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BACKGROUND Trifluralin is widely used in Australia as one of the important pre‐emergence herbicides to control annual ryegrass (Lolium rigidum Gaud.) populations. Trifluralin resistance evolution and mechanisms have been identified in some ryegrass populations. RESULTS: In this study, 21 putative resistant field survey populations from Western Australian were screened with trifluralin, and 90% (19 of 21) contained individuals surviving 480 g ha−1 trifluralin treatment. Twelve populations contained individuals possessing the known α‐tubulin resistance mutations at Val‐202, Thr‐239 and Arg‐243 in TUA4 (alpha‐tubulin 4 n), plus multiple potential resistance mutations in TUA4 pending genetic confirmation. Three populations had only individuals carrying newly identified (but uncharacterized) mutations in TUA3/TUA4. Radioactive work found that six populations evolved metabolic resistance to trifluralin, and at least four of them also possessed the known and/or putative target‐site mutations. CONCLUSION: These results confirm that a high incidence of resistance to the dinitroaniline herbicide (trifluralin) is present, and target‐site tubulin mutations make a major contribution to resistance in these annual ryegrass populations. Co‐evolution of both target‐site and non‐target‐site resistance to per‐emergence herbicides warrants diverse management tactics. [ABSTRACT FROM AUTHOR]

BACKGROUND: Wild radish (Raphanus raphanistrum) is a globally important weed of crops. Two atrazine‐resistant wild radish populations (R1 and R2), collected from the Western Australia grain belt, were investigated for resistance to photosystem II (PSII) herbicides. RESULTS: Sequencing of the full‐length psbA gene revealed the well‐known Ser264–Gly substitution in population R1, whereas population R2 displayed a novel Phe274–Val substitution. Herbicide dose–response studies confirmed that the population with the Ser264–Gly mutation exhibited high‐level resistance to atrazine, but super‐sensitivity to bromoxynil. Plants possessing the novel Phe274–Val mutation exhibited a modest level of resistance to atrazine, metribuzin and diuron, and were bromoxynil susceptible. Structural modelling of the mutant D1 proteins predicts that the Ser264–Gly mutation endows atrazine resistance by abolishing H‐bonds, but confers bromoxynil super‐sensitivity by enhancing hydrogen bonding. The Phe274–Val substitution provides resistance to atrazine and diuron by indirectly affecting H‐bond formation between the Ser264 residue and the herbicides. CONCLUSION: The results demonstrate that the Phe274–Val mutation is likely responsible for resistance to PSII‐inhibiting triazine and urea herbicides. To our knowledge, this is the first evidence of the psbA Phe274–Val mutation in wild radish conferring resistance to PSII herbicides. © 2018 Society of Chemical Industry This study identifies a novel psbA Phe274–Val mutation conferring photosystem II (PSII) herbicide resistance. Structural modelling predicts that this mutation endows resistance by reducing H‐bonds between herbicides and the D1 protein. [ABSTRACT FROM AUTHOR]

BACKGROUND Lolium rigidum populations in Australia and globally have demonstrated rapid and widespread evolution of resistance to acetyl coenzyme A carboxylase ( ACCase)-inhibiting and acetolactate synthase ( ALS)-inhibiting herbicides. Thirty-three resistant L. rigidum populations, randomly collected from crop fields in a most recent resistance survey, were analysed for non-target-site diclofop metabolism and all known target-site ACCase gene resistance-endowing mutations. RESULTS The HPLC profile of [ 14C]-diclofop-methyl in vivo metabolism revealed that 79% of these resistant L. rigidum populations showed enhanced capacity for diclofop acid metabolism (metabolic resistance). ACCase gene sequencing identified that 91% of the populations contain plants with ACCase resistance mutation(s). Importantly, 70% of the populations exhibit both non-target-site metabolic resistance and target-site ACCase mutations. CONCLUSIONS This work demonstrates that metabolic herbicide resistance is commonly occurring in L. rigidum, and coevolution of both metabolic resistance and target-site resistance is an evolutionary reality. Metabolic herbicide resistance can potentially endow resistance to many herbicides and poses a threat to herbicide sustainability and thus crop production, calling for major research and management efforts. © 2015 Society of Chemical Industry [ABSTRACT FROM AUTHOR]

BACKGROUND Lolium rigidum (annual ryegrass) is a widespread annual crop weed that has evolved high levels of resistance to selective herbicides. Anecdotal evidence suggests that intensive cropping also leads to higher seed dormancy in L. rigidum. This was quantified by measuring dormancy levels in L. rigidum populations collected from paired sites (one with nil to low cropping intensity, the other intensively cropped) located throughout the Western Australian grain belt. RESULTS Populations from non-cropped fields or those with low cropping intensity showed higher and faster germination than populations from fields with a medium- or high-intensity cropping regime. Resistance to selective herbicides was also higher in the medium- and high-intensity cropping fields than in the low-intensity cropping fields. CONCLUSION High-intensity cropping systems are likely to impose greater selection pressures for seed dormancy and selective herbicide resistance, because late-emerging seedlings avoid preplanting weed control practices (tillage and non-selective herbicide application) but are exposed to selective in-crop herbicides. © 2014 Society of Chemical Industry [ABSTRACT FROM AUTHOR]

This study investigates mechanisms of multiple resistance to glyphosate, acetyl-coenzyme A carboxylase (ACCase) and acetolactate synthase (ALS)-inhibiting herbicides in two Lolium rigidum populations from Australia. When treated with glyphosate, susceptible (S) plants accumulated 4- to 6-fold more shikimic acid than resistant (R) plants. The resistant plants did not have the known glyphosate resistance endowing mutation of 5-enolpyruvylshikimate-3 phosphate synthase (EPSPS) at Pro-106, nor was there over-expression of EPSPS in either of the R populations. However, [14C]-glyphosate translocation experiments showed that the R plants in both populations have altered glyphosate translocation patterns compared to the S plants. The R plants showed much less glyphosate translocation to untreated young leaves, but more to the treated leaf tip, than did the S plants. Sequencing of the carboxyl transferase domain of the plastidic ACCase gene revealed no resistance endowing amino acid substitutions in the two R populations, and the ALS in vitro inhibition assay demonstrated herbicide-sensitive ALS in the ALS R population (WALR70). By using the cytochrome P450 inhibitor malathion and amitrole with ALS and ACCase herbicides, respectively, we showed that malathion reverses chlorsulfuron resistance and amitrole reverses diclofop resistance in the R population examined. Therefore, we conclude that multiple glyphosate, ACCase and ALS herbicide resistance in the two R populations is due to the presence of distinct non-target site based resistance mechanisms for each herbicide. Glyphosate resistance is due to reduced rates of glyphosate translocation, and resistance to ACCase and ALS herbicides is likely due to enhanced herbicide metabolism involving different cytochrome P450 enzymes. [ABSTRACT FROM AUTHOR]

The acetyl-coenzyme A carboxylase (ACCase)-inhibiting cyclohexanedione herbicide clethodim is used to control grass weeds infesting dicot crops. In Australia clethodim is widely used to control the weed Lolium rigidum. However, clethodim-resistant Lolium populations have appeared over the last 5 years and now are present in many populations across the western Australian wheat (Triticuin aestivum) belt. An aspartate-2078-glycine (Gly) mutation in the plastidic ACCase enzyme has been identified as the only known mutation endowing clethodim resistance. Here, with 14 clethodim-resistant Lolium populations we revealed diversity and complexity in the molecular basis of resistance to ACCase-inhibiting herbicides (clethodim in particular). Several known ACCase mutations (isoleucine-1781-leucine [Leu], tryptophan-2027-cysteine [Cys], isoleucine-2041-asparagine, and aspartate-2078-Gly) and in particular, a new mutation of Cys to arginine at position 2088, were identified in plants surviving the Australian clethodim field rate (60 g ha-1). Twelve combination patterns of mutant alleles were revealed in relation to clethodim resistance. Through a molecular, biochemical, and biological approach, we established that the mutation 2078-Gly or 2088-arginine endows sufficient level of resistance to clethodim at the field rate, and in addition, combinations of two mutant 1781-Leu alleles, or two different mutant alleles (i.e. 1781-Leu/2027-Cys, 1781-Leu/2041-asparagine), also confer clethodim resistance. Plants homozygous for the mutant 1781, 2078, or 2088 alleles were found to be clethodim resistant and cross resistant to a number of other ACCase inhibitor herbicides including clodinafop, diclofop, fluazifop, haloxyfop, butroxydim, sethoxydim, tralkoxydim, and pinoxaden. We established that the specific mutation, the homo/heterozygous status of a plant for a specific mutation, and combinations of different resistant alleles plus herbicide rates all are important in contributing to the overall level of herbicide resistance in genetically diverse, cross-pollinated Lolium species. [ABSTRACT FROM AUTHOR]