{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,29]],"date-time":"2026-04-29T16:29:40Z","timestamp":1777480180390,"version":"3.51.4"},"reference-count":173,"publisher":"Springer Science and Business Media LLC","issue":"9","license":[{"start":{"date-parts":[[2021,2,27]],"date-time":"2021-02-27T00:00:00Z","timestamp":1614384000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.springer.com\/tdm"},{"start":{"date-parts":[[2021,2,27]],"date-time":"2021-02-27T00:00:00Z","timestamp":1614384000000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/www.springer.com\/tdm"}],"funder":[{"DOI":"10.13039\/501100001871","name":"Funda\u00e7\u00e3o para a Ci\u00eancia e a Tecnologia","doi-asserted-by":"publisher","award":["PD\/BD\/131030\/2017"],"award-info":[{"award-number":["PD\/BD\/131030\/2017"]}],"id":[{"id":"10.13039\/501100001871","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100001871","name":"Funda\u00e7\u00e3o para a Ci\u00eancia e a Tecnologia","doi-asserted-by":"publisher","award":["UIDB\/04046\/2020, UIDP\/04046\/2020, PTDC\/BIA-BQM\/28539\/2017"],"award-info":[{"award-number":["UIDB\/04046\/2020, UIDP\/04046\/2020, PTDC\/BIA-BQM\/28539\/2017"]}],"id":[{"id":"10.13039\/501100001871","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100001871","name":"Funda\u00e7\u00e3o para a Ci\u00eancia e a Tecnologia","doi-asserted-by":"publisher","award":["IF\/00819\/2015"],"award-info":[{"award-number":["IF\/00819\/2015"]}],"id":[{"id":"10.13039\/501100001871","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":["Cell. Mol. Life Sci."],"published-print":{"date-parts":[[2021,5]]},"DOI":"10.1007\/s00018-021-03791-0","type":"journal-article","created":{"date-parts":[[2021,2,27]],"date-time":"2021-02-27T14:03:01Z","timestamp":1614434581000},"page":"4399-4415","update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":55,"title":["Speaking the language of lipids: the cross-talk between plants and pathogens in defence and disease"],"prefix":"10.1007","volume":"78","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-8364-655X","authenticated-orcid":false,"given":"Ana Rita","family":"Cavaco","sequence":"first","affiliation":[]},{"ORCID":"https:\/\/orcid.org\/0000-0002-3495-2195","authenticated-orcid":false,"given":"Ana Rita","family":"Matos","sequence":"additional","affiliation":[]},{"ORCID":"https:\/\/orcid.org\/0000-0001-8156-7700","authenticated-orcid":false,"given":"Andreia","family":"Figueiredo","sequence":"additional","affiliation":[]}],"member":"297","published-online":{"date-parts":[[2021,2,27]]},"reference":[{"key":"3791_CR1","doi-asserted-by":"publisher","DOI":"10.3389\/fpls.2014.00624","author":"P-Y Huang","year":"2014","unstructured":"Huang P-Y, Zimmerli L (2014) Enhancing crop innate immunity: new promising trends. Front Plant Sci. https:\/\/doi.org\/10.3389\/fpls.2014.00624","journal-title":"Front Plant Sci"},{"key":"3791_CR2","doi-asserted-by":"publisher","first-page":"487","DOI":"10.1146\/annurev-arplant-050213-040012","volume":"66","author":"H Cui","year":"2015","unstructured":"Cui H, Tsuda K, Parker JE (2015) Effector-triggered immunity: from pathogen perception to robust defense. Annu Rev Plant Biol 66:487\u2013511. https:\/\/doi.org\/10.1146\/annurev-arplant-050213-040012","journal-title":"Annu Rev Plant Biol"},{"key":"3791_CR3","doi-asserted-by":"publisher","first-page":"520","DOI":"10.1016\/j.pbi.2013.06.011","volume":"16","author":"JW Walley","year":"2013","unstructured":"Walley JW, Kliebenstein DJ, Bostock RM, Dehesh K (2013) Fatty acids and early detection of pathogens. Curr Opin Plant Biol 16:520\u2013526. https:\/\/doi.org\/10.1016\/j.pbi.2013.06.011","journal-title":"Curr Opin Plant Biol"},{"key":"3791_CR4","doi-asserted-by":"publisher","DOI":"10.3390\/plants6040057","author":"B Bakan","year":"2017","unstructured":"Bakan B, Marion D (2017) Assembly of the cutin polyester: from cells to extracellular cell walls. Plants (Basel). https:\/\/doi.org\/10.3390\/plants6040057","journal-title":"Plants (Basel)"},{"key":"3791_CR5","doi-asserted-by":"publisher","first-page":"180","DOI":"10.1007\/BF00199748","volume":"191","author":"H Winter","year":"1993","unstructured":"Winter H, Robinson DG, Heldt HW (1993) Subcellular volumes and metabolite concentrations in barley leaves. Planta 191:180\u2013190","journal-title":"Planta"},{"key":"3791_CR6","doi-asserted-by":"publisher","first-page":"419","DOI":"10.1146\/annurev-phyto-080615-100204","volume":"54","author":"TY Toru\u00f1o","year":"2016","unstructured":"Toru\u00f1o TY, Stergiopoulos I, Coaker G (2016) Plant\u2013pathogen effectors: cellular probes interfering with plant defenses in spatial and temporal manners. Annu Rev Phytopathol 54:419\u2013441. https:\/\/doi.org\/10.1146\/annurev-phyto-080615-100204","journal-title":"Annu Rev Phytopathol"},{"key":"3791_CR7","doi-asserted-by":"publisher","first-page":"24","DOI":"10.1186\/1471-2229-13-24","volume":"13","author":"B Delaunois","year":"2013","unstructured":"Delaunois B, Colby T, Belloy N et al (2013) Large-scale proteomic analysis of the grapevine leaf apoplastic fluid reveals mainly stress-related proteins and cell wall modifying enzymes. BMC Plant Biol 13:24. https:\/\/doi.org\/10.1186\/1471-2229-13-24","journal-title":"BMC Plant Biol"},{"key":"3791_CR8","doi-asserted-by":"publisher","first-page":"22","DOI":"10.3390\/proteomes4030022","volume":"4","author":"L Guerra-Guimar\u00e3es","year":"2016","unstructured":"Guerra-Guimar\u00e3es L, Pinheiro C, Chaves I et al (2016) Protein dynamics in the plant extracellular space. Proteomes 4:22. https:\/\/doi.org\/10.3390\/proteomes4030022","journal-title":"Proteomes"},{"key":"3791_CR9","doi-asserted-by":"publisher","DOI":"10.3389\/fpls.2015.00478","author":"LL Guerra-Guimar\u00e3es","year":"2015","unstructured":"Guerra-Guimar\u00e3es LL, Tenente RER, Pinheiro CC et al (2015) Proteomic analysis of apoplastic fluid of Coffea arabica leaves highlights novel biomarkers for resistance against Hemileia vastatrix. Front Plant Sci. https:\/\/doi.org\/10.3389\/fpls.2015.00478","journal-title":"Front Plant Sci"},{"key":"3791_CR10","doi-asserted-by":"publisher","DOI":"10.3389\/fpls.2016.00323","author":"BB Misra","year":"2016","unstructured":"Misra BB (2016) The black-box of plant apoplast lipidomes. Front Plant Sci. https:\/\/doi.org\/10.3389\/fpls.2016.00323","journal-title":"Front Plant Sci"},{"key":"3791_CR11","doi-asserted-by":"publisher","first-page":"553","DOI":"10.1093\/jxb\/erm329","volume":"59","author":"M Regente","year":"2008","unstructured":"Regente M, Monz\u00f3n GC, de la Canal L (2008) Phospholipids are present in extracellular fluids of imbibing sunflower seeds and are modulated by hormonal treatments. J Exp Bot 59:553\u2013562. https:\/\/doi.org\/10.1093\/jxb\/erm329","journal-title":"J Exp Bot"},{"key":"3791_CR12","doi-asserted-by":"publisher","first-page":"2026","DOI":"10.1080\/19440049.2014.968810","volume":"31","author":"M Ludovici","year":"2014","unstructured":"Ludovici M, Ialongo C, Reverberi M et al (2014) Quantitative profiling of oxylipins through comprehensive LC-MS\/MS analysis of Fusarium verticillioides and maize kernels. Food Addit Contam Part A 31:2026\u20132033. https:\/\/doi.org\/10.1080\/19440049.2014.968810","journal-title":"Food Addit Contam Part A"},{"key":"3791_CR13","doi-asserted-by":"publisher","first-page":"1","DOI":"10.1038\/s41598-018-32559-z","volume":"8","author":"G Laureano","year":"2018","unstructured":"Laureano G, Figueiredo J, Cavaco AR et al (2018) The interplay between membrane lipids and phospholipase a family members in grapevine resistance against Plasmopara viticola. Sci Rep 8:1\u201315. https:\/\/doi.org\/10.1038\/s41598-018-32559-z","journal-title":"Sci Rep"},{"key":"3791_CR14","doi-asserted-by":"publisher","first-page":"1340","DOI":"10.1094\/PHYTO-12-13-0338-R","volume":"104","author":"V M\u00fcller","year":"2014","unstructured":"M\u00fcller V, Am\u00e9 MV, Carrari V et al (2014) Lipoxygenase activation in peanut seed cultivars resistant and susceptible to Aspergillus parasiticus colonization. Phytopathology 104:1340\u20131348","journal-title":"Phytopathology"},{"key":"3791_CR15","doi-asserted-by":"publisher","first-page":"1296","DOI":"10.1021\/acs.jafc.7b05273","volume":"66","author":"JH Suh","year":"2018","unstructured":"Suh JH, Niu YS, Wang Z et al (2018) Metabolic analysis reveals altered long-chain fatty acid metabolism in the host by huanglongbing disease. J Agric Food Chem 66:1296\u20131304. https:\/\/doi.org\/10.1021\/acs.jafc.7b05273","journal-title":"J Agric Food Chem"},{"key":"3791_CR16","doi-asserted-by":"publisher","DOI":"10.3389\/fpls.2017.01524","author":"G Chitarrini","year":"2017","unstructured":"Chitarrini G, Soini E, Riccadonna S et al (2017) Identification of biomarkers for defense response to Plasmopara viticola in a resistant grape variety. Front Plant Sci. https:\/\/doi.org\/10.3389\/fpls.2017.01524","journal-title":"Front Plant Sci"},{"key":"3791_CR17","doi-asserted-by":"publisher","first-page":"4064","DOI":"10.1021\/acs.jafc.8b06316","volume":"67","author":"L Righetti","year":"2019","unstructured":"Righetti L, Lucini L, Giorni P et al (2019) Lipids as key markers in maize response to fumonisin accumulation. J Agric Food Chem 67:4064\u20134070. https:\/\/doi.org\/10.1021\/acs.jafc.8b06316","journal-title":"J Agric Food Chem"},{"key":"3791_CR18","doi-asserted-by":"publisher","DOI":"10.3389\/fpls.2018.00360","author":"L Negrel","year":"2018","unstructured":"Negrel L, Halter D, Wiedemann-Merdinoglu S et al (2018) Identification of lipid markers of Plasmopara viticola infection in grapevine using a non-targeted metabolomic approach. Front Plant Sci. https:\/\/doi.org\/10.3389\/fpls.2018.00360","journal-title":"Front Plant Sci"},{"key":"3791_CR19","doi-asserted-by":"publisher","first-page":"260","DOI":"10.1016\/j.tplants.2007.04.003","volume":"12","author":"C Br\u00e9h\u00e9lin","year":"2007","unstructured":"Br\u00e9h\u00e9lin C, Kessler F, van Wijk KJ (2007) Plastoglobules: versatile lipoprotein particles in plastids. Trends Plant Sci 12:260\u2013266. https:\/\/doi.org\/10.1016\/j.tplants.2007.04.003","journal-title":"Trends Plant Sci"},{"key":"3791_CR20","doi-asserted-by":"publisher","first-page":"1","DOI":"10.1038\/ncomms8658","volume":"6","author":"NM Cecchini","year":"2015","unstructured":"Cecchini NM, Steffes K, Schl\u00e4ppi MR et al (2015) Arabidopsis AZI1 family proteins mediate signal mobilization for systemic defence priming. Nat Commun 6:1\u201312. https:\/\/doi.org\/10.1038\/ncomms8658","journal-title":"Nat Commun"},{"key":"3791_CR21","doi-asserted-by":"publisher","first-page":"48","DOI":"10.1016\/j.jprot.2016.10.012","volume":"152","author":"A Figueiredo","year":"2017","unstructured":"Figueiredo A, Martins J, Sebastiana M et al (2017) Specific adjustments in grapevine leaf proteome discriminating resistant and susceptible grapevine genotypes to Plasmopara viticola. J Proteom 152:48\u201357. https:\/\/doi.org\/10.1016\/j.jprot.2016.10.012","journal-title":"J Proteom"},{"key":"3791_CR22","doi-asserted-by":"publisher","first-page":"230","DOI":"10.1016\/j.plantsci.2019.05.007","volume":"285","author":"J Li","year":"2019","unstructured":"Li J, Yang J, Zhu B, Xie G (2019) Overexpressing OsFBN1 enhances plastoglobule formation, reduces grain-filling percent and jasmonate levels under heat stress in rice. Plant Sci 285:230\u2013238. https:\/\/doi.org\/10.1016\/j.plantsci.2019.05.007","journal-title":"Plant Sci"},{"key":"3791_CR23","doi-asserted-by":"publisher","first-page":"971","DOI":"10.1007\/s00425-016-2585-4","volume":"244","author":"TA Salminen","year":"2016","unstructured":"Salminen TA, Blomqvist K, Edqvist J (2016) Lipid transfer proteins: classification, nomenclature, structure, and function. Planta 244:971\u2013997. https:\/\/doi.org\/10.1007\/s00425-016-2585-4","journal-title":"Planta"},{"key":"3791_CR24","doi-asserted-by":"publisher","first-page":"13","DOI":"10.4161\/psb.6.1.14037","volume":"6","author":"J Canonne","year":"2011","unstructured":"Canonne J, Froidure-Nicolas S, Rivas S (2011) Phospholipases in action during plant defense signaling. Plant Signal Behav 6:13\u201318. https:\/\/doi.org\/10.4161\/psb.6.1.14037","journal-title":"Plant Signal Behav"},{"key":"3791_CR25","doi-asserted-by":"publisher","first-page":"348","DOI":"10.1016\/j.celrep.2014.03.032","volume":"7","author":"C Wang","year":"2014","unstructured":"Wang C, El-Shetehy M, Shine MB et al (2014) Free radicals mediate systemic acquired resistance. Cell Rep 7:348\u2013355. https:\/\/doi.org\/10.1016\/j.celrep.2014.03.032","journal-title":"Cell Rep"},{"key":"3791_CR26","doi-asserted-by":"publisher","first-page":"249","DOI":"10.1016\/B978-0-12-818606-0.00014-6","volume-title":"Oxidative stress","author":"E Niki","year":"2020","unstructured":"Niki E (2020) Chapter 14\u2014dual stressor effects of lipid oxidation and antioxidants. In: Sies H (ed) Oxidative stress. Academic Press, Cambridge, pp 249\u2013262"},{"key":"3791_CR27","doi-asserted-by":"publisher","first-page":"1263","DOI":"10.1094\/MPMI-06-13-0184-R","volume":"27","author":"SA Christensen","year":"2014","unstructured":"Christensen SA, Nemchenko A, Park Y-S et al (2014) The novel monocot-specific 9-lipoxygenase ZmLOX12 is required to mount an effective jasmonate-mediated defense against Fusarium verticillioides in maize. Mol Plant Microbe Interact 27:1263\u20131276. https:\/\/doi.org\/10.1094\/MPMI-06-13-0184-R","journal-title":"Mol Plant Microbe Interact"},{"key":"3791_CR28","doi-asserted-by":"publisher","first-page":"565","DOI":"10.3109\/10715762.2014.1000318","volume":"49","author":"G Griffiths","year":"2015","unstructured":"Griffiths G (2015) Biosynthesis and analysis of plant oxylipins. Free Radic Res 49:565\u2013582. https:\/\/doi.org\/10.3109\/10715762.2014.1000318","journal-title":"Free Radic Res"},{"key":"3791_CR29","doi-asserted-by":"publisher","DOI":"10.3389\/fgene.2018.00244","author":"D Botero","year":"2018","unstructured":"Botero D, Vald\u00e9s I, Rodr\u00edguez M-J et al (2018) A genome-scale metabolic reconstruction of Phytophthora infestans with the integration of transcriptional data reveals the key metabolic patterns involved in the interaction of its host. Front Genet. https:\/\/doi.org\/10.3389\/fgene.2018.00244","journal-title":"Front Genet"},{"key":"3791_CR30","doi-asserted-by":"publisher","first-page":"1514","DOI":"10.1093\/pcp\/pcz058","volume":"60","author":"TL Shimada","year":"2019","unstructured":"Shimada TL, Betsuyaku S, Inada N et al (2019) Enrichment of phosphatidylinositol 4,5-bisphosphate in the extra-invasive hyphal membrane promotes Colletotrichum infection of Arabidopsisthaliana. Plant Cell Physiol 60:1514\u20131524. https:\/\/doi.org\/10.1093\/pcp\/pcz058","journal-title":"Plant Cell Physiol"},{"key":"3791_CR31","doi-asserted-by":"publisher","first-page":"995","DOI":"10.1186\/s12864-017-4372-4","volume":"18","author":"S Iizasa","year":"2017","unstructured":"Iizasa S, Iizasa E, Watanabe K, Nagano Y (2017) Transcriptome analysis reveals key roles of AtLBR-2 in LPS-induced defense responses in plants. BMC Genom 18:995. https:\/\/doi.org\/10.1186\/s12864-017-4372-4","journal-title":"BMC Genom"},{"key":"3791_CR32","doi-asserted-by":"publisher","first-page":"1962","DOI":"10.1038\/s41467-018-04434-y","volume":"9","author":"M J\u00e4rv\u00e5","year":"2018","unstructured":"J\u00e4rv\u00e5 M, Lay FT, Phan TK et al (2018) X-ray structure of a carpet-like antimicrobial defensin\u2013phospholipid membrane disruption complex. Nat Commun 9:1962. https:\/\/doi.org\/10.1038\/s41467-018-04434-y","journal-title":"Nat Commun"},{"key":"3791_CR33","doi-asserted-by":"publisher","first-page":"e82485","DOI":"10.1371\/journal.pone.0082485","volume":"8","author":"US Sagaram","year":"2013","unstructured":"Sagaram US, El-Mounadi K, Buchko GW et al (2013) Structural and functional studies of a phosphatidic acid-binding antifungal plant defensin MtDef4: identification of an RGFRRR motif governing fungal cell entry. PLoS ONE 8:e82485. https:\/\/doi.org\/10.1371\/journal.pone.0082485","journal-title":"PLoS ONE"},{"key":"3791_CR34","doi-asserted-by":"publisher","first-page":"169","DOI":"10.1016\/S0378-1097(03)00590-1","volume":"226","author":"K Thevissen","year":"2003","unstructured":"Thevissen K, Fran\u00e7ois IEJA, Takemoto JY et al (2003) DmAMP1, an antifungal plant defensin from dahlia (Dahlia merckii), interacts with sphingolipids from Saccharomyces cerevisiae. FEMS Microbiol Lett 226:169\u2013173. https:\/\/doi.org\/10.1016\/S0378-1097(03)00590-1","journal-title":"FEMS Microbiol Lett"},{"key":"3791_CR35","doi-asserted-by":"publisher","first-page":"346","DOI":"10.1104\/pp.114.236737","volume":"165","author":"A Bl\u00fcmke","year":"2014","unstructured":"Bl\u00fcmke A, Falter C, Herrfurth C et al (2014) Secreted fungal effector lipase releases free fatty acids to inhibit innate immunity-related callose formation during wheat head infection. Plant Physiol 165:346\u2013358. https:\/\/doi.org\/10.1104\/pp.114.236737","journal-title":"Plant Physiol"},{"key":"3791_CR36","doi-asserted-by":"publisher","first-page":"20558","DOI":"10.1074\/jbc.M117.811398","volume":"292","author":"R Darwiche","year":"2017","unstructured":"Darwiche R, Atab OE, Baroni RM et al (2017) Plant pathogenesis\u2013related proteins of the cacao fungal pathogen Moniliophthora perniciosa differ in their lipid-binding specificities. J Biol Chem 292:20558\u201320569. https:\/\/doi.org\/10.1074\/jbc.M117.811398","journal-title":"J Biol Chem"},{"key":"3791_CR37","doi-asserted-by":"publisher","first-page":"210","DOI":"10.1111\/mpp.12391","volume":"18","author":"SC Lambie","year":"2017","unstructured":"Lambie SC, Kretschmer M, Croll D et al (2017) The putative phospholipase lip2 counteracts oxidative damage and influences the virulence of Ustilago maydis. Mol Plant Pathol 18:210\u2013221. https:\/\/doi.org\/10.1111\/mpp.12391","journal-title":"Mol Plant Pathol"},{"key":"3791_CR38","doi-asserted-by":"publisher","first-page":"2576","DOI":"10.1093\/pcp\/pcy177","volume":"59","author":"M Nakano","year":"2018","unstructured":"Nakano M, Mukaihara T (2018) Ralstonia solanacearum type III effector RipAL targets chloroplasts and induces jasmonic acid production to suppress salicylic acid-mediated defense responses in plants. Plant Cell Physiol 59:2576\u20132589. https:\/\/doi.org\/10.1093\/pcp\/pcy177","journal-title":"Plant Cell Physiol"},{"key":"3791_CR39","doi-asserted-by":"publisher","DOI":"10.3389\/fpls.2014.00017","author":"CM Rojas","year":"2014","unstructured":"Rojas CM, Senthil-Kumar M, Tzin V, Mysore K (2014) Regulation of primary plant metabolism during plant\u2013pathogen interactions and its contribution to plant defense. Front Plant Sci. https:\/\/doi.org\/10.3389\/fpls.2014.00017","journal-title":"Front Plant Sci"},{"key":"3791_CR40","doi-asserted-by":"publisher","DOI":"10.3389\/fpls.2018.01088","author":"C Ziv","year":"2018","unstructured":"Ziv C, Zhao Z, Gao YG, Xia Y (2018) Multifunctional roles of plant cuticle during plant\u2013pathogen interactions. Front Plant Sci. https:\/\/doi.org\/10.3389\/fpls.2018.01088","journal-title":"Front Plant Sci"},{"key":"3791_CR41","doi-asserted-by":"publisher","first-page":"551","DOI":"10.1016\/j.tplants.2015.05.009","volume":"20","author":"E Dom\u00ednguez","year":"2015","unstructured":"Dom\u00ednguez E, Heredia-Guerrero JA, Heredia A (2015) Plant cutin genesis: unanswered questions. Trends Plant Sci 20:551\u2013558. https:\/\/doi.org\/10.1016\/j.tplants.2015.05.009","journal-title":"Trends Plant Sci"},{"key":"3791_CR42","doi-asserted-by":"publisher","DOI":"10.1199\/tab.0161","author":"Y Li-Beisson","year":"2013","unstructured":"Li-Beisson Y, Shorrosh B, Beisson F et al (2013) Acyl-lipid metabolism. Arabidopsis Book. https:\/\/doi.org\/10.1199\/tab.0161","journal-title":"Arabidopsis Book"},{"key":"3791_CR43","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pone.0160631","author":"C Morineau","year":"2016","unstructured":"Morineau C, Gissot L, Bellec Y et al (2016) Dual Fatty acid elongase complex interactions in Arabidopsis. PLoS ONE. https:\/\/doi.org\/10.1371\/journal.pone.0160631","journal-title":"PLoS ONE"},{"key":"3791_CR44","doi-asserted-by":"publisher","first-page":"182","DOI":"10.1016\/s0163-7827(01)00023-6","volume":"41","author":"S Rawsthorne","year":"2002","unstructured":"Rawsthorne S (2002) Carbon flux and fatty acid synthesis in plants. Prog Lipid Res 41:182\u2013196. https:\/\/doi.org\/10.1016\/s0163-7827(01)00023-6","journal-title":"Prog Lipid Res"},{"key":"3791_CR45","doi-asserted-by":"publisher","first-page":"236","DOI":"10.1016\/j.tplants.2008.03.003","volume":"13","author":"M Pollard","year":"2008","unstructured":"Pollard M, Beisson F, Li Y, Ohlrogge JB (2008) Building lipid barriers: biosynthesis of cutin and suberin. Trends Plant Sci 13:236\u2013246. https:\/\/doi.org\/10.1016\/j.tplants.2008.03.003","journal-title":"Trends Plant Sci"},{"key":"3791_CR46","doi-asserted-by":"publisher","first-page":"5339","DOI":"10.1093\/jxb\/erx327","volume":"68","author":"W Arag\u00f3n","year":"2017","unstructured":"Arag\u00f3n W, Reina-Pinto JJ, Serrano M (2017) The intimate talk between plants and microorganisms at the leaf surface. J Exp Bot 68:5339\u20135350. https:\/\/doi.org\/10.1093\/jxb\/erx327","journal-title":"J Exp Bot"},{"key":"3791_CR47","doi-asserted-by":"publisher","first-page":"833","DOI":"10.1104\/pp.110.161646","volume":"154","author":"Y Xia","year":"2010","unstructured":"Xia Y, Yu K, Navarre D et al (2010) The glabra1 mutation affects cuticle formation and plant responses to microbes. Plant Physiol 154:833\u2013846. https:\/\/doi.org\/10.1104\/pp.110.161646","journal-title":"Plant Physiol"},{"key":"3791_CR48","doi-asserted-by":"publisher","first-page":"151","DOI":"10.1016\/j.chom.2009.01.001","volume":"5","author":"Y Xia","year":"2009","unstructured":"Xia Y, Gao Q-M, Yu K et al (2009) An intact cuticle in distal tissues is essential for the induction of systemic acquired resistance in plants. Cell Host Microbe 5:151\u2013165. https:\/\/doi.org\/10.1016\/j.chom.2009.01.001","journal-title":"Cell Host Microbe"},{"key":"3791_CR49","doi-asserted-by":"publisher","first-page":"1151","DOI":"10.1111\/j.1365-3059.2011.02467.x","volume":"60","author":"A Hansjakob","year":"2011","unstructured":"Hansjakob A, Riederer M, Hildebrandt U (2011) Wax matters: absence of very-long-chain aldehydes from the leaf cuticular wax of the glossy11 mutant of maize compromises the prepenetration processes of Blumeria graminis. Plant Pathol 60:1151\u20131161. https:\/\/doi.org\/10.1111\/j.1365-3059.2011.02467.x","journal-title":"Plant Pathol"},{"key":"3791_CR50","doi-asserted-by":"publisher","first-page":"4127","DOI":"10.1093\/jxb\/erw187","volume":"67","author":"A Kumar","year":"2016","unstructured":"Kumar A, Yogendra KN, Karre S et al (2016) WAX INDUCER1 (HvWIN1) transcription factor regulates free fatty acid biosynthetic genes to reinforce cuticle to resist Fusarium head blight in barley spikelets. J Exp Bot 67:4127\u20134139. https:\/\/doi.org\/10.1093\/jxb\/erw187","journal-title":"J Exp Bot"},{"key":"3791_CR51","doi-asserted-by":"publisher","first-page":"621","DOI":"10.1080\/10286020902942350","volume":"11","author":"T Arif","year":"2009","unstructured":"Arif T, Bhosale JD, Kumar N et al (2009) Natural products\u2013antifungal agents derived from plants. J Asian Nat Prod Res 11:621\u2013638. https:\/\/doi.org\/10.1080\/10286020902942350","journal-title":"J Asian Nat Prod Res"},{"key":"3791_CR52","doi-asserted-by":"publisher","first-page":"27","DOI":"10.1016\/j.phymed.2017.10.018","volume":"37","author":"SA Zacchino","year":"2017","unstructured":"Zacchino SA, Butassi E, Liberto MD et al (2017) Plant phenolics and terpenoids as adjuvants of antibacterial and antifungal drugs. Phytomedicine 37:27\u201348. https:\/\/doi.org\/10.1016\/j.phymed.2017.10.018","journal-title":"Phytomedicine"},{"key":"3791_CR53","first-page":"1329","volume":"1861","author":"LV Michaelson","year":"2016","unstructured":"Michaelson LV, Napier JA, Molino D, Faure JD (2016) Plant sphingolipids their importance in cellular organization and adaption. Biochim et Biophys Acta (BBA) Mol Cell Biol Lipids 1861:1329\u20131335","journal-title":"Biochim et Biophys Acta (BBA) Mol Cell Biol Lipids"},{"key":"3791_CR54","doi-asserted-by":"publisher","first-page":"2255","DOI":"10.1104\/pp.15.01126","volume":"169","author":"M Magnin-Robert","year":"2015","unstructured":"Magnin-Robert M, Bourse DL, Markham J et al (2015) Modifications of sphingolipid content affect tolerance to hemibiotrophic and necrotrophic pathogens by modulating plant defense responses in Arabidopsis. Plant Physiol 169:2255\u20132274. https:\/\/doi.org\/10.1104\/pp.15.01126","journal-title":"Plant Physiol"},{"key":"3791_CR55","doi-asserted-by":"publisher","DOI":"10.3389\/fpls.2012.00068","author":"R Berkey","year":"2012","unstructured":"Berkey R, Bendigeri D, Xiao S (2012) Sphingolipids and plant defense\/disease: the \u201cdeath\u201d connection and beyond. Front Plant Sci. https:\/\/doi.org\/10.3389\/fpls.2012.00068","journal-title":"Front Plant Sci"},{"key":"3791_CR56","doi-asserted-by":"publisher","first-page":"574","DOI":"10.1016\/j.bbrc.2011.06.028","volume":"410","author":"KP Alden","year":"2011","unstructured":"Alden KP, Dhondt-Cordelier S, McDonald KL et al (2011) Sphingolipid long chain base phosphates can regulate apoptotic-like programmed cell death in plants. Biochem Biophys Res Commun 410:574\u2013580. https:\/\/doi.org\/10.1016\/j.bbrc.2011.06.028","journal-title":"Biochem Biophys Res Commun"},{"key":"3791_CR57","doi-asserted-by":"publisher","first-page":"1086","DOI":"10.1111\/j.1469-8137.2012.04351.x","volume":"196","author":"S K\u00f6nig","year":"2012","unstructured":"K\u00f6nig S, Feussner K, Schwarz M et al (2012) Arabidopsis mutants of sphingolipid fatty acid \u03b1-hydroxylases accumulate ceramides and salicylates. New Phytol 196:1086\u20131097. https:\/\/doi.org\/10.1111\/j.1469-8137.2012.04351.x","journal-title":"New Phytol"},{"key":"3791_CR58","doi-asserted-by":"publisher","first-page":"1862","DOI":"10.1105\/tpc.107.057851","volume":"20","author":"M Chen","year":"2008","unstructured":"Chen M, Markham JE, Dietrich CR et al (2008) Sphingolipid long-chain base hydroxylation is important for growth and regulation of sphingolipid content and composition in Arabidopsis. Plant Cell 20:1862\u20131878. https:\/\/doi.org\/10.1105\/tpc.107.057851","journal-title":"Plant Cell"},{"key":"3791_CR59","doi-asserted-by":"publisher","first-page":"45","DOI":"10.1016\/j.plantsci.2018.05.021","volume":"279","author":"J Li","year":"2019","unstructured":"Li J, Wang X (2019) Phospholipase D and phosphatidic acid in plant immunity. Plant Sci 279:45\u201350. https:\/\/doi.org\/10.1016\/j.plantsci.2018.05.021","journal-title":"Plant Sci"},{"key":"3791_CR60","doi-asserted-by":"publisher","first-page":"899","DOI":"10.1046\/j.1365-313X.2003.01680.x","volume":"33","author":"E Babiychuk","year":"2003","unstructured":"Babiychuk E, M\u00fcller F, Eubel H et al (2003) Arabidopsis phosphatidylglycerophosphate synthase 1 is essential for chloroplast differentiation, but is dispensable for mitochondrial function. Plant J 33:899\u2013909. https:\/\/doi.org\/10.1046\/j.1365-313X.2003.01680.x","journal-title":"Plant J"},{"key":"3791_CR61","doi-asserted-by":"publisher","first-page":"6003","DOI":"10.1074\/jbc.M109.071928","volume":"285","author":"E Dubots","year":"2010","unstructured":"Dubots E, Audry M, Yamaryo Y et al (2010) Activation of the chloroplast monogalactosyldiacylglycerol synthase mgd1 by phosphatidic acid and phosphatidylglycerol. J Biol Chem 285:6003\u20136011. https:\/\/doi.org\/10.1074\/jbc.M109.071928","journal-title":"J Biol Chem"},{"key":"3791_CR62","doi-asserted-by":"publisher","first-page":"759","DOI":"10.1111\/j.1365-313X.2011.04536.x","volume":"66","author":"R Roston","year":"2011","unstructured":"Roston R, Gao J, Xu C, Benning C (2011) Arabidopsis chloroplast lipid transport protein TGD2 disrupts membranes and is part of a large complex. Plant J 66:759\u2013769. https:\/\/doi.org\/10.1111\/j.1365-313X.2011.04536.x","journal-title":"Plant J"},{"key":"3791_CR63","doi-asserted-by":"publisher","first-page":"1233","DOI":"10.1111\/j.1600-0854.2008.00742.x","volume":"9","author":"MG Roth","year":"2008","unstructured":"Roth MG (2008) Molecular mechanisms of PLD function in membrane traffic. Traffic 9:1233\u20131239. https:\/\/doi.org\/10.1111\/j.1600-0854.2008.00742.x","journal-title":"Traffic"},{"key":"3791_CR64","doi-asserted-by":"publisher","first-page":"2428","DOI":"10.1002\/1873-3468.13563","volume":"593","author":"MA Zhukovsky","year":"2019","unstructured":"Zhukovsky MA, Filograna A, Luini A et al (2019) Phosphatidic acid in membrane rearrangements. FEBS Lett 593:2428\u20132451. https:\/\/doi.org\/10.1002\/1873-3468.13563","journal-title":"FEBS Lett"},{"key":"3791_CR65","doi-asserted-by":"publisher","first-page":"515","DOI":"10.1016\/j.pbi.2006.07.011","volume":"9","author":"BOR Bargmann","year":"2006","unstructured":"Bargmann BOR, Munnik T (2006) The role of phospholipase D in plant stress responses. Curr Opin Plant Biol 9:515\u2013522. https:\/\/doi.org\/10.1016\/j.pbi.2006.07.011","journal-title":"Curr Opin Plant Biol"},{"key":"3791_CR66","doi-asserted-by":"publisher","first-page":"2357","DOI":"10.1105\/tpc.108.062992","volume":"21","author":"Y Zhang","year":"2009","unstructured":"Zhang Y, Zhu H, Zhang Q et al (2009) Phospholipase D\u03b11 and phosphatidic acid regulate nadph oxidase activity and production of reactive oxygen species in ABA-mediated stomatal closure in Arabidopsis. Plant Cell 21:2357\u20132377. https:\/\/doi.org\/10.1105\/tpc.108.062992","journal-title":"Plant Cell"},{"key":"3791_CR67","doi-asserted-by":"publisher","first-page":"15","DOI":"10.1016\/j.jplph.2015.06.007","volume":"184","author":"M Nakano","year":"2015","unstructured":"Nakano M, Yoshioka H, Ohnishi K et al (2015) Cell death-inducing stresses are required for defense activation in DS1-phosphatidic acid phosphatase-silenced Nicotiana benthamiana. J Plant Physiol 184:15\u201319. https:\/\/doi.org\/10.1016\/j.jplph.2015.06.007","journal-title":"J Plant Physiol"},{"key":"3791_CR68","doi-asserted-by":"publisher","first-page":"1029","DOI":"10.1111\/pce.12666","volume":"39","author":"Q Hou","year":"2016","unstructured":"Hou Q, Ufer G, Bartels D (2016) Lipid signalling in plant responses to abiotic stress. Plant Cell Environ 39:1029\u20131048. https:\/\/doi.org\/10.1111\/pce.12666","journal-title":"Plant Cell Environ"},{"key":"3791_CR69","doi-asserted-by":"publisher","first-page":"804","DOI":"10.1126\/science.1846707","volume":"251","author":"AV Smrcka","year":"1991","unstructured":"Smrcka AV, Hepler BKO, Sternweis PC (1991) Regulation of polyphosphoinositide-specific phospholipase C activity by purified Gq. Science 251:804\u2013807. https:\/\/doi.org\/10.1126\/science.1846707","journal-title":"Science"},{"key":"3791_CR70","doi-asserted-by":"publisher","first-page":"667","DOI":"10.1016\/j.biochi.2012.10.009","volume":"95","author":"A Grzelczyk","year":"2013","unstructured":"Grzelczyk A, Gendaszewska-Darmach E (2013) Novel bioactive glycerol-based lysophospholipids: new data\u2014new insight into their function. Biochimie 95:667\u2013679. https:\/\/doi.org\/10.1016\/j.biochi.2012.10.009","journal-title":"Biochimie"},{"key":"3791_CR71","doi-asserted-by":"publisher","first-page":"789","DOI":"10.1093\/pcp\/pcp023","volume":"50","author":"FC K\u00fcpper","year":"2009","unstructured":"K\u00fcpper FC, Gaquerel E, Cosse A et al (2009) Free fatty acids and methyl jasmonate trigger defense reactions in Laminaria digitata. Plant Cell Physiol 50:789\u2013800. https:\/\/doi.org\/10.1093\/pcp\/pcp023","journal-title":"Plant Cell Physiol"},{"key":"3791_CR72","doi-asserted-by":"publisher","DOI":"10.1111\/nph.16766","author":"C-W Yu","year":"2020","unstructured":"Yu C-W, Lin Y-T, Li H (2020) Increased ratio of galactolipid MGDG:DGDG induces jasmonic acid overproduction and changes chloroplast shape. New Phytol. https:\/\/doi.org\/10.1111\/nph.16766","journal-title":"New Phytol"},{"key":"3791_CR73","doi-asserted-by":"publisher","first-page":"1681","DOI":"10.1016\/j.celrep.2014.10.069","volume":"9","author":"Q Gao","year":"2014","unstructured":"Gao Q, Yu K, Xia Y et al (2014) Mono- and digalactosyldiacylglycerol lipids function nonredundantly to regulate systemic acquired resistance in plants. Cell Rep 9:1681\u20131691. https:\/\/doi.org\/10.1016\/j.celrep.2014.10.069","journal-title":"Cell Rep"},{"key":"3791_CR74","doi-asserted-by":"publisher","first-page":"491","DOI":"10.1016\/j.plaphy.2009.02.011","volume":"47","author":"AR Matos","year":"2009","unstructured":"Matos AR, Pham-Thi A-T (2009) Lipid deacylating enzymes in plants: old activities, new genes. Plant Physiol Biochem 47:491\u2013503. https:\/\/doi.org\/10.1016\/j.plaphy.2009.02.011","journal-title":"Plant Physiol Biochem"},{"key":"3791_CR75","doi-asserted-by":"publisher","first-page":"470","DOI":"10.1016\/j.bbabio.2013.09.007","volume":"1837","author":"L Boudi\u00e8re","year":"2014","unstructured":"Boudi\u00e8re L, Michaud M, Petroutsos D et al (2014) Glycerolipids in photosynthesis: composition, synthesis and trafficking. Biochim Biophys Acta (BBA) Bioenerg 1837:470\u2013480","journal-title":"Biochim Biophys Acta (BBA) Bioenerg"},{"key":"3791_CR76","doi-asserted-by":"publisher","first-page":"329","DOI":"10.1007\/s11103-013-0137-x","volume":"84","author":"DS Kim","year":"2014","unstructured":"Kim DS, Jeun Y, Hwang BK (2014) The pepper patatin-like phospholipase CaPLP1 functions in plant cell death and defense signaling. Plant Mol Biol 84:329\u2013344. https:\/\/doi.org\/10.1007\/s11103-013-0137-x","journal-title":"Plant Mol Biol"},{"key":"3791_CR77","doi-asserted-by":"publisher","first-page":"693","DOI":"10.1016\/j.tplants.2010.09.005","volume":"15","author":"GFE Scherer","year":"2010","unstructured":"Scherer GFE, Ryu SB, Wang X et al (2010) Patatin-related phospholipase a: nomenclature, subfamilies and functions in plants. Trends Plant Sci 15:693\u2013700. https:\/\/doi.org\/10.1016\/j.tplants.2010.09.005","journal-title":"Trends Plant Sci"},{"key":"3791_CR78","doi-asserted-by":"publisher","first-page":"48","DOI":"10.1016\/j.phytochem.2014.04.009","volume":"104","author":"SJ Wi","year":"2014","unstructured":"Wi SJ, Seo S, yeon, Cho K, et al (2014) lysophosphatidylcholine enhances susceptibility in signaling pathway against pathogen infection through biphasic production of reactive oxygen species and ethylene in tobacco plants. Phytochemistry 104:48\u201359. https:\/\/doi.org\/10.1016\/j.phytochem.2014.04.009","journal-title":"Phytochemistry"},{"key":"3791_CR79","doi-asserted-by":"publisher","first-page":"869","DOI":"10.1016\/j.bbalip.2009.04.006","volume":"1791","author":"SA Arisz","year":"2009","unstructured":"Arisz SA, Testerink C, Munnik T (2009) Plant PA signaling via diacylglycerol kinase. Biochim Biophys Acta (BBA) Mol Cell Biol Lipids 1791:869\u2013875","journal-title":"Biochim Biophys Acta (BBA) Mol Cell Biol Lipids"},{"key":"3791_CR80","doi-asserted-by":"publisher","first-page":"959","DOI":"10.1016\/j.jplph.2014.02.008","volume":"171","author":"G Gonorazky","year":"2014","unstructured":"Gonorazky G, Ramirez L, Abd-El-Haliem A et al (2014) The tomato phosphatidylinositol-phospholipase C2 (SlPLC2) is required for defense gene induction by the fungal elicitor xylanase. J Plant Physiol 171:959\u2013965. https:\/\/doi.org\/10.1016\/j.jplph.2014.02.008","journal-title":"J Plant Physiol"},{"key":"3791_CR81","doi-asserted-by":"publisher","first-page":"1721","DOI":"10.1093\/jxb\/eru540","volume":"66","author":"J Zhao","year":"2015","unstructured":"Zhao J (2015) Phospholipase D and phosphatidic acid in plant defence response: from protein\u2013protein and lipid\u2013protein interactions to hormone signalling. J Exp Bot 66:1721\u20131736. https:\/\/doi.org\/10.1093\/jxb\/eru540","journal-title":"J Exp Bot"},{"key":"3791_CR82","doi-asserted-by":"publisher","first-page":"1057","DOI":"10.1104\/pp.010928","volume":"128","author":"C Qin","year":"2002","unstructured":"Qin C, Wang X (2002) The Arabidopsis phospholipase D family. characterization of a calcium-independent and phosphatidylcholine-selective PLD\u03b61 with distinct regulatory domains. Plant Physiol 128:1057\u20131068. https:\/\/doi.org\/10.1104\/pp.010928","journal-title":"Plant Physiol"},{"key":"3791_CR83","doi-asserted-by":"publisher","first-page":"49685","DOI":"10.1074\/jbc.M209598200","volume":"277","author":"C Qin","year":"2002","unstructured":"Qin C, Wang C, Wang X (2002) Kinetic analysis of Arabidopsis phospholipase D\u03b4 substrate preference and mechanism of activation by Ca2+ and phosphatidylinositol 4,5-bisphosphate. J Biol Chem 277:49685\u201349690. https:\/\/doi.org\/10.1074\/jbc.M209598200","journal-title":"J Biol Chem"},{"key":"3791_CR84","doi-asserted-by":"publisher","first-page":"371","DOI":"10.1104\/pp.19.01292","volume":"183","author":"MA Schl\u00f6ffel","year":"2020","unstructured":"Schl\u00f6ffel MA, Salzer A, Wan W-L et al (2020) The BIR2\/BIR3-associated phospholipase D\u03b31 negatively regulates plant immunity. Plant Physiol 183:371\u2013384. https:\/\/doi.org\/10.1104\/pp.19.01292","journal-title":"Plant Physiol"},{"key":"3791_CR85","doi-asserted-by":"publisher","first-page":"260","DOI":"10.1016\/j.tplants.2012.02.010","volume":"17","author":"JS Thaler","year":"2012","unstructured":"Thaler JS, Humphrey PT, Whiteman NK (2012) Evolution of jasmonate and salicylate signal crosstalk. Trends Plant Sci 17:260\u2013270. https:\/\/doi.org\/10.1016\/j.tplants.2012.02.010","journal-title":"Trends Plant Sci"},{"key":"3791_CR86","doi-asserted-by":"publisher","DOI":"10.3389\/fpls.2015.00239","author":"Y Zhang","year":"2015","unstructured":"Zhang Y, Maximova SN, Guiltinan MJ (2015) Characterization of a stearoyl-acyl carrier protein desaturase gene family from chocolate tree. Theobroma cacao L Front Plant Sci. https:\/\/doi.org\/10.3389\/fpls.2015.00239","journal-title":"Theobroma cacao L Front Plant Sci"},{"key":"3791_CR87","doi-asserted-by":"publisher","first-page":"127","DOI":"10.1134\/S2079086420020024","volume":"10","author":"MA Berestovoy","year":"2020","unstructured":"Berestovoy MA, Pavlenko OS, Goldenkova-Pavlova IV (2020) Plant fatty acid desaturases: role in the life of plants and biotechnological potential. Biol Bull Rev 10:127\u2013139. https:\/\/doi.org\/10.1134\/S2079086420020024","journal-title":"Biol Bull Rev"},{"key":"3791_CR88","doi-asserted-by":"publisher","first-page":"257","DOI":"10.1007\/s11103-006-9086-y","volume":"63","author":"A Kachroo","year":"2006","unstructured":"Kachroo A, Shanklin J, Whittle E et al (2006) The Arabidopsis stearoyl-acyl carrier protein-desaturase family and the contribution of leaf isoforms to oleic acid synthesis. Plant Mol Biol 63:257\u2013271. https:\/\/doi.org\/10.1007\/s11103-006-9086-y","journal-title":"Plant Mol Biol"},{"key":"3791_CR89","doi-asserted-by":"publisher","DOI":"10.1038\/s41467-018-03310-z","author":"F Jing","year":"2018","unstructured":"Jing F, Zhao L, Yandeau-Nelson MD, Nikolau BJ (2018) Two distinct domains contribute to the substrate acyl chain length selectivity of plant acyl-ACP thioesterase. Nat Commun. https:\/\/doi.org\/10.1038\/s41467-018-03310-z","journal-title":"Nat Commun"},{"key":"3791_CR90","doi-asserted-by":"publisher","first-page":"12","DOI":"10.1006\/mben.2001.0204","volume":"4","author":"JJ Thelen","year":"2002","unstructured":"Thelen JJ, Ohlrogge JB (2002) Metabolic engineering of fatty acid biosynthesis in plants. Metab Eng 4:12\u201321. https:\/\/doi.org\/10.1006\/mben.2001.0204","journal-title":"Metab Eng"},{"key":"3791_CR91","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pone.0149917","author":"C-J Dong","year":"2016","unstructured":"Dong C-J, Cao N, Zhang Z-G, Shang Q-M (2016) Characterization of the fatty acid desaturase genes in cucumber: structure, phylogeny, and expression patterns. PLoS ONE. https:\/\/doi.org\/10.1371\/journal.pone.0149917","journal-title":"PLoS ONE"},{"key":"3791_CR92","doi-asserted-by":"publisher","first-page":"e0189759","DOI":"10.1371\/journal.pone.0189759","volume":"12","author":"X Chi","year":"2017","unstructured":"Chi X, Zhang Z, Chen N et al (2017) Isolation and functional analysis of fatty acid desaturase genes from peanut (Arachis hypogaea L.). PLoS ONE 12:e0189759. https:\/\/doi.org\/10.1371\/journal.pone.0189759","journal-title":"PLoS ONE"},{"key":"3791_CR93","doi-asserted-by":"publisher","DOI":"10.3389\/fpls.2017.01789","author":"AA Dar","year":"2017","unstructured":"Dar AA, Choudhury AR, Kancharla PK, Arumugam N (2017) The FAD2 gene in plants: occurrence, regulation, and role. Front Plant Sci. https:\/\/doi.org\/10.3389\/fpls.2017.01789","journal-title":"Front Plant Sci"},{"key":"3791_CR94","doi-asserted-by":"publisher","DOI":"10.3389\/fpls.2020.00390","author":"M He","year":"2020","unstructured":"He M, Qin C-X, Wang X, Ding N-Z (2020) Plant unsaturated fatty acids: biosynthesis and regulation. Front Plant Sci. https:\/\/doi.org\/10.3389\/fpls.2020.00390","journal-title":"Front Plant Sci"},{"key":"3791_CR95","doi-asserted-by":"publisher","first-page":"4237","DOI":"10.1104\/pp.104.052951","volume":"136","author":"I Heilmann","year":"2004","unstructured":"Heilmann I, Mekhedov S, King B et al (2004) Identification of the Arabidopsis palmitoyl-monogalactosyldiacylglycerol \u03947-desaturase gene fad5, and effects of plastidial retargeting of Arabidopsis desaturases on the fad5 mutant phenotype. Plant Physiol 136:4237\u20134245. https:\/\/doi.org\/10.1104\/pp.104.052951","journal-title":"Plant Physiol"},{"key":"3791_CR96","doi-asserted-by":"publisher","first-page":"1025","DOI":"10.1093\/pcp\/pcz017","volume":"60","author":"\u00c1 Soria-Garc\u00eda","year":"2019","unstructured":"Soria-Garc\u00eda \u00c1, Rubio MC, Lagunas B et al (2019) Tissue distribution and specific contribution of Arabidopsis FAD7 and FAD8 plastid desaturases to the JA- and ABA-mediated cold stress or defense responses. Plant Cell Physiol 60:1025\u20131040. https:\/\/doi.org\/10.1093\/pcp\/pcz017","journal-title":"Plant Cell Physiol"},{"key":"3791_CR97","doi-asserted-by":"publisher","first-page":"3209","DOI":"10.1021\/acs.jafc.8b05857","volume":"67","author":"J-U An","year":"2019","unstructured":"An J-U, Lee I-G, Ko Y-J, Oh D-K (2019) Microbial synthesis of linoleate 9 S-lipoxygenase derived plant C18 oxylipins from C18 polyunsaturated fatty acids. J Agric Food Chem 67:3209\u20133219. https:\/\/doi.org\/10.1021\/acs.jafc.8b05857","journal-title":"J Agric Food Chem"},{"key":"3791_CR98","doi-asserted-by":"publisher","first-page":"105","DOI":"10.1104\/pp.113.230185","volume":"164","author":"TL Shimada","year":"2014","unstructured":"Shimada TL, Takano Y, Shimada T et al (2014) Leaf oil body functions as a subcellular factory for the production of a phytoalexin in Arabidopsis. Plant Physiol 164:105\u2013118. https:\/\/doi.org\/10.1104\/pp.113.230185","journal-title":"Plant Physiol"},{"key":"3791_CR99","doi-asserted-by":"publisher","first-page":"2127","DOI":"10.1016\/j.phytochem.2008.04.023","volume":"69","author":"K Kishimoto","year":"2008","unstructured":"Kishimoto K, Matsui K, Ozawa R, Takabayashi J (2008) Direct fungicidal activities of C6-aldehydes are important constituents for defense responses in Arabidopsis against Botrytis cinerea. Phytochemistry 69:2127\u20132132. https:\/\/doi.org\/10.1016\/j.phytochem.2008.04.023","journal-title":"Phytochemistry"},{"key":"3791_CR100","doi-asserted-by":"publisher","first-page":"1351","DOI":"10.1007\/s00425-012-1705-z","volume":"236","author":"E Kombrink","year":"2012","unstructured":"Kombrink E (2012) Chemical and genetic exploration of jasmonate biosynthesis and signaling paths. Planta 236:1351\u20131366. https:\/\/doi.org\/10.1007\/s00425-012-1705-z","journal-title":"Planta"},{"key":"3791_CR101","doi-asserted-by":"publisher","first-page":"171","DOI":"10.1038\/nchembio.2540","volume":"14","author":"A Chini","year":"2018","unstructured":"Chini A, Monte I, Zamarre\u00f1o AM et al (2018) An OPR3-independent pathway uses 4,5-didehydrojasmonate for jasmonate synthesis. Nat Chem Biol 14:171\u2013178. https:\/\/doi.org\/10.1038\/nchembio.2540","journal-title":"Nat Chem Biol"},{"key":"3791_CR102","doi-asserted-by":"publisher","first-page":"2479","DOI":"10.3390\/ijms20102479","volume":"20","author":"J Ruan","year":"2019","unstructured":"Ruan J, Zhou Y, Zhou M et al (2019) Jasmonic acid signaling pathway in plants. Int J Mol Sci 20:2479. https:\/\/doi.org\/10.3390\/ijms20102479","journal-title":"Int J Mol Sci"},{"key":"3791_CR103","doi-asserted-by":"publisher","first-page":"120","DOI":"10.1016\/j.jplph.2015.12.008","volume":"191","author":"K Yoshitomi","year":"2016","unstructured":"Yoshitomi K, Taniguchi S, Tanaka K et al (2016) Rice terpene synthase 24 (OsTPS24) encodes a jasmonate-responsive monoterpene synthase that produces an antibacterial \u03b3-terpinene against rice pathogen. J Plant Physiol 191:120\u2013126. https:\/\/doi.org\/10.1016\/j.jplph.2015.12.008","journal-title":"J Plant Physiol"},{"key":"3791_CR104","doi-asserted-by":"publisher","first-page":"388","DOI":"10.1111\/nph.14376","volume":"214","author":"Y He","year":"2017","unstructured":"He Y, Zhang H, Sun Z et al (2017) Jasmonic acid-mediated defense suppresses brassinosteroid-mediated susceptibility to Rice black streaked dwarf virus infection in rice. New Phytol 214:388\u2013399. https:\/\/doi.org\/10.1111\/nph.14376","journal-title":"New Phytol"},{"key":"3791_CR105","doi-asserted-by":"publisher","first-page":"602","DOI":"10.1094\/PHYTO-05-17-0172-R","volume":"108","author":"Q Wang","year":"2017","unstructured":"Wang Q, Shao B, Shaikh FI et al (2017) Wheat resistances to Fusarium root rot and head blight are both associated with deoxynivalenol- and jasmonate-related gene expression. Phytopathology 108:602\u2013616","journal-title":"Phytopathology"},{"key":"3791_CR106","doi-asserted-by":"publisher","first-page":"1","DOI":"10.1016\/j.jplph.2016.10.006","volume":"208","author":"V Herbel","year":"2017","unstructured":"Herbel V, Sieber-Frank J, Wink M (2017) The antimicrobial peptide snakin-2 is upregulated in the defense response of tomatoes (Solanum lycopersicum) as part of the jasmonate-dependent signaling pathway. J Plant Physiol 208:1\u20136. https:\/\/doi.org\/10.1016\/j.jplph.2016.10.006","journal-title":"J Plant Physiol"},{"key":"3791_CR107","doi-asserted-by":"crossref","unstructured":"Ayala A, Mu\u00f1oz MF, Arg\u00fcelles S (2014) Lipid peroxidation: production, metabolism, and signaling mechanisms of malondialdehyde and 4-hydroxy-2-nonenal. In: Oxidative medicine and cellular longevity. https:\/\/www.hindawi.com\/journals\/omcl\/2014\/360438\/. Accessed 13 May 2020","DOI":"10.1155\/2014\/360438"},{"key":"3791_CR108","doi-asserted-by":"publisher","first-page":"65","DOI":"10.1016\/j.phytochem.2014.01.020","volume":"101","author":"AK Nilsson","year":"2014","unstructured":"Nilsson AK, Johansson ON, Fahlberg P et al (2014) Formation of oxidized phosphatidylinositol and 12-oxo-phytodienoic acid containing acylated phosphatidylglycerol during the hypersensitive response in Arabidopsis. Phytochemistry 101:65\u201375. https:\/\/doi.org\/10.1016\/j.phytochem.2014.01.020","journal-title":"Phytochemistry"},{"key":"3791_CR109","doi-asserted-by":"publisher","first-page":"31528","DOI":"10.1074\/jbc.M604820200","volume":"281","author":"MX Andersson","year":"2006","unstructured":"Andersson MX, Hamberg M, Kourtchenko O et al (2006) Oxylipin profiling of the hypersensitive response in Arabidopsis thaliana formation of a novel oxo-phytodienoic acid-containing galactolipid, arabidopside e. J Biol Chem 281:31528\u201331537. https:\/\/doi.org\/10.1074\/jbc.M604820200","journal-title":"J Biol Chem"},{"key":"3791_CR110","doi-asserted-by":"publisher","first-page":"185","DOI":"10.1146\/annurev.phyto.42.040803.140421","volume":"42","author":"WE Durrant","year":"2004","unstructured":"Durrant WE, Dong X (2004) Systemic acquired resistance. Annu Rev Phytopathol 42:185\u2013209. https:\/\/doi.org\/10.1146\/annurev.phyto.42.040803.140421","journal-title":"Annu Rev Phytopathol"},{"key":"3791_CR111","doi-asserted-by":"publisher","first-page":"5587","DOI":"10.1093\/jxb\/ery319","volume":"69","author":"AJ Schmitt","year":"2018","unstructured":"Schmitt AJ, Sathoff AE, Holl C et al (2018) The major nectar protein of Brassica rapa is a non-specific lipid transfer protein, BrLTP2.1, with strong antifungal activity. J Exp Bot 69:5587\u20135597. https:\/\/doi.org\/10.1093\/jxb\/ery319","journal-title":"J Exp Bot"},{"key":"3791_CR112","doi-asserted-by":"publisher","first-page":"64","DOI":"10.1016\/j.plaphy.2015.02.008","volume":"89","author":"H Safi","year":"2015","unstructured":"Safi H, Saibi W, Alaoui MM et al (2015) A wheat lipid transfer protein (TdLTP4) promotes tolerance to abiotic and biotic stress in Arabidopsis thaliana. Plant Physiol Biochem 89:64\u201375. https:\/\/doi.org\/10.1016\/j.plaphy.2015.02.008","journal-title":"Plant Physiol Biochem"},{"key":"3791_CR113","doi-asserted-by":"publisher","first-page":"e98150","DOI":"10.1371\/journal.pone.0098150","volume":"9","author":"A Kiba","year":"2014","unstructured":"Kiba A, Galis I, Hojo Y et al (2014) SEC14 Phospholipid transfer protein is involved in lipid signaling-mediated plant immune responses in Nicotiana benthamiana. PLoS ONE 9:e98150. https:\/\/doi.org\/10.1371\/journal.pone.0098150","journal-title":"PLoS ONE"},{"key":"3791_CR114","doi-asserted-by":"publisher","first-page":"1017","DOI":"10.1016\/j.jplph.2012.04.002","volume":"169","author":"A Kiba","year":"2012","unstructured":"Kiba A, Nakano M, Vincent-Pope P et al (2012) A novel Sec14 phospholipid transfer protein from Nicotiana benthamiana is up-regulated in response to Ralstonia solanacearum infection, pathogen associated molecular patterns and effector molecules and involved in plant immunity. J Plant Physiol 169:1017\u20131022. https:\/\/doi.org\/10.1016\/j.jplph.2012.04.002","journal-title":"J Plant Physiol"},{"key":"3791_CR115","doi-asserted-by":"publisher","first-page":"540","DOI":"10.1016\/j.plaphy.2009.01.004","volume":"47","author":"JJ Reina-Pinto","year":"2009","unstructured":"Reina-Pinto JJ, Yephremov A (2009) Surface lipids and plant defenses. Plant Physiol Biochem 47:540\u2013549. https:\/\/doi.org\/10.1016\/j.plaphy.2009.01.004","journal-title":"Plant Physiol Biochem"},{"key":"3791_CR116","doi-asserted-by":"publisher","first-page":"640","DOI":"10.1080\/14786419.2010.488230","volume":"25","author":"Q-M Xu","year":"2011","unstructured":"Xu Q-M, Liu Y-L, Li X-R et al (2011) Three new fatty acids from the roots of Boehmeria nivea (L.) Gaudich and their antifungal activities. Nat Prod Res 25:640\u2013647. https:\/\/doi.org\/10.1080\/14786419.2010.488230","journal-title":"Nat Prod Res"},{"key":"3791_CR117","doi-asserted-by":"publisher","first-page":"931","DOI":"10.1111\/j.1365-313X.2004.02260.x","volume":"40","author":"T Yaeno","year":"2004","unstructured":"Yaeno T, Matsuda O, Iba K (2004) Role of chloroplast trienoic fatty acids in plant disease defense responses. Plant J 40:931\u2013941. https:\/\/doi.org\/10.1111\/j.1365-313X.2004.02260.x","journal-title":"Plant J"},{"key":"3791_CR118","doi-asserted-by":"publisher","DOI":"10.3389\/fpls.2014.00267","author":"C-Y Hung","year":"2014","unstructured":"Hung C-Y, Aspesi P Jr, Hunter MR et al (2014) Phosphoinositide-signaling is one component of a robust plant defense response. Front Plant Sci. https:\/\/doi.org\/10.3389\/fpls.2014.00267","journal-title":"Front Plant Sci"},{"key":"3791_CR119","doi-asserted-by":"publisher","first-page":"228","DOI":"10.1111\/nph.12256","volume":"199","author":"J Zhao","year":"2013","unstructured":"Zhao J, Devaiah SP, Wang C et al (2013) Arabidopsis phospholipase D\u03b21 modulates defense responses to bacterial and fungal pathogens. New Phytol 199:228\u2013240. https:\/\/doi.org\/10.1111\/nph.12256","journal-title":"New Phytol"},{"key":"3791_CR120","doi-asserted-by":"publisher","DOI":"10.1038\/s41598-017-03907-2","author":"A Gupta","year":"2017","unstructured":"Gupta A, Hisano H, Hojo Y et al (2017) Global profiling of phytohormone dynamics during combined drought and pathogen stress in Arabidopsis thaliana reveals ABA and JA as major regulators. Sci Rep. https:\/\/doi.org\/10.1038\/s41598-017-03907-2","journal-title":"Sci Rep"},{"key":"3791_CR121","doi-asserted-by":"publisher","first-page":"153","DOI":"10.1146\/annurev-phyto-080508-081820","volume":"47","author":"A Kachroo","year":"2009","unstructured":"Kachroo A, Kachroo P (2009) Fatty acid-derived signals in plant defense. Annu Rev Phytopathol 47:153\u2013176. https:\/\/doi.org\/10.1146\/annurev-phyto-080508-081820","journal-title":"Annu Rev Phytopathol"},{"key":"3791_CR122","doi-asserted-by":"publisher","first-page":"267","DOI":"10.1146\/annurev-phyto-081211-172955","volume":"50","author":"T Mengiste","year":"2012","unstructured":"Mengiste T (2012) Plant immunity to necrotrophs. Annu Rev Phytopathol 50:267\u2013294. https:\/\/doi.org\/10.1146\/annurev-phyto-081211-172955","journal-title":"Annu Rev Phytopathol"},{"key":"3791_CR123","doi-asserted-by":"publisher","first-page":"205","DOI":"10.1146\/annurev.phyto.43.040204.135923","volume":"43","author":"J Glazebrook","year":"2005","unstructured":"Glazebrook J (2005) Contrasting mechanisms of defense against biotrophic and necrotrophic pathogens. Annu Rev Phytopathol 43:205\u2013227. https:\/\/doi.org\/10.1146\/annurev.phyto.43.040204.135923","journal-title":"Annu Rev Phytopathol"},{"key":"3791_CR124","doi-asserted-by":"publisher","first-page":"39","DOI":"10.1016\/j.mib.2010.12.011","volume":"14","author":"A Block","year":"2011","unstructured":"Block A, Alfano JR (2011) Plant targets for Pseudomonas syringae type III effectors: virulence targets or guarded decoys? Curr Opin Microbiol 14:39\u201346. https:\/\/doi.org\/10.1016\/j.mib.2010.12.011","journal-title":"Curr Opin Microbiol"},{"key":"3791_CR125","doi-asserted-by":"publisher","first-page":"291","DOI":"10.1038\/nrmicro.2017.171","volume":"16","author":"P Poole","year":"2018","unstructured":"Poole P, Ramachandran V, Terpolilli J (2018) Rhizobia: from saprophytes to endosymbionts. Nat Rev Microbiol 16:291\u2013303. https:\/\/doi.org\/10.1038\/nrmicro.2017.171","journal-title":"Nat Rev Microbiol"},{"key":"3791_CR126","doi-asserted-by":"publisher","first-page":"9858","DOI":"10.1074\/jbc.RA119.007600","volume":"294","author":"S Haroth","year":"2019","unstructured":"Haroth S, Feussner K, Kelly AA et al (2019) The glycosyltransferase UGT76E1 significantly contributes to 12-O-glucopyranosyl-jasmonic acid formation in wounded Arabidopsis thaliana leaves. J Biol Chem 294:9858\u20139872. https:\/\/doi.org\/10.1074\/jbc.RA119.007600","journal-title":"J Biol Chem"},{"key":"3791_CR127","doi-asserted-by":"publisher","first-page":"363","DOI":"10.1146\/annurev-arplant-042817-040440","volume":"69","author":"C Wasternack","year":"2018","unstructured":"Wasternack C, Feussner I (2018) The oxylipin pathways: biochemistry and function. Annu Rev Plant Biol 69:363\u2013386. https:\/\/doi.org\/10.1146\/annurev-arplant-042817-040440","journal-title":"Annu Rev Plant Biol"},{"key":"3791_CR128","doi-asserted-by":"publisher","first-page":"645","DOI":"10.1007\/s10658-015-0634-7","volume":"142","author":"A Figueiredo","year":"2015","unstructured":"Figueiredo A, Monteiro F, Sebastiana M (2015) First clues on a jasmonic acid role in grapevine resistance against the biotrophic fungus Plasmopara viticola. Eur J Plant Pathol 142:645\u2013652. https:\/\/doi.org\/10.1007\/s10658-015-0634-7","journal-title":"Eur J Plant Pathol"},{"key":"3791_CR129","doi-asserted-by":"publisher","DOI":"10.3389\/fpls.2016.00565","author":"A Guerreiro","year":"2016","unstructured":"Guerreiro A, Figueiredo J, Sousa Silva M, Figueiredo A (2016) Linking jasmonic acid to grapevine resistance against the biotrophic oomycete Plasmopara viticola. Front Plant Sci. https:\/\/doi.org\/10.3389\/fpls.2016.00565","journal-title":"Front Plant Sci"},{"key":"3791_CR130","doi-asserted-by":"publisher","first-page":"355","DOI":"10.1146\/annurev.arplant.48.1.355","volume":"48","author":"RA Creelman","year":"1997","unstructured":"Creelman RA, Mullet JE (1997) Biosynthesis and action of jasmonates in plants. Annu Rev Plant Physiol Plant Mol Biol 48:355\u2013381. https:\/\/doi.org\/10.1146\/annurev.arplant.48.1.355","journal-title":"Annu Rev Plant Physiol Plant Mol Biol"},{"key":"3791_CR131","doi-asserted-by":"publisher","first-page":"80","DOI":"10.1126\/science.252.5002.80","volume":"252","author":"C Somerville","year":"1991","unstructured":"Somerville C, Browse J (1991) Plant lipids: metabolism, mutants, and membranes. Science 252:80\u201387. https:\/\/doi.org\/10.1126\/science.252.5002.80","journal-title":"Science"},{"key":"3791_CR132","doi-asserted-by":"publisher","first-page":"967","DOI":"10.1007\/s10529-008-9639-z","volume":"30","author":"RG Upchurch","year":"2008","unstructured":"Upchurch RG (2008) Fatty acid unsaturation, mobilization, and regulation in the response of plants to stress. Biotechnol Lett 30:967\u2013977. https:\/\/doi.org\/10.1007\/s10529-008-9639-z","journal-title":"Biotechnol Lett"},{"key":"3791_CR133","doi-asserted-by":"publisher","first-page":"625","DOI":"10.1016\/j.jplph.2014.01.007","volume":"171","author":"S Taniguchi","year":"2014","unstructured":"Taniguchi S, Miyoshi S, Tamaoki D et al (2014) Isolation of jasmonate-induced sesquiterpene synthase of rice: product of which has an antifungal activity against Magnaporthe oryzae. J Plant Physiol 171:625\u2013632. https:\/\/doi.org\/10.1016\/j.jplph.2014.01.007","journal-title":"J Plant Physiol"},{"key":"3791_CR134","doi-asserted-by":"publisher","DOI":"10.3389\/fpls.2015.00055","author":"M Saucedo-Garc\u00eda","year":"2015","unstructured":"Saucedo-Garc\u00eda M, Gavilanes-Ru\u00edz M, Arce-Cervantes O (2015) Long-chain bases, phosphatidic acid, MAPKs, and reactive oxygen species as nodal signal transducers in stress responses in Arabidopsis. Front Plant Sci. https:\/\/doi.org\/10.3389\/fpls.2015.00055","journal-title":"Front Plant Sci"},{"key":"3791_CR135","doi-asserted-by":"publisher","first-page":"13099","DOI":"10.1038\/ncomms13099","volume":"7","author":"L Liu","year":"2016","unstructured":"Liu L, Sonbol F-M, Huot B et al (2016) Salicylic acid receptors activate jasmonic acid signalling through a non-canonical pathway to promote effector-triggered immunity. Nat Commun 7:13099. https:\/\/doi.org\/10.1038\/ncomms13099","journal-title":"Nat Commun"},{"key":"3791_CR136","doi-asserted-by":"publisher","first-page":"176","DOI":"10.1016\/j.cell.2019.11.037","volume":"180","author":"JE Jeon","year":"2020","unstructured":"Jeon JE, Kim J-G, Fischer CR et al (2020) A pathogen-responsive gene cluster for highly modified fatty acids in tomato. Cell 180:176-187.e19. https:\/\/doi.org\/10.1016\/j.cell.2019.11.037","journal-title":"Cell"},{"key":"3791_CR137","doi-asserted-by":"publisher","first-page":"1377","DOI":"10.1073\/pnas.1614204114","volume":"114","author":"Z Guo","year":"2017","unstructured":"Guo Z, Lu J, Wang X et al (2017) Lipid flippases promote antiviral silencing and the biogenesis of viral and host siRNAs in Arabidopsis. PNAS 114:1377\u20131382. https:\/\/doi.org\/10.1073\/pnas.1614204114","journal-title":"PNAS"},{"key":"3791_CR138","doi-asserted-by":"publisher","first-page":"801","DOI":"10.1111\/nph.13087","volume":"205","author":"N Alkan","year":"2015","unstructured":"Alkan N, Friedlander G, Ment D et al (2015) Simultaneous transcriptome analysis of Colletotrichum gloeosporioides and tomato fruit pathosystem reveals novel fungal pathogenicity and fruit defense strategies. New Phytol 205:801\u2013815. https:\/\/doi.org\/10.1111\/nph.13087","journal-title":"New Phytol"},{"key":"3791_CR139","doi-asserted-by":"publisher","first-page":"1233","DOI":"10.1007\/s00709-015-0877-3","volume":"253","author":"JPR Marques","year":"2016","unstructured":"Marques JPR, Amorim L, Sp\u00f3sito MB, Appezzato-da-Gl\u00f3ria B (2016) Ultrastructural changes in the epidermis of petals of the sweet orange infected by Colletotrichum acutatum. Protoplasma 253:1233\u20131242. https:\/\/doi.org\/10.1007\/s00709-015-0877-3","journal-title":"Protoplasma"},{"key":"3791_CR140","doi-asserted-by":"publisher","first-page":"121","DOI":"10.1007\/s10126-014-9600-1","volume":"17","author":"K-L Pang","year":"2015","unstructured":"Pang K-L, Lin H-J, Lin H-Y et al (2015) Production of arachidonic and eicosapentaenoic acids by the marine Oomycete halophytophthora. Mar Biotechnol 17:121\u2013129. https:\/\/doi.org\/10.1007\/s10126-014-9600-1","journal-title":"Mar Biotechnol"},{"key":"3791_CR141","doi-asserted-by":"publisher","first-page":"163","DOI":"10.1007\/s00122-009-1167-2","volume":"120","author":"D Bellin","year":"2009","unstructured":"Bellin D, Peressotti E, Merdinoglu D et al (2009) Resistance to Plasmopara viticola in grapevine \u2018Bianca\u2019 is controlled by a major dominant gene causing localised necrosis at the infection site. Theor Appl Genet 120:163\u2013176. https:\/\/doi.org\/10.1007\/s00122-009-1167-2","journal-title":"Theor Appl Genet"},{"key":"3791_CR142","doi-asserted-by":"publisher","first-page":"330","DOI":"10.1094\/MPMI-07-12-0184-R","volume":"26","author":"F Sun","year":"2012","unstructured":"Sun F, Kale SD, Azurmendi HF et al (2012) Structural basis for interactions of the Phytophthora sojae RxLR effector Avh5 with phosphatidylinositol 3-phosphate and for host cell entry. MPMI 26:330\u2013344. https:\/\/doi.org\/10.1094\/MPMI-07-12-0184-R","journal-title":"MPMI"},{"key":"3791_CR143","doi-asserted-by":"publisher","first-page":"3163","DOI":"10.1105\/tpc.108.060053","volume":"20","author":"W Wang","year":"2008","unstructured":"Wang W, Yang X, Tangchaiburana S et al (2008) An Inositolphosphorylceramide synthase is involved in regulation of plant programmed cell death associated with defense in Arabidopsis. Plant Cell 20:3163\u20133179. https:\/\/doi.org\/10.1105\/tpc.108.060053","journal-title":"Plant Cell"},{"key":"3791_CR144","doi-asserted-by":"publisher","first-page":"3449","DOI":"10.1105\/tpc.114.127050","volume":"26","author":"F-C Bi","year":"2014","unstructured":"Bi F-C, Liu Z, Wu J-X et al (2014) Loss of ceramide kinase in Arabidopsis impairs defenses and promotes ceramide accumulation and mitochondrial H2O2 bursts. Plant Cell 26:3449\u20133467. https:\/\/doi.org\/10.1105\/tpc.114.127050","journal-title":"Plant Cell"},{"key":"3791_CR145","doi-asserted-by":"publisher","first-page":"193","DOI":"10.1007\/s00425-002-0902-6","volume":"216","author":"BP Thomma","year":"2002","unstructured":"Thomma BP, Cammue BP, Thevissen K (2002) Plant defensins. Planta 216:193\u2013202. https:\/\/doi.org\/10.1007\/s00425-002-0902-6","journal-title":"Planta"},{"key":"3791_CR146","doi-asserted-by":"publisher","first-page":"1705","DOI":"10.1016\/j.peptides.2003.09.014","volume":"24","author":"K Thevissen","year":"2003","unstructured":"Thevissen K, Ferket KKA, Fran\u00e7ois IEJA, Cammue BPA (2003) Interactions of antifungal plant defensins with fungal membrane components. Peptides 24:1705\u20131712. https:\/\/doi.org\/10.1016\/j.peptides.2003.09.014","journal-title":"Peptides"},{"key":"3791_CR147","doi-asserted-by":"publisher","first-page":"11202","DOI":"10.1073\/pnas.1607855113","volume":"113","author":"M Kvansakul","year":"2016","unstructured":"Kvansakul M, Lay FT, Adda CG et al (2016) Binding of phosphatidic acid by NsD7 mediates the formation of helical defensin-lipid oligomeric assemblies and membrane permeabilization. Proc Natl Acad Sci USA 113:11202\u201311207. https:\/\/doi.org\/10.1073\/pnas.1607855113","journal-title":"Proc Natl Acad Sci USA"},{"key":"3791_CR148","doi-asserted-by":"publisher","first-page":"e01808","DOI":"10.7554\/eLife.01808","volume":"3","author":"IK Poon","year":"2014","unstructured":"Poon IK, Baxter AA, Lay FT et al (2014) Phosphoinositide-mediated oligomerization of a defensin induces cell lysis. Elife 3:e01808. https:\/\/doi.org\/10.7554\/eLife.01808","journal-title":"Elife"},{"key":"3791_CR149","doi-asserted-by":"publisher","first-page":"161","DOI":"10.1016\/j.imbio.2007.10.004","volume":"213","author":"M Livaja","year":"2008","unstructured":"Livaja M, Zeidler D, von Rad U, Durner J (2008) Transcriptional responses of Arabidopsis thaliana to the bacteria-derived PAMPs harpin and lipopolysaccharide. Immunobiology 213:161\u2013171. https:\/\/doi.org\/10.1016\/j.imbio.2007.10.004","journal-title":"Immunobiology"},{"key":"3791_CR150","doi-asserted-by":"publisher","first-page":"505","DOI":"10.1111\/j.1365-2672.2010.04669.x","volume":"109","author":"TJ Evans","year":"2010","unstructured":"Evans TJ, Ind A, Komitopoulou E, Salmond GPC (2010) Phage-selected lipopolysaccharide mutants of Pectobacterium atrosepticum exhibit different impacts on virulence. J Appl Microbiol 109:505\u2013514. https:\/\/doi.org\/10.1111\/j.1365-2672.2010.04669.x","journal-title":"J Appl Microbiol"},{"key":"3791_CR151","doi-asserted-by":"publisher","first-page":"1001","DOI":"10.1016\/j.bbrc.2006.03.216","volume":"344","author":"NM Sanabria","year":"2006","unstructured":"Sanabria NM, Dubery IA (2006) Differential display profiling of the Nicotiana response to LPS reveals elements of plant basal resistance. Biochem Biophys Res Commun 344:1001\u20131007. https:\/\/doi.org\/10.1016\/j.bbrc.2006.03.216","journal-title":"Biochem Biophys Res Commun"},{"key":"3791_CR152","doi-asserted-by":"publisher","first-page":"e1000160","DOI":"10.1080\/15592324.2014.1000160","volume":"10","author":"K-H Mohamed","year":"2015","unstructured":"Mohamed K-H, Daniel T, Aur\u00e9lien D et al (2015) Deciphering the dual effect of lipopolysaccharides from plant pathogenic Pectobacterium. Plant Signal Behav 10:e1000160. https:\/\/doi.org\/10.1080\/15592324.2014.1000160","journal-title":"Plant Signal Behav"},{"key":"3791_CR153","doi-asserted-by":"publisher","first-page":"33660","DOI":"10.1074\/jbc.M506254200","volume":"280","author":"A Silipo","year":"2005","unstructured":"Silipo A, Molinaro A, Sturiale L et al (2005) The elicitation of plant innate immunity by lipooligosaccharide of Xanthomonas campestris. J Biol Chem 280:33660\u201333668. https:\/\/doi.org\/10.1074\/jbc.M506254200","journal-title":"J Biol Chem"},{"key":"3791_CR154","doi-asserted-by":"publisher","first-page":"51","DOI":"10.1016\/j.plaphy.2014.10.011","volume":"85","author":"S Proietti","year":"2014","unstructured":"Proietti S, Giangrande C, Amoresano A et al (2014) Xanthomonas campestris lipooligosaccharides trigger innate immunity and oxidative burst in Arabidopsis. Plant Physiol Biochem 85:51\u201362. https:\/\/doi.org\/10.1016\/j.plaphy.2014.10.011","journal-title":"Plant Physiol Biochem"},{"key":"3791_CR155","doi-asserted-by":"publisher","first-page":"3259","DOI":"10.1007\/978-3-540-77587-4_247","volume-title":"Handbook of hydrocarbon and lipid microbiology","author":"C Gaillardin","year":"2010","unstructured":"Gaillardin C (2010) Lipases as pathogenicity factors of fungi. In: Timmis KN (ed) Handbook of hydrocarbon and lipid microbiology. Springer, Berlin, pp 3259\u20133268"},{"key":"3791_CR156","doi-asserted-by":"publisher","first-page":"357","DOI":"10.1104\/pp.106.079129","volume":"141","author":"DM Rhoads","year":"2006","unstructured":"Rhoads DM, Umbach AL, Subbaiah CC, Siedow JN (2006) Mitochondrial reactive oxygen species. contribution to oxidative stress and interorganellar signaling. Plant Physiol 141:357\u2013366. https:\/\/doi.org\/10.1104\/pp.106.079129","journal-title":"Plant Physiol"},{"key":"3791_CR157","doi-asserted-by":"publisher","first-page":"859","DOI":"10.1186\/1471-2164-14-859","volume":"14","author":"N Peeters","year":"2013","unstructured":"Peeters N, Carr\u00e8re S, Anisimova M et al (2013) Repertoire, unified nomenclature and evolution of the type III effector gene set in the Ralstonia solanacearum species complex. BMC Genomics 14:859. https:\/\/doi.org\/10.1186\/1471-2164-14-859","journal-title":"BMC Genomics"},{"key":"3791_CR158","doi-asserted-by":"publisher","first-page":"1854","DOI":"10.1093\/pcp\/pcw107","volume":"57","author":"N Inada","year":"2016","unstructured":"Inada N, Betsuyaku S, Shimada TL et al (2016) Modulation of plant RAB GTPase-mediated membrane trafficking pathway at the interface between plants and obligate biotrophic pathogens. Plant Cell Physiol 57:1854\u20131864. https:\/\/doi.org\/10.1093\/pcp\/pcw107","journal-title":"Plant Cell Physiol"},{"key":"3791_CR159","doi-asserted-by":"publisher","first-page":"2162","DOI":"10.1111\/mpp.12690","volume":"19","author":"P Battilani","year":"2018","unstructured":"Battilani P, Lanubile A, Scala V et al (2018) Oxylipins from both pathogen and host antagonize jasmonic acid-mediated defence via the 9-lipoxygenase pathway in Fusarium verticillioides infection of maize. Mol Plant Pathol 19:2162\u20132176. https:\/\/doi.org\/10.1111\/mpp.12690","journal-title":"Mol Plant Pathol"},{"key":"3791_CR160","doi-asserted-by":"publisher","DOI":"10.1038\/ncomms13823","author":"E Mart\u00ednez","year":"2016","unstructured":"Mart\u00ednez E, Campos-G\u00f3mez J (2016) Oxylipins produced by Pseudomonas aeruginosa promote biofilm formation and virulence. Nat Commun. https:\/\/doi.org\/10.1038\/ncomms13823","journal-title":"Nat Commun"},{"key":"3791_CR161","doi-asserted-by":"publisher","first-page":"153","DOI":"10.1111\/j.1365-3040.1994.tb00278.x","volume":"17","author":"A Brune","year":"1994","unstructured":"Brune A, Urbach W, Dietz K-J (1994) Compartmentation and transport of zinc in barley primary leaves as basic mechanisms involved in zinc tolerance. Plant Cell Environ 17:153\u2013162. https:\/\/doi.org\/10.1111\/j.1365-3040.1994.tb00278.x","journal-title":"Plant Cell Environ"},{"key":"3791_CR162","doi-asserted-by":"publisher","first-page":"1935","DOI":"10.1104\/pp.103.029215","volume":"133","author":"MM Fecht-Christoffers","year":"2003","unstructured":"Fecht-Christoffers MM, Braun H-P, Lemaitre-Guillier C et al (2003) Effect of manganese toxicity on the proteome of the leaf apoplast in cowpea. Plant Physiol 133:1935\u20131946. https:\/\/doi.org\/10.1104\/pp.103.029215","journal-title":"Plant Physiol"},{"key":"3791_CR163","doi-asserted-by":"publisher","DOI":"10.1111\/ppl.13198","author":"J Figueiredo","year":"2020","unstructured":"Figueiredo J, Cavaco AR, Guerra-Guimar\u00e3es L et al (2020) An apoplastic fluid extraction method for the characterization of grapevine leaves proteome and metabolome from a single sample. Physiol Plant. https:\/\/doi.org\/10.1111\/ppl.13198","journal-title":"Physiol Plant"},{"key":"3791_CR164","doi-asserted-by":"publisher","first-page":"66","DOI":"10.1016\/S1360-1385(97)82565-4","volume":"2","author":"J-C Kader","year":"1997","unstructured":"Kader J-C (1997) Lipid-transfer proteins: a puzzling family of plant proteins. Trends Plant Sci 2:66\u201370. https:\/\/doi.org\/10.1016\/S1360-1385(97)82565-4","journal-title":"Trends Plant Sci"},{"key":"3791_CR165","doi-asserted-by":"publisher","first-page":"399","DOI":"10.1038\/nature00962","volume":"419","author":"AM Maldonado","year":"2002","unstructured":"Maldonado AM, Doerner P, Dixon RA et al (2002) A putative lipid transfer protein involved in systemic resistance signalling in Arabidopsis. Nature 419:399\u2013403. https:\/\/doi.org\/10.1038\/nature00962","journal-title":"Nature"},{"key":"3791_CR166","doi-asserted-by":"publisher","DOI":"10.3389\/fpls.2012.00126","author":"J Jung","year":"2012","unstructured":"Jung J, Kumar K, Lee HY et al (2012) Translocation of phospholipase A2\u03b1 to apoplasts is modulated by developmental stages and bacterial infection in Arabidopsis. Front Plant Sci. https:\/\/doi.org\/10.3389\/fpls.2012.00126","journal-title":"Front Plant Sci"},{"key":"3791_CR167","doi-asserted-by":"publisher","first-page":"172","DOI":"10.1016\/j.tcb.2016.11.003","volume":"27","author":"SLN Maas","year":"2017","unstructured":"Maas SLN, Breakefield XO, Weaver AM (2017) Extracellular vesicles: unique intercellular delivery vehicles. Trends Cell Biol 27:172\u2013188. https:\/\/doi.org\/10.1016\/j.tcb.2016.11.003","journal-title":"Trends Cell Biol"},{"key":"3791_CR168","doi-asserted-by":"publisher","first-page":"728","DOI":"10.1104\/pp.16.01253","volume":"173","author":"BD Rutter","year":"2017","unstructured":"Rutter BD, Innes RW (2017) Extracellular vesicles isolated from the leaf apoplast carry stress-response proteins. Plant Physiol 173:728\u2013741. https:\/\/doi.org\/10.1104\/pp.16.01253","journal-title":"Plant Physiol"},{"key":"3791_CR169","doi-asserted-by":"publisher","first-page":"7654","DOI":"10.1073\/pnas.151262398","volume":"98","author":"LJ Szabo","year":"2001","unstructured":"Szabo LJ, Bushnell WR (2001) Hidden robbers: the role of fungal haustoria in parasitism of plants. Proc Natl Acad Sci 98:7654\u20137655. https:\/\/doi.org\/10.1073\/pnas.151262398","journal-title":"Proc Natl Acad Sci"},{"key":"3791_CR170","doi-asserted-by":"publisher","first-page":"511","DOI":"10.1046\/j.1469-8137.1997.00760.x","volume":"136","author":"D \u0160kalamera","year":"1997","unstructured":"\u0160kalamera D, Jibodhand S, Heath MC (1997) Callose deposition during the interaction between cowpea (Vigna unguiculata) and the monokaryotic stage of the cowpea rust fungus (Uromyces vignae). New Phytol 136:511\u2013524. https:\/\/doi.org\/10.1046\/j.1469-8137.1997.00760.x","journal-title":"New Phytol"},{"key":"3791_CR171","doi-asserted-by":"publisher","first-page":"986","DOI":"10.1111\/j.1365-313X.2008.03743.x","volume":"57","author":"D Meyer","year":"2009","unstructured":"Meyer D, Pajonk S, Micali C et al (2009) Extracellular transport and integration of plant secretory proteins into pathogen-induced cell wall compartments. Plant J 57:986\u2013999. https:\/\/doi.org\/10.1111\/j.1365-313X.2008.03743.x","journal-title":"Plant J"},{"key":"3791_CR172","doi-asserted-by":"publisher","first-page":"5485","DOI":"10.1093\/jxb\/erx355","volume":"68","author":"M Regente","year":"2017","unstructured":"Regente M, Pinedo M, San Clemente H et al (2017) Plant extracellular vesicles are incorporated by a fungal pathogen and inhibit its growth. J Exp Bot 68:5485\u20135495. https:\/\/doi.org\/10.1093\/jxb\/erx355","journal-title":"J Exp Bot"},{"key":"3791_CR173","doi-asserted-by":"publisher","first-page":"1375","DOI":"10.1104\/pp.19.00381","volume":"180","author":"N Movahed","year":"2019","unstructured":"Movahed N, Cabanillas DG, Wan J et al (2019) Turnip mosaic virus components are released into the extracellular space by vesicles in infected leaves. Plant Physiol 180:1375\u20131388. https:\/\/doi.org\/10.1104\/pp.19.00381","journal-title":"Plant Physiol"}],"container-title":["Cellular and Molecular Life Sciences"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/link.springer.com\/content\/pdf\/10.1007\/s00018-021-03791-0.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/link.springer.com\/article\/10.1007\/s00018-021-03791-0\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/link.springer.com\/content\/pdf\/10.1007\/s00018-021-03791-0.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2021,5,29]],"date-time":"2021-05-29T04:22:57Z","timestamp":1622262177000},"score":1,"resource":{"primary":{"URL":"https:\/\/link.springer.com\/10.1007\/s00018-021-03791-0"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2021,2,27]]},"references-count":173,"journal-issue":{"issue":"9","published-print":{"date-parts":[[2021,5]]}},"alternative-id":["3791"],"URL":"https:\/\/doi.org\/10.1007\/s00018-021-03791-0","relation":{},"ISSN":["1420-682X","1420-9071"],"issn-type":[{"value":"1420-682X","type":"print"},{"value":"1420-9071","type":"electronic"}],"subject":[],"published":{"date-parts":[[2021,2,27]]},"assertion":[{"value":"4 November 2020","order":1,"name":"received","label":"Received","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"21 January 2021","order":2,"name":"revised","label":"Revised","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"12 February 2021","order":3,"name":"accepted","label":"Accepted","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"27 February 2021","order":4,"name":"first_online","label":"First Online","group":{"name":"ArticleHistory","label":"Article History"}},{"order":1,"name":"Ethics","group":{"name":"EthicsHeading","label":"Declarations"}},{"value":"The authors declare no competing interests.","order":2,"name":"Ethics","group":{"name":"EthicsHeading","label":"Conflict of interest"}},{"value":"All the authors gave their consent for publication.","order":3,"name":"Ethics","group":{"name":"EthicsHeading","label":"Consent for publication"}}]}}