D376E, A205V and A122S substitutions recently found in A. palmeri confer cross-resistance to ALS-inhibiting herbicides

Abstract

Background

Amaranthus palmeri S. Watson is a serious problem in soybean crops from Argentina. This weed has evolved high level of resistance to (ALS)-inhibiting herbicides mainly due to a target-site mechanism by an altered ALS enzyme. In an A. palmeri population from Totoras with cross-resistance to (ALS)-inhibiting herbicides, six allelic versions of the ALS enzyme were identified.

Objective

The aim of this study was to evaluate plants from that resistant population carrying the ALS substitutions A122S, D376E or A205V, which had not been characterized before for this species.

Methods

Subpopulations with each substitution were produced by a vegetative cloning procedure or by cross-pollination and dose-response assays and herbicide single-dose tests were performed to evaluate in vivo resistance levels to (ALS)-inhibiting herbicides.

Results

Dose-response experiments showed that all the resistant subpopulations survived at the highest doses tested (32 X) for imidazolinones, triazolopyrimidines and sulfonylureas, while the susceptible population was completely controlled at considerably lower doses. Furthermore, an analysis of the novel A122S substitution showed that it provides cross-resistance to five classes of (ALS)-inhibiting herbicides, excluding the entire ALS herbicide group as an effective control tool in weed populations carrying this substitution.

Conclusions

The results indicated that D376E, A205V and A122S substitutions found for the first time in A. palmeri confer cross-resistance to the most used chemical families from herbicide group 2. Interestingly, it was confirmed that the A205V substitution conferred resistance to herbicides in the triazolopyrimidines family. Data generated should be considered in management strategies for delaying the spread of resistance.

ALS isoforms; herbicide resistant weeds; Amaranthus palmeri; propagative cloning

1.Introduction

Palmer amaranth (Amaranthus palmeri S. Watson) is an extremely competitive weed given its huge stress tolerance, genetic variability, high growth rate, and reproduction capacity (Ward et al., 2013). It is a dioecious species, therefore its reproductive biology favors the dispersion and recombination of alleles, speeding up herbicide resistance evolution along withother traits. For instance, the transfer of glyphosate resistance from resistant males to susceptible female plants by pollen has been demonstrated up to a distance of 300 m (Culpepper et al., 2006). In addition, A. palmeri can hybridize with other species of the genus (Franssen et al., 2001; Gaines et al., 2012; Trucco et al., 2007). This property also increases the probability of finding populations with multiple herbicide resistance.

In most cases, resistance to (ALS)-inhibiting herbicides in Amaranthus spp. is caused by changes in the sequence of the ALS gene (Ashigh et al., 2009; Larran et al., 2018; McNaughton et al., 2005; Molin et al., 2016; Nakka et al., 2017; Singh et al., 2019; Trucco et al., 2006). However, although many of these substitutions reduce ALS enzyme sensitivity in vitro (Yu, Powles, 2014), not all of them provide robust protection against herbicide damage. For instance, the level of in vitro resistance to thifensulfuron for ALS with S653N substitution from Amaranthus tuberculatus was 4-fold higher than the wild type enzyme, but this substitution was not enough to confer resistance to ALS inhibitors herbicides in vivo (Patzoldt, Tranel, 2007).

Weed populations are infrequently composed of only resistant or only susceptible individuals to a specific herbicide (Cousens, Mortimer, 1995). In cross-pollinated weeds, and even in self-pollinated species, a great diversity of ALS mutations is often found. Thus, to confirm the level of resistance for a specific ALS mutation, plants carrying exclusively a specific substitution must be selected or generated, and then tested.

The generation of purified subpopulations (from homozygous individuals) is one of the most widespread methodologies to study herbicide resistance in weeds (Deng et al., 2017; Yu et al., 2012). However, this practice is hard for cross-pollinated weeds species with different ALS substitutions, such A. palmeri. For that reason, Teaster and Hoagland (2014) developed a macro-vegetative propagation method that facilitates long-term studies in selected cloned lines of A. palmeri.

Over the past few years, we found a target-site resistance due to specific ALS mutations in an A. palmeri population from Totoras (Santa Fe, Argentina) (Larran et al., 2017). In this work, we selected, cloned and evaluated plants from that resistant population of A. palmeri carrying the ALS substitutions A122S (Larran et al., 2017), or D376E and A205V, which had not been characterized before for this species. Even more, this is the first characterization of the novel A122S substitution in plants. The resistance profile to different (ALS)-inhibiting herbicides was elucidated. Data generated can be useful to make the right weed management recommendations for delaying the spread of resistance.

2.Materials and Methods

2.1 Plant material

The original A. palmeri population (R) was collected from a field in Totoras (32° 34’ 59.88”S, 61° 10’ 59.88”W) in which DERBY® (a.i. imazethapyr 10% w/v; Gleba, La Plata, Argentina) had been continuously used for at least ten years. The susceptible population (S) was collected in a field from Tucumán (27° 17’ 45.36”S, 65° 0’ 3.37”W), where (ALS)-inhibiting herbicides had never been used.

2.2 Plant selection with the D376E, A205V or A122S ALS substitutions

Plants from the resistant population were selected by application of DERBY at dose 1X (100 g ai ha^-1) as described in Larran et al. (2017). Surviving plants were sampled for ALS gene sequencing and/or marker analysis to define the resistance mutation of each individual.

The complete ALS gene of each plant was amplified and cloned in pGEM®-T easy vector (Life Technologies, Grand Island, NY, USA) as described in Larran et al. (2017). Then, these recombinant DNA molecules were sequenced (Macrogen Inc., Seoul, Korea).

Derived cleaved amplified polymorphic sequence (dCAPS) markers were developed for the identification of A122S substitution by screening 50 surviving plants. The primers used were ALSdcaps122f (5´-CTAAACCTCC TTCCGCTACTATAACTCAATCACC-3´) and ALSdcaps122r (5´-CGAGTAAGAGCTTGATGGATTTCCATGCATG-3´). The amplification reactions were performed in a final volume of 12 μl, containing: 0.2 mM dNTPs mix, 0.5 μM primers, 1X amplification buffer and 0.48 U of the GoTaq® DNA Polymerase enzyme (Promega). The PCR program was 95°C for 2 min; 35 cycles of 95°C for 30 s, 58°C for 30 s, 72°C for 30 s and a final step at 72°C for 5 min. Restriction digestions were carried out with SphI enzyme (Biolabs New England) which recognizes and cuts the sequence GCATG^C present in WT sequence. The WT sequence produces a 171-bp digested band, whereas sequence with A122S substitution produces a 202-bp undigested band. DNA bands were visualized on 6% w/v polyacrylamide gels stained with SYBR safe (Invitrogen®).

2.3 Vegetative cloning of plants carrying the D376E, A205V or A122S ALS substitutions

A vegetative cloning procedure was used to achieve homogeneous material (three subpopulations). Each selected plant was multiplied using the protocol described by Teaster and Hoagland (2014), which, briefly, is based on isolating cuttings, coating the cut end with rooting hormone powder, planting them in moistened vermiculite/peat/loam mixture and incubating them under continuous light (150 μmol m^-2s^-1) for 7 days. Clone cultivation was carried out under normal growth conditions (25ºC, photoperiod 16:8 hours day/night, light intensity of 400 μmol m^-2s^-1).

2.4 Chemical compounds

Five herbicides were used in different assays: DERBY® (a.i. imazethapyr 10% w/v; Gleba, imidazolinones), VRILEC® (a.i. chlorimuron-ethyl 25% w/w; Agrofina, sulfonylureas), SPIDER® (a.i. diclosulam 84% w/w; Dow Agro-Sciences, triazolopyrimidines), EVEREST 70WDG® (a.i. flucarbazone sodium 70% w/w, Arysta LifeScience, sulfonylaminocarbonyltriazolinone) and NOMINEE GOLD® (bispyribac sodium 40% w/v, SummitAgro, pyrimidinylthiobenzoates).

2.5 Dose-response assays

At least 120 vegetative clones from each subpopulation R1 (D376E), R2 (A205V) and R3 (A122S) and plants from population S were grown in 500 cm³ pots as described in Larran et al. (2017). Commercial herbicide formulations were applied when plants reached 8-10 cm height at the following doses: imazethapyr (50, 100, 200, 400, 800, 1,600 and 3,200 g ai ha^-1), chlorimuron-ethyl (25, 50, 100, 200, 400, 800 and 1,600 g ai ha^-1) and diclosulam (15, 30, 60, 120, 240, 480 and 960 g ai ha^-1). The dose-response curves were analyzed as described in Larran et al. (2017). The experiment was conducted using six replicates per dose.

2.6 Herbicide single-dose test on the R3.2 population

A population of A. palmeri (here in after referred as R3.2) carrying the A122S substitution in homozygosis was generated by crossing two homozygous plants (a female and a male) for such substitution. Seeds were harvested and stored until use.

To remove physiological dormancy, seeds from both R3.2 and S populations were imbibed for 7 days on agar solution (0.1% w/v) at 4°C. After that, plants were grown and separately sprayed at recommended field doses (1X) of the next herbicides: imazethapyr (100 g ai ha^-1), chlorimuron-ethyl (50 g ai ha^-1), diclosulam (30 g ai ha^-1), flucarbazone sodium (150 g ai ha^-1) and bispyribac sodium (40 ml ha^-1). Ten replicated pots from each R3.2 and S populations, for each herbicide were used. Twenty one days after treatment (DAT), the number of surviving plants and their fresh biomass were recorded. Data were analyzed by t-Student tests using SigmaPlot software (version 11.0; Systat Software, Inc).

3.Results and Discussion

3.1 Herbicide resistance in R1, R2 and R3 subpopulations

In vivo resistance levels to (ALS)-inhibiting herbicides were evaluated in vegetative clones carrying the D376E, A205V or A122S ALS substitutions (R1, R2 and R3 subpopulations, respectively). These subpopulations were produced by a vegetative cloning procedure to develop homogeneous material (Figure 1). Plants selected for cloning were screened from a resistant population of A. palmeri (Larran et al., 2017) by ALS sequencing (D376E, A205V) or by dCAPS (A122S) (Figure 2), according to each genotype frequency.

Figure 1
Vegetative cloning procedure of plants of A. palmeri carrying the D376E, A205V or A122S ALS substitutions

Figure 2
Scheme of ALS sequences of A. palmeri from R1 (a) and R2 (b) subpopulations and dCAPS analysis for screening the A122S substitution to produce R3 subpopulation (c)

Dose-response experiments showed that all the R subpopulations survived at the highest doses tested (32X) for each herbicide, while the S population was completely controlled at considerably lower doses (Figure 3 a-c). However, S population seems to be slightly less sensitive to chlorimuron-ethyl, since the LD₅₀ (73 g ai ha^-1) is higher than the recommended field dose (50 g ai ha^-1). Therefore, this population might carry a non–target site resistance to ALS inhibitors, since it has wild-type ALS (data not shown) and is not fully sensitive to chlorimuron-ethyl (GR₅₀ is 86 g ai ha^-1), if other susceptible populations of A. palmeri are considered (Burgos et al., 2001; Nakka et al., 2017).

Figure 3
Dose-response curves with ALS-inhibiting herbicides in vegetative clones of A. palmeri (R1, R2 and R3 subpopulations)

Although the R subpopulations survived at all herbicides doses, the growth rate was decreased, affecting the biomass after each treatment (Figure 3 d-f). Resistant Factors (Rf) estimated from GR₅₀ ranged from 10-21 to 19-83 for imazethapyr and diclosulam, respectively (Table 1). Regarding chlorimuron-ethyl, only R2 subpopulation showed a significant but low Rf (1.6). This may be caused by the S population not being completely susceptible to chlorimuron-ethyl, leading to an under-estimation of genuine resistance levels to this chemical family.

Table 1
Dose-response curve parameters of A. palmeri

Herbicide (family)	Vegetal material	Parameters
		LD50	Rf	GR50	Rf
Imazethapyr (IMI)	R1	>3200	>290	58±10*	15.3
	R2	>3200	>290	83±3*	21.8
	R3	>3200	>290	39±12*	10.3
	S	11±3	-	3.8±0.6	-
Diclosulam (TP)	R1	>960	>80	607±142*	83.1
	R2	>960	>80	564±114*	77.3
	R3	>960	>80	137±17*	18.8
	S	12±2	-	7.3±0.8	-
Chlorimuron-ethyl (SU)	R1	>1600	>22	89±19	1
	R2	>1600	>22	140±14*	1.6
	R3	>1600	>22	71±36	0.8
	S	73±17	-	86±11	-

• Resistance factors (Rfs) were calculated using LD₅₀ or GR₅₀ of R subpopulations and S population. * indicate statistically significant differences between R subpopulations and S population (t-Student, p < 0.05).

In summary, these results indicate that these substitutions found for the first time in A. palmeri confer cross-resistance to the most used chemical families from herbicide group 2 [imidazolinones (IMI), triazolopyrimidines (TP) and sulfonylureas (SU)].

The cross-resistance conferred by the D376E substitution is consistent to previous reports from other weed species (Ashigh et al., 2009; Whaley et al., 2007; Yu et al., 2012). Concerning the A205V substitution, this had been proved to provide in vivo resistance to IMI and SU families in A palmeri, as well as in other weeds (Ashigh, Tardif, 2007; Matzrafi et al., 2015; McNaughton et al., 2005). In this work, we show that A205V also confers resistance to TP, a chemical family not evaluated before for this mutation.

Finally, the novel A122S substitution showed cross-resistance to the three chemical families evaluated, similarly to other mutations at the same position, such as A122Y and A122N, reported in Raphanus raphanistrum and Echinochloa crus-galli, respectively (Han et al., 2012; Panozzo et al., 2017).

3.2 Deeping on the in vivo characterization of the novel A122S ALS substitution

The macro-vegetative propagation technique allows obtaining numerous clones that can be used as replicates in resistance tests. It has been used to study resistance to multiple herbicides in different Amaranthus species, as well as to characterize the response of A. palmeri to abiotic stress (Korres et al., 2017; Ma et al., 2013; Shergill et al., 2018; Teaster, Hoagland, 2014).

Herbicide single-dose tests were performed using plants from seeds of the R3.2 population obtained to discard any artifact of the technique on the resistance phenotype observed in the clones. Also, two additional herbicides from other families (flucarbazone sodium and bispyribac sodium) were included to assess them as possible control tools for this population.

Treatments with imazethapyr, diclosulam and flucarbazone sodium at 1X doses failed to control the R3.2 population while plant survival in S population decreased (100% vs 50-60%) (Table 2). On the other hand, chlorimuron-ethyl and bispyribac sodium applications did not control individuals from the R3.2 population, suggesting resistance; however, these doses did not control the S population. Once more, the lower susceptibility to chlorimuron-ethyl in the S population could explain part of these results. Curiously, if considering treated vs untreated plants from the R3.2 population, only chlorimuron-ethyl showed significant effects on biomass (Table 2). Regarding bispyribac sodium, it is possible that the appropriate 1X dose for A. palmeri should be higher than the 1X dose indicated for other weed species, given that experiments with a 4X dose allowed a differential survival rate between R3.2 (100%) and S population (60%) (data not shown).

Table 2
Plant survival and fresh biomass 21 DAT of A. palmeri S and R3.2 populations

Treatment	Plant survival (% of untreated)		Fresh biomass (g)
	S	R3.2	S	R3.2
Untreated			1.0±0.2	1.2±0.3
Imazethapyr	50±16	100*	0.22±0.08*	0.7±0.1
Chlorimuron-ethyl	70±15	75±18	0.5±0.2	0.5±0.1*
Diclosulam	60±16	100*	0.4±0.1*	0.87±0.08
Flucarbazone sodium	60±16	100*	0.3±0.1*	0.6±0.1
Bispyribac sodium	90±10	100	0.52±0.09*	0.65±0.04

• * indicate statistically significant differences as compared to S population (plant survival) and to untreated samples (fresh biomass) (t-Student, p < 0.05).

Thus, we confirmed that macro-vegetative propagation is a reliable tool to evaluate herbicide resistance in A. palmeri, since the results from in vivo tests with plants obtained from seeds are consistent with those observed using clones. In addition, we proved that the novel substitution A122S endows cross-resistance to five classes of (ALS)-inhibiting herbicides, excluding this herbicide group as an effective control tool in weed populations carrying this substitution.

4.Conclusions

In vivo resistance to (ALS)-inhibiting herbicides was confirmed in A. palmeri plants carrying the ALS substitutions D376E, A205V or A122S, which had not been characterized before for this species. These three amino acid substitutions confer cross-resistance to SU, IMI and TP, the most used chemical families from herbicide group 2. Additionally, a deeper analysis of the A122S substitution supported two main conclusions: i) this novel substitution endows cross-resistance to five classes of (ALS)-inhibiting herbicides; and ii) the macro-vegetative propagation is a reliable tool to evaluate herbicide resistance in A. palmeri. Data generated should be considered to support weed management recommendations.

Acknowledgements

We appreciate Daniel Tuesca´s and Nicolás Montico´s collaborations during the dose-response assays.

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• Funding: This work was supported by grants D-TEC0001/13 from ANPCyT/MINCyT and Resolution 119/2015-Project 2010-149-14 from SECTEI- Santa Fe Province. VEP, AKM, and ASL are fellows of IICAR-CONICET, VEP and HRP are Professors of the Universidad Nacional de Rosario (UNR) and HRP is researcher of IICAR-CONICET.

Edited by

Approved by:

Editor in Chief: Anderson Luis Nunes

Associate Editor: Todd Gaines

Publication Dates

• Publication in this collection
  14 Jan 2022
• Date of issue
  2022

History

• Received
  15 Aug 2021
• Accepted
  14 Nov 2021