Cambios fisiológicos y mecanismos genéticos asociados a la marchitez vascular causada por Fusarium en tomate: una revisión actualizada

dc.audienceInvestigadorspa
dc.audience.contentCientíficospa
dc.contributor.authorCarmona, Sandra L.
dc.contributor.authorVillarreal Navarrete, Andrea
dc.contributor.authorDiana Burbano, David
dc.contributor.authorSoto Suárez, Mauricio
dc.coverage.countryColombiaspa
dc.date.accessioned2024-09-20T14:24:04Z
dc.date.available2024-09-20T14:24:04Z
dc.date.created2020-08-10
dc.date.issued2020
dc.description.abstractEl cultivo de tomate (Solanum lycopersicum L.), una de las hortalizas más cultivadas en el mundo, se enfrenta a diferentes patógenos del suelo que afectan su morfología, fisiología, bioquímica y regulación genética de las plantas. El hongo fitopatógeno Fusarium oxysporum f. sp. lycopersici (Fol) agente causal de la marchitez vascular del tomate causa pérdidas superiores al 60% en este cultivo. En esta revisión se presentan los mecanismos fisiológicos, bioquímicos y moleculares desarrollados en la interacción tomate – Fol. La co-evolución entre plantas y patógenos ha facilitado el desarrollo de mecanismos de defensa en las plantas que les permite protegerse frente a los efectos nocivos de la invasión por parte del patógeno, mientras que los patógenos implementan estrategias para imponerse frente a la resistencia de las plantas. Las consecuencias fisiológicas del ataque por Fol incluyen respuestas al déficit hídrico, regulaciones en la conductancia estomática, cambios en la fotosíntesis, así como alteraciones en los contenidos de clorofila y su fluorescencia. Estos cambios pueden ser explicados, en parte, con base en respuestas oxidativas, producción de metabolitos secundarios y activación de vías de señalización hormonales que hacen parte de una compleja red bioquímica activada tras la infección por el patógeno.spa
dc.description.productionsystemsTomatespa
dc.description.scientificnameSolanum lycopersicum
dc.format.mimetypeapplication/pdf
dc.identifierhttps://revistas.unicordoba.edu.co/index.php/temasagrarios/article/view/2457
dc.identifier.doi10.21897/rta.v25i2.2457
dc.identifier.instnameinstname:Corporación colombiana de investigación agropecuaria AGROSAVIAspa
dc.identifier.issn2389-9182
dc.identifier.reponamereponame:Biblioteca Digital Agropecuaria de Colombiaspa
dc.identifier.urihttp://hdl.handle.net/20.500.12324/40148
dc.language.isospa
dc.publisherUniversidad de Córdobaspa
dc.publisher.placeCórdoba (Colombia)spa
dc.relation.citationendpage189
dc.relation.citationissue2
dc.relation.citationstartpage166
dc.relation.citationvolume25
dc.relation.ispartofjournalTemas Agrariosspa
dc.relation.referencesAbbashar, A. M. 2003. Investigations On Fusarium oxysporum f. sp. lycopersici The Casual Agent Of Tomato Wilt (Lycopersicon esculentum Mill) (Issue March). University of Khartoum.spa
dc.relation.referencesÁdám, A., Nagy, Z., Kátay, G., Mergenthaler, E. and Viczián, O. 2018. Signals of Systemic Immunity in Plants: Progress and Open Questions. International Journal of Molecular Sciences, 19(4), 1146. https://doi.org/10.3390/ijms19041146spa
dc.relation.referencesAgronet. 2020. Base Agrícola EVA 2007-2019 (P)_12_02_2020.spa
dc.relation.referencesAkhter, A., Hage-Ahmed, K., Soja, G. and Steinkellner, S. 2015. Compost and biochar alter mycorrhization, tomato root exudation, and development of Fusarium oxysporum f. sp. lycopersici. Frontiers in Plant Science, 6, 529. https://doi.org/10.3389/fpls.2015.00529spa
dc.relation.referencesAlsamir, M., Mahmood, T., Ahmad, N. and Trethowan, R. 2017. Distribution of organic metabolites after Fusarium wilt incidence in tomato (Solanum esculentum L.). Australian Journal of Crop Science, 11(9): 1123–1129. https://doi.org/10.21475/ajcs.17.11.09.pne536spa
dc.relation.referencesAndersen, E., Ali, S., Byamukama, E., Yen, Y. and Nepal, M. 2018. Disease Resistance Mechanisms in Plants. Genes, 9(7): 339. https://doi.org/10.3390/genes9070339spa
dc.relation.referencesArbona, V., Argamasilla, R. and Gómez-cadenas, A. 2010. Common and divergent physiological , hormonal and metabolic responses of Arabidopsis thaliana and Thellungiella halophila to water and salt stress. Journal of Plant Physiology, 167(16):1342–1350. https://doi.org/10.1016/j.jplph.2010.05.012spa
dc.relation.referencesAshraf, M. and Foolad, M. R. 2007. Roles of glycine betaine and proline in improving plant abiotic stress resistance. Environmental and Experimental Botany, 59(2): 206–216. https://doi.org/10.1016/j.envexpbot.2005.12.006spa
dc.relation.referencesAtkinson, N. and Urwin, P. 2012. The interaction of plant biotic and abiotic stresses: from genes to the field. Journal of Experimental Botany, 63(10): 3523–3544. https://doi.org/10.1093/jxb/err313spa
dc.relation.referencesAzcón-Bieto, J. and Talón, M. 2008. Fundamentos de fisiología vegetal. In McGrawHill. https://doi.org/10.1017/CBO9781107415324.004spa
dc.relation.referencesBaker, N. R. 2008. Chlorophyll Fluorescence: A Probe of Photosynthesis In Vivo. Annual Review of Plant Biology, 59(1): 89–113. https://doi.org/10.1146/annurev.arplant.59.032607.092759spa
dc.relation.referencesBasco, M. J., Bisen, K., Keswani, C. y Singh, H. B. 2017. Biological management of Fusarium wilt of tomato using biofortified vermicompost. Mycosphere, 8(3): 467–483. https://doi.org/10.5943/mycosphere/8/3/8spa
dc.relation.referencesBeckers, G. J. and Conrath, U. 2007. Priming for stress resistance: from the lab to the field. Current Opinion in Plant Biology, 10(4): 425–431. https://doi.org/10.1016/J.PBI.2007.06.002spa
dc.relation.referencesBen Rejeb, K., Abdelly, C. and Savouré, A. 2014. How reactive oxygen species and proline face stress together. Plant Physiology and Biochemistry, 80: 278–284. https://doi.org/10.1016/j.plaphy.2014.04.007spa
dc.relation.referencesBerger, S., Papadopoulos, M., Schreiber, U., Kaiser, W. and Roitsch, T. 2004. Complex regulation of gene expression, photosynthesis and sugar levels by pathogen infection in tomato. Physiologia Plantarum, 122(4): 419-428. https://doi.org/10.1111/j.1399-3054.2004.00433.xspa
dc.relation.referencesBoix-Ruíz, A., Gálvez-Patón, L., de Cara-García, M., Palmero-Llamas, D., Camacho-Ferre, F. and Tello-Marquina, J. C. 2015. Comparison of analytical techniques used to identify tomato-pathogenic strains of Fusarium oxysporum. Phytoparasitica, 43(4): 471-483. https://doi.org/10.1007/s12600-014-0444-zspa
dc.relation.referencesBoller, T. and Felix, G. 2009. A renaissance of elicitors: perception of microbe-associated molecular patterns and danger signals by pattern-recognition receptors. Annual Review of Plant Biology, 60, 379–406. https://doi.org/10.1146/annurev.arplant.57.032905.105346spa
dc.relation.referencesBrodersen, C. R. and McElrone, A. J. 2013. Maintenance of xylem Network Transport Capacity: A Review of Embolism Repair in Vascular Plants. Frontiers in Plant Science, 4, 108. https://doi.org/10.3389/fpls.2013.00108spa
dc.relation.referencesCarvalhais, L. C., Dennis, P. G., Badri, D. V., Tyson, G. W., Vivanco, J. M. and Schenk, P. M. 2013. Activation of the Jasmonic Acid Plant Defence Pathway Alters the Composition of Rhizosphere Bacterial Communities. PLoS ONE, 8(2): 1–5. https://doi.org/10.1371/journal.pone.0056457spa
dc.relation.referencesCatanzariti, A. M., Do, H. T. T., Bru, P., de Sain, M., Thatcher, L. F., Rep, M. and Jones, D. A. 2017. The tomato I gene for Fusarium wilt resistance encodes an atypical leucine-rich repeat receptor-like protein whose function is nevertheless dependent on SOBIR1 and SERK3/BAK1. Plant Journal, 89(6): 1195–1209. https://doi.org/10.1111/tpj.13458spa
dc.relation.referencesChaudhary, R. and Atamian, H. 2017. Resistance-Gene-Mediated Defense Responses against Biotic Stresses in the Crop Model Plant Tomato. Journal of Plant Pathology & Microbiology, 8(4): 1–11. https://doi.org/10.4172/2157-7471.1000404spa
dc.relation.referencesChaves, M. M., Flexas, J. and Pinheiro, C. 2009. Photosynthesis under drought and salt stress: Regulation mechanisms from whole plant to cell. Annals of Botany, 103(4): 551–560. https://doi.org/10.1093/aob/mcn125spa
dc.relation.referencesChekali, S., Gargouri, S., Paulitz, T., Nicol, J. M., Rezgui, M. and Nasraoui, B. 2011. Effects of Fusarium culmorum and water stress on durum wheat in Tunisia. Crop Protection, 30(6), 718–725. https://doi.org/10.1016/j.cropro.2011.01.007spa
dc.relation.referencesChoudhary, D. K. and Varma, A. 2016. Microbial-mediated Induced Systemic Resistance in Plants (D. K. Choudhary & A. Varma (Eds.); 1st ed.). Springer India.spa
dc.relation.referencesClayton, E. E. 1923. The Relation of Temperature to the Fusarium Wilt of the Tomato. American Journal of Botany, 10(2): 71. https://doi.org/10.2307/2435575spa
dc.relation.referencesCole, S. J., Yoon, A. J., Faull, K. F. and Diener, A. C. 2014. Host perception of jasmonates promotes infection by Fusarium oxysporum formae speciales that produce isoleucine- and leucine-conjugated jasmonates. Molecular Plant Pathology, 15(6): 589–600. https://doi.org/10.1111/mpp.12117spa
dc.relation.referencesConstantin, M. E., de Lamo, F. J., Vlieger, B. V., Rep, M. and Takken, F. L. W. 2019. Endophyte-Mediated Resistance in Tomato to Fusarium oxysporum Is Independent of ET, JA, and SA. Frontiers in Plant Science, 10, 1–14. https://doi.org/10.3389/fpls.2019.00979spa
dc.relation.referencesCouto, D. and Zipfel, C. 2016. Regulation of pattern recognition receptor signalling in plants. Nature Reviews Immunology, 16(9): 537–552. https://doi.org/10.1038/nri.2016.77spa
dc.relation.referencesDean, R., Van Kan, J. A. L., Pretorius, Z. A., Hammond-kosack, K. E., Di Pietro, A., Spanu, P. D., Rudd, J. J., Dickman, M., Kahmann, R., Ellis, J. and Foster, G. D. 2012. The Top 10 fungal pathogens in molecular plant pathology. Molecular Plant Pathology, 13(4): 414-430. https://doi.org/10.1111/j.1364-3703.2011.00783.xspa
dc.relation.referencesDehgahi, R., Subramaniam, S., Zakaria, L., Joniyas, A., Firouzjahi, F. B., Haghnama, K. and Razinataj, M. 2015. Review of Research on Fungal Pathogen Attack and Plant Defense Mechanism against Pathogen. International Journal of Scientific Research in Agricultural Sciences, 2(8): 197–208. https://doi.org/10.12983/ijsras-2015-p0197-0208spa
dc.relation.referencesDi Pietro, A., Madrid, M. P., Caracuel, Z., Delgado-Jarana, J. and Roncero, M. I. G. 2003. Fusarium oxysporum: Exploring the molecular arsenal of a vascular wilt fungus. Molecular Plant Pathology, 4(5): 315–325. https://doi.org/10.1046/j.1364-3703.2003.00180.xspa
dc.relation.referencesDi, X., Gomila, J. O. and Takken, F. L. W. 2017. Involvement of salicylic acid , ethylene and jasmonic acid signalling pathways in the susceptibility of tomato to Fusarium oxysporum. Molecular Plant Pathology, 18(7): 1024–1035.spa
dc.relation.referencesDmitriev, a P. 2003. Signal Molecules for Plant Defense Responses to Biotic Stress. Text, 50(3): 417-425.spa
dc.relation.referencesDoares, S. H., Syrovetst, T., Weilert, E. W. and Ryan, C. A. 1995. Oligogalacturonides and chitosan activate plant defensive genes through the octadecanoid pathway. 92, 4095-4098. http://www.pnas.org/content/pnas/92/10/4095.full.pdfspa
dc.relation.referencesDong, X., Xiong, Y., Ling, N., Shen, Q. and Guo, S. 2014. Fusaric acid accelerates the senescence of leaf in banana when infected by Fusarium. World Journal of Microbiology and Biotechnology, 30(4): 1399–1408. https://doi.org/10.1007/s11274-013-1564-1spa
dc.relation.referencesDuniway, J. 1971. Water relations of Fusarium wilt. Physiology Plant Pathology, 1, 539–548.spa
dc.relation.referencesFAO. 2020. Faostat: Production quantities of Tomatoes by country.spa
dc.relation.referencesFraire-Velázquez, S., Rodríguez-Guerra, R. and Sánchez-Calderón, L. 2011. Abiotic and Biotic Stress Response Crosstalk in Plants. In A. Shank (Ed.), Abiotic Stress Response in Plants - Physiological, Biochemical and Genetic Perspectives (InTech Eur, p. 346).spa
dc.relation.referencesFrancia, D., Demaria, D., Calderini, O., Ferraris, L., Valentino, D., Arcioni, S., Tamietti, G. and Cardinale, F. 2007. Wounding induces resistance to pathogens with different lifestyles in tomato: Role of ethylene in cross-protection. Plant, Cell and Environment, 30(11): 1357–1365. https://doi.org/10.1111/j.1365-3040.2007.01709.xspa
dc.relation.referencesFreitas De Campos, M., Carvalho, K. De, Suano, F., Souza, D. and Jamil, C. 2011. Drought tolerance and antioxidant enzymatic activity in transgenic ‘ Swingle ’citrumelo plants over-accumulating proline. Environmental and Experimental Botany, 72, 242–250. https://doi.org/10.1016/j.envexpbot.2011.03.009spa
dc.relation.referencesGarcía-Enciso, E. L., Benavides-Mendoza, A., Flores-López, M. L., Robledo-Olivo, A., Juárez-Maldonado, A. and González-Morales, S. 2018. A Molecular Vision of the Interaction of Tomato Plants and Fusarium oxysporum f. sp. lycopersic. In Fusarium - Plant Diseases, Pathogen Diversity, Genetic Diversity, Resistance and Molecular Markers. InTech. https://doi.org/10.5772/intechopen.72127spa
dc.relation.referencesGoltsev, V. N., Kalaji, H. M., Paunov, M., Bąba, W., Horaczek, T., Mojski, J., Kociel, H. and Allakhverdiev, S. I. 2016. Variable chlorophyll fluorescence and its use for assessing physiological condition of plant photosynthetic apparatus. Russian Journal of Plant Physiology, 63(6), 869–893. https://doi.org/10.1134/S1021443716050058spa
dc.relation.referencesGonzalez-Cendales, Y., Catanzariti, A.-M., Baker, B., Mcgrath, D. J. and Jones, D. A. 2016. Identification of I-7 expands the repertoire of genes for resistance to Fusarium wilt in tomato to three resistance gene classes. Molecular Plant Pathology, 17(3): 448–463. https://doi.org/10.1111/mpp.12294spa
dc.relation.referencesHenry, G., Thonart, P. and Ongena, M. 2012. PAMPs, MAMPs, DAMPs and others: an update on the diversity of plant immunity elicitors. Biotechnologie, Agronomie, Société et …, 16(2), 12.spa
dc.relation.referencesHouterman, P. M., Cornelissen, B. J. C. and Rep, M. 2008. Suppression of plant resistance gene-based immunity by a fungal effector. PLoS Pathogens, 4(5):1–6. https://doi.org/10.1371/journal.ppat.1000061spa
dc.relation.referencesHuot, B., Yao, J., Montgomery, B. L. and He, S. Y. 2014. Growth-defense tradeoffs in plants: A balancing act to optimize fitness. Molecular Plant, 7(8): 1267–1287. https://doi.org/10.1093/mp/ssu049spa
dc.relation.referencesInami, K., Yoshioka-Akiyama, C., Morita, Y., Yamasaki, M., Teraoka, T. and Arie, T. 2012. A Genetic Mechanism for Emergence of Races in Fusarium oxysporum f. sp. lycopersici: Inactivation of Avirulence Gene AVR1 by Transposon Insertion. PLoS ONE, 7(8), e44101. https://doi.org/10.1371/journal.pone.0044101spa
dc.relation.referencesIto, S. ichi, Ihara, T., Tamura, H., Tanaka, S., Ikeda, T., Kajihara, H., Dissanayake, C., Abdel-Motaal, F. F. and El-Sayed, M. A. 2007. α-Tomatine, the major saponin in tomato, induces programmed cell death mediated by reactive oxygen species in the fungal pathogen Fusarium oxysporum. FEBS Letters, 581(17): 3217–3222. https://doi.org/10.1016/j.febslet.2007.06.010spa
dc.relation.referencesJayamohan, N. S., Patil, S. V. and Kumudini, B. S. 2018. Reactive oxygen species (ROS) and antioxidative enzyme status in Solanum lycopersicum on priming with fluorescent Pseudomonas spp. against Fusarium oxysporum. Biologia, 73(11): 1073–1082. https://doi.org/10.2478/s11756-018-0125-3spa
dc.relation.referencesJiao, J., Zhou, B., Zhu, X., Gao, Z. and Liang, Y. 2013. Fusaric acid induction of programmed cell death modulated through nitric oxide signalling in tobacco suspension cells. Planta, 238(4): 727–737. https://doi.org/10.1007/s00425-013-1928-7spa
dc.relation.referencesJogaiah, S., Abdelrahman, M., Tran, L. S. P. and Ito, S. I. 2018. Different mechanisms of Trichoderma virens-mediated resistance in tomato against Fusarium wilt involve the jasmonic and salicylic acid pathways. Molecular Plant Pathology, 19(4): 870–882. https://doi.org/10.1111/mpp.12571spa
dc.relation.referencesJones, D. and Takemoto, D. 2004. Plant innate immunity - direct and indirect recognition of general and specific pathogen-associated molecules. Current Opinion in Immunology, 16(1): 48–62. https://doi.org/10.1016/j.coi.2003.11.016spa
dc.relation.referencesJones, J. D. G. and Dangl, J. L. 2006. The plant immune system. Nature Reviews, 444, 323–329. https://doi.org/10.1038/nature05286spa
dc.relation.referencesJones, J. D. G., Vance, R. E. and Dangl, J. L. 2016. Intracellular innate immune surveillance devices in plants and animals. In Science 354 (6316): 1-8. American Association for the Advancement of Science. https://doi.org/10.1126/science.aaf6395spa
dc.relation.referencesKavroulakis, N., Doupis, G., Papadakis, I. E., Ehaliotis, C. and Papadopoulou, K. K. 2018. Tolerance of tomato plants to water stress is improved by the root endophyte Fusarium solani FsK. Rhizosphere, 6, 77–85. https://doi.org/10.1016/j.rhisph.2018.04.003spa
dc.relation.referencesKavroulakis, N., Ntougias, S., Zervakis, G. I., Ehaliotis, C., Haralampidis, K. and Papadopoulou, K. K. 2007. Role of ethylene in the protection of tomato plants against soil-borne fungal pathogens conferred by an endophytic Fusarium solani strain. Journal of Experimental Botany, 58(14): 3853–3864. https://doi.org/10.1093/jxb/erm230spa
dc.relation.referencesKiirika, L. M., Stahl, F. and Wydra, K. 2013. Phenotypic and molecular characterization of resistance induction by single and combined application of chitosan and silicon in tomato against Ralstonia solanacearum. Physiological and Molecular Plant Pathology, 81, 1–12. https://doi.org/10.1016/j.pmpp.2012.11.002spa
dc.relation.referencesKról, P., Igielski, R., Pollmann, S. and Kepczyńska, E. 2015. Priming of seeds with methyl jasmonate induced resistance to hemi-biotroph Fusarium oxysporum f.sp. lycopersici in tomato via 12-oxo-phytodienoic acid, salicylic acid, and flavonol accumulation. Journal of Plant Physiology, 179, 122–132. https://doi.org/10.1016/j.jplph.2015.01.018spa
dc.relation.referencesKumar, A. and Verma, J. P. 2018. Does plant Microbe interaction confer stress tolerance in plants: A review? Microbiological Research, 207, 41–52. https://doi.org/10.1016/j.micres.2017.11.004spa
dc.relation.referencesLatowski, D., Surówka, E. and Strzałka, K. 2010. Regulatory Role of Components of Ascorbate Glutathione Pathway in Plant Stress Tolerance. In N. A. Anjum, S. Umar, & M.-T. Chan (Eds.), Ascorbate-Glutathione Pathway and Stress Tolerance in Plants. 1-443. Springer Netherlands. https://doi.org/10.1007/978-90-481-9404-9spa
dc.relation.referencesLiu, L., Sonbol, F. M., Huot, B., Gu, Y., Withers, J., Mwimba, M., Yao, J., He, S. Y. and Dong, X. 2016. Salicylic acid receptors activate jasmonic acid signalling through a non-canonical pathway to promote effector-triggered immunity. Nature Communications, 7, 1–10. https://doi.org/10.1038/ncomms13099spa
dc.relation.referencesLópez-Díaz, C., Rahjoo, V., Sulyok, M., Ghionna, V., Martín-Vicente, A., Capilla, J., Di Pietro, A. and López-Berges, M. S. 2017. Fusaric acid contributes to virulence of Fusarium oxysporum on plant and mammalian hosts. Molecular Plant Pathology. https://doi.org/10.1111/mpp.12536spa
dc.relation.referencesLorenzini, G., Guidi, L., Nali, C., Ciompi, S. and Soldatini, G. F. 1997. Photosynthetic response of tomato plants to vascular wilt diseases. Plant Science, 124(2): 143–152. https://doi.org/10.1016/S0168-9452(97)04600-1spa
dc.relation.referencesLund, S. T., Stall, R. E. and Klee, H. J. 1998. Ethylene regulates the susceptible response to pathogen infection in tomato. Plant Cell, 10(3): 371–382. https://doi.org/10.1105/tpc.10.3.371spa
dc.relation.referencesMaina, F. M., Hauschild, R. and Sikora, R. 2008. Protection of tomato plants against fusaric acid by resistance induction. In ©Journal of Applied Biosciences.1 (1). www.biosciences.elewa.orgspa
dc.relation.referencesMandal, S., Mallick, N. and Mitra, A. 2009. Salicylic acid-induced resistance to Fusarium oxysporum f. sp. lycopersici in tomato. Plant Physiology and Biochemistry, 47(7):642–649. https://doi.org/10.1016/j.plaphy.2009.03.001spa
dc.relation.referencesManokaran, R. and Jambhulkar, P. P. 2016. Study of induced systemic resistance in tomato against Fusarium oxysporum f. sp lycopersici causing wilt of tomato Study of induced systemic resistance in tomato against Fusarium oxysporum f. sp lycopersici causing wilt of tomato. 69, 539–542.spa
dc.relation.referencesMaqsood, A., Wu, H., Kamran, M., Altaf, H., Mustafa, A., Ahmar, S., Hong, N. T. T., Tariq, K., He, Q. and Chen, J. T. 2020. Variations in growth, physiology, and antioxidative defense responses of two tomato (Solanum lycopersicum L.) cultivars after co-infection of Fusarium oxysporum and Meloidogyne incognita. Agronomy, 10(2):1-25. https://doi.org/10.3390/agronomy10020159spa
dc.relation.referencesMarín-Ortiz, J. C., Gutierrez-Toro, N., Botero-Fernández, V. and Hoyos-Carvajal, L. M. 2020. Linking physiological parameters with visible/near-infrared leaf reflectance in the incubation period of vascular wilt disease. Saudi Journal of Biological Sciences, 27(1): 88–99. https://doi.org/10.1016/j.sjbs.2019.05.007spa
dc.relation.referencesMartínez-Medina, A., Fernández, I., Sánchez-Guzmán, M. J., Jung, S. C., Pascual, J. A. and Pozo, M. J. 2013. Deciphering the hormonal signalling network behind the systemic resistance induced by Trichoderma harzianum in tomato. Frontiers in Plant Science, 4, 1–12. https://doi.org/10.3389/fpls.2013.00206spa
dc.relation.referencesMaxwell, K. and Johnson, G. N. 2000. Chlorophyll a fl uorescence - a practical guide. Journal of Experimental Botany, 51(345): 659–668. https://doi.org/10.1093/jxb/51.345.659spa
dc.relation.referencesMcGovern, R. J. 2015. Management of tomato diseases caused by Fusarium oxysporum. Crop Protection, 73, 78–92. https://doi.org/10.1016/j.cropro.2015.02.021spa
dc.relation.referencesMelgarejo, L. M., Romero, M., Hernandez, S., Barrera, J., Solarte, E., Pérez, V., Rojas, A., Cruz, M., Moreno, L., Crespo, S. and Pérez, W. 2010. Experimentos en Fisiología Vegetal (U. N. de Colombia (Ed.); First edit). Universidad Nacional de Colombia.spa
dc.relation.referencesMes, J. J., Van Doorn, A. A., Wijbrandi, J., Simons, G., Cornelissen, B. J. C. and Haring, M. A. 2000. Expression of the Fusarium resistance gene I-2 colocalizes with the site of fungal containment. Plant Journal, 23(2), 183–193. https://doi.org/10.1046/j.1365-313X.2000.00765.xspa
dc.relation.referencesMichielse, C. B. and Rep, M. 2009. Pathogen profile update: Fusarium oxysporum. Molecular Plant Pathology, 10(3): 311-324. https://doi.org/10.1111/j.1364-3703.2009.00538.xspa
dc.relation.referencesNair, A., Kolet, S. P., Thulasiram, H. V. and Bhargava, S. 2015. Role of methyl jasmonate in the expression of mycorrhizal induced resistance against Fusarium oxysporum in tomato plants. Physiological and Molecular Plant Pathology, 92, 139–145. https://doi.org/10.1016/j.pmpp.2015.10.002spa
dc.relation.referencesNankishore, A. and Farrell, A. D. 2016. The response of contrasting tomato genotypes to combined heat and drought stress. Journal of Plant Physiology, 202, 75–82. https://doi.org/10.1016/j.jplph.2016.07.006spa
dc.relation.referencesNarasimhamurthy, K., Soumya, K., Udayashankar, A. C., Srinivas, C. and Niranjana, S. R. 2019. Elicitation of innate immunity in tomato by salicylic acid and Amomum nilgiricum against Ralstonia solanacearum. Biocatalysis and Agricultural Biotechnology, 22. 1-7 https://doi.org/10.1016/j.bcab.2019.101414spa
dc.relation.referencesNobori, T., Mine, A. and Tsuda, K. 2018. Molecular networks in plant-pathogen holobiont. FEBS Letters. https://doi.org/10.1002/1873-3468.13071spa
dc.relation.referencesNogués, S., Cotxarrera, L., Alegre, L. and Trillas, M. I. 2002. Limitations to photosynthesis in tomato leaves induced by Fusarium wilt. New Phytologist, 154(2): 461–470. https://doi.org/10.1046/j.1469-8137.2002.00379.xspa
dc.relation.referencesPeriyannan, S., Milne, R. J., Figueroa, M., Lagudah, E. S. and Dodds, P. N. 2017. An overview of genetic rust resistance: From broad to specific mechanisms. In PLoS Pathogens 13(7). Public Library of Science. https://doi.org/10.1371/journal.ppat.1006380spa
dc.relation.referencesPieterse, C. M. J., Leon-Reyes, A., van Der Ent, S. and van Wees, S. C. M. 2009. Networking by small-molecule hormones in plant immunity. Nature Chemical Biology, 5(5): 308–316. https://doi.org/10.1038/nchembio.164spa
dc.relation.referencesPieterse, C. M. J., van der Does, D., Zamioudis, C., Leon-Reyes, A. and Van Wees, S. C. M. 2012. Hormonal Modulation of Plant Immunity. Annual Review of Cell and Developmental Biology, 28(1): 489–521. https://doi.org/10.1146/annurev-cellbio-092910-154055spa
dc.relation.referencesPinheiro, C. and Chaves, M. M. 2011. Photosynthesis and drought: Can we make metabolic connections from available data? Journal of Experimental Botany, 62(3): 869–882. https://doi.org/10.1093/jxb/erq340spa
dc.relation.referencesPitzschke, A., Schikora, A. and Hirt, H. 2009. MAPK cascade signalling networks in plant defence. Current Opinion in Plant Biology, 12(4): 421–426. https://doi.org/10.1016/j.pbi.2009.06.008spa
dc.relation.referencesPshibytko, N. L., Zenevich, L. A. and Kabashnikova, L. F. 2006. Changes in the photosynthetic apparatus during Fusarium wilt of tomato. Russian Journal of Plant Physiology, 53(1): 25–31.spa
dc.relation.referencesPusztahelyi, T. 2018. Chitin and chitin-related compounds in plant–fungal interactions. Mycology, 9(3): 189–201. https://doi.org/10.1080/21501203.2018.1473299spa
dc.relation.referencesQi, J., Song, C. P., Wang, B., Zhou, J., Kangasjärvi, J., Zhu, J. K. and Gong, Z. 2018. Reactive oxygen species signaling and stomatal movement in plant responses to drought stress and pathogen attack. Journal of Integrative Plant Biology, 60(9): 805–826. https://doi.org/10.1111/jipb.12654spa
dc.relation.referencesRamírez-Gómez, M. and Rodríguez, A. 2012. Mecanismos de defensa y respuestas de las plantas en la interacción micorrícica: una revisión. Revista Colombiana de Biotecnología, 14(1): 271–284.spa
dc.relation.referencesRep, M., van Der Does, H. C., Meijer, M., Van Wijk, R., Houterman, P. M., Dekker, H. L., De Koster, C. G. and Cornelissen, B. J. C. 2004. A small, cysteine-rich protein secreted by Fusarium oxysporum during colonization of xylem vessels is required for I-3-mediated resistance in tomato. Molecular Microbiology, 53(5): 1373-1383. https://doi.org/10.1111/j.1365-2958.2004.04177.xspa
dc.relation.referencesSaharan, V. and Pal, A. 2016. Chitosan Based Nanomaterials in Plant Growth and Protection. Springer India.spa
dc.relation.referencesSamadi, L. and Behboodi, B. 2006. Fusaric acid induces apoptosis in saffron root-tip cells: roles of caspase-like activity, cytochrome c, and H2O2. Planta, 225(1), 223–234. https://doi.org/10.1007/s00425-006-0345-6spa
dc.relation.referencesShah, J. 2009. Plants under attack: systemic signals in defence. Current Opinion in Plant Biology, 12(4): 459–464. https://doi.org/10.1016/j.pbi.2009.05.011spa
dc.relation.referencesSharif, R., Mujtaba, M., Rahman, M. U., Shalmani, A., Ahmad, H., Anwar, T., Tianchan, D. and Wang, X. 2018. The Multifunctional Role of Chitosan in Horticultural crops: a review. Molecules, 23(872): 1–20. https://doi.org/10.3390/molecules23040872spa
dc.relation.referencesSingh, P., Singh, J., Ray, S., Rajput, R. S., Vaishnav, A., Singh, R. K. and Singh, H. B. 2020. Seed biopriming with antagonistic microbes and ascorbic acid induce resistance in tomato against Fusarium wilt Prachi. Microbiological Research, 237. https://doi.org/10.1016/j.micres.2020.126482spa
dc.relation.referencesSingh, V. K., Singh, H. B. and Upadhyay, R. S. 2017. Role of fusaric acid in the development of ‘Fusarium wilt’ symptoms in tomato: Physiological, biochemical and proteomic perspectives. Plant Physiology and Biochemistry, 118, 320–332. https://doi.org/10.1016/j.plaphy.2017.06.028spa
dc.relation.referencesSingh, V. K. and Upadhyay, R. S. 2014. Fusaric acid induced cell death and changes in oxidative metabolism of Solanum lycopersicum L. Botanical Studies, 55(1): 66. https://doi.org/10.1186/s40529-014-0066-2spa
dc.relation.referencesSoliman, M. H. and El-Mohamedy, R. S. R. 2017. Induction of defense-related physiological and antioxidant enzyme response against powdery mildew disease in okra (Abelmoschus esculentus L.) plant by using chitosan and potassium salts. Mycobiology. https://doi.org/10.5941/MYCO.2017.45.4.409spa
dc.relation.referencesSrinivas, C., Nirmala Devi, D., Narasimha Murthy, K., Mohan, C. D., Lakshmeesha, T. R., Singh, B. P., Kalagatur, N. K., Niranjana, S. R., Hashem, A., Alqarawi, A. A., Tabassum, B., Abd Allah, E. F. and Chandra Nayaka, S. 2019. Fusarium oxysporum f. sp. lycopersici causal agent of vascular wilt disease of tomato: Biology to diversity A review. Saudi Journal of Biological Sciences, 26(7): 1315–1324. https://doi.org/10.1016/j.sjbs.2019.06.002spa
dc.relation.referencesStahl, E., biology, J. B.-C. opinion in plant, and 2000. Plant pathogen arms races at the molecular level. Plant Bioloy. 3(4):299-304. Doi: 10.1016/s1369-5266(00)00083-2spa
dc.relation.referencesTakken, F. and Rep, M. 2010. The arms race between tomato and Fusarium oxysporum. In Molecular Plant Pathology 11(2):309–314. https://doi.org/10.1111/j.1364-3703.2009.00605.xspa
dc.relation.referencesThaler, J. S., Humphrey, P. T. and Whiteman, N. K. 2012. Evolution of jasmonate and salicylate signal crosstalk. Trends in Plant Science, 17(5):260–270. https://doi.org/10.1016/j.tplants.2012.02.010spa
dc.relation.referencesTripathy, B. C. hara. and Oelmüller, R. 2012. Reactive oxygen species generation and signaling in plants. Plant Signaling & Behavior, 7(12): 1621–1633. https://doi.org/10.4161/psb.22455spa
dc.relation.referencesVan der Does, H. C., Constantin, M. ., Houterman, P. M., Takken, F. L. W., Cornelissen, B. J. C., Haring, M. A., van den Burg, H. A. and Rep, M. 2018. Fusarium oxysporum colonizes the stem of resistant tomato plants , the extent varying with the R-gene present. European Journal of Plant Pathology, 154. 55-65.spa
dc.relation.referencesVan Loon, L. C., Rep, M. and Pieterse, C. M. J. 2006. Significance of Inducible Defense-related Proteins in Infected Plants. Annual Review of Phytopathology, 44(1), 135–162. https://doi.org/10.1146/annurev.phyto.44.070505.143425spa
dc.relation.referencesVidhyasekaran, P. 2016. Switching on Plant Innate Immunity Signaling Systems - Bioengineering and Molecular Manipulation of PAMP-PIMP-PRR Signaling Complex (F. Baluška & J. Vivanco (Eds.)). Springer International Publishing AG Switzerland. https://doi.org/10.1007/978-3-319-26118-8spa
dc.relation.referencesVilla-Martínez, A., Morales-morales, Hugo Armando., Pérez-Leal, R. y Soto-parra, Juan Manuel., Basurto-Sotelo, M. and E. M.-E. 2015. Situación actual en el control de Fusarium spp . y evaluación de la actividad antifúngica de extractos vegetales. Acta Agronomica, 64(2): 194-205. https://doi.org/http://dx.doi.org/10.15446/acag.v64n2.43358spa
dc.relation.referencesVillarreal, A. del P. 2013. Evaluación fisiológica de plantas de uchuva (Physalis peruviana L.), en la respuesta al estrés por anegamiento e infección de Fusarium oxysporum. 141.spa
dc.relation.referencesWagner, A., Michalek, W. and Jamiolkowska, A. 2006. Chlorophyll fluorescence measurements as indicators of fusariosis severity in tomato plants. Agronomy Research, 4(Speciel Issue), 461–464.spa
dc.relation.referencesWalters, D. R. 2015. Physiological responses of plants to attack. In Crop & Soil Systems Research Group (Wiley Blac),1. 248spa
dc.relation.referencesWalters, M. 2015. The plant innate immune system. Journal of Endocytobiosis and Cell Research, 26, 8–12.spa
dc.relation.referencesWang, F., Wu, N., Zhang, L., Ahammed, G. J., Chen, X., Xiang, X., Zhou, J., Xia, X., Shi, K., Yu, J., Foyer, C. H. and Zhou, Y. 2018. Light Signaling-dependent Regulation of Photoinhibition and Photoprotection in Tomato. Plant Physiology, 176, 1311–1326. https://doi.org/10.1104/pp.17.01143spa
dc.relation.referencesWiesel, L., Newton, A. C., Elliott, I., Booty, D., Gilroy, E. M., Birch, P. R. J. and Hein, I. 2014. Molecular effects of resistance elicitors from biological origin and their potential for crop protection. Frontiers in Plant Science, 5, 655. https://doi.org/10.3389/fpls.2014.00655spa
dc.relation.referencesYadeta, K. A. and J. Thomma, B. P. H. 2013. The xylem as battleground for plant hosts and vascular wilt pathogens. Frontiers in Plant Science, 4, 1–12. https://doi.org/10.3389/fpls.2013.00097spa
dc.relation.referencesYang, F., Wang, Y., Wang, J., Deng, W., Liao, L. and Li, M. 2011. Different eco-physiological responses between male and female Populus deltoides clones to waterlogging stress. Forest Ecology and Management, 262(11): 1963–1971. https://doi.org/10.1016/j.foreco.2011.08.039spa
dc.relation.referencesZaynab, M., Fatima, M., Abbas, S., Sharif, Y., Umair, M., Zafar, M. H. and Bahadar, K. 2018. Role of secondary metabolites in plant defense against pathogens. In Microbial Pathogenesis 124, 198–202. Academic Press. https://doi.org/10.1016/j.micpath.2018.08.034spa
dc.relation.referencesZehra, A., Meena, M., Dubey, M. K., Aamir, M. and Upadhyay, R. S. 2017. Synergistic effects of plant defense elicitors and Trichoderma harzianum on enhanced induction of antioxidant defense system in tomato against Fusarium wilt disease. Botanical Studies, 58(1). https://doi.org/10.1186/s40529-017-0198-2spa
dc.relation.referencesZhang, H., Zhang, Q., Zhai, H., Gao, S., Yang, L., Wang, Z., Xu, Y., Huo, J., Ren, Z., Zhao, N., Wang, X., Li, J., Liu, Q. and He, S. 2020. IbBBX24 Promotes the Jasmonic Acid Pathway and Enhances Fusarium Wilt Resistance in Sweet Potato. The Plant Cell, tpc.00641.2019. https://doi.org/10.1105/tpc.19.00641spa
dc.rightsAttribution-NonCommercial-ShareAlike 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/*
dc.sourceTemas Agrarios; vol. 25, Núm. 2 (2020): Temas Agrarios (Dec.);p. 166–189.spa
dc.subject.agrovocTomatespa
dc.subject.agrovocEstrés bióticospa
dc.subject.agrovocEstrés osmóticospa
dc.subject.agrovocRegulación de la expresión genéticaspa
dc.subject.agrovocurihttp://aims.fao.org/aos/agrovoc/c_7805
dc.subject.agrovocurihttp://aims.fao.org/aos/agrovoc/c_35769
dc.subject.agrovocurihttp://aims.fao.org/aos/agrovoc/c_35750
dc.subject.agrovocurihttp://aims.fao.org/aos/agrovoc/c_1ce66974
dc.subject.faoGenética vegetal y fitomejoramiento - F30spa
dc.subject.redHortalizas y plantas aromáticasspa
dc.titleCambios fisiológicos y mecanismos genéticos asociados a la marchitez vascular causada por Fusarium en tomate: una revisión actualizadaspa
dc.title.translatedPhysiological and genetic changes associated to vascular wilt of tomato caused by Fusarium: an updated reviewspa
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.type.driverinfo:eu-repo/semantics/article
dc.type.localArtículo científicospa
dc.type.localengarticleeng
dc.type.redcolhttps://purl.org/redcol/resource_type/ART
dc.type.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85

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