Simulating immunosuppressive mechanism of Microplitis bicoloratus bracovirus coordinately fights Spodoptera frugiperda

Parasitoid wasps control pests via a precise attack leading to the death of the pest. However, parasitoid larvae exhibit self-protection strategies against bracovirus-induced reactive oxygen species impairment. This has a detrimental effect on pest control. Here, we report a strategy for simulating Microplitis bicoloratus bracovirus using Mix-T dsRNA targeting 14 genes associated with transcription, translation, cell–cell communication, and humoral signaling pathways in the host, and from wasp extracellular superoxide dismutases. We implemented either one-time feeding to the younger instar larvae or spraying once on the corn leaves, to effectively control the invading pest Spodoptera frugiperda. This highlights the conserved principle of “biological pest control,” as elucidated by the triple interaction of parasitoid-bracovirus-host in a cooperation strategy of bracovirus against its pest host.


Introduction
Symbiotic polydnaviruses do not replicate in host cells, making it is impossible to mass-produce them for use in pest control.Symbiotic polydnavirus in hymenopteran wasps suppresses lepidopteran host immune system to assist the development of parasitoids (1).However, the parasitoid also needs sufficient time to complete its development adapting to the increase in reactive oxygen species (ROS) levels triggered by the bracovirus (2).Bracovirus inhibits host immunity at three levels: a) integration into host DNA, directly damaging important host immune genes; b) the viral protein inhibiting transcription of host immune genes and c) translation of host transcriptome to suppress some of the main cellular signaling pathways (3)(4)(5).Meanwhile, the parasitoid needs resources from the host for its development (3,4).These balances are established through interplay between the bracovirus and its symbiotic parasitoid, which complicates the development of strategies for the utility of bracovirus in biological control.Therefore, novel approaches are necessary to direct pest control in the field of biological control.Indeed, host-parasitoid-bracovirus interactions are welldocumented for individual genes or pathways during the process of parasitism.However, their coordinate involvement in the context of these triple interactions and their utility for biological control are not well understood.Although, the direct release of natural enemies is a traditional, conserved, biological strategy, the important aspect is to devise methods of increased efficiency to control agricultural pests using the pest-killing mechanisms of their natural enemies.In such tri-trophic interactions among bracovirus, host, and parasitoid wasps, the often ignored key question is the attack on the host by bracoviruses and parasitoid wasps in an impaired environment triggered by bracovirus for self-protection.The latter is a negative factor reducing the effectivity of biological control using the parasitoid, contrary to the expected quick killing of the pest.The bracovirus triggers the generation of ROS, which is degraded by the extracellular superoxide dismutases (ecSODs) from parasitoid larvae (2).Alteration of ROS homeostasis affects lifespan as shown previously in the yeast, Saccharomyces cerevisiae (6).
Spodoptera frugiperda (Lepidoptera, Noctuidae), an invasive globally polyphagous pest, is a non-native host of the wasp Microplitis bicoloratus, which in turn is the native parasitoid of Spodoptera litura (Lepidoptera, Noctuidae) and carries the symbiotic bracovirus (7).Even in laboratory, M. bicoloratus demonstrates less parasitism towards S. frugiperda, which is a migratory agricultural pest native to North and South America.It was first discovered in Africa (8) and subsequently spread to Europe and Asia (9), especially to Yunnan in China (10)(11)(12).The genomes of S. litura (13) and S. frugiperda (14) and its Sf9 cell line (15) have been sequenced; they have high sequence similarity and these organisms share common signaling pathways, including those involved in transcription, translation, cell communication, and humoral responses, based on our research using Sf9 cells (3,4).Such similarity between the two hosts prompted us to harness effects of Microplitis bicoloratus bracovirus (MbBV) on host gene expression to control S. frugiperda.
However, a simultaneous inhibition of the four major signaling pathways of S. litura by the bracovirus, which controls the congeneric pest, and the utilization of this mechanism has not been reported yet.We hypothesized that eliminating the negative effect of decreased ROS levels caused by parasitoid self-protection would fully simulate a bracoviral attack to control S. frugiperda by targeting four main signaling pathways, resulting in increased ROS levels and thus pest-killing.Recently, RNA interference (RNAi) technology has been widely used in pest management (17)(18)(19)(20), although RNAi efficiency in lepidopteran species, especially in vivo is still controversial in the community (21,22).Many studies have reported the use of dsRNA to down-regulate insect genes through feeding.Recently, dsRNA feeding was used for downregulating genes in insects, such as dsRNases of corn leafhopper, Dalbulus maidis (23) and the glutamate-gated chloride channel gene of the fall armyworm, Spodoptera frugiperda (24).Further, dsRNA is taken up through an active process involving receptor-mediated endocytosis in Drosophila emanogster S2 cells (25).In this study, we have tested how dsRNA can be specifically used to knock-down host genes targeted by bracovirus and to mimic the immunosuppression of S. frugiperda larvae.We used 14 Mix-T double-stranded RNA (dsRNA) to simulate bracovirus through one-time feeding and found that different pathways performed different functions against S. frugiperda, in coordination.We believe that our approach considers the tri-trophic interactions that enhance the effectiveness of the biological control of the pest.Furthermore, we introduce a novel perspective to develop biocontrol strategies.

Results
Simulating bracovirus by using Mix-T 14 dsRNAs against S. frugiperda through onetime feeding Based on the behavior of S. frugiperda in the field, we designed assays for larvae in colonies from 1 st to 2 nd and for individual larvae from 3 rd to 6 th instars, using continuous and one-time feeding methods (Figure 1A).The residual survival of 1 st to 3 rd instars showed consistent development in controls, H 2 O and egfp dsRNA, and Mix-T 14 dsRNA with both continuous and one-time feeding.We observed that the 4 th instar lasted two days longer (dsRNA feeding than two controls), 5 th instar, one day longer, 6 th instar, two days longer, and the pupation stage lasted one-day longer compared to controls (Figure 1A).The data showed that the residual surviving S. frugiperda larvae had a prolonged lifecycle, implying decreased generations per year.
The survival curves showed that the survival rates of both the dsRNA feeding groups were significantly lower than those of the controls; furthermore, there were no significant differences in both continuous and one-time dsRNA feeding (Figure 1B).These data suggest that, by only feeding one-time before the 4 th instar stage at 9 days, Mix-T 14 dsRNA kills pests with efficiency.From days 9-19, until the end of pupation, the survival percentage of larvae treated with Mix-T dsRNA was significantly lower than that of the control group; however, no significant differences were found upon comparing the two dsRNA treatments and control groups, implying that Mix-T dsRNA showed a sustained effect.Subsequently, the development of the residual surviving S. frugiperda larvae was analyzed based on their head capsule width (7,26).The larvae from both the dsRNA treatment groups showed significantly smaller head capsules than those of the two control groups with no significant differences between continuous and onetime feeding (Figure 1C).These findings suggest that one-time feeding of Mix-T dsRNA kills S. frugiperda larvae in the initial instar stages and sustainably inhibits the development of the residual surviving S. frugiperda larvae, suggesting the utility of Mix-T dsRNA for biocontrol.
Cannibalism of younger 2 nd instar larvae in the colony feeding was observed, which was analyzed using the survival rate assay at 5 days (Figure 1B).To detect whether dsRNA treatment affects cannibalism of S. frugiperda larvae, the 1 st instar larval colonies were fed on dsRNA until 3 rd instar stage.Both the feeding methods of Mix-T dsRNA resulted in a significantly lower survival of larvae compared with the feeding of control egfp dsRNA (Figure 1D), suggesting that dsRNA promoted the cannibalism of lower-stage instars.By the 8 th day, dsRNA treatments and control group showed no significant differences, suggesting that Mix-T dsRNA has no sustained effect on promoting cannibalism beyond the 2 nd instar stage.Furthermore, the cannibalism of the colony's 2 nd instar larvae was not significantly different across the treatment groups until the 3 rd instar (Figure 1E).The data confirmed that true cannibalism (aggressive attitude) of larvae, not an increase in appeal, occurs at the beginning of 1 st instar, implying that Mix-T dsRNA can be used against a newly hatching colony to elevate their cannibalism.
To further confirm the effect of one-time dsRNA feeding on lower instar larval individuals, 1 st instar larvae were separated.The percentage of survival for both dsRNA treatments was significantly lower compared with that of the control egfp dsRNA; furthermore, the percentage of survival with one-time Mix-T dsRNA feeding was significantly lower than with continuous feeding (Figure 1F) at the 22 nd day of pupation end.The number of larvae in Mix-T dsRNAtreated groups were significantly lower than in the control groups, suggesting that Mix-T dsRNA showed a persistent effect on the larvae.Similar results were obtained for the individual 2 nd instars indicating that one-time feeding could kill larvae starting from 2 nd instar stage (Figure 1G).However, this was not the case with the individual 3 rd (Figure S1A), 4 th (Figure S1B), 5 th (Figure S1C) and 6 th (Figure S1D) instar larvae, suggesting that Mix-T 14 dsRNA can be used against S. frugiperda during initial instar larval stages.
Taken together, these findings showed that simulating bracovirus using dsRNA kills S. frugiperda from the lower 3 rd instar stage onwards, inhibits the development of residual surviving S. frugiperda larvae and decreases the progression of generations, emphasizing that 14 Mix-T dsRNA can simulate bracovirus at least partially.

Mix-T dsRNA transiently inhibits four major signaling pathways and increases cellular ROS levels
To verify the molecular mechanisms of Mix-T dsRNA, we first assessed if the mRNA of the 14 genes were indeed silenced after feeding.Based on parasitoid-bracovirus-host interaction, parasitoid larvae require 6 days to complete development in the host hemocoel, and release ecSODs to reduce ROS triggered by MbBV infection throughout the developmental period (2,7).The relationship between ROS and longevity has been reported in Caenorhabditis elegans (27).Mix-T dsRNA silenced 11 related genes involved in four main pathways mentioned above and three genes involved in neutralizing ROS from the host hemocytes (Figure 2A).Genes encoding humoral signaling molecules, PLA2, COX11, and COX20 (Figure 2B), and those encoding antimicrobial peptides, attacin and gloverin, showed decreased expression (Figure 2C); cellular communication was also inhibited, as deduced by measuring the TO-PRO3 dye uptake (Figure 2D).In contrast, the expression of apoptosis-related proteins, p53, CypA, and CypD (Figure 2E), as well as the ROS generation, significantly increased (Figure 2F).These data suggested that four pathways were transiently suppressed, while cell apoptosis and ROS increased to create an impaired environment in the host, implying that Mix-T dsRNA simulates bracovirus and kills S. frugiperda by modulating these pathways.
Cooperative functioning of Dip3, eIFs, PCCPs dsRNAs kills S. frugiperda in the feeding stage Administration of dsRNA against the transcriptional co-factor Dip3 quickly and significantly killed young larvae (Figure 3A, D), although it failed to kill larvae over 2 nd instar stage.On the 15 th day at the end of pupation, the surviving larvae from the Dip3 dsRNA group showed no significant differences compared with the control egfp dsRNA group, implying that Dip3 dsRNA is an efficient pesticide without sustained effects on the larva (Figure 3D).From 2 nd instar to the final larval stage, the percentage of surviving larvae from the eIFs dsRNA group was significantly lower than those from the control egfp dsRNA group (Figure 3B, E).Subsequently, at the end of pupation, the number of surviving larvae treated with eIFs dsRNA was significantly lower compared with that of the control group, implying that eIFs dsRNA sustainably kill different instar larvae until the end of pupation (Figure 3E).Similar results were obtained upon treatment with PCCPs dsRNA (Figure 3C, F).In contrast, Inxs dsRNA administration did not kill the larvae and showed no effect on the pupae (Figure S2A, B).These data suggest the complementary function of these three main pathways to kill S. frugiperda in the feeding stage, and that they are potentially modulated by each other.
PCCPs, eIFs, and Inxs dsRNAs cooperatively function against S. frugiperda larvae in the non-feeding stage Killing pest larvae in the non-feeding stage is also a strategy of biological control.At the end of eclosion, PCCPs dsRNA were observed to kill pupae significantly in the non-feeding stage (Figure 3G), while the downregulation of genes involved in the other three pathways namely though, Inxs dsRNA (Figure 3H), eIFs dsRNA (Figure 3I), and Dip3 dsRNA (Figure S2C), did not kill pupae in the non-feeding stage.Interestingly, PCCPs dsRNAs (Figure 3J) and Dips dsRNA (Figure S2D) did not increase the developmental time; while Inxs dsRNA (Figure 3K) and eIFs dsRNA (Figure 3L) increased.These data suggest that these three main pathways, the humoral signaling, cellular communication, and the translation pathways, function cooperatively against the S. frugiperda larvae in its non-feeding stage.
eIFs, Inxs, and PCCP dsRNAs cause immunosuppression in the residual surviving S. frugiperda larvae Residual surviving S. frugiperda larvae were used for evaluating immunosuppression.Head capsule width and hemocyte apoptosis are hallmarks of immunosuppression mediated by the parasitization of M. bicoloratus (7,28).The head capsule width of larvae from the eIFs dsRNA treatment group was significantly decreased from 5 th to 9 th day after continuous feeding (Figure 4A and Figure S3A).Meanwhile, early apoptosis significantly increased, as measured by flowcytometry (Figure 4D, G).The suppression of intracellular communication pathways resulted in significant immunosuppression in residual surviving S. frugiperda larvae, alongside significantly decreased head capsule width (Figure 4B and Figure S3B) and increased early apoptosis (Figure 4E, H).Similar results were found in the PCCP signaling pathway; the head capsule width of larvae feeding on PCCPs dsRNA was significantly decreased (Figure 4C and Figure S3C) and early apoptosis increased (Figure 4F, I).In contrast, administration of the dsRNA targeting the transcription cofactor Dip3 (Dip3 dsRNA) did not inhibit the immune response of the residual surviving larvae, determined based on the lack of effect on the head capsule (Figure S3D) and significantly higher early apoptosis (Figure S3E, F).These data suggest the common immunosuppressive functions of these three main pathways to cooperatively target the survival of the residual S. frugiperda larvae.Mb-ecSODs dsRNA enhances Mix-T dsRNA against S. frugiperda larvae Next, we investigated whether M. bicoloratus ecSODs dsRNA can enhance the effectiveness of Mix-T dsRNA against S. frugiperda in.Previous results showed that MbBV trigger the increase of ROS, which are reduced by M. bicoloratus ecSODs.Since the 14 Mix-T dsRNA increased ROS (Figure 2F), we wondered whether the addition of ecSOD dsRNA can enhance the death of S. frugiperda.When Mix-T no SODs dsRNA and Mix-T dsRNA were administered and the effects compared, the survival curves of the two dsRNA feeding groups were significantly lower than that the control groups.There were no significant differences between the two control groups and between the two dsRNA feeding groups, but the surviving larvae following treatment with Mix-T no SODs dsRNA were significantly higher than those after Mix-T dsRNA feeding at the 15 th days (Figure 5A).These results suggested that the added ecSOD dsRNA enhanced the death of S. frugiperda, at least partially.The development of the residual surviving S. frugiperda larvae was analyzed based on capsule width.The larvae from both the dsRNA treatment groups showed significantly smaller head capsule widths than those from the two control groups.Furthermore, there were significant differences between the Mix-T no SODs dsRNA and Mix-T dsRNA groups and both control groups (Figure 5B).These results imply that added SODs dsRNA inhibited the growth of S. frugiperda in larval stages and the development of residual larvae.Meanwhile, as per the parallel assays, the survival curves were not significantly different for the only single SODs dsRNA compared with control (Figure 5C).Moreover, there was no effect on the survival larval and pupal stages (Figure 5D, E).Furthermore, the developmental stage of larvae from both the treatments showed no significant differences (Figure 5F), implying that single M. bicoloratus ecSODs dsRNA has no effect on the S. frugiperda.The results supported our hypothesis that the addition of M. bicoloratus SODs dsRNA enhanced the effect of Mix-T dsRNA against S. frugiperda.

Mix-T dsRNA one-time spray can effectively control S. frugiperda in the field
To test the effectivity of Mix-T dsRNA to control S. frugiperda in the field, we performed spray assays on corn.Different instars with the same number of S. frugiperda were put on the heart leaves of corn, and different concentrations of Mix-T dsRNA were sprayed on all the leaves.Five days later, investigation of the corn field showed that, compared with the control groups, H 2 O and egfp dsRNA, the spraying of Mix-T dsRNA could effectively relieve pests, and the protective effect of Mix-T dsRNA on corn was dosedependent (Figure 6A).The disaster situation of each maize was graded according to Davis survey method (Figure S4), and further statistical analysis showed that spraying 500 ng/µL Mix-T dsRNA could significantly control the pests.However, administration of other concentrations showed no significant difference compared with that of H 2 O.The number of plants with lower leaf damage after spraying 250 ng/µL dsRNA mixture was significantly less than that of the control group, i.e., only one-time spraying of 500 ng/µL dsRNA mixture could effectively control S. frugiperda (Figure 6B).This data suggests that Mix-T dsRNA simulated bracovirus can be a highly efficient pesticide to control S. frugiperda.

Discussion
In the present study, we propose that simulating bracoviruses that are symbiotic with wasp by "one-time sting", reduce pests with high efficiency and accuracy, and is a potential bio control strategy.Here, we used Mix-T dsRNA to target 14 genes, thereby simulating the wasp one-time sting to control S. frugiperda efficiency and accuracy by transiently suppressing four key pathways and increasing ROS.Eleven genes targeting four main pathways modulated by bracovirus and three genes from parasitoid larvae against ROS triggered by bracovirus have been used.Working in coordination, Dip3, eIFs, and PCCPs dsRNAs kill young instar larvae; eIFs, Inxs, and PCCP dsRNAs cause immunosuppression in the residual surviving S. frugiperda larvae; eIFs, Inxs, and PCCP dsRNAs function against S. frugiperda in its non-feeding stage.Collectively, our findings indicate that simulation of a bracoviral attack by using dsRNA is a promising biocontrol strategy.
Mix-T dsRNA instantly suppresses four main signaling pathways and eliminates SOD, thereby creating an impaired environment with higher apoptosis and ROS, which is a strategy of bracoviruses.Previous studies have also shown that appropriate ROS can prolong the lifespan of nematodes by inducing methylation of H3K4 to improve REDOX homeostasis in nematodes (29).However, research has shown that ROS imbalances lead to a decrease in longevity and cause disease in yeast and mice (30,31).In the yeast, Saccharomyces cerevisiae, alteration of ROS homeostasis decreased its lifespan (30), implying that ROS is involved in its life-cycle regulation.These strategies appear to be utilized by bracovirus in the multi-trophic interactions of the polydnavirus-parasitoid-host.Moreover, ROS generation has been ignored in bio control tool development.M. bicoloratus parasitoid larvae secrete three proteins to reduce SOD and maintain lower ROS levels.
The simulation of bracoviral attack using one-time feeding dsRNA functions against lower instar S. frugiperda larvae.S. frugiperda larvae live in colonies during 1 st -2 nd instars, and separate when the larvae molt into 3 rd instar.We used these behaviors to design the feeding mixture of 14 dsRNAs.One-time feeding of Mix-T dsRNA shows a high efficiency against S. frugiperda by killing larvae, inhibiting development of residual surviving larvae and prolonging the life cycle.Surprisingly, dsRNAs further triggered the 1 st instar larval cannibalism in the colony commonly found in the lepidoptera.This is the first report describing an additional role of dsRNA-mediated gene silencing, beyond the known general effects.This is similar to imidacloprid and acetamiprid, which can affect neurotransmitter transmission and nerve conduction in insects (5,32).An interesting research found that starved male cells consume their own proteins (33).Serotonergic neurons in the brain of larval S. frugiperda are involved in multiple effects in a variety of behaviors, like feedingrelated modulation (34).The stress caused by dsRNA administration may have triggered the nervous system to promote this cannibalism; excluding the cannibalism of 1 st instar, one-time feeding kills individual larva in 1 st and 2 nd instar.Importantly, Mix-T dsRNA works against S. frugiperda in different stages in various ways, highlighting the relevance of these strategies based on bracovirus-wasp-host interactions.The efficiency of simulation by RNAi technique can be further improved, and the technique can then be used in biological control.Similar to RNAi silencing, lepidopteran insects perform substance exchange and immune functions through the circulation of hemolymph in the body, giving dsRNA a chance to pass through the insect gut to the hemolymph and to be delivered into the cell to perform its functions (35)(36)(37).Needless to say, targeting key genes for growth and development is better at eliminating pests.Therefore, the genes selected in this study are those that have been proven to affect larval development and immunity and were based on the immunosuppressive mechanism of insect parasitism.In the

A B
Mix-T dsRNA can effectively control S. frugiperda in the field (A, B) Mix-T dsRNAs showed dose-dependent effects against S. frugiperda in the field.*p < 0.05, **p < 0.01, ns, no significance; the error bars represent the SEM.David's scale was used for statistics and unpaired Student's t-test with Holm-Sidak method for multiple t test, n = 3.
parasitic system, the significant downregulation of these genes resulted in growth retardation and immunosuppression of larvae (38).Collectively considering all functions of 14 Mix-T dsRNA, in the fields, one-time spraying reduced the damage of maize plant.Four main pathways, transcription, translation, PGE 2 regulation, and intracellular communication, play different roles against S. frugiperda during both the feeding and non-feeding stages, and their cooperative interactions improve the efficiency of our method.Three pathways blocked by dsRNA individually, directly kill lower instar S. frugiperda.The most important target of the bracovirus is the transcriptional pathway as evidenced by Dip3 dsRNA killings S. frugiperda lower instar quickly.This is because Dip3, as a transcription factor, regulates the expression of multiple immune-phase genes.For example, Dip3 regulates the expression of eIF4E through the NF-kB pathway (5).Interestingly, Dip3 dsRNA-mediated pest-killing has not been reported yet.Dip3 regulates transcription of genes, involved in survival.This effect is fast as well as short as seen only in lower 2 nd instar stage and has no effect on the residual larvae that survived.Fortunately, eIFs dsRNA and PCCPs dsRNA kill larva over 2 nd instar until the end of pupation.The cessation of peptide translation is fatal to living organisms, and PGE 2 is necessary for the maintenance of immunity in insects (39).Furthermore, eIFs and PCCPs dsRNA affect the development and immunity of armyworm in many ways.In the feeding stage, these three pathways coordinate to present a "no gap" coordination.
Inhibition of three other pathways involving eIFs, Inxs, and PCCPs, causes immunosuppression in residual surviving S. frugiperda larvae.Silencing of these three pathways decreased development and increased the degree of early apoptosis, both of which are hallmarks of immunosuppression by bracovirus.This is not surprising because the bracovirus inhibits host immunosuppression in S. litura (4,40).However, hosts only infected by bracovirus without a parasitoid are not known.Here, our results fill the gaps in which a truly immunosuppressive function of bracovirus is noted in different larval stages and not just at the lower instar stage.In the feeding stage, these three pathways present a unit coordination towards immunosuppression in residual S. frugiperda larvae.
eIFs, Inxs, and PCCP dsRNAs co-operatively function against S. frugiperda in its non-feeding stage; their dsRNA silence four pathways involving PCCPs, eIFs, Inxs, and Dip3, which undertake different functions against S. frugiperda.It is wellknown that the intricate signaling pathways are not independent of each other.The occurrence of tumors, formation of autophagosomes, activation of immune signals, damage and repair of DNA, and the process of aging are all completed through the cooperation of multiple signaling pathways (41,42).Similar to the bracovirus, 14 Mix-T dsRNA worked together to block the immune pathway in the larvae of armyworm and eventually led to immunosuppression throughout the life cycle.Only PCCPs dsRNA can kill the non-feeding pupal stage.Blocking humoral immunity reduced the antimicrobial peptide expression.This is because the absence of antimicrobial peptides is fatal to an insect's innate immunity (43).PCCPs dsRNA specifically regulates the synthesis of PGE 2 and thus reduces the production of antimicrobial peptides.Inxs and eIFs dsRNA increased the time of development of the residual surviving larvae.Increased time for the completion of life cycle leads to reduced generations.It is yet unclear how eIFs and Inxs dsRNA increase the duration of the pupal stage.Recently, it has been reported that the use of triazole can effectively alter the timing of metamorphosis of digger wasps (44).Triazole achieves insecticidal effect mainly by inhibiting enzyme activity in insects, which is quite different from the role of eIFs dsRNA.eIFs dsRNA inhibits the synthesis of many major proteins and ultimately affects the life cycle of armyworm.Similar to the altered life-cycle of crabronid wasp due to the blocking of the neurotransmitter acetylcholine by acetamiprid (45), the blocking of small molecules transmission between insect cells by Inxs dsRNA affects the communication between cells and ultimately alters the life-cycle of armyworm.
Regarding the cost and practically feasibility of dsRNA, the current cost of controlling pests through dsRNA technology is undeniably higher than that of pesticides for weed management in turfgrass systems (46).Spraying dsRNA has been used to control the western flower thrips in greenhouse (36).We believe with advances in research and the maturation of technology, the cost will be reduced, and the use of dsRNA could become practically feasible.
In summary, we have demonstrated that simulating bracovirus by dsRNA provides new insights into understanding the coordination among natural enemies.In addition, our results reveal a truly immunosuppressive function of bracovirus, thereby allowing the avoidance of the self-protection strategy from parasitoids, which are negative factors in biocontrol.Our findings provide a new perspective on bracovirus-parasitoidhost interactions.