A method for obtaining Cordyceps sinensis from host insect bat moth larvae infected by Trichosporum in China
A technology of bat moth larvae, Trichospora chinensis, applied in the fields of botanical equipment and methods, horticulture, agriculture, etc., can solve the problems of shortening the infection rigidity time, low mortality rate, large wound on the surface of the parasite, and shortening the infection rigidity. effect of time, low mortality
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Embodiment 1
[0022] The bat moth used in this example is Thitarodes gonggaensis collected from Sichuan.
[0023] 1. Preparation of Chinese hairy sporozoites
[0024] The medium for cultivating blastospores is PDA medium: each liter contains 20g of glucose, 200g of potato, 5g of peptone, KH 2 PO 4 3g, MgSO 4 ·7H 2 O 1.5g and VB 1 0.02g, the rest is H 2 O (natural pH). After accurate molecular identification, the conidia of Trichosporum sinensis were inserted into the above-mentioned PDA medium, cultured in a shaker (120rpm, 9°C) for 60 days, and the blastospores of Trichosphaera sinensis were collected by centrifugation for injection to infect bat moths larva.
[0025] 2. Breeding of bat moth larvae
[0026] The larvae of the bat moth were mixed and fed with carrots, Polygonum villosa and Potentilla velvet in a mass ratio of 1:1:1 to obtain healthy 5th instar bat moth larvae for infection.
[0027] 3. Injection infection and post-injection care
[0028] Inject the 5th instar bat...
Embodiment 2
[0035] The bat moth used in this example is Thitarodes gonggaensis collected from Sichuan.
[0036] 1. Preparation of Chinese hairy sporozoites
[0037] The medium for cultivating blastospores is PDA medium: each liter contains 20g of glucose, 200g of potato, 5g of peptone, KH 2 PO 4 3g, MgSO 4 ·7H 2 O 1.5g and VB 1 0.02g, the rest is H 2 O (natural pH). After accurate molecular identification, the conidia of Trichosporum sinensis were inserted into the above-mentioned PDA medium, cultured in a shaker (120rpm, 9°C) for 60 days, and the blastospores of Trichosphaera sinensis were collected by centrifugation for injection to infect bat moths larva.
[0038] 2. Breeding of bat moth larvae
[0039]The larvae of the bat moth were mixed and fed with carrots, Polygonum villosa and Potentilla velvet in a mass ratio of 1:1:1 to obtain healthy 5th instar bat moth larvae for infection.
[0040] 3. Injection infection and post-injection care
[0041] Inject the 5th instar bat ...
Embodiment 3
[0048] The bat moth used in this example is Thitarodes gonggaensis collected from Sichuan.
[0049] 1. Preparation of Chinese hairy sporozoites
[0050] The medium for cultivating blastospores is PDA medium: each liter contains 20g of glucose, 200g of potato, 5g of peptone, KH 2 PO 4 3g, MgSO 4 ·7H 2 O 1.5g and VB 1 0.02g, the rest is H 2 O (natural pH). After accurate molecular identification, the conidia of Trichosporum sinensis were inserted into the above-mentioned PDA medium, cultured in a shaker (120rpm, 9°C) for 60 days, and the blastospores of Trichosphaera sinensis were collected by centrifugation for injection to infect bat moths larva.
[0051] 2. Breeding of bat moth larvae
[0052] The larvae of the bat moth were fed with carrots, Polygonum villosa and Potentilla velvet in a mass ratio of 1:1:1 to obtain healthy, infected 2nd instar larvae of the bat moth.
[0053] 3. Injection infection and post-injection care
[0054] The 2nd instar bat moth larvae i...
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