Browse > Article
http://dx.doi.org/10.1080/12298093.2018.1475370

Aspergillus terreus JF27 Promotes the Growth of Tomato Plants and Induces Resistance against Pseudomonas syringae pv. tomato  

Yoo, Sung-Je (Division of Agricultural Microbiology, National Institute of Agricultural Science, Rural Development Administration)
Shin, Da Jeong (Division of Agricultural Microbiology, National Institute of Agricultural Science, Rural Development Administration)
Won, Hang Yeon (Division of Agricultural Microbiology, National Institute of Agricultural Science, Rural Development Administration)
Song, Jaekyeong (Division of Agricultural Microbiology, National Institute of Agricultural Science, Rural Development Administration)
Sang, Mee Kyung (Division of Agricultural Microbiology, National Institute of Agricultural Science, Rural Development Administration)
Publication Information
Mycobiology / v.46, no.2, 2018 , pp. 147-153 More about this Journal
Abstract
Certain beneficial microorganisms isolated from rhizosphere soil promote plant growth and induce resistance to a wide variety of plant pathogens. We obtained 49 fungal isolates from the rhizosphere soil of paprika plants, and selected 18 of these isolates that did not inhibit tomato seed germination for further investigation. Based on a seed germination assay, we selected four isolates for further plant tests. Treatment of seeds with isolate JF27 promoted plant growth in pot tests, and suppressed bacterial speck disease caused by Pseudomonas syringae pathovar (pv.) tomato DC3000. Furthermore, expression of the pathogenesis-related 1 (PR1) gene was higher in the leaves of tomato plants grown from seeds treated with JF27; expression remained at a consistently higher level than in the control plants for 12 h after pathogen infection. The phylogenetic analysis of a partial internal transcribed spacer sequence and the b-tubulin gene identified isolate JF27 as Aspergillus terreus. Taken together, these results suggest that A. terreus JF27 has potential as a growth promoter and could be used to control bacterial speck disease by inducing resistance in tomato plants.
Keywords
Plant growth-promoting fungi; induced resistance; Aspergillus terreus;
Citations & Related Records
연도 인용수 순위
  • Reference
1 Zhang Q, Zhang J, Yang L, et al. Diversity and biocontrol potential of endophytic fungi in Brassica napus. Biol Control. 2014;72:98-108.   DOI
2 Park Y-H, Chung JY, Ahn DJ, et al. Screening and characterization of endophytic fungi of Panax ginseng Meyer for biocontrol activity against ginseng pathogens. Biol Control. 2015;91:71-81.   DOI
3 Syamsia Kuswinanti T, Syam’un E, et al. The potency of endophytic fungal isolates collected from local aromatic rice as indole acetic acid (IAA) producer. Procedia Food Sci. 2015;3:96-103.   DOI
4 Delgado-Sanchez P, Ortega-Amaro MA, Jimenez-Bremont JF, et al. Are fungi important for breaking seed dormancy in desert species? Experimental evidence in Opuntia streptacantha (Cactaceae). Plant Biol. 2011;13:154-159.   DOI
5 Hyakumachi M. Research on biological control of plant diseases: present state and perspectives. J Gen Plant Pathol. 2013;79:435-440.   DOI
6 Waqas M, Khan AL, Hamayun M, et al. Endophytic fungi promote plant growth and mitigate the adverse effects of stem rot: an example of Penicillium citrnum and Aspergillus terreus. J Plant Interact. 2015;10:280-287.   DOI
7 Saha BC, Kennedy GJ. Ninety six well microtiter plate as microbioreactors for production of itaconic acid by six Aspergillus terreus strains. J Microbiol Methods. 2018;144:53-59.   DOI
8 Raina S, De Vizio D, Palonen EK, et al. Is quorum sensing involved in lovastatin production in the filamentous fungus Aspergillus terreus? Process Biochem. 2012;47:843-852.   DOI
9 Jogaiah S, Abdelrahman M, Tran L-SP, et al. Characterization of rhizosphere fungi that mediate resistance in tomato against bacterial wilt disease. J Exp Bot. 2013;64:3829-3842.   DOI
10 Van Loon LC, Bakker PAHM, Pieterse CMJ. Systemic resistance induced by rhizosphere bacteria. Annu Rev Phytopathol. 1998;36:453-483.   DOI
11 Durrant WE, Dong X. Systemic acquired resistance. Annu Rev Phytopathol. 2004;42:185-209.   DOI
12 Lovda T, Lillo C. Reference gene selection for quantitative real-time PCR normalization in tomato subjected to nitrogen, cold, and light stress. Anal Biochem. 2009;387:238-242.   DOI
13 Wani ZA, Mirza DN, Arora P, et al. Molecular phylogeny, diversity, community structure, and plant growth promoting properties of fungal endophytes associated with the corms of saffron plant:an insight into the microbiome of Crocus sativus Linn. Fungal Biol. 2016;120:1509-1524.   DOI
14 Munoz-Espinoza V, Lopez-Climent MF, Casaretto JA, et al. Water stress responses of tomato mutants impaired in hormone biosynthesis reveal absicisic acid, jasmonic acid and salicylic acid interactions. Front Plant Sci. 2015;6:1-13.
15 Priyadharsini P, Muthukumar T. The root endophytic fungus Curvularia geniculate from Parthenium hysterophorus roots improves plant growth through phosphate solubilization and phytohormone production. Fungal Ecol. 2017;27:69-77.   DOI
16 Khan AL, Hamayun M, Kim Y-H, et al. Gibberellins producing endophytic Aspergillus fumigatus sp. LH02 influenced endogenous phytohormonal levels, isoflavonoids production and plant growth in salinity stress. Process Biochem. 2011;46:440-447.   DOI
17 Murali M, Sudisha J, Amruthesh KN, et al. Rhizosphere fungus Penicillium chrysogenum promotes growth and induces defense-related genes and downy mildew disease resistance in pearl millet. Plant Biol. 2013;15:111-118.   DOI
18 Mathys J, De Cremer K, Timmermans P, et al. Genome-wide characterization of ISR induced in Arabidopsis thaliana by Trichoderma hamatum T382 against Botrytis cinerea infection. Front Plant Sci. 2012;3:1025-1081.
19 Nawrocka J, Malolepsza U. Diversity in plant systemic resistance induced by Trichoderma. Biol Control. 2013;67:149-156.   DOI
20 Liu S-I, Wu J, Zhang P, et al. Response of phytohormones and correlation of SAR signal pathway genes to the different resistance levels of grapevine against Plasmopara viticola infection. Plant Physiol Biochem. 2016;107:56-66.   DOI
21 Pikovskaya RI. Mobilization of phosphorus in soil in connection with the vital activity of some microbial species. Mikrobiologiya. 1948;17:362-370.
22 Conrath U. Molecular aspects of defense priming. Trends Plant Sci. 2011;16:524-531.   DOI
23 Lopez-Mondejar R, Ros M, Pascual JA. Mycoparasitism-related genes expression of Trichoderma harzianum isolates to evaluate their efficacy as biological control agent. Biol Control. 2011;56:59-66.   DOI
24 Salas-Marina MA, Silva-Flores MA, Uresti-Rivera EE, et al. Colonization of Arabidopsis roots by Trichoderma atroviride promotes growth and enhances systemic disease resistance through jasmonic acid/ethylene and salicylic acid pathways. Eur J Plant Pathol. 2011;131:15-26.   DOI
25 Shoresh M, Harman GE, Mastouri F. Induced systemic resistance and plant responses to fungal biocontrol agents. Annu Rev Phytopathol. 2010;48:21-43.   DOI
26 Gravel V, Antoun H, Tweddell RJ. 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. 2007;39:1968-1977.   DOI
27 Wang Q, Yang Y-B, Yang X-Q, et al. Lovastatin analogues and other metabolites from soil-derived Aspergillus terreus YIM PH30711. Phytochemistry. 2018;145:146-152.   DOI
28 Mukherjee PK, Horwitz BA, Kenerley CM. Secondary metabolism in Trichoderma-a genomic perspective. Microbiology (Reading, Engl.). 2012;158:35-45.   DOI
29 Baker SE, Perrone G, Richardson NM, et al. Phylogenomic analysis of polyketide synthaseencoding genes in Trichoderma. Microbiology. 2012;158:147-154.   DOI
30 Frisvad JC, Larsen TO. Chemodiversity in the genus Aspergillus. Appl Microbiol Biotechnol. 2015;99:7859-7877.   DOI
31 Guo CJ, Wang CCC. Recent advances in genome mining of secondary metabolites in Aspergillus terreus. Front Microbiol. 2014;5:717.
32 Nesha R, Siddiqui ZA. Effects of Paecilomyces lilacinus and Aspergillus niger alone and in combination on the growth, chlorophyll contents and soft rot disease complex of carrot. Sci Hortic. 2017;218:258-264.   DOI
33 Shoresh M, Harman GE. The molecular basis of shoot responses of maize seedlings to Trichoderma harzianum T22 inoculation of the root: a proteomic approach. Plant Physiol. 2008;147:2147-2163.   DOI
34 Strawn MA, Marr SK, Inoue K, et al. Arabidopsis isochorismate synthase functional in pathogeninduced salicylate biosynthesis exhibits properties consistent with a role in diverse stress responses. J Biol Chem. 2007;282:5919-5933.   DOI
35 Zhang Y, Shi X, Li B, et al. Salicylic acid confers enhanced resistance to Glomerella leaf spot in apple. Plant Physiol Biochem. 2016;106:64-72.   DOI