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Cross- and multiple resistance of diclofop-resistant Lolium spp.

Published online by Cambridge University Press:  20 January 2017

Yong-In Kuk
Affiliation:
Department of Crop, Soil, and Environmental Sciences, University of Arkansas, 276 Altheimer Drive, Fayetteville, AR 72704
Ronald E. Talbert
Affiliation:
Department of Crop, Soil, and Environmental Sciences, University of Arkansas, 276 Altheimer Drive, Fayetteville, AR 72704

Abstract

Eighteen Lolium spp. (ryegrass) accessions collected in 1998 from several locations in Arkansas were tested for resistance (R) to diclofop in both seed and whole-plant response bioassays. Eleven accessions were L. temulentum and eight were L. perenne. Fourteen of eighteen accessions were confirmed resistant to diclofop in whole-plant assay. Three of the susceptible (S) accessions were L. temulentum. The GR50 (diclofop concentration that reduced shoot or root length by 50%) R/S ratios based on whole-plant response were greater than those of the seed bioassay in all test populations, indicating that the whole-plant bioassay was more sensitive than the seed bioassay for determining diclofop resistance in Lolium spp. The most resistant (#18) and most susceptible (#3) accessions of L. temulentum were used for multiple resistance and enzyme assay experiments. Based on whole-plant bioassay, accession #18 was 411 times more resistant to diclofop than the susceptible accession #3. Accession #18 exhibited cross-resistance to fenoxaprop and multiple resistance to chlorsulfuron applied preemergence or postemergence. Resistance to other herbicide families was not observed. Resistance to chlorsulfuron was not detected in the seed bioassay. Acetyl-CoA carboxylase (ACCase) from accession #18 was 833 times more resistant to diclofop and 10 times more resistant to sethoxydim than ACCase from accession #3. Cross-resistance to sethoxydim was not observed at the whole-plant level. Resistance to diclofop among Lolium spp. from Arkansas may be due to an alteration in the target enzyme, ACCase.

Type
Research Article
Copyright
Copyright © Weed Science Society of America 

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References

Literature Cited

Bradford, M. M. 1976. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of proteindye binding. Anal. Biochem. 72:248254.Google Scholar
Bradley, K. W., Wu, J., Hagood, E. S., and Hatzios, K. K. 1999. Investigations on the mechanism of resistance to sethoxydim and quizalofop in a biotype of johnsongrass (Sorghum halepense) from Virginia. Weed Sci. Soc. Am. Abstr. 39:79.Google Scholar
Brewster, B. D., Appleby, A. P., and Spinner, R. L. 1977. Control of Italian ryegrass and wild oats in winter wheat with HOE 23408. Agron. J. 69:911913.Google Scholar
Burnet, M.W.M., Barr, A. R., and Powles, S. B. 1994a. Chloroacetamide resistance in rigid ryegrass (Lolium rigidum). Weed Sci. 42:153157.Google Scholar
Burnet, M.W.M., Hart, Q., Holtum, J.A.M., and Powles, S. B. 1994b. Resistance to nine herbicide classes in a population of rigid ryegrass (Lolium rigidum). Weed Sci. 42:369377.CrossRefGoogle Scholar
Burnet, M.W.M., Hildebrand, O. B., Holtum, J.A.M., and Powles, S. B. 1991. Amitrole, triazine, substituted urea, and metribuzin resistance in a biotype of rigid ryegrass (Lolium rigidum). Weed Sci. 39:317323.CrossRefGoogle Scholar
Burnet, M.W.M., Loveys, B. R., Holtum, J.A.M., and Powles, S. B. 1993. A mechanism of chlorotoluron resistance in Lolium rigidum . Planta 190:182189.Google Scholar
Christopher, J. T., Powles, S. B., Holtum, J.A.M., and Liljegren, D. R. 1991. Cross resistance to herbicides in annual ryegrass (Lolium rigidum) II. Chlorsulfuron resistance involves a wheat-like detoxification system. Plant Physiol. 95:10361043.Google Scholar
Christopher, J. T., Powles, S. B., Liljegren, D. R., and Holtum, J.A.M. 1992. Resistance to acetolactate synthase inhibitors in annual ryegrass (Lolium rigidum) involves at least two mechanisms. Plant Physiol. 100:19091913.Google Scholar
Cotterman, J. C. and Saari, L. L. 1992. Rapid metabolic inactivation is the basis for cross-resistance to chlorsulfuron in diclofop-methyl-resistant rigid ryegrass (Lolium rigidum) biotype SR4/84. Pestic. Biochem. Physiol. 43:182192.Google Scholar
De Prado, R. D., De Prado, J. L., and Menendez, J. 1997. Resistance to substituted urea herbicides in Lolium rigidum biotypes. Pestic. Biochem. Physiol. 57:126136.CrossRefGoogle Scholar
Frie, J. B., Zollinger, R. K., Manthey, F. A., and Durgan, B. R. 1993. Wild oat (Avena fatua L.) resistance to diclofop in Red River Valley. Proc. North Cent. Weed Sci. Soc. 48:16.Google Scholar
Gronwald, J. W., Eberlein, C. V., Betts, K. J., Baerg, R. J., Ehlke, N. J., and Wyse, D. L. 1992. Mechanism of diclofop resistance in an Italian ryegrass (Lolium multiflorum Lam.) biotype. Pestic. Biochem. Physiol. 44:126139.CrossRefGoogle Scholar
Heap, I. M. and Knight, R. 1982. A population of ryegrass tolerant to the herbicide diclofop-methyl. J. Aust. Inst. Agric. Sci. 48:156157.Google Scholar
Heap, I. M. and Knight, R. 1986. The occurrence of herbicide cross resistance in a population of annual ryegrass, Lolium rigidum, resistant to diclofop-methyl. Aust. J. Agric. Res. 37:149156.Google Scholar
Heap, I. M. and Knight, R. 1990. Variation in herbicide cross resistance among populations of annual ryegrass (Lolium rigidum) resistant to diclofop-methyl. Aust. J. Agric. Res. 41:121128.CrossRefGoogle Scholar
Heap, I. M. and Morrison, I. N. 1996. Resistance to aryloxyphenoxypropionate and cyclohexanedione herbicides in green foxtail (Setaria viridis). Weed Sci. 44:2530.CrossRefGoogle Scholar
Heap, I. M., Murray, B. G., Loeppky, H. A., and Morrison, I. N. 1993. Resistance to aryloxyphenoxypropionate and cyclohexanedione herbicides in wild oat (Avena fatua). Weed. Sci. 41:232238.Google Scholar
Holtum, J.A.M., Matthews, J. M., Häusler, R. E., Liljegreen, D. R., and Powles, S. B. 1991. Cross resistance to herbicides in annual ryegrass (Lolium rigidum). III. On the mechanism of resistance to diclofop-methyl. Plant Physiol. 97:10261034.Google Scholar
Kobek, K., Focke, M., and Lichtenthaler, H. K. 1988. Fatty-acid biosynthesis and acetyl-CoA carboxylase as a target of diclofop, fenoxaprop and other aryloxyphenoxypropionic acid herbicides. Z. Naturforsch. 43c:4754.Google Scholar
Kotoula-Syka. 1999. Annual ryegrass (Lolium rigidum) resistant to ACCase inhibitors from Northern Greece. Weed Sci. Soc. Am. Abstr. 39:78.Google Scholar
Kuk, Y. I., Wu, J., Derr, J. F., and Hatzios, K. K. 1999. Mechanism of resistance in a biotype of smooth crabgrass (Digitaria ischaemum), which developed resistance to fenoxaprop. Pestic. Biochem. Physiol. 64:112123.Google Scholar
Leach, G. E., Devine, M. D., Kirkwood, R. C., and Marshall, G. 1995. Target enzyme-based resistance to acetyl-coenzyme A carboxylase inhibitors in Eleusine indica . Pestic. Biochem. Physiol. 51:129136.Google Scholar
Letouzè, A. and Gasquez, J. 1999. A rapid reliable test for screening aryloxyphenoxypropionic acid resistance within Alopecurus myosuroides and Lolium spp. populations. Weed Res. 39:3748.Google Scholar
Ma, G., Burton, J. D., and Coble, H. D. 1998. Herbicide inhibition and characterization of acetyl-coenzyme A carboxylase from diclofop-susceptible and -resistant Italian ryegrass (Lolium multiflorum Lam.) of NC biotype. Weed Sci. Soc. Am. Abstr. 38:51.Google Scholar
Maneechote, C., Holtum, J.A.M., Preston, C., and Powles, S. B. 1994. Resistant acetyl-CoA carboxylase is a mechanism of herbicide resistance in a biotype of Avena sterilis ssp. ludoviciana . Plant Cell Physiol. 35:627635.Google Scholar
Marles, M.A.S., Devine, M. D., and Hall, J. C. 1993. Herbicide resistance in Setaria viridis conferred by a less sensitive form of acetyl coenzyme A carboxylase. Pest. Biochem. Physiol. 46:714.Google Scholar
Matthews, J. M., Holtum, J.A.M., Liljegren, D. R., Furness, B., and Powles, S. B. 1990. Cross resistance to herbicides in annual ryegrass (Lolium rigidum) I. Properties of the herbicide targets acetyl-coenzyme A carboxylase and acetolactate synthase. Plant Physiol. 94:11801186.Google Scholar
Mcalister, F. M., Holtum, J.A.M., and Powles, S. B. 1995. Dinitroaniline herbicide resistance in rigid ryegrass (Lolium rigidum). Weed Sci. 43:5562.Google Scholar
Michael, W.M.B., Loveys, B. R., Holtum, J.A.M., and Powles, S. B. 1993. Increased detoxification is a mechanism of simazine resistance in Lolium rigidum . Pestic. Biochem. Physiol. 46:207218.Google Scholar
Powles, S. B., Lorraine-Colwill, D. F., Dellow, J. J., and Preston, C. 1998. Evolved resistance to glyphosate in rigid ryegrass (Lolium rigidum) in Australia. Weed Sci. 46:604607.Google Scholar
Preston, C., Tardif, F. J., Christopher, J. T., and Powles, S. B. 1996. Multiple resistance to dissimilar herbicide chemistries in a biotype of Lolium rigidum due to enhanced activity of several herbicide degrading enzymes. Pestic. Biochem. Physiol. 54:123134.Google Scholar
[SAS] Statistical Analysis System. 1998. SAS/STAT User's Guide. Version 7. Cary, NC: Statistical Analysis Systems Institute. Electronic version.Google Scholar
Seefeldt, S. S., Fuerst, E. P., Gealy, D. R., Shukla, A., Irzyk, G. P., and Devine, M. D. 1996. Mechanisms of resistance to diclofop of two wild oat (Avena fatua) biotypes from the Willamette Valley of Oregon. Weed Sci. 44:776781.Google Scholar
Seefeldt, S. S., Gealy, D. R., Brewster, B. D., and Fuerst, E. P. 1994. Cross resistance of several diclofop-resistant wild oat (Avena fatua) biotypes from the Willamette Valley of Oregon. Weed Sci. 42:430437.CrossRefGoogle Scholar
Shimabukuro, R. H. and Hoffer, B. L. 1991. Metabolism of diclofop-methyl in susceptible and resistant biotypes of Lolium rigidum . Pestic. Biochem. Physiol. 39:251260.Google Scholar
Shukla, A., Dupont, S., and Devine, M. D. 1997a. Resistance to ACCase-inhibitor herbicides in wild oats: evidence for target site-based resistance in two biotypes from Canada. Pestic. Biochem. Physiol. 57:147155.Google Scholar
Shukla, A., Leach, G. E., and Devine, M. D. 1997b. High-level resistance to sethoxydim conferred by an alteration in the target enzyme, acetyl-CoA carboxylase, in Setaria faberi and Setaria viridis . Plant Physiol. Biochem. 35:803807.Google Scholar
Smeda, R. J., Barrentine, W. L., and Snipes, C. E. 1993. Johnsongrass (Sorghum halepense (L.) Pers) resistance to postemergence grass herbicides. Weed Sci. Soc. Am. Abstr. 33:18 Google Scholar
Smith, E. B. 1994. Keys to the Flora of Arkansas. Fayetville, AR: The University of Arkansas Press. pp. 287, 304.Google Scholar
Stanger, C. E. and Appleby, A. P. 1989. Italian ryegrass (Lolium multiflorum) accessions tolerant to diclofop. Weed Sci. 37:350352.Google Scholar
Stoltenberg, D. E. and Wiederholt, R. J. 1995. Giant foxtail (Setaria faberi) resistance to aryloxyphenoxypropionate and cyclohexanedione herbicides. Weed Sci. 43:527535.Google Scholar
Tal, A., Zarka, S., and Rubin, B. 1996. Fenoxaprop-P resistance in Phalaris minor conferred by an insensitive acetyl-coenzyme A carboxylase. Pestic. Biochem. Physiol. 56:134140.CrossRefGoogle Scholar
Tardif, F. J., Holtum, J.A.M., and Powles, S. B. 1993. Occurrence of a herbicide-resistant acetyl-coenzyme A carboxylase mutant in annual ryegrass (Lolium rigidum) selected by sethoxydim. Planta 190:176181.Google Scholar
Terrell, E. E. 1966. Taxonomic implications of genetics in ryegrass (Lolium). Bot. Rev. 32:138164.Google Scholar
Wiederholt, R. J. and Stoltenberg, D. E. 1995. Cross resistance of a large crabgrass (Digitaria sanguinalis) accession to aryloxyphenoxypropionate and cyclohexanedione herbicides. Weed Technol. 9:518524.CrossRefGoogle Scholar