Abstract
The western corn rootworm (WCR), Diabrotica virgifera virgifera LeConte, is an important pest of maize (Zea mays L.). Published WCR diets contain corn root powder, which is not available for purchase, thereby limiting the practical use of diets containing this ingredient. We applied response surface modeling combined with mixture designs to formulate a WCR diet that does not require corn root powder. We developed the new formulation by systematically exploring eight protein ingredients from animal, plant, and yeast sources based on simultaneous evaluation of three life history parameters (weight, molting, and survival). This formulation (WCRMO-2) without corn root powder supported approximately 97% of larval survival and successful molting. Larval weight gain after 10 days of feeding on WCRMO-2 was 4-fold greater than that of larvae feeding on the current best published WCR diet. Additionally, there was no significant difference in these larval performance traits when larvae were reared on WCRMO-2 and the best proprietary WCR diet. A commercial version of WCRMO-2 was tested and found to perform comparably for these traits. These improvements met our goal of a diet comprised of available ingredients that supports performance of WCR larvae equal to or better than publicly available formulations and proprietary formulations.
Subject terms: Assay systems, Entomology
Introduction
The western corn rootworm (WCR), Diabrotica virgifera virgifera LeConte, is an economically important pest of maize (Zea mays L.) in North America and parts of Europe. The impact of corn rootworm has been estimated at approximately $2 billion annually1. Yield reduction by this pest primarily results from larval feeding on maize roots2,3 that causes detrimental effects on nutrient and water uptake4, facilitation of pathogen infestation5,6, and unharvested grain due to lodging2,3,7. A variety of management tactics [e.g. crop rotation, chemical insecticides, transgenic maize expressing insecticidal proteins from Bacillus thuringiensis Berliner (Bt)] have faltered due to adaptation of WCR populations8–15. Insect resistance management (IRM) plans for western corn rootworm have been directed toward monitoring the development of resistance to each of the Bt products16. Diet bioassays can be a key component of IRM plans. An ideal diet17 used in diet bioassays should be publicly available, compatible with insecticide toxins, easy to use, low in contamination, and support larval development similar to larvae feeding on corn roots.
We previously developed an improved diet for WCR larvae, hereafter referred to as “WCRMO-1”18, an optimization of the ingredients in a previously published diet for WCR. Pleau et al.19 developed the first WCR diet, which was modified from a diet for southern corn rootworm (SCR), D. undecimpunctata howardi Barber20–22, by adding corn root powder, removing formalin, optimizing the pH and changing the concentrations of wheat germ and linseed oils. These modifications resulted in a diet that doubled larval weight gain compared to larvae reared on the SCR formulation19. We improved the Pleau et al. diet by optimizing the concentration of several ingredients (i.e., agar, casein, cellulose, corn root powder, linseed oil, and sucrose) and by adding wheat germ oil18. This resulted in a formulation that supported approximately 99% of larvae for survival and molting and further doubled the weight gain after 11 days compared with larvae reared on the Pleau et al. diet. Additionally, this formulation is publicly available, compatible with each of the four marketed Bt toxins23 and, under our laboratory conditions, resulted in fewer than 1% of infested diet wells becoming contaminated18,24.
Mixture designs combined with response surface modeling have been highly efficient for use in diet improvement for WCR18, northern corn rootworm, D. barberi Smith & Lawrence25, and another coleopteran species, Diaprepes abbreviatus (Linnaeus)26,27. Since insect diets are a mixture of several ingredients, a change in the number of ingredients and in the proportion of any ingredient results in a change in the relative composition of all ingredients. Mixture experiments are commonly analyzed based on Scheffé polynomials28 wherein the proportions of mixture components are varied and total amount of the mixture remains constant. Later, Piepel and Cornell29 developed a mixture-amount experiment expressing the parameters of the Scheffé model while varying the total amount of the mixture. The application of mixture experiments in combination with response surface modeling allows concurrently varying multiple ingredients to identify and characterize key components and predict an optimum formulation that maximizes all desired developmental traits17,18,27,30,31.
Previous diet work for WCR highlighted an important role of corn root powder as a key component that had positive effects on WCR development. Exclusion of this ingredient resulted in a slower development of WCR18,19,32. Corn root powder is the only ingredient that is not available for commercial purchase, thus limiting its use. In order to develop an ideal diet for WCR, this study focused on the development of a WCR diet with improved larval development and without corn root powder, making the WCR diet more widely available for researchers. By applying mixture designs combined with response surface modeling, we explored eight different protein ingredients, which are referred to diet ingredients that contain proteins as major components and may contain other nutritional components, derived from animal, plant, and yeast sources to identify key proteins. We then optimized proteins blends based on WCR life history parameters (weight, molting, and survival) while limiting contamination.
Results
Eight-protein screening experiment
The eight-protein mixture experiment produced significant response surface models for all three measures of life history parameters including weight (p < 0.0001, F9,20 = 42.26) with insignificant lack of fit (LOF) (p = 0.5382), molting (p < 0.0001, F11,18 = 197.99) with significant LOF (p = 0.0397), and survival (p < 0.0001, F9,20 = 50.80) with significant LOF (p = 0.0009) by varying 8 different protein sources: corn gluten meal, cottonseed meal, casein, plant protein, whey protein, perfect amino, yeast extract, and egg powder (see Supplementary Table S4). Pure errors of models for molting (sum of square (SS) of pure error = 0.013) and survival (SS of pure error = 0.0003) were very small, and resulted in significant LOFs. All models had R-squared, predicted R-squared and adjusted R-squared values in reasonable agreement, i.e. the differences between the predicted and adjusted R-squared values were <0.2, indicating good predicted models. The relationships between protein sources and larval performance were shown in trace plots that determine the effects of changeable proportions of one component in relation to a reference blend while all the relative proportions of all other components were held constant30,33 (Fig. 1). The direction and magnitude of influence of the individual components on the measured response variables are indicated by the slope of the line.
All response models revealed that the three components responsible for the greatest effects on all overall larval developmental traits (weight, molting, and survival) were three animal protein sources: casein, egg powder, and whey protein (Fig. 1a–c). For plant protein sources, plant protein and cottonseed meal, to some extent, had positive effects on all three criteria of larval performance, whereas corn gluten meal and Perfect Amino® had negative effects on all response measures. Yeast extract had minor positive effects on all larval performance compared to other positive components tested.
Three-protein mixture-amount experiment
The three-protein mixture-amount (casein, egg powder, and whey protein) yielded significant response surface models for all three measures, including larval weight (p < 0.0001, F4,26 = 12.48) with significant LOF (p < 0.0001), molting (p = 0.0006, F5,25 = 6.44) with significant LOF (p = 0.0011), and survival (p < 0.0001, F4,26 = 23.26) with insignificant LOF (p = 0.0584) (see Supplementary Table S5). Models for weight and molting had significant LOFs due to very small values of pure error. Sums of square of pure error for models for weight and molting were 0.0013 and 0.0110, respectively. The R-squared, predicted R-squared and adjusted R-squared values of all models were clustered in within reasonable agreement (difference <0.2). Ternary plots showed the relationships between protein sources, mixture amount and larval performance by estimating the influences of all possible combinations of mixture components on measured variables (Figs 2 and 3). Color and labelled isobars indicated the magnitude of the response variables in a dimension that can be envisioned as perpendicular to the page.
All response models indicated that egg powder was the most important component to maximize all development traits (Fig. 2a–c). High proportions of egg powder resulted in an increase in all measures of larval performance whereas casein at high proportions resulted in a decrease in all response measures, especially in survival. An increase in the proportion of whey protein resulted in an increase in survival, but whey protein at high proportions had negative effects on weight and molting. There was a synergistic blending effect of egg powder and whey protein on larval molting, indicating an optimal two-component axial blend for egg powder: whey protein at a ratio of 3:2 (see Supplementary Fig. S1).
The contour plots showed interactive effects between egg powder and whey protein and egg powder and casein in relation to varying total amount mixture while proportions of other components (casein or whey protein) were held constant (Fig. 3a–c). The results showed that egg powder at high proportions with higher total amount of mixtures could yield better larval weight, molting, and survival. Since egg powder at high proportions had >95% survival, the minor negative effect of increasing the proportion of egg powder at higher total amount of diet on survival was not considered.
Egg powder optimization
Increases in egg powder up to a proportion of 4% (w/w) and 2% (w/w) resulted in positive larval weight gain (Fig. 4a) and molting (Fig. 4b), respectively, whereas additions of egg powder had no significant effect on survival (Fig. 4c). All diets tested had larval survivorship to 10 d that were higher than 95%, and there were no significant differences in survival. Additions of oil components alone and oil components plus corn root powder to the diet did not yield a better formulation for any developmental traits (Fig. 5a–c).
The egg powder optimization produced a superior formulation, referred to hereafter as WCRMO-2 (Table 1). Compared with previous published WCR diets18,19, WCRMO-2 had no corn root powder, additions of egg powder and glucose, and removal of oil components, casein and sucrose. At 10 days post infestation, larval dry weight increased 4 fold with WCRMO-2 as compared to WCRMO-1 and survival and molting rate of WCR larvae reared on WCRMO-2 were approximately 97%. Additionally, there was no significant difference in all measured developmental traits when WCR larvae were reared on WCRMO-2 or the current best proprietary diet (Fig. 5). A commercial version of WCRMO-2, referred to hereafter as Frontier WCRMO-2, was also created through the collaboration with Frontier Scientific Services (Newark, DE, USA). There was no significant difference between WCRMO-2 and Frontier WCRMO-2 in all life history parameters measured (Fig. 6).
Table 1.
Ingredients | Pleau dieta | WCRMO-1b | WCRMO-2 |
---|---|---|---|
Egg powder | — | — | 4.0 g |
Glucose | — | — | 1.0 g |
Wheat germ (raw, ground) | 5.45 g | 5.5 g | 6.0 g |
Cellulose | 1.38 g | 1.5 g | 1.0 g |
Agar | 1.45 g | 1.5 g | 1.5 g |
Casein | 3.23 g | 2.5 g | — |
Corn root powder | 0.63 g | 1.5 g | — |
Sucrose | 3.85 g | 2.5 g | — |
Linseed oil, raw | 40 µl | 25 µl | — |
Wheat germ oil | — | 25 µl | — |
Cholesterol | 6 mg | 6 mg | 6 mg |
Wesson’s salt mix | 0.93 g | 0.93 g | 0.93 g |
Vanderzant Vitamin mix | 0.9 g | 0.9 g | 0.9 g |
Methyl paraben | 0.1 g | 0.1 g | 0.1 g |
Sorbic acid | 64 mg | 64 mg | 64 mg |
Potassium hydroxide (10%) | 3.5 ml | 3.5 ml | 2.75 ml |
Streptomycin (12.8 mg/ml) | 6.4 mg | 6.4 mg | 6.4 mg |
Chlortetracycline (10.0 mg/ml) | 6.4 mg | 6.4 mg | 6.4 mg |
Distilled water | 88 ml | 88 ml | 88 ml |
Green food coloring | 64 µl | 64 µl | 64 µl |
Contamination
Low rates of contamination on diet bioassays have been achieved by careful attention to clean laboratory practices18,23,24. In this report observed contamination of all experiments was less than 1%.
Discussion
Current published WCR diets require corn root powder as a key component because of its positive influence on larval performance18,19. However, corn root powder is the only ingredient that is not currently commercially available and makes the WCR diet unavailable for many users. We applied response surface methodology combined with n-dimensional mixture designs to develop an improved diet for WCR without corn root powder by systematically exploring the effects of different protein sources on WCR based on life history parameters (weight, molting, and survival). By using geometric and mathematical approaches, we evaluated the influence of eight different protein sources to identify key protein sources and characterized and maximized benefits of the key protein, resulting in an improved formulation that will be more accessible to users.
The eight-protein mixture experiment indicated that animal protein sources supported all larval developmental traits (weight, molting, and survival) better than other protein sources such as plant and yeast proteins (Fig. 1). All three animal proteins had the greatest positive effects on overall larval performance. Increasing proportions of three animal proteins (casein, egg powder, and whey protein) resulted in greater improvements in overall response measures compared with other tested proteins. For plant protein sources, additions of plant protein and cottonseed meal improved all measured responses, but increases in the proportions of corn gluten meal and perfect amino had detrimental effects on the three measured responses. Compared with other proteins tested, yeast protein had the smallest effects on all developmental traits. Pleau et al.19 reported a similar pattern in which WCR larvae performed better with proteins (casein and sodium caseinate) derived from animals compared with proteins (lima bean and pinto beans) derived from plants. Research with lepidopteran insects has also documented similar results. The African cotton leafworm, Spodoptera littoralis (Boisduval), grew better on an artificial diet that contained casein as its protein supplement compared to those reared on a diet formulation that casein was substituted with zein, a maize-derived protein34. Damodaran and Parkin35 documented that nutritional quality in animal proteins are better than that of plant proteins. Animal proteins (e.g., egg yolk, casein) usually provide a complete and balanced level of essential amino acids, while the essential amino acids in proteins of plants (e.g., cereals, legumes) are often not fully presented and are usually not presented at the well-balanced proportions. Bioavailability of proteins of animal origin are better than those of plant origin as well35.
The three-protein mixture-amount experiment to characterize the key protein components revealed that egg powder was the best protein source and egg powder alone at higher amount of diet blends could yield the best formulation based on all developmental traits (weight, molt, and survival) compared to possible combinations of three animal proteins, i.e. casein, egg powder, whey protein (Figs 2 and 3). There was a nonlinear synergy blending effect between egg powder and whey protein on molting (see Supplementary Fig. S1) and this interaction was important when egg powder was at low proportions (Fig. 3b). Casein at high proportions had a negative effect on survival and molting. The similar pattern of the negative effects of casein on larval survival and molting was reported in previous work of WCR diets18,19. These findings suggest that egg powder was the single best protein source. Egg powder used in the current study is derived from whole eggs and therefore is itself a complex mixture that mainly contains proteins but also additional nutritional components (e.g., lipids, vitamins, minerals). Further efforts to identify which components in egg powder are driving the effect would require fractionating egg powder into its components followed by a series of multivariate experiments.
The application of mixture experiments with response surface modeling has shown value in insect diet improvement by identifying and maximizing key ingredients in existing coleopteran diets17,18,25–27. By using this approach, we characterized eight different protein ingredients from animal, plant and yeast sources and maximized the key protein component based on all larval response measures. This resulted in a superior formulation (WCRMO-2) with the addition of egg powder, removal of corn root powder, removal of lipid components (linseed oils and wheat germ oils) and a substitution of sucrose with glucose compared with WCRMO-118. At 10 days post infestation, the level of diet improvement included a 4-fold increase in larval weight gain with WCRMO-2 as compared to WCRMO-1 whereas survival and molting rate of WCR larvae on WCRMO-2 at approximately 97%. There was no significant difference on overall larval performance when WCR larvae were reared on WCRMO-2 compared with the current superior proprietary diet (Fig. 5). Additionally, WCRMO-2 without corn root powder had very low levels of contamination. The new formulation significantly improved larval performance and is more widely available for users. This is a significant accomplishment toward the long-term goal to develop the ideal diet that is publicly available, easy to use, and produces insects that are physically similar to WCR larvae fed on corn roots. For the relevant comparison, larval development when reared on WCRMO-2 slightly lags behind those reared on corn roots. The developmental times of 1st instar of WCR on WCRMO-2 at 25 °C averaged 6.1 ± 0.07 d, whereas that of WCR on corn at 24 °C were 4.8 ± 0.09 d for male and 5.3 ± 0.17 d for female36. Further efforts are ongoing to develop an efficiency system for continuous rearing WCR on WCRMO-2 in multiple generations.
Artificial diets for WCR larvae are used in diet assays to detect the susceptibility of WCR populations to Bt toxins and other sources. Currently, each of the major maize seed companies have developed their own proprietary diet formulations and evaluated their own proteins on their own diets. There is considerable variation among proprietary diets and published diets currently in use for rearing rootworm larvae24. Evaluating rootworm toxins on differing diets does not allow direct comparisons between proteins due to differences in artificial diet formulations. In fact, nutrition may have a significant effect on the toxicity of Bt in WCR as has been shown for lepidopteran species37–41. In the cabbage looper, Trichoplusia ni Hübner, previously unexposed insects fed Cry1Ac incorporated diet were less susceptible on diets containing a low protein:carbohydrate (35:65) ratio than diet containing a high protein: carbohydrate ratio (90:10)41. If nutrition similarly affects coleopteran response to toxins, then differences in the artificial diets between individual companies will complicate direct comparisons between assays; and consequently may provide an inaccurate phenotypic picture of the test populations as it relates to toxin susceptibility. A single optimized artificial diet is necessary to facilitate standardized corn rootworm resistance monitoring assays. All researchers, seed companies, and those performing EPA required monitoring should have access to the same diet formulation and preparation method. However, that level of diet standardization will only happen if the diet is commercially produced. We have collaborated with Frontier Scientific Services to establish a commercial version of WCRMO-2 (Frontier WCRMO-2) that is designed to service and be available for all researchers whether they are members of industry or university laboratories. We believe this formulation would facilitate resistance monitoring efforts and new research discoveries.
Materials and Methods
Insects
Eggs of WCR (primary diapausing and non-diapausing strains) were provided by the USDA-ARS laboratories in Brooking, SD and in Columbia, MO. The eggs were surface-sterilized using a procedure described in Pleau et al.19 (see Supplementary Methods).
Diet preparation
The best proprietary WCR diet24 provided by industry was used within a week of receipt. Other diets were poured using a procedure described in Huynh et al.18 (see Supplementary Methods), except for a commercial version of WCRMO-2 (Frontier WCRMO-2, Frontier Scientific Services). A Frontier WCRMO-2 batch includes agar, a dry mix pack, and KOH solution. To make 1 L of Frontier WCRMO-2, agar (15.8 g) was added to 926 ml of cold water the solution was brought to a full boil for 1 minute while stirring regularly or until agar was completely melted. The agar solution was then transferred to a blender placed in a biological safety cabinet. When the agar solution had cooled to 65 °C, 147.4 g of the dry mix pack was added, and the mixture was blended for 1 minute or until mixed thoroughly. Subsequently, 26.3 ml of KOH solution were added and blended for 1 minute or until mix thoroughly. The diet solution was dispensed immediately into a 96-well plate using a repeater pipette (200 µl per well) or proper containers. The diet plate was opened to evaporate excess moisture in the biological cabinet for 10 min, stored in a refrigerator at 4 °C and used for assays within a week.
Insect artificial diet bioassays
The diet bioassays were conducted as described by Huynh et al.18. All materials used in the diet assays were surface-treated via exposure to UV light for 10 min in biological cabinet. Each formulation was randomly assigned to a 12-well row of the 96-well plate and replicated 5 times for a total of 60 larvae per each formulation. Each well was infested with one larva, which hatched within 24 h, using a fine paintbrush. The plate was covered with a sealing film (TSS-RTQ-100, Excel Scientific, Inc., Victorville, CA, USA). For ventilation, a hole was made with a number zero insect pin in the sealing film over each well. The plates were kept in an incubator (03009412, Sheldon Manufacturing Inc., Cornelius, OR, USA) at 25 °C in darkness for 10 days. Larval weight, molting, survival, and evidence of diet contamination were recorded at 10 days. For larval dry weight, all live larvae were pooled per replicate (12 possible) into 95% ethanol, dried in an oven (602752, Blue M Therm Dry Bacteriological Incubator) at 50 °C for 2 days, and weighed using a micro balance (MSU6.6S-000-DM, Sartorius Lab Instruments GmbH & Co. KG, Goettingen, Germany).
Eight-protein screening design for substitutes for corn root powder
Previous work by Pleau et al.19 and Huynh et al.18 illustrated that protein components were key ingredients that had positive effects on overall WCR larval performance. To eliminate corn root powder, we explored contributions of eight different protein sources (i.e., corn gluten meal, cottonseed, casein, egg powder, plant protein, perfect amino, yeast extract, and whey protein) to three life history parameters (weight, molt, and survival) by constructing an eight-component I-optimal mixture design sufficient to satisfy a Scheffé quadratic polynomial response surface model30. I-optimal mixture designs refer to a mathematical algorithm that identifies diet blends that predict precise responses by minimizing the average variance of prediction across the design space42,43. Additional points to estimate lack of fit, which measures how well the model is fitted by the data, and replicated points to obtain sufficient degree of freedom for estimating pure error and to attain a uniform leverage for design spaces44 were also generated. This design was generated with Design-Expert® (Stat-Ease, Inc., Minneapolis, MN, USA) that had 30 design points with 7 model, 17 lack of fit and 5 pure error degrees of freedom (see Supplementary Table S1). Other ingredients were kept constant (see Supplementary Table S2).
Three-protein mixture-amount design for characterizing key protein sources
Based on the results of the first experiment, three proteins that had the greatest effects on WCR larval performance (weight, molt, and survival) were used to construct a D-optimal mixture-amount design sufficient for modeling a Scheffé quadratic-quadratic polynomial response surface model30. D-optimal mixture designs refer to the mathematical algorithm that chooses diet blends that focus on building precise model estimation43,45 by maximizing the determinant of the information matrix, and are appropriate for experimental designs that combine mixture and process variables46. A mixture-amount experiment is a type of mixture experiment that varies both mixture component proportions and the total amount of the mixture30. In this experiment, a three-component mixture design was generated with Design-Expert® (Stat-Ease, Inc.) to characterize the effects of varying three animal proteins (casein, egg powder, and whey protein) from 0 to 1. The amounts of these proteins were varied in blends from 1 gram to 6 grams. This design consisted of 32 design points with 17 model, 6 lack of fit and 8 pure error degrees of freedom (see Supplementary Table S3). Additional design points and replicated points were included in order to satisfy the model terms, estimate lack of fit, attain sufficient degrees of freedom for estimating pure error, and to attain a uniform leverage for design spaces44. Other ingredients were kept constant (see Supplementary Table S2).
Egg powder experiment to identify optimum formulation
The mixture-amount experiment revealed that egg powder alone had the largest effect on larval performance. An experiment to find the optimum amount of egg powder was conducted by varying the concentration of egg powder (i.e., 0%, 1%, 2%, 3%, 4%, 6%, and 10% w/w). Additionally, formulations containing 3% egg powder with additions of lipid components (linseed oils and wheat germ oils) and lipid components plus corn root powder were tested. The amount of lipid components and corn root powder added were the same as in WCRMO-1 diet18. The proportions of water were changed to incorporate changes in egg powder proportions and additions of lipid components and corn root powder. Other ingredients were kept constant (see Supplementary Table S2). Two WCR diets including WCRMO-118 and the current best proprietary diet24 were also included as positive controls.
Statistical analyses
The percentage of larvae surviving and molting was determined by dividing the number of larvae surviving and molting by the number of larvae initially infested and multiplying by 100. Weight per larva was determined by dividing the dry weight by the number of larvae that survived.
In the eight-protein mixture and three-protein mixture-amount experiments, the best fit model for each measured response (weight, molting, and survival) was selected from all possible models from linear to quartic polynomials generated with Design Expert® (Stat-Ease, Inc.). Model selection was based on several criteria including low model P-value, lack of fit P-value, low standard deviation, high R-values (R-squared, adjusted R-squared, and predicted R-squared)26, close agreement between adjusted R-squared and predicted R-squared, and a low PRESS value47,48. Once more than one satisfactory model was generated, adequacy tests were performed to further evaluate the selected model as described by Anderson and Whitcomb49,50.
In the egg powder experiment, all response measures (weight, molting, and survival) were analyzed as a randomized complete block design using PROC MIXED in SAS51.
Supplementary information
Acknowledgements
The authors would like to thank Monsanto Company (now Bayer Crop Science) for providing financial support through the Corn Rootworm Knowledge Grant program. The authors would also like to thank a major seed company for providing their proprietary diet as a positive control. The authors thank Julie Barry, James Smith and Emily Harrington for technical assistance.
Author contributions
M.P.H., B.E.H. and T.A.C. contributed to writing the first draft of the manuscript. M.P.H., S.L.L., R.P.N. and T.A.C. designed the experiments and performed the analyses. M.P.H. performed the experiments. B.E.H., M.V., K.S.S. and T.A.C. provided materials required for the experiments. All authors edited and approved the final version of the manuscript.
Data availability
All pertinent data are found in the figures and tables. Requests for data and additional information should be submitted to the corresponding author.
Competing interests
Michael Vella, works for Frontier Scientific Services, Newark, Delaware, which intends to market this diet. All other authors declare no competing interests.
Footnotes
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary information
is available for this paper at 10.1038/s41598-019-52484-z.
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