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Pathogenic Interactions of Alternaria crassa and Phenolic Metabolism in Jimsonweed (Datura stramonium L.) Varieties

Published online by Cambridge University Press:  12 June 2017

Robert E. Hoagland  and
C. Douglas Boyette
Robert E. Hoagland
Affiliation:
South. Weed Sci. Lab., Agric. Res. Serv., U.S. Dep. Agric., Stoneville, MS 38776
C. Douglas Boyette
Affiliation:
South. Weed Sci. Lab., Agric. Res. Serv., U.S. Dep. Agric., Stoneville, MS 38776
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Abstract

Alternaria crassa, a mycoherbicide for jimsonweed control, was tested for differential effects on growth, infectivity, and phenolic metabolism of two field-collected jimsonweed varieties. Seeds from field-grown red- and green-stemmed jimsonweed varieties were grown in the greenhouse and spores were applied in aqueous solutions. Infection studies showed no significant differences between the two weed varieties when tested at various growth stages from cotyledonary to 8–leaf stage at 2.5 × 104 spores ml−1. Spore dose response tests with A. crassa spores (6.25 to 100 x 103 spores ml−1) showed no significant varietal differences in disease ratings. Extractable phenylalanine ammonia-lyase activity increased nearly equally (2- to 3-fold above control) in both varieties (8- to 9-leaf stage) 48 to 72 h after treatment with 5 × 104 spores ml−1. The only significant differences between treated varieties occurred 72 h after treatment. Exposure to A. crassa lowered total ethanol-soluble phenolic levels in both varieties 72 h after treatment. Spectrophotometric scans (400 to 700 nm) of ethanol extracts (72 h after treatment) indicated that infection caused some absorbance increases, especially in red-stemmed jimsonweed. Anthocyanin content was about 11-fold higher in red-stemmed than green-stemmed jimsonweed, and A. crassa treatment slightly increased the anthocyanin absorption peak of the red-stemmed variety.

Keywords

Jimsonweed, Datura stramonium L. # DATSTAlternaria crassa (Sacc.) SandsBioherbicidebiological weed controlD. stramonium L. var. stramoniumD. stramonium L. var. tatulamycoherbicidephenylalanine ammonia-lyase [E.C.4.3.1.5]phenylpropanoid metabolismDATST
Type
Weed Biology and Ecology
Information
Weed Science , Volume 42 , Issue 1 , March 1994 , pp. 44 - 49
Copyright
Copyright © 1994 by the Weed Science Society of America 

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References

Literature Cited

1. Bailey, J. A. 1982. Mechanisms of phytoalexin accumulation. Pages 289–318 in Bailey, J. A. and Mansfield, J. W., eds. Phytoalexins. Blackie Press.Google Scholar
2. Blakeslee, A. F. 1921. Types of mutations and their possible significance in evolution. Am. Nat. 55:254–267.CrossRefGoogle Scholar
3. Boyette, C. D. 1986. Evaluation of Alternaria crassa for biological control of jimsonweed: host range and virulence. Plant Sci. 45:223–228.CrossRefGoogle Scholar
4. Boyette, C. D. and Turfitt, L. B. 1988. Factors influencing biocontrol of jimsonweed (Datura stramonium) with Alternaria crassa . Plant Sci. 56:261–264.Google Scholar
5. Boyette, C. D., Weidemann, G. J., TeBeest, D. O., and Quimby, P. C. Jr. 1991. Biological control of jimsonweed (Datura stramonium) with Alternaria crassa . Weed Sci. 39:678–681.Google Scholar
6. Charudattan, R. and Walker, H. L., eds. 1982. Biological Control of Weeds with Plant Pathogens. John Wiley and Sons, New York, 293 pp.Google Scholar
7. Day, E. J. and Dilworth, B. C. 1984. Toxicity of jimsonweed seed and coca shell meal to broilers. Poult. Sci. 63:466–468.Google Scholar
8. Dugan, G. M., Gumbmann, M. R., and Friedman, M. 1989. Toxicological evaluation of jimsonweed (Datura stramonium) seed. Fd. Chem. Toxic. 27:501–510.Google Scholar
9. Felton, W. L. 1974. Control of Datura stramonium L. with oxadiazon under simulated spray and furrow irrigation. Weed Res. 14:209–212.Google Scholar
10. Friend, J. 1979. Phenolic substances and plant disease. Pages 557–588 in Swain, T., Harborne, J. B., and Van Sumere, D. F., eds. Recent Advances in Phytochemistry. Plenum Press, New York.Google Scholar
11. Hagood, E. D. Jr., Bauman, T. T., Williams, J. L., and Schreiber, M. M. 1981. Growth analysis of soybean (Glycine max) in competition with jimsonweed (Datura stramonium). Weed Sci. 29:500–504.Google Scholar
12. Havir, E. A. and Hanson, K. R. 1970. L-Phenylalanine ammonia–lyase (potato tubers). Methods Enzymol. 17a:575–581.CrossRefGoogle Scholar
13. Hoagland, R. E. 1980. Effects of glyphosate on metabolism of phenolic compounds: VI. Effects of glyphosate and glyphosate metabolites on phenylalanine ammonia-lyase activity, growth, and protein, chlorophyll, and anthocyanin levels in soybean (Glycine max) seedlings. Weed Sci. 28:393–400.Google Scholar
14. Hoagland, R. E., ed. 1990. Microbes and Microbial Products as Herbicides. Am. Chem. Soc. Symp. Ser. No. 439. Am. Chem. Soc., Washington, DC. 389 pp.Google Scholar
15. Hoagland, R. E. 1990. Potential Uses of Microbes and Microbial Products as Herbicides—An Overview. Am. Chem. Soc. Symp. Ser. 439:1–52.Google Scholar
16. Hoagland, R. E. 1990. Biochemical Responses of Plants to Pathogens. Am. Chem. Soc. Symp. Ser. 439:161–184.Google Scholar
17. Hoagland, R. E. 1990. Alternaria cassiae alters phenylpropanoid metabolism in sicklepod (Cassia obtusifolia). J. Phytopathol. 130:177–187.Google Scholar
18. Hoagland, R. E., Duke, S. O., and Elmore, C. D. 1979. The effect of glyphosate on metabolism of phenolic compounds. III. Phenylalanine ammonia-lyase activity, free amino acids, soluble protein, and hydroxyphenolic compounds in axes of dark-grown soybeans. Physiol. Plant. 46:357–366.Google Scholar
19. Holm, L. G., Plucknett, D. L., Pancho, J. V., and Herberger, J. P. 1977. Weeds of the World—Distribution and Biology. Univ. Press of Hawaii, Honolulu 609 pp.Google Scholar
20. Kirkpatrick, B. L., Wax, L. M., and Stoller, E. W., 1983. Competition of jimsonweed with soybean. Agron. J. 75:833–837.Google Scholar
21. Manibhushanrao, K., Mohammed, Z., and Matsugama, N. 1988. Phenol metabolism and plant disease resistance. Acta Phytopathol. Entomol. Hung. 23:103–114.Google Scholar
22. Mitchell, J. E. and Mitchell, F. N. 1955. Jimsonweed poisoning in childhood. J. Pediatr. 47:227–233.Google Scholar
23. Mitich, L. W. 1989. Intriguing world of weeds-Jimsonweed. Weed Technol. 3:208–210.CrossRefGoogle Scholar
24. Murphy, J. B. and Kies, M. W. 1960. Note on a spectrophotometric determination of proteins in dilute solutions. Biochim. Biophys. Acta 45:382–384.Google Scholar
25. Oliver, L. R., Chandler, J. M., and Buchanan, G. A. 1991. Influence of geographic region on jimsonweed (Datura stramonium) interference in soybeans (Glycine max) and cotton (Gossypium hirsutum), Weed Sci. 39:585–589.Google Scholar
26. Rathinasabapathi, B. and King, J. 1991. Herbicide resistance in Datura innoxia. Kinetic characterization of acetolactate synthase from wild-type and sulfonylurea-resistant cell variants. Plant Physiol. 96:255–261.Google Scholar
27. Singleton, Y. L. and Rossi, J. A. Jr. 1965. Colorimetry of total phenolics with phosphomolybdic-phosphotunstic acid reagents. Am. J. Enol. Vitic. 16:144–158.Google Scholar
28. Steyermark, J. A. 1963. Flora of Missouri. Publ. Iowa State Univ. Press, Ames, IA. 1728 pp.Google Scholar
29. Weaver, S. E., Dirks, V. A., and Warwick, S. I. 1985. Variation and climatic adaptation in northern populations of Datura stramonium . Can. J. Bot. 63:1303–1308.CrossRefGoogle Scholar
30. Whitehead, I. M., Atkinson, A. L., and Threlfall, D. R. 1990. Studies on the biosynthesis and metabolism of the phytoalexin lubimin and related compounds in Datura stramonium L. Planta 182:81–88.Google Scholar