Control biorracional de hongos del género Fusarium
Los hongos del género Fusarium se encuentran distribuidos de manera universal debido a su capacidad para crecer en gran número de sustratos y a su eficaz mecanismo de dispersión; son de gran importancia a nivel agrícola y económico por los problemas fitosanitarios que ocasiona y las pérdidas de producción, que generalmente pueden llegar hasta el 100%. Investigadores y productores han trabajado conjuntamente para tratar de contrarrestar su impacto, en la búsqueda de soluciones diferentes a los químicos, por cuanto el nivel de resistencia que producen cada vez es más alto. El control biorracional que está referido al manejo inteligente de plagas, utiliza diferentes herramientas disponibles de manera efectiva y compatible entre sí, buscando reducir el impacto ambiental y en consecuencia sobre el ser humano. Los productos que se emplean para este control son aquellos de origen natural, biológicos o de síntesis química que tengan mínimo impacto ambiental.
Vinchira D., & Moreno, N. Control bioló¬gico: Camino a la agricultura moderna. (2019). Revista Colombiana de Biotecno¬logía, 21(1), 2-5. Available from: https://doi.org/10.15446/rev.colomb.biote. v21n1.80860
Acosta C. Control biorracional de plagas en cultivos, con equilibrio biológico. My Press. México (2018). Available from: https://www.mypress.mx/tecnologia/bio-rracionales-que-son-y-beneficios-am¬bientales-3628
Sharma, M., Guleria, S., Singh, K. et al. Mycovirus associated hypovirulence, a potential method for biological control of Fusarium species. VirusDis. 29, 134–140 (2018). Available from: https://ezproxy.unicolmayor.edu.co:2162/10.1007/s13337-018-0438-4
Maryani N, Sandoval-Denis M, Lombard L, Crous PW, Kema GHJ. New endemic Fusa¬rium species hitch-hiking with pathogenic Fusarium strains causing Panama disease in small-holder banana plots in Indone¬sia. Persoonia. (2019); 43: 48–69. Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7085855/
Orbati, M., Arzanlou, M., Sandoval-Denis, M. et al. Multigene phylogeny reveals new fungicolous species in the Fusarium tricinc¬tum species complex and novel hosts in the genus Fusarium from Iran. Mycol Pro¬gress 18, 119–133 (2019). https://ezproxy.unicolmayor.edu.co:2162/10.1007/s11557-018-1422-5
Leiva L, Manejo de problemas fitosanita¬rios del cultivo de gulupa (Passiflora edulis Sims.) medidas para temporada invernal. Instituto Colombiano Agropecuario ICA (2011). 00.09.43.12.C. Available from: https://repository.agrosavia.co/bitstream/handle/20.500.12324/2262/44992_60739.pdf?sequence=1&isAllowed=y
Castañeda E., Sánchez L., Evaluación del crecimiento de cuatro especies del gé¬nero Bacillus sp., primer paso para en¬tender su efecto biocontrolador so¬bre Fusarium sp. NOVA. 2016; 13 (26): 53-65 Available from: http://www.scie-lo.org.co/scielo.php?script=sci_arttex¬t&pid=S179424702016000200006&ln-g=en&nrm=iso&tlng=es
Srivastava S., Kadooka C., Uchida J., Fu¬sarium species as pathogen on orchids, (2018), Vol 207, Pages 188-195. Available from: https://www.sciencedirect.com/science/article/pii/S0944501317307218
Srinivasas C., Devi N., Murthy K., Fusarium oxysporum f. sp. lycopersici causal agent of vascular wilt disease of tomato: Biolo¬gy to diversity– A review. [Internet]. Scin-cedirect.com (2019), Vol 26, Pages 1315- 1324. Available from: https://ezproxy.unicolmayor.edu.co:2163/science/article/pii/S1319562X19301007
Ortiz M, Hoyos L. Description of the symp¬tomatology associated with fusariosis and its comparison with other diseases for the purple passion fruit (Passiflora edulis Sims.) in the Sumapaz region (Colombia). [Internet]. Scielo.org.co. 2012. Available from: http://www.scielo.org.co/pdf/rcch/v6n1/v6n1a11.pdf
Deepa N., Sreenivasa Y., Molecular me¬thods and key genes targeted for the detection of fumonisin producing Fusa¬rium verticillioides – An updated review. [Internet]. Scincedirect.com (2019). Vol 32. Available from: https://ezproxy.uni-colmayor.edu.co:2163/science/article/pii/ S2212429218306801
Villa A., Perez R., Morales H., Basurto M., Situación actual en el control de Fu-sarium spp. y evaluación de la actividad antifúngica de extractos vegetales. [In¬ternet]. Scielo.org.co. (2014) Available from: http://www.scielo.org.co/pdf/acag/v64n2/v64n2a11.pdf
Femenias A., Gatius F., Ramos A, Sanchisa V., Marín S. Use of hyperspectral imaging as a tool for Fusarium and deoxynivale¬nol risk management in cereals: A review. [Internet]. Scincedirect.com (2020). Vol 108. Available from: https://ezproxy.uni-colmayor.edu.co:2163/science/article/pii/ S0956713519304086
Cordoba Diaz J., Gerlach G., Otero T. Hon¬gos endófitos de Stanhopea tricornis (Or-chidaceae) en Colombia. Sociedad Colom¬biana de orquideología (2015). Available from: http://revista.sco.org.co/index.php/ orquideologia/article/view/88/pdf_83
Lopez S., Castaño J. Manejo integrado del mal de Panamá Fusarium oxysporum Schlechtend.: Fr. sp. cubense (E.F. SM.) W.C. Snyder & H.N. Hansen: una revi¬sión. Vol 22 n° 2. [Internet]. Scielo.org.co. 2019 Available from: http://www.scielo. org.co/scielo.php?script=sci_arttext&pi¬d=S0123-42262019000200011
Betancourth Garcia, C., Salazar González, C., Lagos Mora, L., Díaz Rodríguez, V., & Mora Chaves, S. (2020). Caracterización de Fusarium spp. asociado con la pudri¬ción basal de la cebolla de rama. Revista U.D.C.A Actualidad & Divulgación Cientí¬fica, 23(1). https://doi.org/10.31910/rudca. v23.n1.2020.1471
Henao E., Hernández C., Salazar C., Velas¬co M., Gómez E. Identificación molecular de aislamientos de Fusarium asociados a maracuyá en el Valle del Cauca, Colombia. Agron. Mesoam vol.29 n.1 San Pedro Jan./ Apr. 2018. Available from: https://www. scielo.sa.cr/scielo.php?script=sci_arttex¬t&pid=S1659-13212018000100056
Báez-Vallejoa N., Camarena D., Monri¬bot-Villanueva J. Forest tree associated bacteria for potential biological control of Fusarium solani and of Fusarium kuros-hium, causal agent of Fusarium dieback. [Internet]. Scincedirect.com (2020). Vol 235. Available from: https://ezproxy.uni¬colmayor.edu.co:2163/science/article/pii/ S0944501319309218
Medina-Romero, Y.M., Roque-Flores, G. & Macías-Rubalcava, M.L. Volatile organic compounds from endophytic fungi as in¬novative postharvest control of Fusarium oxysporum in cherry tomato fruits. Appl Microbiol Biotechnol 101, 8209–8222 (2017). https://ezproxy.unicolmayor.edu. co:2162/10.1007/s00253-017-8542-8
Guevara-Avendaño, E., Bravo-Castillo, K.R., Monribot-Villanueva, J.L. et al. Diffusible and volatile organic compounds produced by avocado rhizobacteria exhibit antifun¬gal effects against Fusarium kuroshium. Braz J Microbiol (2020). https://ezproxy. unicolmayor.edu.co:2162/10.1007/s42770- 020-00249-6
Bunbury-Blanchette A., Walker A., Tricho¬derma species show biocontrol potential in dual culture and greenhouse bioassays against Fusarium basal rot of onion. [In-ternet]. Scincedirect.com (2019). Vol 130 Pages 127-135. Available from: https://ezproxy.unicolmayor.edu.co:2163/science/article/pii/S1049964418305334
Meng, T., Wang, Q., Abbasi, P. et al. Deci¬phering differences in the chemical and microbial characteristics of healthy and Fusarium wilt-infected watermelon rhi-zosphere soils. Appl Microbiol Biotechnol 103, 1497–1509 (2019). https://ezproxy.unicolmayor.edu.co:2162/10.1007/s00253-018-9564-6
Naing, K.W., Nguyen, X.H., Anees, M. et al. Biocontrol of Fusarium wilt disease in to-mato by Paenibacillus ehimensis KWN38. World J Microbiol Biotechnol 31, 165–174 (2015). https://ezproxy.unicolmayor.edu.co:2162/10.1007/s11274-014-1771-4
Gowtham H., Hariprasad P., Chandra S., Niranjana S. Application of rhizobacteria antagonistic to Fusarium oxysporum f. sp. lycopersici for the management of Fusa-rium wilt in tomato. Vol 2 (2016), Pages 72-74. Available from: https://ezproxy.uni-colmayor.edu.co:2163/science/article/pii/S2452219816300477#
Jangira M. Pathaka R., Sharma S., Sharma S. Biocontrol mechanisms of Bacillus sp., isolated from tomato rhizosphere, against Fusarium oxysporum f. sp. Lycopersici. [Internet]. Scincedirect.com (2018). Vol 123 Pages 60-70. Available from: https://ezproxy.unicolmayor.edu.co:2163/science/article/pii/S1049964418301221
Corrales Ramírez LC, Sánchez Leal LC, Cuervo Andrade PhD JL, Joya JA, Márquez K. Efecto Biocontrolador de ’Bacillus’ spp., Frente a ’Fusarium’ sp., Bajo Condicio¬nes de Invernadero en Plantas de Tomillo (’Thymus Vulgaris l’.).[Internet] Nova. Ju¬nio 2012 Availabre from: https://hemero-teca.unad.edu.co/index.php/nova/article/view/518
Layton C, Maldonado E, Monroy L, Corra¬les Ramírez MSC LC, Sánchez Leal MSC LC. Bacillus spp.; perspectiva de su efec¬to biocontrolador mediante antibiosis en cultivos afectados por fitopatógenos. [Internet] Nova. 15 de diciembre de 2011. Available from: https://hemeroteca.unad.edu.co/index.php/nova/article/view/501
Ariza Y., Sánchez L. Determinación de me¬tabolitos secundarios a partir de Bacillus subtilis con efecto biocontrolador sobre Fusarium sp. Nova - Publicación Científica en Ciencias Biomédicas - Issn: 1794-2470 - Vol. 10 No. 18 Julio - Diciembre de 2012: 135 – 250. Available from: http://www.scielo.org.co/scielo.php?script=sci_arttex-t&pid=S179424702012000200002
Arya, N., Rana, A., Rajwar, A. et al. Bio¬control Efficacy of Siderophore Producing Indigenous Pseudomonas Strains Against Fusarium Wilt in Tomato. Natl. Acad. Sci. Lett. 41, 133–136 (2018). https://ezproxy.unicolmayor.edu.co:2162/10.1007/s40009-018-0630-5
Islam, M.A., Nain, Z., Alam, M.K. et al. In vitro study of biocontrol potential of rhizospheric Pseudomonas aeruginosa against Fusarium oxysporum cucume¬rinum f. sp.. Egypt J Biol Pest Control 28, 90 (2018). https://ezproxy.unicolmayor.edu.co:2162/10.1186/s41938-018-0097-1
Guo Z., Zhang X., Wu J., Yu J. In vitro in¬hibitory effect of the bacterium Serratia marcescens on Fusarium proliferatum growth and fumonisins production. 2020. Vol 143. Available fom: https://ezproxy.unicolmayor.edu.co:2163/science/article/pii/S1049964419306206
Tzu Li Y., Hwang S., Huang Y. Effects of Tri¬choderma asperellum on nutrient uptake and Fusarium wilt of tomato. [Internet]. Scincedirect.com (2018). Vol 110 Pages 275-282. Available from: https://ezproxy.unicolmayor.edu.co:2163/science/article/pii/S0261219417300868
Campanella V., Mandalá C., Angileri V., Meceli C. Management of common root rot and Fusarium foot rot of wheat using Brassica carinata break crop green manu¬re. 2020 Vol 130. Available from: https://ezproxy.unicolmayor.edu.co:2163/science/article/pii/S0261219419304193
Scaglioni, P.T., Pagnussatt, F.A., Lemos, A.C. et al. Nannochloropsis sp. and Spirulina sp. as a Source of Antifungal Compounds to Mitigate Contamination by Fusarium gra¬minearum Species Complex. Curr Micro¬biol 76, 930–938 (2019). https://ezproxy.unicolmayor.edu.co:2162/10.1007/s00284-019-01663-2
Zabka M., Pavela R. Review Chapter: Fu¬sarium Genus and Essential Oils. Natural Antimicrobial Agents. Sustainable Deve¬lopment and Biodiversity. (2018) vol 19. Springer, Cham. Available from: https://ezproxy.unicolmayor.edu.co:2425/chap-ter/10.1007/978-3-319-67045-4_5
Sharma A., Rajendran S., Srivastava A., Sharma S., Antifungal activities of selected essential oils against Fusarium oxysporum f. sp. lycopersici 1322, with emphasis on Syzygium aromaticum essential oil. (2017) Vol. 123 Pages 308-313. Available from: https://ezproxy.unicolmayor.edu.co:2163/science/article/pii/S1389172316303097
Perczak, A., Gwiazdowska, D., Marchwińs¬ka, K. et al. Antifungal activity of selected essential oils against Fusarium culmorum and F. graminearum and their secondary metabolites in wheat seeds. Arch Microbiol 201, 1085–1097 (2019). https://ezproxy.unicolmayor.edu.co:2162/10.1007/s00203-019-01673-5
Pizzolitto R., Jacquat A., Usseglio V., Achi¬món F. Quantitative-structure-activity re¬lationship study to predict the antifungal activity of essential oils against Fusarium verticillioides. [Internet]. Scincedirect.com (2020). Vol 108. Available from: https://ezproxy.unicolmayor.edu.co:2163/science/article/pii/S0956713519304256
Vilaplana R., Pérez K., Valencia S. Essen¬tial oils as an alternative postharvest treatment to control fusariosis, caused by Fusarium verticillioides, in fresh pi-neapples (Ananas comosus) [Internet]. Scincedirect.com (2018). Vol 238 Pages 255-263. Available from: https://ezproxy.unicolmayor.edu.co:2163/science/article/pii/S0304423818303017
La Torre, A., Caradonia, F., Matere, A. et al. Using plant essential oils to control Fusa-rium wilt in tomato plants. Eur J Plant Pa¬thol 144, 487–496 (2016). https://ezproxy.unicolmayor.edu.co:2162/10.1007/s10658-015-0789-2
Kumar, P., Mishra, S., Kumar, A. et al. An¬tifungal efficacy of plant essential oils against stored grain fungi of Fusarium spp. J Food Sci Technol 53, 3725–3734 (2016). https://ezproxy.unicolmayor.edu.co:2162/10.1007/s13197-016-2347-0
Gaffar F., Imani J., Karlovsky P., Koch A. Different Components of the RNA Inter-ference Machinery Are Required for Co¬nidiation, Ascosporogenesis, Virulence, Deoxynivalenol Production, and Fungal Inhibition by Exogenous Double-Stranded RNA in the Head Blight Pathogen Fusa¬rium graminearum. PMCID: PMC6764512 (2019) Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764512/
Son H, Park AR, Lim JY, Shin C, Lee YW (2017) Genome-wide exonic small inter-ference RNA-mediated gene silencing regulates sexual reproduction in the ho-mothallic fungus Fusarium graminearum. PLoS Genet 13 (2): e1006595. https://doi.org/10.1371/journal.pgen.1006595
Johnson, E.T., Proctor, R.H., Dunlap, C.A. et al. Reducing production of fumonisin mycotoxins in Fusarium verticillioides by RNA interference. Mycotoxin Res 34, 29– 37 (2018). https://ezproxy.unicolmayor.edu.co:2162/10.1007/s12550-017-0296-8
Kharbikar, L.L., Shanware, A.S., Saharan, M.S. et al. Fusarium graminearum mi-croRNA-like RNAs and their interactions with wheat genome: a much-needed study. Indian Phytopathology 72, 565–573 (2019). https://ezproxy.unicolmayor.edu.co:2162/10.1007/s42360-019-00139-4
Shanmugam, V., Sharma, V., Bharti, P. et al. RNAi induced silencing of pathogenicity genes of Fusarium spp. for vascular wilt management in tomato. Ann Microbiol 67, 359–369 (2017). https://ezproxy.unicolma-yor.edu.co:2162/10.1007/s13213-017-1265-3
Song X., Gu K., Duan X. A myosin5 dsR¬NA that reduces the fungicide resistance and pathogenicity of Fusarium asiaticum. (2018), Vol 150, Pag 1-9. Available from: https://ezproxy.unicolmayor.edu.co:2163/science/article/pii/S0048357518301172
Bharti, P., Jyoti, P., Kapoor, P. et al. Host-In¬duced Silencing of Pathogenicity Genes Enhances Resistance to Fusarium oxys¬porum Wilt in Tomato. Mol Biotechnol 59, 343–352 (2017). https://ezproxy.unicol¬mayor.edu.co:2162/10.1007/s12033-017-0022-y
Singh, N., Mukherjee, S.K. & Rajam, M.V. Silencing of the Ornithine Decarboxyla¬se Gene of Fusarium oxysporum f. sp. ly¬copersici by Host-Induced RNAi Confers Resistance to Fusarium Wilt in Tomato. Plant Mol Biol Rep (2020). https://ezproxy.unicolmayor.edu.co:2162/10.1007/s11105-020-01205-2
Willforss J. S.Leonova J.Tillander E.An¬dreasson S.Marttila O.Olsson A.Chawade F.Levander. Interactive proteogenomic exploration of response to Fusarium head blight in oat varieties with different resis¬tance. (2020) Vol 218. https://ezproxy.uni-colmayor.edu.co:2163/science/article/pii/S1874391920300567
