Abstract
Constitutive phenolase activity of plants has a profound ability to modulate disease in insects caused by baculoviruses. We investigated the influence of damage-induced plant phenolic oxidases in cotton and tomato on mortality caused by two different baculoviruses in their respective hosts, Heliothis virescens (L.) and Helicoverpa zea (Boddie). For both plant species, peroxidase (POD) and phenolic levels were predictive of larval mortality caused by baculoviruses. The higher the POD activity, the lower the mortality in both hosts. Different classes of phenolics (e.g., monohydroxyphenolics vs. catecholic phenolics) in combination with POD activity had different effects on the severity of viral disease depending upon mixture, which implies that viral efficacy is predictable only if total chemical content of the plants is specified. Inhibition of baculoviral disease by plant phenolase activity has potential implications for the compatibility of baculoviruses with induced resistance in IPM programs.
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REFERENCES
Ahmad, S. 1995. Oxidative Stress and Antioxidant Defenses in Biology. Chapman & Hall, New York.
Ayers, M. D., Howard, S. C., Kuzio, J., Lopezferber, M., and Possee, R. D. 1994. The complete DNA sequence of Autographa californica nuclear polyhedrosis virus. Virology 202:586–605.
Baldwin, I. T. 1994. Chemical changes rapidly induced by folivory, pp. 1–23, in E. A. Bernays (ed.). Insect-Plant Interactions. CRC Press, Boca Raton, Florida.
Barbosa, P. 1988. Natural enemies and herbivore-plant interactions: Influence of plant allelochemicals and host specificity, pp. 201–229, in P. Barbosa and D. K. Letourneau (eds.). Novel Aspects of Insect-Plant Interactions. John Wiley & Sons, New York.
Berenbaum, M. R. 1988. Allelochemicals in insect-microbe-plant interactions: Influence of plant allelochemicals and host specificity, pp. 201–229, in P. Barbosa and D. K. Letourneau (eds.). Novel Aspects of Insect-Plant Interactions. John Wiley & Sons, New York.
Bi, J. L., and Felton, G. W. 1995. Foliar oxidative stress and insect herbivory: Primary compounds, secondary metabolites, and reactive oxygen species as components of oxidative stress. J. Chem. Ecol. 21(10):1511–1530.
Bi, J. L., Murphy, J. B., and Felton, G. W. 1997. Antinutritive and oxidative components as mechanisms of induced resistance in cotton to Helicoverpa zea. J. Chem. Ecol. 23:95–115.
Bloem, K. A., Kelley, K. C., and Duffey, S. S. 1989. Differential effect of tomatine and its alleviation by cholesterol on larval growth and efficiency of food utilization in Heliothis zea and Spodoptera exigua. J. Chem. Ecol. 15:387–398.
Bozer, S. F., Traugott, M. S., and Stamp, N. E. 1996. Combined effects of allelochemical-fed and scarce prey on the generalist insect predator Podisus maculiventris. Ecol. Entomol. 21:328–334.
Broadway, R., Duffey, S. S., Pearce, G., and Ryan, C. A. 1986. Plant proteinase inhibitors: A defense against herbivorous insects. Entomol. Exp. Appl. 41:33–38.
Butt, V. S. 1981. Direct oxidases and related enzymes, pp. 81–123, in P. K. Stumpf and E. E. Conn (eds.). The Biochemistry of Plants: A comprehensive Treatise. Academic Press, New York.
Butt, V. S., and Lamb, J. C. 1981. Oxygenases and the metabolism of plant products, pp. 627–655, in P. K. Stumpf and E. E. Conn. (eds.). The Biochemistry of Plants: A Comprehensive Treatise—Secondary Plant Products. Academic Press, New York.
Caldwell, M. M., Camp, L. B., Warner, C. W., and Flint, S. D. 1986. Action spectra and their key role in assessing biological consequences of solar UV-B radiation damage, pp. 87–111, in R. C. Worrest and M. M. Caldwell (eds.). Stratospheric Ozone Reduction, Solar Ultraviolet Radiation and Plant Life. Springer-Verlag, New York.
Campbell, B. C., and Duffey, S. S. 1979. Tomatine and parasitic wasps: Potential incompatibility of plant-antibiosis with biological control. Science 205:700–702.
Campbell, B. C., and Duffey, S. S. 1981. Alleviation of α-tomatine-induced toxicity to the parasitoid, Hyposoter exiguae, by phytosterols in the diet of the host, Heliothis zea. J. Chem. Ecol. 7:927–946.
Collett, D. 1994. Modelling Survival Data in Medical Research. Chapman and Hall, London.
Conconi, A., Smerdon, M. J., Howe, G. A., and Ryan, C. A. 1996. The octadecanoid signalling pathway in plants mediates a response to ultraviolet radiation. Nature 383:826–829.
Duffey, S. S., and Bloem, K. A. 1986. Plant defense/herbivore/parasite interactions and biological control, pp. 135–183, in M. Kogan (ed.). Ecological Theory and IPM Practice. John Wiley & Sons, London.
Duffey, S. S., and Felton, G. W. 1989. Role of plant enzymes in resistance to insects, pp. 289–313, in J. R. Whitaker and P. E. Sonnet (eds.). Biocatalysis in Agricultural Biotechnology. ACS Symposium Series 389. American Chemical Society, Washington, DC.
Duffey, S. S., and Felton, G. W. 1991. Enzymatic antinutritive defenses of the tomato plant against insects, pp. 167–197, in P. A. Hedin (ed.). Naturally Occurring Pest Bioregulators. ACS Symposium Series 449, American Chemical Society, Washington, DC.
Duffey, S. S., and Stout, M. J. 1996. Antinutritive and toxic components of plant defense against insects. Arch. Insect Biochem. Physiol. 32:3–37.
Duffey, S. S., Bloem, K. A., and Campbell, B. C. 1986. Consequences of sequestration of plant natural products in plant-insect-parasitoid interactions, pp. 31–60, in D. J. Boethel and R. D. Eikenbary (eds.). Interactions of Plant Resistance and Parasitoids and Predators of Insects. Ellis Horwood Limited, New York.
Duffey, S. S., Hoover, K., Bonning, B. C., and Hammock, B. D. 1995. The impact of hostplant on the efficacy of baculoviruses, pp. 137–275, in M. Roe and R. Kuhr (eds.). Reviews in Pesticide Toxicology. CTI Toxicology Communications, Raleigh, North Carolina.
Fazal, F., Rahman, A., Greensill, J., Ainley, K., Hadi, S. M., and Parish, J. H. 1990. Strand scission in DNA by quercetin and Cu(II): Identification of free radical intermediates and the biological consequences of scission. Carcinogenesis 11:2005–2008.
Felton, G. W. 1995. Oxidative stress of vertebrates and invertebrates, pp. 356–434, in S. Ahmad (ed.). Oxidative Stress and Antioxidant Defenses in Biology. Chapman & Hall, New York.
Felton, G. W., and Duffey, S. S. 1990. Inactivation of a baculovirus by quinones formed in insect-damaged plant tissue. J. Chem. Ecol. 16:1211–1236.
Felton, G. W., and Summers, C. B. 1993. Potential role of ascorbate oxidase as a plant defense protein against insect herbivory. J. Chem. Ecol. 19:1553–1568.
Felton, G. W., Duffey, S. S., Vail, P. V., Kaya, H. K., and Manning, J. 1987. Interaction of nuclear polyhedrosis virus with catechols: potential incompatibility for host-plant resistance against noctuid larvae. J. Chem. Ecol. 13:947–957.
Felton, G. W., Donato, K., Del Vecchio, R. J., and Duffey, S. S. 1989. Activation of plant polyphenol oxidases by insect feeding reduces the nutritive quality of foliage for noctuid herbivores. J. Chem. Ecol. 15:2667–2694.
Felton, G. W., Bi, J. L., Summers, C. B., Mueller, A. J., and Duffey, S. S. 1994. Potential role of lipoxygenase in defense against insect herbivory. J. Chem. Ecol. 20:651–666.
Golan-Goldhirsh, A., and Whitaker, J. R. 1984. Relation between structure of polyphenol oxidase and prevention of browning, pp. 437–456, in M. Friedman (ed.). Nutritional and Toxicological Aspects of Food Safety. Plenum Press, New York.
Hoover, K., Schultz, C. M., Lane, S. S., Bonning, B. C., McCutchen, B. F., Duffey, S. S., and Hammock, B. D. 1995. Reduction in damage to cotton plants by a recombinant baculovirus that knocks moribund larvae of Heliothis virescens off the plant. Biol. Control 5:419–426.
Hoover, K., Yee, J. L., Schultz, C. M., Rocke, D. M., Hammock, B. D., and Duffey, S. S. 1998. Effects of plant identity and chemical constituents on the efficacy of a baculovirus against Heliothis virescens. J. Chem. Ecol. 24:221–252.
Huang, M.-T., Ho, C.-T., and Lee, C. Y. 1992. Phenolic Compounds in Food and Their Effects on Health II: Antioxidants and cancer prevention. American Chemical Society, Washington, DC, 402 pp.
Hunter, M. D., and Schultz, J. C. 1993. Induced plant defenses breached? Phytochemical induction protects and herbivore from disease. Oecologia 94:195–203.
Jones, C. G. 1984. Microorganisms as mediators of plant resource exploitation by insect herbivores, pp. 53–99, in P. W. Price, C. N. Slobodchikoff and W. S. Gaud (eds.). Novel Approaches to Interactive Systems. John Wiley & Sons, New York.
Kalbfleisch, J. D., and Prentice, R. L. 1980. The Statistical Analysis of Failure Time Data. Wiley, New York.
Karban, R., and English-Loeb, G. M. 1988. Effects of herbivory and plant conditioning on the population dynamics of spider mites. Exp. Appl. Acarol. 4:225–246.
Karban, R., and Myers, J. H. 1989. Induced plant responses to herbivory. Annu. Rev. Entomol. 20:331–348.
Mayer, A. M. 1987. Polyphenol oxidases in plants-recent progress. Phytochemistry 26:11–20.
McClure, J. W. 1975. Physiology and functions of flavonoids, pp. 970–1055, in J. B. Harborne, T. J. Mabry and H. Mabry (eds.). The Flavonoids. Academic Press, New York.
McEvily, A. J., Iyengar, R., and Gross, A. T. 1992. Inhibition of polyphenol oxidase by phenolic compounds, pp. 318–325. in C.-T. Ho, C. Y. Lee and M.-T. Huang (eds.). Phenolic Compounds in Food and Their Effects on Health: Analysis, Occurrence, and Chemistry. ACS Symposium Series 506, American Chemical Society, Washington, DC.
Mucsi, I., Beladi, I., Pusztai, R., Bakay, M., and Gabor, M. 1977. Antiviral effect of flavonoids, in L. Farkas, M. Gabor and F. Kallay (eds.). Flavonoids and Bioflavonoids-Current Research Trends. Elsevier Scientific, Amsterdam.
Price, J. P., Bouton, C. E., Gross, P., McPheron, B. A., Thompson, J. N., and Weis, A. E. 1980. Interactions among three trophic levels: Influence of plants on interactions between insect herbivores and natural enemies. Annu. Rev. Ecol. System. 11:41–65.
Price, P. W. 1986. Ecological aspects of host plant resistance and biological control: Interactions among three trophic levels, pp. 11–30, in D. J. Boethel and R. D. Eikenbary (eds.). Interactions of Plant Resistance and Parasitoids and Predators of Insects. Ellis Horwood Limited, New York.
Robak, J., and Gryglewski, R. J. 1988. Flavonoids are scavengers of superoxide anions. J. Biochem. Pharmacol. 37:837–841.
Robinson, D. S. 1991. Peroxidases and catalases in foods, pp. 1–47, in D. S. Robinson and N. A. M. Eskin (eds.). Oxidative Enzymes in Foods. Elsevier Applied Science, London.
Ryan, J. D., Gregory, P., and Tingey, W. M. 1982. Phenolic oxidase activities in glandular trichomes of Solanum berthaultii. Phytochemistry 21(8):1185–1187.
Singleton, V. L., and Rossi, J. A., Jr. 1965. Colorimetry of total phenolics with phosphomolyb-dicphosphotungstic acid reagents. Am. J. Enol. Vitic. 16:144–158.
Stamp, N., Yang, Y., and Osier, T. 1997. Response of an insect predator to prey fed multiple allelochemicals under representative thermal regimes. Ecology 78:203–214.
Steel, R. G. D., and Torrie, J. H. 1980. Principles and Procedures of Statistics: A Biometrical Approach, 2nd ed. McGraw-Hill, New York, 633 pp.
Stout, M. J., Workman, K. V., and Duffey, S. S. 1994. Differential induction of tomato foliar proteins by arthropod herbivores. J. Chem. Ecol. 20:2575–2594.
Summers, C. B., and Felton, G. W. 1994. Prooxidant effects of phenolic acids on the generalist herbivore Helicoverpa zea (Lepidoptera: Noctuidae): Potential mode of action for phenolic compounds in plant antiherbivore chemistry. Insect Biochem. Mol. Biol. 24:943–953.
Tallamy, D. W., and Raupp, M. J. (eds.). 1991. Phytochemical Induction by Herbivores. John Wiley & Sons, New York.
Traugott, M., and Stamp, N. 1997. Effects of chlorogenic acid-and tomatine-fed caterpillars on performance of an insect predator. Oecologia 109:265–272.
Wolfson, J. L. 1991. The effects of induced plant proteinase inhibitors on herbivorous insects, pp. 223–243, in D. W. Tallamy and M. J. Raupp. (eds.). Phytochemical Induction by Herbivores. John Wiley & Sons, New York.
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Hoover, K., Stout, M.J., Alaniz, S.A. et al. Influence of Induced Plant Defenses in Cotton and Tomato on the Efficacy of Baculoviruses on Noctuid Larvae. J Chem Ecol 24, 253–271 (1998). https://doi.org/10.1023/A:1022528324344
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DOI: https://doi.org/10.1023/A:1022528324344