Klebsiella pneumoniae (Mannose-sensitive hemagglutination) pilus strain
A Klebsiella, mannose technology, applied in bacteria, antibacterial drugs, allergic diseases, etc., can solve problems such as no medical application value
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Embodiment 1
[0058] Example 1. Source and identification of Klebsiella pneumoniae mannose-sensitive hemagglutination strains
[0059] The inventors established a mannose-sensitive hemagglutination fimbriae strain of Pseudomonas aeruginosa by comparing 6 strains of Klebsiella pneumoniae isolated from clinical specimens, reference (Muxia, Pseudomonas aeruginosa, Acta Microbiology, 26(2): 176-179 , 1986), screened and bred to obtain a Klebsiella pneumoniae mannose-sensitive hemagglutination strain.
[0060] The main identification features are as follows:
[0061] Fermentation of lactose on differential medium to express colored colonies;
[0062] On solid medium, it is a gray-white sticky peptone-like colony;
[0063] After several days in the broth, the liquid is noticeably viscous;
[0064] Gram negative.
[0065] Electron micrographs were performed on this strain, such as figure 1 shown, showing the presence of periphytic fimbriae. Mannose-sensitive hemagglutination and hemagglutina...
Embodiment 2
[0066] Example 2. Strain culture and vaccine preparation
[0067] The Klebsiella pneumoniae mannose-sensitive hemagglutination fimbriae strain of the present invention is cultured on a bacterial plate at 37° C. for 18 hours, the culture is collected, sterilized with a formaldehyde solution, washed repeatedly to prepare a dead bacterin, diluted with Bacterial saline was added with 1% benzyl alcohol as a preservative to prepare a bacterin.
Embodiment 3
[0068] Example 3. Animal experiment of bacterin
[0069] Use bacterial plate culture, kill bacteria with 1% formaldehyde physiological saline, wash 5 times with sterile physiological saline, detect the concentration of bacterial liquid by spectrophotometer, and then check for viable bacteria, dilute to 1.8 to 2 billion / ml, and make bacteria Seedling.
[0070] The experimental animals used in the animal experiments were 18-20 g mice. Subcutaneous injection 3 times, each injection of 0.3ml. The interval between injections is one week. On the 7th day after the last injection, the cross-agglutinated MSHA antibody titer of the immunized mice was detected.
[0071] Table 1. Detection of cross-agglutination titers of antibodies in blood of mice and MSHA antigens of two bacteria after immunization with the "bacterial" of the present invention
[0072]
[0073] A total of 43 mice were immunized successively in the immune protection test. After 17 days of automatic immunization,...
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