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10 March 2022 First Report of ALS Inhibitor–Resistant Green Kyllinga (Kyllinga brevifolia)
David P. Westbury, Patrick E. McCullough, J. Scott McElroy, Claudia A. Rutland, Jinesh Patel
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Abstract

Acetolactate synthase (ALS) inhibitors provide postemergence control of green kyllinga (Kyllinga brevifolia Rottb.) in turfgrass and other cropping systems. A suspected resistant (R) biotype of K. brevifolia was collected from a golf course and evaluated for resistance to ALS inhibitors. In greenhouse experiments, the sulfosulfuron rates required to cause 50% shoot biomass reduction from the nontreated at 4 wk after treatment (WAT) were 10 and 792 g ai ha–1 for the susceptible (S) and R biotypes, respectively. The rates required to cause 50% injury at 4 WAT were 189 and >3,360 g ai ha–1, respectively. In other experiments, shoot mass of the R biotype was not reduced by imazaquin, trifloxysulfuron-sodium, pyrimisulfan, thiencarbazone + foramsulfuron + halosulfuron, florasulam + halauxifen-methyl, and bentazon compared with the nontreated, while sulfentrazone reduced biomass similarly for both R and S biotypes. Gene sequencing of the R biotype revealed a mutation at Asp-376-Glu that has previously conferred resistance to five families of ALS inhibitors. This is the first report of ALS-inhibitor resistance in K. brevifolia.

Introduction

Green kyllinga (Kyllinga brevifolia Rottb.) is a perennial weed in turfgrass throughout the warm-humid region and U.S. transition zone that spreads through rhizomatous growth under turf maintenance (Bryson et al. 1997). Populations also emerge through seed germination that peaks between 20 and 24 C (Molin et al. 1997). Kyllinga brevifolia is difficult to physically remove from turfgrasses, and hand pulling or digging is often ineffective. Kyllinga brevifolia regenerates new plants through rhizomatous growth, enabling populations to escape preemergence herbicides and rapidly infest turfgrasses in summer (Lowe et al. 2000).

Acetolactate synthase (ALS) inhibitors are the most widely utilized herbicides for postemergence control of sedges (Cyperus spp.) in established stands of warm- and cool-season turfgrasses (Lycan and Hart 2004). Sulfonylureas are systemic herbicides that are readily translocated in susceptible plants (Eizenberg et al. 2003; Schloss 1994). These herbicides, such as sulfosulfuron and trifloxysulfuron, control multiple sedge and Kyllinga species, including purple nutsedge (Cyperus rotundus L.), false-green kyllinga (Kyllinga gracillima Miq.), and K. brevifolia (Gannon et al. 2012). Turf managers use several ALS inhibitors for K. brevifolia control due to their efficacy and selectivity in warm-season turfgrasses. However, these herbicides have been overused, and resistance is a concern.

Resistance to ALS-inhibiting herbicides has increased exponentially in turfgrass over recent years (Brosnan et al. 2015; McCullough et al. 2016). ALS-inhibitor resistance has been reported in several sedge species, including, smallflower umbrella sedge (Cyperus difformis L.), yellow nutsedge (Cyperus esculentus L.), rice flatsedge (Cyperus iria L.), and annual sedge (Cyperus compressus L.) (Busi et al. 2006; Kuk et al. 2003; McCullough et al. 2016; Merotto et al. 2010; Riar et al. 2017; Tehranchian et al. 2014; Yu et al. 2020). Cyperus difformis, C. iria, and C. compressus are annuals that reproduce solely from seed. The confirmation of ALS resistance in C. esculentus is concerning due to perennial growth and ability for resistant (R) biotypes to spread asexually. Resistance to ALS inhibitors is often attributed to target-site alteration or enhanced herbicide degradation (Riar et al. 2017; Tranel and Wright 2002). Previous reports of ALS-resistant sedges have been associated with target-site mutations (McCullough et al. 2016; Tehranchian et al. 2014; Yu et al. 2020). Cross-resistance to other ALS inhibitors may further limit the selective herbicides available to practitioners for controlling these weeds (Kuk et al. 2003; Merotto et al. 2009).

A K. brevifolia biotype with suspected resistance to ALS inhibitors was identified on a golf course in Florida. The turf managers had noted reductions in efficacy for K. brevifolia control over time after repeated use of ALS inhibitors. There have been no reports of herbicide resistance in K. brevifolia, which could raise concerns for integrated weed management in turf and other cropping systems. The objectives of this research were to evaluate potential resistance to ALS inhibitors and sequencing of the ALS enzyme of the suspected R biotype.

Materials and Methods

Plant Material

A suspected R K. brevifolia was collected from a golf course in Florida in March 2020. The name and location of the golf course will not be disclosed to protect the privacy of the facility. The turf managers had been using sulfonylurea herbicides for over a decade to control K. brevifolia and had noticed reductions in efficacy over time. A known susceptible (S) population was also collected in April 2020. Plants were potted and placed in a greenhouse set for 30/19 C (high/low). Individual tillers were subsequently planted into potting tubes (3.8-cm diameter, 20-cm depth) filled with sand:peat moss (80:20 v/v). Pots were then irrigated daily to prevent moisture deficiencies.

Herbicide Response

The response of the two biotypes was evaluated from a rate titration of sulfosulfuron (Certainty®, Nufarm, Alsip, IL). Sulfosulfuron was applied at 10 rates, ranging 6.6 to 3,360 g ai ha–1, in a spray chamber calibrated to deliver 374 L ha–1. Nontreated checks of the two biotypes were also included. A nonionic surfactant (Activator 90, Loveland Products, Greenville, MS) was added to the spray solution at 0.25% v/v. Plants were returned to the greenhouse approximately 3 h after treatment (HAT) and did not receive irrigation until 24 HAT. Injury was rated visually at 4 wk after treatment (WAT). Fresh shoot biomass was harvested at 4 WAT and weighed immediately (Table 1).

In a separate experiment, the biotypes were treated with trifloxysulfuron, pyrimisulfan, sulfentrazone, bentazon, imazaquin, thiencarbazone + foramsulfuron + halosulfuron, and florasulam + halauxifen. A nontreated check was included. Herbicide rates are presented in Table 2. All herbicides were applied with the aforementioned surfactant, except sulfentrazone, for which it is not required. Injury was visually evaluated on a percent scale at 4 WAT. Fresh shoot biomass was harvested at 4 WAT and weighed.

Kyllinga Mapping Methods

Detection of possible single-nucleotide polymorphisms (SNPs) were evaluated using Illumina next-generation sequencing, assembly of ALS transcripts, and mapping of reads to known ALS nucleotide AB719979.1. mRNA from R and S biotypes was extracted using the RNeasy Plant Mini Kit (Qiagen, Hilden, Germany,  http://www.qiagen.com). The quantity and quality of mRNA was checked using Nanodrop (Nanodrop One, ThermoFisher Scientific, Waltham, MA,  http://thermofisher.com). Both R and S K. brevifolia biotypes were sequenced using the Illumina HiSeq Platform to generate 150-bp paired-end DNA sequencing reads. Sequencing was conducted by Novogene ( http://en.novogene.com). Reads were first quality checked using FastQC ( https://www.bioinformatics.babraham.ac.uk/projects/fastqc), and adaptors were removed using Trimmomatic,  http://www.usadellab.org/cms/?page=trimmomatic). Transcriptomes of the biotype were assembled using Trinity v. 2.8 ( https://github.com/trinityrnaseq/trinityrnaseq/wiki). Mapping of putative R (KYR2) and S (KYS2) K. brevifolia fastq sequences against a known K. brevifolia ALS nucleotide sequence from NBCI (AB719979.1) was conducted to identify SNPs associated with ALS resistance. The consensus nucleotide transcripts from KYR2 and KYS2 read mappings were also aligned against the AB719979.1 sequence to compare any potential SNPs. All mapping and alignments were performed using Qiagen CLC Genomics Workbench 21.0 ( https://digitalinsights.qiagen.com).

Experimental Design and Data Analysis

The designs in the greenhouse experiments were randomized complete blocks with five replications. A block design was used to reduce the potential variability of greenhouse location on plant responses to herbicides. Three separate runs were conducted for greenhouse experiments.

Data were subjected to ANOVA in SAS v. 9.4 (SAS Institute, Cary, NC) to test for treatment by experimental run interaction. For the dose–response experiments, data were regressed in SigmaPlot v. 11.0 (Systat, San Jose, CA) against the following equation:

e01_287.gif

where f is injury/biomass, β0 is the asymptote, β1 is the slope estimate, and x is the sulfosulfuron rate. Shoot mass reductions were calculated as a percent reduction of the treated against the corresponding nontreated plant per replication.

For the evaluation of various herbicides, shoot biomass data were converted to percent reductions of the nontreated by replication. Means were separated with Fisher's LSD test at α = 0.05. Treatment by experimental run interactions were not detected, and results were therefore combined for presentation.

Results and Discussion

Herbicide Response Experiments

Injury was expressed as tissue chlorosis and stunted growth of the S biotype. The sulfosulfuron rate required to cause 50% injury (I50) was >3,360 g ha–1 and 189 g ha–1 for the R and S biotypes, respectively (Figure 1; Table 1). The rate required to cause 50% shoot mass reductions (SR50) in the R and S biotypes was 792 and 10 g ha–1, respectively (Figure 2). Results support the supposition that the K. brevifolia biotype was resistant to sulfosulfuron.

In the other experiments, shoot biomass of the S biotype was reduced 39% to 61% by the ALS inhibitors evaluated at 4 WAT (Table 2). However, the R biotype did not have reductions in biomass and was significantly different from the S biotype at all treatment levels. Both biotypes responded similarly to other sites of action tested, including bentazon, florasulam + halauxifen, and sulfentrazone. Bentazon and florasulam + halauxifen did not cause a meaningful reduction in biomass for either biotype at the rates tested, but sulfentrazone reduced biomass an average of 54%. Biomass reductions of the R biotype from sulfentrazone were greater than for all ALS inhibitors evaluated.

Within the Cyperaceae family, ALS resistance has been reported in annual sedges (McCullough et al. 2016), C. difformis (Tehranchian et al. 2017), C. iria (Riar et al. 2017), and C. esculentus (Scarabel et al. 2020; Tehranchian et al. 2014). However, the only species with confirmed resistance in established turfgrass stands is C. compressus (McCullough et al. 2016; Yu et al. 2020). Although bentazon and florasulam + halauxifen did not provide meaningful reductions in shoot biomass, sulfentrazone may provide an alternative site of action to ALS inhibitors in selectively controlling K. brevifolia in turfgrass.

Table 1.

Shoot biomass reductions and injury of two Kyllinga brevifolia biotypes at 4 wk after treatment with sulfosulfuron in two greenhouse experiments.a

img-z3-4_287.gif

Figure 1.

Injury of two Kyllinga brevifolia biotypes at 4 wk after treatment. Results were pooled over experimental runs. Vertical bars represent standard errors of the mean. Data were regressed with f = y0 + β0*[1 – exp(–β1*x)], where f is injury, β0 is the asymptote, β1 is the slope estimate, and x is the sulfosulfuron rate.

img-z3-5_287.jpg

Kyllinga Mapping Results

Illumina sequencing allows for the evaluation of all possible SNPs in the ALS gene that are known to confer target-site resistance (TSR). Based on read mapping and alignment of assembled ALS transcripts, an amino acid change from aspartic acid (Asp) to glutamic acid (Glu) at position 376 in the R biotype was observed (GenBank accession numbers MZ558475 and MZ558476 for R and S biotypes, respectively). Both reference AB719979 and S assembled consensus ALS contained only Asp (Figure 3). Asp-376-Glu has been identified previously as a TSR mechanism in ALS resistance.

Implications from These Findings

Repeated use of ALS inhibitors encourages the establishment of R populations through selection pressure (Tranel and Wright 2002). Due to this risk of resistance, a wider variety of techniques must be employed along with herbicide usage. Turf managers should incorporate preemergence herbicides into their integrated weed management programs to help limit the spread of K. brevifolia from seed (Belcher et al. 2002). However, use of these herbicides may be limited by cost, turfgrass injury potential, and limitations for controlling perennial infestations of K. brevifolia.

Table 2.

Shoot biomass reductions of two Kyllinga brevifolia biotypes at 4 wk after treatment from herbicides in three greenhouse experiments, Griffin, GA.a

img-z4-4_287.gif

Figure 2.

Shoot biomass reductions of two Kyllinga brevifolia biotypes at 4 wk after treatment. Results were pooled over experimental runs. Vertical bars represent standard errors of the mean. Data were regressed with f = y0 + β0*[1 – exp(–β1*x)], where f is shoot biomass reductions, β0 is the asymptote, β1 is the slope estimate, and x is the sulfosulfuron rate.

img-z4-7_287.jpg

Figure 3.

Gene sequencing for the ALS enzyme of the two Kyllinga brevifolia biotypes.

img-z4-9_287.jpg

Detecting herbicide resistance in a perennial species has important implications for management programs. Kyllinga brevifolia is able to overwinter in many environments, and postemergence herbicides are often the only means for selective control. Sulfonylureas have been the most selective herbicides for controlling K. brevifolia patches in turfgrass, and resistance to this site of action may limit the options for long-term management. Other control programs may include spot treatment with glyphosate or physically hand pulling K. brevifolia plants with suspected resistance. These options may not be practical or applicable for large areas of turf, such as sod farms and golf courses. Cultural practices, along with herbicide rotation, will be another critical component of managing resistant Kyllinga populations. Factors such as mowing, irrigation, and fertilization could warrant modifications to help reduce infestations and enhance competitive growth of desirable turf with these infestations (Abu-Dieyeh and Watson 2006; Busey 2003).

The main hindrance to controlling the spread of ALS inhibitor–resistant K. brevifolia is the limited number of alternative sites of action available for selective control. This is especially concerning in cool-season turfgrasses, such as bentgrass (Agrostis spp.), that require low use rates of many herbicides to minimize injury potential compared with other turfgrass species. Sulfentrazone appears to have the greatest potential to control ALS-resistant K. brevifolia in turfgrass. Although bentazon offers an alternative site of action to ALS inhibitors, applications did not appear to provide sufficient efficacy for controlling either K. brevifolia biotype at the rate tested. These results are similar to previous experiments on the efficacy of bentazon for control of K. brevifolia in bermudagrass [Cynodon dactylon (L.) Pers.] (McElroy et al. 2005). As resistant populations of K. brevifolia increase through repeated use of ALS inhibitors, further research is needed on application timings, rates, and regimens of herbicides with alternative sites of action, such as sulfentrazone, for selectively controlling infestations in turfgrass and other cropping systems.

Acknowledgments.

The authors would like to thank Vijaya Mantripragada and Catherine McCullough for technical assistance with this research. This research received no specific grant from any funding agency or the commercial or not-for-profit sectors. No conflicts of interest have been declared.

References

1.

Abu-Dieyeh M, Watson A (2006) Impact of mowing and weed control on broadleaf weed population dynamics in turf. J Plant Interact 1:239–252 Google Scholar

2.

Belcher JL, Walker RH, Van Santen E, Wehtje GR (2002) Nontuberous sedge and kyllinga species' response to herbicides. Weed Technol 16:575–579 Google Scholar

3.

Brosnan JT, Vargas JJ, Breeden GK, Grier L, Aponte RA, Tresch S, Laforest M (2015) A new amino acid substitution (Ala-205-Phe) in acetolactate synthase (ALS) confers broad spectrum resistance to ALS-inhibiting herbicides. Planta 243:149–159 Google Scholar

4.

Bryson CT, Carter R, McCarty LB, Yelverton FH (1997) Kyllinga, a genus of neglected weeds in the continental United States. Weed Technol 11:838–842 Google Scholar

5.

Busey P (2003) Cultural management of weeds in turfgrass. Crop Sci 43: 1899–1911 Google Scholar

6.

Busi R, Vidotto F, Fischer AJ, Osuna MD, De Prado M, Ferrero A (2006) Patterns of resistance to ALS herbicides in smallflower umbrella sedge (Cyperus difformis) and ricefield bulrush (Schoenoplectus mucronatus). Weed Technol 20:1004–1014 Google Scholar

7.

Eizenberg H, Goldwasser Y, Achdary G, Hershenhorn J (2003) The potential of sulfosulfuron to control troublesome weeds in tomato. Weed Technol 17:133–137 Google Scholar

8.

Gannon TW, Yelverton F, Tredway LP (2012) Selective exposure of yellow nutsedge (Cyperus esculentus), purple nutsedge (Cyperus rotundus), and false green kyllinga (Kyllinga gracillima) to postemergence herbicides. Weed Technol 26:294–299 Google Scholar

9.

Kuk YI, Kim KH, Kwon OD, Lee DJ, Burgos NR, Jung S, Guh JO (2003) Cross-resistance pattern and alternative herbicides for Cyperus difformis resistant to sulfonylurea herbicides in Korea. Pest Manag Sci 60:85–94 Google Scholar

10.

Lowe DB, Whitwell T, McCarty LB, Bridges WC (2000) Mowing and nitrogen influence green kyllinga (Kyllinga brevifolia) infestation in Tifway bermudagrass (Cynodon dactylon x C. transvaalensis) Turf. Weed Technol 14:471–475 Google Scholar

11.

Lycan DW, Hart SE (2004) Relative tolerance of four cool-season turfgrass species to sulfosulfuron. Weed Sci 18:977–981 Google Scholar

12.

McCullough PE, Yu J, McElroy JS, Chen S, Zhang H, Grey TL, Czarnota MA (2016) ALS-resistant annual sedge (Cyperus compressus) confirmed in turfgrass. Weed Sci 64:33–41 Google Scholar

13.

McElroy JS, Yelverton FH, Warren LS (2005) Control of green and false-green kyllinga (Kyllinga brevifolia and K. gracillima) in golf course fairways and roughs. Weed Technol 19:824–829 Google Scholar

14.

Merotto A, Jasieniuk M, Fischer AJ (2010) Distribution and cross-resistance patterns of ALS-inhibiting herbicide resistance in smallflower umbrella sedge (Cyperus difformis). Weed Sci 58:22–29 Google Scholar

15.

Merotto A, Jasieniuk M, Osuna MD, Vidotto F, Ferrero A, Fischer AJ (2009) Cross-resistance to herbicides of five ALS-inhibiting groups sequencing of the ALS gene in Cyperus difformis. J Agric Food Chem 57:1389–1398 Google Scholar

16.

Molin WT, Khan RA, Barinbaum RB, Kopec DM (1997) Green kyllinga (Kyllinga brevifolia): germination and herbicidal control. Weed Sci 45: 546–550 Google Scholar

17.

Riar DS, Tehranchian P, Norsworthy JK, Nandula V, McElroy S, Srivastava V, Chen S, Bond JA, Scott RC (2017) Acetolactate synthase-inhibiting, herbicide-resistant rice flatsedge (Cyperus iria): cross-resistance and molecular mechanism of resistance. Weed Sci 63:748–757 Google Scholar

18.

Scarabel L, Farinati S, Sattin M (2020) Occurrence of resistance to ALS inhibitors in European Cyperus esculentus L.: characterization and implications for management. Agronomy 10:1133 Google Scholar

19.

Schloss JV (1994) Recent advances in understanding the mechanism and inhibition of acetolactate synthase. Pages 3–14 in Stetter J, ed. Herbicides Inhibiting Branched-Chain Amino Acid Biosynthesis (Chemistry of Plant Protection 10). Berlin: Springer Google Scholar

20.

Tehranchian P, Norsworthy JK, Nandula V, McElroy S, Chen S, Scott RC (2014) First report of resistance to acetolactate-synthase-inhibiting herbicides in yellow nutsedge (Cyperus esculentus): confirmation and characterization. Pest Manag Sci 71:1274–1280 Google Scholar

21.

Tehranchian P, Riar DS, Norsworthy JK, Nandula V, McElroy S, Chen S, Scott RC (2017) ALS-resistant smallflower umbrella sedge (Cyperus difformis) in Arkansas rice: physiological and molecular basis of resistance. Weed Sci 63:561–568 Google Scholar

22.

Tranel PJ, Wright TR (2002) Resistance of weeds to ALS-inhibiting herbicides: what have we learned? Weed Sci 50:700–712 Google Scholar

23.

Yu J, McCullough PE, McElroy JS, Jespersen D, Shilling DG (2020) Gene expression and target-site mutations are associated with resistance to ALS inhibitors in annual sedge (Cyperus compressus) biotypes from Georgia. Weed Sci 68:460–466 Google Scholar
© The Author(s), 2022. Published by Cambridge University Press on behalf of the Weed Science Society of America.
David P. Westbury, Patrick E. McCullough, J. Scott McElroy, Claudia A. Rutland, and Jinesh Patel "First Report of ALS Inhibitor–Resistant Green Kyllinga (Kyllinga brevifolia)," Weed Science 70(3), 287-291, (10 March 2022). https://doi.org/10.1017/wsc.2022.12
Received: 7 October 2021; Accepted: 4 February 2022; Published: 10 March 2022
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