Interaction of almond cystatin with pesticides: Structural and functional analysis

Pesticides are chemical substances that eliminate or control a variety of agricultural pests that damage crops and livestock. They not only affect the targeted pests but also affect the nontargeted systems, raising more concerns for their effect on both plant and animal systems. Cystatins (cysteine protease inhibitor) are ubiquitously present in all living cells and show a variety of important physiological functions. The present study shows the effect of different pesticides (pendimethalin, methoxyfenozide, and Cu^II hydroxide) on purified almond cystatin. Almond cystatin showed concentration‐dependent loss in papain inhibitory activity on interaction with the pesticides, showing maximum loss in the presence of Cu(II) hydroxide and minimum in the case of methoxyfenozide. Native polyacrylamide gel electrophoresis showed maximum degradation of purified cystatin in the presence of Cu(II) hydroxide with insignificant effect in the presence of methoxyfenozide. Structural alterations were significant in the case of Cu(II) hydroxide and less in the case of methoxyfenozide as revealed by UV and fluorescence spectral studies. Secondary structural alterations were further conformed by circular dichroism and Fourier transform infrared spectroscopy. The α‐helix content of almond cystatin decreases from 35.64% (native) to 34.83%, 30.79%, and 29.62% for methoxyfenozide‐, pendimethalin‐, and Cu(II) hydroxide–treated cystatin, respectively. A Fourier transform infrared study shows an amide I band shift for almond cystatin from 1649.15 ± 0.5 to 1646.48 ± 0.6, 1640.44 ± 0.6, and 1635.11 ± 0.3 cm⁻¹ for methoxyfenozide, pendimethalin, and Cu(II) hydroxide, respectively. Values obtained for different thermodynamic parameters (ΔH ⁰, ΔG ⁰, N , and ΔS ⁰) by isothermal titration calorimetric experiments reveal maximum binding of almond cystatin with Cu(II) hydroxide followed by pendimethalin and little interaction with methoxyfenozide.     

Potentialities of methoxyfenozide for the integrated management of Helicoverpa armigera (Lepidoptera: Noctuidae) on cotton in Benin,West Africa

Intensive use of chemical insecticides against Helicoverpa armigera has led to the development of resistance to the major chemical families of insecticides. Consequently, management of H. armigera using conventional chemical insecticides is increasingly difficult. Methoxyfenozide is an agonist of the insect moulting hormone 20-hydroxyecdysone that acts faster than chitin synthesis inhibitors. The present work is aimed to assess the effectiveness of methoxyfenozide for use against H. armigera on cotton in Benin, West Africa. Laboratory tests and field experiments have been carried out. For laboratory studies, topical application of methoxyfenozide was done using L2 and L5 instar larva of H. armigera. Tested methoxyfenozide concentrations varied from 24 μl/ml to 144 μl/ml and the control is water only. For field experiments, a complete randomised block design was used with methoxyfenozide (72 μl/ml) and a control (no spraying). Berthoud Ultra Low Volume sprayer was used to spray methoxyfenozide suspension at 60-l per hectare. Two sprays were applied, 7 days apart. Laboratory tests indicated that 24 h after application of methoxyfenozide, about 100% of treated L2 and L5 larva were morbid or dead compared with 0% for the control larva. There are no significant differences between tested concentrations. Morbid larvae died within 2 days. In field experiments, cotton yield harvested on methoxyfenozide treated plants was double of that obtained on untreated plants (9375 kg and 4875 kg per hectare respectively). Thus methoxyfenozide may be used as component of Integrated Pest Control Programme on cotton in Benin, West Africa.     

Effect of ecdysone agonists on vitellogenesis and the expression of EcR and USP in codling moth (Cydia pomonella)

The effects of tebufenozide and methoxyfenozide on vitellogenin (Vg) synthesis/release in the fat body, translocation in hemolymph, uptake by the ovary, and the expression of the ecdysone receptor (EcR) and its heterodimer partner, ultraspiracle protein (USP) in fat body, were investigated in Cydia pomonella. The results indicated that both ecdysone agonists significantly increased the Vg level in the adult hemolymph when the moths were exposed to agonist-treated surfaces. However, these agonists did not affect Vg release from the fat body nor Vg deposition in the first batch oocytes. Western blot analysis revealed that the expression of EcR and USP was significantly increased in tebufenozide- and methoxyfenozide-treated samples compared to the control, suggesting that ecdysone agonists regulated the Vg synthesis via the EcR and USP proteins complex.     

Fecundity and fertility reductions in adult leafrollers exposed to surfaces treated with the ecdysteroid agonists tebufenozide and methoxyfenozide

The effects on the fecundity and fertility of redbanded leafroller, Argyrotaenia velutinana (Walker), and obliquebanded leafroller,Choristoneura rosaceana (Harris), exposed as adults to surfaces treated with the ecdysone agonists tebufenozide (RH-5992) and methoxyfenozide (RH-2485) were examined. The first part of the study consisted of recently emerged moths being exposed to treated surfaces continuously throughout their lives (including mating and oviposition). Continuous exposure to tebufenozide- or methoxyfenozide-treated surfaces significantly reduced the mean number of eggs laid and the percent of eggs that hatched in both species. The second part of the study involved exposure of recently emerged virgin moths (by sex) to treated surfaces for 24 h, after which, the exposed moths were paired with a nontreated partner to mate and oviposit on nontreated surfaces. In this experiment, for A. velutinana, significant reductions in fecundity occurred only when the female was exposed to methoxyfenozide-treated surfaces. Significant reductions in A. velutinana egg fertility occurred with both male and female exposure in the methoxyfenozide treatments and only female exposure in the tebufenozide treatments. For C. rosaceana, significant reductions in fecundity occurred with both male and female exposure in the tebufenozide and methoxyfenozide treatments. Significant reductions in C. rosaceana egg fertility occurred with both male and female exposure in the tebufenozide treatments and only with female exposure in the methoxyfenozide treatments.     

Effects of methoxyfenozide-treated surfaces on the attractiveness and responsiveness of adult leafrollers

Abstract The attractiveness and responsiveness of the adult redbanded leafroller, Argyrotaenia velutinana (Walker), and obliquebanded leafroller, Choristoneura rosaceana (Harris), exposed to surfaces treated with the ecdysteroid agonist methoxyfenozide were investigated in wind tunnel and orientation tube assays. For both species, when males were exposed to water‐treated surfaces for 48 h, and regardless of what treatment surfaces the females had been exposed to, the mean percentage recaptures of such treated males in the wind tunnel assays were always significantly greater than the recaptures of males that had been exposed to methoxyfenozide. However, exposure to surfaces treated with surfactant (Latron B‐1956) also negatively affected the responsiveness (or attractiveness) of both moth species. In the orientation tube assays, males exposed to methoxyfenozide‐treated surfaces always had significantly lower mean levels of individuals exhibiting sexual excitability, and the mean distances traveled upwind, regardless of females’ exposure. In addition, exposure to surfactant‐treated surfaces did not affect mean levels of sexual excitibility and distances traveled upwind. The two bioassays demonstrated that male A. velutinana and C. rosaceana exposed to methoxyfenozide‐treated surfaces were not as responsive to calling females (treated and non‐treated) as were the non‐treated males. Conversely, females exposed to methoxyfenozide‐treated surfaces were just as attractive to non‐treated males as water‐treated females. It appears that a male's ability to respond to a calling female is more negatively affected by the ecdysone agonist than a female's ability to call and attract males.     

Establishment and characterization of an Ostrinia nubilalis cell line, and its response to ecdysone agonists

Summary A cell line derived from embryonic tissues of the European corn borer, Ostrinia nubilalis (UMC-OnE), was established in EX-CELL 401 medium containing 10% fetal bovine serum. The cells grew in suspension, and were mainly spherical in shape. The cell doubling times at the 17th and 79th passages were 56 and 36 h, respectively. DNA amplification fingerprinting showed that the DNA profile of the OnE cell line was different from that of the southwestern corn borer, Diatraea grandiosella (UMC-DgE), and that of the cotton bollworm, Helicoverpa zea (BCIRL-HZ-AM1). The OnE cell line was responsive to treatments of 20-hydroxyecdysone and the ecdysone agonists, methoxyfenozide (RH-2485) and tebufenozide (RH-5992). These compounds caused similar effects on the cells, which included cell clumping and decreased cell proliferation. The clumps were observed on the third day of incubation, and became larger after 7 d of incubation. After 168 h of incubation, methoxyfenozide and tebufenozide were 35 and 11 times more effective, respectively, in inhibiting proliferation of the OnE cells than was 20-hydroxyecdysone.     

Foliar persistence and residual activity of methoxyfenozide against beet armyworm （Lepidoptera： Noctuidae）

A greenhouse study was conducted to investigate the persistence of methoxyfenozide in pepper （Capsicum annuum L.） foliage. An aqueous suspension of methoxyfenozide was sprayed on pepper plants at concentrations of 72 and 144 mg of active ingredient （a.i.）/L. Foliage was collected at different intervals of time （0, 3, 5, 10, 20, 30, 40, and 50 days） after the treatment, and the methoxyfenozide residue was measured by high-performance liquid chromatography. The foliage was also used in bioas- says to determine the residual toxicity on and the consumption rate of the third-instar larvae of the beet armyworm, Spodoptera exigua （Htibner） （Lepidoptera： Noctuidae）. The methoxyfenozide concentrations observed after 50 days had decreased to 19 and 69μg/g per sample, corresponding to a loss of 61% and 28% from the application concentrations of 72 and 144 mg a.i./L, respectively. When fitting a first-order kinetics degradation model, the half-life （DT50） of this compound was 76 days. Both application concentrations of methoxyfenozide caused a high mortality rate （〉97%） when the larvae were fed the pepper foliage collected at all of the time intervals. Lastly, at all of the time points, the consumption rate by the larvae was reduced to between 57% and 92% for both concentrations that were bioassayed. Our results indicate that, under the present greenhouse conditions, the degradation of methoxyfenozide was slower than that reported by other authors and that its residues were highly toxic to S. exigua larvae. The implications of these results for the management programs of this pest are discussed.     

甲氧虫酰肼对不同抗性棉铃虫种群谷胱甘肽S-转移酶活性和基因表达量的影响

【目的】明确与谷胱甘肽S-转移酶（GST）相关联的棉铃虫 Helicoverpa armigera (Hübner)对甲氧虫酰肼的抗性分子机制, 更有效地开展棉铃虫抗药性的快速监测。【方法】用LC₄₀甲氧虫酰肼处理棉铃虫3龄初幼虫, 测定处理前、后抗性种群GST的活性及5种GST基因的表达量变化, 并比较一种Delta基因GSTd1的编码区序列。【结果】经测序、比对, 抗甲氧虫酰肼种群（R-methoxyfenozide）和同源对照种群（S-methoxyfenozide）GSTd1基因编码区序列相同, 表明其编码的酶结构没有发生改变。甲氧虫酰肼处理前, R-methoxyfenozide种群的GST比活力显著高于S-methoxyfenozide种群; 而药剂处理后, 两种群的GST比活力均降低, 但R-methoxyfenozide种群的活性可以快速回升。药剂处理前, R-methoxyfenozide种群的GST基因表达量显著高于S-methoxyfenozide种群。药剂处理对不同抗性种群GST基因表达量的影响差异较大。除了GSTs1, S-methoxyfenozide种群GST基因表达量均降低, 其中GSTd2和GSTe2可以缓慢回升。GSTs1表达量在36 h内没有明显变化, 但在48 h显著升高。R-methoxyfenozide种群的GST基因表达量均先降低, 然后迅速恢复, 除GSTe2基因外, R-methoxyfenozide种群的基因初始表达量和药剂处理后的最终表达量均显著高于S-methoxyfenozide种群。【结论】棉铃虫对甲氧虫酰肼的抗性与GST比活力增强有关, 而GST比活力的增强主要源于多个GST基因的过量表达。     

Lethal and sublethal effects of abamectin, spinosad, methoxyfenozide and acetamiprid on the predaceous plant bug Deraeocoris brevis in the laboratory

Deraeocoris brevis (Uhler) (Hemiptera: Miridae), an important generalist predator in pome fruits in the western United States, was reared in the laboratory on frozen Ephestia kuehniella (Zeller) (Lepidoptera: Pyralidae) eggs and treated in a Potter spray tower to assess acute toxicity and chronic sublethal effects of abamectin, spinosad, methoxyfenozide, and acetamiprid. Acute toxicity was assessed using topical application. Sublethal effects were examined as the combined result of topical, residual and oral exposure. Two different dose rates, the full field rate and 10% rate of the full field rate, were compared to distilled water as the untreated check. Methoxyfenozide and spinosad had no acute toxicity to nymphs and adults at the 10% and full field rate, and no effect on egg hatch and nymph survival just after hatch. Acetamiprid and abamectin at the full field rate did not affect egg hatch, but the residue had moderate to high toxicity to hatched nymphs. Also, topically applied acetamiprid and abamectin had moderate to high acute toxicity to nymphs and adults at the full field rate, but moderate toxicity at the 10% rate. In sublethal bioassays, abamectin-treated adults (10% field rate) laid 80% fewer and less viable eggs compared with the untreated check. Spinosad-treated (full field rate) adults laid fewer and less viable eggs. Also, egg hatch in the subsequent generation was lower. Methoxyfenozide had no sublethal effects on adults at the full rate, but slowed development of 4th instars following treatment of 2nd instar nymphs, and lowered fecundity by 30% in the subsequent generation compared with the untreated check. Acetamiprid (10% rate) applied to nymphs or adults had no effects on development or reproduction. Results from this study suggest that the newer reduced risk insecticides, which have begun to replace organophosphate insecticides in pome fruits in the United States, are not as selective to natural enemies as initially thought. Their impact on D. brevis varied with chemistry and mode of action from primarily acute toxicity (i.e., acetamiprid) to reproductive and other sublethal effects (i.e., methoxyfenozide, spinosad) or a combination of both (i.e., abamectin). In addition to acute toxicity, sublethal effects need to be quantified in order to accurately predict the total impact of a pesticide on a natural enemy in the field.