High temperature resistant vibrio alginolyticus phage, as well as composition, kit and application thereof
A technology of vibrio alginolyticus and bacteriophage, which is applied in the direction of bacteriophage, virus/phage, medical raw materials derived from virus/phage, etc. effect of proliferation
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Embodiment 1
[0042] Example 1 Separation and purification of Vibrio alginolyticus phage VAP9
[0043] Collect 50ml of Fujian seafood samples and Hainan seawater samples respectively, centrifuge at 5000rpm for 10min, take 20ml of supernatant and sterilize it, mix it with 20ml of 2 times TSB liquid medium and 2ml of Vibrio alginolyticus VAHN1 bacterial solution in logarithmic phase (10 8 cfu / ml) were evenly mixed, and incubated at 150 rpm overnight at 30°C to enrich the phage. The sample enrichment solution was centrifuged at 5000 rpm for 10 min, and the supernatant was sterilized through a 0.22 μm microporous membrane to obtain a filtrate containing phage. Take 50 μl of the filtrate and mix it evenly with 300 μl of the host Vibrio alginolyticus bacteria liquid, and let it stand for 15 minutes to fully bind with the receptors on the surface of the bacteria. Add the above mixed solution to 4ml of semi-solid agar medium cooled to 50°C, spread it on the solidified TSA plate immediately after ...
Embodiment 2
[0045] Example 2 Determination of Vibrio alginolyticus phage VAP9 titer
[0046] Make diluent with SM liquid, the stoste of Vibrio alginolyticus bacteriophage VAP9 (made by embodiment 1) 10 times gradients are diluted step by step to 10 8 times. Take l0 respectively 5 , l0 6 , l0 7 and l0 8 1000 μl of diluted phage culture solution was evenly mixed with 300 μl of its host bacterium Vibrio alginolyticus VAHN1, and left to stand for 15 minutes to allow it to fully bind to the receptors on the surface of the bacteria. Add the above mixed solution to 4ml of semi-solid agar medium cooled to 50°C, mix well and immediately spread on the solidified solid agar plate, and incubate upside down at 30°C for 6-8h after the agar solidifies. Three parallel samples are required for each dilution, and the average of the three parallel samples of this dilution is used for counting. Among them, phage titer (PFU / ml) = average number of plaques × dilution factor
[0047] It can be drawn from...
Embodiment 3
[0050] Example 3 Determination of Vibrio alginolyticus bacteriophage VAP9 on the optimal multiplicity of infection (MOI) of Vibrio alginolyticus
[0051] A single colony of Vibrio alginolyticus was picked, inoculated into a test tube filled with 3 ml of TSB (2% NaCl) culture solution, and cultured with shaking at 150 rpm in a shaker at 30° C. for 12 hours to obtain a host bacterial suspension. The bacterial suspension was transferred to 10ml TSB (2% NaCl) culture solution at a ratio of 1:100, and cultured at 30°C with shaking at 150rpm to the pre-logarithmic phase. The pure culture solution of phage VAP9 (prepared in Example 1) and host bacteria (MOI=number of phages / number of bacteria) were added according to the multiplicity of infection ratio, and TSB liquid medium was added to make the total volume of each tube the same. Shake overnight at 150 rpm in a shaker at 30°C. After the cultivation, centrifuge at 5000 g for 10 min and collect the supernatant to measure the phage t...
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