Biological management of rhizome rot in ginger (Zingiber officinale ) plants and stored ginger seeds

Authors

DOI:

https://doi.org/10.14719/pst.4288

Keywords:

biological control, endospore-forming endophytes, rhizome bacterization, soft rot

Abstract

Two endospore-forming endophytic bacteria (EEB1 A8 and EEB2 B13) were isolated from ginger rhizome collected from the fields of College of Agriculture, Vellayani and identified as Bacillus spp. Their antagonistic potential against Pythium myriotylum , the soft rot pathogen of ginger, was analyzed in vitro by dual culture plate assay and the agar well diffusion method. They tested positive for biocontrol traits such as the production of hydrogen cyanide, siderophore and volatile organic compounds. The bacterial isolates were applied to ginger plants to test biocontrol efficiency against P. myriotylum , individually and in combination with Piriformospora indica , a fungal root endophyte capable of promoting plant growth and enhancing plant defense. A lesser percent disease index (PDI) was observed in plants where the combination of EEB1 A8 and P. indica was applied. The activity of enzymes pertinent to protective mechanisms against pathogens, like peroxidase, phenylalanine ammonia-lyase, super oxide dismutase (SOD) and polyphenol oxidase (PPO) in the plants were analyzed before challenging, 1st, 3rd and 5th day after challenging with pathogen. The values followed the same trend in all treatments as it increased after inoculation up to 3rd day and then decreased for peroxidase (PO) and SOD. The plants treated with EEB1 A8 and combination of EEB1 A8 and P. indica showed the highest values for the level of defense enzyme production. In a storage study, when ginger seed rhizomes were treated with individual bacterial isolates and as a consortium of both, followed by inoculation with the pathogen P. myriotylum , rhizomes treated with consortium were more tolerant to rhizome rot. Applying endospore-forming bacteria with biocontrol properties is a propitious method for controlling rhizome rot in ginger, in the field and during seed storage.

Downloads

Download data is not yet available.

References

Gupta M, Jebasingh T. Diseases of ginger. In: Haiping Wang, editor. Ginger Cultivation and Its Antimicrobial and Pharmaco-logical Potentials [e-book]. London, Intech Open; 2020;305-40. http://dx.doi.org/10.5772/intechopen.88839

Stirling GR, Turaganivalu U, Stirling AM, Lomavatu MF, Smith MK. Rhizome rot of ginger (Zingiber officinale) caused by Pythi-um myriotylum in Fiji and Australia. Plant Pathology. 2009;38: 453-60. https://doi.org/10.1071/AP09023

Anisha C, Radhakrishnan EK. Metabolite analysis of endophytic fungi from cultivars of Zingiber officinale Rosc. identifies myriad of bioactive compounds including tyrosol. 3 Biotech. 2017(2);146. https://doi.org/10.1007/s13205-017-0768-8

Yashaswini MS, Nysanth NS, Anith KN. Endospore-forming bac-terial endophytes from Amaranthus spp. improve plant growth and suppress leaf blight (Rhizoctonia solani Kühn) disease of Amaranthus tricolor L. Rhizosphere. 2021;19:100387. https://doi.org/10.1016/j.rhisph.2021.100387

Melnick RL, Suárez C, Bailey BA, Backman PA. Isolation of endo-phytic endospore-forming bacteria from Theobroma cacao as potential biological control agents of cacao diseases. Biological Control. 2011;57(3):236-45. https://doi.org/10.1016/j.biocontrol.2011.03.005

Varma A, Bakshi M, Lou B, Hartmann A, Oelmueller R. Pirifor-mospora indica: a novel plant growth-promoting mycorrhizal fungus. Agricultural Research. 2012;1:117-31. https://doi.org/10.1007/s40003-012-0019-5

Oelmüller R, Sherameti I, Tripathi S, Varma A. Piriformospora indica, a cultivable root endophyte with multiple biotechnologi-cal applications. Symbiosis. 2009;49:1-7. https://doi.org/10.1007/s13199-009-0009-y

Franken P. The plant strengthening root endophyte Pirifor-mospora indica: potential application and the biology behind. Applied Microbiology and Biotechnology. 2012;96:1455-64. https://doi.org/10.1007/s00253-012-4506-1

Yadav V, Kumar M, Deep DK, Kumar H, Sharma R, Tripathi T, et al. A phosphate transporter from the root endophytic fungus Piriformospora indica plays a role in phosphate transport to the host plant. Journal of Biological Chemistry. 2010;285(34):26532-44. https://doi.org/10.1074/jbc.M110.111021

Andrade-Linares DR, Müller A, Fakhro A, Schwarz D, Franken P. Impact of Piriformospora indica on tomato. Piriformospora indica. 2013;107-17. http://dx.doi.org/10.1007/978-3-642-33802-1_6

Athira S, Anith KN. Plant growth promotion and suppression of bacterial wilt incidence in tomato by rhizobacteria, bacterial endophytes and the root endophytic fungus Piriformospora indica. Indian Phytopathology. 2020;73(4):629-42. http://dx.doi.org/10.1007/s42360-020-00283-2

Anith KN, Faseela KM, Archana PA, Prathapan KD. Compatibility of Piriformospora indica and Trichoderma harzianum as dual inoculants in black pepper (Piper nigrum L.). Symbiosis. 2011;55:11-17. https://doi.org/10.1007/s13199-011-0143-1

Anith KN, Aswini S, Varkey S, Radhakrishnan NV, Nair DS. Root colonization by the endophytic fungus Piriformospora indica improves growth, yield and piperine content in black pepper (Piper nigurm L.). Biocatalysis and Agricultural Biotechnology. 2018;14:215-20. https://doi.org/10.1016/j.bcab.2018.03.012

Anith KN, Sreekumar A, Sreekumar J. The growth of tomato seedlings inoculated with co-cultivated Piriformospora indica and Bacillus pumilus. Symbiosis. 2015;65:9-16. https://doi.org/10.1007/s13199-015-0313-7

Nandana MS, Anith KN. Growth promotion in chilli (Capsicum annuum L.) on inoculation with co-cultured Piriformospora indica and Pseudomonas fluorescens. International Journal of Current Microbiology and Applied Sciences. 2020;9:2015-27. https://doi.org/10.20546/ijcmas.2020.907.231

Le DP, Smith MK, Aitken EA. An assessment of Pythium spp. associated with soft rot disease of ginger (Zingiber officinale) in Queensland, Australia. Plant Pathology. 2016;45:377-87. https://doi.org/10.1007/s13313-016-0424-5

Dennis C, Webster J. Antagonistic properties of species-groups of Trichoderma: I. Production of non-volatile antibiotics. Trans-actions of the British Mycological Society. 1971;57(1):25-IN3. https://doi.org/10.1016/S0048-4059(80)80012-9

Balouiri M, Sadiki M, Ibnsouda SK. Methods for in vitro evaluat-ing antimicrobial activity: A review. Journal of Pharmaceutical Analysis. 2016;6(2):71-79. https://doi.org/10.1016/j.jpha.2015.11.005

Lorck H. Production of hydrocyanic acid by bacteria. Physiolo-gia Plantarum. 1948;1(2):142-46. https://doi.org/10.1111/j.1399-3054.1948.tb07118.x

Schwyn B, Neilands JB. Universal chemical assay for the detec-tion and determination of siderophores. Analytical Biochemis-try. 1987;160(1):47-56. https://doi.org/10.1016/0003-2697(87)90612-9

Anith KN, Radhakrishnan NV, Manomohandas TP. Management of nursery wilt of black pepper (Piper nigrum L.) with antagonis-tic bacteria. Microbiological Research. 2002;83(5):561-62. https://www.cabidigitallibrary.org/doi/full/10.5555/20023178718.

Vinayarani G, Prakash H. Growth promoting rhizospheric and endophytic bacteria from Curcuma longa L. as biocontrol agents against rhizome rot and leaf blight diseases. The Plant Pathology Jornal. 2018;34(3):218. https://doi.org/10.5423/PPJ.OA.11.2017.0225.

Singh AK. Correlation and path analysis for certain metric traits in ginger. Annals of Agricultural Research. 2001;22:285-86. http:/www.cabidigitallibrary.org/doi/full/10.5555/20023013486

Kavitha PG, Thomas G. Population genetic structure of the clon-al plant Zingiber zerumbet (L.) Smith (Zingiberaceae), a wild relative of cultivated ginger, and its response to Pythium apha-nidermatum. Euphytica. 2008;160(1):89-100. https://doi.org/10.1007/s10681-007-9557-5.

Rathmell WG, Sequeira L. Soluble peroxidase in fluid from the intercellular spaces of tobacco leaves. Plant Physiology. 1974;53(2):317-18. https://doi.org/10.1104/pp.53.2.317

Meyer JA, Abdallah MA. The fluorescent pigment of Pseudomo-nas fluorescens: biosynthesis, purification and physicochemical properties. Microbiology. 1978;107(2):319-28. https://doi.org/10.1099/00221287-107-2-319

Brueske CH. Phenylalanine ammonia lyase activity in tomato roots infected and resistant to the root-knot nematode, Meloidogyne incognita. Physiological Plant Pathology.1980;16(3):409-14. https://doi.org/10.1016/S0048-4059(80)80012-9

Beauchamp C, Fridovich I. Superoxide dismutase: improved assays and an assay applicable to acrylamide gels. Analytical Biochemistry.1971;44(1):276-87. https://doi.org/10.1016/0003-2697(71)90370-8

Liu Y, Wisniewski M, Kennedy JF, Jiang Y, Tang J, Liu J. Chitosan and oligochitosan enhance ginger (Zingiber officinale Rosc.) resistance to rhizome rot caused by Fusarium oxysporum in storage. Carbohydr Polym. 2016;151:474-79. https://doi.org/10.1016/j.carbpol.2016.05.103

Omer AM. Bioformulations of Bacillus spores for using as biofer-tilizer. Life Science Journal. 2010;7(4):124-31. http://www.sciencepub.net/publication/26589097729.

Sivapriya SL, Anith KN. Isolation, Characterization and screen-ing of endospore forming endophytic bacteria from cowpea [Vigna unguiculata (L.) Walp.] for plant growth promotion and abiotic stress mitigation. International Journal of Plant and Soil Science. 2024;36(2):214-27. https://doi.org/10.9734/ijpss/2024/v36i24383

Egamberdieva D, Eshboev F, Shukurov O, Alaylar B, Arora NK. Bacterial bioprotectants: biocontrol traits and induced re-sistance to phytopathogens. Microbiology Research. 2023;4(2):689-703. https://doi.org/10.3390/microbiolres14020049

Rana A, Saharan B, Joshi M, Prasanna R, Kumar K, Nain L. Identi-fication of multi-trait PGPR isolates and evaluating their poten-tial as inoculants for wheat. Analytical Microbiology. 2011;61:893-900. https://doi.org/10.1007/s13213-011-0211-z

Shastri B, Kumar R, Lal RJ. Isolation and identification of anti-fungal metabolite producing endophytic Bacillus subtilis (S17) and its in vitro effect on Colletotrichum falcatum causing red rot in sugarcane. Vegetos. 2020;33(3):493-503. https://doi.org/10.1007/s42535-020-00133-6

Flaishman MA, Eyal Z, Zilberstein A, Voisard C, Haas D. Suppres-sion of Septoria tritici blotch and leaf rust of wheat by recombi-nant cyanide-producing strains of Pseudomonas putida. Molec-ular Plant-Microbe Interactions. 1996;9(7):642-45.https://doi.org/10.1094/mpmi-9-0642

Becker JO, Cook RJ. Role of siderophores in suppression of Pythium sp. and production of increased-growth response of wheat by fluorescent pseudomonads. Phytopathology. 1988;78(6):778-82.https://doi.org/10.1094/phyto-78-778

Loper JE. Role of fluorescent siderophore production in biologi-cal control of Pythium ultimum by a Pseudomonas fluorescens strain. Phytopathology. 1988;78(2):166-72.https://doi.org/10.1094/phyto-78-166

Li X, Wang X, Shi X, Wang B, Li M, Wang Q, Zhang S. Antifungal effect of volatile organic compounds from Bacillus velezensis CT32 against Verticillium dahliae and Fusarium oxysporum. Processes. 2020;8(12):1674.https://doi.org/10.3390/pr8121674

Saxena J, Saini A, Ravi I, Chandra S, Garg V. Consortium of phos-phate-solubilizing bacteria and fungi for promotion of growth and yield of chickpea (Cicer arietinum). Journal of Crop Im-provment. 2015;29(3):353-69. https://doi.org/10.1080/15427528.2015.1027979

Varkey S, Anith KN, Narayana R, Aswini S. A consortium of rhizo-bacteria and fungal endophyte suppress the root-knot nema-tode parasite in tomato. Rhizosphere. 2018;1;5:38-42. https://doi.org/10.1016/j.rhisph.2017.11.005

Zhao X, Liu X, Xu X, Fu YV. Microbe social skill: the cell-to-cell communication between microorganisms. Science Bulletin. 2017;15;62(7):516-24. https://doi.org/10.1016/j.scib.2017.02.010.

Jayasinghearachchi HS, Seneviratne G. A bradyrhizobial-Penicillium spp. biofilm with nitrogenase activity improves N2 fixing symbiosis of soybean. Biology and Fertility of Soils. 2004;40:432-34. https://doi.org/10.1007/s00374-004-0796-5

Kaur S, Samota MK, Choudhary M, Choudhary M, Pandey AK, Sharma A, Thakur J. How do plants defend themselves against pathogens-biochemical mechanisms and genetic interventions. Physiology and Molecular Biology of Plants. 2022;28(2):485-504. https://doi.org/10.1007/s12298-022-01146-y.

Appu M, Ramalingam P, Sathiyanarayanan A, Huang J. An over-view of plant defense-related enzymes responses to biotic stresses. Plant Gene. 2021;1(27):100302. https://doi.org/10.1016/j.plgene.2021.100302

Seo DJ, Nguyen DM, Song YS, Jung WJ. Induction of defence response against Rhizoctonia solani in cucumber plants by en-dophytic bacterium Bacillus thuringiensis GS1. Journal Microbi-ology and Biotechnology. 2012;22(3):407-15. https://doi.org/10.4014/jmb.1107.07027

Rai S, Hossain M. Comparative studies of three traditional meth-ods of seed rhizome storage of ginger (Zingiber officinale Rosc.) practiced in Sikkim and Darjeeling hills. Environmental and Ecology.1998;16(1):34-36.

Le DP, Smith M, Hudler GW, Aitken E. Pythium soft rot of ginger: detection and identification of the causal pathogens and their control. Crop Protection. 2014;65:153-67. https://doi.org/10.1016/j.cropro.2014.07.021

Shaik J. In vitro propagation of Zingiber officinale through rhi-zome and effect of plant growth regulators. Journal Pharma-cognosy Phytochem. 2018;7(5):2012-14. 10.22271/phyto.2018.v7.isp5.226

Singh M, Chauhan A, Singh PK. Enhanced growth and suppres-sion of fusarium wilt in tomato plants through the action of Rhizophagus intraradices and Trichoderma viride. Vegetos. 2024;28:1-8. http://dx.doi.org/10.1007/s42535-024-00935-y

Downloads

Published

25-12-2024

How to Cite

1.
Anith KN, Nandana MS. Biological management of rhizome rot in ginger (Zingiber officinale ) plants and stored ginger seeds. Plant Sci. Today [Internet]. 2024 Dec. 25 [cited 2024 Dec. 26];11(sp3). Available from: https://horizonepublishing.com/journals/index.php/PST/article/view/4288

Issue

Section

Special issue on Int Conf Spices