Salmonella phage capable of reducing vertical propagation of salmonella pullorum and application of salmonella phage
A Salmonella, vertical transmission technology, applied in the direction of bacteriophage, virus/bacteriophage, resistance to vector-borne diseases, etc., can solve problems such as large losses, affecting feeding efficiency, and decreasing egg production of laying hens, achieving good purification effect, reducing The effect of vertical transmission and high fermentation efficiency
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Embodiment 1
[0018] Isolation and Purification of Salmonella Phage GSMP2233
[0019] Collect 3 parts of water samples near a chicken farm in Hubei, each 30mL, centrifuge at 5000rpm for 10min, take 15mL supernatant to filter and sterilize, and the filtrate is mixed with 15mL 2×TSB liquid culture medium and 1mL Salmonella bacteria liquid in logarithmic phase (10 8 cfu / mL) were evenly mixed, and cultured overnight at 180 rpm at 37°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 100uL of the filtrate and mix it evenly with 300uL of the host Salmonella bacteria liquid, and let it stand for 15min to fully bind with the receptors on the surface of the bacteria. Add the above mixed solution to 4mL TSB semi-solid agar medium cooled to 50°C, mix well and spread it on the solidified TSA plate immediately, after the agar is solidified, inc...
Embodiment 2
[0022] Determination of titer of Salmonella phage GSMP2233 under different multiplicity of infection and different infection time
[0023] Pick a single bacterium colony of host Salmonella (Salmonella Pullorum), inoculate it into a test tube filled with 3ml TSB culture solution, and shake it at 180rpm in a shaker at 37°C for 12h to obtain a host bacterium suspension. The bacterial suspension was transferred to 10ml TSB culture medium at a ratio of 1:100, and cultured with shaking at 180rpm at 37°C to the pre-logarithmic phase. The phage GSMP2233 and its host Salmonella were diluted to a certain concentration and counted, and mixed cultured according to different multiplicity of infection ratios (MOI=number of phages / number of bacteria), and TSB liquid medium was added to make the total volume of each tube the same. Shake culture at 180rpm in a shaker at 37°C for 12h. Take out part of the culture solution every 2h and carry out 10000g centrifugation for 10min and collect the s...
Embodiment 3
[0029] pH Stability Test of Salmonella Phage GSMP2233
[0030] Take sterile bacterial bottles and add 9 mL of TSB medium with different pH (2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12) respectively, and then place the above bacterial bottles in a constant temperature water bath at 25°C After the temperature was balanced, 1mL of pure phage culture solution was added, and allowed to stand at 25°C for 240min. The samples were taken at 1h, 2h and 4h respectively, and after appropriate dilution, the phage titer was determined by the double-layer plate method. Each point was cultured in duplicate tubes to obtain the average value, and the experiment was repeated 3 times.
[0031] The results are shown in Table 2. Salmonella phage GSMP2233 has no significant change in titer when treated at pH 3-10 for 1 hour, and still has relatively high titer after being treated at pH 4-10 for 4 hours.
[0032] The pH value stability (initial titer: 5.2x10 8 PFU / mL)
[0033]
[0034] Note: ND: not det...
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