Cross protection vaccine
A technology of cross-protection and cross-immunity, which is applied in the field of vaccinology, can solve the problems of single vaccines and achieve the effect of simple preparation and high-efficiency cross-protection effect
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Embodiment 1
[0012] Vaccine construction:
[0013] Plasmid pAQ1 (see Zhang W, Sun K, Cheng S, Sun L.Characterization of DegQ for its construction process Vh , a serine protease and a protective immunogen from a pathogenic Vibrio harveyi strain. Appl Environ Microbiol 2008; 74: 625462.) was transformed into lager by the Hanahan method (Sambrook and Russell: Molecular Cloning: A Laboratory Manual. Cold Spring Harbor Laboratory Press 2001). Edwardsiella ATCC15947 (purchased from ATCC, USA) was obtained from strain Et15VhD, which is a vaccine strain with cross-protective effect on Edwardsiella tarda and Vibrio harveyi.
Embodiment 2
[0015] Vaccine application
[0016] Step 1) Preparation of vaccine preparation liquid. Cultivate the vaccine strain Et15VhD obtained above to OD in LB liquid medium 600 0.8-1, then centrifuge the culture solution (5000g, 4°C, 10min), collect the bacteria, suspend it in PBS to a final concentration of 2x10 8 cfu / ml is the vaccine preparation solution.
[0017] The LB composition is by weight percentage: 1.0% peptone, 0.5% yeast powder, 1.0% sodium chloride, 97.5% distilled water; the PBS composition is by weight percentage: 0.8% NaCl, 0.02% KCl, 0.358% Na 2 HPO 4 .12H 2 O, 0.024% NaH 2 PO 4 , 98.798% distilled water.
[0018] Step 2) Vaccination. 120 flounder (each weighing about 12 g) were randomly divided into 4 groups, 30 in each group. These 4 groups are named A, B, C and D respectively. Each fish in groups A and C was injected intraperitoneally with 100ul of the vaccine preparation solution in step 1) above, and each fish in groups B and D (control group) was inj...
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