Method and device for identifying pathogenic influence of concurrent bacteria infection against poultry influenza virus infection
A technology for virus infection and bacterial infection, applied in tissue cell/virus culture devices, biochemical equipment and methods, microbial measurement/inspection, etc., can solve economic and foreign trade losses and other problems, and achieve low price and easy operation Effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0024] Embodiment 1: Identify the impact of concurrent bacterial infection on the pathogenicity of viral infection (refer to figure 1 )
[0025] 1. Using a cell homogeneous culture device in vitro, culture CEFs with conventional cell culture medium 4 in 3 Kjeldahl cell culture flasks 1 respectively, and inoculate the avian influenza virus to be identified when the CEFs reach 80% fusion;
[0026] 2. Inoculate Bacillus subtilis and tryptase-like bacteria in solid LB culture dishes, culture at 37°C for 12 hours, and pick a single colony;
[0027] 3. the bacteria of Bacillus subtilis and tryptase are inoculated on the a wall 31 insides of 2 bacterial culture chambers 3 respectively (as figure 2 shown). Then put 2 bacterial culture chambers into the culture solution 4 of the 2 cell culture bottles in step 1 respectively, and leave 1 cell culture bottle only inoculated with avian influenza virus as a control group, continue to cultivate, and observe each cell culture bottle Pres...
Embodiment 2
[0033] Referring to Example 1, TOP-10 bacteria were inoculated in a low-salt solid LB culture dish, cultivated at 37°C for 12 hours, picked a single colony, inoculated TOP-10 bacteria in the bacterial culture room on the A wall, and put them into culture for 80 % confluent WCK cell culture flask, continue to culture and observe whether there are lesions.
Embodiment 3
[0035] Referring to Example 1, inoculate DH5α Escherichia coli on a solid LB petri dish, culture at 37°C for 12 hours, pick a single colony, inoculate DH5α Escherichia coli in the bacterial culture room on wall A, and put it into WDCK that has reached 80% fusion In the cell culture flask, continue to culture and observe whether there are lesions.
PUM
Property | Measurement | Unit |
---|---|---|
pore size | aaaaa | aaaaa |
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