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Target-site resistance to cyhalofop-butyl in bearded sprangletop (Diplachne fusca) from China

Published online by Cambridge University Press:  24 June 2019

Shuzhong Yuan
Affiliation:
Associate Professor, College of Horticulture and Plant Protection, Yangzhou University, Yangzhou, China
Yingjie Di
Affiliation:
Graduate Student, College of Horticulture and Plant Protection, Yangzhou University, Yangzhou, China
Yueyang Chen
Affiliation:
Graduate Student, College of Horticulture and Plant Protection, Yangzhou University, Yangzhou, China
Yongrui Chen
Affiliation:
Graduate Student, College of Horticulture and Plant Protection, Yangzhou University, Yangzhou, China
Jingxuan Cai
Affiliation:
Graduate Student, College of Horticulture and Plant Protection, Yangzhou University, Yangzhou, China
Wei Deng*
Affiliation:
Lecturer, College of Horticulture and Plant Protection, Yangzhou University, Yangzhou, China
*
Author for correspondence: Wei Deng, Email: dengwei1990dw@163.com

Abstract

Bearded sprangletop [Diplachne fusca (L.) P. Beauv. ex Roem. & Schult. ssp. fascicularis (Lam.) P. M. Peterson & N. Snow] is a noxious annual grass weed of paddy fields, distributed in coastal regions of the Jiangsu and Hebei provinces in China. Cyhalofop-butyl has been widely used to control grass weeds since 2006 in China. Overreliance on cyhalofop-butyl has led to the evolution of resistant weeds. In this study, the resistance level and cyhalofop-butyl resistance mechanisms were investigated in the putative resistant (JSHH) population. The dose–response experiments showed that the JSHH D. fusca population had evolved 8.9-fold resistance to cyhalofop-butyl. Acetyl-CoA carboxylase (ACCase) sequencing revealed a point mutation (GGC to GCC) at amino acid position 2096, resulting in a Gly-2096-Ala substitution in the resistant population. To our knowledge, this is the first case of cyhalofop-butyl resistance in D. fusca and the first report of a target-site mutation conferring resistance to ACCase-inhibiting herbicides in D. fusca. In addition, the resistant D. fusca population (JSHH) with the Gly-2096-Ala mutation was cross-resistant to the aryloxyphenoxypropionate herbicide metamifop, the cyclohexanedione herbicide sethoxydim, and the phenylpyrazolin herbicide pinoxaden.

Type
Research Article
Copyright
© Weed Science Society of America, 2019 

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References

Chen, G, Xu, H, Zhang, T, Bai, C, Dong, L (2018) Fenoxaprop-P-ethyl resistance conferred by cytochrome P450s and target site mutation in Alopecurus japonicas . Pest Manag Sci 74:16941703 CrossRefGoogle Scholar
Collavo, A, Panozzo, S, Lucchesi, G, Scarabel, L, Sattin, M (2011) Characterisation and management of Phalaris paradoxa resistant to ACCase-inhibitors. Crop Prot 30:293299 10.1016/j.cropro.2010.11.011CrossRefGoogle Scholar
Cruz-Hipolito, H, Domínguez-Valenzuela, JA, Osuna, MD, De Prado, R (2012) Resistance mechanism to acetyl coenzyme a carboxylase inhibiting herbicides in Phalaris paradoxa collected in Mexican wheat fields. Plant Soil 355:121130 10.1007/s11104-011-1085-3CrossRefGoogle Scholar
Délye, C, Zhang, XQ, Michel, S, Matéjicek, A, Powles, SB (2005) Molecular bases for sensitivity to acetyl-coenzyme a carboxylase inhibitors in black-grass. Plant Physiol 137:794806 10.1104/pp.104.046144CrossRefGoogle ScholarPubMed
De Prado, RA, Franco, AR (2004) Cross-resistance and herbicide metabolism in grass weeds in Europe: biochemical and physiological aspects. Weed Sci 52:441447 CrossRefGoogle Scholar
Du, L, Liu, W, Yuan, G, Guo, W, Li, Q, Wang, J (2016) Cross-resistance patterns to ACCase-inhibitors in American sloughgrass (Beckmannia syzigachne Steud.) homozygous for specific ACCase mutations. Pestic Biochem Physiol 126:4248 CrossRefGoogle ScholarPubMed
Guo, W, Chi, Y, Feng, L, Tian, X, Liu, W, Wang, J (2018) Fenoxaprop-P-ethyl and mesosulfuron-methyl resistance status of shortawn foxtail (Alopecurus aequalis Sobol.) in eastern China. Pestic Biochem Physiol 148:126132 CrossRefGoogle Scholar
Han, H, Yu, Q, Owen, MJ, Cawthray, GR, Powles, SB (2016a) Widespread occurrence of both metabolic and target-site herbicide resistance mechanisms in Lolium rigidum populations. Pest Manag Sci 72:255263 10.1002/ps.3995CrossRefGoogle ScholarPubMed
Han, H, Yu, Q, Widderick, MJ, Powles, SB (2016b) Target-site EPSPS Pro-106 mutations: sufficient to endow glyphosate resistance in polyploid Echinochloa colona? Pest Manag Sci 72:264271 CrossRefGoogle ScholarPubMed
Heap, I (2019) The International Survey of Herbicide Resistant Weeds. www.weedscience.com. Accessed: January 25, 2019Google Scholar
Kaundun, SS (2014) Resistance to acetyl-CoA carboxylase-inhibiting herbicides. Pest Manag Sci 70:14051417 CrossRefGoogle ScholarPubMed
Kaundun, SS, Hutchings, SJ, Dale, RP, McIndoe, E (2013) Role of a novel I1781T mutation and other mechanisms in conferring resistance to acetyl-CoA carboxylase inhibiting herbicides in a black-grass population. PLoS One 8:e69568 10.1371/journal.pone.0069568CrossRefGoogle Scholar
Laforest, M, Soufiane, B, Simard, MJ, Obeid, K, Page, E, Nurse, RE (2017) Acetyl-CoA carboxylase overexpression in herbicide-resistant large crabgrass (Digitaria sanguinalis). Pest Manag Sci 73:22272235 CrossRefGoogle Scholar
Letouzé, A, Gasquez, J (2001) Inheritance of fenoxaprop-P-ethyl resistance in a blackgrass (Alopecurus myosuroides Huds.) population. Theor Appl Genet 103:288296 CrossRefGoogle Scholar
Letouzé, A, Gasquez, J (2003) Enhanced activities of several herbicide degrading enzymes: a suggested mechanism responsible for multiple resistance in blackgrass (Alopecurus myosuroides Huds.). Agronomie 23:601608 CrossRefGoogle Scholar
Maneechote, C, Preston, C, Powles, SB (1997) A diclofop-methyl-resistant Avena sterilis biotype with a herbicide-resistant acetyl-coenzyme A carboxylase and enhanced metabolism of diclofop-methyl. Pestic Sci 49:105114 3.0.CO;2-3>CrossRefGoogle Scholar
Nikolau, BJ, Ohlrogge, JB, Wurtele, ES (2003) Plant biotin-containing carboxylases. Arch Biochem Biophys 414:211222 10.1016/S0003-9861(03)00156-5CrossRefGoogle ScholarPubMed
Pan, L, Gao, H, Xia, W, Zhang, T, Dong, L (2016) Establishing a herbicide-metabolizing enzyme library in Beckmannia syzigachne to identify genes associated with metabolic resistance. J Exp Bot 67:17451757 CrossRefGoogle ScholarPubMed
Pan, L, Li, J, Zhang, T, Zhang, D, Dong, LY (2015) Cross-resistance patterns to acetyl coenzyme A carboxylase (ACCase) inhibitors associated with different ACCase mutations in Beckmannia syzigachne . Weed Res 55:609620 CrossRefGoogle Scholar
Papapanagiotou, AP, Paresidou, MI, Kaloumenos, NS, Eleftherohorinos, IG (2015) ACCase mutations in Avena sterilis populations and their impact on plant fitness. Pestic Biochem Physiol 123:4048 10.1016/j.pestbp.2015.01.017CrossRefGoogle ScholarPubMed
Petit, C, Bay, G, Pernin, F, Délye, C (2010) Prevalence of cross- or multiple resistance to the acetyl-coenzyme A carboxylase inhibitors fenoxaprop, clodinafop and pinoxaden in black-grass (Alopecurus myosuroides Huds.) in France. Pest Manag Sci 66:168177 Google Scholar
Powles, SB, Yu, Q (2010) Evolution in action: plants resistant to herbicides. Annu Rev Plant Biol 61:317347 10.1146/annurev-arplant-042809-112119CrossRefGoogle ScholarPubMed
Scarabel, L, Panozzo, S, Varotto, S, Sattin, M (2011) Allelic variation of the ACCase gene and response to ACCase-inhibiting herbicides in pinoxaden-resistant Lolium spp. Pest Manag Sci 67:932941 CrossRefGoogle ScholarPubMed
Seefeldt, SS, Jensen, JE, Fuerst, EP (1995) Log-logistic analysis of herbicide dose response relationships. Weed Technol 9:218227 CrossRefGoogle Scholar
Spies, JJ, Van der Merwe, E, Du Plessis, H, Saayman, EJL (1991) Basic chromosome numbers and polyploid levels in some South African and Australian grasses (Poaceae). Bothalia 21:163170 CrossRefGoogle Scholar
Tian, ZH, Wang, YM, Wu, XY, Gu, CJ, Shen, GH (2017) Diplachne fusca, a newly recorded dominant species in paddy fields in Shanghai. Acta Agr Shanghai 33:5557. ChineseGoogle Scholar
Vila-Aiub, MM, Neve, P, Powles, SB (2005) Resistance cost of a cytochrome P450 herbicide metabolism mechanism but not an ACCase target site mutation in a multiple resistant Lolium rigidum population. New Phytol 167:787796 CrossRefGoogle ScholarPubMed
Wu, X, Li, P, Guo, Y (2018) The resistance of barnyardgrass populations in rice fields from Shanghai to three different action mechanisms of herbicides. World Pestic 40:5962. ChineseGoogle Scholar
Xu, H, Li, J, Zhang, D, Cheng, Y, Jiang, Y, Dong, L (2014) Mutations at codon position 1999 of acetyl-CoA carboxylase confer resistance to ACCase-inhibiting herbicides in Japanese foxtail (Alopecurus japonicus). Pest Manag Sci 70:18941901 10.1002/ps.3753CrossRefGoogle Scholar
Xu, H, Zhu, X, Wang, H, Li, J, Dong, L (2013) Mechanism of resistance to fenoxaprop in Japanese foxtail (Alopecurus japonicus) from China. Pestic Biochem Physiol 107:2531 10.1016/j.pestbp.2013.04.008CrossRefGoogle ScholarPubMed
Yu, J, Gao, H, Pan, L, Yao, Z, Dong, L (2017) Mechanism of resistance to cyhalofop-butyl in Chinese sprangletop (Leptochloa chinensis (L.) Nees). Pestic Biochem Physiol 143:306311 CrossRefGoogle Scholar
Yu, Q, Ahmad-Hamdani, MS, Han, H, Christoffers, MJ, Powles, SB (2013a) Herbicide resistance-endowing ACCase gene mutations in hexaploid wild oat (Avena fatua): insights into resistance evolution in a hexaploid species. Heredity 110:220231 10.1038/hdy.2012.69CrossRefGoogle Scholar
Yu, Q, Collavo, A, Zheng, MQ, Owen, M, Sattin, M, Powles, SB (2007) Diversity of acetyl-coenzyme a carboxylase mutations in resistant Lolium populations: evaluation using clethodim. Plant Physiol 145:547558 CrossRefGoogle ScholarPubMed
Yu, Q, Han, H, Cawthray, GR, Wang, SF, Powles, SB (2013b) Enhanced rates of herbicide metabolism in low herbicide-dose selected resistant Lolium rigidum . Plant Cell Environ 36:818827 CrossRefGoogle ScholarPubMed
Yuan, G (2016) Resistance of Keng Stiffgrass (Pseudosclerochloa kengiana (Ohwi) Tzvel.) to Fenoxaprop-p-Ethyl. M.A. thesis. Tai’an China: Shandong Agricultural University. 91 pGoogle Scholar
Yuan, G, Liu, W, Bi, Y, Du, L, Guo, W, Wang, J (2015) Molecular basis for resistance to ACCase-inhibiting herbicides in Pseudosclerochloa kengiana populations. Pestic Biochem Physiol 119:915 CrossRefGoogle ScholarPubMed
Zagnitko, O, Jelenska, J, Tevzadze, G, Haselkorn, R, Gornicki, P (2001) An isoleucine/leucine residue in the carboxyltransferase domain of acetyl-CoA carboxylase is critical for interaction with aryloxyphenoxypropionate and cyclohexanedione inhibitors. Proc Natl Acad Sci USA 98:66176622 CrossRefGoogle ScholarPubMed
Zhang, P, Wu, H, Xu, H, Gao, Y, Zhang, W, Dong, L (2017) Mechanism of fenoxaprop-P-ethyl resistance in Italian ryegrass (Lolium perenne ssp. multiflorum) from China. Weed Sci 65:710717 CrossRefGoogle Scholar
Zhang, YJ, Zhang, HY (2016) Occurrence, identification and control of Diplachne fusca in coastal saline-alkali paddy area of Eastern Hebei Province. North Rice 46:3637. ChineseGoogle Scholar
Zhao, N, Yan, Y, Ge, LA, Zhu, B, Liu, W, Wang, J (2019) Target site mutations and cytochrome P450s confer resistance to fenoxaprop-P-ethyl and mesosulfuron-methyl in Alopecurus aequalis . Pest Manag Sci 75:204214 CrossRefGoogle ScholarPubMed
Zhu, XL, Ge-Fei, H, Zhan, CG, Yang, GF (2009) Computational simulations of the interactions between acetyl-coenzyme-A carboxylase and clodinafop: resistance mechanism due to active and nonactive site mutations. J Chem Inf Model 49:19361943 CrossRefGoogle ScholarPubMed