Edwardsiella tarda subunit vaccine, and preparation and application thereof
A delayed Edwards, subunit vaccine technology, applied in the field of immunology, can solve the problem of no commercial vaccine, and achieve the effect of simple application method and high immune protection rate
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Embodiment 1
[0019] The construction method of Edwardsiella tarda vaccine expression vector:
[0020] Step 1) Construction of plasmid pGMTD: Edwardsiella tarda LSE40 (preserved in the General Microbiology Center of China Committee for the Collection of Microbial Cultures, preservation number: CGMCC No.7199, taxonomically named Edwardsiella tarda, preservation date: On January 23, 2013, the address of the preservation unit is No. 3, No. 1, Beichen West Road, Chaoyang District, Beijing) Genomic DNA was used as a template, and the primer EDF (5'-GCGC GGATCC GACGACTATCGACAGCGGCAG-3', the underlined base is the BamHI restriction endonuclease point) and EDR (5'-GCGC AAGCTT GGACATGCGTACGCTGCT-3', the underlined base is the HindIII restriction endonuclease as the point) for PCR amplification (the PCR instrument was purchased from Takara Company, model TP600). The volume of the PCR reaction system is 25 μL: 2.5 μL of 10×PCR buffer solution, 0.5 μL of 0.2 mM dNTP, 1.5 mM MgCl 2 2.0 μL, 0.5 μL ea...
Embodiment 2
[0024] The preparation method of Edwardsiella tarda vaccine protein:
[0025] The resulting plasmid pETD was transformed into competent Escherichia coli BL21(DE3) (Tiangen Biochemical Technology Co., Ltd., Beijing), cultured on LB solid medium containing 50 μg / ml kanamycin, screened positive colonies, and named it BL21 / pETD. Culture BL21 / pETD in LB liquid medium containing 50μg / ml kanamycin, culture at 37°C for 12-16 hours, and then transfer to 100ml containing 50μg / ml In the fresh LB liquid medium of kanamycin, culture at 37°C at 120rpm to OD 600 0.6-0.8, add IPTG to a final concentration of 1mmol / L, continue to cultivate for 4-6 hours, then centrifuge at 5000g, 4°C for 10min, collect the bacteria and suspend them in 5-10ml PBS, and the obtained bacteria suspension is lysed by ultrasonic Bacteria until the bacterial suspension is clear (200w, ultrasonic 5s, interval 15s, 20-30min). The obtained clarified bacterial liquid was centrifuged at 10,000 g at 4° C. for 30 min, an...
Embodiment 3
[0028] Use of Edwardsiella tarda subunit vaccine:
[0029] Step 1) Oil emulsion vaccine preparation. Mix 92% (volume ratio) No. 10 white oil, 6% (volume ratio) Siben-80 and 2% (volume ratio) aluminum stearate (heated and melted) to form an oil-emulsion adjuvant. Dilute the vaccine protein purified in Example 2 above to 200 μg / ml in PBS; mix the diluted vaccine protein with oil-emulsion adjuvant in equal volumes to form an oil-emulsion vaccine.
[0030] Step 2) Immunization application of subunit vaccine. Experimental turbot with a body weight of 10-12g was kept temporarily in a 1000L aquarium equipped with a flowing circulating water treatment and purification system, and the culture water temperature was maintained at 16-18°C. After 1 week of temporary breeding, they were randomly divided into 3 groups into a 500L test aquarium, with 50 fish in each group, and continued to be temporarily raised for 1 week. In the test aquarium, the water was changed once a day in the morni...
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