Abstract
On our planet, the customary agricultural operations are influenced by different issues (i.e., disease, pests, drought, diminished soil fertility) because of the utilization of hazardous chemical pesticides, pollution, and climate change. Among these, the fungal genus Trichoderma carries out noteworthy activity in controlling plant maladies. Trichoderma spp. are the best biocontrol agents, as more than 60% of the enlisted biofungicides utilized in present agribusinesses are based on Trichoderma. Plant–Trichoderma–pathogen is a complex community having multiple mechanisms. Proteome and genome examinations have greatly upgraded the capacity for comprehensive and genome-based useful investigations as they have identified and determined the role of a variety of novel genes and gene products, including ABC transporters, enzymes, and various proteins that produce novel elicitors of induced resistance, proteins responsible for a gene-for-gene avirulent interaction between Trichoderma spp. and plants, antagonism-related genes, and plant proteins specifically induced by Trichoderma, but there remains much more to be learned than has already been discovered. Recent methodologies based on molecular science can easily identify, clone, sequence, and express the activity of the genes and can observe their capacities and function in the biocontrol system. Herein we present the comprehensive genetics of interactions of Trichoderma with plants and phytopathogens and their role through different modes of action. The aforementioned variables are required to enhance their efficiency and applications and also demonstrate the possibilities for development of strains of Trichoderma.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Similar content being viewed by others
References
Abbas A, Jiang D, Fu Y (2017) Trichoderma spp. as antagonist of Rhizoctonia solani. J Plant Pathol Microb 8:1000402. https://doi.org/10.4172/2157-7471.1000402
Alabouvette C, Olivain C, Migheli Q, Steinberg C (2009) Microbiological control of soil-borne phytopathogenic fungi with special emphasis on wilt-inducing Fusarium oxysporum. New Phytol Trust 184:529–544
Babychan M, Simon S (2017) Efficacy of Trichoderma spp. against Fusarium oxysporum f. sp. lycopersici (FOL) infecting pre-and post-seedling of tomato. J Pharmacogn Phytochem 6:616–619
Benitez T, Rincon AM, Limon MC, Codon AC (2004) Biocontrol mechanisms of Trichoderma strains. Int Microbiol 7:249–260
Bezuidenhout CN, Van Antwerpen R, Berry SD (2012) An application of principal component analyses and correlation graphs to assess multivariate soil health properties. Soil Sci 177:498–505
Bjorkman T, Blanchard LM, Harman GE (1998) Growth enhancement of shrunken-2 sweet corn when colonized with Trichoderma harzianum 1295-22: effect of environmental stress. J Am Soc Hort Sci 123:35–40
Brotman Y, Landau U, Cuadros-Inostoza A, Takayuki T, Fernie AR et al (2013) Trichoderma–plant root colonization: escaping early plant defense responses and activation of the antioxidant machinery for saline stress tolerance. PLoS Pathog 9:e1003221. https://doi.org/10.1371/journal.ppat.1003221
Cai F, Yu G, Wang P, Wei Z, Fu L, Shen Q, Chen W (2013) Harzianolide, a novel plant growth regulator and systemic resistance elicitor from Trichoderma harzianum. Plant Physiol Biochem 73:106–113
Cardoza RE, Malmierca MG, Hermosa MR, Alexander NJ, McCormick SP, Proctor RH, Tijerino AM, Rumbero A, Monte E, Gutierrez S (2011) Identification of loci and functional characterization of trichothecene biosynthesis genes in filamentous fungi of the genus Trichoderma. Appl Environ Microbiol 77:4867–4877
Chowdappa P, Kumar SPM, Lakshmi MJ, Upreti KK (2013) Growth stimulation and induction of systemic resistance in tomato against early and late blight by Bacillus subtilis OTPB1 or Trichoderma harzianum OTPB3. Biol Control 65:109–117
Contreras-Cornejo HA, Macías-Rodríguez L, Cortés-Penagos C (2009) Trichoderma virens, a plant beneficial fungus enhances biomass production and promotes lateral root growth through an auxin dependent mechanism in Arabidopsis. Plant Physiol 149:1579–1592
Cuevas VC (2006) Soil inoculation with Trichoderma pseudokoningii Rifai enhances yield of rice. Philipp J Sci 135(1):31–37
Daguerre Y, Siegel K, Edel-Hermann V, Steinberg C (2014) Fungal proteins and genes associated with biocontrol mechanisms of soil-borne pathogens: a review. Fungal Biol Rev 28:97–125
Doni F, Isahak A, Radziah C, Zain CM, Ariffin SM, Nurashiqin W, Mohamad W, Mohtar W, Yusoff W (2014) Formulation of Trichoderma sp. SL2 inoculants using different carriers for soil treatment in rice seedling growth. SpringerPlus 3:1–5
Dunlop RW, Simon A, Siwasithamparam D, Ghisalberti EL (1989) An antibiotic from Trichoderma koningii active against soilborne plant pathogens. J Nat Prod 52:67–74
Freitas RS, Steindorff AS, Ramada MHS, Siqueira SJL, Noronha EF, Ulhoa CJ (2014) Cloning and characterization of a protein elicitor Sm1 gene from Trichoderma harzianum. Biotechnol Lett 36(4):783–788
Godio RP, Fouces R, Martín FJ (2007) A squalene epoxidase is involved in biosynthesis of both the antitumor compound clavaric acid and sterols in the basidiomycete H. sublateritium. Cell Press 14:1334–1346
Gravel V, Antoun H, Tweddell RJ (2007) Growth stimulation and fruit yield improvement of greenhouse tomato plants by inoculation with Pseudomonas putida or Trichoderma atroviride: possible role of indole acetic acid (IAA). Soil Biol Biochem 39:1968–1977
Hansen H, Grossmann K (2000) Auxin induced ethylene triggers abscisic acid biosynthesis and growth inhibition. Plant Physiol 124:1437–1448
Haque MM, Ilias GNM, Molla AH (2012) Impact of Trichoderma-enriched biofertilizer on the growth and yield of mustard (Brassica rapa L.) and tomato (Solanum lycopersicum Mill.). Agriculturists 10:109–119
Harman GE (2000) Myths and dogmas of biocontrol changes in perceptions derived from research on Trichoderma harzianum T-22. Plant Dis 84:377–393
Harman GE (2006) Overview of mechanisms and uses of Trichoderma spp. Phytopathology 96:190–194
Harman GE (2011) Multifunctional fungal plant symbionts: new tools to enhance plant growth and productivity. New Phytol 189:647–649
Harman GE, Howell CR, Viterbo A, Chet I, Lorito M (2004) Trichoderma species opportunistic, avirulent plant symbionts. Nat Rev Microbiol 2:43–56
Harman GE, Björkman T, Ondik K, Shoresh M (2008) Changing paradigms on the mode of action and uses of Trichoderma spp. for biocontrol. Outlooks Pest Manag 19:24–29
Hasan EA, Walker F, Buchenauer H (2008) Trichoderma harzianum and its metabolite 6-pentyl-alpha-pyrone suppress fusaric acid produced by Fusarium moniliforme. J Phytopathol 156:79–87
Hermosa R, Botella L, Keck M, Jimenez JA, Montero Barrientos M, Arbona V, Gomez Cadenas A, Monte E, Nicolas C (2011) The over expression in Arabidopsis thaliana of a Trichoderma harzianum gene that modulates glucosidase activity and enhances tolerance to salt and osmotic stresses. J Plant Physiol 168:1295–1302
Hermosa R, Viterbo A, Chet I, Monte E (2012) Plant-beneficial effects of Trichoderma and of its genes. Microbiology 158:17–25
Herrera-Estrella A, Chet I (2004) The biological control agent Trichoderma from fundamentals to applications. In: Arora D (ed) Handbook of fungal biotechnology. Dekker, New York, NY, pp 147–156
Howell CR (2003) Mechanisms employed by Trichoderma species in the biological control of plant diseases: the history and evolution of current concepts. Plant Dis 87:4–10
Howell CR, Hanson LE, Stipanovic RD, Puckhaber LS (2000) Induction of terpenoid synthesis in cotton roots and control of Rhizoctonia solani by seed treatment with Trichoderma virens. Phytopathology 90:248–252
Idowu OO, Olawole OI, Idumu OO, Salami AO (2016) Bio-control effect of Trichoderma asperellum (Samuels) Lieckf. and Glomus intraradices Schenk on okra seedlings infected with Pythium aphanidermatum (Edson) Fitzp. and Erwinia carotovora (Jones). Am J Exp Agric 10:1–12
Inbar J, Abramsky M, Cohe D, Chet I (1994) Plant growth enhancement and disease control by Trichoderma harzianum in vegetable seedlings grown under commercial conditions. Eur J Plant Pathol 100:337–346
Jiang X, Geng A, He N, Li Q (2011) New isolate of Trichoderma viride strain for enhanced cellulolytic enzyme complex production. J Biosci Bioeng 111:121–127
Kubicek CP, Herrera-Estrella A, Seidl-Seiboth V, Martinez DA et al (2011) Comparative genome sequence analysis underscores mycoparasitism as the ancestral life style of Trichoderma. Genome Biol 12:1–15
Kumar A, Scher K, Mukherjee M, Pardovitz-Kedmi E, Sible GV, Singh US, Kale SP, Mukherjee PK, Horwitz BA (2010) Overlapping and distinct functions of two Trichoderma virens MAP kinases in cell wall integrity, antagonistic properties and repression of conidiation. Biochem Biophys Res Commun 398:765–777
Kumar V, Shahid M, Singh A, Srivastava M, Mishra A, Srivastava YK, Pandey S, Sharma A (2014) Effect of biopriming with biocontrol agents Trichoderma harzianum (Th. Azad) and Trichoderma viride on chickpea genotype (Radhey). J Plant Pathol Microb 5:1–4
Latorre BA, Lillo C, Rioja ME (2001) Eficacia de los tratamientos fungicidas para el control de Botrytis cinerea de la vid en función de la época de aplicación. Cienc Invest Agraria 28:61–66
Leong J (1986) Siderophores: their biochemistry and possible role in biocontrol of plant pathogen. Annu Rev Phytopathol 24:187–209
Lorito M, Woo SL, Harman GE, Monte E (2010) Translational research on Trichoderma: from ‘omics to the field. Annu Rev Phytopathol 48:395–417
Losane BK, Kumar PKR (1992) Fungal plant growth regulators. In: Arora DK, Elander KG, Mujerji KG (eds) Handbook of applied mycology: fungal biotechnology, vol 4. Dekker, New York, NY, pp 565–602
Mastouri F, Björkman T, Harman GE (2010) Seed treatment with Trichoderma harzianum alleviates biotic, abiotic and physiological stresses in germinating seeds and seedlings. Phytopathology 100:1213–1221
Meszka B, Broniarek-Niemiec A, Bielenin A (2008) The status of dodine resistance of Venturia inaequalis populations in Poland. Phytopathol Pol 47:57–61
Miethke M (2013) Molecular strategies of microbial iron assimilation: from high affinity complexes to cofactor assembly systems. Metallomics 5:15–28
Migheli Q, González-Candelas L, Dealessi L, Camponogara A, Ramon-Vidal D (1998) Transformants of Trichoderma longibrachiatum over-expressing the beta-1,4-endoglucanase gene egl1 show enhanced biocontrol of Pythium ultimum on cucumber. Phytopathology 88:673–677
Mishra A, Salokhe VM (2011) Rice growth and physiological responses to SRI water management and implications for crop productivity. Paddy Water Environ 9:41–52
Mondejar LR, Ros M, Pascual JA (2011) Mycoparasitism related genes expression of Trichoderma harzianum isolates to evaluate their efficacy as biological control agent. Biol Control 56:59–66
Moran-Diez E, Hermosa R, Ambrosino P, Cardoza RE, Gutierrez S, Lorito M, Monte E (2009) The ThPG1 endopolygalacturonase is required for the Trichoderma harzianum–plant beneficial interaction. Mol Plant Microbe Interact 22:1021–1031
Mukherjee PK, Latha J, Hadar R, Horwitz BA (2004) Role of two G-protein alpha subunits, TgaA and TgaB, in the antagonism of plant pathogens by Trichoderma virens. Appl Environ Microbiol 70:542–549
Mukherjee PK, Wiest A, Ruiz N, Keightley A, Moran-Diez ME, McCluskey K, Pouchus YF, Kenerley CM (2011) Two classes of new peptaibols are synthesized by a single non-ribosomal peptide synthetase of Trichoderma virens. J Biol Chem 286:4544–4554
Mukherjee PK, Horwitz BA, Kenerley CM (2012) Secondary metabolism in Trichoderma: a genomic perspective. Microbiology 158:35–45
Mukherjee PK, Horwitz BA, Singh US, Mukherjee M, Schmoll M (2013) Trichoderma: biology and applications. CAB International, Wallingford. (www.cabi.org)
Mukhtar I (2008) Influence of Trichoderma species on seed germination in okra. Mycopathology 6:47–50
Naznin A, Hossain MM, Anju-ManAra K, Hoque A, Islam M, Hasan T (2015) Influence of organic amendments and bio- control agent on yield and quality of tuberose. J Hort 2:4. https://doi.org/10.4172/2376-0354.1000156
Neumann B, Laing M (2006) Trichoderma: an ally in the quest for soil system sustainability. In: Uphoff N, Fernandes E, Herren H, Husson O, Laing M, Palm C, Pretty J, Sanchez P, Sanginga N, Thies J (eds) Biological approaches to sustainable soil system. Taylor & Francis, Boca Raton, FL, pp 491–500
Newman ME (2006) Modularity and community structure in networks. Proc Natl Acad Sci U S A 103(23):8577–8582
Okoth SA, Otadoh JA, Ochanda OJ (2011) Improved seedling emergence and growth of maize and beans by Trichoderma harziunum. Trop Subtrop Agroecosyst 13:65–71
Omann MR, Lehner S, Escobar-RodrÚguez C, Brunner K, Zeilinger S (2012) The seven-transmembrane receptor Gpr1 governs process relevant for the antagonistic interaction of Trichoderma atroviride with its host. Microbiol 158:107–118. https://doi.org/10.1099/mic.0.052035-0
Pieterse CM, Leon-Reyes A, Vander Ent S, Van Wees SC (2009) Networking by small molecule hormones in plant immunity. Nat Chem Biol 5:308–316
Pozo MJ, Baek JM, García JM, Kenerley CM (2004) Functional analysis of tvsp1, a serine protease-encoding gene in the biocontrol agent Trichoderma virens. Fungal Genet Biol 41:336–348
Rehman SU, Lawrence R, Kumar EJ, Badri ZA (2012) Comparative efficacy of Trichoderma viride, T. harzianum and carbendazim against damping-off disease of cauliflower caused by Rhizoctonia solani Kuehn. J Biopest 5:23–27
Reithner B, Schuhmacher R, Stoppacher N, Pucher M, Brunner K, Zeilinger S (2007) Signaling via the Trichoderma atroviride mitogen-activated protein kinase Tmk1 differentially affects mycoparasitism and plant protection. Fungal Genet Biol 44:1123–1133
Rosado IV, Rey M, Codón AC, Govantes J, Moreno-Mateos MA (2007) QID74 cell wall protein of Trichoderma harzianum is involved in cell protection and adherence to hydrophobic surfaces. Fungal Genet Biol 44:950–964
Saba H, Vibhash D, Manisha M, Prashant KS, Farhan H, Tauseef A (2012) Trichoderma: a promising plant growth stimulator and biocontrol agent. Mycosphere 3:524–531
Sajeesh PK (2015) Cu-Chi-Tri: a triple combination for the management of late blight disease of potato (Solanum tuberosum L.). Dissertation, GBPUA&T, Pantnagar, India
Sarrocco S, Guidi L, Fambrini S, Des I’Innocenti E, Vannacci G (2009) Competition for cellulose exploitation between Rhizoctonia solani and two Trichoderma isolated in the decomposition of wheat straw. J Plant Pathol 91:331–338
Seiboth B, Herold S, Kubicek CP (2012) Metabolic engineering of inducer formation for cellulase and hemicellulase gene expression in Trichoderma reesei. Subcell Biochem 64:367–390
Shayakhmetov IF (2001) Biological activity of metabolites from culture filtrates of Cochliobolus sativus and Fusarium oxysporum in connection with in vitro cellular selection of crop plants for resistance to phytopathogens. Mycol Phytopathol 35:66–71
Shi M, Chen L, Wang XW, Zhang T, Zhao PB, Song XY, Sun CY, Chen X-L, Zhou BC, Zhang YZ (2012) Antimicrobial peptaibols from Trichoderma pseudokoningii induce programmed cell death in plant fungal pathogens. Microbiology 158:166–175
Shoresh M, Gal-On A, Leibman D, Chet I (2006) Characterization of a mitogen-activated protein kinase gene from cucumber required for Trichoderma-conferred plant resistance. Plant Physiol 142:1169–1179
Shukla N, Awasthi RP, Rawat L, Kumar J (2012) Biochemical and physiological responses of rice (Oryza sativa L.) as influenced by Trichoderma harzianum under drought stress. Plant Physiol Biochem 54:78–88
Singh S, Dureja P, Tanwar RS, Singh A (2005) Production and antifungal activity of secondary metabolites of Trichoderma virens. Pest Res J 17:26–29
Singh HB, Singh BN, Singh SP, Singh SR, Sarma BK (2009) Biological control of plant diseases: current status and future prospects. In: Johri JK (ed) Recent advances in biopesticides: biotechnological applications. New India, New Delhi
Srivastava SN, Singh V, Awasthi SK (2006) Trichoderma induced improvement in growth, yield and quality of sugarcane. Sugar Technol 8:166. https://doi.org/10.1007/BF02943654
Stepanova AN, Yun J, Likhacheva AV, Alonso JM (2007) Multilevel interactions between ethylene and auxin in Arabidopsis roots. Plant Cell 19:2169–2185
Steyaert JM, Stewart A, Jaspers MV, Carpenter M, Ridgway HJ (2004) Co-expression of two genes, a chitinase (chit42) and proteinase (prb1), implicated in mycoparasitism by Trichoderma hamatum. Mycologia 96:1245–1252
Swain H, Adak T, Mukherjee AK, Mukherjee PK, Bhattacharya P, Behera S, Bagchi T, Patro R, Shasmita KAK, Bag MK, Danger TK, Lenka S, Jena M (2018) Novel Trichoderma strains isolated from tree barks as potential biocontrol agents and biofertilizers for direct seeded rice. Microbiol Res 214:83–90
Thakur M, Sohal BS (2013) Role of elicitors in inducing resistance in plants against pathogen infection: a review. ISRN Biochem 2013:762412. https://doi.org/10.1155/2013/762412. pp 1–10
Thakur AK, Uphoff N, Antony E (2010) An assessment of physiological effects of system of rice intensification (SRI) practices compared with recommended rice cultivation practices in India. Exp Agric 46:77–98
Tijerino A, Cardoza RE, Moraga J, Malmierca MG, Vicente F, Aleu J, Collado IG, Gutierrez S, Monte E, Hermosa R (2011a) Overexpression of the trichodiene synthase gene tri5 increases trichodermin production and antimicrobial activity in Trichoderma brevicompactum. Fungal Genet Biol 48:285–296
Tijerino A, Hermosa R, Cardoza RE, Moraga J, Malmierca MG, Aleu J, Collado IG, Monte E, Gutierrez S (2011b) Overexpression of the Trichoderma brevicompactum tri5 gene: effect on the expression of the trichodermin biosynthetic genes and on tomato seedlings. Toxins 3:1220–1232
Tucci M, Ruocco M, De Masi L, De Palma M, Lorito M (2011) The beneficial effect of Trichoderma spp. on tomato is modulated by the plant genotype. Mol Plant Pathol 12(4):341–354. https://doi.org/10.1111/j.1364-3703.2010.00674
Van Wees SCM, Van der Ent S, Pieterse CMJ (2008) Plant immune responses triggered by beneficial microbes. Curr Opin Plant Biol 11:443–448
Verma M, Brar SK, Tyagi RD, Surampalli RY, Val’ero JR (2007) Antagonistic fungi, Trichoderma spp.: panoply of biological control. Biochem Eng J 37:1–20
Vinale F, Sivasithamparam K, Ghisalberti EL, Marra R, Woo SL, Lorio M (2008) Trichoderma–plant–pathogen interactions. Soil Biol Biochem 40:1–10
Vinale F, Ghisalberti EL, Sivasithamparam K, Marra R, Ritieni A, Ferracane R, Woo S, Lorito M (2009) Factors affecting the production of Trichoderma harzianum secondary metabolites during the interaction with different plant pathogens. Lett Appl Microbiol 48:705–711
Vinale F, Marra R, Ruocco M (2014) Trichoderma secondary metabolites active on plants and fungal pathogens. Open Mycol J 8:127–139
Viterbo A, Horwitz BA (2010) Mycoparasitism. In: Borkovich K, Ebbole DJ (eds) Cellular and molecular biology of filamentous fungi. ASM Press, Washington, DC, pp 676–693
Yedidia I, Srivastva AK, Kapulnik Y, Chet I (2001) Effect of Trichoderma harzianum on microelement concentrations and increased growth of cucumber plants. Plant and Soil 235:235–242
Yoshioka Y, Ichikawa H, Naznin HA, Kogure A, Hyakumachi M (2012) Systemic resistance induced in Arabidopsis thaliana by Trichoderma asperellum SKT-1, a microbial pesticide of seed borne diseases of rice. Pest Manag Sci 68:60. https://doi.org/10.1002/ps.2220
Zeilinger S, Reithner B, Scala V, Peiss I, Lorito M, Mach RL (2005) Signal transduction by Tga3, a novel G-protein-alpha subunit of Trichoderma atroviride. Appl Environ Microbiol 71:1591–1597
Zhong YH, Wang TH, Wang XL, Zhang GT, Yu HN (2009) Identification and characterization of a novel gene, TrCCD1, and its possible function in hyphal growth and conidiospore development of Trichoderma reesei. Fungal Genet Biol 46:255–263
Acknowledgments
The authors acknowledge the Director, ICAR-National Rice Research Institute, Cuttack, for providing technical support, and the Department of Science and Technology, Govt. of India, New Delhi, for providing an INSPIRE Fellowship (IF140749) to Harekrushna Swain. The authors are also immensely thankful to Dr. Prasun K. Mukherjee, Scientist G and Head of the Environmental Biotechnology Section and group leader of Agricultural Microbiology, Nuclear Agricultural Biotechnology Division, Bhabha Atomic Research Centre, Trombay, Mumbai, for his tremendous support and guidance.
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2020 Springer Nature Singapore Pte Ltd.
About this chapter
Cite this chapter
Swain, H., Mukherjee, A.K. (2020). Host–Pathogen–Trichoderma Interaction. In: Sharma, A., Sharma, P. (eds) Trichoderma. Rhizosphere Biology. Springer, Singapore. https://doi.org/10.1007/978-981-15-3321-1_8
Download citation
DOI: https://doi.org/10.1007/978-981-15-3321-1_8
Published:
Publisher Name: Springer, Singapore
Print ISBN: 978-981-15-3320-4
Online ISBN: 978-981-15-3321-1
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)