Cyclodepsipeptides: Isolation from Endophytic Fungi of Sarcophyton ehrenbergi and Verification of Their Larvicidal Activity via In-Vitro and In-Silico Studies

Culex pipiens mosquitoes are vectors to many viruses and can transmit diseases such as filariasis and avian malaria. The present study evaluated the larvicidal activity of marine-derived endophytic fungi Aspergillus nomius and Aspergillus flavus from the soft coral Sarcophyton ehrenbergi along with two known cyclodepsipeptide compounds, scopularide A (1) and B (2), isolated from A. flavus extract, against third-instar larvae of C. pipiens, using distilled water as a negative control and toosenedanin as a positive control. The structures of the isolated compounds were confirmed by various spectroscopic analyses. The lethal concentrations (LC50 and LC90) were calculated by probit analysis. Scopularide A was the most potent after 96 h treatment, with LC50 and LC90 values of 58.96 and 994.31 ppm, respectively, and with 82.66% mortality at a concentration of 300 ppm. To unravel the biochemical mechanism of the tested extracts and compounds, their effects against protease, chitinase, phenoloxidases and lipase enzymes from the whole-body tissue of C. pipiens were evaluated after 72 h treatment at LC50 dose. Superior activity was observed for A. flavus extract against all tested enzymes. A molecular docking study was conducted for scopularide A and B on the four tested enzymes, to further verify the observed activity. Results revealed good binding affinities for both compounds as compared to the docked ligands, mainly via a number of hydrogen bonds. This was the first study to report the isolation of endophytic fungi A. flavus and A. nomius from the marine soft coral S. ehrenbergi. The endophytic fungal extract of A. flavus was found to be a promising source for a natural larvicidal agent against C. pipiens populations.


Introduction
Insects are vital organisms that have been shown to benefit humans in a variety of ways, including environmental stability, agriculture, and nutrition. Several other insects, on the other hand, are dangerous in terms of causing health problems, crop loss, or even pollution. Pests and vectors are the most harmful organisms, causing major health and productivity problems. Insect pests cause damage to crops by feeding on plants or stored cereals. Increased pest attacks frequently result in lower productivity and, as a result, a weaker economy [1]. Outbreaks of these pests frequently endanger worldwide food safety and, as a result, raise health concerns [2]. Aside from pests, vectors, which include mosquitoes, are another important group of insects that have a major impact on healthcare systems. Mosquitoes are the primary vectors of pathogens such as Zika virus and malarial and dengue virus in tropical and subtropical countries such as India, South Africa, and Brazil [3]. According to WHO, mosquitoes are considered the number one "public enemy" [4]. Mosquito-borne diseases are common in more than one hundred countries across the world, infecting over four billion people every year worldwide [5].
These vectors can only be controlled by manmade insecticides such as organochlorines, organophosphates, carbamates, and DDTs. The misuse of these synthesized insecticides has led to environmental problems, in addition to the emergence of resistant variants [6,7]. To ensure the sustainability of the ecosystem, components with low or no toxicity to non-target organisms should be used [8]. Natural products derived from fungi or other biological sources are inexpensive, environmentally friendly, and play an important role in alleviating these types of problems [9,10]. Natural products provide effective alternatives and promising sources for many bioactivities [11][12][13][14][15]. Discovering larvicides from marine sources with biodiversity may be another approach to mosquito control. Natural-originated and -derived larvicides contain a mixture of metabolites, which act concurrently on both physiological and behavioral processes and may exert actions different from single synthetic larvicides, which may lead to unexpected resistance [16]. Identifying efficient as well as ecofriendly bio-larvicides is crucial for continued efficient mosquito management. Marine organisms provide a reservoir of a vast number of organisms, such as bacteria or fungi, that can live symbiotically within their tissues [17,18]. The bioactive metabolites produced by some seaweeds showed a wide range of biological activities, from insecticidal against arthropods to neurologically active in humans [19,20].
Endophytes are microorganisms, generally fungi and bacteria, that spend part or all their lives in the host marine creature [21]. In healthy and fine tissue, endophytic microorganisms can be discovered. Owing to the biotechnological interest of fungal endophytes as biological control agents, metabolites, and genetic vectors, endophytes have been observed as an excellent reservoir of secondary bioactive metabolites [22]. They are able to defend their hosts against several biotic and abiotic aspects, e.g., the attack of pathogens, insects, and herbivores [23].
Molecular docking is considered as a mockup technique that discovers the best fitting pose between ligands and the active sites of the specific targets. This procedure includes the arrangement of the 3D coordinate space on the binding site of the target, calculation of the binding affinity of the formed complex, and elaboration of the subsequent orientation of a molecule on the ligand's binding site. The largest magnitude negative number signifies the sensitivity of binding affinity, representing the most satisfactory conformation of the formed complex [24][25][26][27]. Here, we reveal the isolation and larvicidal activity of two cyclodepsipeptides, scopularide A and B, along with the crude extracts, from the culture rice media of both endophytic A. flavus and A. nomius, isolated from Sarcophyton ehrenbergi. This is the first study demonstrating the mosquito larvicidal activity of Egyptian marine endophytic fungi.

Compound Identification
Compound 1 was isolated as thin off-white crystals, m.p. 228-232 • C; the purity of the isolated crystals was indicated by the sharp melting point observed. Pure compounds have sharp melting points, which, according to Dent [28], are compounds with melting points within a temperature range of 5 • C. NMR data of compound 1 (Tables 1 and S1) were in accordance with those reported for the cyclodepsipeptide, scopularide A [29]. Compound 2 was isolated as white amorphous powder. Its NMR data (Tables 2 and S2) were in accordance with the reported data for scopularide B [29]. The structures of the isolated compounds are presented in Figure 1.

Larvicidal Activity
To assess the mosquito larvicidal activities of the crude extracts, third-instar larvae of C. pipiens were used. Crude extracts of A. flavus and A. nomius as well as the isolated scopularides A and B were tested against C. Pipiens. Tables 3 and 4 summarize the toxicities of different concentrations of the two isolated compounds and A. flavus and A. nomius crude extracts at various time intervals (24,48,72, and 96 h) and their the LC 50 values. The mortality of C. pipiens larvae was directly proportional to the concentrations of the tested material, i.e., a potential linear relationship between the concentration and mortality percentages exists, also with the extension of the exposure period. The mortality rate after 96 h treatment ranged from 26   As clarified in Figures 2 and 3, these results revealed parallel toxicity regression lines and indicated that all tested materials possess the same mode of action. This might be able to be predicted because both extracts and the isolated compounds were from the same genus, Aspergillus sp. In addition, all tested materials possessed a latent kill effect in which they showed a significant LC 50      It was important to investigate the biochemical changes in the activities of some enzymes (protease, chitinase, phenoloxidases, and lipase) from the whole-body tissue of C. pipiens larvae after 72 h treatment with LC 50 of A. flavus, A. nomius extracts, and isolated compounds.

Determination of Chitinase
Chitinase is a hydrolytic enzyme that breaks down glycosidic bonds in chitin, which is present in the exoskeletons of arthropods. The chitinase activities in the larvae homogenate of C. pipiens treated with LC 50 for 72 h in four examined samples are presented in Table 5. A. flavus extract showed an increase in the enzyme activity as 118 ± 8.6 a mg N-acetylglucosamine/min/mg protein, with a percentage change of 9.3%, compared with 108 ± 5.1 a mg N acetyl glucose amine/min/mg protein in the untreated control group. A. nomius extract, scopularide A, and scopularide B showed an insignificant reduction in enzymatic activity of 95 ± 3.2 b , 86 ± 2.5 b , and 82 ± 2.4 b mg N-acetylglucosamine/min/mg protein, with percentage changes of −12.0%, −24.1%, and −20.3%, respectively.
Means bearing different scripts are significantly different from control at p < 0.01 (Duncan's multiple range test).

Determination of Phenoloxidases
Phenoloxidase is an enzyme produced by insects as a defense system against bacterial and fungal infections. Enzymatic processes generate superoxide, diphenols, hydrogen peroxide, quinones, and reactive nitrogen intermediates, all of which are necessary for defense. The phenoloxidase activities in the larvae homogenate of C. pipiens treated with LC 50 for 72 h for four examined samples are presented in Table 6. The analysis revealed that phenol oxidase was decreased to 1579 ± 14.5 c O.D. units × 10 3 /min/mg protein, equal to −11.88%, with A. flavus extract, compared with 1792 ± 15.6 a O.D. units × 10 3 /min/mg protein in the untreated control group, followed by scopularide B, scopularide A, and A. nomius crude extract.

Determination of Lipase
The lipase activities in the larvae homogenate of C. pipiens treated with LC 50 for four examined samples for 72 h are presented in Table 7. A. flavus crude extract, scopularide A, and scopularide B showed significant increases in enzymatic activity as 4.6 ± 0.22 a , 3.8 ± 0.16 b , and 3.9 ± 0.15 b µM oleic acid liberated/min/gram body weight, with percentage changes of −52.7%, −26%, and −28.3%, respectively, compared with 3 ± 0.12 c µM oleic acid liberated/min/gram body weight in the untreated control group.

Determination of Protease
The protease activities in the larvae homogenate of C. pipiens treated with LC 50 for four examined samples for 72 h are presented in Table 8. Both crude extracts, scopularide A and B, showed an insignificant reduction in enzymatic activity as 3235 ± 106 ab , 2873 ± 61 c , 3116 ± 78 b , and 2277 ± 42 d g protein, compared with 3426 ± 88 a in the untreated control group, with percentage changes of 5.6%, 16.1%, 9.0%, and 33.5%, respectively.

Phenoloxidase Enzyme
The ligand O-methylated saccharide showed -(C-docker interaction energy) = −33.25 kcal/mol with interaction with phenoloxidase via hydrogen bonds with Thr 318 and Thr 340. Meanwhile, scopularide A docked against phenoloxidase showed −43.68 kcal/mol as -(C-docker interaction energy) and the same two hydrogen bonds, with an interaction similar to that of the ligand with Thr 318 and Thr 340. On the other hand, scopularide B's interaction was through hydrogen bonds with Thr 318 and Thr 340 and an extra hydrogen bond with Gly 317, and it also showed -(C-docker interaction energy) = −37.79 Kcal/mol.

Discussion
C. pipiens is the most widely dispersed mosquito species in the world. Mosquitoes in Egypt are vectors of malaria, several forms of filariasis, and numerous arboviruses, such as dengue and yellow fever [30]. Thangum and Kathiresan investigated a wide range of marine creatures for insecticidal activity towards mosquito species; one of their research works, published in 1996, was the first case to look into the larvicidal activity caused by marine resources [31]. Bahgat et al. used spinosadas, made from soil Actinomycete, to investigate the environmental risks of employing synthetic insecticides against mosquitoes [32]. There have been numerous studies focused on terrestrial plants to exert mosquito larvicidal activity [33].
Endophytic fungi have been shown to protect their hosts against pests, insects, pathogens, and even domestic herbivores [34]. A. flavus and Penicillium sublateritium, which live on the host plant, can produce useful metabolites to improve their fitness and fight stress [35]. Biochemical analyses focused on the mosquito larvae's vital enzymes aided us in understanding the toxicity of substances to mosquito larvae. In contrast to synthetically derived insecticides, naturally derived insecticides are gaining popularity because they do not endanger animals or humans [35]. In view of these results, the purified active compounds as well as endophytic isolated fungi extract found in our studies could be effective in killing mosquito third-instar larvae in an economic and safe manner. Many isolated natural chemical compounds and extracts have been reported for their potential biological activities [36][37][38][39]. Our results showed that isolated scopularide A possessed larvicidal activity, with values of LC 50 69.963 and 58.968 ppm after 72 and 96 h treatment, respectively. A. flavus crude extract was the most effective one. Through biochemical analyses of certain enzymes to identify the mode of action by which the tested samples exert their activity, it was noticed that changes in the activities of lipase, chitinase, protease, and phenoloxidase enzymes lead to the death of the mosquito larva. These results suggested that the stereochemistry of both compounds plays an important role in their biological activity, which was also confirmed through in silico molecular docking studies. The findings suggest that the endophytic fungus Aspergillus flavus could be developed as a natural larvicidal product.

Fungal Material and Identification
The soft coral Sarcophyton ehrenbergi was collected in 2015 from Hurghada, Red Sea at 10 m depth, Egypt. It was identified by Dr. Hamada Ali of the National Institute of Oceanography and Fisheries, Hurghada. A voucher sample was kept at Ain Shams University under the voucher sample code of PHG-M-SE-259. The fungal strain was isolated from the coral using the previously described standard technique [40]. Based on DNA amplification and sequencing of the ITS region, the fungus was identified as A. flavus (GenBank accession no. Mk969114) [41,42] and the closest relative strain was A. nomius (GenBank accession no. MK969116).

Cultivation, Extraction, and Isolation
The strains were grown in 12 1 L Erlenmeyer flasks for 30 days at room temperature under static conditions, using a solid rice medium prepared by autoclaving 100 g rice and 120 mL water at 121 • C for 20 min. Following fermentation, EtOAc (3 × 600 mL) was used to extract the fungal culture in each flask. The obtained crude extract of A. flavus (1.2 g) was partitioned between n-hexane and 90% aqueous MeOH, giving 850 mg of 90% aqueous MeOH extract. The latter was subjected to vacuum liquid chromatography (VLC) on silica gel 60 eluting with gradient mobile phase (n-hexane-EtOAc 100:0 to 0:100, DCM-MeOH 100:0 to 0:100) to give eight fractions (V1-V3). Fraction 3 was subjected to Sephadex LH-20 using MeOH and yielded scopularide A and B, as previously isolated [29,42].

Investigation of the Molecular Target Involved in the Larvicidal Activity of the Isolated Compounds
Scopularides A and B were further virtually tested for their activity against chitinase, lipase, protease, and phenoloxidase using Discovery Studio 4.0. The proteins were downloaded from PDB with codes (3CHC, 1GT6, 1NF6, and 6RGG), respectively. All proteins were cleaned, unneeded chains were removed, and hydrogens were added. Simulation using CHARMm forcefield and partial charge MMFF94 was applied and a heavy atom was created. Constraints were turned to be fixed and minimization of proteins took place. Receptor and binding site were identified from the complexed ligand interaction site. For chitinase (3CHC), the crystal structure of Aspergillus fumigatus chitinase B1 in complex with monopeptide ligand -(2S)-2-acetamido-N-methyl-5-[[N-(methyl carbamoyl) carbamimidoyl] amino] pentanamide-was downloaded from PDB. In lung homogenates from a mouse model of chronic asthma, the peptide in complex was found to inhibit chitinase B1 from Aspergillus fumigatus (AfChiB1), human chitotriosidase, and chitinase activity, with potencies ranging from high nanomolar to high micromolar suppression. The linear peptides' conformations were very comparable to those of the natural product, according to X-ray crystallographic examination of the chitinase inhibitor complexes [46]. Lipase (1GT6) was downloaded from PDB as the S146A mutant of Thermomyces (Humicola) lanuginosa lipase in complex with oleic acid [47]. Tricorn protease in complex with Z-Phe-diketo-Arg-Glu-Phe-a trideca-peptide inhibitor modifying the catalytic Ser965 that revealed part of the peptide trapped inside the channel of the beta7 domain-was downloaded from PDB with code (1N6F) [48]. Photorhabdus laumondii lectin PLL2 in complex with O-methylated PGL-1-derived disaccharide was downloaded from PDB with code (6RGG). The O-methylated saccharides interacted with two-propeller lectins, PLL2 from the entomopathogenic bacterium Photorhabdus laumondii and its homologue PHL from the related human pathogen Photorhabdusa symbiotica, in this study. O-methylation is an uncommon sugar alteration with a poorly understood function. Methylated sugars were postulated to constitute a conserved pathogen-associated molecular pattern because of their presence and identification by lectins involved in the immune response. [49]. C-docker was applied between each of the prepared ligands: scopularides A and B and the four minimized proteins. The -(C-docker interaction energy) of the top active conformer out of the resulting 10 and the binding modes were analyzed, visualized, and compared with each of the complexed ligands

Larvicidal Activity
In a series of experiments, the larvicidal activity of the crude extract of A. flavus, A. nomius as well as the isolated scopularides A and B was assayed against the 3rd-instar larvae of C. pipiens using an immersion method as compared to toosenedanin (positive control) according to WHO [4], as follows.
Groups of 25 early 3rd-instar larvae of C. pipiens were transferred into test cups, each containing water (100 mL), under laboratory conditions. Each fungal extract was prepared in five different concentrations, with mortality rates ranging from 20% to 90%. Three replicates for each treatment and one for the untreated control (distilled water) were used in the experiment. Every day, abnormal pupae were removed and placed in labeled glass vials containing 70% ethanol.

Method for Larvicidal Activity Using Biochemical Analysis
The insects were prepared in accordance with the guidelines provided by [50]. The insects were mixed in distilled water (50 mg/1 mL). Homogenates were centrifuged at 8000 rpm for 15 min at 2 • C in a refrigerated centrifuge. The deposits were discarded and the supernatants could be stored for at least one week without considerable damage of activity when stored at 5 • C. All experiments contained 3-4 replicates (insect homogenates), and the results of biochemical investigations were combined from triplicate determinations. The data were examined using statistical software and a one-way analysis of variance (ANOVA) (Cohort software, Berkeley). When the ANOVA data were significant, Duncan's multiple range test (p < 0.01) was used to compare the means.

Protein Preparation
Protein solutions were prepared in 0.15 M NaCl according to [51].

Preparation of Protein Reagent
Protein reagent was prepared by dissolving 100 mg of Coomassie Brilliant Blue G−250 in 50 mL 95% ethanol. To this solution, 100 mL 85% (W/V) phosphoric acid was added. The resulting solution was diluted to a final volume of 1 L. For the sample solution (50 µL) for preparation of the standard curve, 50 µL of serial concentrations containing 10 to 100 µg bovine serum albumin was pipetted into test tubes. The volume in the test tube was adjusted to 1 mL with phosphate buffer (0.1 M pH 6.6). Five millimeters of protein reagent were added to the test tube and the contents were mixed by inversion. The absorbance at λ 595 nm was measured after 2 min and before 1 h against a blank prepared from 1 mL of phosphate buffer and 5 mL protein reagent.

Chitinase Activity
Substrate preparation: According to [52], colloidal chitin was prepared, as follows. First, 4.0 g of purified chitin powder was suspended in 100 mL water at 4 • C and stirred. Conc. H 2 SO 4 (30 mL) at 4 • C was added to the suspension. We then filtered the cold chitin solution through glass wool into 1800 mL ice-cold 50% ethanol while stirring. We washed the precipitated chitin with distilled water to pH 5.
Enzyme assay: The reaction mixture was prepared according to [53], with some modifications; we used 1 mL phosphate buffer (0.2 M, pH 6.5), 200 mL 0.5% colloidal chitin, and 200 mL enzyme solution. Enzyme activity was determined after 1.5 h incubation at 37 • C, by boiling the test tube. At 8000 rpm, undigested chitin was sedimented by centrifugation for 15 min. The supernatant was taken for the determination of N-acetylglucosamine produced as a result of chitin digestion by chitinase.
Determination of N-acetylglucosamine: It was determined by the sensitive method of [54]. The volume of the appropriate aliquot from the supernatant was adjusted to 1 mL with phosphate acetate buffer (0.2 M, pH 6). For each determination, a 1 mL buffer blank and a series of N-acetylglucosamine standards (10, 20, 40, 60, and 80 g) in 1 mL buffer were used. Each tube was shaken and heated in a boiling water bath for 10 min, after the addition of 0.3 mL saturated sodium borate solution. The tubes were then transferred rapidly to cold water, and then 8 mL glacial acetic acid was added to each tube. The tubes were shaken and allowed to stand for 30 min at room temperature. The enzyme activity was expressed as µg N-acetylglucosamine (NAGA) × 10 3 /min/gm fresh weight.

Lipase Activity
Lipase activity was investigated by a slight modification of the procedure of [55]. The approach worked by measuring the decrease in the ester content of triolein as a substrate.
Assay method: 1 mL substrate emulsion, sample solution 100 µL, and 0.4 mL 0.2 M tris buffer (pH 7.5), incubated at 35 • C for exactly 5 min. After incubation, iso-propanol 4 mL and 1M H 2 SO 4 2 mL mixture were added. The reaction products were extracted in 5 mL n-heptane. The mixture was allowed to stand for 5 min after vigorous stirring. One mL of n-heptane layer was transferred to the test tube and the optical density of the ester content was determined as compared to the standard. Lipase activity was expressed as the number of µM oleic acid liberated/min/gram body weight.

Proteolytic Activity
Tatchell et al. described a method for determining proteolytic activity, which we adopted with some modifications [56]. During 1 h incubation at 30 • C, the increase in free amino acids separate from substrate albumin was measured. Reaction mixture: insect homogenate 100 µL, 0.1 M phosphate buffer 1 mL (pH 8), and 0.5% bovine serum albumin 100 µL. First, 1.2 mL 20% TCA was added to end the reaction. The mixture was centrifuged at 3000 rpm for 20 min after standing for 15 min. Then, the supernatant was used for measuring the quantity of the produced amino acids. Amino acids were colorimetrically assayed by ninhydrin reagent according to the method described by [57]. The reaction mixture: supernatant 100 µL, ninhydrin-citrate (pH 5.5) 1.9 mL, 0.5 M citrate buffer (pH 5.5) 0.2 mL, and 1.2 mL glycerol. In a boiling water bath for 12 min, the mixture was heated and cooled by tap water. The developed color was measured at λ 570 nm, zero adjustment was against blank. Standard D,L alanine, and the amino acids were measured in µg alanine/min/g.b.wt.

Phenol Oxidase Activity
The activity of phenol oxidase was measured according to a modification of [58]. Reaction mixture: phosphate buffer (0.1 M, pH 7) 0.5 mL, enzyme solution 200 µL, and catechol solution (2%) 200 µL. Enzyme reaction was initiated by adding catechol solution after 1 min, the optical density (O.D.) was determined, zero adjustment was against blank. The phenol oxidase activity was determined as O.D. units ×10 3 at an absorbance of λ 405 nm.

Statistical Analysis
Mortality data were recorded in a probit regression line and we calculated LC 50, LC 90, slope function, and X 2 [59], and correction for control mortality was conducted using Abbott's formula according to [60]: % corrected mortility = % mortility in treatment − % mortality in untreated 100 − % mortality in untreated × 100

Conclusions
The present study has shown that scopularide A exhibits larvicidal activity against third-instar larvae of C. pipiens with LC 50 values of 69.963 and 58.968 after 72 and 96 h, respectively. The efficacy demonstrated could be encouraging evidence to enhance the existing methods in the vector mosquito control toolkit. The findings of this study reveal that scopularide A is a strong, biodegradable, and natural mosquito larvicidal agent that can be exploited to develop eco-friendly larvicides.