Biostimulants influence the biochemical response in plantain plants (Musa AAB) infected with Ralstonia solanacearum

Autores:: Mateus-Cagua, Diana Mayerly
González-Almario, Adriana
Betancourt-Vásquez, Mónica
Rodríguez-Yzquierdo, Gustavo Adolfo

Tipo de recurso:: Article of journal

Fecha de publicación:: 2026

Institución:: Universidad Pedagógica y Tecnológica de Colombia

Repositorio:: RiUPTC: Repositorio Institucional UPTC

Idioma:: eng

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dc.title.spa.fl_str_mv	Biostimulants influence the biochemical response in plantain plants (Musa AAB) infected with Ralstonia solanacearum
title	Biostimulants influence the biochemical response in plantain plants (Musa AAB) infected with Ralstonia solanacearum
spellingShingle	Biostimulants influence the biochemical response in plantain plants (Musa AAB) infected with Ralstonia solanacearum Chlorophyll Malondialdehyde Moko Osmotic adjustment Musaceae Platain Clorofila Malondialdehído Moko Ajuste osmótico Musáceas Plátano
title_short	Biostimulants influence the biochemical response in plantain plants (Musa AAB) infected with Ralstonia solanacearum
title_full	Biostimulants influence the biochemical response in plantain plants (Musa AAB) infected with Ralstonia solanacearum
title_fullStr	Biostimulants influence the biochemical response in plantain plants (Musa AAB) infected with Ralstonia solanacearum
title_full_unstemmed	Biostimulants influence the biochemical response in plantain plants (Musa AAB) infected with Ralstonia solanacearum
title_sort	Biostimulants influence the biochemical response in plantain plants (Musa AAB) infected with Ralstonia solanacearum
dc.creator.fl_str_mv	Mateus-Cagua, Diana Mayerly González-Almario, Adriana Betancourt-Vásquez, Mónica Rodríguez-Yzquierdo, Gustavo Adolfo
dc.contributor.author.eng.fl_str_mv	Mateus-Cagua, Diana Mayerly González-Almario, Adriana Betancourt-Vásquez, Mónica Rodríguez-Yzquierdo, Gustavo Adolfo
dc.subject.none.fl_str_mv	Chlorophyll Malondialdehyde Moko Osmotic adjustment Musaceae Platain Clorofila Malondialdehído Moko Ajuste osmótico Musáceas Plátano
topic	Chlorophyll Malondialdehyde Moko Osmotic adjustment Musaceae Platain Clorofila Malondialdehído Moko Ajuste osmótico Musáceas Plátano
publishDate	2026
dc.date.accessioned.none.fl_str_mv	2026-08-29 21:18:22 2026-11-10T10:15:10Z
dc.date.available.none.fl_str_mv	2026-08-29 21:18:22
dc.date.issued.none.fl_str_mv	2026-08-29
dc.type.spa.fl_str_mv	Artículo de revista
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dc.identifier.doi.none.fl_str_mv	10.19053/uptc.24223719.19743
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dc.language.iso.eng.fl_str_mv	eng
language	eng
dc.relation.references.eng.fl_str_mv	Alves, A.O., M.M.B. Santos, L.J.N. Souza, E.B. Souza, and R.L.R. Mariano. 2015. Use of silicon for reducing the severity of bacterial wilt of sweet pepper. J. Plant Pathol. 97(3), 419-429. Bates, L.S., R.P. Waldren, and I.D. Teare. 1973. Rapid determination of free proline for water-stress studies. Plant Soil 39(1), 205-207. Doi: https://doi.org/10.1007/BF00018060 Cao, Y., H. Pi, P. Chandrangsu, Y. Li, Y. Wang, H. Zhou, H. Xiong, J.D. Helmann, and Y. Cai. 2018. Antagonism of two plant-growth promoting Bacillus velezensis isolates against Ralstonia solanacearum and Fusarium oxysporum. Sci. Rep. 8, 4360. Doi: https://doi.org/10.1038/s41598-018-22782-z Chauhan, J., M.D. Prathibha, P. Singh, P. Choyal, U.N. Mishra, D. Saha, R. Kumar, H. Anuragi, S. Pandey, B. Bose, B. Mehta, P. Dey, K.K. Dwivedi, N.K. Gupta, and R.K. Singhal. 2023. Plant photosynthesis under abiotic stresses: damages, adaptive, and signaling mechanisms. Plant Stress 10, 100296. Doi: https://doi.org/10.1016/j.stress.2023.100296 Chávez-Arias, C.C., S. Gómez-Caro, and H. Restrepo-Díaz. 2020. Physiological responses to the foliar application of synthetic resistance elicitors in cape gooseberry seedlings infected with Fusarium oxysporum f. sp. physali. Plants 9(2), 176. Doi: https://doi.org/10.3390/plants9020176 Cruz-Lara, D.A., E. Polanco-Díaz, Y.A. Deaquiz-Oyola, M. Betancourt-Vásquez, and G.A. Rodríguez-Yzquierdo. 2024. Evaluation of the effect of biostimulant substances on the growth and physiological response of Dominico-Harton plantain (Musa AAB). Rev. Colomb. Cienc. Hortic. 18(3), e17926. Doi: https://doi.org/10.17584/rcch.2024v18i3.17926 Dien, D.C., T. Mochizuki, and T. Yamakawa. 2019. Effect of various drought stresses and subsequent recovery on proline, total soluble sugar and starch metabolisms in rice (Oryza sativa L.) varieties. Plant Prod. Sci. 22(4), 530-545. Doi: https://doi.org/10.1080/1343943X.2019.1647787 Djaya, L., H. Hersanti, N. Istifadah, S. Hartati, and I.M. Joni. 2019. In vitro study of plant growth promoting rhizobacteria (PGPR) and endophytic bacteria antagonistic to Ralstonia solanacearum formulated with graphite and silica nano particles as a biocontrol delivery system (BDS). Biocatal. Agric. Biotechnol. 19, 101153. Doi: https://doi.org/10.1016/j.bcab.2019.101153 DuBois, M., K.A. Gilles, J.K. Hamilton, P.A. Rebers, and F. Smith. 1956. Colorimetric method for determination of sugars and related substances. Anal. Chem. 28(3), 350-356. Doi: https://doi.org/10.1021/ac60111a017 Fan, X.Y., W.P. Lin, R. Liu, N.-H. Jiang, and K.Z. Cai. 2018. Physiological response and phenolic metabolism in tomato (Solanum lycopersicum) mediated by silicon under Ralstonia solanacearum infection. J. Integr. Agric. 17(10), 2160-2171. Doi: https://doi.org/10.1016/S2095-3119(18)62036-2 Fortunato, A.A., F.Á. Rodrigues, and K.J.T. Nascimento. 2012. Physiological and biochemical aspects of the resistance of banana plants to fusarium wilt potentiated by silicon. Phytopathology 102(10), 957-966. Doi: https://doi.org/10.1094/PHYTO-02-12-0037-R Ghosh, U.K., M.N. Islam, M.N. Siddiqui, and M.A.R. Khan. 2021. Understanding the roles of osmolytes for acclimatizing plants to changing environment: a review of potential mechanisms. Plant Signal. Behav. 16(8), 1913306. Doi: https://doi.org/ 10.1080/15592324.2021.1913306 He, L.Y., L. Sequeira, and A. Kelman. 1983. Characteristics of strains of Pseudomonas solanacearum from China. Plant Dis. 67, 1357-1361. Doi: https://doi.org/10.1094/PD-67-1357 Hodges, D.M., J.M. DeLong, C.F. Forney, and R.K. Prange. 1999. Improving the thiobarbituric acid-reactive-substances assay for estimating lipid peroxidation in plant tissues containing anthocyanin and other interfering compounds. Plants 227, 604-611. Doi: https://doi.org/10.1007/s004250050524 Huang, H., F. Ullah, D.-X. Zhou, M. Yi, and Y. Zhao. 2019. 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Doi: https://doi.org/10.1080/07060661.2019.1654547 Xiao, X.-O., W. Lin, K. Li, W. Li, X. Gao, and L. Lv. 2017. Early burst of reactive oxygen species positively regulates resistance of eggplant against bacterial wilt. J. Phytopathol. 165(10), 652-661. Doi: https://doi.org/10.1111/jph.12604 Ye, P., X. Li, B. Cui, S. Song, F. Shen, X. Chen, G. Wang, X. Zhou, and Y. Deng. (2022). Proline utilization a controls bacterial pathogenicity by sensing its substrate and cofactors. Commun. Biol. 5(1), 496. Doi: https://doi.org/10.1038/s42003-022-03451-4 Zuur, A.F., E.N. Ieno, N. Walker, A.A. Saveliev, and G.M. Smith. 2009. Mixed effects models and extensions in ecology with R. Springer-Verlag, New York, NY. Doi: https://doi.org/10.1007/978-0-387-87458-6
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spelling	Mateus-Cagua, Diana MayerlyGonzález-Almario, AdrianaBetancourt-Vásquez, MónicaRodríguez-Yzquierdo, Gustavo Adolfo2026-08-29 21:18:222026-11-10T10:15:10Z2026-08-29 21:18:222026-08-292011-2173https://repositorio.uptc.edu.co/handle/001/2343210.19053/uptc.24223719.197432422-3719https://doi.org/10.19053/uptc.24223719.19743application/pdfengSociedad Colombiana de Ciencias Hortícolas-SCCH and Universidad Pedagógica y Tecnológica de Colombia-UPTCRevista Colombiana de Ciencias Hortícolas - 2026http://creativecommons.org/licenses/by-nc-sa/4.0info:eu-repo/semantics/openAccessThis work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.http://purl.org/coar/access_right/c_abf2https://revistas.uptc.edu.co/index.php/ciencias_horticolas/article/view/19743ChlorophyllMalondialdehydeMokoOsmotic adjustmentMusaceaePlatainClorofilaMalondialdehídoMokoAjuste osmóticoMusáceasPlátanoBiostimulants influence the biochemical response in plantain plants (Musa AAB) infected with Ralstonia solanacearumArtículo de revistahttp://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1info:eu-repo/semantics/articleJournal articleinfo:eu-repo/semantics/publishedVersionTexthttp://purl.org/coar/version/c_970fb48d4fbd8a85Alves, A.O., M.M.B. Santos, L.J.N. Souza, E.B. Souza, and R.L.R. Mariano. 2015. Use of silicon for reducing the severity of bacterial wilt of sweet pepper. J. Plant Pathol. 97(3), 419-429. Bates, L.S., R.P. Waldren, and I.D. Teare. 1973. Rapid determination of free proline for water-stress studies. Plant Soil 39(1), 205-207. Doi: https://doi.org/10.1007/BF00018060 Cao, Y., H. Pi, P. Chandrangsu, Y. Li, Y. Wang, H. Zhou, H. Xiong, J.D. Helmann, and Y. Cai. 2018. Antagonism of two plant-growth promoting Bacillus velezensis isolates against Ralstonia solanacearum and Fusarium oxysporum. Sci. Rep. 8, 4360. Doi: https://doi.org/10.1038/s41598-018-22782-z Chauhan, J., M.D. Prathibha, P. Singh, P. Choyal, U.N. Mishra, D. Saha, R. Kumar, H. Anuragi, S. Pandey, B. Bose, B. Mehta, P. Dey, K.K. Dwivedi, N.K. Gupta, and R.K. Singhal. 2023. Plant photosynthesis under abiotic stresses: damages, adaptive, and signaling mechanisms. Plant Stress 10, 100296. Doi: https://doi.org/10.1016/j.stress.2023.100296 Chávez-Arias, C.C., S. Gómez-Caro, and H. Restrepo-Díaz. 2020. Physiological responses to the foliar application of synthetic resistance elicitors in cape gooseberry seedlings infected with Fusarium oxysporum f. sp. physali. Plants 9(2), 176. Doi: https://doi.org/10.3390/plants9020176 Cruz-Lara, D.A., E. Polanco-Díaz, Y.A. Deaquiz-Oyola, M. Betancourt-Vásquez, and G.A. Rodríguez-Yzquierdo. 2024. Evaluation of the effect of biostimulant substances on the growth and physiological response of Dominico-Harton plantain (Musa AAB). Rev. Colomb. Cienc. Hortic. 18(3), e17926. Doi: https://doi.org/10.17584/rcch.2024v18i3.17926 Dien, D.C., T. Mochizuki, and T. Yamakawa. 2019. Effect of various drought stresses and subsequent recovery on proline, total soluble sugar and starch metabolisms in rice (Oryza sativa L.) varieties. Plant Prod. Sci. 22(4), 530-545. Doi: https://doi.org/10.1080/1343943X.2019.1647787 Djaya, L., H. Hersanti, N. Istifadah, S. Hartati, and I.M. Joni. 2019. In vitro study of plant growth promoting rhizobacteria (PGPR) and endophytic bacteria antagonistic to Ralstonia solanacearum formulated with graphite and silica nano particles as a biocontrol delivery system (BDS). Biocatal. Agric. Biotechnol. 19, 101153. Doi: https://doi.org/10.1016/j.bcab.2019.101153 DuBois, M., K.A. Gilles, J.K. Hamilton, P.A. Rebers, and F. Smith. 1956. Colorimetric method for determination of sugars and related substances. Anal. Chem. 28(3), 350-356. Doi: https://doi.org/10.1021/ac60111a017 Fan, X.Y., W.P. Lin, R. Liu, N.-H. Jiang, and K.Z. Cai. 2018. Physiological response and phenolic metabolism in tomato (Solanum lycopersicum) mediated by silicon under Ralstonia solanacearum infection. J. Integr. Agric. 17(10), 2160-2171. Doi: https://doi.org/10.1016/S2095-3119(18)62036-2 Fortunato, A.A., F.Á. Rodrigues, and K.J.T. Nascimento. 2012. Physiological and biochemical aspects of the resistance of banana plants to fusarium wilt potentiated by silicon. Phytopathology 102(10), 957-966. Doi: https://doi.org/10.1094/PHYTO-02-12-0037-R Ghosh, U.K., M.N. Islam, M.N. Siddiqui, and M.A.R. Khan. 2021. Understanding the roles of osmolytes for acclimatizing plants to changing environment: a review of potential mechanisms. Plant Signal. Behav. 16(8), 1913306. Doi: https://doi.org/ 10.1080/15592324.2021.1913306 He, L.Y., L. Sequeira, and A. Kelman. 1983. Characteristics of strains of Pseudomonas solanacearum from China. Plant Dis. 67, 1357-1361. Doi: https://doi.org/10.1094/PD-67-1357 Hodges, D.M., J.M. DeLong, C.F. Forney, and R.K. Prange. 1999. Improving the thiobarbituric acid-reactive-substances assay for estimating lipid peroxidation in plant tissues containing anthocyanin and other interfering compounds. Plants 227, 604-611. Doi: https://doi.org/10.1007/s004250050524 Huang, H., F. Ullah, D.-X. Zhou, M. Yi, and Y. Zhao. 2019. 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Doi: https://doi.org/10.1007/978-0-387-87458-6220Revista Colombiana de Ciencias Hortícolashttps://revistas.uptc.edu.co/index.php/ciencias_horticolas/article/download/19743/17605Núm. 2 , Año 2026 : In press/En prensaPublicationOREORE.xmltext/xml2908https://repositorio.uptc.edu.co/bitstreams/6c3da20b-fe7f-425b-99d2-0e78668bf8cb/download3216c16de513bdff4a7315d6c7bbf0beMD51falseAnonymousREAD001/23432oai:repositorio.uptc.edu.co:001/234322026-11-10 05:15:10.88http://creativecommons.org/licenses/by-nc-sa/4.0metadata.onlyhttps://repositorio.uptc.edu.coRepositorio Institucional UPTCbdigital@metabiblioteca.com

Biostimulants influence the biochemical response in plantain plants (Musa AAB) infected with Ralstonia solanacearum

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