Nano-insecticides against the black cutworm Agrotis ipsilon (Lepidoptera: Noctuidae): Toxicity, development, enzyme activity, and DNA mutagenicity

Frequent applications of synthetic insecticides might cause environmental pollution due to the high residue. In addition, increasing insecticide resistance in many insect pests requires novel pest control methods. Nanotechnology could be a promising field of modern agriculture, and is receiving considerable attention in the development of novel nano-agrochemicals, such as nanoinsectticides and nanofertilizers. This study assessed the effects of the lethal and sublethal concentrations of chlorantraniliprole, thiocyclam, and their nano-forms on the development, reproductive activity, oxidative stress enzyme activity, and DNA changes in the black cutworm, Agrotis ipsilon, at the molecular level. The results revealed that A. ipsilon larvae were more susceptible to the nano-forms than the regular forms of both nano chlorine and sulfur within the chlorantraniliprole and thiocyclam insecticides, respectively, with higher toxicities than the regular forms (ca. 3.86, and ca.2.06-fold, respectively). Significant differences in biological parameters, including developmental time and reproductive activity (fecundity and hatchability percent) were also observed. Correspondingly, increases in oxidative stress enzyme activities were observed, as were mutagenic effects on the genomic DNA of A. ipsilon after application of the LC50 of the nano-forms of both insecticides compared to the control. These promising results could represent a crucial step toward developing efficient nanoinsecticides for sustainable control of A. ipsilon.


Introduction
The black cutworm, Agrotis ipsilon (Hufnagel) (Lepidoptera: Noctuidae) is a major insect pest that can destroy many important crops worldwide [1]. Specifically, the insect larvae damage a1111111111 a1111111111 a1111111111 a1111111111 a1111111111 are safe for field administration without significant side effects on human health. Thus, this study's main goal was to evaluate the potential effects of the nano-forms of two new insecticides, chlorantraniliprole and thiocyclam, on A. ipsilon. We also investigated the effects of the lethal and sublethal concentrations of both insecticides and their nano-forms on the development, reproductive activity, and oxidative stress enzyme activities, including; SOD, CAT, lipid peroxidase, and GR of A. ipsilon. This study examined both insecticides for nanoparticleinduced changes in A. ipsilon at the DNA molecular level.

Insect rearing
Agrotis ipsilon was reared for 12 generations in the absence of insecticides in the laboratory in a rearing room at 26 ± 1˚C, 65 ± 5% relative humidity and a photoperiod of 16 L:8 D. The newly hatched larvae were kept in a clean glass jar (1 L) and provided a castor oil leaves daily until the third instar larvae emerged. Then they were transferred to larger, and clean glass jars (2 L) to prevent larval cannibalism. The bottom of each jar was covered with a thick layer of fine sawdust and the usual rearing techniques were performed along with the developing instars larvae until pupation occurred. After pupation, the developed pupae had been transferred to clean jar for the adult emergence. The adult moths (males and females in ratio 7:5) were transferred to a glass jar (5 L) which was supplied with hanged piece of cotton wool soaked in 10% sugar solution as dietary supplement [11].

Insecticides and chemicals
Chlorantraniliprole (Coragen 1 20% SC, suspension concentrate, DuPont) and thiocyclam (Evisect-S 1 75% SC) were tested. All chemicals used in the preparation of the nano-form of the insecticides were purchased from Sigma Chemical Co. (St. Louis, USA) without further purification. The oxidative stress enzymes kits were purchased from Biodiagnostic Company, Egypt.

Nanoinsecticides preparation and size measurements
Nano-chlorine (chlorantraniliprole) and nano-sulfur (thiocyclam) were prepared by De Oliveira et al. [28], Cota-Arriola et al. [29], and Xu et al. [30], with some modifications. Hydrochloric acid (HCl) and orthorhombic bravais were used as a chlorine source, while sodium thiosulphate and sulfuric acid were used as a sulfur source. The nano-chlorine was made from a sedimentary solution of HCl and MnO2 v:v, where hydrochloric acid and manganese oxide were added slowly in a molar ratio (3:2) in the presence of the stabilizing agent PVA using forceful moving for 5 hours continuously. The obtained precipitation was filtered and washed thoroughly with deionized water, then 16 ml of NaCl 0.2 M aquwous solution was added to the suspension solution using forceful moving at a steady rate for 40 min. The reaction fusion was stirred for an additional 3 hours continuously at ambient temperature. The precipitate was mixed with orthorhombic brava by w:w (2:1) in the presence of HCl 90%, then centrifuged at 1500 rpm for 30 min. Then, the solution was cooled in an ice bath, subsequently exposed to 1.5 psi pressure continuously for 6 hours, and the final nano-suspension was ready for examination under transmission electron microscope.
Nano-sulfur was prepared from a sedimentary solution of sodium thiosulphate and sulfuric acid (1:1). Sodium polysulfide and hydrochloric acid solutions were incrementally mixed in a molar ratio of 3:2 under forceful moving for 8 hours discontinuously. The obtained precipitation was filtered and washed methodically with deionized water in a mixed water/toluene system, then washed with ionized water for 3 hours continuously. The precipitation was mixed with oxalic acid 1 M and trimethylammoniumbromide compound solution in molar ratio 1:3 under slow stirring at 33˚C for 6 hours discontinuously. Afterwards, drop benzene sulphonate in molar ratio 2:3 was added, and the obtained solution was kept at 1.5 psi pressure for 3 days discontinuously (7 hours per day). Finally, the solution was dried in an oven at 90˚C for 3 days continuously. The final nano-suspension was prepared in deionized water and left on a shaker for 2 days continuously at 20˚C. The final nano-suspension was ready for examination under transmission electron microscope.

Bioassays
The toxicity of chlorantraniliprole, thiocyclam, and their nano-forms on the second instar larvae were assessed using the leaf dipping technique [31], with some modifications. Briefly, six different concentrations were prepared for each insecticide, while water was used for the control. Castor oil leaves were dipped in each concentration for 20 s then left to air-dry. After drying, the leaves were transferred into a glass jar (0.25 L). Ten larvae were added to each jar with five replications and left to feed for 24 h. Afterwards, all larvae were offered untreated leaves, and the mortality% was recorded four days (96 hours) post-treatment [32] to calculate the lethal and sublethal concentrations for each insecticide form. The bioassay was repeated twice.

Effects on Agrotis ipsilon development
Lethal concentrations that kill 15 and 50% of the larvae exposed to each form of chlorantraniliprole and thiocyclam were applied on the second instar larvae using the method described above. Surviving insects were used to study the effect of each insecticide on larval and pupal development time, pupation%, and adult emergence. Seven days after exposure, the surviving larvae were transferred individually to a clean cup to record the development time of the larval and pupal stages and the pupation%. After pupation, each pupa was sexed, weighed, and kept individually in the same cup to record the emergence%.

Studies on fecundity and fertility
Groups of 5 females and 7 males in 3 replicates [33] were used to calculate the number of eggs and hatching% after the second instar larvae were treated with the LC 15 and LC 50 values of each insecticide and their nano-forms. Deposited eggs were collected and counted on days 2-6 in the mating jars. The eggs were transferred to a clean jar and kept for 5 days to record the hatching%.
Oxidative stress enzyme assays Sample preparation. Seven days after LC 15 and LC 50 equivalent treatment of the second instar larvae, 100 mg fresh body weight of the surviving larvae were transferred to clean and sterile Eppendorf tubes (1.5 ml). The samples were stored immediately at −20˚C until later analysis. Each treatment and control was replicated five times. The treated larvae were homogenized in a potassium phosphate buffer (50 mM, pH 7.0) at 30 μl buffer per 1 mg of body weight. The homogenate was centrifuged for 15 min at 7000 g at 4˚C, and the supernatants were used for further analysis.
Enzymes measurement. SOD activity was determined according to Misra and Fridovich [34] at the absorbance of 560 nm. The CAT enzyme activity was estimated by measuring the rate of H 2 O 2 consumption [35] via absorbance at 510 nm. The level of lipid peroxidase was assayed by monitoring the formation of malondialdehyde (MDA) at 534 nm [36]. GR activity was estimated as the reduced glutathione (GSSG) in the presence of NADPH [37], which oxidizes to NADPH + at 340 nm. The total protein concentration of all samples was measured spectrophotometrically based on the Biuret Method using Protein Biuret Kit (Biodiagnostic, Egypt).

Molecular analysis
DNA extraction. DNA was isolated from both treated and untreated second instar larvae using a G-spin™ total DNA extraction kit (INtRON Biotechnology) following manufacturer's instructions. The DNA was quantified with a Qubit 4 Fluorometer (Thermo Fisher Scientific Inc.). The DNA concentrations were measured and subsequently adjusted in all samples to 10 ng/μL for subsequent molecular analyses.
ISSR polymorphism analysis. For ISSR PCR amplification [38,39], a set of 15 ISSR primers were applied against the 9 treatments. The PCR was carried out in a total volume of 25 μl containing the following components: 25 ng genomic DNA; 1X PCR buffer; 1.5 mM MgCl 2 ; 0.25 mM of each dNTPs; 1 μM of each primer; 1 U Go-Taq Flexi polymerase (Promega).
Thermocycling amplification was performed with a GeneAmp PCR system 9700 (Applied Biosystem, Inc.). The amplification was programmed at 94˚C for 5 min for the initial denaturation cycle, followed by 35 cycles with each cycle comprising 94˚C for 1 min, 50˚C for 1 min, then 72˚C for 90 s; and a final extension at 72˚C for 7 min. The produced PCR amplicons were electrophoresed using 1.5% agarose gel. A 100 bp plus DNA ladder and 1 kb were used as molecular size standards. PCR products were photographed using a Gel Doc™ XR+ System (Bio-Rad1).

Data analyses
Biological and biochemical data analyses. The statistical analysis program LDP line was used to determine the lethal and sublethal concentration values (LC 15 , LC 50 , and LC 90 ) for each insecticide and its nano-forms (with 95% confidence limits). All biological parameters and oxidative stress enzymes activity (SOD, CAT, lipid peroxidase, and GR) were performed using one way ANOVA in addition to Dunnett's multiple comparisons test with Graph Pad Prism 8 statistical analysis software. Moreover, a silhouette analysis was performed to evaluate the quality of the reproductive activity, enzymes, and developmental measurements by testing the cluster distances within and between each cluster [40]. Additionally, we performed a multidimensional preference analysis to disclose the interrelationships among parameters in addition to the similarity classification in terms of dependent and independent variables in different space dimensions [41]. Finally, hierarchical clustering based on the correlation analysis was conducted with two-dimensional heatmap plotting was constructed.
Molecular data analysis. For ISSR data analysis, the generated amplicons were scored visually. To generate a binary data set, the amplicons were scored as absent (0) and present (1). The polymorphism percentage was analyzed by dividing the number of amplified polymorphic bands by the total number of amplified bands separately for each primer [42]. A similarity matrix was built to estimate the genetic distances between all possible treatment pairs. The Jaccard coefficient was used for the pairwise comparisons [43]. The genetic similarity (GS) between each pair of treatments was calculated using GS = a/(n-d), in which n is the total number of fragments; a is the number of positive coincidences; and d is the number of negative coincidences. The genetic distances (GD) between pairs of treatments were estimated using GD = 1-GS. The unweighted pair group method of arithmetic averages (UPGMA) was used to construct the dendrogram [44].

Characterization of nano-(chlorine) chlorantraniliprole and nano-(sulfur) thiocyclam
The nano-suspensions of chlorine (Fig 1) and sulfur (Fig 2) were achieved using top-down molecular chemical techniques. Briefly, a single drop of the nanoparticle solution was spread onto a carbon-coated copper grid, and then was posteriorly dried at room temperature for transmission electron microscope (TEM) analysis. The dimensions of the nanoparticles were established directly from the figure using Image-Pro Plus 4.5 software. The particles were irregular in shape, with dimensions of 3.99 nm for chlorine and 4.05 nm for sulfur (Table 1), as well as 98.5% purity for each element. The nanoparticles' shape and dimension were examined using a JEOL 1010 TEM at 80 kV (JEOL, Japan).

Activities of chlorantraniliprole, thiocyclam, and their nano-forms
The toxicity of chlorantraniliprole, thiocyclam, and their nano-forms on the second instar larvae are presented in Table 2. The LC 50 values were 0.058 and 9.20 mg/l for chlorantraniliprole and thiocyclam, respectively, 96 h post-treatment. In contrast, the nano-forms (nano-chlorantraniliprole and nano-thiocyclam) had significantly higher toxicities than their original compounds, with LC 50 values of 0.015 and 4.46 mg/l, respectively ( Table 2). Table 3 shows the latent effect of chlorantraniliprole, thiocyclam, and their nano-forms on A. ipsilon development (from second instar larvae until the emergence) due to LC 15 and LC 50 exposure. The results showed elongation of the larval developmental period under all LC 50 treatments, while pupal duration was significantly increased in larvae exposed to regular form of both insecticides. The pupation% decreased significantly after LC 15 and LC 50 treatment of nano-thiocyclam at 83.20 ± 4.36% and 85.88 ± 0.56%, respectively ( were found in the female and male pupal weight, sex ratio, or emergence% for all treatments (Table 3).

Fecundity and fertility
Chlorantraniliprole, thiocyclam, and their nano-forms significantly decreased the hatchability percent under LC 15 and LC 50 compared to the control (  50 . In contrast, the number of eggs laid by one female showed no significant differences between treated and untreated larvae ( Table 4).

Activity of oxidative stress enzymes
Exposure to both insecticides and their nano-forms caused a significant increase in SOD activity after treatment with the LC 50 of thiocyclam (40.09 U/g of protein) and nano-thiocyclam  respectively). The highest significance was observed for the LC 50 of chlorantraniliprole and nano-chlorantraniliprole, and the LC 50 of thiocyclam (ca. 5.56, 5.54, and 5.0-fold, respectively). An increase in lipid peroxidase activity was observed under exposure to the LC 50 of nanochlorantraniliprole with 3.75 nmol/g of protein (ca. 16.30-fold). Meanwhile, the lipid peroxidase activity after treatment with the LC 50 of chlorantraniliprole, thiocyclam, and nano-thiocyclam was slightly significant at 2.24, 2.02, and 2.26 nmol/g of protein, respectively. No significant differences in lipid peroxidase activities were observed in any other treatments (Table 5).
Exposure to all investigated insecticides and their nano-forms resulted in significant stimulation of GR activity in the LC 15 and LC 50 of chlorantraniliprole (11.4 and 11.76 U/g of protein) ( Table 5). GR activity was significantly high under the LC 15

Correlation between development, reproductive, and enzyme activity
The plots for silhouette analysis were calculated based on the Euclidean distance metric to assess the cluster quality of the treatments based on reproductive activity, enzymes, and developmental measurements via cluster distance tests within and between each cluster (Fig 3). The results revealed that all parameters, except GR, SOD, and CAT enzymes, exhibited negative values, thus indicating that the clusters were mostly similar, and that the cluster configuration may have too few clusters. Meanwhile, two-dimensional heatmap plotting based on all parameters clustered the LC 15 of thiocyclam, chlorantraniliprole, and nano-chlorantraniliprole as the most similar to the control (1 st cluster), whereas the LC 50 of nano-chlorantraniliprole, nanothiocyclam, chlorantraniliprole, and the LC 15 of nano-thiocyclam were grouped in the second cluster as less-similar relative to the control (Fig 4). Moreover, multidimensional preference analysis was performed to summarize the interrelationships of all treatments, parameters, and classes ( Fig 5). The plot shows that the LC 50 of nano-thiocyclam, chlorantraniliprole, and the LC 15 of nano-thiocyclam deviated the most compared to the control. GR, SOD, and CAT enzymes revealed almost the same pattern.

ISSR analysis
To determine the mutagenic levels of the chlorantraniliprole, thiocyclam, and their nanoforms on the DNA of the second instar larvae, the ISSR marker system was used. The DNA of the untreated second instar larvae and all other treatments were amplified using 15ISSR primers (Fig 6). The 15 ISSR primers yielded a total of 252 scorable amplicons with an average of 16.8 bands/primer ( Table 6). The number of amplified DNA fragments per primer ranged from 11 bands (primer ISSR-18) to 21 bands (primers ISSR-10 and ISSR-12). The number of polymorphic bands per primer ranged from 7 bands (primer ISSR-1) to 19 bands (primer ISSR-5). A narrow range of the expected heterozygosity values was observed between 0.37 to 0. 50 Table 6). The highest GS was observed between the LC 50 of chlorantraniliprole and the LC 15 of thiocyclam. The lowest GS was determined to be between the LC 50 of nano-chlorantraniliprole, and nano-thiocyclam ( Table 7).

Analysis of molecular phylogeny
A dendrogram based on the UPGMA cluster analyses of the ISSR data was constructed for the nine treatments (Fig 7). The dendrogram was comprised of two main clusters: the first cluster included only the LC 50 of chlorantraniliprole, while the second cluster comprised two subclusters. The first sub-cluster consisted of only the LC 50 of nano-thiocyclam, and the second sub-cluster involved two major groups. The first major group included the LC 15 treatments of chlorantraniliprole, and nano-thiocyclam. The second major group consisted of the control, the LC 15 treatments of chlorantraniliprole, nano-chlorantraniliprole, and thiocyclam , and the LC 50 of thiocyclam. Furthermore, the PCA analysis of the ISSR data revealed highly similar results to the cluster analysis. The PCA results indicated that the LC 15 of nano-chlorantraniliprole and the LC 50 of thiocyclam were most similar to the control (Fig 8).

Discussion
Insecticide efficacy depends on the mode of action, insect species, developmental stage, application methods, and the number of days post-treatment [50]. Thus, pesticide nano-   formulations may change the toxicity or residue activity of insecticides, and reducing its application frequency, according to the Environmental Protection Agency's recommendation [51].
In the present study, we investigated the effects of the lethal and sublethal concentrations of Table 7. Genetic similarities between the nine treatments based on Jaccard's similarity coefficient based on ISSR primers data. C15  C50  T15  T50  CN15  CN50  TN15  TN50 CONTROL thiocyclam, chlorantraniliprole, and their nano-forms on A. ipsilon larval and pupal duration, larval mortality, adult emergence, reproductive activity, sex ratio, and oxidative stress enzymes with particular emphasis on DNA mutagenicity. Chlorantraniliprole has a novel mode of action [52] that activates insect ryanodine receptors (RyRs), leading to paralysis and mortality in sensitive species [53]. Thiocyclam is a broadspectrum nereistoxin antagonist that blocks the transmission of cholinergics [52], resulting in insect death. Our results revealed that A. ipsilon larvae were more susceptible to the nanoforms than the regular forms for both insecticides (Table 2). This might be due to (1) the nano chlorine within chlorantraniliprole, since chlorine is a non-selective oxidant with a number of effects on the living biota (e.g., reacts with a variety of cellular components, deactivates enzymatic active sites, decreases the biological functions of proteins, and produces deleterious effects on DNA [54]. In some cases, different layers of protein present in insects, larvae or even spores provide protection against chemical attacks, including chlorine, but we speculate that nano-chlorine has a greater effect on the cytoplasmic membrane permeability, causing the loss of refractivity, separating the spore coats from the cortex, extensively discharging Ca+, dipicolinic acid, and DNA, and finally causing lysis to occur, which can lead to cell death and growth inhibition [55]. The increased susceptibility to the nano-forms may also be due to (2) the nano-sulfur within thiocyclam, since sulfur destroys an insect's normal energy-producing bodily functions [56]. Normal pesticides containing sulfur have some caveats, because sulfur can damage plants during hot, dry weather and is incompatible with some other pesticides. In addition, sulfur should not be used on plants that have been sprayed with horticultural oils, as the induced reaction can damage foliage. Sulfur is non-toxic to humans and animals, unless ingested [57].
Sublethal effects of insecticides could be considered a common toxicological phenomenon and represent a secondary effect of insecticide application [62,64]. This phenomenon may occur in insects due to exposure to degraded insecticide after its initial application on crops [31]. In our results, the developmental rates of the larvae and pupae were substantially extended ( Table 2) after treating the 2 nd instar larvae of A. ipsilon with the original form of both insecticides compared to their nano-forms. These results agree with He et al. [62], Lutz et al. [65], El-Dewy [66], and Han et al. [67], whom found that the development of A. ipsilon, Plutella xylostella (Linnaeus), S. littoralis, and Spodoptera cosmioides (Walker) larvae was prolonged by low concentrations of chlorantraniliprole. In this study, both insecticides and their nano-forms did not show any significant differences in other biological parameters except for the LC 50 of nano-thiocyclam, which exhibits a significant difference in pupation% and emer-gence%. Additionally, the nano-form of both insecticides at LC 50 showed a significant difference in the number of eggs laid per female and fertility.
In the last decade, pesticide-induced oxidative stress has been a focus of toxicological research as a possible toxicity mechanism that causes a final manifestation of a pro-oxidant and antioxidant defense mechanism imbalance [68]. Pesticide intoxication causes a derangement of different antioxidant mechanisms in various tissues [68]; however, exposure to sublethal insecticide concentrations can induce oxidative stress enzymes to increase (e.g., SOD, CAT, and GR) [69]. Our results indicate that the CAT activity was significantly increased in both the insecticides and their nano-forms. Significantly increased SOD activity was observed in the LC 50 of both insecticides and their nano-forms. Also, significantly higher GR activities were observed in nano-chlorantraniliprole and nano-thiocyclam. The antioxidant enzyme systems, such as CAT or SOD, play an essential role in detoxifying harmful agents to counter the damaging effects of ROS [70].
Similar to the elevated antioxidant levels, lipid peroxide activity was significantly increased in MDA, which is the main oxidation result from the peroxidation of unsaturated fatty acids. This represents the oxidative effect on different organisms [71,72] in the LC 50 of both insecticides and their nano-forms. We observed no significant differences between the insecticides and their nano-forms at the lowest tested concentration (LC 15 ), which reflects the protective effects of antioxidants in A. ipsilon larvae. The antioxidant system can reduce MDA levels, which contributes to the accumulation of active oxygen and inhibits antioxidase activity [73]. The accumulation of MDA can be reduced by antioxidant enzymes, such as SOD and CAT. Other studies have demonstrated that toxic oxygen metabolism can mediate lipid peroxidation [74].
The ISSR-PCR technique was used as an effective marker to investigate the genetic mutagenicity levels between the second instar larvae subjected to different insecticidal treatments (chlorantraniliprole, thiocyclam and their nano-forms) compared to the untreated control. One of the benefits of ISSR is that it performs a qualitative evaluation of DNA variability through the differences in amplification profiles [44]. Many studies reported that the exposure of insects to particular insecticides at different concentration levels might lead to damages or changes in genomic DNA sequences (e.g., insertions, deletions, substitutions, or rearrangements), resulting in changes in the ISSR profile (e.g., the presence or absence of certain bands or variations of the band intensity) [25]. In addition, the possible occurrence of point mutations at the oligonucleotide annealing site may cause the absence of bands due to the loss of a priming site [75]. In this study, 15 ISSR primers were used to detect genetic mutagenicity levels and screen the degree of polymorphism between treated and untreated larvae. Furthermore, to establish the relationship between the insecticides, the ISSR study results were used to create a dendrogram. The results showed that the lowest mutagenic insecticidal effects on the insect DNA was observed in the LC 15 of nano-chlorantraniliprole treatment compared to the control. In contrast, the highest mutagenic effect was observed in the LC 50 of nano-chlorantraniliprole, followed by the LC 50 of nano-thiocyclam compared to the control. The PCA analysis of ISSR data revealed a consistent result to that obtained by the dendrogram topology. Moreover, it was found that the LC 15 of nano-chlorantraniliprole and the LC 50 of thiocyclam exhibited almost the same mutagenic effects as the control.
It is expected that the polymorphic differences observed in the ISSR patterns may be attributed to changes in primer binding sites or DNA structures, or to DNA damage caused by insecticide exposure. In addition, it could also be due to the blocking of DNA replication, the presence of a large number of chromosomal lesions, such as large rearrangements (e.g., deletion, inversion, or translocation), or un-repaired DNA damage due to direct exposure to different insecticidal treatments [76]. The ISSR studies demonstrated their ability and effectiveness to detect DNA damage and changes caused by the studied insecticides.

Conclusion
In summary, we developed insecticide nanometerization to improve the biological activity of conventional insecticides. Our obtained results represent a promising step toward developing safe and efficient nano-insecticides. Further investigations are still needed to determine their effects on the environment. To the best of our knowledge, this research is a pioneer case-study that examined and analyzed the genome-wide DNA mutability, biochemical effects, and toxicity levels of chlorantraniliprole, thiocyclam, and their nano-forms for the control of A. ipsilon.