Use of dsrna targeting a gene encoding an antigenic thaumatin-like protein

Abstract

This invention belongs to the field of RNA biocontrol technology, specifically relating to the application of dsRNA targeting genes encoding antigenic sweet proteins. This invention provides the application of dsRNA targeting genes encoding antigenic sweet proteins in the control of crop anthracnose, wherein the dsRNA is encoded by a gene encoding an antigenic sweet protein. CsATLP1 The dsRNA was obtained by partial sequence transcription. By loading the above-mentioned dsRNA onto the nanomaterial layered double hydroxide, the pathogenicity of *Anthracnose rubrum* and *Anthracnose mango* can be significantly reduced, showing promising application prospects for efficient and targeted control of crop anthracnose.

Description

Technical Field

[0001] This invention belongs to the field of RNA biological control technology, specifically involving the application of dsRNA targeting antigenic sweet protein encoding genes. Background Technology

[0002] Anthrax ( genus Anthrax) Colletotrichum genus Anthracnose is one of the world's ten most important fungal plant pathogens. The anthracnose it causes severely damages crops, cash crops, and horticultural plants, often leading to leaf death, fruit rot, and sharp yield reduction. In tropical, subtropical, and Mediterranean regions, anthracnose lowers the quality of exported fruits. Mangoes, as an important export fruit in tropical and subtropical regions, are highly susceptible to anthracnose, severely reducing their commercial value and resulting in economic losses of 60% to 80% or more after harvest. Among cash crops, rubber trees, as the core source of natural rubber, are also severely affected.

[0003] RNA pesticides are novel biological pesticides developed based on RNA interference technology. Essentially, they specifically bind to the mRNA transcribed from specific genes in target organisms. Through the naturally occurring RNAi pathway within the target organism, they cause transcript degradation or inhibit translation, thereby interfering with the normal growth of the target organism and its harm to the host plant, ultimately achieving pest control and plant protection. RNA pesticides are defined as biological pesticides. Compared to traditional chemical pesticides, double-stranded RNA (dsRNA) pesticides have many advantages. First, dsRNA has strong specificity and efficient gene silencing ability without involving transgenic technology. Second, based on target design, dsRNA can inhibit the growth of viruses, bacteria, and fungi, thus controlling the diseases they cause. Furthermore, dsRNA can cross cell membranes and be delivered within the body. Finally, dsRNA is easily degraded in the environment, making it an environmentally friendly pesticide. Based on these advantages, RNA pesticides offer significant benefits for pest and disease control: high specificity, good efficacy, low risk of resistance development, non-toxic, harmless, and residue-free, with low development costs, representing a cutting-edge direction in green agricultural pest control.

[0004] However, the application of RNA pesticides also faces many challenges. For example, naked dsRNA is easily degraded by enzymes and ultraviolet light in the environment, resulting in short-lived efficacy; the epidermis of harmful organisms hinders the absorption of dsRNA, leading to low dsRNA delivery efficiency and affecting the silencing effect of target genes; and large-scale synthesis of dsRNA is costly. Therefore, how to obtain highly efficient and targeted anthrax RNA pesticides is an urgent problem to be solved in this field. Summary of the Invention

[0005] The purpose of this invention is to provide the application of dsRNA targeting antigenic sweet protein encoding genes, which can efficiently and effectively control crop anthracnose.

[0006] To achieve the above objectives, the technical solution adopted by the present invention is as follows:

[0007] The present invention provides a dsRNA that targets the gene encoding an antigenic sweet protein, the nucleotide sequence of which is shown in SEQ ID No. 2.

[0008] Preferably, the dsRNA is derived from anthrax bacteria. CsATLP1 Anthrax bacteria were obtained by transcribing the gene target gene segment. CsATLP1 The nucleotide sequence of the gene target gene segment is shown in SEQ ID No. 1.

[0009] This invention also provides the application of the above-mentioned dsRNA in the prevention and control of crop anthracnose.

[0010] Preferably, the crop includes: rubber and mango.

[0011] Preferably, the pathogen causing anthrax includes: *Anthrax sicca*. Colletotrichum siamense Asian anthrax bacteria Colletotrichum asianum .

[0012] The present invention also provides products for the prevention and control of crop anthracnose, including the above-mentioned dsRNA.

[0013] Preferably, the product further includes layered double hydroxides (LDH) of nanomaterials.

[0014] More preferably, the nanomaterial layered double hydroxide is a magnesium / aluminum layered double hydroxide.

[0015] The present invention also provides a method for controlling crop anthracnose, comprising applying the above-mentioned product to crops.

[0016] More preferably, the product is sprayed onto rubber leaves, mango leaves, or mango fruit.

[0017] The beneficial effects of this invention are as follows:

[0018] This invention first obtains segmental dsRNA of the target gene using in vitro dsRNA synthesis technology, and then combines it with layered double hydroxide (LDH) nanomaterials to obtain a dsRNA nanocomposite for crop control. The dsRNA nanocomposite is sprayed onto rubber leaves, mango leaves, and mango fruits, and then *Anthracis chinensis* is inoculated onto the rubber leaves, mango leaves, and fruits, respectively. Colletotrichum siamense HN08, Asian anthrax bacteria Colletotrichum asianum 02-3, measure the area of ​​lesions, and obtain a combination of target gene dsRNA and nano-LDH for effective control of anthracnose in rubber leaves, mango leaves, and mango fruits. This combination can efficiently and effectively control crop anthracnose. Attached Figure Description

[0019] To more clearly illustrate the technical solutions in the embodiments of the present invention or the prior art, the drawings used in the embodiments will be briefly introduced below. Obviously, the drawings described below are only some embodiments of the present invention. For those skilled in the art, other drawings can be obtained based on these drawings without creative effort.

[0020] Figure 1 for CsATLP1 The diagram shows the protein domain structure and the electrophoresis diagram of the transcript provided by the present invention. Figure a shows the schematic diagram of the position of dsCsATLP1 on the CsATLP1 protein; Figure b shows the electrophoresis diagram of the transcript, with lane M being the DNADL2000 marker and lane 1 being the electrophoresis result of dsCsATLP1.

[0021] Figure 2 The diagrams show the control effect of anthracnose on rubber leaves provided by this invention. Figure a shows the phenotype of anthracnose lesions on rubber leaves after spraying with dsRNA; Figure b shows the area of ​​anthracnose lesions on rubber leaves after spraying with dsRNA.

[0022] Figure 3 The diagrams show the control effect of mango leaf anthracnose provided by the present invention. Figure a shows the phenotype of mango leaf anthracnose lesions after spraying with dsRNA; Figure b shows the area of ​​mango leaf anthracnose lesions after spraying with dsRNA.

[0023] Figure 4 The diagrams show the control effect of mango anthracnose on mango fruit provided by the present invention. Figure a shows the phenotype of anthracnose lesions on mango fruit after spraying with dsRNA; Figure b shows the area of ​​anthracnose lesions on mango fruit after spraying with dsRNA. Detailed Implementation

[0024] Unless otherwise specified, the materials, reagents and equipment used in this invention are all conventional selections.

[0025] This invention provides anthrax bacteria CsATLP1 dsCsATLP1, a gene targeting a specific gene region, was transcribed to control crop anthracnose. Anthracnose fungus. CsATLP1The nucleotide sequence of the gene target gene segment is shown in SEQ ID No. 1, specifically: 5′-ATGCAGCTCTCATCCCTCCTCCTCCCTCTCACCCTCGCCCTCGGCGCCGACGCCCTCGGCCGCGCCGTCGTCGTCAACCGCTGCCCGACCGAAGTCACCCTCTGGTCCGTCGGCGGCTCCGTCTCCGCGGCCAATACGCTCTCGCCCAACGGCGGCTCCTACGGCGAGACCTTTGTGCGGGACGCCACCACCGGCGCAAGTCGCTGAAAGTCACAAACGCGCGGGACGGGCTGTACACGGGCGCCGCGCAGCTGAACTTCGCGTACAACCTCGACGGGAGCCAAGTGTGGTACGATCTG-3′; The nucleotide sequence of dsCsATLP1 is shown in SEQ ID No. As shown in No. 2, specifically: 5′-CAGAUCGUACCACACUUGGCUCCCGUCGAGGUUGUACGCGAAGUUCAGCUGCGCGGCGCCCGUGUACAGCCCGUCCCGCGCGUUUGUGACUUUCAGCGACUUGCCGCCGGUGGUGGCGUCCCGCACAAAGGUCUCGCCGUAGGAGCCGCCGUUGGGCGAGAGCGUAUUGGCCGCGGAGACGGAGCCGCCGACGGACCAGAGGGUGACUUCGGUCGGGCAGCGGUUGACGACGACGGCGCGGCCGAGGGCGUCGGCGCCGAGGGCGAGGGUGAGAGGGAGGAGGAGGAGGAGGAUGAGAGCUGCAU-3′; The dsRNA sequence shown in SEQ ID No. 2 is inversely complementary to the nucleotide sequence shown in SEQ ID No. 1.

[0026] To further illustrate the present invention, the solutions provided by the present invention will be described in detail below with reference to the accompanying drawings and embodiments, but these should not be construed as limiting the scope of protection of the present invention.

[0027] Example 1

[0028] 1. Previous studies have shown that anthrax bacteria have antigenic sweet protein-like proteins. CsATLP1 Gene( CsATLP1 The gene (accessed via NCBI at accession number OQ470641) is an important pathogenic factor of Bacillus anthracis, and this gene may have the potential to serve as a target for anthracis control; according to CsATLP1Genetically designed specific primers dsCsATLP1-F (SEQ ID No. 3) and dsCsATLP1-R (SEQ ID No. 4) were used to extract the highly pathogenic wild-type strain of *Anthracis sinensis*. Colletotrichum siamense Using HN08 DNA (obtained from laboratory sampling and identification) as a template, a DNA fragment (SEQ ID No. 1) was amplified for subsequent dsCsATLP1 synthesis. Primers were designed based on the first 300bp of the CsATLP1 gene to synthesize dsRNA targeting this antigenic sweet protein-encoding gene. This was chosen because it covers the core coding region at the 5' end of the gene, has a length suitable for the optimal silencing range of dsRNA, and has high specificity. Furthermore, it meets the primer design parameters, ensuring silencing efficiency, reducing off-target risks, and facilitating subsequent experimental procedures. Specific primer sequences are shown in Table 1.

[0029] Table 1 Primer Information

[0030]

[0031] 2. Polymerase chain reaction (PCR) amplification was performed using 2× Rapid Taq Master Mix (Nanjing Novizan Biotechnology Co., Ltd., catalog number: P222-03). The reaction system is shown in Table 2. The PCR reaction product was purified and recovered using an agarose gel DNA recovery kit (HiPure Gel Pure DNA Mini Kit, Guangzhou Meiji Biotechnology Co., Ltd., catalog number: D2111-03) to finally obtain the target DNA fragment (SEQ ID No. 1).

[0032] Table 2 50μL reaction system

[0033]

[0034] Note: After mixing, gently pipette to mix thoroughly, and briefly centrifuge the reagent to the bottom of the tube.

[0035] (1) The PCR reaction procedure is as follows:

[0036] (a) Pre-denaturation at 95℃ for 5 min.

[0037] (b) Denaturation at 95°C for 30 s.

[0038] (c) Anneal at 58℃ for 30 s.

[0039] (d)72℃ extended for 10 s.

[0040] (e) Repeat steps (b) to (d) 35 times.

[0041] (f) Extend at 72°C for another 10 min.

[0042] (g) Cycle at 4℃.

[0043] (2) Briefly centrifuge the PCR products. Measure the volume with a pipette and transfer it to a sterile 1.5 mL centrifuge tube.

[0044] (3) Add an equal volume of GDP buffer solution and mix by inverting or vortexing.

[0045] (4) Attach the HiPure DNA column to the collection tube. Transfer the mixture to the DNA column. Centrifuge at 12,000×g for 30 seconds.

[0046] (5) Discard the filtrate and put the column back into the collection tube. Add 600 μL of DW2 buffer to the column. Centrifuge at 12,000 × g for 30 seconds.

[0047] (6) Discard the filtrate and put the column back into the collection tube. Add 300 μL of Buffer DW2 to the column. Centrifuge at 12,000 × g for 2 minutes.

[0048] (7) Place the column into a 1.5 mL centrifuge tube and add 30 μL of elution buffer to the center of the column membrane. Incubate for 2 minutes. Centrifuge at 12,000 × g for 1 minute. Discard the column and store the DNA at -20°C.

[0049] 3. dsRNA was synthesized in vitro using the T7 RNAi Transcription Kit (Nanjing Novizan Biotechnology Co., Ltd., catalog number: TR102-02). T7 RNA polymerase recognizes DNA templates containing the T7 promoter and uses four NTPs as substrates to synthesize dsCsATLP1 in vitro. The specific method is as follows:

[0050] a. Prepare a 20 μL reaction system as shown in Table 3.

[0051] Table 3 20μL reaction system

[0052]

[0053] b. The PCR product dsCsATLP1 (SEQ ID No. 2) was obtained by reacting at 37 ℃ for 6 h in a PCR instrument.

[0054] c. Dilute 100 U / μL RNase T1 to 10 U / μL with RNase T1 dilution buffer, and incubate the transcription product to digest excess template DNA and single-stranded RNA. The incubation system is shown in Table 4.

[0055] Note: RNase T1 specifically degrades single-stranded RNA and the three G bases at the 5′ end. Diluted RNase T1 should be used as soon as possible and should not be stored.

[0056] Table 4 Incubation System

[0057]

[0058] Note: After mixing, gently pipette to mix thoroughly, and briefly centrifuge the reagent to the bottom of the tube.

[0059] d. Incubate at 37 ℃ for 30 min to obtain pure dsCsATLP1 (SEQ ID No.2).

[0060] e. Electrophoretic analysis of the transcription product (i.e., dsCsATLP1 as shown in SEQ ID No. 2), the results are as follows: Figure 1 As shown in Figure b.

[0061] f. Product purification

[0062] RNA was purified using the magnetic bead method.

[0063] (1) Remove the RNA purification beads from 4°C and allow them to equilibrate at room temperature for 30 min. Invert or vortex to mix before use.

[0064] (2) Add 80 μL of magnetic bead solution to the transcription product and pipette to mix the solution thoroughly more than 10 times.

[0065] (3) Incubate at room temperature for 8 min to allow the RNA to fully bind with the magnetic beads.

[0066] (4) Place the PCR tube on the magnetic rack for 5 minutes. After the solution becomes clear, carefully remove the supernatant. When aspirating the supernatant, be careful not to disturb the magnetic beads.

[0067] (5) Keep the PCR tube on the magnetic rack at all times, add 200 μL of freshly prepared 80% ethanol, being careful not to disturb the magnetic beads, incubate at room temperature for 30 seconds, and carefully remove the supernatant. Repeat this step once.

[0068] (6) Open the lid and air dry the magnetic beads for 5-10 minutes. Dry until there is no water on the surface of the magnetic beads. Over-drying will affect the elution of RNA.

[0069] (7) Remove the PCR tube from the magnetic rack, add 40 μL of RNase-free water, use a pipette to blow the magnetic beads off the tube wall, mix thoroughly, and incubate at room temperature for 3 min.

[0070] (8) Place the PCR tube on a magnetic rack. After the solution has clarified, carefully transfer the supernatant to a new RNase-free EP tube, being careful not to pick up the magnetic beads. To avoid the magnetic beads affecting subsequent experiments, reserve 1-2 μL of solution when transferring the product to prevent picking up the magnetic beads.

[0071] (9) Detect the A260 absorbance of the product to determine its concentration, and store the purified product (i.e. dsCsATLP1) at -20℃.

[0072] 4. Preparation of anthrax inoculum: The Siamese anthrax bacteria in the preservation tube... Colletotrichum siamense HN08, Asian anthrax bacteria Colletotrichum asianum 02-3 (obtained from anthracnose-infected mango fruit collected from Hainan during laboratory outreach) was activated on PDA solid medium. Fresh mycelia were scraped from the edges of the activated strain and cultured in PD liquid medium at 28°C for 4 days. The fresh spore suspension was then filtered and diluted to 1×10⁻⁶. 6 per mL.

[0073] 5. Layered double hydroxide (LDH) nanomaterials loaded with dseGFP (dsRNA targeting enhanced Green Fluorescent Protein, a double-stranded RNA molecule encoding enhanced green fluorescent protein GFP).

[0074] Magnesium / aluminum layered double hydroxide MgAl-LDH (purchased from Nanjing Xianfeng Nanomaterials Technology Co., Ltd., product number: XFL02) was dissolved in DEPC water to obtain LDH working solution (200 μg / mL); dseGFP was diluted with LDH working solution to prepare LDH-dseGFP mixture (final concentration of dseGFP in the mixture was 200 ng / μL); the diluted LDH-dseGFP mixture was placed in a 55℃ water bath and allowed to stand for 1 min, then quickly transferred to a high-speed vortex shaker and shaken for 2 min, and allowed to stand for 2 min. At this time, dseGFP was adsorbed on the LDH surface to form stable LDH-dseGFP nanoparticles. dseGFP is artificially synthesized in the laboratory, and its nucleotide sequence is as SEQ ID As shown in No. 7, specifically: 5′-GCAAGCTGACCCTGAAGTTCATCTGCACCACCGGCAAGCTGCCCGTGCCCTGGCCCACCCTCGTGACCACCCTGACCTACGGCGTGCAGTGCTTCAGCCGCTACCCGACCACATGAAGCAGCACGACTTCTTCAAGTCCGCCATGCCCGAAGGCTACGTCCAGGAG CGCACCATCTTCTTCAAGGACGACGGCAACTACAAGACCCGCGCCGAGGTGAAGTTCGAGGGCGACACCCTGGTGAACCGCATCGAGCTGAAGGGCATCGACTTCAAGGAGGACGGCAACATCCTGGGGCACAAGCTGGAGTACAACTACAACAGCCACAACGTCTATATCATGGCCG-3′. Based on the gene SEQ ID No. 7, a pair of specific primers dseGFP-F (SEQ ID No. 5) and dseGFP-R (SEQ ID No. 6) were designed. The primer sequences are shown in Table 1. The specific synthesis method is the same as that for dsCsATLP1.

[0075] 6. dsCsATLP1 supported on layered double hydroxide (LDH) nanomaterials.

[0076] Magnesium / aluminum layered double hydroxide MgAl-LDH was dissolved in DEPC water to obtain LDH working solution (200 μg / mL). dsCsATLP1 was diluted with the LDH working solution to prepare an LDH-dsCsATLP1 mixture (final concentration of dsCsATLP1 in the mixture was 200 ng / μL). The diluted LDH-dsCsATLP1 mixture was placed in a 55 ℃ water bath and allowed to stand for 1 min, then quickly transferred to a high-speed vortex shaker and shaken for 2 min, followed by standing for 2 min. At this point, dsCsATLP1 was adsorbed onto the LDH surface, forming stable LDH-dsCsATLP1 nanoparticles.

[0077] 7. Application of LDH-dsCsATLP1 in the prevention and control of rubber anthrax.

[0078] The preventive effect of LDH-dsCsATLP1 nano-formulation on rubber anthrax bacteria was analyzed, and two treatment groups were designed.

[0079] The first group was sprayed with LDH-dseGFP as a control;

[0080] The second group was treated with LDH-dsCsATLP1.

[0081] Rubber leaves with uniform growth and size were selected, and two treatment groups (LDH-dsCsATLP1 group and control LDH-dseGFP group) were set up for the experiment, with 5 leaves in each group.

[0082] Two groups of leaves were sprayed with the corresponding treatment solution (LDH-dsCsATLP1 or LDH-dseGFP) evenly sprayed on each leaf. After treatment and standing for 24 hours, six evenly distributed inoculation points were selected on each leaf, and 4 μL of a 1×10⁻⁶ solution was added to each inoculation point. 6 The inoculation procedure was completed using a suspension of *Anthrax sicca* HN08 spores per mL. Results are shown below. Figure 2 .

[0083] The results showed a significant difference between the control group LDH-dseGFP and LDH-dsCsATLP1, as shown in Figure 2a. The lesion area in the LDH-dsCsATLP1 treatment (right) was significantly smaller than that in the control treatment (left). Figure 2 As shown in Figure b, the average lesion area of ​​the control group LDH-dseGFP was 0.0388 cm². 2 The average lesion area in the LDH-dsCsATLP1 treatment group was 0.0137 cm². 2Therefore, the dsCsATLP1 treatment resulted in a 64.55% reduction in lesion area compared to the control. This indicates that applying LDH-dsCsATLP1 can effectively reduce anthracnose infection of rubber leaves and provides good protection.

[0084] 8. Application of LDH-dsCsATLP1 in the prevention and control of mango anthracnose.

[0085] The preventive effect of LDH-dsCsATLP1 nano-formulation on mango anthracnose was analyzed, and two treatment groups were designed.

[0086] The first group was sprayed with LDH-dseGFP as a control;

[0087] The second group was treated with LDH-dsCsATLP1.

[0088] Mango leaves of uniform growth and size were selected, and two treatment groups (LDH-dsCsATLP1 group and control LDH-dseGFP group) were set up for the experiment, with 5 leaves in each group.

[0089] Two groups of leaves were sprayed with the corresponding treatment solution (LDH-dsCsATLP1 or LDH-dseGFP) evenly sprayed on each leaf. After treatment and standing for 24 hours, six evenly distributed inoculation points were selected on each leaf, and 4 μL of a 1×10⁻⁶ solution was added to each inoculation point. 6 The inoculation procedure was completed using a suspension of Bacillus anthracis 02-3 spores per mL. Results are shown below. Figure 3 .

[0090] The results showed significant differences between the control LDH-dseGFP and LDH-dsCsATLP1, such as Figure 3 As shown in Figure a, the lesion area in the LDH-dsCsATLP1 treatment (right) was significantly smaller than that in the control treatment (left). Figure 3 As shown in Figure b, the average lesion area of ​​the control group LDH-dseGFP was 0.7711 cm². 2 The average lesion area in the LDH-dsCsATLP1 treatment group was 0.3726 cm². 2 Therefore, the dsCsATLP1 treatment resulted in a 51.17% reduction in lesion area compared to the control. This indicates that applying LDH-dsCsATLP1 can effectively reduce anthracnose infection of mango leaves and has a good protective effect.

[0091] 9. Application of LDH-dsCsATLP1 in the prevention and control of mango anthracnose.

[0092] The preventive effect of LDH-dsCsATLP1 nano-formulation on mango anthracnose was analyzed, and two treatment groups were designed.

[0093] The first group was sprayed with LDH-dseGFP as a control;

[0094] The second group was treated with LDH-dsCsATLP1.

[0095] Mango fruits of uniform growth and size were selected, and two treatment groups (LDH-dsCsATLP1 group and control LDH-dseGFP group) were set up, with 5 fruits in each group.

[0096] Two groups of fruits were sprayed separately: each fruit was evenly sprayed with 150 μL of the corresponding treatment solution (LDH-dsCsATLP1 or LDH-dseGFP). After treatment and standing for 24 h, six evenly distributed inoculation points were selected on each fruit, and 4 μL of a 1×10⁻⁶ solution was added to each inoculation point. 6 The inoculation procedure was completed using a suspension of Bacillus anthracis 02-3 spores per mL. Results are shown below. Figure 4 .

[0097] The results showed significant differences between the control LDH-dseGFP and LDH-dsCsATLP1, such as Figure 4 As shown in Figure a, the lesion area in the LDH-dsCsATLP1 treatment (right) was significantly smaller than that in the control treatment (left). Figure 4 As shown in Figure b, the average lesion area of ​​the control group LDH-dseGFP was 0.2074 cm². 2 The average lesion area in the LDH-dsCsATLP1 treatment group was 0.0851 cm². 2 Therefore, the dsCsATLP1 treatment resulted in a 58.96% reduction in lesion area compared to the control. This indicates that applying LDH-dsCsATLP1 can effectively reduce anthracnose infection of mango fruits and has a good protective effect.

[0098] Obviously, the above embodiments of the present invention are merely examples to illustrate the present invention more clearly, and are not intended to limit the implementation of the present invention. For those skilled in the art, other variations or modifications can be made based on the above description. It is impossible to exhaustively list all implementation methods here. All obvious variations or modifications derived from the technical solutions of the present invention are still within the protection scope of the present invention.

Claims

1. The application of dsRNA targeting antigenic sweet protein-encoding genes in the control of crop anthracnose, characterized in that, The nucleotide sequence of the dsRNA is shown in SEQ ID No.

2. The dsRNA is transcribed from the target gene region of the CsATLP1 gene of Bacillus anthracis. CsATLP1 The nucleotide sequence of the gene target gene segment is shown in SEQ ID No. 1, and the anthrax pathogen is selected from *Anthrax sicca*. Colletotrichum siamense Asian anthrax bacteria Colletotrichum asianum .

2. The application according to claim 1, characterized in that, The crops mentioned include: rubber and mango.

3. A product for the prevention and control of crop anthracnose, characterized in that, Includes the dsRNA of the gene encoding the antigenic sweet protein as described in claim 1.

4. The product according to claim 3, characterized in that, The product also includes layered double hydroxides made of nanomaterials.

5. The product according to claim 4, characterized in that, The nanomaterial layered double hydroxide is a magnesium / aluminum layered double hydroxide.

6. A method for controlling crop anthracnose, characterized in that, This includes applying the product according to any one of claims 3 to 5 to crops, wherein the anthracnose pathogen is selected from *Anthracnose sicca*. Colletotrichum siamense Asian anthrax bacteria Colletotrichum asianum .

7. The method according to claim 6, characterized in that, This includes spraying the product onto rubber leaves, mango leaves, or mango fruit.

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