Control of Virus Diseases of Plants 1677.6 ConclusionWith the precipitous withdrawal of some of the toxic protectants, it may beprofitable to explore <strong>natural</strong> <strong>plant</strong> <strong>products</strong> as alternatives, particularlyaga<strong>in</strong>st virus diseases where all other methods fail. The phytoprote<strong>in</strong>s ortheir smaller peptides may prove valuable as ‘lead structures’ for the developmentof synthetic compounds. It would pay us to explore this rich sourceof antivirals more thoroughly. The value of these antiviral prote<strong>in</strong>s is unlimitedbecause they are quite safe, non-toxic even after repeated and prolongeduse, and substantially enhance <strong>plant</strong> growth and yield. Antiviral phytoprote<strong>in</strong>smay be useful if they are <strong>in</strong>tegrated with other strategies of virus disease<strong>management</strong>.Botanical resistance <strong>in</strong>ducers can be classified as ideal virus-suppress<strong>in</strong>gagents, as they encompass all the characteristics of an ideal antiviral compound.Induced resistance operates through the activation of <strong>natural</strong> defencemechanisms of the host <strong>plant</strong> and <strong>in</strong>duces systemic resistance to viral multiplication<strong>in</strong> <strong>plant</strong>s. The active <strong>products</strong> present <strong>in</strong> these extracts have nodirect effect on viruses; their antiviral activity is mediated by host cells <strong>in</strong>which they <strong>in</strong>duce the antiviral state. Systemic resistance <strong>in</strong>ducers obta<strong>in</strong>edfrom <strong>plant</strong>s have been shown to be effective aga<strong>in</strong>st a wide range of viruses.Plant extracts or the semi-purified prote<strong>in</strong>s from these <strong>plant</strong>s stimulate thehosts to produce a virus <strong>in</strong>hibitory agent, which spreads to surround<strong>in</strong>gtissues and other <strong>plant</strong> parts.ReferencesAlexander, D., Goodman, R.M., Gut-Rella,M., Glascock, C., Weymann, K., Friedrich,L., Maddox, D., Ahi-Goy, P., Lunz,T., Ward, E. and Ryals, J. (1993) Increasedtolerance of two oomycete pathogens<strong>in</strong> transgenic tobacco express<strong>in</strong>gpathogenesis-related prote<strong>in</strong> 1a. Proceed<strong>in</strong>gsof National Academy of Sciences USA90, 7327–7331.Aron, G.M. and Irv<strong>in</strong>, J.D. (1980) Inhibitionof herpes simplex virus multiplicationby the pokeweed antiviral prote<strong>in</strong>.Antimicrobial Agents Chemotherapy 17,1032–1033.Awasthi, L.P., Chowdhury, B. and Verma,H.N. (1984) Prevention of <strong>plant</strong> virus diseaseby Boerhaavia diffusa <strong>in</strong>hibitor. IndianJournal of Tropical Plant Diseases 2, 41–44.Awasthi, L.P., Kluge, S. and Verma, H.N.(1989) Characterstics of antiviral agents<strong>in</strong>duced by Boerhaavia diffusa glycoprote<strong>in</strong><strong>in</strong> host <strong>plant</strong>s. Indian Journal of Virology 3,156–169.Awasthi, L.P., Pathak, S.P., Gautam, N.C. andVerma, H.N. (1985) Control of virusdiseases of vegetable crops by a glycoprote<strong>in</strong>isolated from Boerhaavia diffusa. IndianJournal of PIant Pathology 3, 311–327.Awasthi, L.P. (1981) The purification andnature of an antiviral prote<strong>in</strong> from Cuscutareflexa <strong>plant</strong>s. Archives of Virology 70,215–223.Baranwal, V.K. and Ahmad, N. (1997) Effectof Clerodendrum aculeatum leaf extract ontomato leaf curl virus. Indian Phytopathology50, 297–299.Barbieri, L. and Stirpe, F. (1982) Ribosome<strong>in</strong>activat<strong>in</strong>g prote<strong>in</strong>s from <strong>plant</strong>s propertiesand possible uses. Cancer Survey 1,489–520.
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