Pseudomonas aeruginosa bacteriophage and application thereof in prevention of hemorrhagic pneumonia of mink
A technology for Pseudomonas aeruginosa and hemorrhagic pneumonia, applied in the direction of viruses/phages, medical raw materials derived from viruses/phages, antibacterial drugs, etc., can solve problems such as economic losses in the mink breeding industry, reduce feeding costs, improve The economic benefits of breeding and the effect of improving the effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0016] Phage Screening and Purification
[0017] 1. Preparation of Pseudomonas aeruginosa
[0018] The disease materials of mink suffering from hemorrhagic pneumonia were collected from a mink farm, and Pseudomonas aeruginosa was isolated using a selective medium. Using molecular biology methods, it was determined that the pathogen was Pseudomonas aeruginosa. Use LB medium to amplify and save phages for isolation.
[0019] 2. Treatment of water samples
[0020] Take hospital wastewater, add CaCl 2 The final concentration is 1mol / L, and centrifuged at 5000rpm for 10min to remove the precipitated particles in the sewage. The supernatant was sterilized by filtration with a 0.22 μm filter membrane. Take 20 ml of the filtrate, mix it with 20 ml of 2×LB medium, inoculate 400 μl of Pseudomonas aeruginosa at an inoculum size of 1%, and enrich and culture at 37° C. for 12 hours. Take 5ml of the above bacterial solution, centrifuge at 5000rpm at 4°C for 10min, take the supernatant...
Embodiment 2
[0028] Biological properties of phages
[0029] 1. Electron microscope observation of phage
[0030] Take the phage suspension purified by ultracentrifugation and drop a little on the copper grid covered with polyvinyl formaldehyde film, stain with 2% phosphotungstic acid (pH7.0) for 5-10min, put the copper grid on dry filter paper, and let it dry naturally. Then observe with a Hitachi JEM2100C electron microscope.
[0031] 2. One-step growth curve of phage
[0032] Add phage and early logarithmic host bacteria to make MOI = 0.1, incubate at 37°C for 15 minutes, centrifuge at 10,000×g for 10 minutes, discard the supernatant, suspend the bacteria in LB medium, centrifuge again, suspend the sediment, wash twice, and use 5ml Suspend the preheated LB medium and mix well, quickly place it in a 37°C shaker (140rpm / min) for culture, start timing, sample 100μl at time 0 and every 10min, centrifuge at 10000×g for 5min, and pipette Clear, 10-fold serial dilution to determine the phag...
Embodiment 3
[0036] Phage safety experiment
[0037] Select 12 male Kunming mice weighing 25-30 g, randomly divide them into experimental group and blank control group, and inoculate purified phage lysate (10 10 PFU / ml) and normal saline 20ul, after continuous inoculation for 3 days, the behavioral performance of the mice was observed, and the lungs, liver, and kidneys were removed to make pathological sections to determine whether the purified phage lysate had toxic side effects on the mice.
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com