Advances on Trichoderma-induced Plant Resistance against Diseases

doi:10.16409/j.cnki.2095-039x.2015.05.013

Abstract

Abstract: Trichoderma spp. are widely used biocontol microbe against plant disease with multiple antagonistic mechanism. The significant advances in induced resistance mechanism have been made in recent years. Trichoderma can produce over 20 MAMPs or DAMPs, correspondingly plant roots have about 30 receptors or response genes. The Trichoderma colonization on roots is able to initiate interaction of MAMPs/DAMPs-root receptor or response gene, which then triggers long distance transduction of signals including salicylic acid and jasmonic acid/E tresponsible for induced expression of leaf defense genes against plant disease. Integration of information based on the changes of plant trancriptome, proteome and metabolome after Trichoderma colonization on roots can provide more comprehensive understanding to Trichoderma-plant beneficial interaction associated with the induced resistance against plant disease.

Key words: Trichodema, biological control, induced resistance, MAMPs, metabolome

CLC Number:

S476

CHEN Jie. Advances on Trichoderma-induced Plant Resistance against Diseases[J]. journal1, 2015, 31(5): 733-741.

References

[1] Alonso-Ramirez A, Poveda J, Martin I, et al. Salicylic acid prevents Trichoderma harzianum from entering the vascular system of roots[J]. Molecular Plant Pathology, 2014, 15(8): 823-831.
[2] Mukherjee M, Mukherjee P, Horwitz B, et al. Trichoderma-plant-pathogen nteractions: advances in genetics of biological control[J]. Indian Journal of Microbiology, 2012, 52(4): 522-529.
[3] Fan L, Fu K, Yu C, et al. Thc6 protein, isolated from Trichoderma harzianum, can induce maize defense response against Curvularia lunata[J]. Journal of Basic Microbiology, 2014, 54(1): 1-10.
[4] Vargas W A, Mandawe J C, Kenerley C M. Plant-derived sucrose is a key element in the symbiotic association between Trichoderma virens and maize plants[J]. Plant Physiology, 2009, 151(2): 792-789.
[5] Moran–Diez E, Hermosa R, Ambrosino P, et al. The endopolygalacturonase is required for the Trichoderma harzianum–plant beneficial interaction[J]. Molecular Plant-Microbe Interactions, 2009, 22(10): 1021-1231.
[6] Nawrocka J, Malolepsza U. Diversity in plants systemic resistance induced by Trichoderma[J]. Biological Control, 2013, 67(2): 149-156.
[7] Shoresh M, Gal-On A, Leibmann D, et al. Characterization of mitogen-activated protein kinase gene from cucumber required for Trichoderma-confered plant resistance[J]. Plant Physiology, 2006, 142(3): 1169-1179.
[8] Hermosa R, RubioM B, Cardoza R E, et al. The contribution of Trichoderma to balancing the costs of plant growth and defense[J]. International Microbiology, 2013, 16(2): 69-80.
[9] Nawrocka J, Małolepsza U. Diversity in plant systemic resistance induced by Trichoderma[J]. Biological Control, 2013, 67(2): 149-156.
[10] Atanasova L, LeCrom S, Gruber S, et al. Comparative transcriptomics reveal different strategies of Trichoderma mycoparasitism[J]. BMC Genomics, 2013, 14: 121.
[11] Hemestsberger C, Herrberger C, Zechmann B, et al. The Ustilago maydis effector Pep1 suppresses plant immunity by inhibition of host peroxidase activity[J]. PloS Pathogens, 2012, 8: e10002684.
[12] Lorito M, Woo S L, Harman G E, et al. Translational research on Trichoderma: from ‘omics' to the field[J]. Annual Review of Phytopathology, 2010, 48: 395-417.
[13] Muljerkee P K, Horitz B A, AfredoHerrera-Estrella S, et al. Trichoderma research in the genome Era[J]. Annual Review of Phytopathology, 2013, 51: 105-129.
[14] Buensanteai N, Mukherjee P K, Horwitz B A, et al. Expressison and purification of biologically active Trichoderma virens protein acetous elicitor Sm1 in Pichiapastoris[J]. Protein Expression and Purification, 2010, 72(1): 131-138.
[15] Harman G E, Petzoldt R, Comis A, et al. Interaction between Trichoderma harzianum strain T22 and maize inbred line Mo17 and effects of these interactions on disease caused by Pythium ultimum and Collectrichum gramin icola[J]. Phytopathology, 2004, 94(2): 147-153.
[16] Chen J, Dou k, Gao Y D, et al. Mechanism and application of Trichoderma spp. in biological control of corn diseases[J]. Mycosystema, 2014, 33(6): 1154-1167.
[17] Vargas W A, Djonovic S, Sukno S A, et al. Dimerization controls the activity of fungal elicitors that trigger systemic resistance in plants[J]. Journal of Biological Chemistry, 2008, 283(28): 19804-19815.
[18] Samolski I, Rincon A M, Pinzon L M, et al. The qid74 gene from Trichoderma harzianum has a role in root architechture and plant biofertilization[J]. Microbiology, 2012, 158(1): 129-138.
[19] Horwitz B A, Kosti I, Glaser F, et al. Trichoderma genomes: a vast reservoir of potential elicitor proteins//Mukherjee P K, Horwitz B A, Singh U S, et al, eds. Trichoderma Biology and Application[M]. London: CABI, 2013, 195-208.
[20] de Oliveira A L, Gallo M, Pazzagli L, et al. The structure of the elicitor cerato-platanin (CP), the first member of the CP fungal protein family, reveals a double psi-beta-barrel fold and carbohydrate binding[J]. Journal of Biological Chemistry, 2011, 286(20): 17560-17568.
[21] Bar M, Sharfman M, Ron M, et al. BAK1 is required for the attenuation of ethylene inducing xylanse (Eix)- induced defense responses by the decoy receptor LeEix1[J]. Plant Journal, 2010, 63(5): 791-800.
[22] Ma Y, Han C, Chen J, et al. Fungal cellulase is an elicitor but its enzymatic activity is not required for its elicitor activity[J]. Molecular Plant Pathology, 2015, 16(1): 14-26.
[23] Moran-Diez E, Hermosa R, Ambrosino P, et al. ThPG1 endopolygalacturonase is required for the Trichoderma harzianum-plant beneficial interaction[J]. Molecular Plant-Microbe Interations, 2009, 22(8): 1021-1031.
[24] Shoresh M, Harman G E. The molecular basis of shoot responses of maize seedlings to Trichoderma harzianum T22 inoculation of the root: a proteomic approach[J]. Plant Physiology, 2008, 147(4): 2147-2163.
[25] Contreras-Cornejo H A, Ortiz-Casttro R, Lopez-Bucio J. Promotion of plant growth and induction of systemic defense by Trichoderma: physiology, genetics and gene expression//Mukherjee P K, Horwitz B A, Singh U S, et al, eds. Trichoderma Biology and Application[M]. London: CABI, 2013.
[26] Brotman Y L, Lisec J, Meret M, et al. Transcript and metabolite analysis of the Trichoderma-iduced systemic resistance response to Pseudomonas syringae in Arabidopsis thaliana[J]. Microbiology, 2012, 158(2): 139-146.
[27] Brotman Y. The use of metabolomic approaches to study Trichoderma-plant-interactions//Mukherjee P K, Horwitz B A, Singh U S, et al, eds. Trichoderma Biology and Application[M]. London: CABI, 2013.
[28] 陈捷, 朱洁伟, 张婷, 等. 木霉菌生物防治机制与应用研究进展[J]. 中国生物防治学报, 2012, 27(2): 145-151.
[29] Harman G E, Howell C R, Viterbo A, et al. Trichoderma species: opportunistic, avirulent plants sybiombionts[J]. Nature Reviews of Microbiology, 2004, 2(1): 43-56.
[30] Kanehisa M, Goto S, Sato Y, et al. KEGG for integration and interpretation of large-scale molecular data sets[J]. Nucleic Acids Research, 2012, 40(1): 109-114.
[31] Moran-Diez E, Rubio B, Dominguez S, et al. Transcriptomic response of Arabidopsis thaliana after 24 h inoculation with the biocontrol fungus Trichoderma harzianum[J]. Journal of Plant Physiology, 2012, 169(6): 614-620.