Please wait a minute...
Journal of Integrative Agriculture  2018, Vol. 17 Issue (12): 2714-2723    DOI: 10.1016/S2095-3119(18)62021-0
Plant Protection Advanced Online Publication | Current Issue | Archive | Adv Search |
Non-target-site and target-site resistance to AHAS inhibitors in American sloughgrass (Beckmannia syzigachne)
WANG Jing-jing, LI Xiang-ju, LI Dan, HAN Yu-jiao, LI Zheng, YU Hui-lin, CUI Hai-lan
Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing 100193, P.R.China
Download:  PDF in ScienceDirect  
Export:  BibTeX | EndNote (RIS)      
Abstract  
American sloughgrass (Beckmannia syzigachne (Steud.) Fernald) is one of the most competitive and malignant weeds in rice-wheat rotation fields in China.  American sloughgrass populations in the Jiangsu Province of China became less sensitive to acetohydroxyacid synthase (AHAS) inhibitors after repeated application for many years in these areas.  Two suspected resistant American sloughgrass populations (R1 and R2) collected in the field were detected the resistance to inhibitors of AHAS in whole-plant dose-response assays, compared to the susceptible (S) population.  These assays indicated that R1 showed low resistance to mesosulfuron-methyl (3.32-fold), imazapic (2.84-fold) and pyroxsulam (1.55-fold), moderate resistance to flazasulfuron (4.67-fold) and pyribenzoxim (7.41-fold), and high resistance to flucarbazone (11.73-fold).  However, using a combination of the cytochrome P450 inhibitor, malathion, with mesosulfuron-methyl resulted in a reduction in R1 resistance relative to mesosulfuron-methyl alone.  Furthermore, R2 was highly resistant to flazasulfuron (34.90-fold), imazapic (11.30-fold), flucarbazone (49.20-fold), pyribenzoxim (12.94-fold), moderately resistant to mesosulfuron-methyl (9.77-fold) and pyroxsulam (6.26-fold), and malathion had no effect on R2 resistance to mesosulfuron-methyl.  The full-length of AHAS genes was sequenced and the AHAS enzymes were assayed in vitro in order to clarify the mechanism of resistance to AHAS inhibitors in R1 and R2 populations.  The results demonstrated that R2 had a Pro-197-Ser mutation in the AHAS gene, and the sensitivity of R2 to the five AHAS inhibitors was decreased, which may result in R2 resistance to AHAS inhibitors.  There was no mutation in the AHAS gene of R1, and there were no significant differences in enzyme sensitivity between susceptible (S) and resistant (R1) populations.  An enhanced metabolism may be the main mechanism of R1 resistance to AHAS inhibitors.
Keywords:  American sloughgrass        cross-resistance        gene mutation        non-target-site resistance  
Received: 10 April 2018   Accepted:
Fund: This work was financed by the National Natural Science Foundation of China (31371952) and the Special Fund for Agro-scientific Research in the Public Interest of China (201303031).
Corresponding Authors:  Correspondence CUI Hai-lan, E-mail: cuihailan413@163.com   
About author:  WANG Jing-jing, E-mail:wjj9874561230@163.com

Cite this article: 

WANG Jing-jing, LI Xiang-ju, LI Dan, HAN Yu-jiao, LI Zheng, YU Hui-lin, CUI Hai-lan. 2018. Non-target-site and target-site resistance to AHAS inhibitors in American sloughgrass (Beckmannia syzigachne). Journal of Integrative Agriculture, 17(12): 2714-2723.

Bi Y L, Liu W T, Li L X. 2013. Molecular basis of resistance to mesosulfuron-methyl in Japanese foxtail, Alopecurus japonicus. Journal of Pesticide Sciences, 38, 74–77.
Chaleff R S, Mauvais C J. 1984. Acetolactate synthase is the site of action of two sulfonylurea herbicides in higher plants. Science, 224, 1443–1445.
Délye C. 2005. Weed resistance to acetyl coenzyme A carboxylase inhibitors: An update. Weed Science, 53, 728–746.
Délye C. 2013. Unravelling the genetic bases of non-target-site-based resistance (NTSR) to herbicides: A major challenge for weed science in the forthcoming decade. Pest Management Science, 69, 176–187.
Duhoux A, Carrere S, Gouzy J, Bonin L, Délye C. 2015. RNA-Seq analysis of rye-grass transcriptomic response to an herbicide inhibiting acetolactate-synthase identifies transcripts linked to non-target-site-based resistance. Plant Molecular Biology, 87, 473–487.
Duggleby R G, Pang S S. 2000. Acetohydroxyacid synthase. BMB Reports, 33, 1–36.
Gardin J A C, Gouzy J, Carrère S, Délye C. 2015. ALOMYbase, a resource to investigate non-target-site-based resistance to herbicides inhibiting acetolactate-synthase (ALS) in the major grass weed Alopecurus myosuroides (black-grass). BMC Genomics, 16, 590.
Gerwick B C, Subramanian M V, Loney-gallant V I. 1990. Mechanism of action of the 1, 2, 4-triazolo[1,5-α]pyrimidines. Pest Management Science, 29, 357–364.
Guo J Q, Riggins C W, Hausman N E, Hager A G, Riechers D E, Davis A S, Tranel P J. 2015. Nontarget-site resistance to ALS inhibitors in waterhemp (Amaranthus tuberculatus). Weed Science, 63, 399–407.
Han H P, Yu Q, Purba E, Li M, Walsh M, Friesen S, Powles S B. 2012. A novel amino acid substitution Ala-122-Tyr confers high-level and broad resistance across AHAS-inhibiting herbicides. Pest Management Science, 68, 1164–1170.
Han H P, Yu Q, Vila-Aiub M, Powles S B. 2014. Genetic inheritance of cytochrome P450-mediated metabolic resistance to chlorsulfuron in a multiple herbicide resistant Lolium rigidum population. Crop Protection, 65, 57–63.
Heap I. 2018. The international survey of herbicide resistant weeds. [2018-02-27]. http://www.weedscience.com
Kaloumenos N S, Adamouli V N, Dordas C A, Eleftherohorinos I G. 2011. Corn poppy (Papaver rhoeas) cross-resistance to ALS-inhibiting herbicides. Pest Management Science, 67, 574–585.
Li L X, Du L, Liu W T, Yuan G H, Wang J X. 2014. Target-site mechanism of ACCase-inhibitors resistance in American sloughgrass (Beckmannia syzigachne Steud.) from China. Pesticide Biochemistry Physiology, 110, 57–62.
Li L X, Liu W T, Chi Y C, Guo W L, Luo X Y, Wang J X. 2015. Molecular mechanism of mesosulfuron-methyl resistance in multiply-resistant American sloughgrass (Beckmannia syzigachne). Weed Science, 63, 781–787.
Owen M J, Goggin D E, Powles S B. 2012. Non-target-site-based resistance to ALS inhibiting herbicides in six Bromus rigidus populations from Western Australian cropping fields. Pest Management Science, 68, 1077–1082.
Pan L, Gao H T, Xia W W, Zhang T, Dong L Y. 2016a. Establishing a herbicide-metabolizing enzyme library in Beckmannia syzigachne to identify genes associated with metabolic resistance. Journal of Experimental Botany, 67, 1745–1757.
Pan L, Li J, Zhang W N, Dong L Y. 2015. Detection of the I1781L mutation in fenoxaprop-p-ethy-resistant American sloughgrass (Beckmannia syzigachne Steud.), based on the loop-mediated isothermal amplification method. Pest Management Science, 71, 123–130.
Pan L, Wang Z Y, Cai J, Gao H T, Zhao H W, Dong L Y. 2016b. High-throughput sequencing reveals differential regulation of miRNAs in fenoxaprop-P-ethyl-resistant Beckmannia syzigachne. Scientific Reports, 6, 28725.
Park K W, Mallory-Smith C A. 2004. Physiological and molecular basis for ALS inhibitor resistance in Bromus tectorum biotypes. Weed Research, 44, 71–77.
Petit C, Duhieu B, Boucansaud K, Délye C. 2010. Complex genetic control of non-target-site-based resistance to herbicides inhibiting acetylcoenzyme A carboxylase and acetolactate synthase in Alopecurus myosuroides Huds. Plant Science, 178, 501–509.
Powles S B, Yu Q. 2010. Evolution in action: Plants resistant to herbicides. Annual Review of Plant Biology, 61, 317–347.
Rao N, Dong L Y, Li J, Zhang H. 2008. Influence of environmental factors on seed germination and seeding emergence of American sloughgrass (Beckmannia syzigachne). Weed Science, 56, 529–533.
Rey-Caballero J, Menéndez J, Osuna M D, Salas M, Torra J. 2017. Target-site and non-target-site resistance mechanisms to ALS inhibiting herbicides in Papaver rhoeas. Pesticide Biochemistry Physiology, 138, 57–65.
Santel H J, Bowden B A, Sorensen V M, Mueller K H, Reynolds J. 1999. Flucarbazaone-sodium: a new herbicide for grass control in wheat. Weed Science Society, 52, 124–124.
Seefeldt S S, Jensen J E, Fuerst E P. 1995. Log-logistic analysis of herbicide dose response relationships. Weed Technology, 9, 218–227.
Shaner D L, Anderson P C, Studham M A. 1984. Imidazolinones: Potential inhibitors of acetohydroxidacid synthase. Plant Physiology, 76, 545–546.
Stidham M A. 1991. Herbicides that inhibit acetohydroxidacid synthase. Weed Science, 39, 428–434.
Veldhuis L J, Hall L M, O’Donovan J T, Dyer W, Hall J C. 2000. Metabolism-based resistance of a wild mustard (Sinapis arvensis L.) biotype to ethametsulfuron-methyl. Journal of Agricultural Food Chemistry, 48, 2986–2990.
Xia W W, Pan L, Li J, Wan Q, Feng Y J, Dong L Y. 2015. Molecular basis of ALS-and/or ACCase-inhibitor resistance in shortawn foxtail (Alopecurus aequalis Sobol.). Pesticide Biochemistry and Physiology, 122, 76–80.
Yang Q, Deng W, Li X F, Yu Q, Bai L Y, Zheng M Q. 2016. Target-site and non-target-site based resistance to the herbicide tribenuron-methyl in flixweed (Descurainia sophia L.). BMC Genomics, 17, 551.
Yasuor H, Osuna M D, Ortiz A, Saldaín N E, Eckert J W, Fischer A J. 2009. Mechanism of resistance to penoxsulam in late watergrass [Echinochloa phyllopogon (Stapf) Koss.]. Journal of Agricultural Food Chemistry, 57, 3653–3660.
Yu Q, Frisesen L J S, Zhang X Q, Powles S B. 2004. Tolerance to acetolactate synthase and acetyl-coenzyme A carboxylase inhibiting herbicides in Vulpia bromoides is conferred by two co-existing resistance mechanisms. Pesticide Biochemistry Physiology, 78, 21–30.
Yu Q, Han H P, Li M, Purba E, Walsh M J, Powles S B. 2012. Resistance evaluation for herbicide resistance-endowing acetolactate synthase (ALS) gene mutations using Raphanus raphanistrum populations homozygous for specific ALS mutations. Weed Research, 52, 178–186.
Yu Q, Han H P, Powles S B. 2008. Mutations of the ALS gene endowing resistance to ALS-inhibiting herbicides in Lolium rigidum populations. Pest Management Science, 64, 1229–1236.
Yu Q, Powles S B. 2014. Resistance to AHAS inhibitor herbicides: Current understanding. Pest Management Science, 70, 1340–1350.
Zhao B C, Fu D N, Yu Y, Huang C T, Yan K C, Li P S, Shafi J, Zhu H, Wei S H, Ji M S. 2017. Non-target-site resistance to ALS-inhibiting herbicides in a Sagittaria trifolia L. population. Pesticide Biochemistry Physiology, 140, 79–84.
[1] WANG Ran, WANG Jin-da, CHE Wu-nan, SUN Yan, LI Wen-xiang, LUO Chen .
Characterization of field-evolved resistance to cyantraniliprole in Bemisia tabaci MED from China
[J]. >Journal of Integrative Agriculture, 2019, 18(11): 2571-2578.
[2] DENG Wei, YANG Qian, JIAO Hong-tao, ZHANG Yong-zhi, LI Xue-feng, ZHENG Ming-qi. Cross-resistance pattern to four AHAS-inhibiting herbicides of tribenuron-methyl-resistant flixweed (Descurainia sophia) conferred by Asp-376-Glu mutation in AHAS[J]. >Journal of Integrative Agriculture, 2016, 15(11): 2563-2570.
No Suggested Reading articles found!