A kind of Edwardsiella piscida derived from turbot and its application
A technology of turbot and source, applied in the field of fish-killing Edwardsiella, can solve the problems of high frequency, seriousness and large economic losses of bacterial diseases, and achieve the effect of improving the immune protection rate
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Embodiment 1
[0015] This example relates to the isolation and identification of Edwardsiella piscicida. The Edwardsiella piscicida derived from turbot is Edwardsiella piscicida H4-S18 strain, and its gene sequence is shown in SEQ ID No.1.
[0016] Specific steps are as follows:
[0017] The samples of diseased turbot were collected from the turbot farm in Yantai, Shandong Province. The individual weight ranged from 205 g to 518 g, the average weight was 436±5 g, and the average body length was 29±2 cm. The diseased turbot showed weakened feeding ability, sluggish movement, swollen abdomen, red and swollen anus, congested and red snout, fin rays and base. Autopsy revealed pale yellow ascites in the abdominal cavity, intestinal enlargement, thin intestinal wall with pale yellow liquid, and liver congestion.
[0018] Take dying individuals with typical symptoms, aseptically dissect internal organs, take liver, kidney, spleen, heart and other tissues, rinse with sterile water, grind, streak o...
Embodiment 2
[0025] This embodiment involves the use of Edwardsiella piscicida to prepare inactivated vaccines. The Edwardsiella piscicida derived from turbot is Edwardsiella piscicida H4-S18 strain, the gene sequence of which is shown in SEQ ID No.1.
[0026] Specific steps are as follows:
[0027] Inoculate the Edwardsiella piscicidae H4-S18 strain on a nutrient agar medium (NA) plate, and incubate at 37°C for 24-48h for recovery; pick the above pathogenic bacteria into NB medium, culture with shaking at 37°C for 24h, and collect the culture solution Centrifuge at 5000rpm for 10min at 4°C, wash the centrifuged bacterial cells with PBS buffer solution with pH=7.2 for 3 times, and then use sterile normal saline (containing 2% NaCl) to make the concentration of 10 9 cfu / mL bacterial suspension stock solution; add 37% formalin solution until the final concentration of formaldehyde is 0.2%, inactivate at 37°C and 140r / min, take the inactivated 12h and 24h bacterial solution respectively Dete...
Embodiment 3
[0029] This embodiment relates to the detection of vaccine effects, and the Edwardsiella piscicida derived from turbot is Edwardsiella piscicidae H4-S18 strain.
[0030] Its gene sequence is shown in SEQ ID No.1.
[0031] According to the steps of preparing the vaccine in step 2, Edwardsiella piscicida (ET883) was used as the antigen to prepare the vaccine.
[0032] Adjust the 2 inactivated vaccine concentrations to OD 600 0.1±0.01, intraperitoneal injection of immune turbot, each injection of 0.1mL, the control group injection of the same dose of sterile saline. 20 tails were immunized in each group, with 3 replicates and 1 control. Breeding water temperature 18±1℃, inflated throughout the day, daily water change 30%; 30 days after immunization, it was challenged with Edwardsiella piscicida, and the concentration of each tail was 8.9×10 10 CFU / mL of bacterial solution 0.1mL; observe and record the number of deaths in each experimental group every day, and calculate the im...
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