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Molecular analysis of cloransulam resistance in a population of giant ragweed

Published online by Cambridge University Press:  20 January 2017

William L. Patzoldt
Affiliation:
Department of Crop Sciences, University of Illinois, Urbana, IL 61801

Abstract

A population of giant ragweed not controlled by cloransulam was identified near Seymour, IN, during the first year of that herbicide's commercialization in 1998. Results from acetolactate synthase (ALS) activity assays performed by Dow AgroSciences showed that resistance was caused by an altered ALS. Studies were conducted to define more precisely the molecular basis of resistance and to determine cross-resistance to other ALS-inhibiting herbicides. Sixteen greenhouse-grown giant ragweed plants from the Seymour population were tested individually with postemergence (POST) applications of cloransulam, imazethapyr, or chlorimuron, or by using a nondestructive leaf disk assay to determine resistant or sensitive herbicide responses. All plants identified from the Seymour population as resistant to cloransulam were cross-resistant to imazethapyr and chlorimuron. Two DNA fragments, totaling 804 nucleotide base pairs, within ALS were sequenced from each of the 16 plants. Sequence data, combined with phenotypic data, showed that a tryptophan to leucine substitution at amino acid position 574 of ALS (based on numbering of the Arabidopsis ALS) was responsible for ALS-inhibitor resistance. Among 11 resistant and 5 sensitive giant ragweed plants analyzed from the Seymour population, at least 15 different ALS alleles were identified. Of these 15 alleles, two alleles, at an average frequency of 0.25, contained a leucine at position 574 and conferred resistance. The 13 alleles that conferred susceptibility to ALS-inhibiting herbicides occurred at an average frequency of 0.04.

Type
Research Article
Copyright
Copyright © Weed Science Society of America 

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References

Literature Cited

Bernasconi, P., Woodworth, A. R., Rosen, B. A., Subramanian, M. V., and Siehl, D. L. 1995. A naturally occurring point mutation confers broad range tolerance to herbicides that target acetolactate synthase. J. Biol. Chem. 270:1738117385.Google Scholar
Boutsalis, P., Karotam, J., and Powles, S. B. 1999. Molecular basis of resistance to acetolactate synthase-inhibiting herbicides in Sisymbrium orientale and Brassica tournefortii . Pestic. Sci. 55:507516.Google Scholar
Doyle, J. J. and Doyle, J. L. 1990. Isolation of plant DNA from fresh tissue. Focus 12:1315.Google Scholar
Foes, M. J., Liu, L., Tranel, P. J., Wax, L. M., and Stoller, E. W. 1998. A biotype of common waterhemp (Amaranthus rudis) resistant to triazine and ALS herbicides. Weed Sci. 46:514520.Google Scholar
Foes, M. J., Liu, L., Vigue, G., Stoller, E. W., Wax, L. M., and Tranel, P. J. 1999. A kochia (Kochia scoparia) biotype resistant to triazine and ALS-inhibiting herbicides. Weed Sci. 47:2027.CrossRefGoogle Scholar
Gutteri, M. J., Eberlein, C. V., Mallory-Smith, C. A., and Thill, D. C. 1996. Molecular genetics of target-site resistance to acetolactate synthase inhibiting herbicides. Pages 1016 In Brown, T. M., ed. Molecular Genetics and Evolution of Pesticide Resistance. Washington, DC: American Chemical Society.Google Scholar
Hattori, J., Brown, D., Mourad, G., Labbe, H., Ouellet, T., Sunohara, G., Rutledge, R., King, J., and Miki, B. 1995. An acetohydroxy acid synthase mutant reveals a single site involved in multiple herbicide resistance. Mol. Gen. Genet. 246:419425.Google Scholar
Heap, I. 2001. International Survey of Herbicide Resistant Weeds. Web page: www.weedscience.com. Accessed: September 12, 2001.Google Scholar
Jasieniuk, M., Brûlé-Babel, A. L., and Morrison, I. N. 1996. The evolution and genetics of herbicide resistance in weeds. Weed Sci. 44:176193.Google Scholar
Mourad, G., Haughn, G., and King, J. 1994. Intragenic recombination in the CSR1 locus of Arabidopsis . Mol. Gen. Genet. 243:178184.Google Scholar
Murashige, T. and Skoog, F. 1962. A revised medium for rapid growth and bioassay with tobacco tissue cultures. Physiol. Plant 15:473497.Google Scholar
Ott, K., Kwagh, J., Stockton, G. W., Sidorov, V., and Kakefuda, G. 1996. Rational molecular design and genetic engineering of herbicide resistant crops by structure modeling and site-directed mutagenesis of acetohydroxyacid synthase. J. Mol. Biol. 263:359368.Google Scholar
Patzoldt, W. L., Tranel, P. J., Alexander, A. L., and Schmitzer, P. R. 2001. A common ragweed population resistant to cloransulam-methyl. Weed Sci. 49:485490.CrossRefGoogle Scholar
Sathasivan, K., Haughn, G. W., and Murai, N. 1990. Nucleotide sequence of a mutant acetolactate synthase gene from an imidazolinone-resistant Arabidopsis thaliana var. Columbia . Nucleic Acids Res. 18:2188.Google Scholar
Saunders, J. W., Acquaah, G., Renner, K. A., and Doley, W. P. 1992. Monogenic dominant sulfonylurea resistance in sugarbeet from somatic cell selection. Crop Sci. 32:13571360.Google Scholar
Schultz, M. E., Schmitzer, P. R., Alexander, A. L., and Dorich, R. A. 2000. Identification and management of resistance to ALS-inhibiting herbicides in giant ragweed (Ambrosia trifida) and common ragweed (Ambrosia artemisiifolia). Weed Sci. Soc. Am. Abstr. 40:42.Google Scholar
Woodworth, A. R., Rosen, B. A., and Bernasconi, P. 1996. Broad range resistance to herbicides targeting acetolactate synthase (ALS) in a field isolate of Amaranthus sp. is conferred by a Trp to Leu mutation in ALS gene. Plant Physiol. 111:1353.Google Scholar
Wright, T. R., Bascomb, N. E., Sturner, S. F., and Penner, D. 1998. Biochemical mechanism and molecular basis for ALS-inhibiting herbicide resistance in sugarbeet (Beta vulgaris) somatic cell selection. Weed Sci. 46:1323.CrossRefGoogle Scholar
Wright, T. R. and Penner, D. 1998. Cell selection and inheritance of imidazolinone resistance in sugarbeet (Beta vulgaris). Theor. Appl. Genet. 96:612620.Google Scholar