Unraveling the Mechanism of Resistance in a Glufosinate-Resistant Palmer Amaranth (Amaranthus palmeri) Accession

• Published in: Weed science Vol. 70; no. 4; pp. 370 - 379
• Main Authors: Carvalho-Moore, Pamela, Norsworthy, Jason K., González-Torralva, Fidel, Hwang, Jeong-In, Patel, Jinesh D., Barber, L. Tom, Butts, Thomas R., McElroy, J. Scott
• Format: Journal Article
• Language: English
• Published: New York, USA The Weed Science Society of America 01.07.2022; Cambridge University Press
• Subjects: Absorption; Amaranth; Amaranthus palmeri; Amino acids; Copy number; Enzymes; Experiments; Gene amplification; Gene expression; Glufosinate; Glutamate-ammonia ligase; Glutamine; Glutamine synthetase; Herbicide resistance; Herbicides; Isoforms; Leaves; Mutation; Nitrogen; Peptides; Polymerase chain reaction; Proteins; Roots; Seeds; Translocation; Weeds; United States > US; Arkansas; Glutamine synthetase; gene amplification; herbicide resistance
• ISSN: 0043-1745; 1550-2759
• DOI: 10.1017/wsc.2022.31

Glufosinate resistance in Palmer amaranth (Amaranthus palmeri S. Watson) was recently detected in three accessions from Arkansas, USA. Amaranthus palmeri is the first and only broadleaf weed species resistant to this herbicide, and the resistance mechanism is still unclear. A previous study characterized the glufosinate resistance level in the accessions from Arkansas. A highly glufosinate-resistant accession was further used to investigate the mechanism conferring glufosinate resistance in A. palmeri. Experiments were designed to sequence the herbicide target enzyme cytosolic and chloroplastic glutamine synthetase isoforms (GS1 and GS2, respectively) and quantify copy number and expression. Absorption, translocation, and metabolism of glufosinate using the 14C-labeled herbicide were also evaluated in the resistant and susceptible accessions. The glufosinate-resistant accession had an increase in copy number and expression of GS2 compared with susceptible plants. All accessions showed only one GS1 copy and no differences in expression. No mutations were identified in GS1 or GS2. Absorption (54% to 60%) and metabolism (13% to 21%) were not different between the glufosinate-resistant and glufosinate-susceptible accessions. Most residues of glufosinate (94% to 98%) were present in the treated leaf. Glufosinate translocation to tissues above the treated leaf and in the roots was not different among accessions. However, glufosinate translocation to tissues below the treated leaf (not including roots) was greater in the resistant A. palmeri (2%) compared with the susceptible (less than 1%) accessions. The findings of this paper strongly indicate that gene amplification and increased expression of the chloroplastic glutamine synthetase enzyme are the mechanisms conferring glufosinate resistance in the A. palmeri accession investigated. Thus far, no additional resistance mechanism was observed, but further investigations are ongoing.