Suppression of seedling diseases of silk cotton (Bombax Ceiba) and eucalyptus (Euclayptus tereticornis) by Pleurotus Sajorcaju decomposed coir pith and Plant Growth Promoting Rhizobacteria (PGPR) based potting media
DOI:
https://doi.org/10.14719/pst.6502Keywords:
Forest tree seedling, PGPR , Potting medium, Suppression of disease , Yeasts slurryAbstract
The studies on the decomposition of coir waste by yeast slurry and Pleurotus Sojar caju showed that it was found to decompose the coir waste effectively. The nutrient analysis of the decomposed coir pith showed that the Pleurotus decomposed coir pith (PDCP) recorded a higher nutrient status than the yeast slurry decomposed coir pith (YDCP). The effect of decomposed coir pith, biocontrol agents and Plant growth promoting Rhizobacteria (PGPR) based potting media on forest tree seedling disease and their growth was studied. Furthermore, the various combinations of normal nursery mix and P. Sojar caju decomposed coir pith (PDCP) used were 0:100, 25:75, 50:50 and 100:0. The media with equal proportions of normal media mix (NMM) and (PDCP) at 50:50 recorded maximum germination in forest tree seeds, viz., Eucalyptus (Euclayptus tereticornis), Silk cotton (Bombax ceiba). The treated seeds with Trichoderma viride were sown in a PDCP 50:50 ratio along with the amendment of Pseudomonas fluorescens+ Azospirillium + Phosphobacteria @ 10 % (v/v) were recorded the maximum shoot and root growth in both the seedlings of silk cotton and eucalyptus and also resulted in a minimum disease incidence of 2.36 and 1.36 percent in Eucalyptus wilt (Fusarium oxysporum) and silk cotton root rot (Verticillium albo-atrum), respectively. These findings highlight an eco-friendly approach to disease suppression in forest nurseries, offering a sustainable alternative to chemical fungicides.
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References
Zakalyukina YV, Zenova GM. Antagonistic activity of soil acidophilic actinomycetes. Biol Bull. 2007;34:329-32. https://doi.org/10.1134/S1062359007040036
Cook RJ. The nature and practice of biological control of plant pathogens. American Phytopathological Society. 1983;539. https://doi.org/10.1094/Phyto-75-25
Kloepper JW, Schroth MN, Miller TD. Effects of rhizosphere colonization by plant growth-promoting rhizobacteria on potato plant development and yield. Phytopathol. 1980;70(11):1078-82. https://doi.org/10.1094/Phyto-70-1078
Weller DM. Biological control of soilborne plant pathogens in the rhizosphere with bacteria. Annu Rev Phytopathol. 1988;26(1):379-407. https://doi.org/10.1146/annurev.py.26.090188.002115
Liu L, Kloepper JW, Tuzun S. Induction of systemic resistance in cucumber by plant growth-promoting rhizobacteria: duration of protection and effect of host resistance on protection and root colonization. Phytopathol. 1995;86(10):1064-68. https://doi.org/10.1094/Phyto-85-1064
Backer R, Rokem JS, Ilangumaran G, Lamont J, Praslickova D, Ricci E, et al. Plant growth-promoting rhizobacteria: context, mechanisms of action and roadmap to commercialization of biostimulants for sustainable agriculture. Front Plant Sci. 2018;9(1473):1-17. https://doi.org/10.3389/fpls.2018.01473
Li X, Zhao G, Huang Y, Li B. Distinct rhizobacteria recruitment under copper stress contributes to the different copper-accumulating capacities of two Elsholtzia species (Lamiaceae). Plant Soil. 2023;489(1):295-307. https://doi.org/10.1007/s11104-023-06017-3
Mashabela MD, Piater LA, Dubery IA, Tugizimana F, Mhlongo MI. Rhizosphere tripartite interactions and PGPR-mediated metabolic reprogramming towards ISR and plant priming: A metabolomics review. Biology. 2022;11(3):346. https://doi.org/10.3390/biology11030346
Pantelides IS, Stringlis IA, Finkel OM, Mercado-Blanco J. Organic amendments: microbial communities and their role in plant fitness and disease suppression. Front Plant Sci. 2023;14:1213092. https://doi.org/10.3389/fpls.2023.1213092
Mohanan C, Sharma JK. Seed pathology of forest tree species in India-present status, practical problems and future prospects. Commonw For Rev. 1991:133-51.
Kwa?na H, Bateman GL. Aberrant growth and conidiation in wild?type cultures of Fusarium species from wheat. J Phytopathol. 2006;154(1):29-34. https://doi.org/10.1111/j.1439-0434.2005.01054.x
Johnsen K, Nielsen P. Diversity of Pseudomonas strains isolated with King's B and Gould's S1 agar determined by repetitive extragenic palindromic-polymerase chain reaction, 16S rDNA sequencing and fourier transform infrared spectroscopy characterisation. FEMS Microbiology Letters. 1999 Apr 1;173(1):155-62. https://doi.org/10.1111/j.1574-6968.1999.tb13497.x
Papavizas GC, Lumsden RD. Biological control of soilborne fungal propagules. Annu Rev Phytopathol. 1980;18(1):389-413. https://doi.org/10.1146/annurev.py.18.090180.002133
Sendhilvel V, Marimuthu T, Samiappan R. Talc-based formulation of Pseudomonas fluorescens-induced defense genes against powdery mildew of grapevine. Arch Phytopathol Plant Prot. 2007;40(2):81-89. https://doi.org/10.1080/03235400500321677
Dennis C, Webster J. Antagonistic properties of species-groups of Trichoderma: I. Production of non-volatile antibiotics. Transactions of the British Mycological Society. 1971;57(1):25-39. https://doi.org/10.1016/S0007-1536(71)80077-3
Nagarajan R, Manickam TS, Kothandaraman GV. Manurial value of coir pith. Madras Agric J. 1985;72(6):533-35. https://doi.org/10.5281/zenodo.4568256
Muthurayar T, Dhanarajan MS. Biochemical changes during composting of coir pith waste as influenced by different agro industrial wastes. Agricultural Sciences. 2013 May 1;4(5B):28. DOI:10.4236/as.2013.45B005
Kloepper JW, Schroth MN. Development of a powder formulation of rhizobacteria for inoculation of potato seed pieces. Phytopathol. 1981;71(6):590-92. https://doi.org/10.1094/Phyto-71-590
Kloepper JW. Plant growth-promoting rhizobacteria as biological control agents. New York. 1933;6:255-74.
Sivakumar S, Ravi V, Subburam V. The effects of coir pith compost on the growth and quality of leaves of the mulberry plant Morus alba L. Bioresour Technol. 2000;72(1):95-97. https://doi.org/10.1016/S0960-8524(99)90100-1
Holl FB, Chanway CP. Rhizosphere colonization and seedling growth promotion of lodgepole pine by Bacillus polymyxa. Can J Microbiol. 1992;38(4):303-08. https://doi.org/10.1139/m92-050
De Meyer G, Höfte M. Salicylic acid produced by the rhizobacterium Pseudomonas aeruginosa 7NSK2 induces resistance to leaf infection by Botrytis cinerea on bean. Phytopathol. 1997;87(6):588-93. https://doi.org/10.1094/PHYTO.1997.87.6.588
Duffy BK, De?fago G. Environmental factors modulating antibiotic and siderophore biosynthesis by Pseudomonas fluorescens biocontrol strains. Appl Environ Microbiol. 1999;65(6):2429-38. https://doi.org/10.1128/AEM.65.6.2429-2438.1999
Maurhofer M, Keel C, Haas D, Défago G. Pyoluteorin production by Pseudomonas fluorescens strain CHA0 is involved in the suppression of Pythium damping-off of cress but not of cucumber. Eur J Plant Pathol. 1994;100:221-32. https://doi.org/10.1007/BF01876237
Chanway CP, Radley RA, Holl FB, Axlerrood PE. Effect of Bacillus strains on the growth of pine, spruce and Douglas-fir. In: Keister DL, Cregan, editors. The rhizosphere and plant growth. Kluwer, Netherlands; 1991. p. 366.
https://doi.org/10.1007/978-94-011-3336-4_77
Hendromono H. Improvement of growth and quality of Acacia mangium seedlings by using several types of medium. 1986;502:17-26. https://www.cabidigitallibrary.org/doi/full/10.5555/19900645079
Bahuguna VK, Maithani GP, Dhaundiyal UD, Unnikrishnan KP. Standardization of nursery techniques of Acacia albida Del. under North Indian moist climatic condition. 1987;113:95-100. https://www.cabidigitallibrary.org/doi/full/10.555 5/19880620040
Shah A, Nazari M, Antar M, Msimbira LA, Naamala J, Lyu D, et al. PGPR in agriculture: A sustainable approach to increasing climate change resilience. Front Sustain Food Syst. 2021;5:667546. https://doi.org/10.3389/fsufs.2021.667546

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