CN110628771A

CN110628771A - Kit for preventing and treating harmonia axyridis

Info

Publication number: CN110628771A
Application number: CN201910718239.5A
Authority: CN
Inventors: 潘慧鹏; 吕晶; 郭威; 杨春晓; 郭木娟; 陈诗敏; 邱宝利; 刘卓琦
Original assignee: South China Agricultural University
Current assignee: South China Agricultural University
Priority date: 2019-08-05
Filing date: 2019-08-05
Publication date: 2019-12-31
Anticipated expiration: 2039-08-05
Also published as: CN110628771B

Abstract

The invention discloses a kit for preventing and treating ladybug. The invention obtains a high lethal gene zetacOPI of the harmonia axyridis by screening, and researches show that the expression of the silent gene zetacOPI can obviously inhibit the growth and development of the harmonia axyridis and can efficiently prevent and control the harmonia axyridis. Meanwhile, dszetacoPI of a silent target gene zetacoPI is designed, and the target gene can be directly fed to achieve the purpose of preventing and treating the harmonia axyridis. The method has the advantages of convenient operation, good effectiveness and sensitivity, high insecticidal efficiency, environmental friendliness and the like, and has good application prospect.

Description

Kit for preventing and treating harmonia axyridis

Technical Field

The invention belongs to the technical field of insect pest prevention and control. More particularly relates to a kit for preventing and treating ladybug.

Background

The harmonia axyridis (Fabricius) belongs to the family of Coleoptera axyridis, is an important agricultural pest, has wide host plants, and is mainly harmful to solanaceae vegetables such as eggplants, potatoes, tomatoes and the like. The larvae and adults all feed on leaves, prefer to gather on the back of the leaves, and eat down the epidermis and mesophyll, so that the damaged leaves usually form irregular transparent spots or perforations, and the plant wilts or even the whole plant dies when the disease is serious. The distribution range of the harmonia axyridis in China is wide, and particularly the occurrence density of the harmonia axyridis in the south of Yangtze river is high. In recent years, due to the warming of climate, the development of trade and the enlargement of vegetable cultivation area in protected areas, the occurrence and the harm of the ladybug are increasingly serious because of the continuous foodstuff all the year round. In 2015, the potato staple food strategy is started in China, the planting area of potatoes in China must be further enlarged, and the prevention and control of the ladybug are not slow.

At present, the control of the harmonia axyridis comprises artificial capture, attractant trapping and chemical pesticide. Wherein, the manual capture has poor effect and very heavy labor problem; the trapping effect of the attractant is not satisfactory and not thorough; therefore, chemical pesticides are still relied on more, but the chemical pesticides cause environmental pollution and quality safety of agricultural products.

RNA interference (RNAi) is an evolutionarily conserved mechanism of action that relies on the production of short stretches of RNAs (sirnas) to promote degradation or inhibit translation of homologous mrnas. RNAi provides an important tool for functional genomics research in insects, and lays a foundation for developing an environment-friendly pest control method. As RNAi technology can specifically inhibit the expression of genes, the technology is widely applied to target interference of pest genes so as to achieve the purpose of preventing and controlling pests, but the research on the functions of the gene of the harmonia axyridis is less at home and abroad at present, and no target gene report with insecticidal activity exists.

The earlier-stage research of the inventor team shows that (201710949193.9), the toxicity to the ladybug can be realized by directly feeding proper exogenous dsRNA, so that the exogenous dsRNA product suitable for preventing and treating the physalis alkekengi is developed from a gene level, the use is convenient, the cost is low, the accurate and excellent prevention and treatment effect can be realized due to the specificity of the gene, the environment is protected, and the application prospect in the prevention and treatment of the physalis alkekengi is great. However, the screening of related target genes and the design of specific and stable dsRNA with good control effect are the biggest difficult problems and key problems.

Disclosure of Invention

The invention aims to solve the technical problem of overcoming the defects and shortcomings of the existing technology for preventing and controlling the harmonia axyridis and provides a high lethal gene of the harmonia axyridis, namely a zetacOPI gene. And a technology capable of efficiently preventing and controlling the harmonia axyridis is developed based on the gene, namely, the technology is directly fed with a target gene dsRNA with high lethal capacity to the harmonia axyridis, and the lethal effect of dszetacoPI on the harmonia axyridis is utilized to achieve the purpose of preventing and controlling. The method has the advantages of convenient operation, good effectiveness and sensitivity, high insecticidal efficiency, environmental friendliness and the like, and has good application prospect.

The invention aims to provide a harmonia axyridis zetacoPI gene and application thereof in preventing and treating harmonia axyridis.

The invention also aims to provide dsRNA of the zetacOPI gene for preventing and treating the ladybug and application thereof.

The invention further aims to provide a method and a kit for preventing and treating the harmonia axyridis.

The above purpose of the invention is realized by the following technical scheme:

the invention screens and obtains a high lethal gene-zetacOPI gene based on the transcriptome library of the harmonia axyridis, and develops the technology for preventing and treating the harmonia axyridis by feeding dsRNA (dszetacOPI) of the zetacOPI gene. The method comprises the steps of respectively soaking eggplant leaves in dszetacoPI and dsGFP solutions synthesized by a kit, taking out the eggplant leaves, airing the eggplant leaves, feeding 1-instar larvae of the ladybug for 2 days, feeding the 1-instar larvae with the eggplant leaves which are not treated by dsRNA, and observing and recording the mortality rate and the development state of the ladybug; in addition, the lethality of the dszetacoPI to 1-year and 3-year ladybug and adults is determined by using a method for expressing the dszetacoPI by using a bacterial liquid, so that the insecticidal activity of the exogenous dszetacoPI to the ladybug is comprehensively evaluated. Finally, the method of fluorescent quantitative PCR (qPCR) is used for detecting and analyzing the expression quantity change of the zetacoPI gene in dszetacoPI and dsGFP ladybug eating. The result shows that the direct feeding of the exogenous dszetacOPI can obviously inhibit the zetacOPI gene expression of the harmonia axyridis, and the direct feeding of the exogenous dszetacOPI has obvious lethal effect on the harmonia axyridis. Therefore, the following subject matters and applications should be considered to be within the protection scope of the present invention:

a gene of the zetacoPI of the harmonia axyridis has a sequence shown in SEQ ID NO. 1.

The zetacOPI gene is applied to the prevention and treatment of the harmonia axyridis or the preparation of products for preventing and treating the harmonia axyridis.

The zetacOPI gene is applied to inhibiting the growth of the ladybug or preparing products for inhibiting the growth of the ladybug.

The zetacOPI gene is applied to promotion of death of the harmonia axyridis or preparation of products for promoting death of the harmonia axyridis.

The zetacOPI gene inhibitor is applied to the prevention and treatment of the harmonia axyridis or the preparation of products for preventing and treating the harmonia axyridis.

dsRNA can be used for preventing and controlling ladybug, and can target and silence zetacoPI gene. Preferably, the dsRNA sequence is shown as SEQ ID NO. 1.

A kit for preventing and treating ladybug contains zetacoPI gene inhibitor. Preferably, the inhibitor is the above-described dsRNA.

Specifically, one of the ways of preventing and treating the harmonia axyridis by the zetacoPI gene is used, namely the method for preventing and treating the harmonia axyridis, exogenous dsRNA is directly fed, so that dszetacoPI enters the body of the harmonia axyridis, the dsRNA can silence/inhibit the zetacoPI gene expression of the harmonia axyridis, inhibit the growth of the harmonia axyridis and promote the death of the harmonia axyridis, and the aim of preventing and treating the harmonia axyridis is fulfilled.

The invention has the following beneficial effects:

the invention obtains a high lethal gene zetacoPI gene of the ladybug through screening, develops the high-efficiency silencing dsRNA of the gene, and develops a technology capable of efficiently preventing and treating the ladybug, namely directly feeding the target gene dsRNA with high lethal capability to the ladybug, and achieving the purpose of preventing and treating by utilizing the lethal effect of dszetacoPI on the ladybug. The method has the advantages of convenient operation, good effectiveness and sensitivity, high insecticidal efficiency, environmental friendliness and the like, and has good application prospect.

Drawings

FIG. 1 is an electrophoretogram of dsGFP and dszetacOPI expressed from bacterial fluid.

FIG. 2 is a graph showing the effect of dszetacOPI at various concentrations on mortality of Laimiria serrulata larvae. Survival curves were established using Cox regression procedures using larval mortality data 10 days after the start of the experiment. Different letters (e.g., a, b) indicate significant differences between the control and treatment curves.

FIG. 3 is a graph showing the effect of dszetacOPI expressed in the inoculum solution on the survival rate of E.varivestis (graph A: survival rate of 1 st larva; graph B: survival rate of 3 rd larva; graph C: survival rate of adult). Survival curves were established using Cox regression programs using mortality data for 1 st, 3 rd and adult larvae at 10, and 14 days, respectively. Different letters (e.g., a, b) indicate significant differences between the control and treatment curves.

FIG. 4 shows the phenotypic differences between a normally developed dsGFP control group (A) and a dead dszetacOPI-treated group (B) on day 3 from dsRNA feeding.

FIG. 5 shows the change in zetacoPI gene expression level in E.physaloidis at day 2 and day 4 after feeding dszetacoPI and dsGFP.

Detailed Description

The invention is further described with reference to the drawings and the following detailed description, which are not intended to limit the invention in any way. Reagents, methods and apparatus used in the present invention are conventional in the art unless otherwise indicated.

Unless otherwise indicated, reagents and materials used in the present invention are commercially available.

The ladybug, used in the examples below, was bred at the department of insects at southern agricultural university of south China. The eggplants for breeding the harmonia axyridis are Tengsheng Maruashuai round eggplant seedlings, the harmonia axyridis is placed in a culture dish containing filter paper, the filter paper is moisturized by a cotton ball, and the harmonia axyridis is placed in an artificial climate box (the temperature is 25 +/-1 ℃, the humidity is 70-80%, and the photoperiod L: D is 14: 10) for propagation.

RNA extraction Using TRIzol extraction (Invitrogen, USA), reverse transcription reagent (PrimeScript)^TMRT reagent Kit with gDNA Eraser) from TAKARA Biotechnology Ltd, dsRNA synthesis Kit (MEGAscript)^TMT7) from Thermo Fisher Scientific, kit for PCR reaction System (EX Taq^TM) Purchased from TAKARA Biotechnology Ltd, and DNA Purification recovery Kit (Universal DNA Purification Kit) purchased from Tiangen Biochemical technology (Beijing) Ltd.

The data processing method of the following example: for the result analysis of the bioassay of the two types of dsRNA on the harmonia axyridis, the survival rate of the harmonia axyridis is counted by using Excel 2010, the SPSS 19.0 software is used for drawing by adopting Cox regression analysis, and the difference analysis among different concentrations is used for single factor analysis. Analyzing the change of target gene expression after RNA interference, wherein qPCR data adopts 2^-△△CtThe method (Ct represents the number of cycles) was performed. Data analysis was performed using single factor analysis of variance using SPSS 19.0 software.

Example 1 acquisition of ZetacoPIdsRNA, a growth and development-related gene

A transcriptome library of the harmonia axyridis is constructed according to the genome of the harmonia axyridis, genes related to growth and development of the harmonia axyridis are researched and screened based on the constructed transcriptome library, and a zetacOPI gene fragment is obtained through screening, wherein the zetacOPI gene fragment is shown as SEQ ID NO. 1. The dsRNA is then synthesized.

1. Extracting total RNA of the harmonia axyridis and synthesizing first strand cDNA.

Taking 10 2-instar larvae of the harmonia axyridis to be placed in a 2ml centrifuge tube, and extracting the total RNA of the harmonia axyridis by using a TRIzol method, wherein the concentration sum of the RNAQuality utilization of NanoDropOne^CThe measurement was carried out using a reverse transcription kit (PrimeScript)^TMRT reagent Kit with gDNA Eraser, TAKARA) reverse transcription was performed according to the instruction to synthesize the first strand cDNA.

2. Primer design

The zetacoPI gene sequence was obtained from the transcriptome library of E.variegatus, and the dsRNA primer P1 (Table 1) of the zetacoPI gene was designed, the green fluorescent protein Gene (GFP) was amplified from a GFP-containing plasmid stored in the laboratory, and the dsRNA primer P2 (Table 1) of the GFP gene was designed. Homology arms related to enzyme cutting sites are added to a dszetacoPI primer P1 and a dsGFP primer P2 respectively, and a dszetacoPI construction expression vector related primer P3 and a dsGFP construction expression vector related primer P4 are designed (Table 1). Based on the sequence of zetacorpi gene, qPCR primer P5 for zetacorpi gene and qPCR primer P6 for reference gene GAPDH were designed (table 1).

Table 1: dsRNA synthesis and qPCR primers

3. Kit for synthesizing zetacOPI gene and dsRNAs of GFP gene

PCR amplification was performed using primers P1 and P2 in Table 1, with the reaction system of 10 XEX Taq Buffer 5. mu.L, TaKaRa EX Taq 0.25. mu.L, dNTP mix 4. mu.L, upstream primer (10. mu. moL/L) 1. mu.L, downstream primer (10. mu. moL/L) 1. mu. L, cDNA/GFP plasmid 1. mu.L, ddH₂The content of O is filled to 50 mu L. The reaction program of PCR amplification is pre-denaturation at 94 ℃ for 3 min; denaturation at 94 ℃ for 30s, annealing at 55 ℃ for 30s, and extension at 72 ℃ for 1min for 30 cycles; extension at 72 ℃ for 5 min. The amplification product was stored at 4 ℃. And after the program reaction is finished, detecting the amplification result by using an agarose gel electrophoresis method.

Recovering and purifying the two PCR products by using a DNA Purification recovery Kit (TIANGEN) as templates for in vitro transcription of dsRNA, wherein the in vitro transcription system of the dsRNA is 10x reaction buffer 5 muL, solutions of (ATP, GTP, CTP and UTP) are respectively 5 muL, Enzyme mix 5 muL, a template 20 muL and ddH₂O make up to 50. mu.L.The mixture was left at 37 ℃ for 4 hours. After the reaction, 2.5. mu.L of TURBO DNase was added to remove the residual template DNA and single-stranded RNA, then the dsRNA was purified, and finally 50. mu.L of ddH was used₂O dissolves the dsRNA to give dszetacOPI and dsGFP, respectively, and the band of dsRNA was verified by electrophoresis on a 1.5% agarose gel.

The zetacoPIdsRNA (dszetacoPI) of the harmonia axyridis is double-stranded RNA and consists of a sense strand and an antisense strand, wherein the nucleotide sequence of the sense strand is SEQ ID NO.1 in a sequence table, the nucleotide sequence of the antisense strand is a reverse complementary sequence of SEQ ID NO.1 in the sequence table, and the nucleotide sequence of a zetacoPIdsRNA encoding gene is SEQ ID NO.1 in the sequence table. The GFP dsRNA is double-stranded RNA and consists of a sense strand and an antisense strand, wherein the nucleotide sequence of the sense strand is SEQ ID NO.2 in a sequence table, and the nucleotide sequence of the antisense strand is a reverse complementary sequence of the SEQ ID NO.2 in the sequence table.

4. Obtaining of dsRNA expressed by zetacOPI bacterial liquid of growth and development related gene

Two cleavage sites were selected on the sequence of L4440, BamHI (GGATCC) and SacI (GAGCTC), respectively. According to the sequence information of L4440 (the sequence information is disclosed), homology arms related to two enzyme cutting sites are added to a dszetacoPI primer P1 and a dsGFP primer P2, respectively, and a dszetacoPI construction expression vector related primer P3 and a dsGFP construction expression vector related primer P4 are designed (Table 1). The cDNA template, reaction system and amplification procedure of PCR amplification are shown above, and the target fragments of dszetacoPI and dsGFP for constructing the vector are obtained, and the two PCR products obtained above are recovered by using a DNA Purification recovery Kit (Universal DNA Purification Kit, TIANGEN). Utilizing Quickcut according to the sequence of two enzyme cutting sites^TMSacI and Quickcut^TMThe L4440 vector was linearized with BamHI, the reaction system for the enzyme digestion is described in the specification, and after the enzyme digestion reaction was completed, the linearized L4440 vector was recovered with a DNA Purification recovery Kit (Universal DNA Purification Kit, TIANGEN).

Utilizing Trelief of Guangzhou Ongke Biotech Co., Ltd^TMThe SoSoSoSoSoo Cloning Kit Ver.2 Kit separately reacts dsGFP and dszetacOPI with linearized L4440 vector for 20min at 50 ℃ for recombination. Then will contain dszetacOPI and dsGFPIntroducing the recombinant expression vector into HT115 competent cells, placing on ice for 30min, and then performing heat shock at 37 ℃ for 1 min; after standing on ice for 3min, 700. mu.L of LB liquid medium containing no ampicillin was added, and the mixture was incubated at 37 ℃ and 210rpm for 1h, followed by overnight incubation with LB plates containing ampicillin and tetracycline. Single colonies were picked and placed in 4mL of LB liquid medium containing ampicillin (100. mu.g/mL) and tetracycline (10. mu.g/mL) and cultured at 37 ℃ and 210rpm for 12 hours, then 50. mu.L of the single colonies were transferred to 5mL of LB liquid medium containing ampicillin (100. mu.g/mL) and tetracycline (10. mu.g/mL) and cultured at 37 ℃ and 210rpm for 3 hours so that the OD of the resulting culture was between 0.5 and 0.8, 1mM IPTG was added thereto and cultured at 37 ℃ and 120rpm for 5 hours, and dsRNA was induced. Both of the bacterial solutions containing dsGFP and dszetacOPI were subjected to hyphal collection at 4 ℃ and 5000rpm, RNA was extracted by TRIzol extraction (Invitrogen, USA), and 1.5% agarose gel electrophoresis was performed to confirm successful induction of dsRNA.

5. Results

Amplifying by using a P1 primer to obtain a PCR amplification product with the size of 396bp, sequencing and deleting a T7 promoter sequence to obtain a nucleotide sequence with the size of 356bp, namely the target gene zetacOPI, as shown in SEQ ID NO. 1. The plasmid carrying GFP is used as a template, P2 primer is used for amplification, a PCR product with the size of 507bp is obtained, and the target bands of dsGFP and dszetacOPI are consistent with the sequencing result.

The dsRNA of the target gene is expressed by using bacterial liquid, the RNA of the hyphae is extracted, agarose gel electrophoresis is used for verifying whether the dsRNA of the target gene is successfully induced, and the target bands for successfully inducing the dsGFP and the dszetacoPI can be seen according to the electrophoresis result (figure 1).

Example 2 inhibition of ladybug by dsRNA

1. Application of dsRNA (double-stranded ribonucleic acid) synthesized by kit in inhibiting growth and development of harmonia axyridis

The harmonia axyridis dszetacorpi feeding group: 10 1 st larvae of the ladybug were placed in a petri dish with filter paper and humidified cotton balls. Soaking round eggplant leaf disks with the diameter of 12mm in dszetacoPI solutions with the concentration of 30 ng/mu L, 5 ng/mu L and 3 ng/mu L for 1min, air-drying at room temperature for 1h, feeding larvae, replacing the leaf disks every 24h, continuously feeding the leaf disks soaked by the dszetacoPI, and feeding the larvae with normal eggplant leaves after two days.

Wintercherry ladybug dsGFP feeding group: 10 1 st larvae of the ladybug were placed in a petri dish with filter paper and humidified cotton balls. Soaking a round eggplant leaf disc with the diameter of 12mm in a dsGFP solution with the concentration of 30ng/uL synthesized by the kit for 1min, air-drying for 1h, feeding larvae, replacing the leaf disc every 24h, continuously feeding the leaf disc soaked with the dsGFP for two days, and feeding the larvae with untreated eggplant leaves.

Each group is set to be 5 times, the death number of the harmonia axyridis in each culture dish is counted every 24 hours, the new leaf is replaced, and the culture dishes are placed in an artificial climate box (the temperature is 25 +/-1 ℃, the humidity is 70-80%, and the light period L: D is 14: 10). And counting the death number of the harmonia axyridis in each culture dish of each group, and calculating the survival rate change of the harmonia axyridis under the treatment of the control group and the dsRNA with different concentrations.

2. Application of dszetacOPI expressed by bacterial liquid to lethal effect of harmonia axyridis

The harmonia axyridis dszetacorpi feeding group: 10 1-instar larvae, 10 3-instar larvae and 5 adults are placed in a culture dish with filter paper and a humidifying cotton ball, 3 groups of experiments are set in total, and 5 replicates are set in each group. Soaking a circular eggplant leaf disc with the diameter of 12mm for 1min by using a bacterial liquid expressing dszetacoPI, and feeding larvae after air drying for 1h at room temperature. 2 leaf discs are placed in each culture dish of 1-instar larvae in the treatment group; 5 leaf discs are placed in each culture dish of 3-instar larvae; adult dishes were placed with 5 leaf discs. Changing the leaf disc every 24h, continuously feeding the leaf disc soaked by the dszetacOPI bacterial liquid for two days, and feeding the leaf disc by using normal eggplant leaves.

Wintercherry ladybug dsGFP feeding group: 10 1-instar larvae, 10 3-instar larvae and 5 adults are placed in a culture dish containing filter paper and a humidifying cotton ball, 3 groups of controls are arranged in total, and 5 replicates are arranged in each group. Round eggplant leaves with the diameter of 12mm are soaked for 1min by using dsGFP-expressing bacterial liquid, and the round eggplant leaves are air-dried for 1h at room temperature and then fed to larvae. 2 leaf discs are placed in each culture dish of 1-instar larvae in the control group; 5 leaf discs are placed in each culture dish of 3-instar larvae; adult dishes were placed with 5 leaf discs. And replacing the leaf disc every 24 hours, continuously feeding the leaf disc soaked by the dsGFP bacterial liquid for two days, and feeding the leaf disc by using normal eggplant leaves.

Counting the death number of the harmonia axyridis in each culture dish every 24h, replacing new leaves, and placing the culture dishes in an artificial climate box (the temperature is 25 +/-1 ℃, the humidity is 70-80%, and the light period L: D is 14: 10). And counting the death number of the harmonia axyridis in each culture dish of each group, and calculating the change of the survival rate of the harmonia axyridis of the control group and the different treatment groups.

3. According to the statistical results, after continuously feeding leaf discs containing dszetacoPI to 1 st larvae of the harmonia axyridis for two days, the survival rate of the 1 st larvae of the harmonia axyridis shows a trend of decreasing along with the increase of time, the feeding concentrations of the treatment groups are 3 ng/mu L, 5 ng/mu L and 30 ng/mu L respectively, and the feeding concentration of the control group is 30 ng/mu L. From the results of fig. 2, significant differences were found between the treatment groups and the control group at different concentrations (χ 2 ═ 112.807, df ═ 3, P < 0.0001). There was a significant difference between 30ng/μ L (P <0.0001, exp (b) ═ 37.277) and 5ng/μ L (P <0.0001, exp (b) ═ 11.503) and 3ng/μ L (P <0.0001, exp (b) ═ 8.443), respectively, and there was no significant difference between the treatment groups at the other two concentrations. From the statistical results, it can be concluded that the mortality increased 8.443-fold, 11.503-fold and 37.277-fold when the concentration of the treatment group was 3 ng/. mu.L, 5 ng/. mu.L and 30 ng/. mu.L, respectively, compared to the control group.

According to the statistical results (as shown in fig. 3), after continuously feeding dszetaCOPI expressed by the strain liquid of the harmonia axyridis, the survival rates of 1 st larva (P <0.0001, exp (b) ═ 16.497), 3 rd larva (P <0.0001, exp (b) ═ 9.267) and adult (P ═ 0.035, exp (b) ═ 5.150) were significantly different from those of the control group, and the mortality rates of the 1 st larva, the 3 rd larva and the adult of the treatment group were increased by 16.497 times, 9.267 times and 5.150 times, respectively, compared with the control group.

In addition, changes in phenotypic characteristics of E.varivestis were observed with a dissecting mirror two days after feeding dszetacoPI. It was found that, on day 3 from the feeding of dszetacoPI, the ladybug in the dsGFP control group normally entered the 2-instar stage, and the larvae in the treatment group failed to normally molt into the 2-instar stage and died, and the phenotypic characteristics were shown that the branches and spots of the anterior dorsal lamella of the larvae failed to form as shown in FIG. 4, indicating that feeding of dszetacoPI could induce a strong RNAi effect in vivo in the ladybug, resulting in the death of the ladybug.

Example 3 dszetacoPI inhibition of expression of the zetacoPI Gene in Lasiosphaera sp

1. Experimental methods

On days 2 and 4 after the onset of dsRNA feeding, respectively, 1 st larvae of E.paduligera treated with 5 ng/. mu.L dszetacoPI and dsGFP were collected, 3 biological replicates per treatment were collected. And extracting and collecting RNA of the harmonia axyridis, then carrying out reverse transcription on the RNA into cDNA, and diluting the cDNA by 10 times to obtain a qPCR template. qPCR analysis was performed with P5 and P6 as primers. The qPCR system (15. mu.L) contained 5.25. mu.L of ddH₂O, 7.5. mu.L of 2 XSSYBR Green MasterMix (BIO-RAD Inc, Hercules, Calif.), 4. mu.M primer and 1.0. mu.L of cDNA first strand template. The qPCR reaction apparatus Bio-Rad C1000Real-Time PCR system (BIO-RAD, USA). The reaction condition is 95 ℃ for 5 min; the reaction was performed in 96 well plates (BIO-RAD, USA) with 95 ℃ for 10s, 60 ℃ for 30s, 39 cycles, and 3 technical replicates per sample.

2. Results of the experiment

Relative changes in zetacoPI gene expression in E.varivestis were counted at day 2 and 4 after dszetacoPI feeding, respectively, using dsGFP feeding as a control (as shown in FIG. 5). The expression level of zetacoPI gene in the ladybug fed with dszetacoPI is obviously reduced compared with the expression level of zetacoPI gene in the ladybug fed with dsGFP. Further shows that the feeding of dszetacoPI can cause strong RNAi effect in the body of the ladybug, so that the expression level of the zetacoPI gene in the body is obviously reduced, and the death or the development of the ladybug is inhibited. On day 2 from the feeding of dszetacorpi, the expression amount of zetacorpi was decreased 2.12-fold compared with the control group (F)_1,414.455, P0.019); on day 4 from the feeding of dszetacorpi, the expression amount of zetacorpi decreased 4.24-fold compared with the control group (F)_1,4＝618.240,P<0.0001), further indicates that the feeding of dszetacoPI can cause strong RNAi effect in the body of the harmonia axyridis, so that the expression level of the zetacoPI in the body is obviously reduced, and the development of the harmonia axyridis is inhibited or killed.

The above embodiments are preferred embodiments of the present invention, but the present invention is not limited to the above embodiments, and any other changes, modifications, substitutions, combinations, and simplifications which do not depart from the spirit and principle of the present invention should be construed as equivalents thereof, and all such changes, modifications, substitutions, combinations, and simplifications are intended to be included in the scope of the present invention.

SEQUENCE LISTING

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<213> P6-F

<400> 13

ctgatatcat cgatgaattc aagttcagcg tgtccggcga g 41

<210> 14

<211> 40

<212> DNA

<213> P6-R

<400> 14

cgaattcctg cagcccgggt tcacgttgat gccgttcttc 40

Claims

1. A gene of zetacoPI of the harmonia axyridis is characterized in that the sequence is shown as SEQ ID NO. 1.

2. A dsRNA useful for controlling ladybug, wherein the dsRNA silencing target gene is the zetacorpi gene of claim 1.

3. Use of the zetaCOPI gene of claim 1 or the dsRNA of claim 2 for control of or in the manufacture of a product for control of sabina japonica.

4. Use of the zetaCOPI gene of claim 1 or the dsRNA of claim 2 for inhibiting the growth of ladybug or for preparing a product for inhibiting the growth of ladybug.

5. Use of the zetaCOPI gene of claim 1 or the dsRNA of claim 2 for promoting death of or for preparing a product for promoting death of sabina.

6. The use of the zetacorpi gene expression inhibitor of claim 1 for controlling or preparing a product for controlling harmonia axyridis.

7. The use according to claim 6, wherein the inhibitor of zetacorpi gene expression is the dsRNA of claim 2.

8. A kit for controlling Laurencia grandis, comprising the zetacoPI gene expression inhibitor according to claim 1.

9. The kit of claim 8, wherein the expression inhibitor is the dsRNA of claim 2.

10. A method of controlling harmonia axyridis, characterized in that it is fed with exogenous dsRNA which silences/inhibits the expression of the zetacorpi gene of claim 1.