Evaluating Trichoderma viride for enhancing oil palm growth and biochemical defense against fusarium wilt caused by Fusarium oxysporum f. sp. elaeidis

. 2025 May 27 ; () : . [epub] 20250527

Status Publisher Jazyk angličtina Země Spojené státy americké Médium print-electronic

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid40423921
Odkazy

PubMed 40423921
DOI 10.1007/s12223-025-01273-5
PII: 10.1007/s12223-025-01273-5
Knihovny.cz E-zdroje

This work aimed to evaluate the antagonist effect of Trichoderma viride against Fusarium oxysporum and its ability to promote growth and resistance defence of oil palm. The antagonistic effect of T. viride was tested by paired culture, cellophane plate, and micro-atmosphere methods. In the nursery, 30-day-old oil palm plants were inoculated with T. viride, and 30 days after growing, the roots of plants were infected with the spores of Fusarium oxysporum. Ninety days after infection, plants were harvested, and a series of morphological (height, fresh root and shoot) and biochemical changes (total chlorophyll, phenol compounds, soluble proteins and oxidative enzymes), which are considered to be part of the plant defence response, were evaluated. Results showed that, in dual culture, T. viride significantly reduced mycelial growth of Fusarium oxysporum and released non-volatile and volatile compounds that inhibited the pathogen. In the nursery, there was a significant reduction in disease impact (severity index and incidence) in oil palm inoculated with T. viride and infected with Fusarium oxysporum. A significant increase in plant root and shoot fresh weights, as well as chlorophyll, soluble proteins, and phenol content, was noticed in comparison with non-inoculated control plants. A significant increase in peroxidase, polyphenol oxidase, and phenylalanine ammonia lyase activities was recorded in inoculated and infected plants, compared to control. There was a significant and positive correlation between disease incidence and the activity of these oxidative enzymes. These findings suggest that these compounds play a vital role in plant defence. T. viride could serve as a biological agent to manage vascular wilt in oil palm. However, analysis of its effects on mass production and field application is needed.

Zobrazit více v PubMed

Assoumo MMR, Tchouamo IR, Baudouin M (2023) Adoption of the Tenera Hybrid of Oil Palm (Elaeis guineensis Jacquin) among Smallholder Farmers in Cameroon. Tropicultura 31:103–109

Awan ZA, Shoaib A (2019) Combating early blight infection by employing Bacillus subtilis in combination with plant fertilizers. Curr Plant Biol 20:100125 DOI

Bedine BMA, Sameza ML, Iacomi B, Tchameni NS, Fekam BF (2020) Screening, identification and evaluation of Trichoderma spp. for biocontrol potential of common bean damping-off pathogens. Biocontrol Sci Technol 30:228–242 DOI

Bradford MM (1976) A rapid and sensitive method for quantification of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248–254 PubMed DOI

Chakraborty N, Chandra S, Acharya K (2017) Biochemical basis of improvement of defense in tomato plant against Fusarium wilt by CaCl PubMed DOI PMC

Chakraborty N, Chandra S, Sarkar A, Ghosh A, Dasgupta A, Acharya K (2023) An in planta approach for understanding defense responses in tomato plants against Fusarium oxysporum Schltdl. J Plant Pathol 105:129–136. https://doi.org/10.1007/s42161-022-01224-w DOI

Chidi NI, Adekunle AA, Samuel TO, Eziashi EI (2020) Molecular identification of secreted effector genes involved in African Fusarium oxysporum f.sp. Elaeidis Strains pathogenesis during screening nigerian susceptible and tolerant oil palm (Elaeis guineensis Jacq.) Genotypes. Front Cell Infect Microbiol 10:552394. https://doi.org/10.3389/fcimb.2020.552394 PubMed DOI PMC

Concellün A, Aòün MC, Chaves AR (2004) Characterization and changes in polyphenol oxidase from eggplant fruit (Solanum melongena L.) during storage at low temperature. Food Chem 88:17–24 DOI

Cooper RM, Rusli MH (2014) Threat from Fusarium wilt disease of oil palm to south-east Asia and suggested control measures. J Oil Palm Res 26:109–119

Hammerschmidt R, Nuckles EM, Kuc J (1982) Association of enhanced peroxidase activity with induced systemic resistance of cucumber to Colletotrichum lagenarium. Physiol Plant Pathol 20:73–82 DOI

Hermosa R, Viterb A, Chet I, Monte E (2012) Plant-beneficial effects of Trichoderma and of its genes. Microbiology 158:17–25 PubMed DOI

Hermosa R, Rubio MB, Cardoza RE, Nicolás C, Monte E, Gutiérrez S (2023) The contribution of Trichoderma to balancing the costs of plant growth and defense. Int Microbiol 16(2):69–80. https://doi.org/10.2436/20.1501.01.181 DOI

Imran A, Arif M, Shah Z, Bari A (2020) Soil application of Trichoderma and peach (Prunus persica L.) residues possesses biocontrol potential for weeds and enhances growth and profitability of soybean (Glycine max). Sarhad J Agric 36: 10–20

Karthikeyan M, Radhika K, Mathiyazhagan S, Bhaskaran R, Samiyappan R, Velazhahan R (2006) Induction of phenolics and defense-related enzymes in coconut (Cocos nucifera) roots treated with biocontrol agents. Braz J Plant Physiol 18:367–377 DOI

Khan MIR, Poor P, Janda T (2022) Salicylic acid: a versatile signaling molecule in plants. J Plant Growth Regul 41(5):1887–1890

Leslie JF, Summerel BA (2006) The Fusarium Laboratory Manual. Blackwell Publishing Hoboken 1–2. https://doi.org/10.1002/9780470278376

Lichtenthaler HK, Wellburn RR (1987) Determination of total carotenoids and chlorophylls A and B of extracts in different solvents. Biochem Soc Trans 603:591–592

Masso C, Mukhongo R, Thuita M, Abaidoo R, Ulzen J, Kariuki G, Kalumuna M (2016) Biological Inoculants for Sustainable Intensification of Agriculture in Sub-Saharan Africa Smallholder Farming Systems. Climate change and multi-dimensional sustainability in African agriculture. Springer, Cham, pp 639–658 DOI

Modrzewska M, Bryła M, Kanabus J, Pierzgalski AJPP (2022) Trichoderma as a biostimulator and biocontrol agent against Fusarium in the production of cereal crops: Opportunities and possibilities. Plant Pathol 71:1471–1485. https://doi.org/10.1111/ppa.13578 DOI

Moghaddam GA, Rezayatmand Z, Nasr-Esfahani M, Khozaei M (2019) Genetic defense analysis of tomatoes in response to early blight disease, Alternaria alternata. Plant Physiol Biochem 142:500–509 PubMed DOI

Ngadze E, Icishahayo D, Coutinho TA, Van der Waals JE (2012) Role of polyphenol oxidase, peroxidase, phenylalanine ammonia lyase, chlorogenic acid, and total soluble phenols in resistance of potatoes to soft rot. Plant Dis 96(2):186–192. https://doi.org/10.1094/PDIS-02-11-0149 PubMed DOI

Nicholson RL, Hammerschmidt R (1992) Phenolic compounds and their role in disease resistance. Annu Rev Phytopathol 30:369–389 DOI

Ntah A, Ayong M, Ambata ATH, Bedine BAM, Siebatcheu E, Youassi YO, Tchameni NS, Sameza ML, Wansi JP (2023) Appraisement of antimicrobial potential of organic extracts of Trichoderma virens an Trichoderma asperellum against Phytophthora colocasiae, the causal agent of taro leaf blight. Int J Adv Agric Res 11:16–26

Ntah A, Ayong M, Tchameni NS, Siebatcheu EC, Ambata AHT, Sameza ML, Wansi JD (2018) Efficacy of Trichoderma harzianum (Edtm) and Trichoderma aureoviride (T4) as potential bio-control agent of taro leaf blight caused by Phytophthora colocasiae. Int J Appl Microbiol Biotechnol Res 6:115–126

Ntsomboh-Ntsefong G, Madi G, Nyaka NA, Nsimi MA, Epoh GT, Namuene KS, Fontem LA, Ngando Ebongue GF (2015) Vascular wilt disease tolerance status of some oil palm (Elaeis guineensis Jacq.) Progenies in relation to local strains of Fusarium oxysporum f. sp. elaeidis in cameroon. Int J Curr Res Biosci Plant Biol 2:111–122

Nuangmek W, Aiduang W, Kumla J, Lumyong S, Suwannarach N (2021) Evaluation of a newly identified endophytic fungus, Trichoderma phayaoense for plant growth promotion and biological control of gummy stem blight and wilt of muskmelon. Front Microbiol 12:634772. https://doi.org/10.3389/fmicb.2021.634772 PubMed DOI PMC

Pelagio-Flores R, Esparza-reynoso S, Garnica-vergara A, López-Bucio J, Herrera-Estrella A (2017) Trichoderma-induced acidification is an early trigger for changes in Arabidopsis root growth and determines fungal phytostimulation. Front Plant Sci 8:822. https://doi.org/10.3389/fpls.2017.00822 PubMed DOI PMC

Pomwee A, Yenjit P, Issarakraisila M, Intana W, Chamswarng C (2017) Efficacy of indigenous Trichoderma harzianum in controlling Phytophthora leaf fall (Phytophthora palmivora) in Thai rubber trees. J Plant Dis Prot 124:41–50 DOI

Ponsankar A, Senthil-Nathan S, Vasantha-Srinivasan P, Pandiyan R, Karthi S et al (2023) Systematic induced resistance in Solanum lycopersicum (L.) against vascular wilt pathogen (Fusarium oxysporum f. sp. lycopersici) by Citrullus colocynthis and Trichoderma viride. PLoS One 18:e0278616. https://doi.org/10.1371/journal PubMed DOI PMC

Ren Y, Armstrong M, Qi Y, McLellan H, Zhong C, Du B et al (2019) Phytophthora infestans RXLR effectors target parallel steps in an immune signal transduction pathway. Plant Physiol 180(4):2227–2239. https://doi.org/10.1104/pp.18.00625 PubMed DOI PMC

Rivera-Méndez W, Obregón M, Morán-Diez ME, Hermosa R, Monte E (2020) Trichoderma asperellum biocontrol activity and induction of systemic defenses against Sclerotium cepivorum in onion plants under tropical climate conditions. Biol Cont 141:104145 DOI

Ross WW, Sederoff RR (1992) Pheylalanini ammonia lyase from lo bololly pine; Purification of the enzyme and isolation of complementary DNA clones. Plant Physiol 98:380–386 DOI

Rudresh DL, Shivaprakash MK, Prasad RD (2005) Tricalcium phosphate solubilizing abilities of Trichoderma spp. in relation to P uptake and growth and yield parameters of chickpea (Cicer arietinum L.). Can J Microbiol 51(3):217–222

Saikia R, Kumar R, Singh T, Srivastava AK, Arora DK, Lee MW (2004) Induction of defense related enzymes and pathogenesis related proteins in Pseudomonas fluorescens-treated chickpea in response to infection by Fusarium oxysporum f. sp. ciceri. Mycobiology 32:47–53. https://doi.org/10.4489/MYCO.2004.32.1.047 DOI

Shoresh M, Harman GE, Mastouri F (2010) Induced systemic resistance and plant responses to fungal biocontrol agents. Annu Rev Phytopathol 48:21–43 PubMed DOI

Siebatcheu EC, Wetadieu D, Youassi YO, Bedine Boat AM, Kibrom G B, Tchameni NS, Sameza ML (2023) Secondary metabolites from an endophytic fungus Trichoderma erinaceum with antimicrobial activity towards Pythium ultimum. Nat Prod Res 37:657–662 PubMed DOI

Singh BN, Singh A, Singh SP, Singh HB (2011) Trichoderma harzianum mediated reprogramming of oxidative stress response in root apoplast ofsun ower enhances defence against Rhizoctonia solani. Eur J Plant Pathol 131:121–134 DOI

Singleton VL, Rossi JA (1965) Colorimetry of total phenolics with phosphomolybdicphosphotungstic acid reagents. Am J Enol Viticul 16:144–158 DOI

Sood M, Kapoor D, Kumar V, Sheteiwy MS, Ramakrishnan M, Landi M, Araniti F, Sharma A (2020) Trichoderma: the “Secrets” of a multitalented biocontrol agent. Plants 9:762. https://doi.org/10.3390/plants9060762 PubMed DOI PMC

Tchameni SN, Sameza ML, O’donovan A, Fokom R, Mangaptche ELN, Wakam Nana L, Etoa L, Nwaga D (2017) Antagonism of Trichoderma asperellum against Phytophthora megakarya and its potential to promote cacao growth and induce biochemical defence. Mycology 8(2):84–92 DOI

Tchameni NS, Cotârleț M, Ghinea OI, Bedine BMA, Sameza ML, Borda G, Dinica RM (2020) Involvement of lytic enzymes and secondary metabolites produced by Trichoderma spp. in the biological control of Pythium myriotylum. Int Microbiol 23:179–188 PubMed DOI

Yuan M, Huang Y, Ge W, Jia Z, Song S, Zhang L, Hua Y (2019) Involvement of jasmonic acid, ethylene and salicylic acid signaling pathways behind the systemic resistance induced by Trichoderma longibrachiatum H9 in cucumber. BMC Genom 20:144 DOI

Zheng R, Li S, Zhang X, Zhao C (2021) Biological activities of some new secondary metabolites isolated from endophytic fungi: a review study. Int J Mol Sci 22:959. https://doi.org/10.3390/ijms22020959 PubMed DOI PMC

Zhou Y, Zhao W, Lai Y, Zhang B, Zhan D (2020) Edible Plant Oil: Global status, health issues, and perspectives. Front Plant Sci 11:1315. https://doi.org/10.3389/fpls.2020.01315 PubMed DOI PMC

Zin AW, Badaluddin AN (2020) Biological functions of Trichoderma spp. for agriculture applications. Ann Agri Sci 65:168–178 DOI

Najít záznam

Citační ukazatele

Pouze přihlášení uživatelé

Možnosti archivace

Nahrávání dat ...