Gnotobiotic system for selecting microorganisms with biocontrol potential against Fusarium oxysporum f. sp. physali

dc.audienceInvestigadorspa
dc.audience.contentCientíficospa
dc.contributor.authorGarcía, Diana
dc.contributor.authorDávila Mora, Liseth Lorena
dc.contributor.authorGonzález, Adriana
dc.contributor.authorCaro Quintero, Alejandro
dc.contributor.authorCotes Prado, Alba Marina
dc.coverage.countryColombiaspa
dc.date.accessioned2024-03-06T14:28:34Z
dc.date.available2024-03-06T14:28:34Z
dc.date.created2021
dc.date.issued2021
dc.description.abstractThe cape gooseberry (Physalis peruviana) is a Solanaceae species with enormous economic importance in Colombia; it is the second most exported fruit, after bananas. Vascular wilt caused by Fusarium oxysporum f. sp. physali (Fox) is the most limiting factor of this crop, with losses of up to 80% of production. Biological control is a promising alternative for controlling this pathogen. Bacteria and fungi, originally isolated from potentially suppressive soils of cape gooseberry crops in Nariño, Colombia with different management (organic and conventional), were evaluated as biocontrol agents of Fox using a gnotobiotic model (seedlings cultured under axenic conditions with defined microbial strains). Of the 64 isolated microorganisms, 37.5% (15 bacteria and 9 fungi) were discarded because of toxicological risks and an unknow potential biological control. The remaining 62.5% of the microorganisms, 14 bacteria and 26 fungi, were evaluated to assess their potential as biological control agents against Fox. The gnotobiotic model system evaluated the protection and plant growth promotion characteristics. Response variables were used to group the microorganism using a principal component analysis (PCA), and five clusters were obtained. Cluster number four concentrated the 10 microorganisms (three bacteria and seven fungi) with the highest protection values against Fox, with a positive effect on growth. The isolates were identified as two Bacillus subtilis strains, Rhodococcus sp., Podospora setosa, Debaryomyces vindobonensis, Plectosphaerella plurivora, Acinetobacter rhizosphaerae, Umbelopsis sp. and two strains of Trichoderma koningiopsis. The gnobiotic system offered clear advantages for evaluating and selecting microorganisms with a biological control potential against Fusarium oxysporum f. sp. physalis.spa
dc.description.productionsystemsUchuvaspa
dc.description.scientificnamePhysalis peruviana L.
dc.format.mimetypeapplication/pdf
dc.identifierhttps://revistas.uptc.edu.co/index.php/ciencias_horticolas/article/view/11699
dc.identifier.doi10.17584/rcch.2021v15i1.11699
dc.identifier.instnameinstname:Corporación colombiana de investigación agropecuaria AGROSAVIAspa
dc.identifier.issn2422-3719
dc.identifier.reponamereponame:Biblioteca Digital Agropecuaria de Colombiaspa
dc.identifier.urihttp://hdl.handle.net/20.500.12324/38973
dc.language.isospa
dc.publisherUniversidad Pedagógica y Tecnológica de Colombia - UPTCspa
dc.publisher.placeBogotá (Colombia)spa
dc.relation.citationendpage18
dc.relation.citationissue1
dc.relation.citationstartpage1
dc.relation.citationvolume15
dc.relation.ispartofjournalRevista Colombiana de Ciencias Hortícolasspa
dc.relation.referencesAgronet. 2018. Área, producción y rendimiento nacional por cultivo. In: https://www.agronet.gov.co/estadisti ca/Paginas/home.aspx?cod=1; consulted: April, 20spa
dc.relation.referencesAkköprü, A. and S. Demir. 2005. Biological control of Fu sarium wilt in tomato caused by Fusarium oxys f. sp. lycopersici by AMF Glomus intraradices and some rhizobacteria. J. Phytopathol. 153(9), 544-550. Doi: 10.1111/j.1439-0434.2005.01018.xspa
dc.relation.referencesAnastasiadis, I.A., I.O. Giannakou, D.A. Prophetou-Atha nasiadou, and S.R. Gowen. 2008. The combined effect of the application of a biocontrol agent Paecilomyces lilacinus, with various practices for the control of root knot nematodes. Crop Prot. 27(3-5), 352-361. Doi: 10.1016/j.cropro.2007.06.008spa
dc.relation.referencesArrebola, E., R. Jacobs, and L. Korsten. 2010. Iturin: A is the principal inhibitor in the biocontrol activity of Bacillus amyloliquefaciens PPCB004 against postharvest fungal pathogens. J. Appl. Microbiol. 108(2), 386-395. Doi: 10.1111/j.1365-2672.2009.04438.xspa
dc.relation.referencesAsaka, O. and M. Shoda. 2002. Biocontrol of Rhizoctonia solani damping-off of tomato with Bacillus subtilis RB14. Appl. Environ. Microbiol. 62(11), 4081-4085. Doi: 10.1128/aem.62.11.4081-4085.1996spa
dc.relation.referencesBais, H.P., R. Fall, and J.M. Vivanco. 2004. Biocontrol of Ba cillus subtilis against infection of arabidopsis roots by Pseudomonas syringae is facilitated by biofilm forma tion and surfactin production. Plant Physiol. 134(1), 307-319. Doi: 10.1104/pp.103.028712spa
dc.relation.referencesBanaay, C.G.B., C.V. Cuevas, and C.M. Vera. 2012. Tricho derma ghanense promotes plant growth and controls disease caused by Pythium arrhenomanes in seedlings of aerobic rice variety Apo. Philipp. Agric. Scientist 95(2), 175-184.spa
dc.relation.referencesBayman, P., L.L. Lebron, R.L. Tremblay, and D.J. Lodge. 1997. Variation in endophytic fungi from roots and leaves of Lepanthes (Orchidaceae). New Phytol. 135(1), 143-149. Doi: 10.1046/j.1469-8137.1997.00618.xspa
dc.relation.referencesBennett, R.S., W. O’neill, L. Smith, R.B. Hutmacher, and R.S. Bennett. 2011. Plant pathology and nematology: Activity of commercial detergents against conidia and chlamydospores of Fusarium oxysporum f. sp. vasinfec tum. J. Cotton Sci. 15(2), 162-169.spa
dc.relation.referencesBlankenberg, D., A. Gordon, G. Von Kuster, N. Coraor, J. Taylor, A. Nekrutenko, and G. Team. 2010. Manipu lation of FASTQ data with galaxy. Bioinformatics 26(14), 1783-1785. Doi: 10.1093/bioinformatics/ btq281spa
dc.relation.references1 Bleve, G., F. Grieco, G. Cozzi, A. Logrieco, and A. Viscon ti. 2006. Isolation of epiphytic yeasts with potential for biocontrol of Aspergillus carbonarius and A. niger on grape. Int. J. Food Microbiol. 108(2), 204-209. Doi: 10.1016/j.ijfoodmicro.2005.12.004spa
dc.relation.referencesBubici, G., M. Kaushal, M.I. Prigigallo, C.G.L. Cabanás, and J. Mercado-Blanco. 2019. Biological control agents against Fusarium wilt of banana. Front. Microbiol. 10, 616. Doi: 10.3389/fmicb.2019.00616spa
dc.relation.referencesCaporaso, J.G., C.L. Lauber, W.A. Walters, D. Berg-Lyons, C.A. Lozupone, P.J. Turnbaugh, N. Fierer, and R. Kni ght. 2011. Global patterns of 16S rRNA diversit a depth of millions of sequences per sample. Proc. Natl. Acad. Sci. USA 108(Suppl. 1), 4516-4522. Doi: 10.1073/pnas.1000080107spa
dc.relation.referencesCarmarán, C.C. and M.V. Novas. 2003. A review of Spe gazzini taxa of Periconia and Sporocybe after over 115 years. Fungal Divers. 14, 67-76.spa
dc.relation.referencesCarvalho, D.D.C., M. Lobo Junior, I. Martins, P.W. In glis, and S.C.M. Mello. 2014. Biological control of fusarium oxysporum f. sp. phaseoli by Trichoderma har zianum and its use for common bean seed treatment. Trop. Plant Pathol. 39(5), 384-391. Doi: 10.1590/ S1982-56762014000500005spa
dc.relation.referencesCatara, V. 2007. Pseudomonas corrugata: plant pathogen and/ or biological resource? Mol. Plant Pathol. 8(3), 233- 244. Doi: 10.1111/j.1364-3703.2007.00391.xspa
dc.relation.referencesChastre, J. 2003. Infections due to Acinetobacter baumannii in the ICU. Semin. Respir. Crit. Care Med. 24(1), 069- 078. Doi: 10.1055/s-2003-37918spa
dc.relation.referencesChen, F., Y.B. Guo, J.H. Wang, J.Y. Li, and H.M. Wang. 2007. Biological control of grape crown gall by Rahnella aquatilis HX2. Plant Dis. 91(8), 957-963. Doi: 10.1094/ PDIS-91-8-0957spa
dc.relation.referencesChin-A-Woeng, T.F.C., G.V. Bloemberg, and B.J.J. Lugten berg. 2003. Phenazines and their role in biocontrol by Pseudomonas bacteria. New Phytol. 157(3), 503-523. Doi: 10.1046/j.1469-8137.2003.00686.xspa
dc.relation.referencesCotes, A.M., C.A. Moreno-Velandia, C. Espinel, L. Villami zar, and M. Gómez. 2018. Biological control of tomato Fusarium wilt and whiteflies with two fungal biopes ticides. Acta Hortic. 1207, 129-138. Doi: 10.17660/ ActaHortic.2018.1207.17spa
dc.relation.referencesCreason, A.L., O.M. Vandeputte, E.A. Savory, E.W. II Da vis, M.L. Putnam, E. Hu, D. Swader-Hines, A. Mol, M. Baucher, E. Prinsen, M. Zdanowska, S.A. Givan, M. El Jaziri, J.E. Loper, T. Mahmud, and J.H. Chang. 2014. Analysis of genome sequences from plant pathoge nic Rhodococcus reveals genetic novelties in virulence loci. PLoS ONE 9(7), e101996. Doi: 10.1371/journal. pone.0101996spa
dc.relation.referencesDe Boer Sietske, A. and B. Diderichsen. 1991. On the safe ty of Bacillus subtilis and B. amyloliquefaciens: a review. Appl. Microbiol. Biotechnol. 36(1), 1-4. Doi: 10.1007/ BF00164689spa
dc.relation.referencesDe Hoog, G.S., S.A. Ahmed, M.J. Najafzadeh, D.A. Sutton, M.S. Keisari, A.H. Fahal, U. Eberhardt, G.J. Verkleij, L. Xin, B. Stielow, and W.W.J. van de Sande. 2013. Phylogenetic findings suggest possible new habitat and routes of infection of human eumyctoma. PLoS Negl. Trop. Dis. 7(5), e2229. Doi: 10.1371/journal. pntd.0002229spa
dc.relation.referencesDeng, W., B.A. Vallance, Y. Li, J.L. Puente, and B.B. Finlay. 2003. Citrobacter rodentium translocated intimin re ceptor (Tir) is an essential virulence factor needed for actin condensation, intestinal colonization and colo nic hyperplasia in mice. Mol. Microbiol. 48(1), 95-115. Doi: 10.1046/j.1365-2958.2003.03429.xspa
dc.relation.referencesDi Pietro, A., M. Gut-Rella, J.P. Pachlatko, and F.J. Schwinn. 1992. Role of Antibiotics Produced by Chaetomium glo bosum in biocontrol of Pythium ultimum, a causal agent of damping-off. Phytopathology 82(2), 131. Doi: 10.1094/phyto-82-131spa
dc.relation.referencesDorman, H.J.D. and S.G. Deans. 2000. Antimicrobial agents from plants: Antibacterial activity of plant volatile oils. J. Appl. Microbiol. 88(2), 308-316. Doi: 10.1046/j.1365-2672.2000.00969.xspa
dc.relation.referencesDruzhinina, I.S., V. Seidl-Seiboth, A. Herrera-Estrella, B.A. Horwitz, C.M. Kenerley, E. Monte, P.K. Mukherjee, S. Zeilinger, I.V. Grigoriev, and C.P. Kubicek. 2011. Trichoderma: The genomics of opportunistic success. Nat. Rev. Microbiol. 9(10), 749-759. Doi: 10.1038/ nrmicro2637spa
dc.relation.referencesEl-Tarabily, K.A. 2006. Rhizosphere-competent isolates of streptomycete and non-streptomycete actinomycetes capable of producing cell-wall-degrading enzymes to control Pythium aphanidermatum damping-off disease of cucumber. Can. J. Bot. 84, 211-222. Doi: 10.1139/ B05-153spa
dc.relation.referencesEnciso-Rodríguez, F.E., C. González, E.A. Rodríguez, C.E. López, D. Landsman, L.S. Barrero, and L. Mariño-Ra mírez. 2013. Identification of immunity related genes to study the Physalis peruviana - Fusarium oxysporum pathosystem. PLoS ONE 8(7), 68500. Doi: 10.1371/ journal.pone.0068500spa
dc.relation.referencesEshraghi, L., J.P. Anderson, N. Aryamanesh, J.A. McComb, B. Shearer, and G.E. Giles. 2014. Defence signalling pathways involved in plant resistance and phos phite-mediated control of Phytophthora cinnamomi. Plant Mol. Biol. Rep. 32(2), 342-356. Doi: 10.1007/ s11105-013-0645-5spa
dc.relation.referencesFelestrino, E.B., I.F. Santiago, L.S. Freitas, L.H. Rosa, S.P. Ri beiro, and L.M. Moreira. 2017. Plant growth promoting bacteria associated with Langsdorffia hypogaea-Rhizos phere-Host biological interface: A neglected model of bacterial prospection. Front. Microbiol. 8, 172. Doi: 10.3389/fmicb.2017.00172spa
dc.relation.referencesFischer, G. and L.M. Melgarejo. 2020. The ecophysiology of cape gooseberry (Physalis peruviana L.) - an Andean fruit crop. A review. Rev. Colomb. Cienc. Hortic. 14(1), 76-89. Doi: 10.17584/rcch.2020v14i1.10893spa
dc.relation.referencesGalindo, J.R. and L.M. Pardo. 2010. Uchuva (Physalis peru viana): Producción y manejo poscosecha. Cámara de Comercio, Bogota.spa
dc.relation.referencesGalindo-Flores, H., J.C. Martínez-Álvarez, E. Nava-Pérez, R.S. García-Estrada, and I.E. Maldonado-Mendo za. 2005. A saprotrophic fungal isolate from nor thern Sinaloa, Mexico, with homology to members of the chaetomiaceae behaves as an antagonist of phytopathogenic fungi in vitro. Rev. Mex. Fitopatol. 23(2), 130-139.spa
dc.relation.referencesGally, T., B.A. González, and F. Pantuso. 2006. Efecto con junto de Fusarium sp. y Phomopsis sp., patógenos trans mitidos por las semillas en plántulas de soja [Glycine max (L.) Merrill]. Rev. Mex. Fitopatol. 24(2), 156-158spa
dc.relation.referencesGhelardi, E., F. Celandroni, S. Salvetti, E. Fiscarelli, and S. Senesi. 2007. Bacillus thuringiensis pulmonary infec tion: critical role for bacterial membrane-damaging toxins and host neutrophils. Microb. Infect. 9(5), 591- 598. Doi: 10.1016/j.micinf.2007.02.001spa
dc.relation.referencesGiraldo-Betancourt, C., E.A. Velandia-Sánchez, G. Fischer, S. Gómez-Caro, and L.-J. Martínez. 2020. Hyperspec tral response of cape gooseberry (Physalis peruviana L.) plants inoculated with Fusarium oxysporum f. sp. phy sali for vascular wilt detection. Rev. Colomb. Cienc. Hortic. 14(3). Doi: 10.17584/rcch.2020v14i3.10938spa
dc.relation.referencesGonzález, C. and L.S. Barrero. 2011. Estudio de la marchi tez vascular de la uchuva para el mejoramiento genéti co del cultivo. Cámara de Comercio, Bogspa
dc.relation.referencesGrohskopf, L., V. Roth, D. Feikin, M. Arduino, L. Carson, J. Tokars, S.C. Holt, B.J. Jensen, R.E. Hoffman, and W.R. Jarvis. 2001. Serratia liquefaciens bloodstream infec tions from contamination of epoetin alfa at a hemo dialysis center. N. Engl. J. Med. 344, 1491-1497. Doi: 10.1056/nejm200105173442001spa
dc.relation.referencesGunther IV, N.W., A. Nuñez, W. Fett, and D.K.Y. Solai man. 2005. Production of rhamnolipids by Pseudomo nas chlororaphis, a nonpathogenic bacterium. Appl. Environ. Microbiol. 71(5), 2288-2293. Doi: 10.1128/ AEM.71.5.2288-2293.2005spa
dc.relation.referencesGutiérrez-Luna, F.M., J. López-Bucio, J. Altamirano-Her nández, E. Valencia-Cantero, H.R. De La Cruz, and L. Macías-Rodríguez. 2010. Plant growth-promoting rhi zobacteria modulate root-system architecture in Ara bidopsis thaliana through volatile organic compound emission. Symbiosis 51(1), 75-83. Doi: 10.1007/ s13199-010-0066-2spa
dc.relation.referencesGutiérrez, E. 2017. Caracterización de los mecanismos anta gónicos de Debaryomyces hansenii contra Colletotrichum gloersporioides y su efecto en la protección poscosecha en papaya var. Maradol. MSc thesis. Centro de Inves tigaciones Biológicas del Noroeste, La Paz, Mexico.spa
dc.relation.referencesHaglund, W.A. and J.M. Kraft. 2001. Fusarium wilt. In: Compendium of pea diseases and pests. American Phytopathological Society, St. Paul, MN.spa
dc.relation.referencesHandelsman, J., S. Raffel, E.H. Mester, L. Wunderlich, and C.R. Grau. 1990. Biological control of damping-off of alfalfa seedlings with Bacillus cereus UW85. Appl. Environ. Microbiol. 56(3), 713-718. Doi: 10.1128/ aem.56.3.713-718.1990spa
dc.relation.referencesHassanien, M.F.R. 2011. Physalis peruviana: A rich source of bioactive phytochemicals for functional foods and pharmaceuticals. Food Rev. Int. 27(3), 259-273. Doi: 10.1080/87559129.2011.563391spa
dc.relation.referencesHe, H., L.A. Silo-Suh, J. Handelsman, and J. Clardy. 1994. Zwittermicin A: an antifungal and plant protection agent from Bacillus cereus. Tetrahedron Lett. 35(16), 2499-2502. Doi: 10.1016/S0040-4039(00)77154-1spa
dc.relation.referencesHoppe, J.E., M. Herter, S. Aleksic, T. Klingebiel, and D. Niethammer. 1993. Catheter-related Rahnella aquati lis bacteremia in a pediatric bone marrow transplant recipient. J. Clin. Microbiol. 31(7), 1911-1912. Doi: 10.1128/JCM.31.7.1911-1912.1993spa
dc.relation.referencesHowell, C.R. 2003. Mechanisms employed by Trichoderma species in the biological control of plant diseases: The history and evolution of current concepts. Plant Dis. 87(1), 4-10. Doi: 10.1094/PDIS.2003.87.1.4spa
dc.relation.referencesHuang, P., L. de-Bashan, T. Crocker, J.W. Kloepper, and Y. Bashan. 2017. Evidence that fresh weight measu rement is imprecise for reporting the effect of plant growth-promoting (rhizo)bacteria on growth promo tion of crop plants. Biol. Fert. Soils 53(2), 199-208. Doi: 10.1007/s00374-016-1160-2spa
dc.relation.referencesHubbard, J.P., G.E. Harman, and C.J. Eckenrode. 1982. In teraction of a biological control agent, Chaetomium globosum, with seed coat microflora. Can. J. Microbiol. 28(4), 431-437. Doi: 10.1139/m82-065spa
dc.relation.referencesICA, Instituto Colombiano Agropecuario. 2020. Fertilizantes y bioinsumos agrícolas. In: https://www. ica.gov.co/getdoc/d3612ebf-a5a6-4702-8d4b-8427c1c daeb1/registros-nacionales-pqua-15-04-09.aspx; con sulted: December, 2020.spa
dc.relation.referencesIndiragandhi, P., R. Anandham, M. Madhaiyan, and T.M. As. 2008. Characterization of plant growth-promo ting traits of bacteria isolated from larval guts of Diamondback moth Plutella xylostella (Lepidoptera: Plutellidae). Curr. Microbiol. 56(4), 327-333. Doi: 10.1007/s00284-007-9086-4spa
dc.relation.referencesKalbe, C., P. Marten, and G. Berg. 1996. Strains of the genus Serratia as beneficial rhizobacteria of oilseed rape with antifungal properties. Microbiol. Res. 151(4), 433-439. Doi: 10.1016/S0944-5013(96)80014-0spa
dc.relation.referencesKloepper, J.W., F.M. Scher, M. Laliberté, and B. Tipping. 1986. Emergence-promoting rhizobacteria: Des cription and implications for agriculture. pp. 155- 164. In: Swinburne, T.R. (eds.). Iron, siderophores, and plant diseases. NATO ASI Series (Series A: Life Sciences). Vol. 117. Springer, Boston, MA. Doi: 10.1007/978-1-4615-9480-2_17spa
dc.relation.referencesKöhl, J., R. Kolnaar, and W.J. Ravensberg. 2019. Mode of action of microbial biological control agents against plant diseases: Relevance beyond efficacy. Front. Plant Sci. 10, 845. Doi: 10.3389/fpls.2019.00845spa
dc.relation.referencesKorolev, N., J. Katan, and T. Katan. 2000. Vegetative compatibility groups of Verticillium dahliae in Israel: Their distribution and association with pathogeni city. Phytopathology 90(5), 529-536. Doi: 10.1094/ PHYTO.2000.90.5.529spa
dc.relation.referencesKůdela, V., V. Krejzar, and I. Pánková. 2010. Pseudomonas corrugata and Pseudomonas marginalis associated with the collapse of tomato plants in Rockwool slab hy droponic culture. Plant Prot. Sci. 46(1), 1-11. Doi: 10.17221/44/2009-PPSspa
dc.relation.referencesKuhls, K., E. Lieckfeldt, T. Börner, and E. Guého. 1999. Molecular reidentification of human pathogenic Tri choderma isolates as Trichoderma longibrachiatum and Trichoderma citrinoviride. Med. Mycol. 37(1), 25-33. Doi: 10.1046/j.1365-280X.1999.00197.xspa
dc.relation.referencesKumar, R.M., G. Kaur, A. Kumar, M. Bala, N.K. Singh, N. Kaur, N. Kumar, and S. Mayilraj. 2015. Taxonomic description and genome sequence of Bacillus campisalis sp. nov., a member of the genus Bacillus isolated from a solar saltern. Int. J. Syst. Evol. Microbiol. 65(10), 3235-3240. Doi: 10.1099/ijsem.0.000400spa
dc.relation.referencesKurze, S., H. Bahl, R. Dahl, and G. Berg. 2001. Biological control of fungal strawberry diseases by Serratia ply muthica HRO-C48. Plant Dis. 85(5), 529-534. Doi: 10.1094/PDIS.2001.85.5.529spa
dc.relation.referencesLagier, J.C., F. Armougom, M. Million, P. Hugon, I. Pag nier, C. Robert, F. Bittar, G. Fournous, G. Gimenez, M. Maraninchi, J.-F. Trape, E.V. Koonin, B. La Sco la, and D. Raoult. 2012. Microbial culturomics: Pa radigm shift in the human gut microbiome study. Clin. Microbiol. Infect. 18(12), 1185-1193. Doi: 10.1111/1469-0691.12023spa
dc.relation.referencesLópez, J.R., A.L. Diéguez, A. Doce, E. de la Roca, R. de la Herran, J.I. Navas, A.E. Toranzo, and J.L. Romalde. 2012. Pseudomonas baetica sp. nov., a fish pathogen isolated from wedge sole, Dicologlossa cuneata (Mo reau). Int. J. Syst. Evol. Microb. 62(4), 874-882. Doi: 10.1099/ijs.0.030601-0spa
dc.relation.referencesLorito, M., S.L. Wood, M. D’Ambrosio, G.E. Harman, C.K. Hayes, C.P. Kubicek, and F. Scala. 1996. Synergistic interaction between cell wall degrading enzymes and membrane affecting compounds. Mol. Plant Microbe Interact. 9(3), 206-213. Doi: 10.1094/MPMI-9-0206spa
dc.relation.referencesLucy, M., E. Reed, and B.R. Glick. 2004. Applications of free living plant growth-promoting rhizobacteria. Antonie van Leeuwenhoek 86(1), 1-25. Doi: 10.1023/B:ANTO. 0000024903.10757.6espa
dc.relation.referencesLuongo, L., M. Galli, L. Corazza, E. Meekes, L. De Haas, C.L. Van Der Plas, and J. Köhl. 2005. Potential of fungal antagonists for biocontrol of Fusarium spp. in wheat and maize through competition in crop debris. Biocontrol Sci. Techn. 15(3), 229-242. Doi: 10.1080/09583150400016852spa
dc.relation.referencesMarinho, A.M.R., E. Rodrigues-Filho, M.D.L.R. Moitinho, and L.S. Santos. 2005. Biologically active polyketides produced by Penicillium janthinellum isolated as an endophytic fungus from fruits of Melia azedarach. J. Braz. Chem. Soc. 16(2), 280-283. Doi: 10.1590/ s0103-50532005000200023spa
dc.relation.referencesMartínez, S.A. and J. Dussán. 2018. Lysinibacillus sphaericus plant growth promoter bacteria and lead phytoreme diation enhancer with Canavalia ensiformis. Environ. Prog. Sustain. Energy 37(1), 276-282. Doi: 10.1002/ ep.12668spa
dc.relation.referencesMartínez-Medina, A., M. Del Mar Alguacil, J.A. Pascual, and S.C.M. Van Wees. 2014. Phytohormone profi les induced by Trichoderma isolates correspond with their biocontrol and plant growth-promoting activity on melon plants. J. Chem. Ecol. 40(7), 804-815. Doi: 10.1007/s10886-014-0478-1spa
dc.relation.referencesMayorga-Cubillos, F., J. Arguelles, E. Rodriguez, C. Alma rio, C. Ariza, and L. Barrero. 2019. Yield and physico chemical quality of Physalis peruviana L. fruit related to the resistance response against Fusarium oxysporum f. sp. physali. Agron. Colomb. 37(2), 120-128. Doi: 10.15446/agron.colomb.v37n2.77550spa
dc.relation.referencesMcGovern, R.J. 2015. Management of tomato diseases cau sed by Fusarium oxysporum. Crop Prot. 73, 78-92. Doi: 10.1016/j.cropro.2015.02.021spa
dc.relation.referencesMelnick, R.L., C. Suárez, B.A. Bailey, and P.A. Backman. 2011. Isolation of endophytic endospore-forming bacteria from Theobroma cacao as potential biological control agents of cacao diseases. Biol. Control 57(3), 236-245. Doi: 10.1016/j.biocontrol.2011.03.005spa
dc.relation.referencesMichielse, C.B. and M. Rep. 2009. Pathogen profile update: Fusarium oxysporum. Mol. Plant Pathol. 10(3), 311-324. Doi: 10.1111/j.1364-3703.2009.00538.xspa
dc.relation.referencesMoreno, C.A., F. Castillo, A. González, D. Bernal, Y. Jaimes, M. Chaparro, C. González, F. Rodriguez, S. Restrepo, and A.M. Cotes. 2009. Biological and molecular cha racterization of the response of tomato plants treated with Trichoderma koningiopsis. Physiol. Mol. Plant Pa thol. 74(2), 111-120. Doi: 10.1016/j.pmpp.2009.10.0spa
dc.relation.referencesMoreno, C.A., J. Kloepper, M. Ongena, and A.M. Cotes. 2014. Biotic factors involved in biological control acti vity of Bacillus amyloliquefaciens (Bs006) against Fusa rium oxysporum in cape gooseberry (Physalis peruviana). pp. 129-136. In: Pertot, I., D.F. Jensen, M. Hökeberg, M. Karlsson, I. Sundh, and Y. Elad (eds.). Proc. XIII Meeting Biocontrol of Plant Diseases: From the Field to the Laboratory and Back Again. IOBC-WPRS Bull. 115. Zürich Switzerland.spa
dc.relation.referencesMoreno-Limón, S., L.N. González-Solís, S.M. Salcedo-Mar tínez, M.L. Cárdenas-Avila, and A. Perales-Ramírez. 2011. Efecto antifúngico de extractos de goberna dora (Larrea tridentata L.) sobre la inhibición in vitro de Aspergillus flavus y Penicillium sp. Polibotánica 32, 193-205.spa
dc.relation.referencesNRCS, National Resources Conservation Service. 2020. Physalis peruviana L.: Peruvian groundcherry. In: United States Department of Agriculture USDA, https://plants.sc.egov.usda.gov/core/profile?sym bol=PHPE4; consulted: November, 2020.spa
dc.relation.referencesNicoletti, R., A. Carella, and E. Cozzolino. 2008. Investiga tion on fungal antagonists of root rot agents from the rhizosphere of white lupin (Lupinus albus). Dyn. Soil Dyn. Plant 2(1), 69-72.spa
dc.relation.referencesOpelt, K., V. Chobot, F. Hadacek, S. Schönmann, L. Eberl, and G. Berg. 2007. Investigations of the structure and function of bacterial communities associated with Sphagnum mosses. Environ. Microbiol. 9(11), 2795- 2809. Doi: 10.1111/j.1462-2920.2007.01391.xspa
dc.relation.referencesOsburn, R.M., J.L. Milner, E.S. Oplinger, R.S. Smith, and J. Handelsman. 1995. Effect of Bacillus cereus UW85 on the yield of soybean at two field sites in Wisconsin. Plant Dis. 79(6), 551-556. Doi: 10.1094/PD-79-0551spa
dc.relation.referencesOwnley, B.H., M.R. Griffin, W.E. Klingeman, K.D. Gwinn, J.K. Moulton, and R.M. Pereira. 2008. Beauveria bassia na: Endophytic colonization and plant disease control. J. Invertebr. Pathol. 98(3), 267-270. Doi: 10.1016/j. jip.2008.01.010spa
dc.relation.referencesPalma-Guerrero, J., H.B. Jansson, J. Salinas, and L.V. Lo pez-Llorca. 2008. Effect of chitosan on hyphal growth and spore germination of plant pathogenic and bio control fungi. J. Appl. Microbiol. 104(2), 541-553. Doi: 10.1111/j.1365-2672.2007.03567.xspa
dc.relation.referencesPieterse, C.M.J., C. Zamioudis, R.L. Berendsen, D.M. We ller, S.C.M. Van Wees, and P.A.H.M. Bakker. 2014. Induced systemic resistance by beneficial microbes. Annu. Rev. Phytopathol. 52, 347-375. Doi: 10.1146/ annurev-phyto-082712-102340spa
dc.relation.referencesPloper, L.D., P.A. Backman, C. Stevens, V.A. Khan, and R. Rodriguez-Kábana. 1992. Effects of soil mulch, row cover, and biological and chemical foliar treatments on early blight of tomato. Biol. Cult. Test. 7, 38.spa
dc.relation.referencesPrescott, J.F. 1991. Rhodococcus equi: An animal and hu man pathogen. Clin. Microbiol. Rev. 4(1), 20-34. Doi: 10.1128/CMR.4.1.20spa
dc.relation.referencesRaaijmakers, J.M. and D.M. Weller. 1998. Natural plant protection by 2,4-diacetylphloroglucinol-produ cing Pseudomonas spp. in Take-all decline soils. Mol. Plant-Microb. Interact. 11(2), 144-152. Doi: 10.1094/ MPMI.1998.11.2.144spa
dc.relation.referencesRai, J.N. and V.C. Saxena. 1975. Sclerotial mycoflora and its role in natural biological control of ‘white-rot’ disease. Plant Soil 43(1), 509-513. Doi: 10.1007/BF01928513spa
dc.relation.referencesRashid, S., T.C. Charles, and B.R. Glick. 2012. Isolation and characterization of new plant growth-promoting bac terial endophytes. Appl. Soil Ecol. 61, 217-224. Doi: 10.1016/j.apsoil.2011.09.011spa
dc.relation.referencesRefai, M., H.A. El-Yazid, and W. Tawakkol. 2015. Mono graph on the genus Penicillium. A guide for historical, classification and identification of penicilli, their in dustrial applications and detrimental effects. Cairo University, Cairo.spa
dc.relation.referencesRete, A. 2011. Caracterización molecular de Streptomyces spp. asociadas a la sarna común y evaluación in vi tro de antagonistas nativos de la rizosfera de papa en Sinaloa. MSc thesis. Instituto Politécnico Nacional, Guasave, Mexico.spa
dc.relation.referencesRickerts, V., A. Böhme, A. Viertel, G. Behrendt, V. Jacobi, K. Tintelnot, and G. Just-Nübling. 2000. Cluster of pul monary infections caused by Cunninghamella bertho lletiae in immunocompromised patients. Clin. Infect. Dis. 31(4), 910-913. Doi: 10.1086/318144spa
dc.relation.referencesRodriguez, E. 2010. Aislamiento y caracterización de cepas de Fusarium oxysporum en uchuva (Physalis peruviana) y evaluación de la patogenicidad en invernadero. Un dergraduate thesis. Universidad de Cundinamaca, Fu sagasuga, Colombiaspa
dc.relation.referencesRodriguez, E. 2010. Aislamiento y caracterización de cepas de Fusarium oxysporum en uchuva (Physalis peruviana) y evaluación de la patogenicidad en invernadero. Un dergraduate thesis. Universidad de Cundinamaca, Fu sagasuga, Colombiaspa
dc.relation.referencesRodríguez, E.A. 2013. Caracterización de aislamientos de Fusarium spp. obtenidos de zonas productoras de uchuva (Physalis peruviana) en Cundinamarca y Bo yacá. MSc tesis. Facultad de Agronomía, Universidad Nacional de Colombia. Bogota.spa
dc.relation.referencesRodríguez, P., A. Cerda, X. Font, A. Sánchez, and A. Artola. 2019. Valorisation of biowaste digestate through so lid state fermentation to produce biopesticides from Bacillus thuringiensis. Waste Manage. 93, 63-71. Doi: 10.1016/j.wasman.2019.05.026spa
dc.relation.referencesRokhbakhsh-Zamin, F., D. Sachdev, N. Kazemi-Pour, A. Engineer, K.R. Pardesi, S. Zinjarde, P.K. Dhakephalk ar, and B.A. Chopade. 2011. Characterization of plant-growth-promoting traits of Acinetobacter spe cies isolated from rhizosphere of Pennisetum glaucum. J. Microbiol. Biotechnol. 21(6), 556-566. Doi: 10.4014/ jmb.1012.12006spa
dc.relation.referencesSahebani, N. and N. Hadavi. 2008. Biological control of the root-knot nematode Meloidogyne javanica by Trichoder ma harzianum. Soil Biol. Biochem. 40(8), 2016-2020. Doi: 10.1016/j.soilbio.2008.03.011spa
dc.relation.referencesSandoval-Denis, M., J. Guarro, J.F. Cano-Lira, D.A. Sut ton, N.P. Wiederhold, G.S. de Hoog, S.P. Abbott, C. Decock, L. Sigler, and J. Gené. 2016. Phylogeny and taxonomic revision of Microascaceae with emphasis on synnematous fungi. Stud. Mycol. 83, 193-233. Doi: 10.1016/j.simyco.2016.07.002spa
dc.relation.referencesSchirmböck, M., M. Lorito, Y.L. Wang, C.K. Hayes, I. Ari san-Atac, F. Scala, G.E. Harman, and C.P. Kubicek. 1994. Parallel formation and synergism of hydrolytic enzymes and peptaibol antibiotics, molecular mecha nisms involved in the antagonistic action of Trichoder ma harzianum against phytopathogenic fungi. Appl. Environ. Microbiol. 60(12), 4364-4370. Doi: 10.1128/ aem.60.12.4364-4370.1994spa
dc.relation.referencesShishido, M., C. Miwa, T. Usami, Y. Amemiya, and K.B. Jo hnson. 2005. Biological control efficiency of Fusarium wilt of tomato by nonpathogenic Fusarium oxysporum Fo-B2 in different environments. Phytopathology 95(9), 1072-1080. Doi: 10.1094/PHYTO-95-1072spa
dc.relation.referencesShoda, M. 2000. Bacterial control of plant diseases. J. Biosci. Bioeng. 89(6), 515-521. Doi: 10.1016/ S1389-1723(00)80049-3spa
dc.relation.referencesSiegel-Hertz, K., V. Edel-Hermann, E. Chapelle, S. Terrat, J.M. Raaijmakers, and C. Steinberg. 2018. Compara tive microbiome analysis of a Fusarium wilt suppres sive soil and a Fusarium wilt conducive soil from the Châteaurenard region. Front. Microbiol. 9, 568. Doi: 10.3389/fmicb.2018.00568spa
dc.relation.referencesSingh, R.K., D.P. Kumar, P. Singh, M.K. Solanki, S. Srivasta va, P.L. Kashyap, S. Kumar, A.K. Srivastava, P.K. Sin ghal, and D.K. Arora. 2014. Multifarious plant growth promoting characteristics of chickpea rhizosphere as sociated Bacilli help to suppress soil-borne pathogens. Plant Growth Regulation, 73(1), 91-101. Doi: 10.1007/ s10725-013-9870-zspa
dc.relation.referencesSingh, N.P., R.K. Singh, V.S. Meena, and R.K. Meena. 2015. Can we use maize (Zea mays) rhizobacteria as plant growth promoter? Vegetos 28(1), 86-99. Doi: 10.5958/2229-4473.2015.00012.9spa
dc.relation.referencesSmith, A. 2012. Reconocimiento de las enfermedades y pla gas en el cultivo de uchuva. pp. 9-12. In: Días, A. (ed.). Avances en el manejo y control de Fusarium oxysporum en el cultivo de uchuva (Physalis peruviana). Corpoica, Bogota, DC.spa
dc.relation.referencesSobita, S. and A. Anamika. 2011. Agro-based waste pro ducts as a substrate for mass production of Trichoderma spp. J. Agric. Sci. 3(4), 168-171. 10.5539/jas.v3n4p168spa
dc.relation.referencesSpencer, R.C. 2003. Bacillus anthracis. J. Clin. Pathol. 56(3), 182-187. Doi: 10.1136/jcp.56.3.182spa
dc.relation.referencesSzaniszlo, P.J. and J.L. Harris (eds.). 1985. Fungal di morphism: With emphasis on fungi pathoge nic for humans. Springer, Boston, MA. Doi: 10.1007/978-1-4684-4982-2spa
dc.relation.referencesTena, D., C. Fernández, and M.R. Lago. 2015. Alcaligenes faecalis: An unusual cause of skin and soft tissue infec tion. Jap. J. Infect. Dis. 68(2), 128-130. Doi: 10.7883/ yoken.JJID.2014.164spa
dc.relation.referencesToju, H., A.S. Tanabe, S. Yamamoto, and H. Sato. 2012. High-coverage ITS primers for the DNA-based iden tification of Ascomycetes and Basidiomycetes in en vironmental samples. PLoS ONE 7(7), e40863. Doi: 10.1371/journal.pone.0040863spa
dc.relation.referencesToloza-Moreno, D.L., L.M. Lizarazo-Forero, and D. Uri be-Vélez. 2020. Antagonist capacity of bacteria isolated from cape gooseberry cultures (Physalis pe ruviana L.) for biological control of Fusarium oxys porum. Trop. Plant Pathol. 45(1), 1-12. Doi: 10.1007/ s40858-019-00313-zspa
dc.relation.referencesUrrea, R., L. Cabezas, R. Sierra, M. Cárdenas, S. Restrepo, and P. Jiménez. 2011. Selection of antagonistic bacte ria isolated from the Physalis peruviana rhizosphere against Fusarium oxysporum. J. Appl. Microbiol. 111(3), 707-716. Doi: 10.1111/j.1365-2672.2011.05092.xspa
dc.relation.referencesVelivelli, S.L.S., P. Kromann, P. Lojan, M. Rojas, J. Franco, J.P. Suarez, and B.D. Prestwich. 2015. Identification of mVOCs from andean rhizobacteria and field evalua tion of bacterial and mycorrhizal inoculants on grow th of potato in its center of origin. Microbiol. Ecol. 69(3), 652-667. Doi: 10.1007/s00248-014-0514-2spa
dc.relation.referencesVerma, P.S. and C.C. Allison. 1970. Possible modification of susceptibility of tomato to Fusarium wilt by a Chaeto mium sp. Phytopathology 60, 1318spa
dc.relation.referencesVillarreal-Navarrete, A., G. Fischer, L.M. Melgarejo, G. Correa, and L. Hoyos-Carvajal. 2017. Growth res ponse of the cape gooseberry (Physalis peruviana L.) to waterlogging stress and Fusarium oxysporum in fection. Acta Hortic. 1178, 161-168. Doi: 10.17660/ ActaHortic.2017.1178.28spa
dc.relation.referencesVon Der Weid, I., D.S. Alviano, A.L.S. Santos, R.M.A. Soares, C.S. Alviano, and L. Seldin. 2003. Antimicro bial activity of Paenibacillus peoriae strain NRRL BD-62 against a broad spectrum of phytopathogenic bacteria and fungi. J. Appl. Microbiol. 95(5), 1143-1151. Doi: 10.1046/j.1365-2672.2003.02097.xspa
dc.relation.referencesXu, L., S. Ravnskov, J. Larsen, R.H. Nilsson, and M. Nico laisen. 2012. Soil fungal community structure along a soil health gradient in pea fields examined using deep amplicon sequencing. Soil Biol. Biochem. 46, 26-32. Doi: 10.1016/j.soilbio.2011.11.010spa
dc.relation.referencesZacky, F.A. and A.S.Y. Ting. 2013. Investigating the bioac tivity of cells and cell-free extracts of Streptomyces griseus towards Fusarium oxysporum f. sp. cubense race 4. Biol. Control 66(3), 204-208. Doi: 10.1016/j. biocontrol.2013.06.001spa
dc.relation.referencesZahid, M., M. Kaleem Abbasi, S. Hameed, and N. Rahim. 2015. Isolation and identification of indigenous plant growth promoting rhizobacteria from Himalayan re gion of Kashmir and their effect on improving growth and nutrient contents of maize (Zea mays L.). Front. Microbiol. 6, 207. Doi: 10.3389/fmicb.2015.00207spa
dc.relation.referencesZhang, X., P.R. Harvey, B.E. Stummer, R.A. Warren, G. Zhang, K. Guo, J. Li, and H. Yang. 2015. Antibiosis functions during interactions of Trichoderma afrohar zianum and Trichoderma gamsii with plant pathogenic Rhizoctonia and Pythium. Funct. Integr. Genomics 15, 599-610. Doi: 10.1007/s10142-015-0456-xspa
dc.relation.referencesZhao, S., D. Liu, N. Ling, F. Chen, W. Fang, and Q. Shen. 2014. Bio-organic fertilizer application significantly reduces the Fusarium oxysporum population and alters the composition of fungi communities of watermelon Fusarium wilt rhizosphere soil. Biol. Fertil. Soils 50(5), 765-774. Doi: 10.1007/s00374-014-0898-7spa
dc.rights.licenseAttribution-ShareAlike 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-sa/4.0/
dc.sourceRevista Colombiana de Ciencias Hortícolas; Vol. 15, Núm. 1 (2021): Revista Colombiana de Ciencias Hortícolas;p. 1 -18.spa
dc.subject.agrovocFusarium oxysporumspa
dc.subject.agrovocUchuvaspa
dc.subject.agrovocControl biológicospa
dc.subject.agrovocMarchitamientospa
dc.subject.agrovocurihttp://aims.fao.org/aos/agrovoc/c_16244
dc.subject.agrovocurihttp://aims.fao.org/aos/agrovoc/c_3b22c756
dc.subject.agrovocurihttp://aims.fao.org/aos/agrovoc/c_918
dc.subject.agrovocurihttp://aims.fao.org/aos/agrovoc/c_8390
dc.subject.faoPlagas de las plantas - H10spa
dc.subject.redFrutalesspa
dc.titleGnotobiotic system for selecting microorganisms with biocontrol potential against Fusarium oxysporum f. sp. physalispa
dc.title.translatedGnotobiotic system for selecting microorganisms with biocontrol potential against Fusarium oxysporum f. sp. physalieng
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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