Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Crucian herpes virus disease compound vaccine preparation, preparation method and application

A crucian carp herpes virus and preparation technology, applied in antiviral agents, biochemical equipment and methods, viral peptides, etc., can solve the problems of high-efficiency expression of heterogeneous biological cells, difficulty of exogenous genes, etc.

Active Publication Date: 2015-04-22
YANGTZE RIVER FISHERIES RES INST CHINESE ACAD OF FISHERY SCI
View PDF2 Cites 12 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Codon bias makes it difficult for cloned foreign genes to be expressed efficiently in heterogeneous biological cells

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Crucian herpes virus disease compound vaccine preparation, preparation method and application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0068] Acquisition of JDORF25, JDORF25C, JDORF25D gene encoded proteins:

[0069] 1. Truncated region screening

[0070] The antigenic region, hydrophilic region and surface display probability of ORF25, ORF25C, ORF25D genes of carp herpesvirus type II were analyzed, and the hydrophilic sequences with concentrated antigenic determinants and strong antigenicity were selected as the proposed expression genes.

[0071] 2. Codon optimization

[0072] According to the yeast codon preference, codon optimization was performed on the proposed expression gene sequence, and the GC content was kept moderate, and the optimized sequence was synthesized. Compared with the original sequence of the optimized ORF25, ORF25C, ORF25D gene (JDORF25, JDORF25C, JDORF25D) coding sequence, 20%-30% of the bases in the sequence are optimized and the low-frequency codons of Pichia pastoris are all replaced by high-frequency or sub-high frequency codons.

[0073] 3. Amplification of JDORF25, JDORF25C, ...

Embodiment 2

[0121] A preparation method of crucian carp herpes virus disease vaccine, the steps are as follows:

[0122] Pick Pichia pastoris Km71 / CyHV-2-25, Pichia pastoris Km71 / CyHV-2-25C, and Pichia pastoris Km71 / CyHV-2-25D strains, and inoculate them into 100mL BMGY culture medium, 30°C, 250r / min shaking culture to OD 600 When the value reaches about 6, centrifuge at room temperature at 1500g for 5min, resuspend the bacteria in 20mL of BMMY medium, transfer the obtained bacterial solution into a 100mL shake flask, seal the bottle, add 100% methanol to a final concentration of 0.5%, and store at 30°C, 250r / The culture was induced under the condition of 1 min, and methanol was added every 24 hours to maintain the concentration of methanol at 0.5%. After continuous induction for 3 days, the yeast in the induction solution was removed by centrifugation (removing the precipitate and leaving the supernatant), and the content of the target protein (recombinant protein JDORF25, JDORF25C, JD...

Embodiment 3

[0127] The application of a crucian carp herpes virus disease compound vaccine preparation in the preparation of carp herpes virus type II vaccine is as follows:

[0128] The vaccine prepared in Example 2 was used to immunize crucian carp (250 ± 20 grams) with basically no difference in body weight, good mental condition, and negative carp herpes virus type II, and a positive control and a normal saline control (100 microliters of each crucian carp intramuscularly injected, 200 microliters, 300 microliters, the specific concentration is shown in Table 1), after 15 days after boosting immunization with the same dose, each fish was intraperitoneally injected with 500 microliters of 1×10 6 . 5 TCID 50 / ml of carp herpesvirus type Ⅱ for challenge experiments to detect whether the antibodies produced are protective.

[0129] Table 1 Grouping of crucian carp herpes virus disease yeast immune protection experiment

[0130] test group

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention discloses a crucian herpes virus disease compound vaccine preparation, a preparation method and application. An applicant provides three strains of recombinant saccharomycetes, including pichia pastoris Km71 / CyHV-2-25, CCTCC NO:M2014570, pichia pastoris Km71 / CyHV-2-25C, CCTCC NO:M2014571 and pichia pastoris Km71 / CyHV-2-25D, CCTCC NO:M2014572. Proteins produced by utilizing the saccharomycetes through fermentation have the characteristics of high activity and yield; and immunity protective experiments prove that the crucian herpes virus disease compound vaccine preparation prepared by mixing the three proteins is capable of effectively preventing crucian herpes virus diseases.

Description

technical field [0001] The invention belongs to the field of biotechnology, and relates to a compound vaccine preparation for crucian carp herpes virus disease, a preparation method and application. Background technique [0002] Cyprinid herpesvirus Ⅱ (CyHV-2) infection of heterogeneous gibel carp is a serious viral disease emerging in recent years, which has caused significant economic losses. Carp herpesvirus type Ⅱ was first discovered in ornamental goldfish, known as "goldfish herpesvirus hematopoietic organ necrosis". Because the virus is the second herpesvirus isolated from carps, the International Committee on Taxonomy and Nomenclature of Viruses named it Cyprus herpesvirus type II (CyHV-2). CyHV-2 is closely related to Carp pox herpesvirus (Cyprinid herpesvirus Ⅰ, CyHV-1) and Koi herpesvirus (Koi herpesvirus, Cyp rinid herpesvirus 3, CyHV-3). The whole genome sequencing and annotation research of CyHV-2 has been completed, and the research on the important function...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
IPC IPC(8): A61K39/245A61P31/22C12N1/19C12P21/02C07K14/03C12R1/84
Inventor 周勇曾令兵范玉顶徐进马杰
Owner YANGTZE RIVER FISHERIES RES INST CHINESE ACAD OF FISHERY SCI
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

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