Stress-Mediated Responses of Aedes aegypti (Diptera: Culicidae) Larvae When Exposed to Metarhizium brunneum (Hypocreales: Clavicipitaceae) and Toxorhynchites brevipalpis (Diptera: Culicidae)

Abstract Aedes aegypti mosquitoes are capable of vectoring a wide range of diseases including dengue, yellow fever, and Zika viruses, with approximately half of the worlds’ population at risk from such diseases. Development of combined predator–parasite treatments for the control of larvae consistently demonstrates increased efficacy over single-agent treatments, however, the mechanism behind the interaction remains unknown. Treatments using the natural predator Toxorhynchites brevipalpis and the entomopathogenic fungus Metarhizium brunneum were applied in the laboratory against Ae. aegypti larvae as both individual and combined treatments to determine the levels of interaction between control strategies. Parallel experiments involved the removal of larvae from test arenas at set intervals during the course of the trial to record whole body caspase and phenoloxidase activities. This was measured via luminometric assay to measure larval stress factors underlying the interactions. Combined Metarhizium and Toxorhynchites treatments were seen to drastically reduce lethal times as compared to individual treatments. This was accompanied by increased phenoloxidase and caspase activities in combination treatments after 18 h (p < 0.001). The sharp increases in caspase and phenoloxidase activities suggest that combined treatments act to increase stress factor responses in the larvae that result in rapid mortality above that of either control agent individually. This work concludes that the underlying mechanism for increased lethality in combined parasite–predator treatments may be related to additive stress factors induced within the target host larvae.

including, coleoptera, diptera, hemiptera, and odonata (Shaalan et al. 2009). These have the advantage that they can naturally proliferate within the environment, offering potential sustained background control, albeit with a reduced efficacy as compared to insecticidal applications. Of the entomopathogenic biological control agents available, entomopathogenic fungi are of significant interest for commercial development. Several strains of Metarhizium brunneum and M. anisopliae (Hypocreales: Clavivipitaceae) have been developed that effectively kill a wide range of arthropod hosts, including those of relevance to agro-forestry and vectors of human and animal disease (Scholte et al. 2007, Brunner-Mendoza et al. 2019. Both species show much promise for vector control as they, unlike bacterial pathogens, can infect all developmental stages (adults, eggs, larvae, pupae) of the mosquito (Alkhaibari et al. 2017, Carolino et al. 2019, Choi et al. 2020, de Paula et al. 2021. Another advantage of EPF is that they can work in concert with aquatic natural predators, with the latter usually being more tolerant of Metarhizium than Aedes larvae (Alkhaibari et al. 2018, Belevich et al. 2018). Recently, it was shown that M. brunneum and the natural predator Toxorhynchites brevipalpis, applied as simultaneous control agents, significantly increase mortality of Ae. aegypti larvae within a shorter time-frame than either agent acting alone (Alkhaibari et al. 2018). The underlying mechanism for this interaction remains to be elucidated, but may be useful in facilitating significantly reduced application requirements for the fungal biocontrol agents, especially given residual natural predator populations within the environment.
Insect stress responses are known to alter immunological pathways through redirection of resources away from immune systems; conserving resources for physiologically demanding activities (Adamo 2014). This effect can increase insect susceptibility to disease, thereby offering a potential route for improved insecticidal control. Earlier work has shown that M. brunneum conidia do not adhere to the larval cuticle, rather, the spores are ingested, and the spore bound protease Pr1 induced stress which leads to larval mortality , Greenfield et al. 2015. This response may in part be explained by the pro-inflammatory state induced by insect stress responses, while ostensibly likely to enhance early immune response (Adamo 2017), this state may facilitate apoptotic cell death, leading to mortality, as described in Butt et al. 2013. Aquatic invertebrate predator species are known to cause a range of direct and indirect effects, including stress amplification in prey species such as mosquito larvae, for which shortened lifespans are an indirect stress-related consequence (Cinel et al. 2020, Alomar andAlto, 2021). Introduction of additional stress factors, in the form of natural predators may, therefore, serve to amplify stress responses of mosquito larvae leading to rapid mortality. This may explain why laboratory application rates of M. brunneum can be significantly reduced in the presence of Tx. brevipalpis, offering potential cost-reductions relating to entomopathogen applications, alongside significantly reduced nontarget effects Garrido-Jurado et al. 2016). Caspases are excellent stress markers, their levels are elevated in mosquito larvae, and other aquatic invertebrates exposed to EPF and their metabolites (Garrido-Jurado et al. 2016. Caspases are cysteine proteases that play a pivotal role in regulating inflammation and apoptosis and their levels can be raised before there is manifestation of damage . Injury triggers several defense reactions, most notable is the activation of prophenoloxidase to its active form phenoloxidase, a key enzyme that leads to the formation of melanin at wound sites and around invading microbes in the hemolymph (Lu et al. 2014;Butt et al. 2016). Melanin will inhibit growth of invading microbes, but its constant production may have fitness costs, reducing egg production, and shortening the mosquito's lifespan (Ferdig et al. 1993).
The aim of this article was to elucidate upon the mechanisms driving interactions between M. brunneum and Tx. brevipalpis in relation to increased pathogenicity against Ae. aegypti larvae. Improved understanding of these entomopathogen-predator interactions within target species will allow for improved modelling, application, and control strategy design within the natural environment, both for entomopathogenic fungi and natural predator applications

Mosquito Larvae
The eggs of Ae. aegypti (strain: AeAe) and Tx. brevipalpis were obtained from the London School of Hygiene and Tropical Medicine (LSHTM). Ae. aegypti were reared to fourth instar using crushed guinea pig pellets (Pets at Home, UK) in a controlled temperature room at 25 ± 2°C, 65% RH, and a photoperiod of 12:12 (L:D) h. Tx. brevipalpis larvae were reared to fourth instar in the same controlled temperature room. These were fed on a separate colony of size appropriate Ae. aegypti larvae, while being fed on size appropriate Ae. Aegypti larvae; Ae. aegypti feed stock was at the same instar as the Tx. Brevipalpis larvae.

Fungal Production
M. brunneum isolate ARSEF 4556, identified as an effective pathogen of Ae. aegypti , Greenfield et al. 2015) was produced and maintained on broken basmati rice (Ansari and Butt 2011). Conidial viability was determined using the plate count technique after 18 h incubation (Vega et al. 2009). Only batches with viability above 90% were used for further experimentation. The concentration of conidia was determined using an improved Neubauer haemocytometer and diluted to the desired concentration using 0.03% aqueous Tween 80.
Susceptibility of Ae. aegypti and Tx. brevipalpis larvae to M. brunneum Larvae of Tx. brevipalpis and Ae. aegypti were tested for individual susceptibility to M. brunneum prior to testing as combined treatments. Protocols were modified from that in Greenfield et al. (2015); 15 Ae. aegypti larvae were assessed in 250 ml round plastic tubs (diameter 92 mm) using 150 ml of tap water, 10 Tx. brevipalpis larvae were assessed in 1.5 liters. plastic containers (230 × 230 mm) in 1 liter-tap water. Larvae were exposed to three different concentrations of M. brunneum (10 5 , 10 6 , 10 7 conidia ml −1 ) in two formulations; 'dry conidia', consisting of a dried spores applied to the surface of the water without adjuvant; and 'wet conidia', whereby conidia were suspended in 0.03% (v/v) aqueous Tween 80 (Sigma Aldrich, UK) before being applied at the water's surface. 'Dry' conidial applications will remain at the surface of the water for an extended period, whereas 'wet' conidia immediately suspend within the water column. Mortality was recorded each 24 h period for duration of the trials and individuals' status was determined as 'dead' via physiological stimulation. Trials were conducted in triplicate and repeated three times as biological replicates for each of the treatments. All experiments were conducted in a controlled temperature room at 25 ± 2°C, with a photoperiod of 14:10 (L:D) h.

Tx. brevipalpis and M. brunneum
Bioassays were conducted according to the protocol set for Aedes larvae during the initial susceptibility assays within this study. Assays for combined treatment were conducted at concentrations of 1 × 10 5 , 1 × 10 6 , and 1x10 7 viable conidia mL -1 , both with and without the introduction of 1 Tx. brevipalpis larvae. Control treatments were carried out using 0.03 % aqueous Tween 80 in lieu of conidial suspension, both with and without the addition of a Toxorhynchites larva. Mortality was recorded every 24 h throughout the duration of the experiment, with larval status determined via physiological stimulation. Aedes larvae that were no longer present within the test arena were counted as consumed by the Toxorhynchites larva. All experiments were conducted in a controlled temperature room at 25 ± 2°C, with photoperiod of 14:10 (L:D) h. As with previous assays, all experiments were conducted in triplicate and repeated three times overall.
The Spatio-chemical Effects of Tx. brevipalpiss Additional assays were conducted to determine whether Aedes mortality seen in initial bioassays was influenced by chemicals released by Toxorhynchites, or through direct physical exposure; either through feeding related damages inflicted by Tx. brevipalpis or through behavioural response to constant predator evasion. For this, 250 ml plastic containers (diameter: 92 mm) were modified with a mesh barrier to separate Aedes and Toxorhynchites larvae. Experiments were otherwise carried out according to the protocol established in the previous bioassays; using concentrations of 1 × 10 6 , and 1 × 10 7 viable conidia ml −1 . Mortality was recorded every 24 h until the conclusion of the experiment, larval status was determined through physiological stimulation. All experiments were conducted in a controlled temperature room at 25 ± 2°C, with a photoperiod of 14:10 (L:D) h. As with previous assays, all experiments were conducted in triplicate and repeated three times overall.

Effects of Tx. brevipalpis Density on the Survival of Ae. aegypti Larvae When Treated With M. brunneum
Bioassays were also completed to determine the effects Toxorhynchites population density may have on Aedes mortality using combined applications. In these, larger square plastic tubs (Width 260 mm), each containing 1-liter water and 100 Aedes larvae were inoculated with M. brunneum at 1 × 10 6 conidia ml −1 . 1, 5, 10, or 20 Toxorhynchites larvae were introduced in combination with M. brunneum. An additional treatment consisting of 1 × 10 6 conidia ml −1 was completed to demonstrate control efficacy using M. brunneum only. Control experiments used an application of 0.03% Tween 80 only. Experimental subsets conducted in triplicate were set up according to the reduced Latin square randomization tables described in WHO 2013. Mortality was recorded every 24 h until the conclusion of the experiment, larval status was determined through physiological stimulation. Aedes larvae that were no longer present within the test arena were counted as consumed by the Toxorhynchites larva. All experiments were conducted in a controlled temperature room at 25 ± 2°C, with a photoperiod of 14:10 (L:D) h. As with previous assays, all experiments were conducted in triplicate and repeated three times overall.

Caspase Activity
Activity of caspases 2, 3, 7, and 8 was assessed over time in whole body homogenates of Aedes larvae (n = 10 per treatment) exposed to M. Metarhizium and Tx. brevipalpis using a BioTek Synergy H1 hybrid reader (Agilent, CA) in three replicate wells for each sample. All samples were exposed to control assays as per methodology described in Section 2.3. Due to rapid mortality, insects were assayed at the lower dose (1 × 10 6 conidia ml −1 ) and removed for assay at 0, 5, 10, and 18 h post inoculation (PI). Control Aedes larvae and those exposed to M. brunneum and Tx. brevipalpis were also assayed.
Aedes larvae were removed from their respective treatments and frozen under liquid nitrogen at each specified time-point before homogenization using a micropestle and mortar. Resuspension of homogenates in 500 μL 0.5% triton lysis buffer (Tris 20 mM, NaCl 100 mM, EDTA 500 mM, 0.5% Triton X-100) was followed by gentle agitation before being incubated on ice for 10 min. Homogenates were centrifuged at 14,000 g for 10 min and 35 μL aliquots of the resultant supernatant added to 4 replicate wells in a white walled 96-well microtiter plate (Grenier Bio-one). Luminometric assays for each of Caspases-2, 3/7, and 8 activity were then performed in accordance with manufacturer protocol using Caspase Glo 2, Caspase Glo 3-7, and Caspase Glo 8 assay kits (Promega) through addition of 35 μL of Caspase Glo reagent to each supernatant aliquot. Microtiter plates were agitated gently for 10 s at 180 rpm before incubating at 25°C. Endpoint luminescence was measured after 1 h.

Phenoloxidase Activity
Phenoloxidase (PO) activity was monitored in total larval homogenates from groups of 15 larvae exposed to combined Metarhizium and Toxorhynchites treatments as described in Butt et al. 2013. Experiments were conducted, as per the caspase assessments described above, throughout a time course study PI (0 h, 10 min, 20 min, 30 min, 40 min, 50 min, 60 min, 6 h, 12 h, 18h, and 24 h). Larvae were removed at each interval and frozen under liquid nitrogen. 15 Larvae were homogenized in 200 μL of phosphate buffer saline (PBS, pH 7.8) in a 1.5 ml microfuge tube, per replicate. Homogenate was made up to 800 μL with PBS and centrifuged at 3,000 g for 20 min. Supernatants were removed and stored at −80°C until required. 5 Replicates were in parallel, the experiment was independently repeated three times. L-DOPA (3, 4-dihydroxy-L-phenyl-alanine, Sigma) was the substrate used to determine PO activity, which was expressed as changes in absorbance/min/mg protein . 20 μL of homogenate was added to 180 μL of L-DOPA (4 mg mL −1 ) in a 96-well plate and incubated for 30 min at room temperature. Absorbance was measured at 490 nm at each time point. Homogenate protein contents were determined using Bradford's method; all assays were made with Biotek Synergy H1 plate reader.

Statistical Analyses
Survival rates of 1) Ae. aegypti and Tx. brevipalpis larvae exposed to the different concentrations of M. brunneum ARSEF 4556 conidia, 2) Ae. aegypti larvae exposed to three concentrations of fungal treatment in presence and absence of Tx. brevipalpis, 3) Ae. aegypti larvae exposed to M. brunneum at 1 × 10 6 and 1 × 10 7 conidia ml −1 with or without Tx. brevipalpis larvae, and 4) Ae. aegypti larvae exposed to M. brunneum at 1 × 10 6 conidia ml −1 with varied ratios of Tx. brevipalpis were analysed using Cox regression, with the resulting hazard ratio values used to assess mortality rates (Greenfield et al. 2015). Survival curves were generated via Kaplan−Meier survival analysis, with pairwise comparisons performed using the log-rank tests (Ansari et al. 2011). LT 50 and LC 50 values were estimated for each of the insect species by fitting probit regression models to the quantal response data. Log transformations were applied to the dosage and time independent variables, with an additional parameter fitted to the LC 50 model to account for the natural mortality rates of Toxorhynchites larvae under control conditions. Differences in LT 50 and LC 50 were compared by ANOVA and significance levels adjusted where appropriate by application of Tukey's multiple comparisons post-test. Biochemical data sets were analysed through two-way ANOVA with Bonferroni's post-hoc -tests. Data sets for both caspase and phenoloxidase analyses were evaluated through two-way ANOVA with Bonferroni's post-tests. Data were log 10 transformed to meet ANOVA assumptions of homogeneity of variance. All analyses were carried out using SPSS v22.0 (IMB Corporation, USA) and GraphPad Prism v5.0 (Graphpad Software, USA).

Results
Susceptibility of Ae. aegypti and Tx. brevipalpis Larvae to M. brunneum Both Ae. aegypti and Tx. brevipalpis were susceptible to infection with both wet and dry M. brunneum conidia (ARSEF 4556). In both wet and dry applications, Aedes mortality was significantly higher than control samples at 1 × 10 6 conidia ml −1 and 1 × 10 7 conidia ml −1 (p < 0.001). Applications at 1 × 10 5 conidia ml −1 did not cause mortality significantly above that of the control samples (p = 0.189) (Fig. 1B and  D). Toxorhynchites larvae demonstrate similar susceptibilities ( Fig. 1A and C) excepting that no significant mortality was observed for dry applications at 1 × 10 6 conidia ml −1 (Fig. 1C; Table 1). No significant differences in LT 50 were observed between 'wet' and 'dry' spore application (Table 2) for either Tx. brevipalpis or Ae. aegypti. Between the two species, however, Tx. brevipalpis was seen to have a lower susceptibility to M. brunneum application, demonstrated by the higher LT 50 values recorded as compared to Ae. aegypti larvae (Table 2).
In both Ae. aegypti and Tx. brevipalpis, no significant differences in LC 50 values were recorded between wet and dry conidial applications (Table 2). In wet applications, fungal applications resulted in higher LC 50 values for Tx. brevipalpis than Ae. aegypti, dry applications produced no significant differences between the LC 50 values for Tx. brevipalpis and Ae. aegypti.

Ae. aegypti Survival Postexposure to Fungal Conidia With or Without Toxorhynchites Larva
LT 50 values were estimated for all assays (Table 3). Significant differences were found between all treatments except Ae. aegypti treated with 1 × 10 5 conidia ml −1 either with or without the addition of Tx. brevipalpis larvae (Fig. 2). Ae. aegypti larvae were highly susceptible to M. brunneum at concentrations of 1 × 10 6 conidia ml −1 and 1 × 10 7 conidia ml −1 . In both cases mortality was significantly higher in larvae exposed to M. brunneum than in untreated controls at (p < 0.01). Likewise, Ae. aegypti larvae exposed to a Tx. brevipalpis larva suffered significant mortality as compared to controls, reaching 90% mortality after 168 h (p < 0.001). The rate of Aedes mortality caused by Tx. brevipalpis was similar to that of M. brunneum treatments of 1 × 10 6 and 1 × 10 7 conidia ml −1 (p = 0.187 & p = 0.678 respectively). When Ae. aegypti larvae were treated with combinations of M. brunneum and Tx. brevipalpis; mean survival times were significantly lower as compared other treatments and controls (p < 0.001). Combined treatments with fungal concentrations of 1 × 10 6 and 1 × 10 7 conidia ml −1 reached 96.3% and 100% mortality, respectively, after just 24 h. Treatments consisting of Tx. brevipalpis larvae applied in combination with M. brunneum at 1 × 10 5 conidia ml −1 resulted in Aedes mortality at similar levels to treatments consisting of Tx. brevipalpis additions only (p = 1.000), however, both of these resulted in significantly higher mortality than control experiments (p < 0.001).

Assessment of the Spatio-chemical Effects of Tx. brevipalpis Larvae on Ae. aegypti Survival
During experiments in which Toxorhynchites larvae were physically separated from the Aedes larvae, no spatio-chemical effects were observed that would suggest chemical markers were responsible for increased lethality in combined treatments (Fig. 3). Treatment efficacy was seen to be similar for those Aedes larvae : Survival curves of Aedes aegypti and Toxorhynchites brevipalpis exposed to different concentrations of 'wet and dry' formulated Metarhizium brunneum conidia (ARSEF 4556). Percentage cumulative survival of Tx. brevipalpis exposed 'wet' (A) and 'dry' (C) conidia and Ae. aegypti exposed to the same 'wet' (B) and 'dry' (D) formulations of M. brunneum using three different concentrations (10 5 , 10 6 , 10 7 conidia ml −1 ) for 7 d. Controls were exposed to Tween 80 (0.03%) only. Error is represented as 95% CI. Key: Mb -Metarhizium brunneum. exposed to combined Toxorhynchites and Metarhizium treatments and those Aedes larvae that were treated with Metarhizium only (p < 0.001). No significant difference in LT 50 values was recorded for combined or individual treatments at either 1 × 10 6 conidia ml −1 (F (2,18) = 2.043 p = 0.893) or 1 × 10 7 conidia ml −1 (F (2,18) = 3.019 p = 0.657). All combined treatments were significantly different to untreated controls (p < 0.001) and controls with 1 physically separated Toxorhynchites larva (p < 0.001).
During experiments in which the Toxorhynchites were physically separated from the Aedes larvae, mortality rates were the same for those Aedes larvae exposed to combined Toxorhynchites (without barrier) and Metarhizium treatments, and those Aedes larvae that were treated with Metarhizium with one physically separated Toxorhynchites larva (p < 0.001).

Effect of Tx. brevipalpis Density on Aedes Larvae Survival in Treatments
Toxorhynchites density, relative to Aedes abundance, was seen to have an impact on survival (Fig. 4). Treatment densities comprising 1(Tx):10(Ae) larvae resulted in similar mortality levels to those recorded during previous experiments. 97.8% mortality was recorded within 24 h, significantly higher than either untreated controls or those treated solely with 1 × 10 6 conidia ml −1 (p < 0.001). When LT 50 estimates were compared between treatment groups, Toxorhynchites: Aedes densities of 1:5, 1:10, & 1:20 all produced LT 50 values significantly lower than the Metarhizium only positive controls (F (5,45) = 44.598 p = <0.001). Only a ratio of 1(Tx):100(Ae) resulted in a significantly higher LT 50 as compared to other treatment densities, although in comparison to the Metarhizium only treatments, the LT 50 value remained significantly lower (p < 0.001). Cannibalism amongst Tx. brevipalpis was only seen to occur after consumption of all Ae. aegypti larvae present in treatments.

Caspase Activity
Overall caspase activity for caspases 2, 3/7, and 8 was consistently higher in Ae. aegypti larvae exposed to combined M. brunneum and Tx. brevipalpis treatments (F (3,81) = 343.15, p < 0.001). These effects were seen to be most prominent for caspases 3/7 and 8 ( Fig. 5A-C). Groups individually treated with M. brunneum or Tx. brevipalpis larvae did not express caspase activities significantly different to those in control assays (p = 0.994 and p = 0.068 respectively). Within the treatment groups, Ae. aegypti larvae exposed to Toxorhynchites as a sole control agent demonstrated the lowest caspase activity response after 18 h, followed by those treated with M. brunneum only.

Phenoloxidase Activity
Phenoloxidase activity was not significantly modified by the combined treatments including M. brunneum and Tx. brevipalpis over the course of the experiment until 18 h PI, concurrent with death (F (3,81) = 168.241, p = <0.001). In individual treatments, no significant differences were detected in comparison to control samples (Fig. 6).
is exacerbated to a significant degree when combination treatments are applied. These combination treatments elicit a clear caspase and phenoloxidase cascade, implying predator-associated stress factors are key components in the control agent interaction. While both species were seen to be susceptible to M. brunneum, 'wet' applications were seen to affect Tx. brevipalpis to a lesser degree than 'dry' spore inoculation. Counter to this, the same 'wet' applications were seen to elicit a greater response in Ae. aegypti larvae. This is likely due to behavior, Toxorhynchites species predominantly spend their time at the water surface, where they will ambush nearby larvae of a similar size. Aedes larvae, by contrast, are preferential substrate feeders, often moving down in the water column to feed off of settled particulate matter (Merritt et al. 1992). Given that wet applications of M. brunneum sediment quickly, much of the available inoculum would be removed from Toxorhynchites preferential level within the water column, simultaneously, this inoculum would readily aggregate in preferential feeding areas for Aedes larvae. Such considerations to formulation, therefore, must be considered in systems whereby surface dwelling beneficials are present in treatment areas.
The mode of pathogenesis of Metarhizium in terrestrial applications is well understood to be through cuticular invasion followed by colonisation of the haemocoel  alongside fungal metabolite induced pathogenic activities such as destruxin release (Crisan 1971, Lacey et al. 1988. It had been assumed that the same processes were also the primary mode of pathogenesis in the aquatic environment (Riba et al. 1986, Lacey et al. 1988, and Bukhari et al. 2010, however, Butt et al. (2013) demonstrated mortality can be largely mediated through protease induced stress, leading to apoptotic cell death, and eventually organismal death. While previous studies have focused on increasing fungal pathogenicity Roberts 1982, Shah et al. 2005, and Wang and St. Leger 2007) and viability (Daoust and Roberts 1983), few, if any, have focused on increasing external stress factors. Predator−prey interactions often dominate confined aquatic environments, with organisms under environmental stress shown to be less long-lived, smaller, and often less successful reproductively (Alomar and Alto, 2021). By creating a 'landscape of fear', predators could potentially be used to influence prey behavior and physiology, thereby increasing biological control potential and reducing vector capacity. This study shows for the first time that stress factors within the aquatic environment can be increased using predatory species, resulting in increased lethality beyond the capabilities of a single control agent such as M. brunneum.
Mosquito larvae have been seen to be effectively controlled with several strains of M. brunneum as singular agent (Bukhari et al. 2010), albeit with significant differences in control rates based Caspase activity for caspases 2 (A), 3/7 (B), and 8 (C) in total body homogenates of Aedes aegypti larvae exposed to Metarhizium brunneum and Toxorhynchites brevipalpis. Caspase activities in Ae. aegypti larvae under treatment conditions utilizing Tx. brevipalpis and M. brunneum as individual and combined treatments. 'Wet' formulated M. brunneum was applied at a concentration of 1 × 10 6 conidia ml −1 ; treatments utilizing Tx. brevipalpis used one larva per replicate. Controls were exposed to Tween 80 (0.03%) applications only. Error is represented as 95% CI. Key: Mb -Metarhizium brunneum; Tx -Toxorhynchites brevipalpis. Fig. 6. Phenoloxidase activity associated with assays combining Metarhizium brunneum and Toxorhynchites brevipalpis over time. Phenoloxidase activity, as an indicator of phenoloxidase cascade initiation, in total body homogenates of Ae. aegypti larvae after exposure to M. brunneum (1 × 10 6 conidia ml −1 ) in the presence of one Tx. brevipalpis larva. Controls were exposed to Tween 80 (0.03%) applications only. Error is represented as 95% CI. Key: Mb -Metarhizium brunneum; Tx -Toxorhynchites brevipalpis. on strain and formulation (Greenfield et al. 2015, Alkhaibari et al. 2017. Such methods require relatively high concentrations of conidia to be applied to cause 100% mortality in less than 48 h. The mortality enhancing effects seen in combined Metarhizium and Toxorhynchites treatment on Aedes larvae corroborates the work of Alkhaibari et al. (2018), while adding to the growing list of efficacy enhancing interactions reported between entomopathogenic fungi and other biocontrol agents including bacteria, entomopathogenic nematodes, and predatory mites (Ansari et al. 2008, Dogan et al. 2017, Imperiali et al. 2017, Wakil et al. 2017. Such effects have the potential to not only reduce biological control application requirements, but also offer a chemical-free approach to such techniques. Although it is generally accepted that stress can increase the host's susceptibility to infection the biochemical pathways have not been well elucidated . It is tempting to speculate that the apoptotic responses in Aedes larvae, previously described in association with Metarhizium, may have been exacerbated by presence of the Tx. brevipalpis larvae, resulting in rapid mortality with significantly lower concentrations of the fungus. Indeed, the caspase assays support this hypothesis. Both initiator (caspases 2 and 8) and effector (caspases 3 and 7) caspase activity increased with time, suggesting a continued increase in stress response that could lead to exacerbated apoptotic cell death as per Butt et al. (2013), eventually leading to death.
The efficacy enhancing interactions between M. brunneum and Tx. brevipalpis have the potential to not only reduce conidial application requirements, but have been shown to significantly accelerate Aedes mortality under laboratory conditions. The experiments described herein demonstrate temporal larvicidal efficacy comparable with, or superior to, conventional chemical pesticides and the biopesticide Bacillus thurungiensis israelensis (Bti) (Bacillales: Bacillaceae) (Kovendan et al. 2011, Mansour et al. 2012, and Araújo et al. 2013. Given that widespread adoption of Metarhizium usage is dependent on the length of time required to kill target invertebrates, increases in mortal rapidity produced through control agent interactions have the potential to improve the outlook for future adoption. Furthermore, M. brunneum and Tx. brevipalpis offer an alternative to Bti and chemical insecticides to which Ae. aegypti and other mosquito vectors have developed resistance (Gan et al. 2021), while reduced application requirements for M. brunneum will reduce the risks to nontarget aquatic invertebrates (Garrido-Jurado et al. 2016).
Although both Metarhizium and Toxorhynchites species could work alone, the combination treatments have many benefits, as outlined above. The limitation is the predator, application of these organisms would be less easy than that of Metarhizium pesticide spraying of environments. Due to the persistence of Toxorhynchites species, and other predators, within the natural environments of Aedes larvae, naturalized populations may reduce the requirements for direct human intervention. Furthermore, human assisted introduction of Toxorhynchites larvae may result in over-abundance of the predators, which are known to become cannibalistic at high densities (Donald et al. 2020, Collins andBlackwell, 2000). Through reliance on natural populations, these effects may be mitigated to some extent, while data accumulated about natural localized populations could be used in tandem with information presented herein to reduce application requirements for Metarhizium.