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Inheritance of resistance in eastern black nightshade (Solanum nigrum) to acetolactate synthase inhibitors

Published online by Cambridge University Press:  20 January 2017

Dean S. Volenberg  and
David E. Stoltenberg
David E. Stoltenberg
Affiliation:
Department of Agronomy, University of Wisconsin, Madison, WI 53706
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Abstract

Experiments were conducted to determine the inheritance of resistance in a Wisconsin accession of eastern black nightshade to acetolactate synthase (ALS) inhibitors. ALS-inhibitor–susceptible (S) and ALS-inhibitor–resistant (R) plants were crossed (S × R), and inheritance was characterized in F1 and F2 generations. Inheritance was characterized further in progeny of reciprocal crosses (R × S) and backcrosses (BCs) (S × F1 and R × F1). In dose–response experiments, three- to four-leaved F1 plants were intermediate in response to imazethapyr compared with parent R and S plants. The imazethapyr ED50 value (the effective dose that reduced shoot dry biomass by 50% compared with nontreated plants) was 99.6 ± 13.6, 32.5 ± 8.9, 24.5 ± 3.3, and 0.6 ± 0.1 g ae ha−1 for R, F1 (R × S), F1 (S × R), and S plants, respectively. Similarly, the response of in vivo ALS activity in F1 plants to imazethapyr was intermediate compared with that of parent R and S plants. To differentiate among phenotypes in F2 generations and in BC generations, the response of three- to four-leaved plants to imazethapyr applied in a single dose was scored 21 d after treatment as R (no imazethapyr symptomology), S (total plant necrosis), or intermediate (I, severely stunted plants with chlorotic and twisted leaves at the apical meristem). R, I, and S phenotypes segregated in a 1:2:1 ratio in the F2 generation. S and I phenotypes segregated in a 1:1 ratio in progeny from F1 BCs to the S parent. Similarly, R and I phenotypes segregated in a 1:1 ratio in progeny from BCs to the R parent. Eastern black nightshade resistance to ALS inhibitors is associated with a single, nuclear, incompletely dominant allele, which codes for an insensitive form of the target ALS enzyme.

Keywords

Imazethapyreastern black nightshade, Solanum ptycanthum L. SOLPTImidazolinone
Type
Research Article
Information
Weed Science , Volume 50 , Issue 6 , December 2002 , pp. 731 - 736
Copyright
Copyright © Weed Science Society of America 

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References

Literature Cited

Amann, A., Feucht, D., and Wellmann, A. 2000. A new herbicide for grass control in winter wheat, winter rye and triticale. Zeitschrift-fuer-Pflan-zenkrankheiten-und-Pflanzenschutz. 17 (Special Issue): 545–553.Google Scholar
Bauer, T. A., Renner, K. A., Penner, D., and Kelly, J. D. 1995. Pinto bean (Phaseolus vulgaris) varietal tolerance to imazethapyr. Weed Sci. 43:417–424.Google Scholar
Boutsalis, P. and Powles, S. B. 1995. Inheritance and mechanism of resistance to herbicides inhibiting acetolactate synthase in Sonchus oleraceus L. Theor. Appl. Genet. 91:242–247.Google Scholar
Box, G. E. and Cox, D. R. 1964. An analysis of transformation. J. R. Stat. Soc. B 26:211–252.Google Scholar
Buchmann, S. L. and Cane, J. H. 1989. Bees assess pollen returns while sonicating Solanum flowers. Oecologia 81:289–309.Google Scholar
Christopher, J. T., Preston, C., and Powles, S. B. 1994. Malathion antagonizes metabolism-based chlorsulfuron resistance in Lolium rigidum . Pestic. Biochem. Physiol. 49:172–182.Google Scholar
Draper, N. R. and Smith, H. 1980. Applied Regression Analysis. New York: J. Wiley. pp. 458–517.Google Scholar
Fisher, R. A. 1970. Statistical Methods for Research Workers. Edinburgh: Oliver and Boyd. pp. 78–113.Google Scholar
Gerwick, B. C., Mireles, L. C., and Eilers, R. J. 1993. Rapid diagnosis of ALS/AHAS-resistant weeds. Weed Technol. 7:519–524.CrossRefGoogle Scholar
Heap, I. 2001. International Survey of Herbicide-Resistant Weeds. Herbicide Resistance Action Committee and Weed Science Society of America. Available only at www.weedscience.com. Accessed: May 2001.Google Scholar
Hermanutz, L. 1991. Outcrossing in the weed Solanum ptycanthum (Solanaceae): a comparison of agrestal and ruderal populations. Am. J. Bot. 78:638–646.Google Scholar
Jasieniuk, M. and Maxwell, B. D. 1993. Population genetics and the evolution of herbicide resistance in weeds. Phytoprotection 75 (Suppl.): 25–35.CrossRefGoogle Scholar
Levin, D. A. 1971. The origin of reproductive isolating mechanisms in flowering plants. Taxon 20:91–113.Google Scholar
Lovell, S. T., Wax, L. M., Horak, M. J., and Peterson, D. A. 1996. Imidazolinone and sulfonylurea resistance in a biotype of common waterhemp (Amaranthus rudis). Weed Sci. 44:789–794.CrossRefGoogle Scholar
Mackenzie, R., Mortimer, A. M., Putwain, P. D., Bryan, I. B., and Hawkes, T. R. 1995. The inheritance of chlorsulfuron resistance in perennial ryegrass: strategic implications for management of resistance. Pages 769–774 In Brighton Crop Protection-Weeds. Farnham, U.K.: British Crop Protection Council.Google Scholar
Mallory-Smith, C., Hendrickson, P., and Mueller-Warrant, G. 1999. Cross-resistance of primisulfuron-resistant Bromus tectorum L. (downy brome) to sulfosulfuron. Weed Sci. 47:256–257.CrossRefGoogle Scholar
Mallory-Smith, C. A., Thill, D. C., Dial, M. J., and Zemetra, R. S. 1990. Inheritance of sulfonylurea herbicide resistance in Lactuca spp. Weed Technol. 4:787–790.CrossRefGoogle Scholar
Maxwell, B. D. and Mortimer, A. M. 1994. Selection for herbicide resistance. Pages 1–26 In Powles, S. B. and Holtum, J.A.M., eds. Herbicide Resistance in Plants: Biology and Biochemistry. Boca Raton, FL: Lewis Publishers.Google Scholar
Maxwell, B. D., Roush, M. L., and Radosevich, S. R. 1990. Predicting the evolution and dynamics of herbicide resistance in weed populations. Weed Technol. 4:2–13.Google Scholar
Milliman, L. D., Riechers, D. E., Simmons, F. W., and Wax, L. M. 2000. Two biotypes of eastern black nightshade that are resistant to ALS-inhibiting herbicides. Proc. N. Cent. Weed Sci. Soc. 55:86.Google Scholar
Mourad, G., Pandey, B., and King, J. 1993. Isolation and genetic analysis of a triazolopyrimidine-resistant mutant of Arabidopsis . J. Heredity 84:91–96.CrossRefGoogle Scholar
Mulligan, G. A. 1961. Chromosome numbers of Canadian weeds III. Can. J. Bot. 39:1057–1066.Google Scholar
Ohmes, G. A. Jr. and Kendig, J. A. 1999. Inheritance of an ALS-cross resistant common cocklebur (Xanthium strumarium) biotype. Weed Technol. 13:100–103.Google Scholar
Ray, T. B. 1984. Site of action of chlorsulfuron: inhibition of valine and isoleucine biosynthesis in plants. Plant Physiol. 75:827–831.Google Scholar
Saari, L. L., Cotterman, J. C., and Thill, D. C. 1994. Resistance to acetolactate synthase inhibiting herbicides. Pages 83–140 In Powles, S. B. and Holtum, J.A.M., eds. Herbicide Resistance in Plants: Biology and Biochemistry. Boca Raton, FL: Lewis Publishers.Google Scholar
Schilling, E. E. 1981. Systematics of Solanum sect. Solanum (Solanaceae) in North America. Syst. Bot. 6:172–185.CrossRefGoogle Scholar
Schilling, E. E. Jr. and Heiser, C. B. Jr. 1979. Crossing relationships among diploid species of the Solanum nigrum complex in North America. Am. J. Bot. 66:709–716.Google Scholar
Simpson, D. M., Stoller, E. W., and Wax, L. M. 1995. An in vivo acetolactate synthase assay. Weed Technol. 9:17–22.Google Scholar
Snedecor, G. W. and Cochran, W. G. 1989. Statistical Methods. 8th ed. Ames, IA: Iowa State University Press. pp. 53–63.Google Scholar
Stoltenberg, D. E. and Wiederholt, R. J. 1995. Giant foxtail (Setaria faberi) resistance to aryloxyphenoxypropionate and cyclohexanedione herbicides. Weed Sci. 48:527–535.Google Scholar
Veldhuis, L. J., Hall, L. M., O’Donovan, J. T., Dyer, W., and Hall, J. C. 2000. Metabolism-based resistance of a wild mustard (Sinapsis arvensis L.) biotype to ethametsulfuron-methyl. J. Agric. Food Chem. 48:2986–2990.Google Scholar
Volenberg, D. S., Stoltenberg, D. E., and Boerboom, C. M. 2000a. Outcrossing and inheritance of herbicide-resistance traits in giant foxtail. Proc. N. Cent. Weed Sci. Soc. 55:83.Google Scholar
Volenberg, D. S., Stoltenberg, D. E., and Boerboom, C. M. 2000b. Solanum ptycanthum resistance to acetolactate synthase inhibitors. Weed Sci. 48:399–401.Google Scholar
Whalen, M. D. 1978. Reproductive character displacement and floral diversity in Solanum section Androceras . Syst. Bot. 3:77–86.Google Scholar
Wright, T. R. and Penner, D. 1998. Cell selection and inheritance of imidazolinone resistance in sugarbeet (Beta vulgaris). Theor. Appl. Genet. 96:612–620.Google Scholar