Identiﬁcation and Characterization of a Double-Stranded RNA Degrading Nuclease Inﬂuencing RNAi Efﬁciency in the Rice Leaf Folder Cnaphalocrocis medinalis

: Rice leaf folder Cnaphalocrocis medinalis is one of the most serious pests of rice in rice-planting regions worldwide. DsRNA-degrading nucleases (dsRNases) are important factors in reducing the efﬁciency of RNA interference (RNAi) in different insects. In this study, a dsRNase gene from C. medinalis ( CmdsRNase ) was cloned and characterized. The CmdsRNase cDNA was 1395 bp in length, encoding 464 amino acids. The CmdsRNase zymoprotein contains a signal peptide and an endonuclease NS domain that comprises six active sites, three substrate-binding sites, and one Mg 2+ -binding site. The mature CmdsRNase forms a homodimer with a total of 16 α -helices and 20 β -pleated sheets. Homology and phylogenetic analyses revealed that CmdsRNase is closely related to dsRNase2 in Ostrinia nubilalis . Expression pattern analysis by droplet digital PCR indicated that the expression levels of CmdsRNase varied throughout the developmental stages of C. medinalis and in different adult tissues, with the highest expression levels in the fourth-instar larvae and the hemolymph. CmdsRNase can degrade dsRNA to reduce the efﬁciency of RNAi in C. medinalis . Co-silencing of CmCHS ( chitin synthase from C. medinalis ) and CmdsRNase affected signiﬁcantly the growth and development of C. medinalis and thus improved RNAi efﬁcacy, which increased by 27.17%. These ﬁndings will be helpful for green control of C. medinalis and other lepidopteran pests by RNAi.


Introduction
RNA interference (RNAi) is a highly conserved mechanism triggered by doublestranded RNA (dsRNA) in the evolutionary process; therefore, homologous mRNAs are degraded efficiently and specifically. The essence of RNAi is post-transcriptional gene silencing. The transcription of the silenced genes continues to proceed normally, but the transcribed messenger RNA (mRNA) undergoes sequence-specific degradation in the cytoplasm, with the result that these genes cannot be normally expressed as proteins [1]. RNAi exists in most eukaryotes, but the efficiency of RNAi varies greatly among different species [2][3][4][5]. RNAi has high efficiency, specificity, and transmissibility, and is widely used as a powerful tool in the exploration of gene function analysis, biomedical research, biological pest control, and other fields. The use of RNAi technology to control pests is currently one of the hotspots in scientific research. The difference in RNAi efficiency among different species of insects limits the use of RNAi technology in basic insect research and pest control; for example, the RNAi efficiency in most coleopteran insects is high and longlasting [6][7][8][9], whereas the RNAi efficiency in most dipteran, hemipteran, and lepidopteran insects is variable and unstable [10][11][12]. There are many factors that affect the efficiency of RNAi in insects, including delivery methods [13][14][15], dsRNA transport in cells [16], target is a holometabolous insect, undergoing four developmental stages in its life cycle: egg, larva, pupa, and adult. C. medinalis larvae generally go through five instars and adults can migrate over long distances. This insect is a migratory rice pest and widely distributed in rice-planting regions worldwide [36]. Larvae feed on mesophyll tissues of rice leaves, which severely affects the photosynthesis of rice, leading to approximately 10-20% yield loss or even total crop failure. In this study, dsRNase from C. medinalis, named CmdsRNase, was cloned with reverse transcription-polymerase chain reaction (RT-PCR) and characterized with bioinformatics methods and digital PCR (dPCR). Functional analysis of CmdsRNase was performed using RNAi technology.

Characteristics of CmdsRNase
The open reading frame (ORF) of the CmdsRNase cDNA is 1395 bp in length, encoding 464 amino acids ( Figure 1). The molecular formula of CmdsRNase was C 2330 H 3534 N 676 O 663 S 17 , with a molecular weight of 52.17 kDa and a theoretical isoelectric point (pI) of 8.88. This zymoprotein contains a signal peptide of 16 amino acids at the N-terminus. Functional domain analysis revealed that CmdsRNase possesses an endonuclease NS domain (Figure 2a) that comprises six active sites, three substrate-binding sites, and one Mg 2+ -binding site ( Figure 2b). The mature CmdsRNase contains four O-glycosylation (S8, S123, S140, and S208) and two N-glycosylation sites (N36 and N297). CmdsRNase includes 36 negatively charged amino acid residues (Asp + Glu) and 43 positively charged amino acid residues (Arg + Lys), with a calculated instability index (II) of 39.05, which indicates that it is a stable protein since a protein with an II greater than 40 is unstable. The aliphatic index of CmdsRNase was predicted to be 75.71 and the grand average of hydropathicity (GRAVY) to be −0.31. Homology modeling showed that the mature CmdsRNase (amino acids 159-440) forms a homodimer, with a total of 16 α-helices, 20 β-pleated sheets, and 36 random coils ( Figure 3a). As shown in Figure 3b, deep red indicates the evolutionarily conserved amino acids that are of vital importance in the structure and function of CmdsRNase.
reported as a notorious insect pest of rice in Asian rice-growing areas [34,35]. This spe is a holometabolous insect, undergoing four developmental stages in its life cycle: larva, pupa, and adult. C. medinalis larvae generally go through five instars and adults migrate over long distances. This insect is a migratory rice pest and widely distribute rice-planting regions worldwide [36]. Larvae feed on mesophyll tissues of rice lea which severely affects the photosynthesis of rice, leading to approximately 10-20% y loss or even total crop failure. In this study, dsRNase from C. medinalis, named CmdsRN was cloned with reverse transcription-polymerase chain reaction (RT-PCR) and cha terized with bioinformatics methods and digital PCR (dPCR). Functional analys CmdsRNase was performed using RNAi technology.

Characteristics of CmdsRNase
The open reading frame (ORF) of the CmdsRNase cDNA is 1395 bp in length, en ing 464 amino acids ( Figure 1). The molecular formula of CmdsRNase C2330H3534N676O663S17, with a molecular weight of 52.17 kDa and a theoretical isoele point (pI) of 8.88. This zymoprotein contains a signal peptide of 16 amino acids at th terminus. Functional domain analysis revealed that CmdsRNase possesses an endonu ase NS domain (Figure 2a) that comprises six active sites, three substrate-binding s and one Mg 2+ -binding site ( Figure 2b). The mature CmdsRNase contains four O-glyco ation (S8, S123, S140, and S208) and two N-glycosylation sites (N36 and N297). Cm Nase includes 36 negatively charged amino acid residues (Asp + Glu) and 43 positi charged amino acid residues (Arg + Lys), with a calculated instability index (II) of 3 which indicates that it is a stable protein since a protein with an II greater than 40 is stable. The aliphatic index of CmdsRNase was predicted to be 75.71 and the grand ave of hydropathicity (GRAVY) to be −0.31. Homology modeling showed that the ma CmdsRNase (amino acids 159-440) forms a homodimer, with a total of 16 α-helices, 2 pleated sheets, and 36 random coils ( Figure 3a). As shown in Figure 3b, deep red indic the evolutionarily conserved amino acids that are of vital importance in the structure function of CmdsRNase.  Blue inverted triangles represent active sites of six key amino acid residues, the yellow triangle indicates Mg 2+ -binding sites, and black triangles mark substrate-binding sites. (a)

Homology Comparison and Cluster Dendrogram
CmdsRNase showed 75.37% similarity with dsRNase2 from O. nubilalis base BLAST against the NCBI NR database containing its amino acid sequence. The phy netic tree of 36 dsRNases from 25 insect species showed that dsRNases from the s order grouped into a clade and CmdsRNase clustered together with dsRNA-degra nuclease from O. nubilalis ( Figure 4). These results indicate that dsRNase is conse during evolution and that C. medinalis is the cloest relative of O. nubilalis.

Homology Comparison and Cluster Dendrogram
CmdsRNase showed 75.37% similarity with dsRNase2 from O. nubilalis based on BLAST against the NCBI NR database containing its amino acid sequence. The phylogenetic tree of 36 dsRNases from 25 insect species showed that dsRNases from the same order grouped into a clade and CmdsRNase clustered together with dsRNA-degrading nuclease from O. nubilalis ( Figure 4). These results indicate that dsRNase is conserved during evolution and that C. medinalis is the cloest relative of O. nubilalis. Int. J. Mol. Sci. 2022, 23, x FOR PEER REVIEW 6 of 17

Gene Expression Profiles
The droplet digital PCR (ddPCR) results showed that CmdsRNase was expressed in the larvae, with the highest level in the fourth-instar larvae, and was almost not expressed in the eggs, pupae, and adults ( Figure 5). This gene was expressed in the tissues tested from C. medinalis adults, with the highest level in the hemolymph, followed by the midgut, and with the lowest level in the head and integument. The CmdsRNase expression level in the hemolymph was 59 times that in the head and integument ( Figure 6).

Gene Expression Profiles
The droplet digital PCR (ddPCR) results showed that CmdsRNase was expressed the larvae, with the highest level in the fourth-instar larvae, and was almost not express in the eggs, pupae, and adults ( Figure 5). This gene was expressed in the tissues test from C. medinalis adults, with the highest level in the hemolymph, followed by the midg and with the lowest level in the head and integument. The CmdsRNase expression leve the hemolymph was 59 times that in the head and integument ( Figure 6). tively. E, Egg; 1-5, first-fifth-instar larvae; P, Pupa; A, Adult. Each bar represents the mean ± S Different letters above the bars indicate significant differences at p < 0.05 based on Duncan's test

Degradation of dsRNA by Crude CmdsRNase
The agarose gel electrophoresis assay showed that 120 ng of dsRNA was totally degraded by 10 μg of crude CmdsRNase in 1 min at 28 °C (

Effect of dsCmdsRNase Injection on RNAi Efficiency
To further verify the function of dsRNase in C. medinalis, dsRNAs of CmRNase and CmCHS (chitin synthase gene from C. medinalis) were jointly injected into the third-instar larvae to verify whether this enzyme can degrade dsRNA in the hemolymph. The expression level of CmCHS after co-injection of dsCmdsRNase + dsCmCHS was significantly lower than that of CmCHS at the third and fourth days after injection of dsCmCHS alone. The CmCHS expression level at the third day post co-injection was reduced by 2 times compared with the dsCmCHS-injected group, in which the CmCHS level was reduced by 2.3 times compared with the control. The CmCHS level at the fourth day post co-injection Each bar represents the mean ± SD. Different letters above the bars indicate significant differences at p < 0.05 based on Duncan's test.

Degradation of dsRNA by Crude CmdsRNase
The agarose gel electrophoresis assay showed that 120 ng of dsRNA was totally degraded by 10 µg of crude CmdsRNase in 1 min at 28 • C (

Degradation of dsRNA by Crude CmdsRNase
The agarose gel electrophoresis assay showed that 120 ng of dsRNA was totally degraded by 10 μg of crude CmdsRNase in 1 min at 28 °C (

Effect of dsCmdsRNase Injection on RNAi Efficiency
To further verify the function of dsRNase in C. medinalis, dsRNAs of CmRNase and CmCHS (chitin synthase gene from C. medinalis) were jointly injected into the third-instar larvae to verify whether this enzyme can degrade dsRNA in the hemolymph. The expression level of CmCHS after co-injection of dsCmdsRNase + dsCmCHS was significantly lower than that of CmCHS at the third and fourth days after injection of dsCmCHS alone. The CmCHS expression level at the third day post co-injection was reduced by 2 times compared with the dsCmCHS-injected group, in which the CmCHS level was reduced by 2.3 times compared with the control. The CmCHS level at the fourth day post co-injection

Effect of dsCmdsRNase Injection on RNAi Efficiency
To further verify the function of dsRNase in C. medinalis, dsRNAs of CmRNase and CmCHS (chitin synthase gene from C. medinalis) were jointly injected into the third-instar larvae to verify whether this enzyme can degrade dsRNA in the hemolymph. The expression level of CmCHS after co-injection of dsCmdsRNase + dsCmCHS was significantly lower than that of CmCHS at the third and fourth days after injection of dsCmCHS alone. The CmCHS expression level at the third day post co-injection was reduced by 2 times compared with the dsCmCHS-injected group, in which the CmCHS level was reduced by 2.3 times compared with the control. The CmCHS level at the fourth day post co-injection decreased by 2.4 times compared with the dsCmCHS-injected group, in which the CmCHS level decreased by 2 times compared with the control (Figure 8). Three days after co-injection of dsCmdsRNase + dsCmCHS and injection of dsCmCHS, RNAi efficiency of CmCHS in C. medinalis reached 78.04% and 56.84%, respectively; this efficiency increased by 27.17% (Figure 9). The corrected mortality of the dsCmCHS-injected larvae (53.3%) was 6.4 times that of the dsGFP-injected larvae (8.3%) at the seventh day after injection, and the corrected mortality of larvae injected with dsCmdsRNase + dsCmCHS (81.7%) was 1.5 times that of the dsCmCHS-injected larvae (53.3%), whereas dsGFP had little influence on larval survival ( Figure 10).  (Figure 8). Three days after co-injection of dsCmdsRNase + dsCmCHS and injection of dsCmCHS, RNAi efficiency of CmCHS in C. medinalis reached 78.04% and 56.84%, respectively; this efficiency increased by 27.17% (Figure 9). The corrected mortality of the dsCmCHS-injected larvae (53.3%) was 6.4 times that of the dsGFP-injected larvae (8.3%) at the seventh day after injection, and the corrected mortality of larvae injected with dsCmdsRNase + dsCmCHS (81.7%) was 1.5 times that of the dsCmCHS-injected larvae (53.3%), whereas dsGFP had little influence on larval survival ( Figure 10). Larvae injected with dsGFP were used as the control group. Each bar represents the mean ± SD. One asterisk above bars indicates a significant difference at p < 0.05 and two asterisks indicate a very significant difference at p < 0.01 according to Duncan's test.  Larvae injected with dsGFP were used as the control group. Each bar represents the mean ± SD. One asterisk above bars indicates a significant difference at p < 0.05 and two asterisks indicate a very significant difference at p < 0.01 according to Duncan's test.  (Figure 8). Three days after co-injection of dsCmdsRNase + dsCmCHS and injection of dsCmCHS, RNAi efficiency of CmCHS in C. medinalis reached 78.04% and 56.84%, respectively; this efficiency increased by 27.17% (Figure 9). The corrected mortality of the dsCmCHS-injected larvae (53.3%) was 6.4 times that of the dsGFP-injected larvae (8.3%) at the seventh day after injection, and the corrected mortality of larvae injected with dsCmdsRNase + dsCmCHS (81.7%) was 1.5 times that of the dsCmCHS-injected larvae (53.3%), whereas dsGFP had little influence on larval survival ( Figure 10). The CmCHS expression levels in the third-instar C. medinalis larvae were detected with ddPCR four days after injection of dsCmCHS or the mixture of dsCmdsRNase and dsCmCHS. Larvae injected with dsGFP were used as the control group. Each bar represents the mean ± SD. One asterisk above bars indicates a significant difference at p < 0.05 and two asterisks indicate a very significant difference at p < 0.01 according to Duncan's test.   Corrected mortality of the third-instar C. medinalis larvae was calculated within seven days after injection with dsCmCHS or the mixture of dsCmdsRNase and dsCmCHS. Larvae injected with dsGFP were used as the control group. Different letters above the broken lines indicate significant differences between treatments on the same day (p < 0.05, Duncan's test).

Effect of RNAi on Phenotypes of C. medinalis
After CmCHS was silenced, phenotypic changes of C. medinalis were recorded. Larvae injected with dsCmCHS or dsCmdsRNase + dsCmCHS displayed phenotypic alterations, such as lower vitality, smaller body size, and lighter weight. The abdomen of larvae shrank ( Figure 11D), the body color turned black ( Figure 11E), and the head got bigger ( Figure 11D,F). Some larvae with CmCHS gene knockdown died. In addition, CmCHS RNAi larvae could not molt and pupate normally; however, the larvae in the control group grew normally and there were no obvious phenotypic changes. Some pupae from larvae with CmCHS RNAi blackened and exhibited deformed phenotypes ( Figure 12). RNAi also caused adult deformities, such as abnormal wing folding and unfolding (Figure 13B,C), and malformation, with pupa-shaped abdomens observed in adults ( Figure  13D). In the experimental group injected with dsCmdsRNase + dsCmCHS, it was observed that there were normal-sized adults without wing deformities, but they had no ability to fly. These results indicate that co-silencing of both CmCHS and CmdsRNase can lead to serious developmental disorders and death of C. medinalis. Figure 10. Corrected mortality of larvae within seven days after dsRNA injection. Corrected mortality of the third-instar C. medinalis larvae was calculated within seven days after injection with dsCmCHS or the mixture of dsCmdsRNase and dsCmCHS. Larvae injected with dsGFP were used as the control group. Different letters above the broken lines indicate significant differences between treatments on the same day (p < 0.05, Duncan's test).

Effect of RNAi on Phenotypes of C. medinalis
After CmCHS was silenced, phenotypic changes of C. medinalis were recorded. Larvae injected with dsCmCHS or dsCmdsRNase + dsCmCHS displayed phenotypic alterations, such as lower vitality, smaller body size, and lighter weight. The abdomen of larvae shrank ( Figure 11D), the body color turned black ( Figure 11E), and the head got bigger ( Figure 11D,F). Some larvae with CmCHS gene knockdown died. In addition, CmCHS RNAi larvae could not molt and pupate normally; however, the larvae in the control group grew normally and there were no obvious phenotypic changes. Some pupae from larvae with CmCHS RNAi blackened and exhibited deformed phenotypes ( Figure 12). RNAi also caused adult deformities, such as abnormal wing folding and unfolding ( Figure 13B,C), and malformation, with pupa-shaped abdomens observed in adults ( Figure 13D). In the experimental group injected with dsCmdsRNase + dsCmCHS, it was observed that there were normal-sized adults without wing deformities, but they had no ability to fly. These results indicate that co-silencing of both CmCHS and CmdsRNase can lead to serious developmental disorders and death of C. medinalis.  Figure 10. Corrected mortality of larvae within seven days after dsRNA injection. Corrected mortality of the third-instar C. medinalis larvae was calculated within seven days after injection with dsCmCHS or the mixture of dsCmdsRNase and dsCmCHS. Larvae injected with dsGFP were used as the control group. Different letters above the broken lines indicate significant differences between treatments on the same day (p < 0.05, Duncan's test).

Effect of RNAi on Phenotypes of C. medinalis
After CmCHS was silenced, phenotypic changes of C. medinalis were recorded. Larvae injected with dsCmCHS or dsCmdsRNase + dsCmCHS displayed phenotypic alterations, such as lower vitality, smaller body size, and lighter weight. The abdomen of larvae shrank ( Figure 11D), the body color turned black ( Figure 11E), and the head got bigger ( Figure 11D,F). Some larvae with CmCHS gene knockdown died. In addition, CmCHS RNAi larvae could not molt and pupate normally; however, the larvae in the control group grew normally and there were no obvious phenotypic changes. Some pupae from larvae with CmCHS RNAi blackened and exhibited deformed phenotypes ( Figure 12). RNAi also caused adult deformities, such as abnormal wing folding and unfolding (Figure 13B,C), and malformation, with pupa-shaped abdomens observed in adults ( Figure  13D). In the experimental group injected with dsCmdsRNase + dsCmCHS, it was observed that there were normal-sized adults without wing deformities, but they had no ability to fly. These results indicate that co-silencing of both CmCHS and CmdsRNase can lead to serious developmental disorders and death of C. medinalis.

Discussion
The analysis of the overall expression pattern of CmdsRNase, especially the high expression in the hemolymph and midgut of the larvae, showed that the activity of the nuclease increased during the larval stage, and the high level of dsRNase in the hemolymph and midgut may help reduce larval RNAi efficiency. Recent research on S. litura supports this view [28]. However, in Spodoptera exigua, the nuclease activity of the intestinal supernatant at different developmental stages is relatively low, and the lower level of dsRNase may be one of the factors leading to the higher RNAi response of this insect [37]. With tissue specificity, almost all insect dsRNases are highly expressed in the intestine and hemolymph [31,33]; the expression profile of CmdsRNase in C. medinalis is consistent with

Discussion
The analysis of the overall expression pattern of CmdsRNase, especially the high expression in the hemolymph and midgut of the larvae, showed that the activity of the nuclease increased during the larval stage, and the high level of dsRNase in the hemolymph and midgut may help reduce larval RNAi efficiency. Recent research on S. litura supports this view [28]. However, in Spodoptera exigua, the nuclease activity of the intestinal supernatant at different developmental stages is relatively low, and the lower level of dsRNase may be one of the factors leading to the higher RNAi response of this insect [37]. With tissue specificity, almost all insect dsRNases are highly expressed in the intestine and hemolymph [31,33]; the expression profile of CmdsRNase in C. medinalis is consistent with

Discussion
The analysis of the overall expression pattern of CmdsRNase, especially the high expression in the hemolymph and midgut of the larvae, showed that the activity of the nuclease increased during the larval stage, and the high level of dsRNase in the hemolymph and midgut may help reduce larval RNAi efficiency. Recent research on S. litura supports this view [28]. However, in Spodoptera exigua, the nuclease activity of the intestinal supernatant at different developmental stages is relatively low, and the lower level of dsRNase may be one of the factors leading to the higher RNAi response of this insect [37]. With tissue specificity, almost all insect dsRNases are highly expressed in the intestine and hemolymph [31,33]; the expression profile of CmdsRNase in C. medinalis is consistent with the general pattern, indicating the function of CmdsRNase to degrade dsRNA that enters the gut lumen or hemolymph.
It has been reported that LmdsRNase1 in L. migratoria can effectively degrade dsRNA at pH5 and is highly expressed in blood cells, but the physiological pH value of hemolymph (7.0) strongly inhibits the activity of LmdsRNase1, making dsRNA stable in the hemolymph for a long time. Therefore, although dsRNase is expressed in different tissues, some may not degrade dsRNA due to physiological pH or substrate-specific factors [26]. Our results showed that the hemolymph and the crude CmdsRNase extracted from the hemolymph had similar ability to degrade dsRNA; this may be because the hemolymph contained dsR-Nases that degrade dsRNA. Although CmdsRNase is mainly expressed in the hemolymph, dsRNase in the hemolymph of C. medinalis is active, which is consistent with the results of the study on dsRNase in the hemolymph of Manduca sexta [38]. The conditions for dsRNase to degrade dsRNA are different in different insects.
In insects, dsRNases reduce RNAi efficiency by degrading dsRNA. In S. gregaria, interfering with dsRNase2 improved RNAi efficiency, while interfering with other dsRNases had no effect [26,32]. In C. puncticollis, only dsRNase3 could affect RNAi efficiency [33]; however, in S. litura, the combined action of multiple dsRNases led to a decrease in RNAi efficiency [28,30], indicating that the number of dsRNases and their mechanisms of action may be different in various insects. In the present study, by co-injecting dsCmCHS and dsCmRNase + dsCmCHS in C. medinalis, the degrading activity of CmdsRNase on dsRNA was confirmed and the RNAi efficiency in this pest was significantly elevated. This experiment was only a preliminary study on the function of a single dsRNase; it does not rule out the existence of a synergistic effect between this enzyme and other dsRNases of C. medinalis. In the next step, we will try to silence multiple enzymes simultaneously so as to further improve the efficacy of RNAi in C. medinalis.

Insect-Rearing and Sample Preparation
C. medinalis was collected from a rice field in Guiyang, Guizhou, China, and maintained in an insectary of the Institute of Entomology, Guizhou University, at 26 ± 1 • C and 75 ± 5% relative humidity under a 14:10 h light: dark photoperiod. After three consecutive generations, insects at the same developmental stage were collected and stored in RNAlater (Qiagen, Duesseldorf, Germany) at −20 • C until use. These samples included eggs, firstfifth-instar larvae, pupa, adults, and imaginal tissues (the head, hemolymph, fat bodies, testis, ovary, midgut, and integument).

RNA Extraction and cDNA Synthesis
Total RNA was extracted at different developmental stages and from various imaginal tissues of C. medinalis using an Eastep Super Total RNA Kit (Promega, Madison, WI, USA) according to the manufacturer's instructions. The quality and purity of the isolated RNA were determined by using agarose gel electrophoresis and a NanoDrop 2000 spectrophotometer (Thermo Fisher Scientific, Waltham, MA, USA), respectively. Then, cDNA was synthesized using a PrimeScript First-Strand cDNA Synthesis Kit (Takara Bio, Beijing, China) according to the manufacturer's instructions and stored at −20 • C.

Cloning CmdsRNase
Specific primers were designed based on the CmdsRNase sequence using Primer Premier 6.0 (PREMIER Biosoft, Palo Alto, CA, USA). The CmdsRNase ORF was then amplified using RT-PCR with cDNA from C. medinalis as a template. RT-PCR was performed with 2× Taq PCR Star Mix (GenStar, Beijing, China) under the following conditions: 2 min at 94 • C; 32 cycles of 30 s at 94 • C, 30 s at 55 • C, and 60 s at 72 • C; and 10 min at 72 • C. Subsequently, the PCR products were run on a 1% agarose gel for 25 min at 130 V, and the expected band was excised from the gel and purified using a DiaSpin DNA Gel Extraction Kit (Sangon Biotech, Shanghai, China). The recovered PCR products were cloned into a pMD18-T vector (Takara Bio, Dalian, China) and the recombinant pMD-18-T-CmdsRNase vector was transformed into E. coli DH5α competent cells (Invitrogen, Carlsbad, CA, USA), which were plated on Luria-Bertani agar plates and incubated at 37 • C overnight. Finally, the colony PCR was performed to identify positive clones that were submitted to Sangon Biotech (Shanghai, China) for sequencing.

Gene Expression Analyses Using ddPCR
The mRNA expression levels of CmdsRNase were detected using a QX200 Droplet Digital PCR system (ddPCR) (Bio-Rad, Hercules, CA, USA) at different developmental stages and in various adult tissues. The disposable eight-channel DG8 cartridge was placed in the cartridge holder, and 20 µL of PCR mixtures were transferred to the middle wells of the cartridge. The lower wells were filled with 70 µL of droplet-generation oil. The cartridge containing the PCR mixtures and oil was placed into a Droplet Generator (Bio-Rad, Hercules, CA, USA) to generate individual droplets. Then, 40 µL of droplets were transferred into wells of a 96-well PCR plate, which was heat-sealed at 180 • C for 5 s with a permeable foil using a PX1 PCR Plate Sealer and loaded into a C1000 Touch Thermal Cycler (Bio-Rad, Hercules, CA, USA). The PCR reaction system and conditions are listed in Table 1. After PCR was complete, the sealed plate was placed into a Droplet Reader (Bio-Rad, Hercules, CA, USA) to count the positive and negative droplets. The ddPCR experiment was repeatedly performed three times for each sample. Data were analyzed using QuantaSoft software (Bio-Rad, Hercules, CA, USA) and SPSS 22.0 (SPSS Inc., Chicago, IL, USA). 4.6. Crude CmdsRNase Extraction and dsRNA Degrading Assay C. medinalis larvae were torn using dissecting forceps and put into a 0.8 mL centrifuge tube with four holes at its bottom. This small tube was then put into a 1.5 mL tube containing 1 mM phenylthiourea and 1 mM phenylmethylsulfonyl fluoride (PMSF). The double-tube device was centrifuged at 2500× g for 10 min at 4 • C and the collected hemolymph was centrifuged at 12,000× g for 10 min at 4 • C to remove cells for obtaining serum. Next, 0.1 M NaOH was added to the serum to adjust the pH to 8.8 (the isoelectric point of CmdsRNase), and the precipitate was collected by centrifugation at 12,000× g for 10 min at 4 • C and dissolved with 0.01 M phosphate-buffered saline (PBS) to obtain crude CmdsRNase.
The concentration of the crude CmdsRNase zymoprotein was measured using a BCA Protein Quantification Kit (Yesea, Shanghai, China) according to the manufacturer's instructions in a Multiskan GO (Thermo Fisher Scientific, Waltham, MA, USA). For an in vitro incubation assay, 1 µL of dsCmCHS solution (containing 120 ng of dsRNA, 381 bp) was mixed with 10 µg of the crude CmdsRNase in 1.5 mL centrifuge tubes and incubated at 28 • C for 1, 10, 20, 4, and 60 min, respectively. Then, 120 ng of dsCmCHS was mixed separately with 1, 5, 10, 15, and 20 µg of the crude CmdsRNase in 1.5 mL centrifuge tubes and incubated at 28 • C for 5 min. After incubation, these samples were subjected to 1.5% agarose gel electrophoresis to evaluate the integrity of residual dsRNA.

RNA Interference
According to the ORFs of CmdsRNase and CmCHS (chitin synthase gene from C. medinalis), two online RNAi design tools, including siDirect (http://sidirect2.rnai.jp) and DSIR (http://biodev.extra.cea.fr/DSIR/DSIR.html) (accessed on 6 May 2021), were used to search for fragments targeting CmdsRNase and CmCHS mRNAs. The green fluorescent protein gene (GFP) (GenBank: CAA58789) from Aequorea victoria was used as the internal control. The target fragments were amplified using CmdsRNase-iF/CmdsRNase-iR, CmCHS-iF/CmCHS-iR, and GFP-iF/GFP-iR primers, respectively. After purification, the PCR products were inserted into the pMD18-T vector (Takara Bio, Dalian, China) for sequencing. Clones containing the correct sequences were cultured. Plasmids were extracted and used as templates to separately amplify target fragments with CmdsRNase-dsF/CmdsRNase-dsR, CmCHS-dsF/CmCHS-dsR, and GFP-dsF/GFP-dsR primers. After the PCR product was purified, DNA at a high concentration (not less than 300 ng/µL) was used for the template-synthesis of dsCmdsRNase, dsCmCHS, and dsGFP using a Tran-scriptAid T7 High Yield Transcription Kit (Thermo Fisher Scientific, Waltham, MA, USA). Briefly, the in vitro transcription system (20 µL) contained 2 µL of nuclease-free water, 4 µL of 5 × reaction buffer, 8 µL of ATP/CTP/GTP/UTP mix, 4 µL of DNA template (with T7 at both ends), and 2 µL of enzyme mix. After vortexing and briefly spinning, the tubes were incubated at 37 • C for 6 h. The dsRNA was purified using a GeneJET RNA Purification Kit (Thermo Fisher Scientific, Waltham, MA, USA) and then detected by agarose gel electrophoresis and a NanoDrop 2000 spectrophotometer (Thermo Fisher Scientific, Waltham, MA, USA) to evaluate its integrity and quality. The primers used in this study are listed in Table 2. Twenty healthy third-instar larvae were selected for each RNAi experiment in each group. One-point-five micrograms of dsCmCHS or the mixture of dsCmdsRNase and dsCmCHS were injected into the eighth abdominal segment of each larva using a Nanoliter 2020 Injector (World Precision Instruments, Sarasota, FL, USA), then the larvae were moved onto fresh rice leaves inside glass tubes and cultured in an artificial climate box. The feeding, phenotype, and survival of the larvae were observed each day, and the leaves were replaced with fresh ones every two days. Larvae injected with the same amount of dsGFP were used as the control. These experiments were replicated 4 times for each group. Two surviving larvae were collected from each group every day over four days to detect the expression level of CmCHS by ddPCR.

Statistical Analyses
Data are expressed as the means ± SD from at least three independent experiments. Statistical analyses were performed with one-way analysis of variance followed by Duncan's multiple range test using SPSS 22.0 (SPSS Inc., Chicago, IL, USA). Statistical significance was set at p < 0.05.

Conclusions
In this study, a dsRNase in C. medinalis was cloned and characterized using PCR and bioinformatics technologies. CmdsRNase can degrade dsRNA to reduce the efficiency of RNAi in C. medinalis. Co-silencing of the target genes CmCHS and CmdsRNase can significantly improve the RNAi effect on C. medinalis. This research provides a new strategy for RNAi-mediated insect pest control and will be helpful in promoting green control of lepidopteran pests by RNAi.