Oviposition-Stimulant and Ovicidal Activities of Moringa oleifera Lectin on Aedes aegypti

Background Natural insecticides against the vector mosquito Aedes aegypti have been the object of research due to their high level of eco-safety. The water-soluble Moringa oleifera lectin (WSMoL) is a larvicidal agent against A. aegypti. This work reports the effects of WSMoL on oviposition and egg hatching of A. aegypti. Methodology/Principal Findings WSMoL crude preparations (seed extract and 0–60 protein fraction), at 0.1 mg/mL protein concentration, did not affect oviposition, while A. aegypti gravid females laid their eggs preferentially (73%) in vessels containing isolated WSMoL (0.1 mg/mL), compared with vessels containing only distilled water (control). Volatile compounds were not detected in WSMoL preparation. The hatchability of fresh eggs deposited in the solutions in the oviposition assay was evaluated. The numbers of hatched larvae in seed extract, 0–60 protein fraction and WSMoL were 45±8.7 %, 20±11 % and 55±7.5 %, respectively, significantly (p<0.05) lower than in controls containing only distilled water (75–95%). Embryos were visualized inside fresh control eggs, but not within eggs that were laid and maintained in WSMoL solution. Ovicidal activity was also assessed using stored A. aegypti eggs. The protein concentrations able to reduce the hatching rate by 50% (EC50) were 0.32, 0.16 and 0.1 mg/mL for seed extract, 0–60 protein fraction and WSMoL, respectively. The absence of hatching of stored eggs treated with WSMoL at 0.3 mg/mL (EC99) after transfer to medium without lectin indicates that embryos within the eggs were killed by WSMoL. The reduction in hatching rate of A. aegypti was not linked to decrease in bacteria population. Conclusions/Significance WSMoL acted both as a chemical stimulant cue for ovipositing females and ovicidal agent at a given concentration. The oviposition-stimulant and ovicidal activities, combined with the previously reported larvicidal activity, make WSMoL a very interesting candidate in integrated A. aegypti control.


Introduction
Aedes aegypti Linnaeus is a domestic, daytime mosquito that breeds preferably in water storage containers, discarded plastic vials, and automobile tyres [1]. This mosquito has great importance in tropical and subtropical countries, since it is the vector of yellow and dengue fevers. Currently, dengue is the vector-borne disease that spreads most rapidly worldwide, with over two-fifths of the world's population at risk of infection [2,3]. The absence of an effective vaccine makes the control of vector population the only way to minimize dengue spreading.
Worldwide, synthetic chemicals, mainly pyrethroids, carbamates and organophosphates are used to control adults, larvae, pupae and eggs of A. aegypti. These compounds pose high environmental risks, due to adverse effects on human and nontarget organisms [4,5]. In addition, their widespread usage has lead to mosquito resistance, compromising the effectiveness of control strategies [6]. It was also demonstrated that the presence of residual herbicides in ecosystems can reduce the sensitiveness of mosquito larvae to insecticides [7]. Due to their biodegradability, insecticides extracted from plants have been considered environmentally friendly substitutes for synthetic insecticides [8].
Plant extracts, secondary metabolites, essential oils and lectins (carbohydrate-binding and hemagglutinating proteins) have been shown to exert deleterious effect on A. aegypti, delaying development, impairing growth and digestive enzyme activities, reducing egg hatching and larval survival, as well as deterring feeding and oviposition activities [9][10][11][12][13][14][15]. The deleterious effects of lectins on insects have been associated with interaction of lectin with Nacetylglucosamine residues of chitin, a structural component in insects being found in peritrophic matrices, epidermal cuticles and tracheas [16].
Oviposition behavior of mosquitoes is a useful tool in determining female preference for oviposition sites. The acceptance or rejection by gravid females of a site for oviposition can be related to chemosensory cues (semiochemicals) which the insects detect through specialized cuticular structures, sensilla and chemosensory neurons in antennae, mouthparts, wing margins and legs [17]. Olfactory sensilla detect airborne volatiles, while gustatory sensilla respond to the treatment with chemicals of lowvolatility [17].
Oviposition repellents have been the object of research designed to discover ways to eliminate oviposition sites and ward off A. aegypti gravid females from human hosts. Monoterpenes and sesquiterpenes present in essential oils act as repellant to females [18,19]. Compounds that elicit increased A. aegypti oviposition have also been searched, an attractive property that may be used in ovitraps in combination with larvicidal agents [20]. Secondary metabolites produced by fungus Trichoderma viride and infusions obtained by fermentation of organic materials (e.g. sod, hay, grass, leaves, senescent bamboo and pelletized plant-based animal feeds) were shown to act as oviposition stimulants to gravid Aedes and Culex mosquitoes [21][22][23][24].
A. aegypti eggs are the main dispersion form of mosquito. Eggs resist dry conditions and manage to survive for many months or years in adverse environments [25]. They also afford these insects to rapidly reconstitute populations, even if the other stages have been eliminated by control measures. Thus, it is important to search for insecticides that act also against this developmental stage of the mosquito. Different plant species have been investigated for ovicidal activity on A. aegypti. Organic solvent extracts, as well as essential oils have been found to impair egg hatching [14,26,27].
Moringa oleifera Lamarck is a tree widely cultivated throughout the tropics and subtropics. In developing countries, its seeds are used to treat water for human consumption. Its seeds also contain a water-soluble lectin (WSMoL), which showed similarity with M02.1 and M02.2 (identification number gi|127215) proteins [9]. Using cell-free plasmid DNA and Salmonella typhimurium assays, a study on genotoxicity of WSMoL demonstrated that the lectin was non-mutagenic, indicating its safety for use in water treatment [28]. This lectin also acted as coagulant and antibacterial against Staphylococcus aureus, and effectively reduced lake water bacteria growth [29]. WSMoL exerted larvicidal activity (LC 50 of 0.197 mg/mL) against A. aegypti fourth-stage larvae. The larvae treated with WSMoL lost the underlying epithelium, and showed increased gut lumen and hypertrophic segments [9]. Due to the high solubility in water and larvicidal activity against A. aegypti, WSMoL may become a potential candidate in A. aegypti control.
This work evaluated the effects of crude preparations (seed extract and 0-60 protein fraction) containing WSMoL and isolated lectin on A. aegypti oviposition. The hatchability of the freshly laid eggs obtained from the oviposition assay as well as of stored eggs was assessed. The presence of volatiles in WSMoL solution and the possibility that the effect of WSMoL on hatching involved embryo death and reduction of bacteria population in incubation medium were investigated. In addition, fresh and stored eggs from control and WSMoL treatments were examined on a stereomicroscope.

Breeding and rearing of A. aegypti in laboratory
The mosquitoes and eggs used were obtained from the colony (Rockfeller strain) maintained at the Laboratório de Ecologia Química of the Universidade Federal de Pernambuco (Recife, Brazil) since 2003. The insectary room was kept at 2761uC, 7862% relative humidity and 14:10 (light/dark) photoperiod. The larvae were reared in plastic bowls containing water and cat food (WhiskasH). Adult mosquitoes were reared in cages (30630630 cm) covered with a fine mesh cloth and fed a 10% glucose solution. Females took blood meal from chicken blood acquired from local farms and dispensed from a common artificial feeder. The eggs laid by females were collected and used to restart the cycle for maintaining the colony or used to assess ovicidal activity. Crude preparations of WSMoL were obtained according to Coelho et al. [9]. Seeds were milled to a fine powder and homogenized (10 g) with distilled water (100 mL) using a magnetic stirrer for 16 h at 4uC. After filtration through gauze and centrifugation (9,000 g, 15 min, 4uC), the clear supernatant (seed extract) was submitted to protein precipitation using ammonium sulphate at saturation of 60% according to Green and Hughes [30]. The 0-60 precipitate collected after centrifugation (9,000 g, 15 min, 4uC) was dialyzed (3.5 kDa cut-off membrane) against distilled water (4 h) for use in bioassays and additionally with 0.15 M NaCl (4 h) for use in chromatography step. The dialysed fraction corresponded to the 0-60 protein fraction. The presence of residual ammonium sulphate in the 0-60 protein fraction was evaluated adding 50 mL of this sample to 0.5 mL of a 10 mg/mL barium chloride solution acidified to pH 4.0 with 1.0 M HCl. The formation of precipitates indicates that there is ammonium sulphate in sample [31].

Isolation of WSMoL
WSMoL was isolated according to the procedure described by Coelho et al. [9]. The 0-60 protein fraction was loaded (40 mg of proteins) onto a chitin column (7.561.5 cm) equilibrated (0.3 mL/ min flow rate) with 0.15 M NaCl, a salt concentration which does not interfere on A. aegypti oviposition [32]. After washing with the equilibrating solution, WSMoL was recovered by elution with 1.0 M acetic acid and dialysed (3.5 kDa cut-off membrane) against distilled water (4 h) at 4uC for eluent elimination. The presence of residual sodium chloride in WSMoL was evaluated according to the classic Mohr's method for determination of chloride by precipitation titration with silver nitrate. The detection limit of the method was 5610 24 M.

Protein and carbohydrate contents
The protein concentration was determined according to Lowry et al. [33] using bovine serum albumin (31.25-500 mg/mL) as standard. Carbohydrate concentration was determined according to Dubois et al. [34] using mannose (10-500 mg/mL) as standard.

Hemagglutinating activity
Hemagglutinating activity of seed extract, 0-60 protein fraction and erythrocytes treated with glutaraldehyde [36]. One hemagglutination unit (titer) was defined as the reciprocal of the highest dilution of the sample promoting full agglutination of erythrocytes [11]. Specific hemagglutinating activity (unit WSMoL was assessed aiming to quantify and monitor lectin activity. The assay was performed in microtiter plates (Kartell S.P.A., Italy) according to Paiva and Coelho [35] using suspension (2.5% v/v) of rabbit /mg) was defined as the ratio between the titer and protein concentration.

Oviposition assay
Oviposition assay was performed according to Navarro et al. [32]. Oviposition assays were carried out using A. aegypti gravid females 3 days after blood meal. Twenty-five females were placed in a bioassay cage (33621630 cm) containing two glass vessels (10 cm diameter), each containing 50 mL of distilled water and placed at diagonally opposite corners of the cage. Aliquot (1 mL, 5.1 mg/mL of protein) of seed extract, 0-60 protein fraction or WSMoL was added to a vessel, resulting in a final protein concentration of 0.1 mg/mL. The same volume of distilled water was added to the control vessel. A disk shaped piece of filter paper (18 cm in diameter) folded into a cone was placed covering the inside of each vessel, to provide a support for oviposition ( Figure 1). The females were maintained at 2760.5uC with 7360.4% relative humidity for 14 h in the dark. After this period, eggs in oviposition paper sheets were manually counted using a stereomicroscope (Leica M80). The oviposition response was expressed as follows: % oviposition = 1006 [(number of eggs in sample vessel) / (number of eggs in sample and control vessels)]. For each treatment (seed extract, 0-60 protein fraction or WSMoL), three independent experiments were performed in quintuplicate, on different dates.

Volatiles analysis by headspace analysis
WSMoL preparation was enclosed within a glass vessel from which the air was drawn for 30 min by a battery-operated membrane pump (ASF Thomas) at a constant flow rate of 200 mL/min through sorbent traps containing a mixture of 0.05 g of Tenax TA (80/100 mesh, Macherey-Nagel 706318) and 0.05 g of Carbopack X (20/40 mesh, Supleco 1-0435). Blanks corresponded to the air drawn from empty vessel. The traps were eluted with 150 mL acetone, which was kept under 224uC refrigeration until analysis.
The presence of trapped volatiles was analyzed by combined gas-chromatography-mass spectrometry (GC-MS) on a Thermo Finnigan Voyager Mass Spectrometer coupled with a Thermo Trace GC 2000 (Thermo Fisher Scientific) equipped with a CP-Wax 52CB column (Varian; 30 m60.25 mm60.25 mm). The sample eluted from traps (1.0 mL) was injected in the column in splitless mode, and the temperature of the inlet was 250uC. GC oven temperature was set at 60uC for 3 min, increased by 2.5uC/ min to 240uC, and then held steady for 10 min. Helium carrier gas flow was maintained at a constant pressure of 100 kPa. The MS interface was 200uC, and mass spectra were taken at 70 eV in EI mode) with a scanning speed of 0.5 scan/s from m/z 20-350.
Hatchability of fresh eggs laid on seed extract, 0-60 protein fraction and WSMoL Aiming to determine if M. oleifera seed preparations affect hatchability, fifty fresh eggs from each vessel from oviposition assays (including controls) were selected considering their integrity using a stereomicroscope and placed again in the same solutions where they were deposited. The number of hatched larvae present in solution was determined after 144 h of incubation at 28uC. For each treatment (seed extract, 0-60 protein fraction or WSMoL), three independent experiments were performed in quintuplicate on different dates.

Ovicidal assay using stored eggs
Ovicidal assay was performed according to Prajapati et al. [37]. A. aegypti eggs stored for 3 months at 28uC were selected considering their integrity using a stereomicroscope. Seed extract was diluted in filtered tap water to provide test solutions with protein concentrations of 0.  Controls contained distilled water, in a volume equivalent to that of sample used to achieve each concentration, completed to 20 mL with filtered tap water. The number of hatched larvae was determined after 72 h of incubation at 28uC. Three independent experiments were run in triplicate.
Aiming to evaluate whether WSMoL inhibits hatching and/or kills embryos, stored eggs submerged for 72 h in a 0.3 mg/mL lectin solution were rinsed with distilled water and transferred to another vessel filled with filtered tap water. The hatching of larvae was assessed after 24 and 48 h.

Evaluation of bacteria population in ovicidal assays medium
Fresh and stored eggs were incubated with WSMoL at 0.1 and 0.3 mg/mL, respectively. After 144 (fresh eggs) or 72 h (stored eggs), the media (50 mL) from treatments or controls were smeared on petri dishes containing nutrient agar. The plates were incubated at 37uC for 16 h. After, the number of bacterial colony forming units (CFU) was determined.

Visualization of embryos in fresh and stored eggs from ovicidal assays
Fresh and stored eggs were incubated with WSMoL at 0.1 and 0.3 mg/mL, respectively. After 144 h (fresh) or 72 h (stored), the eggs were placed in solution of 5% sodium hypochlorite until all the chorion had dissolved, leaving the vitelline membrane intact [38]. The eggs were then rinsed with distilled water to prevent complete dissolution by sodium hypoclorite and visualized in a Leica KL300 stereomicroscope (Leica Microsystems, Wetzlar, Germany). Fresh eggs incubated with water and stored eggs not incubated with any solution were also observed.

Statistical analysis
Standard deviations (s.d.) were calculated using GraphPad Prism version 4.0 for Windows (GraphPad Software, San Diego, California, USA) and data were expressed as a mean of replicates 6 s.d. Significant differences between treatment groups were analysed by Student's t-test (significance at p,0.05) using Origin 6.0 program. The effective concentrations required to reduce the hatching of A. aegypti eggs by 50% and 99% (EC 50 and EC 99 ) in 72 h were calculated by probit analysis with a reliability interval of 95% (degrees of freedom of 5, 4 and 4 for tests with seed extract, 0-60 protein fraction and WSMoL, respectively) using the computer software IBM SPSS Statistics (IBM Corporation, New York, USA).

Results
In seed extract, protein concentration was 4.1 mg/mL and specific hemagglutinating activity was 15. In 0-60 protein fraction, protein concentration was 21.0 mg/mL and specific hemagglutinating activity was 97. No precipitate formation was observed after addition of 0-60 protein fraction to acidified barium chloride solution, revealing that no residual ammonium sulphate remained in the sample. WSMoL was isolated by chitin chromatography and was the most hemagglutinating preparation (specific hemagglutinating activity of 2,915). The results from Mohr's method did not reveal the presence of chloride ions in solution, indicating absence of residual sodium chloride content. Carbohydrate contents in seed extract, 0-60 protein fraction were 0.2 and 0.008 mg/mL, respectively and no detected in WSMoL.
The effects of M. oleifera seed preparations on A. aegypti oviposition are shown in Fig. 2A. The difference between the amount of eggs deposited in seed extract and control vessels was not significant (p.0.05), showing that this preparation was not able to attract or repel A. aegypti females. Similarly to the results found for seed extract, A. aegypti gravid females did not show (p.0.05) preference or rejection for vessels containing the 0-60 protein fraction. The number of eggs laid in vessels containing WSMoL was significantly (p,0.05) higher than that laid in control vessels, showing that the lectin exerts an oviposition-stimulant activity.
Volatile compounds were not detected in WSMoL preparation by dynamic headspace analysis since chromatograms from GC-MS did not reveal the presence of any such compound.
The effect of M. oleifera preparations on A. aegypti eggs from oviposition assay (fresh eggs) was evaluated aiming at determining if the hatchability of eggs laid on lectin solution would be affected. Fig. 2B shows that hatching rates of fresh eggs from seed extract, 0-60 protein fraction and WSMoL assays at concentration of 0.1 mg/mL were 45%, 20% and 55%, respectively. Significant reductions (p,0.05) in hatching rate of fresh eggs were observed after 144-h incubation with seed extract, 0-60 protein fraction and WSMoL in comparison with their respective controls.
The hatching rate of stored eggs was also reduced after treatment with seed extract, 0-60 protein fraction and WSMoL in a dose-dependent manner (Fig. 3). The values of EC 50 are shown in Table 1. When eggs submerged for 72 h in WSMoL at EC99 (0.3 mg/mL) were transferred to medium containing only tap water, the hatching rate was zero after 24 and 48 h. The absence of dead larvae in WSMoL solutions at 0.03, 0.05, 0.08, 0.1, 0.13, 0.15 mg/mL and no hatching of eggs treated with WSMoL at EC 99 reflect the ovicidal, not the larvicidal activity of lectin.
The numbers of CFU from ovicidal assays using fresh and stored eggs incubated with WSMoL were 1.46103628 and 1.36103673 CFU/mL, respectively. Media from controls of assays with fresh and stored eggs presented 1.561036135 and 1.36103694 CFU/mL, respectively.
The visualization on stereomicroscope of fresh eggs deposited in distilled water (control) or WSMoL (0.1 mg/mL) and maintained for 72 h in these same solutions revealed the presence of embryo head inside eggs from control treatment ( Figure 4A), but the embryo could not be visualized through the vitelline membrane in eggs from WSMoL treatment ( Figure 4B). Embryos were visualized in stored eggs incubated with WSMoL for 72 h and from control ( Figure 4C and 4D).

Discussion
The results obtained for WSMoL isolation were similar to those obtained by the protocol previously described by Coelho et al. [9]. The lower values of specific hemagglutinating activity in seed extract and 0-60 protein fraction, in comparison with isolated lectin, indicate the lowest concentration of WSMoL. The measurement of the biological activity of a protein is essential to assure that it is active before determination of a biological activity. In lectinology, the hemagglutinating assay is the classic tool to assess the carbohydrate-binding property of a lectin, making sure that it is active. Increased specific hemagglutinating activity reveals lectin concentration and purification [39].
Ammonium sulphate precipitation is a rapid and inexpensive method broadly used to concentrate proteins. This salt does not affect structure and function, and can be easily removed from the protein solution by exhaustive dialysis [9][10][11]30,34,40]. The absence of precipitate species after treatment of 0-60 protein fraction with acidified barium chloride solution proved the absence of residual ammonium sulphate in this preparation.
The results from oviposition assays revealed that WSMoL at 0.1 mg/mL with specific hemagglutinating of 2,915 acted as a chemical cue for A. aegypti gravid females, eliciting increased oviposition response. The absence of oviposition-stimulant activity in seed extract and 0-60 protein fraction was probably due to the lowest specific hemagglutinating activity of these preparations. To the best of our knowledge, there are no reports of oviposition deterrent, attractive or stimulant response from mosquitoes induced by plant lectins. The 0.1 mg/mL (or 100 ppm) concentration was selected, since this value is often used in oviposition bioassays [18,41,42].
Prabhu et al. [43] reported that methanolic extract from M. oleifera seeds (0.5, 1.0 and 2.0 mg/cm2) repelled Anopheles stephensi. The authors observed a decrease in number of bites in arms of human volunteers treated with the extract. The fact that the seed extract used here did not exert repellent activity reveals that repellent compounds were not extracted in water or that, if present at all, concentrations were below the detection threshold by females.
Oviposition-stimulant activity of WSMoL can be due to gustatory stimuli, since non-volatile chemicals such as proteins are perceived by gustatory system of insects [44]. The stimulus in oviposition can be unchained by WSMoL adsorption onto gustatory sensillas of A. aegypti female, as reported in a study on the detection of sex pheromones and protein kairomones by Glossina spp. and Diadromus pulchellus, respectively [45,46]. Volatile compounds were not detected by dynamic headspace analysis in WSMoL preparation indicating that, if present, they occurred in trace amounts. Olfactory stimuli by volatile compounds were described for selection of oviposition sites by Culex quinquefasciatus, A. aegypti and Aedes triseriatus [47].
WSMoL from chitin column was dialysed against distilled water aiming to eliminate acetic acid used in elution as well as residues of 0.15 M NaCl (0.85%) used in washing steps of chromatography. TianFu et al. [48] reported that acetic acid (0.001 mg/L) acted as an oviposition attractant to Aedes albopictus gravid females. In the present study, GC-MS analysis did not identify acetic acid in WSMoL. Thus, the effect of lectin preparation was not due to contamination by this compound. Chloride ions were not detected by Mohr's method in WSMoL, indicating that the ovipositionstimulant effect of lectin cannot be linked to salt contamination. Also, Navarro et al. [32] demonstrated that NaCl at 0 to 5% concentrations did not interfere on A. aegypti oviposition.
Frings and Hamrum [49] reported that sugars can be detected through contact receptors present in labella of A. aegypti mosquito. Thus, M. oleifera preparations were evaluated for presence of these compounds. The results reveal that carbohydrates from M. oleifera seed preparations were not attractive components, since WSMoL, which showed the highest oviposition rate, was free of carbohydrates. WSMoL can be included in the group of non-volatile proteins with oviposition-stimulant activity on A. aegypti.
Since the embryogenesis of A. aegypti eggs is completed between 77-96 h and acquisition of egg resistance occurs 48 h after postoviposition [25,50] the effect on hatchability of eggs from oviposition assay was assessed. The hatching rates were determined after 144 h to guarantee that the eggs had a reasonable time to complete embryonic development. The results showed that besides stimulating oviposition by females, WSMoL at 0.1 mg/mL was also able to impair hatching, an advantage if it will be used in ovitraps.
The effect of WSMoL preparations on stored eggs was also evaluated during an incubation period of 72 h. Incubation periods between 72 and 120 h have been used to assess ovicidal activity on eggs which have already completed their embryogenesis [51][52][53][54][55][56]. The detection of lowest EC 50 value for WSMoL suggests that the lectin is an active principle in seed extract and 0-60 protein fraction against stored eggs, although a proportional correlation between increase in specific hemagglutinating activity and ovicidal effect (decrease in EC 50 ) was not observed. The absence of hatching of stored eggs treated with WSMoL at 0.3 mg/mL (EC 99 ) after transfer to medium without lectin indicates that embryos within the eggs were killed by WSMoL. The absence of contaminant traces of acetic acid, sodium chloride and ammonium sulphate in 0-60 protein fraction and WSMoL assure that the adverse effects of these preparations on hatching rates were not due to residues of these chemicals.
It has been reported that the presence of bacteria is a hatchingstimulant factor for A. aegypti eggs and in the absence of bacteria the hatchability is lower than 5% [57]. Since it is known that WSMoL exerts antibacterial effect [29], it was evaluated whether the lower hatching rate could have been also a consequence of reduction in bacteria population. The numbers of CFU/mL in media from ovicidal assays using WSMoL was not lower than that detected in media from control assays. This result reveals that, in this case, lower hatching rates in WSMoL treatment were not linked to decrease in bacterial population. So, it is possible to conclude that impairment of egg hatching by WSMoL was due to embryo death.
It was also evaluated if the sensitiveness of freshly laid eggs to M. oleifera preparations was different from that of stored eggs. According to probit analysis of results from ovicidal assays using stored eggs, the egg hatching rates after treatment with seed extract, 0-60 protein fraction and WSMoL at concentration of 0.1 mg/mL would be 65%, 54% and 50%, respectively. Comparison of data from ovicidal assays using fresh and stored eggs and protein concentration of 0.1 mg/mL reveals that stored eggs were less sensitive to seed extract and 0-60 protein fraction, while WSMoL reduced similarly the hatching rates of fresh and stored eggs. These findings indicate the presence of other ovicidal agents in seed extract and 0-60 protein fraction that were eliminated in the WSMoL isolation procedure. Ferreira et al. [58] did not detect ovicidal activity from aqueous extract from dehulled M. oleifera seeds (5.2 mg/mL) using stored eggs. The authors attributed this fact to the high resistance of eggs. Differently, WSMoL showed similar ovicidal activity against fresh and stored eggs, indicating that the completion of embryogenesis and egg maturation processes was not accompanied by reduction in sensitiveness to lectin. This is an interesting and advantageous property concerning A. aegypti control strategies targeting the eggs, the most resistant stage of mosquito life cycle.
The EC 50 of WSMoL on stored eggs was lower than values determined for essential oils from Juniperus macropoda, Zingiber officinale and Pimpinella anisum, whose EC 50 ranged from 0.15 to 0.18 mg/mL and leaf extracts of Eclipta alba, whose EC 50 ranged from 0.10 to 0.20 mg/mL [27,37]. The ovicidal activity of WSMoL was compared with those from essential oils and plant extracts because there are no previous reports on ovicidal activity of lectins on insects.
Ovicidal compounds are able to interrupt embryo development, impair the survival of larva inside the egg or block egg hatching [27]. Fresh eggs from control treatment showed embryogenesis in progress while impairment of embryo development was detected in fresh eggs treated with WSMoL, reflecting the ovicidal activity.
Chitin is present in oocytes, eggshell and eggs of A. aegypti and this polysaccharide has an important role in egg viability [50]. The ovicidal activity of WSMoL may be linked to binding of lectin to chitin present in eggshells, blocking the hatching process by promoting disruption of this structure. Also, the fact that stored  eggs transferred to water after incubation with WSMoL for 72 h did not hatch reveals that embryos, observed inside eggs using a stereomicroscope, are dead. It is possible that WSMoL gets inside the egg, interfering in embryo development through the same mechanisms which kill A. aegypti larvae. The previously described larvicidal activity of WSMoL, combined with its oviposition-stimulant and ovicidal activities described here make this lectin a very interesting candidate for use in integrated mosquito control programs. The WSMoL concentration in which oviposition-stimulant (0.1 mg/mL) and ovicidal (EC 50 of 0.1 mg/mL) activities were detected was lower than that in which the lectin promotes larvicidal activity (LC 50 of 0.197 mg/ mL). This finding is interesting, because if WSMoL is applied in an A. aegypti breeding site aiming at killing the larvae, it will also attract gravid females and will impair the hatching of new eggs laid by females.
In summary, WSMoL is a sustainable and environmentally friendly alternative for A. aegypti control, since one same concentration of WSMoL acts as a chemical stimulant cue for ovipositing females and ovicidal agent at the same time. Further studies will be performed on oviposition response of gravid females under field conditions as well as on the development of effective formulations for WSMoL and its large-scale production based on genetic engineering techniques.