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RNA Interference in Insects: Protecting Beneficials and Controlling Pests

Elise Vogel, Dulce Santos, Lina Mingels and 2 more

Frontiers in Physiology · 2019 · Review · CC BY

doi:10.3389/fphys.2018.01912

Abstract

Insects constitute the largest and most diverse group of animals on Earth with an equally diverse virome. The main antiviral immune system of these animals is the post-transcriptional gene-silencing mechanism known as RNA(i) interference. Furthermore, this process can be artificially triggered via delivery of gene-specific double-stranded RNA molecules, leading to specific endogenous gene silencing. This is called RNAi technology and has important applications in several fields. In this paper, we review RNAi mechanisms in insects as well as the potential of RNAi technology to contribute to species-specific insecticidal strategies. Regarding this aspect, we cover the range of strategies considered and investigated so far, as well as their limitations and the most promising approaches to overcome them. Additionally, we discuss patterns of viral infection, specifically persistent and acute insect viral infections. In the latter case, we focus on infections affecting economically relevant species. Within this scope, we review the use of insect-specific viruses as bio-insecticides. Last, we discuss RNAi-based strategies to protect beneficial insects from harmful viral infections and their potential practical application. As a whole, this manuscript stresses the impact of insect viruses and RNAi technology in human life, highlighting clear lines of investigation within an exciting and promising field of research.

Full text

From PubMed Central, U.S. National Library of Medicine, as current on Oct 24, 2026. Paragraph numbers are ours, so an answer can point at one.

Introduction to Cell-Autonomous, Environmental and Systemic RNAi in Insects

The discovery of RNA interference (RNAi) constitutes an important milestone in the study of regulatory RNAs. In this process, small (s)RNA molecules of 18–31 nucleotides (nt) long effectuate a sequence-specific gene silencing response, acting at the post-transcriptional level through cleavage or blockage of longer RNAs containing a matching sequence. Based on their origin, biogenesis, structure and role in distinct biological processes, small RNAs are classified in three main cell-autonomous pathways: (1) genome encoded microRNAs (miRNAs), which regulate a multitude of biological processes; (2) PIWI-interacting (pi)RNAs, which silence transcripts derived from selfish genomic elements, such as transposons; and (3) small interfering (si)RNAs, which defend the organism against invading viruses. However, recent studies revealed that some level of functional crosstalk can occur between the different sRNA-mediated pathways. A fascinating example is found in insects, where an important antiviral role of the piRNA pathway has been described in mosquitoes.

In insects, the siRNA pathway is activated when double-stranded (ds)RNA molecules, as products of viral replication, are recognized in the cytoplasm and processed into siRNAs of 18-24 nt by the RNase type III enzyme Dicer-2. Cleavage of viral RNA targets is then further exerted by an Argonaute-2 (Ago2) containing ‘RNA induced silencing complex’ (RISC), which encompasses the siRNA guide strand. Interestingly, this RNA silencing mechanism can also be triggered by artificial administration of gene-specific long dsRNA, a technique that is generally designated as RNAi. This dsRNA treatment can result in functional knockdown effects that in fact can be considered as auto-immune defects, since the siRNA pathway, an antiviral immune defense mechanism of insects, is being misled to target an endogenous transcript of the host. As such, RNAi has become the most widely used reverse genetics research tool in insects and holds great potential to contribute to novel strategies for species-specific control of insect pests and to combat viral infections in disease-vectoring and beneficial insects.

An interesting aspect of the RNAi response in insects is its potential systemic character, also known as systemic (sys)RNAi. Specifically, in some insects administration of dsRNA can result in the generation of an RNAi response throughout the entire body. However, the precise mechanism of both short- and long-distance intercellular transfer of the sysRNAi-signal, as well as the exact nature of this signal, still remain elusive. Different reports indicate that the cellular uptake of dsRNA in insects, also referred to as environmental (env)RNAi, occurs via scavenger receptor-mediated endocytosis both in cultured cells and in vivo. It is also known that the uptake of naked dsRNA is length-dependent. It occurs efficiently for long dsRNA molecules of around 200–500 base pairs (bp) and even of up to circa 1000 bp. However, for shorter constructs such as siRNAs, this efficiency decreases. Furthermore, it has been shown that lipophorins can adhere to dsRNA fragments in the insect hemolymph, suggesting a possible role of these proteins in either protection, transport, or both, throughout the body. In addition, two main findings have been reported for Drosophila melanogaster. First, viral infection of cultured Drosophila cells increased the formation of nanotube-like structures through which short-distance transport of dsRNA and RISC components can occur. Second, it has been shown that flies use hemocyte-derived exosome-like vesicles to systemically spread an antiviral siRNA signal in the hemolymph. At present, it is still unclear how all these separate findings might fit together and whether they can be extrapolated to other conditions and species (Figure 1).

In this review article, we start by discussing the potential of the RNAi technique to contribute to insect pest control. On this matter, we review several application strategies that have been tried, their limitations and the most promising approaches described in the available scientific literature thus far. On a parallel perspective, we summarize relevant insect viral infections and review the use of viruses as bio-insecticides. Finally, with perspective to the natural antiviral role of the RNAi mechanism, we discuss the potential use of RNAi for protecting beneficial insects from harmful viral diseases.

RNAi-Based Insect Pest Control

Despite frequent use of insecticides, approximately 18–20% of the global crop harvest is still lost due to damage caused by pest insects. A major underlying cause is insect population resistance against the most commonly used insecticides, posing a persistent challenge to agriculture. Furthermore, the devastating impact of chemical insecticides on the environment and other organisms, such as beneficial insects, can no longer be ignored. Taking the previous statements into account, it becomes evident that the current array of insect pest combatting methods is insufficient to secure global food production for the next decades. Finding alternative options to improve plant protection strategies is therefore critical.

In this context, an interesting perspective is represented by the RNAi technique. The potential of this mechanism is inherent in its mode-of-action, namely the subsequent degradation of complementary target mRNA upon entry of specific dsRNA into the cell. Therefore, by delivering dsRNA targeting any endogenous gene transcript to the intended pest organism, expression of this gene can be knocked down at the post-transcriptional level. Thus, through careful selection of an essential target gene, this mechanism can lead to insect mortality. The sequence-specific nature and the possibility to theoretically target any non-conserved, ‘lethal’ gene, make RNAi an ideal candidate for further application as a species-specific insecticide.

A proof-of-concept study was executed in 2007 by Baum et al. In this research, a transgenic corn crop was genetically engineered to express dsRNA against the V-ATPase A transcript of the Western corn rootworm Diabrotica virgifera virgifera. Feeding D. virgifera virgifera with this modified plant resulted in larval stunting and in the premature death of the insect. Additionally, dsRNA functioned as a crop protectant as feeding damage to the transgenic corn was greatly reduced. A similar study was executed for the cotton bollworm Helicoverpa armigera. In this research, showed that plant-mediated expression of dsRNA targeting the cytochrome P450 monooxygenase gene (CYP6AE14) could increase the toxic effects of gossypol, a cotton metabolite that is otherwise tolerated by the cotton bollworm. Silencing of CYP6AE14 led to delayed larval growth when gossypol was supplemented in the diet. It should be noted that another research has since shown that CYP6AE14 is likely not directly involved in gossypol metabolism but rather plays a more general role in the insect stress response to ingestion of plant toxins. Nonetheless, the research of Mao et al. remains an interesting example of the application potential of dsRNA-mediated plant protection.

This section will continue by reviewing the predominant theories regarding the variable nature of the RNAi response across the class Insecta. Bearing in mind the promising use of RNAi technology as an insecticide, an overview of dsRNA delivery systems is given next. Finally, current use of RNAi-based insecticides will be summarized.

Variable Efficiency of the RNAi Response

Although an RNAi response has been detected at least once in most economically important insect orders, such as Coleoptera, Diptera, Orthoptera, Lepidoptera, and Hemiptera, the efficiency of the induced response may vary between species and even within the same organism. Whereas some insects, such as the Colorado potato beetle Leptinotarsa decemlineata, and the western corn rootworm D. virgifera virgifera, are consistently able to generate a systemic RNAi response; other species, such as the tobacco cutworm Spodoptera litura, and the silkworm Bombyx mori, show a more variable and generally less efficient response. The nature of this variable efficiency has been the subject of much speculation and it is likely that a lot remains to be discovered.

Extracellular Nucleases Inhibit the Efficiency of the RNAi Response

Some insect species, such as the desert locust Schistocerca gregaria, and the migratory locust Locusta migratoria, are able to display an efficient systemic RNAi response after injection of dsRNA into the body cavity. However, when dsRNA is fed to these insects, they appear to be refractory. As most food sources contain nucleic acids, it follows that nucleases are an integral part of the insect digestive system. In addition, it has been suggested that nucleases in the digestive track may also exert a function of protection against viruses. Unfortunately, presence of high nuclease activity can have an inhibitory effect on the RNAi response.

showed that a digestive enzyme solution, collected from the midgut of S. gregaria, had the ability to quickly degrade dsRNA (i.e., 150 nanograms of dsRNA within 5 min). Subsequently, four different sequences coding for dsRNases were identified from S. gregaria transcriptome data. In several other species, such as the pea aphid Acyrthosiphon pisum, the tarnished plant bug Lygus lineolaris, B. mori, and L. migratoria, the limited RNAi response after feeding with dsRNA has been linked to the presence of dsRNA-degrading enzymes in the digestive system.

The limiting effect of nucleases is not unique to the digestive tract. In fact, their activity in the hemolymph has been linked to a lowered RNAi efficiency in a number of species. Whereas dsRNA remained stable in the hemolymph of the RNAi efficient German cockroach Blattella germanica, injection of dsRNA into the body cavity of the RNAi refractory tobacco hornworm Manduca sexta, led to its swift degradation. Furthermore, in the Asian corn borer Ostrinia furnacalis, the nuclease Rease was found to be upregulated in the hemolymph after administration of dsRNA. Reducing transcript levels of this gene led to a significantly improved RNAi response in this insect. Phylogenetic analysis revealed homologous genes in seven other lepidopteran species, suggesting that this nuclease might be Lepidoptera-specific.

Surprisingly, the presence of dsRNases has even been recorded in insects which generally show an efficient RNAi response after feeding with dsRNA, such as the Colorado potato beetle L. decemlineata. showed that an enzyme solution collected from the gut of this beetle was capable of degrading dsRNA. Additionally, the induced RNAi response after feeding dsRNA could still be significantly increased after the knockdown of two dsRNA degrading enzymes, Ld_dsRNase1 and Ld_dsRNase2. Although it has become clear that most insect orders contain species wherein the efficiency of the RNAi response is somehow limited by the presence of dsRNases, not all species appear to be equally affected. It is therefore likely that differences in the activity of dsRNA degrading enzymes contribute to the tissue-, stage- and species-dependent variability in RNAi sensitivity observed in insects. In this context, it is notable that extracellular nuclease activity will additionally influence dose-dependence of the RNAi response as it conditions the quantity of dsRNA that remains available for uptake. Certainly, it appears that the role of dsRNases in limiting the RNAi response cannot be ignored. Moreover, since reducing transcript levels of dsRNases already led to an improved RNAi sensitivity in some insect species, these nucleases may have to be taken into account when considering future RNAi-based insect pest control strategies.

Tissue-Dependence of the RNAi Response

The fruit fly D. melanogaster, is a well-known example of an insect that is recalcitrant to external administration of dsRNA. Remarkably, this is a generalization that does not apply to the whole insect: D. melanogaster hemocytes can take up extracellular dsRNA and generate an RNAi response. This sensitivity can also be observed in the hemocyte-derived D. melanogaster S2 cell line, a commonly used in vitro model for RNAi research.

While this inconsistency is striking, the fruit fly is not the only organism in which the sensitivity of the RNAi response appears to be cell type or tissue-dependent. Another striking example presents itself in S. gregaria; independent studies in this species have proven that an efficient RNAi response can be induced in various tissues, ranging from the brain to the Malpighian tubules. Nevertheless, have observed that the ovaries and testes of this locust species showed a lower RNAi efficiency when compared to these other tissues. Further examples can be found in the African malaria mosquito Anopheles gambiae, and the yellow fever mosquito Aedes aegypti. In the former, a reduced RNAi susceptibility was observed in the salivary glands, whereas in the latter both head and ovarian tissues responded less efficiently than other tissues to external application of dsRNA. Finally, lepidopterans are known to have a variable RNAi susceptibility and tissue-dependency has also been observed for a number of species in this order. Particularly wing-disk and larval epidermal tissues appear to be problematic.

Little is known about the exact causes of the tissue-dependency of the RNAi response, and as such they may vary between and within species. Research using the lepidopteran Sf9 and Hv-E6 cell lines showed that dsRNA molecules are unable to escape after endosomal uptake. Thus, in these insect cells, the RNAi response is not induced because the dsRNA cannot enter the cytoplasm. In this context, it has been suggested that this inability might contribute to the poor susceptibility and possibly to the tissue-dependency often observed in this insect order. Similarly, in L. migratoria it was found that a reduced uptake of dsRNA in oocytes and follicle cells resulted in a less efficient ovarian RNAi response. In S. gregaria, the reduced responsiveness of ovaries and testes could be attributed to reduced expression levels of argonaute-2 and dicer-2, two crucial RNAi genes. Likewise, in several lepidopteran species it was also suggested that variable expression of core RNAi components might be linked to the inconsistent RNAi response observed in these insects.

Intra-Species Differential Sensitivity and Resistance

To fully understand the problem of variable RNAi efficiency in insects, intraspecies variations also need to be considered. Indeed, some populations of the same species appear to be differentially sensitive to external administration of dsRNA. This was most recently observed in L. migratoria by. In this research, four different lab strains of the migratory locust were examined, each originating from a geographically isolated location in Japan. Two of the tested lab strains were found to be very sensitive to injection with dsRNA, while the other two appeared to be completely refractory. Even within the same lab strain, different individuals could respond with different degrees of sensitivity. In a comparable research, three phenotypically different field populations of D. virgifera virgifera were given the same dsRNA treatment to see whether they would respond in a similar way. The efficiency of the RNAi treatment varied between the three populations, indicating that the RNAi susceptibility differed for each population. It has been suggested that a similar phenomenon could be occurring in the red flour beetle, Tribolium castaneum. While some lab strains of this species show a highly sensitive response to feeding with dsRNA, other lab strains appear to be unresponsive to this method of administration.

The cause for these intraspecies variations in RNAi sensitivity remains uncertain. proposed that in locusts these intraspecies differences could be attributed to a genetic component. They postulate that RNAi sensitivity is regulated by an incompletely dominant gene or several genes that remain to be determined. On the other hand, another theory suggests persistent viral infections as a key-determining factor in the establishment of variable RNAi efficiencies between insect populations of the same or different species. hypothesize that these infections could reduce insect RNAi sensitivity through the expression of viral suppressors of RNAi, the saturation of the RNAi machinery by viral siRNAs, or the manipulation of host gene expression. However, this remains speculative as the effect of specific persistent viral infections on the efficiency of the RNAi response in lepidopteran cells remains to be demonstrated. Thus, further investigation is necessary to verify this hypothesis.

Taken together, observations regarding the variation of RNAi efficiency suggest that the potential emergence of RNAi-resistance in currently RNAi-sensitive insects is a real possibility. Indeed, in a recent study, an RNAi-resistant insect population was created. Resistance was induced by consistently feeding a field population of the Western corn rootworm with transgenic maize plants expressing DvSnf7 dsRNA. showed that resistant insects displayed reduced dsRNA uptake from the gut lumen after feeding. Furthermore, the researchers were able to determine that the resistance was not limited to DvSnf7 dsRNA, since the insects displayed cross-resistance to feeding with several different dsRNAs. Further research into the underlying mechanisms causing the development of resistance in RNAi-sensitive insects could provide important insights into the efficient application of RNAi as an insecticide.

Target Selection and Construct Design

Taking the aforementioned variabilities into account, it is unsurprising that the set-up of RNAi technology experiments requires careful consideration. Selection of the target gene of interest, for instance, is crucial to their success or failure. The ideal target gene should be abundantly transcribed, produce an mRNA with a high turnover rate and translate into a protein with a low half-life. To become applicable as an insecticide, transcript reduction of the intended target gene must additionally lead to mortality in the insect. Furthermore, off-target effects should always be considered. With regard to this, dsRNA constructs should preferably be chosen in non-conserved regions of the target mRNA to avoid cross-silencing among other species or isoforms of the gene of interest. Correspondingly, research has shown that RNAi can be highly species-specific if the dsRNA construct is well-designed. By targeting the variable 3′-UTR region of the greatly conserved γ-Tubulin transcript, showed that a species-specific knockdown could even be achieved in four closely related Drosophila species. Similarly, could induce very specific transcript reductions for three highly similar CYP genes in the Tobacco hornworm Manduca sexta.

Moreover, the length of the dsRNA construct should be contemplated as the optimal length for dsRNA uptake varies from insect to insect. Research has shown that for most insects this optimum lies between 200 and 520 bp (reviewed by ). A last criterium that should be taken into account is the dosage of dsRNA that is administrated. This concentration should be adjusted according to the abundance of target mRNA. As most genes are not stably expressed during the entire life cycle of the insect, temporal expression according to life and developmental stage should be taken into account. In addition, this concentration can be species dependent. In insect species where dsRNAses limit RNAi efficiency in the gut, for instance, an overdose of dsRNA may be required to induce an RNAi signal. This was extensively reviewed by.

RNAi Delivery Systems

Clearly the obstacles of insufficient RNAi sensitivity must be solved before RNAi technology can be further applied as a universal insecticide. An elegant solution is presented by packaging dsRNA in such a way that it is protected against degradation and uptake is facilitated. This may be achieved through the use of delivery systems. Many different strategies have already been proposed in the existing literature and will be discussed here. An important feat to keep in mind is that the specificity of these systems has to be prudently considered. As such, the effect of all proposed delivery strategies on other animals and on human consumption has to be investigated thoroughly before they can be applied as vehicles for insecticidal dsRNA. Regardless, the great potential of these systems is undeniable. An overview of all delivery systems reported so far can be found in Table 1.

Micro-Organisms

The bacterial system, in its simplicity, is one of the most successful methods of dsRNA delivery in insects. This system makes use of the genetically modified HT115 bacterial strain, which lacks the dsRNA-degrading bacterial endonuclease RNase III. Furthermore, this strain contains the T7 polymerase gene, controlled by the inducible lac operon. HT115 is often combined with L4440, a plasmid specifically designed to contain two T7 promoters flanking its multiple cloning site. Transformation of the bacteria with L4440 will lead to expression of dsRNA within the cell. This method was first utilized in the nematode Caenorhabditis elegans. Since then it has also been applied to insects, as described below.

first fed bacteria expressing Chitin synthase A (SeChsA) dsRNA to the beet armyworm Spodoptera exigua in 2009. They found that this delivery method not only lead to an efficient knockdown but also to reduced larval growth and insect death. Moreover, feeding dsRNA in this way induced sysRNAi as reduced transcript levels were observed in the trachea and epidermis of treated insects. A similar experiment was performed in L. decemlineata, where a knockdown was achieved for several target genes after the insects were fed with dsRNA-expressing bacteria. In addition, the insects showed increased mortality as well as reduced weight gain. Finally, bacterial delivery of dsRNA targeting the ultraspiracle gene transcript was shown to improve the RNAi efficiency through feeding in H. armigera.

The mechanism through which this bacterial system facilitates dsRNA-uptake remains elusive. It is likely, however, that packaging dsRNA in a protective bacterial shell may have a stabilizing effect on the presence of dsRNA in the lumen of the digestive system. With regard to this, pre-treatment of the bacteria was shown to improve release of dsRNA in insects. Specifically, research has shown that sonication improved the efficiency of the induced RNAi response in S. exigua. Therefore, it is possible that in this case weakening the bacterial cell wall through pretreatment stimulated dsRNA-uptake. However, there is no concrete evidence for this and it remains to be proven.

The potential pathogenicity of Escherichia coli to several insect species implies that beneficial insects could be negatively affected by the use of this delivery system. Therefore, it has been suggested that a more appropriate approach might be achieved by focusing on symbiotic bacteria or yeasts. In the bloodsucking insect Rhodnius prolixus, and the western flower thrips Frankliniella occidentalis, knockdowns were achieved by delivering genetically engineered symbiotic bacteria capable of expressing dsRNA. Furthermore, research suggests that this method of feeding might potentially lead to horizontal transfer of the RNAi signal in R. prolixus through symbiont-contaminated feces. More specifically, the eGFP-tagged symbiont could be detected in untreated younger instar insects after they had been fed with feces from treated insects. This implies that, through the use of this symbiont, possibly whole colonies could be targeted with only a minimal amount of bacteria. Likewise, in the spotted wing fruit fly, Drosophila suzukii, it was found that feeding with a genetically modified symbiotic yeast led to induction of the RNAi response and resulted in reduced larval fitness. Finally, it was shown that a knockdown could be achieved by feeding larvae of the mosquito species Anopheles stephensi, with a dsRNA delivery system consisting of transgenic microalgae. These alternative delivery vehicles were suggested to have a negligible pathogenic impact on non-target insects, making them attractive options for application as ecologically friendly insecticides in the field.

Viruses

Viruses are extremely efficient at infecting cells and thus at delivering nucleic acid material into the intracellular environment. As RNAi is known to play a vital part in insect antiviral immunity, the use of viral delivery systems becomes an intriguing pitch, since the natural path of dsRNA cell entry is simulated. Furthermore, as many viruses have a very specific host range, a high degree of species-specificity could be achieved through careful virus screening and selection. However, despite its many positive facets, viral delivery of dsRNA is still faced with a number of obstacles. Since many viruses have developed counter-measures against the RNAi mechanism, such as viral suppressors of RNAi, it is likely that not all viruses will be equally applicable as a delivery system. Some examples of successful experimental use of a viral delivery system are given below.

found that a recombinant BmNPV baculovirus, encoding a juvenile hormone esterase specific hairpin, could induce gene-specific knockdown phenotypic effects in the Mediterranean corn borer, Sesamia nonagrioides. Surprisingly, despite careful selection of the viral carrier, the virus itself also seemed to affect the vitality of the insect. Therefore, it is likely that not all observed phenotypic effects could be attributed to the knockdown. In B. mori, it was discovered that injection with a recombinant Sindbis virus (SINV) could achieve a knockdown of the transcription factor Broad-Complex (Br-C). determined that engineering SINV to express an antisense RNA strand for Br-C led to reduced Br-C mRNA levels in this insect. This resulted in decreased rates of larval to pupal molting as well as developmental defects in those larvae that were able to reach adulthood. It is of interest to mention that recombinant strains of SINV have additionally been used as a viral delivery system in the mosquito, Aedes aegypti, as a control measure for the RNAi-induced inhibition of dengue virus.

While viral delivery systems show a lot of potential and are generally considered to be among the most efficient methods for dsRNA delivery, their in vivo application has not been widely investigated yet. This may be due to the many safety issues that accompany this method of delivery. As not all insect viruses have a specific host range, a biosafety issue that needs to be thoroughly considered is cross-infection of beneficial insects with these highly virulent delivery systems. Furthermore, the ecological implications of releasing transgenic viruses into the field will need to be carefully considered, especially with regard to stability and turn-over time. A last point that will need to be evaluated is the possibility of transgene transfer from recombinant viral vesicles to wild type viruses.

Nanoparticles

In order to increase stability and uptake efficiency, dsRNA can also be incorporated into a nanoparticle. Nanoparticles are polyplex-based delivery systems, consisting of either natural or synthetic polymer subunits. The most utilized nanoparticles are chitosan-derived.

Chitosan is a non-toxic, biodegradable molecule that can be obtained by deacetylation of chitin, one of the most abundant biopolymers in nature that is especially known for its structural function in the exoskeleton of arthropods. Due to its poly-cationic character and many amino groups, chitosan is able to bind dsRNA through electrostatic interaction. Chitosan:dsRNA nanoparticles are thus formed through self-assembly during the binding process. Incorporation of dsRNA into such a nanoparticle complex increases stability and uptake of the dsRNA in vivo. This method of oral dsRNA delivery appeared to be especially effective in the African malaria mosquito A. gambiae, and the yellow fever mosquito A. aegypti. In these two species successful application of chitosan-mediated dsRNA delivery led to a knockdown in various independent experiments.

Additionally, nanoparticles can consist of synthetically modified polymers. An interesting example is presented by, who generated a fluorescent nanoparticle (FNP) to facilitate dsRNA uptake in the Asian corn borer Ostrinia furnacalis. FNP consists of a core chromophore, allowing FNP uptake to be observed through fluorescence microscopy, and two outer shell layers that facilitate binding to dsRNA and prevent aggregation in water. Complexation of FNP with dsRNA targeting the chitinase-like gene CHT10 caused RNAi silencing after feeding of the Asian corn borer larvae. The treatment resulted in molting defects, reduced larval weight and, eventually, death. Finally, developed a series of nanoparticles designed to specifically shield dsRNA from the degrading effects of the highly basic conditions (high pH) that are typical of the lepidopteran gut. In this research, nanoparticle stability in this alkaline environment was enhanced by modifying cationic polymethacrylate derivatives with protective guanidine side groups. Feeding larvae of the beet armyworm S. exigua with chitin synthase B dsRNA packaged in these pH-stable nanoparticles, led to the swift knockdown of the target gene as well as increased mortality in the experimental insects.

Liposomes

Another means to obtain an increased RNAi efficiency is through the use of lipid-based transfection agents; these vesicles are collectively referred to as liposomes. Liposomes form naturally when transfection agents are brought into an aqueous environment. During this process, the positively charged lipids envelop the negatively charged nucleic acid material, forming compact lipid bilayer particles similar to the phospholipid bilayer of the cell membrane. Cell entry of the liposome-encapsulated dsRNA is then achieved through lipofection.

first used liposomes to improve the RNAi efficiency in four distinctive drosophilid species: D. melanogaster, D. sechellia, D. yakuba, and D. pseudoobscura. By creating liposomes using commercial transfection agents, such as Lipofectamine 2000 and Cellfectin (both available at Invitrogen), the dsRNA-induced mortality was increased. Furthermore, mRNA silencing could be improved in the mosquito species A. aegypti by feeding it dsRNA packaged in Effectene-liposomes. Notably, a similar approach also led to liposome-mediated uptake of dsRNA in the tick species Rhipicephalus haemaphysaloides.

Proteinaceous Delivery Systems

The use of carrier proteins as delivery systems for dsRNA also provides an interesting prospect. Although research within this category remains limited, the best studied protein carriers are represented by the so-called cell-penetrating peptides or CPPs. One of the characterizing traits of these peptides is that they are able to facilitate entry into the intracellular environment while transporting molecular cargo, such as dsRNA. CPPs are short chain cationic peptides that usually consist of 10 – 30 amino acids with a high prevalence of basic residues, such as lysine and arginine. Although there is still some speculation about the exact cellular mechanisms of CPP-mediated delivery, the most commonly accepted theory is that endocytosis plays an important part.

To induce an RNAi response through feeding in the Cotton boll weevil Anthonomus grandis, a fusion protein was designed containing a peptide transduction domain (PTD) as well as the dsRNA binding domain (DRBD) from the human protein kinase R. PTD is an enhanced version of the arginine-rich CPP trans-activating transcriptional activator (TAT) of the human Immunodeficiency Virus 1 (HIV-1), engineered to have additional properties that promote endosomal escape of the fusion protein and its cargo into the cytoplasm. PTD-DRBD, in combination with dsRNA, forms a ribonucleoprotein particle (RNP) that is able to swiftly facilitate uptake in the insect gut. Furthermore, after feeding RNPs to A. grandis, found that the knockdown for chitin synthase II was significantly increased compared to feeding with naked dsRNA.

The CPPs may represent an intriguing solution to the problem of RNAi sensitivity. This category of compounds encompasses a wide diversity of untested candidates and, therefore, many potentially interesting carriers for oral dsRNA delivery remain to be discovered. However, some caution must be exercised as these CPPs belong to a class of very general protein carriers, able of entering mammalian cells as well as arthropod cells.

Chemical Modifications of Small RNA Oligonucleotides

Although the RNAi response is not effective upon exposure to short dsRNA duplexes such as siRNAs, it is known that chemical modifications of these molecules can improve their stability and uptake. In fact, feeding of modified siRNAs targeting vital genes can lead to mortality in the diamondback moth, Plutella xylostella. Furthermore, the use of modified synthetic miRNA inhibitors, antagomirs and agomirs is an interesting approach that requires further investigation.

Plastids: A Plant-Based Delivery System

dsRNA delivery through genetically engineered plants has been achieved for many insect species, often resulting in reduced growth and developmental delay. Since plants possess their own RNAi machinery, transgenic dsRNAs produced in planta are swiftly diced into siRNAs instead of accumulating. However, efficient uptake of dsRNA in insects requires that administrated duplexes have a minimum length of 60 bp. Therefore, as insects take up siRNAs much less efficiently than long dsRNAs, the corresponding toxicity of the transgenic plant will also be reduced.

While it is debatable whether plants really can be classified as typical delivery systems, an interesting cross-over presents itself in the research of. In their research, a potato plant was genetically engineered to produce dsRNAs in chloroplasts, a plant organelle that lacks the RNAi pathway thus allowing long dsRNAs to accumulate here. The dsRNA molecules expressed in these transgenic plants targeted β-actin and Shrub. Feeding larvae of the Colorado potato beetle with leaves from this modified potato plant resulted in 100% RNAi-induced mortality. Thus, the chloroplasts function as a kind of delivery system within the plant, ensuring that dsRNA of the correct length reaches the target insect. Naturally, this discovery has major implications for the further mode of application of RNAi insecticides in the field.

Current RNAi-Based Insecticides

The RNAi response has been thoroughly researched in the Western corn rootworm (WCR) D. virgifera virgifera. The WCR is a well-known pest insect with a significant economic impact on the maize harvest in the United States, as well as in Europe. In fact, it is estimated that in the United States alone, crop losses due to this plague amount to more than $1 billion annually. The WCR has a very sensitive RNAi response to oral administration of dsRNA and many target genes with lethal or detrimental effects have already been identified in this insect. It is therefore not so surprising that the first RNAi-based insecticides for the control of this insect have already been approved by the United States Environmental Protection Agency (EPA)1.

The proposed RNAi insecticide, developed by Monsanto and Dow Agrosciences, will be known as SmartStax Pro®. This plant-incorporated protectant (PIP) will employ a pyramid strategy: several different Bt-proteins, as well as dsRNA targeting the WCR Snf7 gene, will be expressed in this plant. Bt-proteins, also known as crystalline toxins, insert themselves into the gut epithelium of the insect, causing gut paralysis and resulting in the death of the insect. On the other hand, downregulation of Snf7, a gene that plays an essential role in protein trafficking, will also result in mortality. This combined strategy is designed to lead to the swift death of the insect, while also reducing the chances that insects will develop resistance against this PIP. As RNAi is a budding technology within the field of agriculture, it is likely only a matter of time before SmartStax Pro® and other, yet to be discovered insecticidal strategies, will appear on the market.

Insect Viral Infections and RNAi-Based Antiviral Immunity

Insects represent the largest group of animals on Earth in terms of biodiversity, with an estimated number of 5.5 million different species. This diversity reflects in a matching range of infecting viruses, which in addition to positively or negatively affecting insect populations, can also have a major impact on human well-being. In this section, important concepts regarding the patterns of viral infection pathogenesis will be addressed. Then, relevant insect disease-causing and persistent viral infections will be reviewed. At last, the use of viruses for insect biological control, as well as the potential use of the RNAi technology to protect beneficial insects from harmful viral infections will be discussed.

Patterns of Viral Infection – From Lethality to Non-pathogenicity

Viral infections can be classified according to their effect on the host, ranging from presenting no obvious harmful symptoms to being highly pathogenic or even lethal. These distinct outcomes exist in a variable range and are generally linked to different levels of viral particle production. Therefore, although this classification is not established beyond doubt, efforts have been made to classify them in three main groups, namely: acute, persistent and latent. Acute infections are characterized by high levels of viral replication and increased viral particle production. Generally, these infections are limited in time; either by the death of the host or by the clearance of the virus by the host immune system. On the other hand, persistent infections are characterized by constant, but relatively low, levels of viral replication and of viral particle production. These infections can manifest themselves for longer periods of time as often an equilibrium is established between the attack and counterattack strategies of the virus-host system. Although some persistent infections have the potential to cause variable levels of pathogenic effects, clear effects on fitness are often not observed. Finally, latent infections consist in the presence of the viral genome in the host cell without actual production of viral particles. The viral genome (in DNA form) can remain latent either as an episome or can be integrated in the host genome as a provirus. During this latency, viruses maintain the potential to resume viral replication and start producing viral particles, a process which is referred to as reactivation.

Additionally, the terms chronic and slow infection are often used, although mostly in the context of human viral diseases. A chronic infection is generally defined as the outcome of an acute infection in which neither host mortality nor virus clearance occur, meaning a persistent or latent outcome derived from an acute infection. In a slow infection, viral replication and particle production are slow but not constant, increasing overtime. Figure 2 summarizes these different patterns of viral infection.

Acute Viral Infections in Insects – Disease in Beneficials and Control Strategies for Pests

Clear examples of acute viral infections are the ones affecting beneficial insects, such as bees and economically important lepidopteran species. Recently, worrying losses in bee populations have been observed. These are typically associated with environmental pollution, specific pesticides or the presence of parasitic infections. However, the impact of diseases caused by different viruses, though often overlooked, cannot be ignored. In fact, several studies have identified multiple harmful viruses infecting honeybees and bumblebees. In addition, in the specific case of honeybees, losses have also been linked to the so-called Colony Collapse Disorder (CCD) which, in general terms, results in the sudden death of colonies. Although the specific causes of this phenomenon are still to be unraveled, it is thought that the aforementioned factors have been correlated with it, including the prevalence of several viral diseases. Another relevant example can be found in silkworms, whose viral diseases often cause sizeable economic losses to the sericulture industry in Asiatic countries. Table 2 presents an overview of viruses with significant impact on bees and silkworms. In addition, viruses affecting economically important shrimps are also contemplated.

In addition to the viruses that cause harmful infections in beneficial insects, others can use insects as vectors to infect other animals or plants – arthropod-borne viruses, or arboviruses. Important examples are the ones responsible for human diseases, transmitted via mosquitoes (e.g., Chikungunya Virus, Dengue Virus, Yellow Fever Virus, West Nile virus, Japanese Encephalitis Virus and Zika Virus); and plant viruses which may be deleterious to crops.

Insect viruses can also have a positive impact on human wellbeing. This is the case for viruses whose hosts are considered pest species. Because of this, insect viruses have long been researched for use as pest control agents. Some examples of viruses as delivery systems for RNAi were already discussed. Until recently, the use of microbial bio-insecticides has remained stagnant. However, increased concern about health and pollution hazards, environmental awareness, increased governmental restrictions on synthetic pesticides, advances in farming technology and other factors are fueling a solid growth in the biopesticide market. To be applicable as biopesticides, the viruses must comply with several requirements: they must be specific, highly virulent, and lethal to the targeted pest insect, while preferably also inducing epizootics. Despite the large diversity in entomopathogenic viruses, commercial research and use is mainly restricted to the family of Baculoviridae. Even though baculoviruses can infect arthropods belonging to several insect orders, only Lepidoptera-specific viruses belonging to the genera Nucleopolyhedrosis virus (Alphabaculovirus) and Granulovirus (Betabaculovirus) have been developed into commercial products. The widescale use of Baculoviruses can be explained by the already extant knowledge and expertise on this family of viruses as well as their useful characteristics. Baculoviruses display remarkable specificity and infections are highly lethal. During the late stage of infection, Baculoviruses produce occlusion bodies (OBs). These OBs increase resistance to the environment and make baculoviral insecticides easier to store and apply in the field. The major drawbacks of viral biopesticides are: the current absence of practical mass production systems resulting in high production costs; the (relatively) slow kill rate; short shelf-life and inconsistent field performance.

To date, the most widely used viral biopesticide is the H. armigera NPV, with over 10 manufacturers in China alone and new product registrations occurring on a yearly basis2. Other important viral agents are the S. exigua NPV, S. litura NPV and Cydia pomonella GV. A comprehensive list of virus-based commercial insecticide products has been assembled by and.

Virome and Insect Persistent Viral Infections

The idea that persistent viral infections are ubiquitous has recently started to emerge. In fact, the word ‘virome’ is often used nowadays and this field of research has gained a lot of interest in insects. This is due to three main reasons: (1) the advent of genomic and transcriptomic techniques; (2) the growing idea that the microbiome, including the virome, has the potential to interfere (both positively and negatively) in many biological processes; (3) and the establishment of viruses as crucial drivers of evolution. The latter has gained interest not only due to the ability of genetic mobile elements to cause mutagenesis, but also due to their potential capacity of providing hosts with beneficial gene-regulatory machinery.

In addition to the major direct impact of insect viruses on human life, as reviewed above; insect viral infections might play crucial roles on the ecological equilibrium of our planet. Therefore, it is of great interest to understand the mechanisms underlying the establishment and maintenance of insect viromes. In this context, persistent viral infections gain special relevance. Since these do not always cause obvious pathogenesis, their existence is often neglected. However, recently, identification of persistent viruses in insects has become recurring, with several reported cases both in vivo and in cultured cells. Interestingly, whether an infection is persistent or acute does not depend only on the virus itself, but also on the host. As demonstrated by several loss-of-function and deep sequencing studies, the role of RNAi in the established equilibrium between the persistent virus and the insect host is clear. However, the possible role of still unidentified factors has to be considered. A particularly interesting example is the Flock House Virus (FHV), which is known to cause persistent infections in lepidopteran cell lines and acute infections in crickets and flies. Remarkably, and by still unknown mechanisms, FHV is able to cause the two types of infection in D. melanogaster S2 cells. Further research regarding the diversity of insect viromes and the (RNAi-based) mechanisms involved in persistent-to-acute viral-host interactions would be of great value to understand their influence on several physiological processes; as well as their potential to contribute to efficient strategies to protect beneficial insects from harmful pathogens and to control dangerous pest insects.

RNAi-Based Antiviral Immunity to Protect Beneficial Insects

As discussed in the previous sections, it is clear that a deep understanding of the interactions between insects and their viruses is of great value. In addition, the current demand to control insect viral infections stresses the need to search for original approaches to fight these infections. Since RNAi is the main insect antiviral immune response, it is only logical to think of this mechanism as a potential form to protect beneficial insects against harmful viral infections.

In this context, the use of virus specific dsRNA aiming to trigger the RNAi pathway against viral infections has already been explored in bees. More specifically, delivery of targeted virus dsRNA by injection or feeding has been demonstrated to be effective in protecting honeybees against several relevant viral infections. In line with these findings, feeding virus-specific dsRNA to bumblebees has been demonstrated to act against the IAPV infection. Surprisingly, delivery of non-specific dsRNA has revealed to trigger an antiviral response in both honeybees and bumblebees.

Similar approaches have been investigated in lepidopteran insects with promising results. First, transfection or expression of virus-specific dsRNA in cell lines was shown to result in lower viral levels. Then, transgenic B. mori silkworms expressing virus-specific dsRNA have been reported to exhibit higher survival rates upon NPV infection on several occasions. In fact, this approach has been demonstrated to be effective in a commercially valuable silkworm strain. In addition, a similar strategy has been successfully tested to obtain protection of the silkworm to the B. mori cytoplasmic polyhedrosis virus (BmCPV). At last, injection of virus-specific dsRNA has been demonstrated to protect the mealworm beetle, Tenebrio molitor, against viral infection as well. Notably, comparable approaches have also been successfully applied in two economically relevant crustacean species. Recently, Trichoplusia ni High Five cells overexpressing key components of the RNAi machinery, namely B. mori Dicer2 and Argonaute2, have been reported to present reduced CrPV-induced mortality. This tactic remains to be tested in vivo and with regard to infections by other viruses. However, since RNAi is a broadly-acting antiviral immune mechanism in insects and considering that improvement of the RNAi response is observed in transgenic B. mori larvae overexpressing Argonaute2, this constitutes a promising approach. Table 3 presents a summary of the investigated strategies to obtain improved antiviral defense in insects, as well as in economically relevant crustacean species.

Considering these potential strategies to control insect viral diseases, the use of genetically engineered insects deserves special attention due to the risks of environmental contamination. In fact, up to date, the release of transgenic insects has been limited to sterile animals, with the aim of reducing pest species populations. However, the use of genetically engineered beneficial insects, as would be the eventual goal for various species of bees, would mostly require the maintenance of viable populations and therefore the use of fertile transgenic animals. On the other hand, the breeding of domestic silkworms closely depends on humans and is, therefore, highly controlled. Thus, the use of transgenic moths in sericulture is more feasible and might hold great potential with lower risks compared to the creation of other valuable transgenic species. In this context, it is important to keep in mind that several challenges will need to be overcome before such innovative strains can be obtained. For example, special regard should be payed to the productivity and fitness of such transgenic lines, as well as to the maintenance of the phenotype throughout several generations. Furthermore, a last consideration should be given to the eventual development of resistance by these viruses. Thus, before actual implementation, approaches to minimize this issue should be contemplated, such as the use of inducible expression systems which would be activated only in the case of viral disease, or the alternate expression of different transgenes.

Conclusion and Future Prospects

It is clear that the impact of RNAi technology and of insect viral infections on human life cannot be underestimated. In fact, in agricultural and industrial contexts, this is likely to become even more prominent in the years to come. In the first place, RNAi technology poses great potential to contribute to highly specific insect control strategies through delivery of dsRNA to pest species. Although the application of this technique has so far been limited by the variable RNAi efficiency amongst economically important insects, delivery systems provide a promising solution. Of these, an incredible wealth of options is available, with encouraging success rates. In the second place, insect baculoviruses form an interesting class of highly species-specific insecticides, which are currently under use. Due to the increasing knowledge on insect virus diversity, the potential use of other viral families cannot be excluded. In addition, the RNAi mechanism shows great potential as a combatant against viruses, which form an undeniable threat to beneficial insects. The efficient delivery of virus-specific dsRNA is a promising approach to protect beneficial insects such as pollinators. In addition, in the case of silkworms, the use of transgenic lines, resistant against such viral infections seems possible in the foreseeable future. This paper reviews the current literature on practical applications based on insect viruses and RNAi, as summarized in Figure 3. Although some of the described aspects still need to be thoroughly researched and therefore have to be considered with caution, this is an undeniably exciting field of research, full of potential.

Author Contributions

EV, DS, LM, T-WV, and JB conceived the manuscript. EV, DS, LM, and T-WV wrote the parts of the text. EV and DS worked on the structure and prepared the final version of the manuscript. EV, DS, and LM prepared the figures. EV, DS, and T-WV prepared the tables. JB corrected the manuscript and suggested further improvements.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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    Head G. P. Carroll M. W. Evans S. P. Rule D. M. Willse A. R. Clark T. L. (2017 ). Evaluation of SmartStax and SmartStax PRO maize against western corn rootworm and northern corn rootworm: efficacy and resistance management. Pest Manag. Sci. 73 1883–1899.

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    Isobe R. Kojima K. Matsuyama T. Quan G. X. Kanda T. Tamura T. (2004 ). Use of RNAi technology to confer enhanced resistance to BmNPV on transgenic silkworms. Arch. Virol. 149 1931–1940.

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    Iwanaga M. Hitotsuyama T. Katsuma S. Ishihara G. Daimon T. Shimada T. (2012 ). Infection study of Bombyx mori macula-like virus (BmMLV) using a BmMLV-negative cell line and an infectious cDNA clone. J. Virol. Methods 179 316–324.

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    Kontogiannatos D. Swevers L. Maenaka K. Park E. Y. Iatrou K. Kourti A. (2013 ). Functional characterization of a juvenile hormone esterase related gene in the moth Sesamia nonagrioides through RNA interference. PLoS One 8:e73834.

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    Koonin E. V. (2016 ). Viruses and mobile elements as drivers of evolutionary transitions. Philos. Trans. R. Soc. B Biol. Sci. 371:20150442.

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    Krempl C. Heidel-Fischer H. M. Jiménez-Alemán G. H. Reichelt M. Menezes R. C. Boland W. (2016 ). Gossypol toxicity and detoxification in Helicoverpa armigera and Heliothis virescens. Insect Biochem. Mol. Biol. 78 69–77.

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    Kumar A. Wang S. Ou R. Samrakandi M. Beerntsen B. T. T. Sayre R. T. T. (2013 ). Development of an RNAi based microalgal larvicide to control mosquitoes. Malar. World J. 4:6.

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    Kumar D. R. Kumar P. S. Gandhi M. R. Al-Dhabi N. A. Paulraj M. G. Ignacimuthu S. (2016 ). Delivery of chitosan/dsRNA nanoparticles for silencing of wing development vestigial (vg) gene in Aedes aegypti mosquitoes. Int. J. Biol. Macromol. 86 89–95.

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    Kumar P. Pandit S. S. Baldwin I. T. (2012 ). tobacco rattle virus vector: a rapid and transient means of silencing Manduca sexta genes by plant mediated RNA interference. PLoS One 7:e31347.

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    Labreuche Y. Veloso A. de la Vega E. Gross P. S. Chapman R. W. Browdy C. L. (2010 ). Non-specific activation of antiviral immunity and induction of RNA interference may engage the same pathway in the Pacific white leg shrimp Litopenaeus vannamei. Dev. Comp. Immunol. 34 1209–1218.

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    Lacey L. A. Grzywacz D. Shapiro-Ilan D. I. Frutos R. Brownbridge M. Goettel M. S. (2015 ). Insect pathogens as biological control agents: back to the future. J. Invertebr. Pathol. 132 1–41.

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    Lenaerts C. Cools D. Verdonck R. Verbakel L. Vanden Broeck J. Marchal E. (2017a ). The ecdysis triggering hormone system is essential for successful moulting of a major hemimetabolous pest insect, Schistocerca gregaria. Sci. Rep. 7:46502.

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    Lenaerts C. Palmans J. Marchal E. Verdonck R. Vanden Broeck J. (2017b ). Role of the venus kinase receptor in the female reproductive physiology of the desert locust, Schistocerca gregaria. Sci. Rep. 7:11730.

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    Lenaerts C. Van Wielendaele P. Peeters P. Vanden Broeck J. Marchal E. (2016 ). Ecdysteroid signalling components in metamorphosis and development of the desert locust, Schistocerca gregaria. Insect Biochem. Mol. Biol. 75 10–23.

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    Li T.-C. Scotti P. D. Miyamura T. Takeda N. (2007 ). Latent infection of a new alphanodavirus in an insect cell line. J. Virol. 81 10890–10896.

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    Longdon B. Fabian D. K. Hurst G. D. D. Jiggins F. M. (2012 ). Male-killing Wolbachia do not protect Drosophila bifasciata against viral infection. BMC Microbiol. 12(Suppl. 1):S8.

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    Marchal E. Badisco L. Verlinden H. Vandersmissen T. Van Soest S. Van Wielendaele P. (2011a ). Role of the Halloween genes, Spook and Phantom in ecdysteroidogenesis in the desert locust, Schistocerca gregaria. J. Insect Physiol. 57 1240–1248.

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    Marchal E. Verlinden H. Badisco L. Van Wielendaele P. Vanden Broeck J. (2012 ). RNAi-mediated knockdown of Shade negatively affects ecdysone-20-hydroxylation in the desert locust, Schistocerca gregaria. J. Insect Physiol. 58 890–896.

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    Meyering-Vos M. Müller A. (2007 ). RNA interference suggests sulfakinins as satiety effectors in the cricket Gryllus bimaculatus. J. Insect Physiol. 53 840–848.

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    Mysore K. Flannery E. M. Tomchaney M. Severson D. W. Duman-Scheel M. (2013 ). Disruption of Aedes aegypti olfactory system development through chitosan/siRNA nanoparticle targeting of semaphorin-1a. PLoS Negl. Trop. Dis. 7:e2215.

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    Shukla J. N. Kalsi M. Sethi A. Narva K. E. Fishilevich E. Singh S. (2016 ). Reduced stability and intracellular transport of dsRNA contribute to poor RNAi response in lepidopteran insects. RNA Biol. 13 656–669.

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