Swine Streptococcosis trivalent inactivated vaccine and preparation method thereof
A technology of Streptococcus suis and inactivated vaccine, applied in the direction of antibacterial drugs, bacterial antigen components, etc., can solve the problems of reduced feed rate, economic loss of pig industry, and large stress of pigs, and achieves improvement of piglet survival rate, The effect of reducing pig stress and reducing morbidity
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Embodiment 1
[0044] Example 1: Isolation and identification of Streptococcus suis 2-LT strain.
[0045] The disease material to be separated—the tissue disease material was obtained by the applicant's inventor in September 2004 from a pig farm with neurological symptoms and acute death in a pig farm in Luotian, Hubei. The specific separation method is as follows: aseptically collect heart blood and inoculate it on a TSA plate (purchased from BD Company, USA), and observe after incubating at 37° C. for 12-24 hours. Pick small colonies with a diameter of 0.1mm-1.0mm, off-white, translucent, smooth, round, and with neat edges, and inoculate them in TSB liquid medium for overnight culture on a shaker at 37°C. Purely cultured bacteria were subjected to Gram staining for microscopic examination. Then observed with an optical microscope, Gram staining was positive, doubled or short streptococci, which were subcultured and purified.
[0046] The classification and identification of Streptococcus...
Embodiment 2
[0067] Example 2: Isolation and identification of Streptococcus suis 7-YZ.
[0068] Isolation of Streptococcus suis type 7 YZ
[0069] The disease material to be separated—the disease material of each tissue was obtained by the applicant's inventor in August 2005 from the disease material submitted for inspection by a pig farm in Yongzhou City, Hunan Province. The specific separation method is as follows: aseptically collect heart blood, lung tissue, spleen tissue, and synovial fluid, inoculate them on a TSA plate, and observe after culturing at 37°C for 12-24 hours. Pick small colonies with a diameter of 0.1mm-1.0mm, off-white, translucent, smooth, round, and with neat edges, and inoculate them in TSB liquid medium for overnight culture on a shaker at 37°C. Purely cultured bacteria were subjected to Gram staining for microscopic examination. Then observed with an optical microscope, Gram staining was positive, double or short streptococcus, which was subcultured and purifie...
Embodiment 3
[0092] Example 3: Isolation and identification of Streptococcus equi subspecies zooepidemicus XS
[0093] The diseased material to be separated—the diseased material of each tissue was obtained by the inventor of the applicant in April 2001 from a diseased pig joint in a pig farm in Xiaoshan, Zhejiang. The specific separation method is as follows: aseptically take samples from heart blood, lung tissue, spleen tissue, joint fluid and other disease materials of suspected diseased pigs, first inoculate them by streaking on TSA solid medium, culture them at 37°C for 24-48 hours, and then pick them. Take a single colony and perform a pure culture. Pick the smear of the above-mentioned pure culture colony, it can be seen that Gram staining is positive, double or short streptococci. It was named Streptococcus equi subsp. zooepidemicus XS.
[0094] Taxonomic identification of Streptococcus equi subspecies zooepidemicus XS
[0095] The latex agglutination test, biochemical identific...
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