Turbot pathogenic strain and inactivated vaccine for ascites disease
An inactivated vaccine, turbot technology, applied in the directions of bacteria, antibacterial drugs, bacterial antigen components, etc., can solve the problems of destroying ecological balance, drug residues, anorexia, etc., to curb the occurrence and prevalence, simple preparation process, and yield. stable effect
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Embodiment 1
[0029] Example 1: Inactivated vaccine of Acinetobacter ruckeri CCTCC M 2010372
[0030] 1. Preparation of inactivated vaccine of Acinetobacter ruckeri CCTCC M 2010372
[0031] First, the Acinetobacter ruckerii screened by the present invention was inoculated in 500ml high-salt common LB liquid medium (tryptone 10g / L, yeast extract juice 5g / L, sodium chloride 30g / L), and cultured with shaking at 28°C After 12 hours, the concentration of the bacterial liquid detected by the hemocytometer reaches 10 9 CFU / ml, or when the OD600 value reaches 0.6 or more, the culture is terminated, and the expanded culture medium of Acinetobacter ruckerii is obtained;
[0032] Add 25ml formaldehyde solution by volume ratio 0.5% afterward, inactivate 12 hours at room temperature to the expanded culture solution of bacterial strain, shake 3 times during this period; Obtain the inactivated bacterium solution of bacterial strain Acinetobacter ruckerii;
[0033] Finally, centrifuge the inactivated bac...
Embodiment 2
[0036] Embodiment 2: Acinetobacter ruckeri and pseudoalteromonas tetrodotoxin and / or Pseudomonas make the inactivated vaccine of mixed strain
[0037] 1. Preparation of inactivated vaccine
[0038] First, the Acinetobacter ruckerii screened by the present invention was inoculated in 500ml high-salt common LB liquid medium (tryptone 10g / L, yeast extract juice 5g / L, sodium chloride 30g / L), and cultured with shaking at 28°C After 12 hours, the concentration of the bacterial liquid detected by the hemocytometer reaches 10 9 CFU / ml, or when the OD600 value reaches 0.6 or more, the culture is terminated, and the expanded culture medium of Acinetobacter ruckerii is obtained;
[0039] Then one or both of the tetrodotoxin pseudoalteromonas or pseudomonas were inoculated in 500ml high-salt ordinary LB liquid medium (tryptone 10g / L, yeast extract juice 5g / L, sodium chloride 30g / L), cultured with shaking at 28°C for 16 hours, and the concentration of bacteria liquid detected by the hemo...
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