Bacillus megaterium strain NBAII 63: A potential biocontrol agent for the management of bacterial wilt of tomato caused by Ralstonia solanacearum


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Authors

  • G SIVAKUMAR National Bureau of Agriculturally Important Insects, Bangalore, Karnataka 560 024
  • R RANGESHWARAN National Bureau of Agriculturally Important Insects, Bangalore, Karnataka 560 024
  • S SRIRAM National Bureau of Agriculturally Important Insects, Bangalore, Karnataka 560 024
  • P RAVEENDRAN National Bureau of Agriculturally Important Insects, Bangalore, Karnataka 560 024

https://doi.org/10.56093/ijas.v84i10.44224

Keywords:

Bacillus megaterium, Bioefficacy, Ralstonia solanacearum, Tomato

Abstract

Among 100 isolates of Bacillus spp. screened under in vitro condition, ten of them were found inhibitory against Ralstonia solanacearum which causes bacterial wilt of tomato. Bacillus isolate NBAII-63 was selected as promising one based on in vitro and in vivo screening. The promising Bacillus isolate NBAII 63 was identified as Bacillus megaterium by 16S rDNA analysis. The bio-efficacy of talc formulation of B. megaterium strain NBAII-63 was evaluated under green house and field for plant growth promotion and suppression of bacterial wilt in tomato. A combined application of seed treatment, soil application, seedling root dip and foliar spray was found effective for the management of bacterial wilt of tomato. Combined application resulted in reduction of wilt incidence to 59.9% and 56.0% under green house and field conditions respectively. Streptomycin sulphate application recorded 75.0% reduction in wilt under green house and 69.0% under field conditions. Significant increase in growth parameters, viz. root length (26.2 cm) and shoot length (74.1 cm) of tomato plants were recorded under field condition due to application B. megaterium as compared to control where it was 13.0 cm and 33.2 cm respectively. The per cent increase in root and shoot length of tomato plants due to application of B. megaterium over control was 50.3 and 55.2 respectively. Highest rhizosphere population B.megaterium of 71.2×106 cfu/g was recorded in field condition at 40 days after transplanting when the antagonist was applied as a combination of seed treatment, seedling root dip, soil application and foliar spray. Application of B. megaterium strain NBAII-63 in a combination approach such as seed treatment, seedling root dip, soil application and foliar spray significantly reduced the wilt incidence of tomato. This organism shows potential for use as a promising biological control agent in tomato.

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References

Brooks S D, Gonzalez C F, Appel D N and Filer T H. 1994. Evaluation of endophytic bacteria as potential biological control agents for oak wilt. Biological Control 4: 373–81. DOI: https://doi.org/10.1006/bcon.1994.1047

Buddenhagen I W, Sequeira L and Kelman A. 1962. Designation of races in Pseudomonas solanacearum. Phytopathology 52: 726.

Dhingra O D and Sinclair J B. 1995. Basic Plant Pathology Methods, 2nd Ed. CRC Press, Boca Raton, FL, USA.

Doan T T and Nguyen T H. 2006. Status of research on biological control of tomato and groundnut bacterial wilt in Vietnam. (In) 1st International Symposium on Biological Control of Bacterial Plant Diseases, Darmstadt, Germany, 2005, pp 105–110

Emami S S, Asilia J, Rahimizadeh M, Fazly-Bazzaz B S and Hassanzadeh-Khayyat M. 2006. Chemical and antimicrobial studies of Cupressus sempervirens L. and C. horizentalis Mill. essential oils. Iranian Journal of Pharmaceutical Sciences 2(2): 103–8.

Han H S Lee K D. 2005. Phosphate and potassium solubilising bacteria effect on mineral uptake, soil availability and growth of eggplant. Research Journal of Agriculture and Biological Sciences 1: 176–80.

Han H S, Supanjani Lee K D. 2006. Effect of co-inoculation with phosphate and potassium solubilising bacteria on mineral uptake and growth of pepper and cucumber. Plant and Soil Environment 52: 130–6. DOI: https://doi.org/10.17221/3356-PSE

Liu Z L and Sinclair J B. 1993. Population dynamics of Bacillus megaterium strain B153–2-2 in the rhizosphere of soybean. Phytopathology 82: 1 297–1301. DOI: https://doi.org/10.1094/Phyto-82-1297

Lwin M and Ranamukhaarachchi S L. 2006. Development of biological control of Ralstonia solanacearum through antagonistic microbial populations. International Journal of Agriculture and Biology 8: 657–60.

Norris J R, Berkeley R C W, Logan N A and O’Donnell A G. 1981. The genera Bacillus and Sporolactobacillus, pp 1711-42. (In) The Prokaryotes, vol. 2, pp 1711–42 Star M P, Stolp A, Truper A G, Balows A. and Schlegel H G (Eds). Springer, Berlin.

Nguyen M T, Ranamukhaarachchi S L and David B Hannaway. 2011. Efficacy of antagonist strains of Bacillus megaterium, Enterobacter cloacae, Pichia guilliermondii and Candida ethanolica against bacterial wilt disease of tomato. Journal of Phytology 3: 1–10.

Rangeshwaran R, Vajid N V, Ramanujam B, Sriram S, Bhaskaran T V and Satendar Kumar. 2010. Additives in powder based formulation for enhanced shelf life of Pseudomonas fluorescens and Bacillus spp. Journal of Biological Control 24: 158–63.

Roberts T and Hitchins A. 1969. Resistance of spores, (In) The Bacterial Spore, pp 611–71 Gould G W and Hurst A (Eds). Academic Press, London UK.

Sneath P H A. 1986. Endospore- forming Gram-positive rods and cocci. (In) Bergeys Manual of Systematic Bacteriology, Vol 2, 9th ed. Sneath P H A, Nair N S, Sharpe M E and Holt J G (Eds), pp 1104–9. M D Willaims and Wilkins, Baltimore.

Sivaprasad P. 2002. Microbial inoculant technology for plant disease management, pp 23–30. (In) Research Extension interface, Farm Information bureau. Government of Kerala, pp 23–30.

Sivakumar G, Rangeshwaran R and Sriram S. 2011. Screening and identification of potential Bacillus spp. for the management of bacterial wilt of brinjal (egg plant). Journal of Biological Control 25: 229–35.

Subbarao N S. 1988. Phosphate solubilizing micro-organism, (In) Biofertilizer in agriculture and forestry pp 133–42. Regional Biofertilizer Development Centre, Hisar.

Weller D M. 1998. Biological control of soil borne plant pathogens in the rhizoshere with bacteria. Annual Review of Phytopathology 26: 379–407. DOI: https://doi.org/10.1146/annurev.py.26.090188.002115

Winstead N N and Kelman A. 1952. Inoculation techniques for evaluating resistance to Pseudomonas solanacearum. Phytopathology 42: 628–34.

Wu S C, Cao Z H, Li Z G, Cheung K C and Wong M H. 2005. Effects of biofertilizer containing N-fixer, P and K solubilizers and AM fungi on maize growth: a greenhouse trial. Geoderma 125: 155–66. DOI: https://doi.org/10.1016/j.geoderma.2004.07.003

Yabuuchi E, Kosako Y, Yano I, Hotta H, Nishiuchi Y. 1995. Transfer of two Burkholderia and an Alcaligenes species to Ralstonia gen. nov.: proposal of Ralstonia pickettii (Ralston, Palleroni and Doudoroff 1973) comb. nov, Ralstonia solanacearum (Smith 1896) comb. nov and Ralstonia eutropha (Davis 1969) comb. nov. Microbiol. Immunology 39: 897–904. DOI: https://doi.org/10.1111/j.1348-0421.1995.tb03275.x

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Submitted

2014-10-15

Published

2014-10-15

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Short-Communication

How to Cite

SIVAKUMAR, G., RANGESHWARAN, R., SRIRAM, S., & RAVEENDRAN, P. (2014). Bacillus megaterium strain NBAII 63: A potential biocontrol agent for the management of bacterial wilt of tomato caused by Ralstonia solanacearum. The Indian Journal of Agricultural Sciences, 84(10), 1288–92. https://doi.org/10.56093/ijas.v84i10.44224
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