Identification of disease suppressive potential of Trichoderma virens and Jasmonic acid against fusarium wilt and damping-off in “Seed Primed” tomato plants

Authors

  • Monika Sood Department of Botany, School of Bioengineering and Biosciences, Lovely Professional University, Delhi-Jalandhar Highway Phagwara, 144411, Punjab, India https://orcid.org/0000-0002-8673-3162
  • Sarvjeet Kukreja Department of Agronomy, School of Agriculture, Lovely Professional University, Delhi-Jalandhar Highway Phagwara, 144411, Punjab, India https://orcid.org/0000-0001-7107-4849
  • Vipul Kumar Department of Plant Pathology, School of Agriculture, Lovely Professional University, Delhi-Jalandhar Highway Phagwara, 144411, Punjab, India

DOI:

https://doi.org/10.14719/pst.2325

Keywords:

Biotic stress, Seed priming, Biocontrol, Disease incidence, Plant defence

Abstract

Disease causing phytopathogens are responsible for an approximately 15% reduction in worldwide food production. Therefore, for efficient management of plant diseases, a systematic understanding of the harmful impacts of pathogens on economic crops is essential. The practice of sustainable agriculture aims at the development of a system that supports the growth of plants but simultaneously induces adverse effects on the existence of pathogens. Therefore, the current research was designed to monitor the seed priming effects of Trichoderma virens (as Biocontrol Agent, BCA) and Jasmonic acid (a chemical inducer) in tomato plants infected with two devastating soil-borne pathogens viz., Fusarium oxysporum lycopersici (Fol) and Rhizoctonia solani. Application of these agents in infected plants alone or together leads to the establishment of various disease-suppressive mechanisms in the host plants as observed in the form of enhanced seedling vigour index, percentage germination, morphological growth, and a substantial decrease in the percentage of disease incidence. Furthermore, pathogen inoculation in diseased plants enhances the content of two compatible osmolytes i.e., proline and glycine betaine which themselves serve as defensive molecules by acting as osmoprotectants and signalling molecules in the induction of various defence-related pathways in the stressed plants. Our study provides important insights into the effectiveness of T. virens and JA in the amelioration of pathogen-induced damage in the host plants. The
inferences obtained from this research highlight the better efficiency of combined applications of T. virens and JA against these two soil-borne pathogens.

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References

Panno S, Davino S, Caruso AG, Bertacca S, Crnogorac A, Mandi? A et al. A review of the most common and economically important diseases that undermine the cultivation of tomato crop in the Mediterranean basin. Agronomy 2021 Nov 1 ;11(11):2188. https://doi.org/10.3390/agronomy11112188

Joshi R. A review of Fusarium oxysporum on its plant interaction and industrial use. J Med Pl Studies. 2018;6(3):112-15. https://doi.org/10.22271/plants.2018.v6.i3b.07

Clocchiatti A, Hannula SE, Rizaludin MS, Hundscheid MPJ, Klein Gunnewiek PJA, Schilder MT et al. Impact of cellulose-rich organic soil amendments on growth dynamics and pathogenicity of Rhizoctonia solani. Microorganisms. 2021 Jun 1;9(6). https://doi.org/10.3390/microorganisms9061285

Ghosh UK, Islam MN, Siddiqui MN, Khan MAR. Understanding the roles of osmolytes for acclimatizing plants to changing environment: A review of potential mechanism. Plant Signal Behav Aug;16(8):1913306. https://doi.org/10.1080/15592324.2021.1913306

Giri J. Glycinebetaine and abiotic stress tolerance in plants.Plant Signal Behav 2011 Nov 6(11):1746-51

Huang J, Hirji R, Adam L, Rozwadowski KL, Hammerlindl JK, Keller WA et al. Genetic engineering of glycinebetaine production toward enhancing stress tolerance in plants: metabolic limitations. Plant Physiol 1;122(3):747-56

Suprasanna P, Rai AN, Hima Kumari P, Kumar SA, Kavi Kishor PB. Modulation of proline: implications in plant stress tolerance and development. In: Anjum NA, Gill SS, Gill R, editors. Plant Adaptation to Environmental UK: CABI Publishers. 2014; p. 68-93.

Meena RS, Kumar S, Datta R, Lal R, Vijayakumar V, Brtnicky M et al. Impact of agrochemicals on soil microbiota and management: A review. 2020 Jan 23;9(2):34. https://doi.org/10.3390/land9020034

Panth M, Hassler SC, Baysal-Gurel F. Methods for management of soilborne diseases in crop production. Agriculture. 2020 Jan 11;10(1):16. https://doi.org/10.3390/agriculture10010016

Collinge DB, Jensen DF, Rabiey M, Sarrocco S, Shaw MW, Shaw RH. Biological control of plant diseases – What has been achieved and what is the direction?. Plant Pathol 2022 Jun 1. https://doi.org/10.1111/ppa.13555

Fenibo EO, Ijoma GN, Matambo T. Biopesticides in sustainable agriculture: A critical sustainable development driver governed by green chemistry principles. Front Sustain Food Syst. 2021 Jun 11;5:141. https://doi.org/10.3389/fsufs.2021.619058

Lahlali R, Ezrari S, Radouane N, Kenfaoui J, Esmaeel Q, el Hamss H et al. Biological control of plant pathogens: A global perspective. Microorganisms.2022. https://doi.org/10.3390/microorganisms10030596

Sood M, Kapoor D, Kumar V, Sheteiwy MS, Ramakrishnan M, Landi M et al. Trichoderma: The “Secrets” of a multitalented biocontrol agent. Plants (Basel). 2020

Mishra J, Dutta V, Arora NK. Biopesticides in India: technology and sustainability linkages. 3 Biotech. 2020 May 1. https://doi.org/10.1007/s13205-020-02192-7

Zhang L, Zhang F, Melotto M, Yao J, He SY. Jasmonatesignaling and manipulation by pathogens and insects. J Exp Bot. 2017 Mar 3. https://doi.org/10.1093/jxb/erw478

Wang Y, Mostafa S, Zeng W, Jin B. Function and mechanism of jasmonicacid in plant responses to abiotic and biotic stresses. Int J Mol Sci. 2021 Aug. https://doi.orger/10.3390/ijms22168568

Morton DJ, Stroube WH. Antagonistic and stimulatory effects of soil microorganisms upon Sclerotium rolfsii. Phytopath. 1955; 45(8) 417-20

Garrett S. Biology of root-infecting fungi. Cambridge University Press. 1956; 294 p. https://doi.org/10.1097/00010694-195607000-00011

Agrawal T, Kotasthane AS. Chitinolytic assay of indigenous Trichoderma isolates collected from different geographical locations of Chhattisgarh in Central India. Springerplus. 2012. https://doi.org/10.1186/2193-1801-1-73

Roberts WK, Selitrennikoff CP. Plant and bacterial chitinases differ in antifungal activity. Microbiology (N Y). 1988 Jan 1. https://doi.org/10.1099/00221287-134-1-169

Abdul-Baki AA, Anderson JD. Vigor determination in soybean seed by multiple criteria1. Crop Sci. 1973 Nov 1. https://doi.org/10.2135/cropsci1973.0011183X001300060013x

Jain A, Singh S, Kumar Sarma B, Bahadur Singh H. Microbial consortium-mediated reprogramming of defence network in pea to enhance tolerance against Sclerotinia sclerotiorum. J Appl Microbiol]. 2012 Mar. https://doi.org/10.1111/j.1365-2672.2011.05220.x

Jensen B, Knudsen IMB, Madsen M, Jensen DF. Biopriming of infected carrot seed with an antagonist, Clonostachys rosea, selected for control of seedborne Alternaria spp. Phytopathology.2004. https://doi.org/10.1094/PHYTO.2004.94.6.551

Nirmaladevi D, Venkataramana M, Srivastava RK, Uppalapati SR, Gupta VK, Yli-Mattila T et al. Molecular phylogeny, pathogenicity and toxigenicity of Fusarium oxysporum f. sp. lycopersici. Scientific Reports. 2016 Feb 17 https://doi.org/10.1038/srep21367

Manganiello G, Sacco A, Ercolano MR, Vinale F, Lanzuise S, Pascale A et al. Modulation of tomato response to Rhizoctonia solani by Trichoderma harzianum and its secondary metabolite Harzianic acid. Front Microbiol. 2018 Aug 30;9(AUG):1966. https://doi.org/10.3389/fmicb.2018.01966

Bates LS, Waldren RP, Teare ID. Rapid determination of free proline for water-stress studies. Plant and Soil. 1973 Aug. https://doi.org/doi.org/10.1007/BF00018060

Grieve CM, Grattan SR. Rapid assay for determination of water soluble quaternary ammonium compounds. Plant Soil. 1983 Jun;70(2):303-07. https://doi.org/10.1007/BF02374789

Tamburino R, Sannino L, Cafasso D, Cantarella C, Orrù L, Cardi T et al. Cultivated tomato (Solanum lycopersicumL.) suffered a severe cytoplasmic bottleneck during domestication: Implications from chloroplast genomes. Plants. 2020 Oct https://doi.org/10.3390/plants9111443

Singh VK, Singh AK, Kumar A. Disease management of tomato through PGPB: current trends and future perspective. 3 Biotech. 2017 Jul 20. https://doi.org/10.1007/s13205-017-0896-1

Adhikari TB, Gao A, Ingram T, Louws FJ. Pathogenomics characterization of an emerging fungal pathogen, Fusarium oxysporum f. sp. lycopersiciin greenhouse tomato productionsystems. Front Microbiol. 2020 Aug 27;11:1995. https://doi.org/10.3389/fmicb.2020.01995

Abdelghany MMA, Kurikawa M, Watanabe M, Matsui H, Yamamoto M, Ichinose Y et al. Surveillance of pathogenicity of Rhizoctonia solani Japanese isolates with varied anastomosis groups and subgroups on Arabidopsis thaliana. Life. 2022 Jan 1. https://doi.org/10.3390/life12010076

Heflish AA, Abdelkhalek A, Al-Askar AA, Behiry SI. Protective and curative effects of Trichoderma asperelloides ta41 on tomato root rot caused by Rhizoctonia solani Rs33. Agronomy. 2021 Jun 1;11(6). https://doi.org/10.3390/agronomy11061162

Larousse M, Rancurel C, Syska C, Palero F, Etienne C, Industri B et al. Tomato root microbiota and Phytophthora parasitica-associated disease. Microbiome. 2017;5(1). https://doi.org/10.1186/s40168-017-0273-7

Chaturvedi H, Singh B, Jajoo A, Prakash A. Shielding of photosynthetic apparatus by consortia of bacterial endophytes in tomato plants suffering from Fusarium wilt. Frontiers in Agronomy. 2022 May 18;4:33. https://doi.org/10.3389/fagro.2022.831731

Ajayi-Oyetunde OO, Bradley CA. Rhizoctonia solani: taxonomy, population biology and management of Rhizoctonia seedling disease of soybean. Plant Pathol. 2018 Jan 1. https://doi.org/10.1111/ppa.12733

Halifu S, Deng X, Song X, Song R, Liang X. Inhibitory mechanism of Trichoderma virens ZT05 on Rhizoctonia solani. Plants. 2020 Jul 19 . https://doi.org/10.3390/plants9070912

Zehra A, Meena M, Dubey MK, Aamir M, Upadhyay RS. Activation of defense response in tomato against Fusarium wilt disease triggered by Trichoderma harzianum supplemented with exogenous chemical inducers (SA and MeJA). Revista Brasil Botanica. 2017 Sep 1;40(3):651-64. https://doi.org/10.1007/s40415-017-0382-3

Ayub MA, Rehman MZU, Umar W, Farooqi ZUR, Sarfraz M, Ahmad HR et al. Role of glycine betaine in stress management in plants. Emerging Plant Growth Regulators in Agriculture: Roles in Stress Tolerance. https://doi.org/10.1016/B978-0-323-91005-7.00005-9

Aydi-Ben-Abdallah R, Jabnoun-Khiareddine H, Daami-Remadi M. Fusarium wilt biocontrol and tomato growth stimulation, using endophytic bacteria naturally associated with Solanum sodomaeum and S. bonariense plants. Egypt J Biol Pest Control. 2020 Dec 1. https://doi.org/10.1186/s41938-020-00313-1

Sood M, Kumar V, Rawal R. Seed biopriming a novel method to control seed borne diseases of crops. Biocontrol Agents and Secondary Metabolites. 2021 Jan 1; 181-223. https://doi.org/10.1016/B978-0-12-822919-4.00008-9

Abbas A, Mubeen M, Zheng H, Sohail MA, Shakeel Q, Solanki MK et al. Trichoderma spp. genes involved in the biocontrol activity against Rhizoctonia solani. Front Microbiol. 2022 May 25 .https://doi.org/10.3389/fmicb.2022.884469

Howell CR. Mechanisms employed by Trichodermaspecies in the biological control of plant diseases: The history and evolution of current concepts.2007 Feb 23. https://doi.org/10.1094/PDIS.2003.87.1.4

Harwoko H, Daletos G, Stuhldreier F, Lee J, Wesselborg S, Feldbrügge M et al. Dithiodiketopiperazine derivatives from endophytic fungi Trichoderma harzianum and Epicoccum nigrum. Nat Prod Res. 2021. https://doi.org/10.1080/14786419.2019.1627348

Wang J, Song L, Gong X, Xu J, Li M. Functions of jasmonicacid in plant regulation and response to abiotic stress. Int J Mol Sci 2020. Feb 1. https://doi.org/10.3390/ijms21041446

Ameye M, Audenaert K, de Zutter N, Steppe K, van Meulebroek L, Vanhaecke L et al. Priming of wheat with the green leaf volatile Z-3-hexenyl acetate enhances defense against Fusarium graminearum but boosts deoxynivalenol production. Plant Physiol. 2015 Apr 1;167(4):1671-84. https://doi.org/10.1104/pp.15.00107

Mei C, Qi M, Sheng G, Yang Y. Inducible overexpression of a rice allene oxide synthase gene increases the endogenous jasmonic acid level, PR gene expression and host resistance to fungal infection. Mol Plant Microbe Interact. 2006 Oct. https://doi.org/10.1094/MPMI-19-1127

Zhao S, Li Y. Current understanding of the interplays between host hormones and plant viral infections. PLoSPathog. 2021 Feb 25;17(2). https://doi.org/10.1371/journal.ppat.1009242

Moosa A, Sahi S, Khan S, Horticulturae AMF, 2019 undefined. Salicylic acid and jasmonic acid can suppress green and blue moulds of citrus fruit and induce the activity of polyphenol oxidase and peroxidase. researchgate.net. 2019 Jun 1. https://doi.org/10.2478/fhort-2019-0014

Motallebi P, Niknam V, Ebrahimzadeh H, Hashemi M, Enferadi ST. Exogenous methyl jasmonatetreatment induces defenseresponse against Fusarium culmorum in wheat seedlings. J Plant Growth Regul. 2017 Mar 1;36(1):71-82. https://doi.org/10.1007/s00344-016-9620-3

Published

07-08-2023 — Updated on 10-09-2023

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1.
Sood M, Kukreja S, Kumar V. Identification of disease suppressive potential of Trichoderma virens and Jasmonic acid against fusarium wilt and damping-off in “Seed Primed” tomato plants. Plant Sci. Today [Internet]. 2023 Sep. 10 [cited 2024 Nov. 4];10(sp1):30-45. Available from: https://horizonepublishing.com/journals/index.php/PST/article/view/2325

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