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Glyphosate-Resistant Junglerice (Echinochloa colona) from Mississippi and Tennessee: Magnitude and Resistance Mechanisms

Published online by Cambridge University Press:  11 September 2018

Vijay K. Nandula*
Affiliation:
Research Plant Physiologist, Crop Production Systems Research Unit, USDA-ARS, Stoneville, MS, USA
Garret B. Montgomery
Affiliation:
Graduate Student, Department of Plant Sciences, University of Tennessee, Knoxville, TN, USA
Amaranatha R. Vennapusa
Affiliation:
Postdoctoral Fellow, Department of Agronomy, Kansas State University, Manhattan, KS, USA
Mithila Jugulam
Affiliation:
Associate Professor, Department of Agronomy, Kansas State University, Manhattan, KS, USA
Darci A. Giacomini
Affiliation:
Research Assistant Professor, Department of Crop Sciences, University of Illinois, Urbana, IL, USA
Jeffery D. Ray
Affiliation:
Research Geneticist (Plants), Crop Genetics Research Unit, USDA-ARS, Stoneville, MS, USA
Jason A. Bond
Affiliation:
Professor, Delta Research and Extension Center, Mississippi State University, Stoneville, MS, USA
Lawrence E. Steckel
Affiliation:
Professor, Department of Plant Sciences, University of Tennessee, Knoxville, TN, USA
Patrick J. Tranel
Affiliation:
Professor, Department of Crop Sciences, University of Illinois, Urbana, IL, USA
*
*Author for correspondence: Vijay K. Nandula, USDA-ARS, 141 Experiment Station Road, Stoneville, MS 38776. (Email: vijay.nandula@ars.usda.gov)

Abstract

Recently, several incidents of glyphosate failure on junglerice [Echinochloa colona (L.) Link] have been reported in the midsouthern United States, specifically in Mississippi and Tennessee. Research was conducted to measure the magnitude of glyphosate resistance and to determine the mechanism(s) of resistance to glyphosate in E. colona populations from Mississippi and Tennessee. ED50 (dose required to reduce plant growth by 50%) values for a resistant MSGR4 biotype, a resistant TNGR population, and a known susceptible MSGS population were 0.8, 1.62, and 0.23 kg ae ha−1 of glyphosate, respectively. The resistance index calculated from the these ED50 values indicated that the MSGR4 biotype and TNGR population were 4- and 7-fold, respectively, resistant to glyphosate relative to the MSGS population. The absorption patterns of [14C]glyphosate in the TNGR and MSGS populations were similar. However, the MSGS population translocated 13% more [14C]glyphosate out of the treated leaf compared with the TNGR population at 48 h after treatment. EPSPS gene sequence analyses of TNGR E. colona indicated no evidence of any point mutations, but several resistant biotypes, including MSGR4, possessed a single-nucleotide substitution of T for C at codon 106 position, resulting in a proline-to-serine substitution (CCA to TCA). Results from quantitative polymerase chain reaction analyses suggested that there was no amplification of the EPSPS gene in the resistant populations and biotypes. Thus, the mechanism of resistance in the MSGR population (and associated biotypes) is, in part, due to a target-site mutation at the 106 loci of the EPSPS gene, while reduced translocation of glyphosate was found to confer glyphosate resistance in the TNGR population.

Type
Physiology/Chemistry/Biochemistry
Copyright
© Weed Science Society of America, 2018 

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References

Alarcón-Reverte, R, García, A, Urzúa, J Fischer, AJ (2013) Resistance to glyphosate in junglerice (Echinochloa colona) from California. Weed Sci 61:4854 Google Scholar
Alarcón‐Reverte, R, García, A, Watson, SB, Abdallah, I, Sabaté, S, Hernández, MJ, Dayan, FE Fischer, AJ (2015) Concerted action of target‐site mutations and high EPSPS activity in glyphosate‐resistant junglerice (Echinochloa colona) from California. Pest Manag Sci 71:9961007 Google Scholar
Bakkali, Y, Ruiz-Santaella, JP, Osuna, MD, Wagner, J, Fischer, AJ De Prado, R (2007) Late watergrass (Echinochloa phyllopogon): mechanisms involved in the resistance to fenoxaprop-p-ethyl. J Agric Food Chem 55:40524058 Google Scholar
Corpet, F (1988) Multiple sequence alignment with hierarchical clustering. Nucleic Acids Res 16:1088110890 Google Scholar
Dinelli, G, Marotti, I, Bonetti, A, Minelli, M, Catizone, P Barnes, J (2006) Physiological and molecular insight on the mechanisms of resistance to glyphosate in Conyza canadensis (L.) Cronq. biotypes. Pestic Biochem Physiol 86:3041 Google Scholar
Dinelli, G, Marotti, I, Catizone, P, Bonetti, A, Urbano, JM Barnes, J (2008) Physiological and molecular basis of glyphosate resistance in C. bonariensis (L.) Cronq. biotypes from Spain. Weed Res 48:257265 Google Scholar
Feng, PC, Tran, M, Chiu, T, Sammons, RD, Heck, GR CaJacob, CA (2004) Investigation into GR horseweed (Conyza canadensis): retention, uptake, translocation and metabolism. Weed Sci 52:498505 Google Scholar
Gaines, TA, Cripps, A Powles, SB (2012) Evolved resistance to glyphosate in junglerice (Echinochloa colona) from the Tropical Ord River Region in Australia. Weed Technol 26:480484 Google Scholar
Ge, X, d’Avignon, DA, Ackerman, JJH, Collavo, A, Sattin, M, Ostrander, EL, Hall, EL, Sammons, RD Preston, C (2012) Vacuolar glyphosate-sequestration correlates with glyphosate resistance in ryegrass (Lolium spp.) from Australia, South America, and Europe: a 31P NMR investigation. J Agric Food Chem 60:12431250 Google Scholar
Ge, X, d’Avignon, DA, Ackerman, JJH Sammons, RD (2010) Rapid vacuolar sequestration: the horseweed glyphosate resistance mechanism. Pest Manag Sci 66:345348 Google Scholar
Godar, AS, Varanasi, VK, Nakka, S, Prasad, PV, Thompson, CR Mithila, J (2015) Physiological and molecular mechanisms of differential sensitivity of Palmer amaranth (Amaranthus palmeri) to mesotrione at varying growth temperatures. PLoS ONE 10:e0126731 Google Scholar
Han, H, Yu, Q, Widderick, MJ Powles, SB (2016) Target-site EPSPS Pro-106 mutations: sufficient to endow glyphosate resistance in polyploid Echinochloa colona? Pest Manag Sci 72:264271 Google Scholar
Heap, I (2018) The International Survey of Herbicide Resistant Weeds. www.weedscience.org. Accessed: February 12, 2018Google Scholar
Holm, LG, Pancho, JV, Herberger, JP Plucknett, DL (1991) A Geographic Atlas of World Weeds. Malabar, FL: Krieger Google Scholar
Koger, CH Reddy, KN (2005) Role of absorption and translocation in the mechanism of glyphosate resistance in horseweed (Conyza canadensis). Weed Sci 53:8489 Google Scholar
Latasa, MAG (2014) Glyphosate-resistant Echinochloa colona: Response to Glyphosate, Investigation into the Mechanisms and Distribution in Perennial Crops of the Central Valley of California. Ph.D dissertation. Davis, CA: University of California. 125 pGoogle Scholar
Lorraine-Colwill, DF, Powles, SB, Hawkes, TR, Hollinshead, PH, Warner, SAJ Preston, C (2003) Investigations into the mechanism of glyphosate resistance in Lolium rigidum . Pestic Biochem Physiol 74:6272 Google Scholar
Nandula, VK, Ray, JD, Ribeiro, DN, Pan, Z Reddy, KN (2013) Glyphosate resistance in tall waterhemp (Amaranthus tuberculatus) from Mississippi is due to both altered target site and non-target site mechanisms. Weed Sci 61:374383 Google Scholar
Nandula, VK, Reddy, KN, Poston, DH, Rimando, AM Duke, SO (2008) Glyphosate-tolerance mechanisms in Italian ryegrass (Lolium multiflorum) from Mississippi. Weed Sci 56:344349 Google Scholar
Nandula, VK Vencill, WK (2015) Herbicide absorption and translocation in plants using radioisotopes. Weed Sci 63(SP1): 140151 Google Scholar
Nguyen, TH, Malone, JM, Boutsalis, P, Shirley, N Preston, C (2016) Temperature influences the level of glyphosate resistance in barnyardgrass (Echinochloa colona). Pest Manag Sci 72:10311039 Google Scholar
Perez-Jones, A, Park, K-W, Polge, N, Colquhoun, J Mallory-Smith, CA (2007) Investigating the mechanisms of glyphosate resistance in Lolium multiflorum . Planta 226:395404 Google Scholar
Pfaffl, MW (2001) A new mathematical model for relative quantification in real-time RT–PCR. Nucleic Acids Res 29:e45e45 Google Scholar
Powles, SB Preston, C (2006) Evolved glyphosate resistance in plants: biochemical and genetic basis of resistance. Weed Technol 20:282289 Google Scholar
Salas, RA, Dayan, FE, Pan, Z, Watson, SB, Dickson, JW, Scott, RC Burgos, NR (2012) EPSPS gene amplification in glyphosate‐resistant Italian ryegrass (Lolium perenne ssp. multiflorum) from Arkansas. Pest Manag Sci 68:12231230 Google Scholar
Schmittgen, TD Livak, KJ (2008) Analyzing real-time PCR data by the comparative CT method. Nature Protocols 3:1101 Google Scholar
Shaner, DL (2009) Role of translocation as a mechanism of resistance to glyphosate. Weed Sci 57:118123 Google Scholar
Steckel, LE, Bond, JA, Montgomery, GB, Phillips, TL Nandula, V (2017) Glyphosate-resistant barnyardgrass in Tennessee and Mississippi. Page 183 in Proceedings of the Southern Weed Science Society 70th Annual Meeting. Birmingham, AL: Southern Weed Science SocietyGoogle Scholar
Wakelin, AM, Lorraine-Colwill, DF Preston, C (2004) Glyphosate resistance in four different populations of Lolium rigidum as associated with reduced translocation of glyphosate to meristematic zones. Weed Res 44:453459 Google Scholar
Wright, AA, Nandula, VK, Grier, L, Showmaker, KC, Bond, JA, Peterson, DG, Ray, JD Shaw, DR (2016) Characterization of fenoxaprop-P-ethyl-resistant junglerice (Echinochloa colona) from Mississippi. Weed Sci 64:588595 Google Scholar
Wright, AA, Rodriguez-Carres, M, Sasidharan, R, Koski, L, Peterson, DG, Nandula, VK, Ray, JD, Bond, JA Shaw, DR (2018) Multiple herbicide–resistant junglerice (Echinochloa colona): identification of genes potentially involved in resistance through differential gene expression analysis. Weed Sci 66:347354 Google Scholar
Yu, Q, Jalaludin, A, Han, H, Chen, M, Sammons, RD Powles, SB (2015) Evolution of a double amino acid substitution in the 5-enolpyruvylshikimate-3-phosphate synthase in Eleusine indica conferring high-level glyphosate resistance. Plant Physiol 167:14401447 Google Scholar