Hexanoic Acid Treatment Prevents Systemic MNSV Movement in Cucumis melo Plants by Priming Callose Deposition Correlating SA and OPDA Accumulation

dc.contributor.affiliationInstituto Universitario Mixto de Biología Molecular y Celular de Plantas
dc.contributor.authorFernandez-Crespo, E.es_ES
dc.contributor.authorNAVARRO-BOHIGUES, JOSE-ANTONIO
dc.contributor.authorSerra Soriano, Martaes_ES
dc.contributor.authorFiniti, I.es_ES
dc.contributor.authorGarcía Agustín, Pilares_ES
dc.contributor.authorPallás Benet, Vicente
dc.contributor.authorGonzalez-Bosch, C.es_ES
dc.contributor.funderEuropean Regional Development Fundes_ES
dc.contributor.funderMinisterio de Ciencia e Innovaciónes_ES
dc.contributor.funderMinisterio de Economía y Competitividades_ES
dc.date.accessioned2020-07-30T03:35:30Z
dc.date.available2020-07-30T03:35:30Z
dc.date.issued2017-10-20es_ES
dc.description.abstract[EN] Unlike fungal and bacterial diseases, no direct method is available to control viral diseases. The use of resistance-inducing compounds can be an alternative strategy for plant viruses. Here we studied the basal response of melon to Melon necrotic spot virus (MNSV) and demonstrated the efficacy of hexanoic acid (Hx) priming, which prevents the virus from systemically spreading. We analysed callose deposition and the hormonal profile and gene expression at the whole plant level. This allowed us to determine hormonal homeostasis in the melon roots, cotyledons, hypocotyls, stems and leaves involved in basal and hexanoic acid-induced resistance (Hx-IR) to MNSV. Our data indicate important roles of salicylic acid (SA), 12-oxo-phytodienoic acid (OPDA), jasmonic-isoleucine, and ferulic acid in both responses to MNSV. The hormonal and metabolites balance, depending on the time and location associated with basal and Hx-IR, demonstrated the reprogramming of plant metabolism in MNSV-inoculated plants. The treatment with both SA and OPDA prior to virus infection significantly reduced MNSV systemic movement by inducing callose deposition. This demonstrates their relevance in Hx-IR against MNSV and a high correlation with callose deposition. Our data also provide valuable evidence to unravel priming mechanisms by natural compounds.en_EN
dc.description.accrualMethodSes_ES
dc.description.bibliographicCitationFernandez-Crespo, E.; Navarro Bohigues, JA.; Serra Soriano, M.; Finiti, I.; García Agustín, P.; Pallás Benet, V.; Gonzalez-Bosch, C. (2017). Hexanoic Acid Treatment Prevents Systemic MNSV Movement in Cucumis melo Plants by Priming Callose Deposition Correlating SA and OPDA Accumulation. Frontiers in Plant Science. 8:1-15. https://doi.org/10.3389/fpls.2017.01793es_ES
dc.description.referencesAlazem, M., & Lin, N. (2014). Roles of plant hormones in the regulation of host–virus interactions. Molecular Plant Pathology, 16(5), 529-540. doi:10.1111/mpp.12204es_ES
dc.description.referencesAndo, S., Obinata, A., & Takahashi, H. (2014). WRKY70 interacting with RCY1 disease resistance protein is required for resistance to Cucumber mosaic virus in Arabidopsis thaliana. Physiological and Molecular Plant Pathology, 85, 8-14. doi:10.1016/j.pmpp.2013.11.001es_ES
dc.description.referencesAnfoka, G. H. (2000). Benzo-(1,2,3)-thiadiazole-7-carbothioic acid S-methyl ester induces systemic resistance in tomato (Lycopersicon esculentum. Mill cv. Vollendung) to Cucumber mosaic virus. Crop Protection, 19(6), 401-405. doi:10.1016/s0261-2194(00)00031-4es_ES
dc.description.referencesAranega-Bou, P., de la O Leyva, M., Finiti, I., García-Agustín, P., & González-Bosch, C. (2014). Priming of plant resistance by natural compounds. Hexanoic acid as a model. Frontiers in Plant Science, 5. doi:10.3389/fpls.2014.00488es_ES
dc.description.referencesBellés, J. M., López-Gresa, M. P., Fayos, J., Pallás, V., Rodrigo, I., & Conejero, V. (2008). Induction of cinnamate 4-hydroxylase and phenylpropanoids in virus-infected cucumber and melon plants. Plant Science, 174(5), 524-533. doi:10.1016/j.plantsci.2008.02.008es_ES
dc.description.referencesBolwell, G. P., Davies, D. R., Gerrish, C., Auh, C.-K., & Murphy, T. M. (1998). Comparative Biochemistry of the Oxidative Burst Produced by Rose and French Bean Cells Reveals Two Distinct Mechanisms. Plant Physiology, 116(4), 1379-1385. doi:10.1104/pp.116.4.1379es_ES
dc.description.referencesCamañes, G., Scalschi, L., Vicedo, B., González-Bosch, C., & García-Agustín, P. (2015). An untargeted global metabolomic analysis reveals the biochemical changes underlying basal resistance and priming in Solanum lycopersicum, and identifies 1-methyltryptophan as a metabolite involved in plant responses to Botrytis cinerea and Pseudomonas sy. The Plant Journal, 84(1), 125-139. doi:10.1111/tpj.12964es_ES
dc.description.referencesClarke, S. F., Guy, P. L., Burritt, D. J., & Jameson, P. E. (2002). Changes in the activities of antioxidant enzymes in response to virus infection and hormone treatment. Physiologia Plantarum, 114(2), 157-164. doi:10.1034/j.1399-3054.2002.1140201.xes_ES
dc.description.referencesCollum, T. D., & Culver, J. N. (2016). The impact of phytohormones on virus infection and disease. Current Opinion in Virology, 17, 25-31. doi:10.1016/j.coviro.2015.11.003es_ES
dc.description.referencesConti, G., Rodriguez, M. C., Venturuzzi, A. L., & Asurmendi, S. (2016). Modulation of host plant immunity by Tobamovirus proteins. Annals of Botany, mcw216. doi:10.1093/aob/mcw216es_ES
dc.description.referencesCulver, J. N., & Padmanabhan, M. S. (2007). Virus-Induced Disease: Altering Host Physiology One Interaction at a Time. Annual Review of Phytopathology, 45(1), 221-243. doi:10.1146/annurev.phyto.45.062806.094422es_ES
dc.description.referencesDong, C.-J., Li, L., Shang, Q.-M., Liu, X.-Y., & Zhang, Z.-G. (2014). Endogenous salicylic acid accumulation is required for chilling tolerance in cucumber (Cucumis sativus L.) seedlings. Planta, 240(4), 687-700. doi:10.1007/s00425-014-2115-1es_ES
dc.description.referencesEllinger, D., Naumann, M., Falter, C., Zwikowics, C., Jamrow, T., Manisseri, C., … Voigt, C. A. (2013). Elevated Early Callose Deposition Results in Complete Penetration Resistance to Powdery Mildew in Arabidopsis. Plant Physiology, 161(3), 1433-1444. doi:10.1104/pp.112.211011es_ES
dc.description.referencesFiniti, I., de la O. Leyva, M., Vicedo, B., Gómez-Pastor, R., López-Cruz, J., García-Agustín, P., … González-Bosch, C. (2014). Hexanoic acid protects tomato plants againstBotrytis cinereaby priming defence responses and reducing oxidative stress. Molecular Plant Pathology, 15(6), 550-562. doi:10.1111/mpp.12112es_ES
dc.description.referencesFlors, V., Leyva, M. de la O., Vicedo, B., Finiti, I., Real, M. D., García-Agustín, P., … González-Bosch, C. (2007). Absence of the endo-β-1,4-glucanases Cel1 and Cel2 reduces susceptibility toBotrytis cinereain tomato. The Plant Journal, 52(6), 1027-1040. doi:10.1111/j.1365-313x.2007.03299.xes_ES
dc.description.referencesFlors, V., Ton, J., Van Doorn, R., Jakab, G., García-Agustín, P., & Mauch-Mani, B. (2007). Interplay between JA, SA and ABA signalling during basal and induced resistance against Pseudomonas syringae and Alternaria brassicicola. The Plant Journal, 54(1), 81-92. doi:10.1111/j.1365-313x.2007.03397.xes_ES
dc.description.referencesFriedrich, L., Lawton, K., Ruess, W., Masner, P., Specker, N., Rella, M. G., … Ryals, J. (1996). A benzothiadiazole derivative induces systemic acquired resistance in tobacco. The Plant Journal, 10(1), 61-70. doi:10.1046/j.1365-313x.1996.10010061.xes_ES
dc.description.referencesFurch, A. C. U., Zimmermann, M. R., Kogel, K.-H., Reichelt, M., & Mithöfer, A. (2014). Direct and individual analysis of stress-related phytohormone dispersion in the vascular system ofCucurbita maximaafter flagellin 22 treatment. New Phytologist, 201(4), 1176-1182. doi:10.1111/nph.12661es_ES
dc.description.referencesGarcía, J. A., & Pallás, V. (2015). Viral factors involved in plant pathogenesis. Current Opinion in Virology, 11, 21-30. doi:10.1016/j.coviro.2015.01.001es_ES
dc.description.referencesGarcia-Marcos, A., Pacheco, R., Manzano, A., Aguilar, E., & Tenllado, F. (2013). Oxylipin Biosynthesis Genes Positively Regulate Programmed Cell Death during Compatible Infections with the Synergistic Pair Potato Virus X-Potato Virus Y and Tomato Spotted Wilt Virus. Journal of Virology, 87(10), 5769-5783. doi:10.1128/jvi.03573-12es_ES
dc.description.referencesGenovés, A., Navarro, J. A., & Pallás, V. (2006). Functional analysis of the five melon necrotic spot virus genome-encoded proteins. Journal of General Virology, 87(8), 2371-2380. doi:10.1099/vir.0.81793-0es_ES
dc.description.referencesGenovés, A., Navarro, J. A., & Pallás, V. (2009). A self-interacting carmovirus movement protein plays a role in binding of viral RNA during the cell-to-cell movement and shows an actin cytoskeleton dependent location in cell periphery. Virology, 395(1), 133-142. doi:10.1016/j.virol.2009.08.042es_ES
dc.description.referencesGhoshroy, S., Freedman, K., Lartey, R., & Citovsky, V. (1998). Inhibition of plant viral systemic infection by non‐toxic concentrations of cadmium. The Plant Journal, 13(5), 591-602. doi:10.1046/j.1365-313x.1998.00061.xes_ES
dc.description.referencesGosalvez, B., Navarro, J. ., Lorca, A., Botella, F., Sánchez-Pina, M. ., & Pallas, V. (2003). Detection of Melon necrotic spot virus in water samples and melon plants by molecular methods. Journal of Virological Methods, 113(2), 87-93. doi:10.1016/s0166-0934(03)00224-6es_ES
dc.description.referencesGOSALVEZ‐BERNAL, B., GENOVES, A., ANTONIO NAVARRO, J., PALLAS, V., & SANCHEZ‐PINA, M. A. (2008). Distribution and pathway for phloem‐dependent movement of Melon necrotic spot virus in melon plants. Molecular Plant Pathology, 9(4), 447-461. doi:10.1111/j.1364-3703.2008.00474.xes_ES
dc.description.referencesHanley-Bowdoin, L., Bejarano, E. R., Robertson, D., & Mansoor, S. (2013). Geminiviruses: masters at redirecting and reprogramming plant processes. Nature Reviews Microbiology, 11(11), 777-788. doi:10.1038/nrmicro3117es_ES
dc.description.referencesHernandez, J. A., Diaz-Vivancos, P., Rubio, M., Olmos, E., Ros-Barcelo, A., & Martinez-Gomez, P. (2006). Long-term plum pox virus infection produces an oxidative stress in a susceptible apricot, Prunus armeniaca, cultivar but not in a resistant cultivar. Physiologia Plantarum, 126(1), 140-152. doi:10.1111/j.1399-3054.2005.00581.xes_ES
dc.description.referencesHipper, C., Brault, V., Ziegler-Graff, V., & Revers, F. (2013). Viral and Cellular Factors Involved in Phloem Transport of Plant Viruses. Frontiers in Plant Science, 4. doi:10.3389/fpls.2013.00154es_ES
dc.description.referencesInaba, J., Kim, B. M., Shimura, H., & Masuta, C. (2011). Virus-Induced Necrosis Is a Consequence of Direct Protein-Protein Interaction between a Viral RNA-Silencing Suppressor and a Host Catalase. Plant Physiology, 156(4), 2026-2036. doi:10.1104/pp.111.180042es_ES
dc.description.referencesLange, L., & Insunza, V. (1977). Root-inhabiting Olpidium species: The O. radicale complex. Transactions of the British Mycological Society, 69(3), 377-384. doi:10.1016/s0007-1536(77)80074-0es_ES
dc.description.referencesLee, J.-Y., Wang, X., Cui, W., Sager, R., Modla, S., Czymmek, K., … Lakshmanan, V. (2011). A Plasmodesmata-Localized Protein Mediates Crosstalk between Cell-to-Cell Communication and Innate Immunity in Arabidopsis. The Plant Cell, 23(9), 3353-3373. doi:10.1105/tpc.111.087742es_ES
dc.description.referencesLeyva, M. O., Vicedo, B., Finiti, I., Flors, V., Del Amo, G., Real, M. D., … González-Bosch, C. (2008). Preventive and post-infection control ofBotrytis cinereain tomato plants by hexanoic acid. Plant Pathology, 57(6), 1038-1046. doi:10.1111/j.1365-3059.2008.01891.xes_ES
dc.description.referencesLi, J., Brader, G., Kariola, T., & Tapio Palva, E. (2006). WRKY70 modulates the selection of signaling pathways in plant defense. The Plant Journal, 46(3), 477-491. doi:10.1111/j.1365-313x.2006.02712.xes_ES
dc.description.referencesManacorda, C. A., Mansilla, C., Debat, H. J., Zavallo, D., Sánchez, F., Ponz, F., & Asurmendi, S. (2013). Salicylic Acid Determines Differential Senescence Produced by Two Turnip mosaic virus Strains Involving Reactive Oxygen Species and Early Transcriptomic Changes. Molecular Plant-Microbe Interactions®, 26(12), 1486-1498. doi:10.1094/mpmi-07-13-0190-res_ES
dc.description.referencesMandadi, K. K., & Scholthof, K.-B. G. (2013). Plant Immune Responses Against Viruses: How Does a Virus Cause Disease? The Plant Cell, 25(5), 1489-1505. doi:10.1105/tpc.113.111658es_ES
dc.description.referencesMauch-Mani, B., & Mauch, F. (2005). The role of abscisic acid in plant–pathogen interactions. Current Opinion in Plant Biology, 8(4), 409-414. doi:10.1016/j.pbi.2005.05.015es_ES
dc.description.referencesMayers, C. N., Lee, K.-C., Moore, C. A., Wong, S.-M., & Carr, J. P. (2005). Salicylic Acid-Induced Resistance to Cucumber mosaic virus in Squash and Arabidopsis thaliana: Contrasting Mechanisms of Induction and Antiviral Action. Molecular Plant-Microbe Interactions®, 18(5), 428-434. doi:10.1094/mpmi-18-0428es_ES
dc.description.referencesMittler, R. (2017). ROS Are Good. Trends in Plant Science, 22(1), 11-19. doi:10.1016/j.tplants.2016.08.002es_ES
dc.description.referencesMiura, K., & Tada, Y. (2014). Regulation of water, salinity, and cold stress responses by salicylic acid. Frontiers in Plant Science, 5. doi:10.3389/fpls.2014.00004es_ES
dc.description.referencesNaumann, M., Somerville, S. C., & Voigt, C. A. (2013). Differences in early callose deposition during adapted and non-adapted powdery mildew infection of resistantArabidopsislines. Plant Signaling & Behavior, 8(6), e24408. doi:10.4161/psb.24408es_ES
dc.description.referencesNavarro, J. A., Genovés, A., Climent, J., Saurí, A., Martínez-Gil, L., Mingarro, I., & Pallás, V. (2006). RNA-binding properties and membrane insertion of Melon necrotic spot virus (MNSV) double gene block movement proteins. Virology, 356(1-2), 57-67. doi:10.1016/j.virol.2006.07.040es_ES
dc.description.referencesNicaise, V. (2014). Crop immunity against viruses: outcomes and future challenges. Frontiers in Plant Science, 5. doi:10.3389/fpls.2014.00660es_ES
dc.description.referencesNieto, C., Morales, M., Orjeda, G., Clepet, C., Monfort, A., Sturbois, B., … Bendahmane, A. (2006). AneIF4Eallele confers resistance to an uncapped and non-polyadenylated RNA virus in melon. The Plant Journal, 48(3), 452-462. doi:10.1111/j.1365-313x.2006.02885.xes_ES
dc.description.referencesNováková, S., Flores-Ramírez, G., Glasa, M., Danchenko, M., Fiala, R., & Skultety, L. (2015). Partially resistant Cucurbita pepo showed late onset of the Zucchini yellow mosaic virus infection due to rapid activation of defense mechanisms as compared to susceptible cultivar. Frontiers in Plant Science, 6. doi:10.3389/fpls.2015.00263es_ES
dc.description.referencesOhki, T., Akita, F., Mochizuki, T., Kanda, A., Sasaya, T., & Tsuda, S. (2010). The protruding domain of the coat protein of Melon necrotic spot virus is involved in compatibility with and transmission by the fungal vector Olpidium bornovanus. Virology, 402(1), 129-134. doi:10.1016/j.virol.2010.03.020es_ES
dc.description.referencesPacheco, R., García-Marcos, A., Manzano, A., de Lacoba, M. G., Camañes, G., García-Agustín, P., … Tenllado, F. (2012). Comparative Analysis of Transcriptomic and Hormonal Responses to Compatible and Incompatible Plant-Virus Interactions that Lead to Cell Death. Molecular Plant-Microbe Interactions®, 25(5), 709-723. doi:10.1094/mpmi-11-11-0305es_ES
dc.description.referencesPadmanabhan, M. S., Shiferaw, H., & Culver, J. N. (2006). The Tobacco mosaic virus Replicase Protein Disrupts the Localization and Function of Interacting Aux/IAA Proteins. Molecular Plant-Microbe Interactions®, 19(8), 864-873. doi:10.1094/mpmi-19-0864es_ES
dc.description.referencesPallas, V., & García, J. A. (2011). How do plant viruses induce disease? Interactions and interference with host components. Journal of General Virology, 92(12), 2691-2705. doi:10.1099/vir.0.034603-0es_ES
dc.description.referencesPark, S.-W., Li, W., Viehhauser, A., He, B., Kim, S., Nilsson, A. K., … Lawrence, C. B. (2013). Cyclophilin 20-3 relays a 12-oxo-phytodienoic acid signal during stress responsive regulation of cellular redox homeostasis. Proceedings of the National Academy of Sciences, 110(23), 9559-9564. doi:10.1073/pnas.1218872110es_ES
dc.description.referencesPeng, H., Li, S., Wang, L., Li, Y., Li, Y., Zhang, C., & Hou, X. (2013). Turnip mosaic virus induces expression of the LRR II subfamily genes and regulates the salicylic acid signaling pathway in non-heading Chinese cabbage. Physiological and Molecular Plant Pathology, 82, 64-72. doi:10.1016/j.pmpp.2013.01.006es_ES
dc.description.referencesRodrigo, G., Carrera, J., Ruiz-Ferrer, V., del Toro, F. J., Llave, C., Voinnet, O., & Elena, S. F. (2012). A Meta-Analysis Reveals the Commonalities and Differences in Arabidopsis thaliana Response to Different Viral Pathogens. PLoS ONE, 7(7), e40526. doi:10.1371/journal.pone.0040526es_ES
dc.description.referencesRodriguez, M. C., Conti, G., Zavallo, D., Manacorda, C. A., & Asurmendi, S. (2014). TMV-Cg Coat Protein stabilizes DELLA proteins and in turn negatively modulates salicylic acid-mediated defense pathway during Arabidopsis thalianaviral infection. BMC Plant Biology, 14(1). doi:10.1186/s12870-014-0210-xes_ES
dc.description.referencesScalschi, L., Sanmartín, M., Camañes, G., Troncho, P., Sánchez-Serrano, J. J., García-Agustín, P., & Vicedo, B. (2014). Silencing ofOPR3in tomato reveals the role of OPDA in callose deposition during the activation of defense responses againstBotrytis cinerea. The Plant Journal, 81(2), 304-315. doi:10.1111/tpj.12728es_ES
dc.description.referencesScalschi, L., Vicedo, B., Camañes, G., Fernandez-Crespo, E., Lapeña, L., González-Bosch, C., & García-Agustín, P. (2012). Hexanoic acid is a resistance inducer that protects tomato plants againstPseudomonas syringaeby priming the jasmonic acid and salicylic acid pathways. Molecular Plant Pathology, 14(4), 342-355. doi:10.1111/mpp.12010es_ES
dc.description.referencesSerra-Soriano, M., Pallás, V., & Navarro, J. A. (2014). A model for transport of a viral membrane protein through the early secretory pathway: minimal sequence and endoplasmic reticulum lateral mobility requirements. The Plant Journal, 77(6), 863-879. doi:10.1111/tpj.12435es_ES
dc.description.referencesTaheri, P., & Tarighi, S. (2010). Riboflavin induces resistance in rice against Rhizoctonia solani via jasmonate-mediated priming of phenylpropanoid pathway. Journal of Plant Physiology, 167(3), 201-208. doi:10.1016/j.jplph.2009.08.003es_ES
dc.description.referencesTaheri, P., & Tarighi, S. (2011). A survey on basal resistance and riboflavin-induced defense responses of sugar beet against Rhizoctonia solani. Journal of Plant Physiology, 168(10), 1114-1122. doi:10.1016/j.jplph.2011.01.001es_ES
dc.description.referencesTamogami, S., Noge, K., Abe, M., Agrawal, G. K., & Rakwal, R. (2012). Methyl jasmonate is transported to distal leaves via vascular process metabolizing itself into JA-Ile and triggering VOCs emission as defensive metabolites. Plant Signaling & Behavior, 7(11), 1378-1381. doi:10.4161/psb.21762es_ES
dc.description.referencesUeki, S., & Citovsky, V. (2002). The systemic movement of a tobamovirus is inhibited by a cadmium-ion-induced glycine-rich protein. Nature Cell Biology, 4(7), 478-486. doi:10.1038/ncb806es_ES
dc.description.referencesVatén, A., Dettmer, J., Wu, S., Stierhof, Y.-D., Miyashima, S., Yadav, S. R., … Helariutta, Y. (2011). Callose Biosynthesis Regulates Symplastic Trafficking during Root Development. Developmental Cell, 21(6), 1144-1155. doi:10.1016/j.devcel.2011.10.006es_ES
dc.description.referencesVicedo, B., Flors, V., de la O Leyva, M., Finiti, I., Kravchuk, Z., Real, M. D., … González-Bosch, C. (2009). Hexanoic Acid-Induced Resistance Against Botrytis cinerea in Tomato Plants. Molecular Plant-Microbe Interactions®, 22(11), 1455-1465. doi:10.1094/mpmi-22-11-1455es_ES
dc.description.referencesVlot, A. C., Dempsey, D. A., & Klessig, D. F. (2009). Salicylic Acid, a Multifaceted Hormone to Combat Disease. Annual Review of Phytopathology, 47(1), 177-206. doi:10.1146/annurev.phyto.050908.135202es_ES
dc.description.referencesWang, X., Sager, R., Cui, W., Zhang, C., Lu, H., & Lee, J.-Y. (2013). Salicylic Acid Regulates Plasmodesmata Closure during Innate Immune Responses in Arabidopsis. The Plant Cell, 25(6), 2315-2329. doi:10.1105/tpc.113.110676es_ES
dc.description.referencesZhu, F., Xi, D.-H., Yuan, S., Xu, F., Zhang, D.-W., & Lin, H.-H. (2014). Salicylic Acid and Jasmonic Acid Are Essential for Systemic Resistance Against Tobacco mosaic virus in Nicotiana benthamiana. Molecular Plant-Microbe Interactions®, 27(6), 567-577. doi:10.1094/mpmi-11-13-0349-res_ES
dc.description.referencesZhu, S., Gao, F., Cao, X., Chen, M., Ye, G., Wei, C., & Li, Y. (2005). The Rice Dwarf Virus P2 Protein Interacts with ent-Kaurene Oxidases in Vivo, Leading to Reduced Biosynthesis of Gibberellins and Rice Dwarf Symptoms. Plant Physiology, 139(4), 1935-1945. doi:10.1104/pp.105.072306es_ES
dc.description.sponsorshipThis work has been supported by grants from the Spanish Ministry of Science and Innovation (AGL2010-22300-C03-01-02, AGL2013-49023-C03-01-02-R and BIO2014-54862-R), co-funded by the European Regional Development Fund.es_ES
dc.description.upvformatpfin15es_ES
dc.description.upvformatpinicio1es_ES
dc.description.volume8es_ES
dc.identifier.doi10.3389/fpls.2017.01793es_ES
dc.identifier.eissn1664-462Xes_ES
dc.identifier.pmcidPMC5655017es_ES
dc.identifier.pmid29104580es_ES
dc.identifier.urihttps://riunet.upv.es/handle/10251/148904
dc.languageIngléses_ES
dc.publisherFrontiers Media SAes_ES
dc.relation.ispartofFrontiers in Plant Sciencees_ES
dc.relation.pasarelaS\357672es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/MINECO//BIO2014-54862-R/ES/INTERACCIONES ENTRE FACTORES VIRALES Y DEL HUESPED IMPLICADOS EN LOS PROCESOS DE MOVIMIENTO Y PATOGENESIS EN CULTIVOS DE INTERES AGRONOMICO/es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/MINECO//AGL2013-49023-C3-1-R/ES/DETERMINACION DE PROTEINAS, MARCADORES DE ESTRES OXIDATIVO Y MODIFICACIONES EPIGENETICAS COMO POTENCIALES BIOMARCADORES PARA LA DETECCION TEMPRANA DE ESTRESES EN CULTIVOS ECON/es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/MICINN//AGL2010-22300-C03-02/ES/INMUNIDAD INDUCIDA POR EL ACIDO HEXANOICO EN SOLANACEAS Y CITRICOS PARA EL DESARROLLO DE UNA AGRICULTURA SOSTENIBLE. UNA APROXIMACION METABOLOMICA./es_ES
dc.relation.publisherversionhttps://doi.org/10.3389/fpls.2017.01793es_ES
dc.relation.references10.1111/mpp.12204es_ES
dc.relation.references10.1016/j.pmpp.2013.11.001es_ES
dc.relation.references10.1016/S0261-2194(00)00031-4es_ES
dc.relation.references10.3389/fpls.2014.00488es_ES
dc.relation.references10.1016/j.plantsci.2008.02.008es_ES
dc.relation.references10.1104/pp.116.4.1379es_ES
dc.relation.references10.1111/tpj.12964es_ES
dc.relation.references10.1034/j.1399-3054.2002.1140201.xes_ES
dc.relation.references10.1016/j.coviro.2015.11.003es_ES
dc.relation.references10.1093/aob/mcw216es_ES
dc.relation.references10.1146/annurev.phyto.45.062806.094422es_ES
dc.relation.references10.1007/s00425-014-2115-1es_ES
dc.relation.references10.1104/pp.112.211011es_ES
dc.relation.references10.1111/mpp.12112es_ES
dc.relation.references10.1111/j.1365-313X.2007.03299.xes_ES
dc.relation.references10.1111/j.1365-313X.2007.03397.xes_ES
dc.relation.references10.1046/j.1365-313X.1996.10010061.xes_ES
dc.relation.references10.1111/nph.12661es_ES
dc.relation.references10.1016/j.coviro.2015.01.001es_ES
dc.relation.references10.1128/JVI.03573-12es_ES
dc.relation.references10.1099/vir.0.81793-0es_ES
dc.relation.references10.1016/j.virol.2009.08.042es_ES
dc.relation.references10.1046/j.1365-313X.1998.00061.xes_ES
dc.relation.references10.1016/S0166-0934(03)00224-6es_ES
dc.relation.references10.1111/j.1364-3703.2008.00474.xes_ES
dc.relation.references10.1038/nrmicro3117es_ES
dc.relation.references10.1111/j.1399-3054.2005.00581.xes_ES
dc.relation.references10.3389/fpls.2013.00154es_ES
dc.relation.references10.1104/pp.111.180042es_ES
dc.relation.references10.1016/S0007-1536(77)80074-0es_ES
dc.relation.references10.1105/tpc.111.087742es_ES
dc.relation.references10.1111/j.1365-3059.2008.01891.xes_ES
dc.relation.references10.1111/j.1365-313X.2006.02712.xes_ES
dc.relation.references10.1094/MPMI-07-13-0190-Res_ES
dc.relation.references10.1105/tpc.113.111658es_ES
dc.relation.references10.1016/j.pbi.2005.05.015es_ES
dc.relation.references10.1094/MPMI-18-0428es_ES
dc.relation.references10.1016/j.tplants.2016.08.002es_ES
dc.relation.references10.3389/fpls.2014.00004es_ES
dc.relation.references10.4161/psb.24408es_ES
dc.relation.references10.1016/j.virol.2006.07.040es_ES
dc.relation.references10.3389/fpls.2014.00660es_ES
dc.relation.references10.1111/j.1365-313X.2006.02885.xes_ES
dc.relation.references10.3389/fpls.2015.00263es_ES
dc.relation.references10.1016/j.virol.2010.03.020es_ES
dc.relation.references10.1094/MPMI-11-11-0305es_ES
dc.relation.references10.1094/MPMI-19-0864es_ES
dc.relation.references10.1099/vir.0.034603-0es_ES
dc.relation.references10.1073/pnas.1218872110es_ES
dc.relation.references10.1016/j.pmpp.2013.01.006es_ES
dc.relation.references10.1371/journal.pone.0040526es_ES
dc.relation.references10.1186/s12870-014-0210-xes_ES
dc.relation.references10.1111/tpj.12728es_ES
dc.relation.references10.1111/mpp.12010es_ES
dc.relation.references10.1111/tpj.12435es_ES
dc.relation.references10.1016/j.jplph.2009.08.003es_ES
dc.relation.references10.1016/j.jplph.2011.01.001es_ES
dc.relation.references10.4161/psb.21762es_ES
dc.relation.references10.1038/ncb806es_ES
dc.relation.references10.1016/j.devcel.2011.10.006es_ES
dc.relation.references10.1094/MPMI-22-11-1455es_ES
dc.relation.references10.1146/annurev.phyto.050908.135202es_ES
dc.relation.references10.1105/tpc.113.110676es_ES
dc.relation.references10.1094/MPMI-11-13-0349-Res_ES
dc.relation.references10.1104/pp.105.072306es_ES
dc.rightsReconocimiento (by)es_ES
dc.rights.accessRightsAbiertoes_ES
dc.subjectMNSVes_ES
dc.subjectCucumis meloes_ES
dc.subjectPriming by natural compoundses_ES
dc.subjectHexanoic acides_ES
dc.subjectOPDAes_ES
dc.subjectSalicylic acides_ES
dc.titleHexanoic Acid Treatment Prevents Systemic MNSV Movement in Cucumis melo Plants by Priming Callose Deposition Correlating SA and OPDA Accumulationes_ES
dc.typeArtículoes_ES
dc.type.versioninfo:eu-repo/semantics/publishedVersiones_ES
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person.identifier246872
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upv.uuide6c7239f-2c95-4cd7-bc9f-ff3b4865737bes_ES

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