Porcine epidemic diarrhea, porcine delta coronavirus bivalent inactivate vaccine and preparation method thereof
A dual inactivated vaccine, porcine epidemic diarrhea technology, applied in biochemical equipment and methods, vaccines, viruses, etc., can solve the problems of pig industry losses, lack of effective treatment measures and vaccines, etc., to reduce the cost of epidemic prevention , the effect of simple immunization methods
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0026] The source of embodiment 1 strain
[0027] 1. Porcine epidemic diarrhea virus PEDV-KB2013-4 strain
[0028] The disease material collected from a pig farm in Shaanxi and tested positive for porcine epidemic diarrhea antigen by RT-PCR was added to PBS at a ratio of 1:10 (weight: volume). Filter twice with a 0.22 μm filter, and store the filtrate below -20°C for future use.
[0029] The Vero cells covered with a dense monolayer were inoculated with the filtrate at a dose of 10%, and after adsorption, the maintenance solution containing trypsin was added, and cultured at 37°C. At the same time, blank cells were set as a negative control. Obvious cytopathic changes in the second passage ( figure 1 ), the lesions were basically stable after the fifth passage.
[0030] Using Primer Premier 5.0 gene analysis software, refer to the PEDV M protein gene in Genbank to design detection primer pairs: upstream primer PEDV-F: 5'-AACGGTTCTATTCCCGTTGATG-3'; downstream primer PEDV-R: ...
Embodiment 2
[0040] The characteristic of embodiment 2 virus strains
[0041] 1. Specificity
[0042] Dilute porcine epidemic diarrhea virus and porcine deltacoronavirus to 200 TCID with MEM medium respectively 50 / 0.1ml, mixed with the corresponding equivalent amount of PEDV and PDCoV specific positive serum, neutralized at 37°C for 1 hour, inoculated into a 96-well cell culture plate of Vero cells and ST cells that had grown into a good monolayer, and inoculated into 4 wells , 200μl / well, set normal cell control and unneutralized serum control at the same time, set at 37℃, containing 5% CO 2 The cells were cultured in an incubator for 7 days, and the cytopathic changes were observed and recorded daily. Neither the positive serum neutralizing group nor the normal cell control group had cytopathic changes; all the non-neutralizing serum control groups had cytopathic changes.
[0043] 2. Virulence
[0044] A total of 10 healthy susceptible piglets aged 17-19 days (both antigens and antibo...
Embodiment 3
[0047] Example 3 Preparation and inspection of porcine epidemic diarrhea and porcine deltacoronavirus dual inactivated vaccine
[0048] 1. Materials and methods
[0049] 1.1 cells
[0050] Vero cells and ST cells were purchased from China Veterinary Drug Administration.
[0051] 1.2 Preparation of virus liquid for seedling production
[0052] Preparation of Porcine Epidemic Diarrhea Virus Seeds: The virus was prepared by the spinner bottle cell culture method. Inoculate Vero cells covered with dense monolayer with 0.2% dose of qualified porcine epidemic diarrhea virus seed virus, and add MEM with a final concentration of 10 μg / mL of trypsin, 100 U / ml of penicillin, and 100 μg / ml of streptomycin The maintenance solution was cultured at 37°C for 48-72 hours. When the cytopathic effect reached more than 80%, the virus liquid was harvested, frozen and thawed twice, and kept below -20°C for later use.
[0053] Preparation of porcine deltacoronavirus seed: the virus was prepared...
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