Metarhizium anisopliae MANGS71814 and application of metarhizium anisopliae MANGS71814 in prevention and treatment of phthorimaea operculella
A technology of MANGS71814 and Metarhizium anisopliae, which is applied in the field of microorganisms, can solve problems such as human and animal safety hazards, pesticide residues, ecological environment impacts, etc., and achieve the effects of high spore germination rate, difficult production, and large spore production
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Embodiment 1
[0019] Example 1. Isolation and identification of Metarhizium anisopliae MANGS71814
[0020] 1.1 Materials
[0021] 1.1.1 Tested strains
[0022] The strain was collected from pupae of diseased Lepidoptera pests in Nangong Mountain, Mengyuan Town, Xishuangbanna Autonomous Prefecture, Yunnan Province on August 8, 2019.
[0023] 1.1.2 Isolation and cultivation of strains
[0024] The collected 3rd instar larvae of the diseased potato tuber moth were placed in a 5mL sterile EP tube and brought back to the laboratory. Using the streaking method, in the SDAY medium (glucose 40g, peptone 10g, yeast extract powder 10g, Agar 20g, pH natural), cultivated in a light incubator at (25±1)°C, L / / D=16h / / 8h, humidity 80%. After 7 days of culture, the conidia were transferred to a new medium for purification. Purified strains were stored in a 4°C refrigerator using SDAY slant medium.
[0025] 1.1.3 Colony morphology observation
[0026] Inoculate the isolated and purified fungi into SDAY...
Embodiment 2
[0030] Example 2. Determination of pathogenicity of Metarhizium anisopliae MANGS71814 to potato tuber moth eggs, larvae and pupae
[0031] 1 material
[0032] 1.1.1 Tested insects
[0033] Potato tuber moths were collected in the potato field of Xuanwei City, Yunnan Province, and were continuously raised indoors for 5 generations. The experiment was carried out under the conditions of temperature 25±1°C, relative humidity (RH) 60±5%, and photoperiod L:D=16:8. carried out in the intelligent artificial incubator (RG-300). Potato tuber moths are reared on fresh potato cubes and leaves.
[0034] 1.1 Preparation of spore suspension
[0035] Inoculate the isolated bacterial strains on the SDAY medium, and after it produces a large number of conidia (about 20 days), scrape the conidia on the surface of the medium with a sterile scalpel and place them in 0.02% sterile Tween-80 , formulated as 2 x 10 3 – 2×10 8 individual / mL spore suspension.
[0036] 1.1.2 Dipping method
[00...
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