Agricultural Science Digest

  • Chief EditorArvind kumar

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Agricultural Science Digest, volume 41 special issue (april 2021) : 163-168

Usage of Non-chemical Methods to Counter the Damages Caused by Tomato Mosaic Virus

Suleman Saleem, Muhammad Ahmad Zeshan, Yasir Iftikhar, Muhammad Asif Shabbir, Ashara Sajid, Sonum Bashir, Muhammad Usman Ghani
1Department of Plant Pathology, College of Agriculture, University of Sargodha, Pakistan. 40100.
Cite article:- Saleem Suleman, Zeshan Ahmad Muhammad, Iftikhar Yasir, Shabbir Asif Muhammad, Sajid Ashara, Bashir Sonum, Ghani Usman Muhammad (2021). Usage of Non-chemical Methods to Counter the Damages Caused by Tomato Mosaic Virus. Agricultural Science Digest. 41(2021): 163-168. doi: 10.18805/ag.D-292.
Background: Tomato mosaic virus (ToMV) is the most common and important pathogen of tomato crop. The infected plants show mosaic, mottle, wrinkling, reduced leaf size and uneven ripening of fruits. ToMV is transmitted mechanically, by cultural operations, farm implements and also through seed. 
Methods: The present study was planned to evaluate environment friendly strategies for the management of ToMV disease. Different non-chemical means viz., Elephant Ear plant extract, Eucalyptus extract, Zinc and Boron solution, NPK solution, Milk and Urea were used on four tomato varieties (Tanja, Chico, Manik and Sahil). All the treatments were used at three different concentrations (1%, 2% and 3%) and replicated three times. 
Result: The maximum disease reduction was recorded in plants treated with NPK solution (16.35%) and minimum in plants treated with Elephant Ear plant extract (29.65%). The maximum mean disease severity was recorded at 1 percent concentration of all the treatments (32.46%) which was statistically significant from that of 2 and 3% (24.74% and 19.23%), respectively. Among the varieties, minimum disease severity was recorded in Manik (24.64%) variety and maximum in Chico (31.27%) variety. All the treatments contributed towards reduction in disease severity of which NPK solution being most efficient.
  1. Ahn, I.P., Kim, S. and Lee, Y.H. (2005). Vitamin B1 functions as an activator of plant disease resistance. Plant Physiology. 138(3): 1505-1515.
  2. Akhtar, K.P., Ullah, N., Saleem, M.Y., Iqbal, Q., Asghar, M. and Khan, A.R. (2019). Evaluation of tomato genotypes for early blight disease resistance caused by Alternaria solani in Pakistan. Journal of Plant Pathology. 101: 1159-1170.
  3. Arinaitwe, W., Ochwo-Ssemakula, M., Mbewe, W.K., Sseruwagi, P., Kyamanywa, S., Erbaugh, M., Miller, S. and Qu, F. (2018). Molecular characteristics of tomato mosaic virus infecting tomato in Uganda. African Crop Science Journal. 26(3): 433-455.
  4. Aseel, D.G., Rashad, Y.M. and Hammad, S.M. (2019). Arbuscular mycorrhizal fungi trigger transcriptional expression of flavonoid and chlorogenic acid biosynthetic pathways genes in tomato against tomato mosaic virus. Scientific Reports. 9: 9692-9702. 
  5. Bachir, R.G. and Benali, M. (2012). Antibacterial activity of the essential oils from the leaves of Eucalyptus globulus against Escherichia coli and Staphylococcus aureus. Asian Pacific Journal of Tropical Biomedicine. 2(9): 739-742.
  6. Bawden, F.C. and Pirie, N.W. (1940). The inactivation of some plant viruses by urea. Biochemical Journal. 34(9): 1258-1277.
  7. Benkerroum, N. (2008). Antimicrobial activity of lysozyme with special relevance to milk. African Journal of Biotechnology. 7(25). 
  8. Bonafe, C.F.S., Vital, C.M.R., Telles, R.C.B., Gonçalves, M.C. Matsuura, M.S.A., Pessine, F.B.T., Freitas, D.R.C. and Vega, J. (1998). Tobacco mosaic virus disassembly by high hydrostatic pressure in combination with urea and low temperature. Biochemistry. 37: 11097-11105.
  9. Brown, P.H., Bellaloui, N., Wimmer, M., Bassil, E.S., Ruiz, J., Hu, H. and Römheld, V. (2002). Boron in plant biology. Plant Biology. 4(02): 205-223. 
  10. Cerda, R., Avelino, J., Gary, C., Tixier, P., Lechevallier, E. and Allinne, C. (2017). Primary and secondary yield losses caused by pests and diseases: assessment and modelling in coffee. PLoS One. 12(1): 1-17.
  11. Chakraborty, P., Deb, P., Chakraborty, S., Chatterjee, B., and Abraham, J. (2015). Cytotoxicity and antimicrobial activity of Colocasia esculenta. Journal of Chemistry and Pharmacy Research. 7(12): 627-635. 
  12. Datnoff, L.E., Elmer, W.H. and Huber, D.M. (2007). Mineral nutrition and plant disease. American Phytopathological Society (APS Press). USA.
  13. Ditengou, F.A. and Lapeyrie, F. (2000). Hypaphorine from the ectomycorrhizal fungus Pisolithus tinctorius counteracts activities of indole-3-­acetic acid and ethylene but not synthetic auxins in eucalypt seedlings. Molecular Plant Microbe Interaction. 13: 151-158.
  14. Dordas, C. (2008). Role of nutrients in controlling plant diseases in sustainable agriculture. A review. Agronomy for Sustainable Development. 28(1): 33-46. 
  15. Giri, B.K. and Mishra, M.D. (1990). Effect of tomato mosaic virus on pollen viability and yield of tomatoes. Indian Phytopathology. 43: 487-490.
  16. GOP (2018). Agricultural statistics of Pakistan, Government of Pakistan , Ministry of Food, Agriculture and Livestock, Economics Wing, Islamabad.
  17. Hanssen, I.M., Gutierrez Aguirre, I., Paeleman, A., Goen, K., Wittemans, L., Lievens, B., Vanachter, A.C.R.C., Ravnikar, M. and B.P.H.J. Thomma (2010). Cross protection or enhanced symptom display in greenhouse tomato co infected with different Pepino mosaic virus isolates. Plant Pathology. 59: 13-21.
  18. Henery, M., Wallis, I., Stone, C. and Foley, W. (2008). Methyl jasmonate does not induce changes in Eucalyptus grandis leaves that alter the effect of constitutive defences on larvae of a specialist herbivore. Oecologia. 156: 847-859.
  19. Huber, D. and Arny, D. (1985). Interactions of potassium with plant disease. In: Potassium in Agriculture. (R.D. Munson and W.D. Bishop Eds.). Proceedings of an Internatinal Symposium. Madison Wisconson : American Society Agronomy, pp. 467-488.
  20. Imran, M., Khan, M.A., Azeem, M., Ahmed, N., Binyamin, R. and Riaz, A. (2012). Screening of tomato germplasm for the source of resistance and its management against ToMV. Pakistan Journal of Phytopathology. 24(1): 53-57.
  21. Kim, K.S., Min, J.Y. and Dickman, M.B. (2008). Oxalic acid is an elicitor of plant programmed cell death during Sclerotinia sclerotiorum disease development. Molecular Plant-Microbe Interactions. 21(5): 605-612.
  22. Kirkby, E. and Mengel, K. (1967). Ionic balance in different tissues of the tomato plant in relation to nitrate, urea, or ammonium nutrition. Plant Physiology. 42(1): 6-14.
  23. Kumar, S., Udaya-Shankar, A.C., Nayaka, S.C., Lund, O.S. and Prakash, H.S. (2011). Detection of tobacco mosaic virus and tomato mosaic virus in pepper and tomato by multiplex RT-PCR. Letters in Applied Microbiology. 53: 359-363.
  24. Letschert, B., Gunter, A., Dietrich-Eckhardt, L., Willingmann, P. and Heinze, C. (2002). Detection and differentiation of serologically cross-reacting tobamoviruses of economical importance by RT-PCR and RT-PCR-RFLP. Journal of Virological Methods. 106: 1-10. 
  25. Li, Z., Fan, Y., Gao, L., Cao, X., Ye, J. and Li, G. (2016). The dual roles of zinc sulfate in mitigating peach gummosis. Plant disease. 100(2): 345-351. 
  26. Marshall, K. (2004). Therapeutic applications of whey protein. Alternative Medicine Review. 9: 136-156.
  27. Naidoo, R., Ferreira, L., Berger, D.K., Myburg, A.A., Naidoo, S. (2013). The identification and differential expression of Eucalyptus grandis pathogenesis-related genes in response to salicylic acid and methyl jasmonate. Frontier in Plant Science. 4: 43.
  28. Pfitzner, A.J. (2006). Resistance to tobacco mosaic virus and tomato mosaic virus in tomato. In: Natural resistance mechanisms of plants to viruses. (J. Carr and G. Loebenstein Eds.). Springer, Berlin, Germany, pp. 399-413.
  29. Regassa, D., Tigre, W. and Shiferaw, A. (2016). Tomato (Lycopersicon esculentum Mill.) varieties evaluation in Borana zone, Yabello district, Southern Ethiopia. Journal of Plant Breeding and Crop Science. 8(10): 206-210.
  30. Rosa, D.D., Furtado, E.L., Boava, L.P., Marino, C.L., Mori, E.S., Guerrini, I.A., Veline, E.D. and Wilcken, C.F. (2010). ESTs involved in mechanisms against plant pathogens and environmental stresses. Summa Phytopathology. 36: 282-290.
  31. Saikia, R., Yadav, M., Varghese, S., Singh, B.P., Gogoi, D.K., Kumar, R. and Arora, D.K. (2006). Role of riboflavin in induced resistance against Fusarium wilt and charcoal rot diseases of chickpea. The Plant Pathology Journal. 22(4): 339-347. 
  32. Santos, J.L.R., Aparicio, R., Joekes, I., Silva, J.L., Bispo, J.A.C. and Bonafe, C.F.S. (2008). Different urea stoichiometries between the dissociation and denaturation of tobacco mosaic virus as probed by hydrostatic pressure. Biophysical Chemistry. 134: 214-224.
  33. Snoeijers, S.S., Perez-Garcia, A., Joosten, M.H. and De-Wit, P.J. (2000). The effect of nitrogen on disease development and gene expression in bacterial and fungal plant pathogens. European Journal of Plant Pathology. 106(6): 493-506.
  34. Spence, N.J., Scaly, I., Mills, P.R. and Foster, G.D. (2001). Detection of different strains of potato virus Y and their mixed infections using competitive fluorescent RT-PCR. Journal of Virological Methods. 91: 167-173. 
  35. Sui, X., Zheng, Y., Li, R., Padmanabhan, C., Tian, T., Groth-Helms, D., Keinath, A.P., Fei, Z., Wu, Z. and Kai-Shu, L. (2017). Molecular and biological characterization of tomato mottle mosaic virus and development of RT-PCR detection. Plant Disease. 101: 704-711.
  36. Sun, Y., Wang, M., Mur, L.A.J., Shen, Q. and Guo, S. (2020). Unravelling the roles of nitrogen nutrition in plant disease defences. International Journal of Molecular Sciences. 21(2): 572. 
  37. Tewodros, M. and Asfaw, K. (2013). Promotion and evaluation of improved technologies through participatory approach in South Ethiopia: Experience from hot pepper. Unique Research Journal of Agricultural Science. 1(4): 57-62.
  38. Ullah, N., Ali, A., Ahmad, M., Fahim, M., Din., N., Ahmad, F. (2017). Evaluation of tomato genotypes against tomato mosaic virus (tomv) and its effect on yield contributing parameters. Pakistan Journal of Botany. 49(4): 1585-1592.
  39. Ullah, N., Akhtar, K.P., Saleem, M.Y., and Habib, M. (2019). Characterization of tomato mosaic virus and search for its resistance in Solanum species. European Journal of Plant Pathology. 155: 1195-1209. 
  40. Waarts, B., Aneke, O.J., Smit, J.M., Kimata, K., Bittman, R. and Meijer, D.K.F. (2005). Antiviral activity of human lactoferrin: Inhibition of alphavirus interaction with heparan sulfate. Virology. 333: 284-292.
  41. Zheng, S., Chen, B., Qiu, X., Chen, M., Ma, Z. and Yu, X. (2016). Distribution and risk assessment of 82 pesticides in Jiulong River and estuary. Chemosphere. 144: 1177-1192.

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