,"languages":1301,"translateLanguages":24,"viewCount":25,"primaryUrl":1302,"fullTextUrl":24,"authors":1303,"publicationType":282,"publisherRelationship":1342,"citationCount":1375,"citationInfo":1376,"publishDate":1378,"publishYear":1379,"citationAnalyzeStatus":23,"lastCitationAnalyze":24,"indexDatabases":24,"openAccess":24,"references":1380,"isForceReanalyzing":563},"b219d942-325f-48e4-87c2-8e210d195520","2024-09-27T23:28:19.818+00:00",[],"Ethylene-Signaling-Modulates-Herbivore-Induced-Defense-Responses-in-the-Model-Legume-i-Medicago-truncatula-i-",{"mag":1285,"keywords":1287,"openalex":1288,"abstract":1290,"title":1292,"pm":1294,"doi":1296},{"VOID":1286},"2061399295",{},{"VOID":1289},"W2061399295",{"EN":1291},"\u003Cjats:p> One or more effectors in the labial saliva (LS) of generalist Noctuid caterpillars activate plant signaling pathways to modulate jasmonate (JA)-dependent defense responses; however, the exact mechanisms involved have yet to be elucidated. A potential candidate in this phytohormone interplay is the ethylene (ET) signaling pathway. We compared the biochemical and molecular responses of the model legume Medicago truncatula and the ET-insensitive skl mutant to herbivory by fourth instar Spodoptera exigua (Hübner) caterpillars with intact or impaired LS secretions. Cellular oxidative stress increases rapidly after herbivory, as evidenced by changes in oxidized-to-reduced ascorbate (ASC) and glutathione (GSH) ratios. The caterpillar-specific increase in GSH ratios and the LS-specific increase in ASC ratios are alleviated in the skl mutant, indicating that ET signaling is required. Ten hours postherbivory, markers of the JA and JA\u002FET pathways are differentially expressed; MtVSP is induced and MtHEL is repressed in a caterpillar LS- and ET-independent manner. In contrast, expression of the classic marker of the systemic acquired resistance pathway, MtPR1, is caterpillar LS-dependent and requires ET signaling. Caterpillar LS further suppresses the induction of JA-related trypsin inhibitor activity in an ET-dependent manner. 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Interaction of a plant with a fungal pathogen is an encounter with hundreds of molecules. In contrast to this, a single molecule often decides between the disease and resistance. In the present article, we describe the defense responses triggered by AvrLm1, an avirulence gene from a hemibiotrophic ascomycete, Leptosphaeria maculans, responsible for an incompatible interaction with Brassica napus. Using multiple hormone quantification and expression analysis of defense-related genes, we investigated signaling events in Rlm1 plants infected with two sister isolates of L. maculans differentiated by the presence or absence of AvrLm1. Infection with the isolate carrying AvrLm1 increased the biosynthesis of salicylic acid (SA) and induced expression of the SA-associated genes ICS1, WRKY70, and PR-1, a feature characteristic of responses to biotrophic pathogens and resistance gene–mediated resistance. In addition to SA-signaling elements, we also observed the induction of ASC2a, HEL, and CHI genes associated with ethylene (ET) signaling. Pharmacological experiments confirmed the positive roles of SA and ET in mediating resistance to L. maculans. The unusual cooperation of SA and ET signaling might be a response to the hemibiotrophic nature of L. maculans. Our results also demonstrate the profound difference between the natural host B. napus and the model plant Arabidopsis in their response to L. maculans infection. \u003C\u002Fjats:p>",{"EN":1676},"Recognition of Avirulence Gene \u003Ci>AvrLm1\u003C\u002Fi> from Hemibiotrophic Ascomycete \u003Ci>Leptosphaeria maculans\u003C\u002Fi> Triggers Salicylic Acid and Ethylene Signaling in \u003Ci>Brassica 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Functional characterization of Mi-odr-1, Mi-odr-3, Mi-tax-2, and Mi-tax-4 via RNA interference revealed behavioral defects in M. incognita and perturbed attraction to host roots in Pluronic gel medium. Knockdown of Mi-odr-1, Mi-odr-3, Mi-tax-2, and Mi-tax-4 resulted in defective chemotaxis of M. incognita to various volatile compounds (alcohol, ketone, aromatic compound, ester, thiazole, pyrazine), nonvolatiles of plant origin (carbohydrate, phytohormone, organic acid, amino acid, phenolic), and host root exudates in an agar-Pluronic gel–based assay plate. In addition, ascaroside-mediated signaling was impeded by downregulation of chemosensory genes. 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To further confirm that the miR844-mediated defense response was due to the decrease in CDS3 mRNA level, the disease response of a CDS3 loss-of-function mutant was analyzed upon pathogen challenge. Increased susceptibility of both cds3 mutant and 35S::miR844 plants to pathogens confirmed that miR844 affected the defense response by downregulating CDS3 mRNA. The expression of miR844 was decreased, and the CDS3 transcript level increased upon pathogen challenge. 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