dsRNA of wing growth related gene decapentaplegic and application thereof in pest control
A gene and DNA molecular technology, applied in the field of Bactrocera dorsalis control, can solve problems such as heavy workload, impact of import and export trade, difficult and efficient governance, etc., to achieve prevention and control of invasion and spread, good ecological security, good effect on human health
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Embodiment 1
[0050] Embodiment 1, the acquisition of dsRNA of wing development gene decapentaplegic (abbreviated as dpp)
[0051] 1. Samples of Bactrocera dorsalis for testing
[0052] The insect source Bactrocera dorsalis used in this experiment is the indoor population of the Plant Quarantine and Invasion Biology Laboratory of China Agricultural University. The indoor breeding conditions: the temperature is 25°C; the relative humidity is kept at about 70%; D). The breeding method of Bactrocera dorsalis is as follows: Bactrocera dorsalis is reared uniformly in the insect cage, and the larval feed (the formula of the larval feed is shown in Table 1) is added to 500mL distilled water, boiled and bottled for later use, and it is frozen after being cooled. ; Adult feed (adult feed is obtained by mixing sucrose and soybean peptone in a mass ratio of 1:3) is fed to adults after adding water to moisten them. After feeding on the feed, the larvae burrow into the soil to pupate after they are ma...
Embodiment 2
[0157] Embodiment 2, the application of the dsRNA of wing development gene decapentaplegic in the control of Bactrocera dorsalis
[0158] 1. Feeding dsRNA
[0159] The 1st instar healthy and normally developing Bactrocera dorsalis larvae were selected as experimental materials. The experiment was set up with blank control group, dsGFP (irrelevant gene) control group and treatment group. Each group had three replicates, with 40 larvae in each replicate.
[0160] 1. Blank control group (CK)
[0161] Take 20 1.5mL centrifuge tubes, add about 0.15g crushed B. dorsalis larva feed and 4 μL ddHO to each centrifuge tube 2O, mix well. Two larvae were placed in each centrifuge tube for feeding. The feeding and growth of larvae were observed daily. After 48 hours, the feed is completely eaten, and then only supplementary feed is sufficient until the larvae grow to the end of the third instar. One of the surviving larvae in the centrifuge tube was picked into the soil to pupate and e...
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