Streptococcus suis type 3 vaccine strain and application thereof
A technology of Streptococcus suis and vaccine strains, applied in vaccines, veterinary vaccines, bacteria, etc., can solve the problems of Streptococcus suis being prone to drug resistance, lack of efficient Streptococcus suis type 3 vaccine, etc., to achieve effective resistance to virulent Attack, good growth performance and immunogenicity, effect of excellent immunogenicity
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Embodiment 1
[0024] 1. Bacterial Isolation
[0025] The disease material was collected from the lungs of acutely dead pigs from a pig farm in Jiangsu. After aseptically treating the surface of the collected lungs, a small piece of internal tissue was aseptically cut out and placed in THB liquid medium. Pick up the enrichment solution from the inoculation loop and inoculate it on the THB plate, and incubate at 37°C for 24 hours. Pick milky white, translucent, circular suspected colonies with a diameter of 1-2 mm, and then inoculate them in THB liquid medium for enrichment, then draw the enrichment solution on THB plates, and then pick single colonies and culture them on THB plates until a single pure colony. Pure cultures of several strains were finally obtained.
[0026] 2. Identification
[0027] (1) Gram staining identification of isolates
[0028] The pure cultures of each strain were picked, and Gram staining was carried out according to the method of "The Veterinary Pharmacopoeia ...
Embodiment 2
[0059] Embodiment 2 immune protection test
[0060] Preparation of Streptococcus suis type 3 oil emulsion vaccine: Take Streptococcus suis type 3 JSHZ strain out of the -70°C refrigerator, streak on THB solid medium, culture in a 37°C incubator for 24 hours, and pick 3 single colonies In 5mL THB liquid medium, place on a shaker at 37°C, shake the bacteria at a speed of 200rpm overnight, take 4mL of the bacterial liquid from it and add it to 200mL THB liquid medium, place it on a shaker at 37°C, 200rpm, and cultivate 6 Hour. Take a small amount of bacterial liquid to carry out plate counting of viable bacteria, and the result shows that the concentration of bacterial liquid is 2.5×10 9 cfu / mL. Add formaldehyde with a final concentration (volume percentage) of 0.3% to the rest of the bacterial solution, place it in a constant temperature shaker at 37° C. with a rotation speed of 100 rpm for 48 hours for inactivation, and then place it at 4° C. for use. Take 200 μL of inactiva...
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