12.07.2015 Views

natural-products-in-plant-pest-management

natural-products-in-plant-pest-management

natural-products-in-plant-pest-management

SHOW MORE
SHOW LESS

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

162 H.N. Verma and V.K. BaranwalVerma and Awasthi (1980) reported that the synthesis of VIA is <strong>in</strong>hibitedif AMD is applied soon after extract treatment. The VIA synthesized is neithervirus specific nor host specific. Extracts conta<strong>in</strong><strong>in</strong>g VIA when <strong>in</strong>cubated withthe virus reduced their <strong>in</strong>fectivity. VIAs from a few hosts have been characterized.The VIA synthesized <strong>in</strong> the leaves of N. glut<strong>in</strong>osa, treated with B.diffusa root extract reduced <strong>in</strong>fectivity of TMV on N. glut<strong>in</strong>osa, Datura stramoniumand D. metel (Verma and Awasthi, 1980). It was, however, less effective<strong>in</strong> <strong>in</strong>hibit<strong>in</strong>g TRSV and GMV on C. amaranticolor. The VIA production wasmaximum after 24 h treatment with the extract. The VIA has a prote<strong>in</strong>aceousnature (Verma and Awasthi, 1980). VIA synthesized <strong>in</strong> C. tetragonoloba <strong>plant</strong>sfollow<strong>in</strong>g treatment with B. spectabilis leaf extract prevented <strong>in</strong>fection oftobamoviruses <strong>in</strong> seven hypersensitive hosts (Verma and Dwivedi, 1984) andits production was maximum after 48 h treatment. The VIA showed characteristicsof a prote<strong>in</strong> (Verma and Dwivedi, 1984). VIA produced <strong>in</strong> the samehost upon treatment with Pseuderanthemum bicolor extract completely prevented<strong>in</strong>fection of SHRV, TMV, CGMMV, and PVX on C. tetragonoloba, D.stramonium, C. amaranticolor and G. globosa, respectively (Khan and Verma,1990).VIA and the antiviral state are <strong>in</strong>duced concomitantly with the systemicresistance <strong>in</strong>duction <strong>in</strong> host <strong>plant</strong>s, follow<strong>in</strong>g treatment with certa<strong>in</strong> <strong>plant</strong>extracts. VIA is an <strong>in</strong>ducible gene product like AVF, IVR and PR prote<strong>in</strong>s. Thephytoprote<strong>in</strong>s occurr<strong>in</strong>g <strong>in</strong> the root / leaf extracts of Boerhaavia diffusa, Clerodendrumaculeatum, Clerodendrum <strong>in</strong>erme and B. spectabilis etc. possess strongsystemic-resistance-<strong>in</strong>duc<strong>in</strong>g properties (Verma and Prasad, 1992).Clerodendrum aculeatum and Boerhaavia diffusa, the two potentantiviral <strong>plant</strong>sClerodendrum and Boerhaavia are economically important <strong>plant</strong>s becausemany of their species possess medic<strong>in</strong>al properties. Almost every part ofthese <strong>plant</strong>s is credited with some medic<strong>in</strong>al properties and is employed <strong>in</strong>traditional Indian system of <strong>natural</strong> therapy.Virus <strong>in</strong>hibitors from Boerhaavia diffusa and Clerodendrum aculeatum<strong>in</strong>hibit several <strong>plant</strong> viruses. These <strong>in</strong>hibitors modify the susceptibility ofhost <strong>plant</strong>s towards virus <strong>in</strong>fection. The roots of B. diffusa are a rich source ofa basic prote<strong>in</strong>, which has been used for <strong>in</strong>duc<strong>in</strong>g systemic resistance <strong>in</strong>many susceptible crops aga<strong>in</strong>st commonly occurr<strong>in</strong>g viruses (Verma andAwasthi, 1979, 1980; Verma et al., 1979; Awasthi et al., 1984, 1985, 1989; Vermaet al., 1995, 1999). This prote<strong>in</strong> or antiviral agent was active aga<strong>in</strong>st sphericaland tubular viruses <strong>in</strong> hypersensitive hosts such as Datura metel, Nicotianatabacum var Ky-58, N. glut<strong>in</strong>osa / TMV, Cyamopsis tetragonoloba / SHRV, Vignas<strong>in</strong>ensis / SHRV, and systemic hosts such as Nicotiana tabacum c.v NP-31 / TMV,Crotolaria juncea / SHRV, N.glut<strong>in</strong>osa / TRSV, when applied a few hours (17–24h) before virus <strong>in</strong>oculation or when tested after mix<strong>in</strong>g with virus <strong>in</strong>oculum(Verma and Awasthi, 1979; Awasthi et al., 1984). The <strong>in</strong>hibitor is a basic glycoprote<strong>in</strong>(70–80% prote<strong>in</strong>, 8–13% carbohydrate) with a molecular weight of

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!