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Control of Fusarium wilt of tomato caused by Fusarium oxysporum f. sp. lycopersici using leaf extract of Piper betle L.: a preliminary study

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Abstract

The main objective of this study was to evaluate the effectiveness of crude chloroform extract of Piper betle L. (PbC) in controlling Fusarium wilt of tomato (Lycopersicon esculentum) caused by Fusarium oxysporum f. sp. lycopersici. It was observed that 1% (w/w) amendment of the PbC in soil was more efficient in reducing the Fusarium population in soil than carbendazim and the combined amendment of carbendazim and PbC. Fusarium wilt control studies were carried out in a greenhouse. Variation in different parameters like shoot growth, root growth and mean fresh weights of tomato seedlings in all the treatments were recorded. Accumulation of total phenolics was also studied from the root tissues of tomato. Higher accumulation of total phenolics was observed in the Fusarium-infested plants as compared to that of healthy control and PbC-treated plants. Moreover, it was observed that the extract could reduce the symptoms and disease development. Electron microscopy studies were also done to observe the Fusarium infestation in the vascular bundles and to show the accumulation of total phenolics in the vacuoles of root tissue.

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References

  • Agrios GN (2005) Plant pathology. Elsevier Academic Press, NewYork

    Google Scholar 

  • Alabouvette C (1999) Fusarium wilt suppressive soils: an example of disease suppressive soils. Australas Plant Pathol 28:47–64

    Article  Google Scholar 

  • Aneja KR (2005) Experiments in microbiology, plant pathology and biotechnology. New Age International (P) Ltd, New Delhi

    Google Scholar 

  • Benner JP (1993) Pesticidal compounds from higher plants. Pest Sci 39:95–102

    Article  Google Scholar 

  • Bennet RN, Wallsgrove RM (1994) Secondary metabolites in plant defence mechanisms. New Phytol 127:617–633

    Article  Google Scholar 

  • Booth C (1971) The genus Fusarium. Commonwealth Mycological Institute, Kew

    Google Scholar 

  • Bowers JH, Locke JC (2000) Effect of botanical extracts on the population density of Fusarium oxysporum in soil and control of Fusarium wilt in the greenhouse. Plant Dis 84:300–305

    Article  Google Scholar 

  • De Vecchi L, Matta A (1989) An ultrastructural and cytochemical study of peroxidase, polyphenoloxidases and phenols in xylem of tomato plant infected with Fusarium oxysporum f. sp. lycopersici or Fusarium oxysporum f. sp. melonis. Caryologia 42:103–114

    Google Scholar 

  • DeVay JE, Garber RH, Wakeman RJ (1988) Field management of cotton seedling diseases in California using chemical and biological seed treatments. In: Proceedings of Beltwiae cotton conference, National Cotton Council of Americana, Memphis, TN, USA, pp 29–35

  • Diehl T, Fehrmann H (1999) Wheat fusarioses: Influence of infection date, tissue injury and aphids on leaf and ear attack. J Plant Dis Prot 96:393–407

    Google Scholar 

  • Garibaldi A, Guglielmone L, Gullino ML (1990) Rhizosphere competence of antagonistic Fusaria isolated from suppressive soils. Symbiosis 9:401–404

    Google Scholar 

  • Lewis NG, Yamamoto E (1990) Lignin: occurrence, biogenesis and biodegradation. Annu Rev Plant Physiol Plant Mol Biol 41:455–496

    Article  CAS  Google Scholar 

  • Liggit J, Jenkinson P, Parry DW (1997) The role of saprophytic microflora in the development of Fusarium ear blight of winter wheat caused by Fusarium culmorum. Crop Prot 16:679–685

    Article  Google Scholar 

  • Lumsden RD, Locke JC (1989) Biological control of damping-off caused by Pythium ultimum and Rhizoctonia solani with Gliocladium virens in soilless mix. Phytopathology 79:361–366

    Article  Google Scholar 

  • Matta A, Ferraris L, Abbattista GI (1988) Variation of phenoloxidase activities and the consequence of stress induced resistance to Fusarium wilt of tomato. J Phytopathol 122:45–53

    Article  Google Scholar 

  • Minerdi D, Bossi S, Gullino ML, Garibaldi A (2009) Volatile organic compounds: a potential direct long-distance mechanism for antagonistic action of Fusarium oxysporum strain MSA 35. Environ Microbiol 11:844–854

    Article  CAS  Google Scholar 

  • Minton EB (1986) Half a century dynamics and control of cotton disease. In: Proceedings of Beltwiae cotton conference, National Cotton Council of America, Memphis, TN, USA, pp 33–35

  • Nash SN, Snyder WC (1962) Quantitative estimations by plate counts of propagules of the bean rot Fusarium in field soils. Phytopathology 52:567–572

    Google Scholar 

  • Nicholson RL, Hammerschmidt R (1992) Phenolic compound and their role in disease resistance. Annu Rev Phytopathol 30:369–389. doi:10.1146/annurev.py.30.090192.002101

    Article  CAS  Google Scholar 

  • Parmar VS, Jain SC, Gupta S, Talwar S et al (1998) Polyphenols and alkaloids from Piper species. Phytochemistry 38(3):958–967

    Google Scholar 

  • Policegoudra RS, Swaroop Kumar MH, Aradhya MS (2007) Accumulation of bioactive compounds during growth and development of Mango ginger (Curcuma amada Roxb.) rhizomes. J Agric Food Chem 55:8105–8111. doi:10.1021/jf0715469

    Article  CAS  Google Scholar 

  • Randhir R, Shetty K (2005) Developmental stimulation of total phenolics and related antioxidant activity in light and dark-germinated corm by natural elicitors. Process Biochem 40:1721–1732. doi:10.1016/j.procbio.2004.06.064

    Article  CAS  Google Scholar 

  • Singha IM, Unni BG, Kakoty Y, Das J, Wann SB, Singh L, Kalita MC (2010) Evaluation of in vitro antifungal activity of medicinal plants against phytopathogenic fungi. Arch Phytopathol Plant Prot. doi:10.1080/03235401003672913

  • Song W, Zhou L, Yang C, Cao X, Zhang L, Liu X (2004) Tomato Fusarium wilt and its chemical control strategies in a hydroponic system. Crop Prot 23:243–247

    Article  CAS  Google Scholar 

  • Summeral BA, Salleh B, Leslie JF (2003) A utilitarian approach to Fusarium identification. Plant Dis 87:117–128

    Article  Google Scholar 

  • Vakalounakis DJ, Fragkiadakis GA (1999) Genetic diversity of Fusarium oxysporum isolates from cucumber: differentiation by pathogenecity, vegetative compatibility and RAPD fingerprinting. Phytopathology 89:161–168. doi:org/10.1094/PHYTO.1999.89.2.161

    Article  CAS  Google Scholar 

  • Vance CP, Kirk TK, Sherwood RT (1980) Lignifications as a mechanism of disease resistance. Annu Rev Phytopathol 18:259–288. doi:abs/10.1146/annurev.py.18.090180.001355

    Article  CAS  Google Scholar 

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Acknowledgments

We thank Dr. P. G. Rao, Director, NEIST, Jorhat and Dr. R. B. Srivastava, former Directorate of Life Sciences, DRDO, New Delhi for constant support and encouragement. We thank Dr. P. Chattopadhyay and Dr. R. S. Policegoudra for valuable guidance. Dr. B. G. Unni gratefully acknowledges Defence Research and Development Organization (DRDO), Govt. of India for financial support. I. M. Singha acknowledges DRDO for the SRF fellowship.

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Correspondence to Bala Gopalan Unni.

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Singha, I.M., Kakoty, Y., Unni, B.G. et al. Control of Fusarium wilt of tomato caused by Fusarium oxysporum f. sp. lycopersici using leaf extract of Piper betle L.: a preliminary study. World J Microbiol Biotechnol 27, 2583–2589 (2011). https://doi.org/10.1007/s11274-011-0730-6

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