Despite local Bt resistance, growers still have options

The development of resistance to Bt Cry toxins by the western corn rootworm is a growing concern, highlighted by the recent confirmation of field-evolved resistance to Cry34/35Ab1 in Iowa (https://www.agriculture.com/crops/corn/why-managing-corn-rootworm-just-became-more-complicated). Across the Corn Belt there are western corn rootworm populations with resistance to multiple Bt Cry toxins expressed in Bt corn. In Illinois, Bt resistance can be found in western corn rootworms from both continuous and first-year cornfields; rotation-resistant populations are vulnerable to Bt resistance. Since the first report of western corn rootworm Bt resistance in 2011, resistance to each of the Bt toxins expressed in Bt corn hybrids (i.e. Cry3Bb1, mCry3A, eCry3.1Ab and Cry34/35Ab1) has been documented at multiple Corn Belt locations (Gassmann et al. 2016: https://doi.org/10.1093/jee/tow110, Zukoff et al. 2016: https://doi.org/10.1093/jee/tow073). Repeated use of the same Bt trait(s) in the same continuous (or rotated) fields imposed strong selection for rootworm resistance to those traits. This problem is not limited to rootworms; Tabashnik and Carrière (2017) have recently documented examples of increasing Bt resistance around the globe (https://doi.org/10.1038/nbt.3974).

The introduction of corn hybrids that expressed two different Bt toxins was an important innovation in Bt technology that offered a way to slow the development of resistance and manage rootworms already resistant to a Bt trait. Because these “pyramided” Bt corn hybrids expressed Bt proteins with two different modes of action, a larva feeding on a pyramid’s roots must have resistance to both Bt proteins to survive.  Thus, pyramided hybrids provided a “second line of defense” against western corn rootworms in areas where some Bt resistance may already be present.

Cross-resistance among the structurally similar “Cry3” family of Bt Cry proteins (Cry3Bb1, mCry3A, and eCry3.1Ab) has further complicated rootworm management (Gassmann et al. 2014: https://doi.org/10.1073/pnas.1317179111). With cross-resistance, rootworms with resistance to one Cry3 toxin were also resistant to the other two. This significantly reduces grower options, as despite the availability of many different commercial Bt corn hybrids, there are functionally only two different Bt modes of action with activity against western corn rootworm beetles. Choosing an effective hybrid requires information about which traits work well against the rootworm populations in a particular field or area and information about which Bt Cry toxins are expressed in different Bt corn hybrids. Information about the Bt traits expressed in commercial Bt corn hybrids can be found in the “Handy Bt Trait Table” (https://www.texasinsects.org/bt-corn-trait-table.html).

Though western corn rootworm Bt resistance is increasing across the Corn Belt, field efficacy trials and bioassays reveal that some susceptibility to one or more proteins remains in most populations.  Furthermore, a recent publication from University of Nebraska (Reinders et al. 2018: https://doi.org/10.1371/journal.pone.0208266), showed that the level of resistance to a particular Bt protein(s) could vary from field-to-field even within a portion of a county. In east central Illinois, we have conducted a series of experiments to examine the susceptibility of local western corn rootworm populations to Bt traits.

Measuring local patterns of Bt susceptibility.

Local western corn rootworm populations have been periodically assessed for their susceptibility to the Cry toxins expressed in Bt corn hybrids.  Last spring, a variety of single trait-, pyramided- and non-Bt corn hybrids were planted for a Bt efficacy trial at the UI Agricultural and Biological Engineering (ABE) Farm in Urbana, Illinois.  Laboratory Bt resistance bioassays were also conducted using the offspring (larvae) of rootworm populations collected from the ABE farm during 2017.

Local field efficacy of Bt traits.  Bt corn hybrids expressing three of the four Bt toxins commercially available for corn rootworm management (Cry3Bb1, mCry3A, and Cry34/35Ab1; eCry3.1Ab Duracade®, a Cry3 toxin, was not tested) were evaluated as single trait hybrids and in pyramided hybrids with one other Bt protein (i.e. Cry34/35Ab1 + Cry3Bb1 proteins and Cry34/35Ab1 + mCry3A) (Table 1).

 

Table 1. Hybrid number and corn rootworm Bt trait(s) expressed in single- and pyramided Bt corn hybrids evaluated for node injury in 2018 ABE Farm Bt field efficacy trials.

aStandard commercial seed treatments were present on all hybrids. CRW: corn rootworm.

 

Local rootworm pressure has been low for several years. To assure significant western corn rootworm pressure for the efficacy trial, in 2017, the site was late-planted with corn and pumpkins to attract egg-laying adults. The 2018 trial was planted on May 2nd in a 6 x 6 grid of 8r x 9m plots. On July 18th, five roots were dug from each plot and evaluated for rootworm larval feeding injury using the Iowa State University 0-3 Node-Injury Scale (NIS)(Oleson et al. 2005: https://doi.org/10.1093/jee/98.1.1).

Western corn rootworm larval pressure in the trial was only modest leading to a pattern of variable results. The roots of non-CRW Bt hybrids sustained nearly two full nodes of injury (NIS = 1.987 ± 0.335; mean ± SE) (Table 2) which was greater than injury to all of the Bt corn hybrids, except the Cry3Bb1 single trait hybrid. The injury to roots of the mCry3A-expressing single-trait hybrid was not significantly different from injury to the Cry3Bb1- or the Cry34/35Ab1-expressing single trait hybrids.  The lowest NIS (=best root protection) occurred on the two pyramided hybrids, though this was not significantly different from the NIS for the single trait Cry34/35Ab1-expressing hybrid.

While a significant contribution of Cry34/35Ab1 to better root protection is evident from these data, the level of root protection provided by Cry3 traits (i.e. Cry3Bb1- and mCry3A-expressing single trait hybrids) compared to unprotected roots (i.e. non-CRW Bt) would be unacceptable in a commercial setting. Unsatisfactory Cry3 toxin performance is hardly surprising, given Cry3 cross-resistance, prior local evidence of reduced Cry3 Bt toxin efficacy, and current bioassay data (below). In single trait hybirds, Cry3 traits are unlikely to meet root protection expectations.

 

Table 2. Node Injury Scores (NIS) for Bt corn hybrids from the field efficacy trial. There were n=5 roots evaluated per replicate and n=6 replicates per each of the six corn hybrids; n=180 total roots evaluated.

aAll hybrids also expressed Lepidopteran-specific Bt traits. b Data were Log10 (NIS + 0.5) transformed before ANOVA and comparison of Least Squares Means with Tukey HSD using JMP Pro 13; untransformed means are shown. NIS scores sharing the same letter are not significantly different at alpha <0.05.

 

The importance of the Cry34/35Ab1 Bt toxin can be highlighted by pooling the NIS data according to whether the Cry34/35Ab1 Bt toxin was or was not expressed in a Bt hybrid (regardless of Cry3Bb1 or mCry3A expression) (Table 3).  After a re-analysis, the pooled Cry34/35Ab1 (+) hybrids are found to experience significantly less root injury than the two Cry34/35Ab1 (-) hybrids or the non-Bt control.

 

Table 3. Node Injury Scores (NIS) for the field efficacy trial from Table 2, data were pooled according to Bt-corn hybrid Cry34/35Ab1 protein expression category. Five roots were evaluated per replicate and n=6 replicates per each of the six corn hybrids; n=180 total roots.

aData were Log10 (NIS + 0.5) transformed before ANOVA and comparison of Least Squares Means with Tukey HSD using JMP Pro 13; untransformed means are shown.

 

Western corn rootworm Bt resistance bioassays. Single-plant Bt resistance bioassays compared the survival of larvae from a suspected-Bt resistant population and a Bt-susceptible population from a USDA laboratory colony (Brookings, SD). Larval survival was measured using corn hybrids expressing single Bt toxins (Cry3Bb1, mCry3A, or Cry34/35Ab1) and their respective non-Bt near-isoline hybrids. The suspected-Bt resistant rootworm larvae were the offspring of adults collected from the ABE field during 2017. Because, these larvae were the siblings of those attacking the plants in the field efficacy trial, we expected similar results.

Corn hybrids were obtained from the respective trait licensees and greenhouse-grown singly in 1-liter cups. When plants reached the V5-V6 stage, they were each inoculated with n=10 newly-emerged larvae. Twelve cups were inoculated for each of the six treatments, for a total of n=72 cups per rootworm population. Inoculated cups incubated for 17d at 25°C before transfer to Berlese funnels to recover surviving larvae. The bioassay was replicated twice.

 

 Table 4. Mean proportion larval survival for western corn rootworm on the roots of Bt- and non-Bt isoline hybrids in single-plant Bt-resistance bioassays.

aANOVA was performed on Log10(proportion survival + 0.5) transformed data. Untransformed data are depicted; JMP Pro 13 (2013 SAS Institute) was used to perform analyses. Means sharing the same letter within a trait family do not differ significantly (P<0.05) based on least-squares means (Tukey HSD).

 

Survival of larvae from the suspected-resistant, Urbana population on Cry3Bb1- and mCry3A-expressing corn was significantly higher than the Bt-susceptible population. The Urbana population survived as well on the Cry3 hybrids as they did on the non-Bt isoline hybrids indicating that they were resistant and had little if any susceptibility to either of the Cry3 proteins. In contrast, survival of larvae from the same population on Cry34/35Ab1-expressing corn was low and did not differ from that of Bt-susceptible WCR populations indicating that the Urbana field population was susceptible to the Cry34/35Ab1 toxin.

Results from field efficacy trials and Bt-resistance bioassays suggest that the Urbana, Illinois western corn rootworm population is susceptible to the Cry34/35Ab1 toxin, but resistant, or nearly so, to the Cry3 toxins (i.e. Cry3Bb1 and mCry3A).  Based on these data, growers anticipating economic populations of western corn rootworm should select Bt corn hybrids (pyramided hybrids) that express the Cry34/35Ab1 toxin. Whenever possible, rotating to soybean (a recommended Best Management Practice or BMP) should also be a first choice when an economic population is anticipated. The Urbana population’s minimal susceptibility (only in the field efficacy trial) to Cry3 toxins was too low to prevent significant injury to single trait hybrids and did not add to the efficacy of the Cry34/35Ab1 toxin expressed in pyramided corn hybrids.

Conclusions. Local populations of western corn rootworm in east central Illinois are still mostly susceptible to Cry34/35Ab1, despite the recent confirmation of resistance to this toxin in Iowa. The efficacy of pyramided hybrids in our area is largely dependent on this toxin, as local populations are mostly resistant to the “Cry3” toxins.  Western corn rootworm abundance monitoring is the first step when initiating an integrated pest management approach to corn rootworm. Rotating with a non-Bt alternative (e.g. non-host soybeans, a seed treatment or liquid/granular soil-applied insecticide) rather than using a Bt hybrid in every field every year helps to preserve the efficacy of Bt traits. When a Bt hybrid is used, planting pyramided Bt corn hybrids that express Cry34/35Ab1 is also an appropriate response. Finally, when field-specific monitoring indicates that rootworm populations will be below economically damaging levels in continuous or rotated cornfields, forgoing rootworm control helps to prevent needless selection of Bt-resistant individuals.  Using pest monitoring to guide selection of the appropriate management techniques fosters long-term strategies that are justified by data and responsive to field-specific pest threats.

Given evidence for field-evolved resistance to Cry3 and/or Cry34/35Ab1 traits elsewhere in the Corn Belt, it is important to protect local Bt trait efficacy by adopting IPM-based approaches. Remember that local adoption of BMPs can help mitigate resistance in problem fields. When the next generation of rootworm protection products reach the market, the new RNAi-based mode of action is slated to be pyramided with existing Cry3Bb1 and Cry34/35Ab1 Bt traits in a product called “SmartStax®Pro”. Careful stewardship of current Bt traits is in the best interest of growers. Not only does it preserve the remaining management options, but it will help to prolong and reinforce the efficacy of new products.

Joe Spencer and Nick Seiter

 

Links to helpful scientific literature:

Gassmann, A.J., J.L. Petzold-Maxwell, R.S. Keweshan, and M.W. Dunbar. 2011. Field-evolved resistance to Bt maize by western corn rootworm. PLOS ONE 6:e22629.  https://doi.org/10.1371/journal.pone.0022629

Gassmann, A.J., J.L. Petzold-Maxwell, E.H. Clifton, M.W. Dunbar, A.M. Hoffmann, D.A. Ingber, and R.S. Keweshan. 2014. Field-evolved resistance by western corn rootworm to multiple Bacillus thuringiensis toxins in transgenic maize. PNAS, 111 (14):5141-5146. https://doi.org/10.1073/pnas.1317179111

Gassmann, A.J., R.B. Shrestha, S.R.K. Jakka, M.W. Dunbar, E.H. Clifton, A.R. Paolino, D.A. Ingber, B.W. French, K.E. Masloski, J.W. Dounda, and C.R. St. Clair. 2016. Evidence of Resistance to Cry34/35Ab1 corn by western corn rootworm (Coleoptera: Chrysomelidae): root injury in the field and larval survival in plant-based bioassays. J. Economic Entomology, 109(4): 1872–1880. https://doi.org/10.1093/jee/tow110

Oleson, J.D., Y.L. Park, T.M. Nowatzki, and J.J. Tollefson. 2005. Node-injury scale to evaluate root injury by corn rootworms (Coleoptera: Chrysomelidae). J. Economic Entomology, 98:1–8. https://doi.org/10.1093/jee/98.1.1

Reinders J.D., B.D. Hitt, W.W. Stroup, B.W. French, and L.J. Meinke. 2018. Spatial variation in western corn rootworm (Coleoptera: Chrysomelidae) susceptibility to Cry3 toxins in Nebraska. PLoS ONE 13(11): e0208266. https://doi.org/10.1371/journal.pone.0208266

Tabashnik, B. and Y. Carriere. 2017. Surge in insect resistance to transgenic crops and prospects for sustainability. Nature Biotechnology. 35(10):926-935. https://doi.org/10.1038/nbt.3974

Zukoff, S.N., K.R. Ostlie, B. Potter, L.N. Meihls, A.L. Zukoff, L.French, M.R. Ellersieck, B.W. Wade French, and B.E. Hibbard. 2016. Multiple assays indicate varying levels of cross resistance in Cry3Bb1-selected field populations of the western corn rootworm to mCry3A, eCry3.1Ab, and Cry34/35Ab1. J. Economic Entomology, 109(3):1387-1398. https://doi.org/10.1093/jee/tow073


Managing Corn Rootworm Populations in Illinois: Considerations for 2018

 

Authors: Nick Seiter, Joe Spencer, and Kelly Estes

Rootworm management is a yearly consideration for most corn producers in central and northern Illinois. Western corn rootworm (Fig. 1) is the primary pest species throughout most of the state, but areas in northern IL can experience pest pressure from the northern corn rootworm (Fig. 2) as well. Adult population densities have been low in recent years compared with historical averages, although they did creep up a bit in 2017. The overall reduction in corn rootworm pressure is likely due to a combination of unfavorable weather (or at least unfavorable to rootworm larvae) and widespread adoption of corn hybrids expressing combinations of Bt toxins for rootworm control.

Fig. 1. Western corn rootworm adult. Photo: J. Spencer

Over the last few years, western corn rootworm populations with resistance to Cry3Bb1 and mCry3A (two commonly expressed toxins in Bt corn hybrids) have been documented in Illinois. Research published in 2016 on Iowa1 and Minnesota2 western corn rootworm populations showed that resistance to these toxins also confers resistance to the structurally-similar eCry3.1Ab toxin.  Cross-resistance among these “Cry3” Bt toxins should be expected for Illinois western corn rootworm populations.  Resistance to pest control practices in the western corn rootworm is nothing new; this insect is notorious for developing resistance to control tactics such as insecticides and crop rotation. Part of the concern with these recent developments is that there are relatively few Bt toxins available to combat corn rootworm. Furthermore, all available hybrids with pyramided traits for corn rootworm use either Cry3Bb1 or mCry3A in combination with a second toxin (either Cry34/35Ab1 or eCry3.1Ab). This means that, where resistance is present in the population, there might in fact be at best only one effective toxin at work. (If you have trouble keeping all of these toxins straight, a good resource is the “Handy Bt Trait Table” produced by Dr. Chris DiFonzo at Michigan State University: https://www.texasinsects.org/bt-corn-trait-table.html).

Fig. 2. Northern corn rootworm adult. Photo: J. Spencer.

There are steps producers can take to manage corn rootworm and hopefully slow the further development of resistance. The best way to delay resistance to any control tactic is to reduce exposure of the target insect to that tactic in the environment. Specific ways to accomplish this with Bt toxins include:

  • Apply rootworm control (whether in the form of a Bt hybrid or a soil insecticide) only where it is economically justified based on sampling rootworm adults the previous year. If you monitor using a yellow sticky trap, the economic threshold is 2 rootworm beetles per trap per day in corn following corn. For rotated corn, the economic threshold is 1.5 western corn rootworm beetles per trap per day in soybean3. (These thresholds are based on a recent study in Iowa, which recalculated economic thresholds for corn rootworm based on updated crop values and control costs3).
  • Rotating corn with soybean or another non-host crop remains an effective management strategy in the southern portion of the state. While crop rotation is no longer a reliable method to protect first-year corn from western corn rootworm damage in central and northern Illinois, all larvae that hatch into soybean still die, and every acre planted to soybean is an acre where larvae are not being exposed to Bt toxins or soil insecticides.
  • Where monitoring indicates that control is justified in corn, rotate the control measures used from year to year. This means rotating among Bt hybrids with different trait combinations and non-Bt hybrids treated with a soil insecticide.
  • Follow all refuge requirements for any Bt corn hybrids you plant. In many cases, the “refuge in a bag” or “RIB” approach is now used, but check with your seed distributor on specific requirements for your hybrids.

Finally, an important step is to monitor the performance of your control methods. While lodging is often the cue we look out for to identify rootworm damage, keep in mind that (1) corn can take a lot of damage without lodging depending on soil type and weather conditions and (2) plenty of factors other than rootworm damage can lead plants to lodge. The best approach to evaluating rootworm damage is to dig a representative sample of roots in late July and evaluate them for feeding damage: unpleasant work, but necessary if we want to understand the true extent of the damage.  Consider planting a small area or a portion of a row with a non-Bt/untreated hybrid as a check strip. Having an untreated patch in your field will allow you to compare the efficacy of your management tactic vs. the background level of damage where no rootworm protection was used. Finally, if you experience greater damage than expected in Bt corn hybrids in 2018, please let us know at the email address below; your reports will help us to document the status of resistance in Illinois and provide updated information to producers.

Correspondence:

Nick Seiter: nseiter@illinois.edu Research Assistant Professor, Field Crop Entomologist,University of Illinois Department of Crop Sciences

Joe Spencer: spencer1@illinois.edu Principal Research Scientist and Research Program Leader in Insect Behavior, University of Illinois, Illinois Natural History Survey
1Jakka, S.R.K., et al. Scientific Reports 6: 27860. DOI: 10.1038/srep27860

2Zukoff, S. N. et al. 2016. Journal of Economic Entomology 109: 1387-1398. DOI: 10.1093/jee/tow073

3Dunbar, M. W. and Gassmann, A. J. 2013. Journal of Economic Entomology 106: 168-180. DOI: 10.1603/EC11291