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

Avian influenza virus-like particle antigen, vaccine, preparation method of avian influenza virus-like particle antigen and application of avian influenza virus-like particle antigen or vaccine

An avian influenza virus and particle antigen technology, applied in the field of vaccines, can solve problems such as endogenous virus contamination, insufficient supply of chicken embryos, and inability to induce cellular immunity.

Active Publication Date: 2020-12-15
YANGZHOU UNIV
View PDF4 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, traditional inactivated vaccines rely on chicken embryos for production, which has disadvantages such as insufficient supply of chicken embryos during disease outbreaks, and the production of a large amount of waste causing environmental pollution and endogenous virus contamination.
In addition, inactivated vaccines can only induce antibody immunity but not cellular immunity

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
  • Avian influenza virus-like particle antigen, vaccine, preparation method of avian influenza virus-like particle antigen and application of avian influenza virus-like particle antigen or vaccine
  • Avian influenza virus-like particle antigen, vaccine, preparation method of avian influenza virus-like particle antigen and application of avian influenza virus-like particle antigen or vaccine
  • Avian influenza virus-like particle antigen, vaccine, preparation method of avian influenza virus-like particle antigen and application of avian influenza virus-like particle antigen or vaccine

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0047] Embodiment 1: Construction of recombinant shuttle plasmid

[0048] The H7N9 subtype avian influenza virus A / Chicken / Guangdong / GD15 / 2016 (hereinafter referred to as GD15 strain) used in this experiment was preserved and provided by the Key Open Laboratory of Livestock and Poultry Infectious Diseases, Ministry of Agriculture, Yangzhou University. The strain has been published on the genebank sequence, the sequence number is: PB2 (KY751288), PB1 (KY751256), PA (KY751233), HA (KY751058), NP (KY751157), NA (KY751124), M (KY751091), NS (KY751190). Primers are designed according to the nucleic acid sequences of the HA, NA, and M1 genes of the H7N9 GD15 strain of the avian influenza virus, and are used for gene amplification. The primers used in the construction were designed with Primer Premier 5.0 software and synthesized by Shanghai Bioengineering Technology Co., Ltd. The primer information is shown in Table 1.

[0049] Table 1 Primer information for amplifying the target...

Embodiment 2

[0055] Example 2: Rescue of recombinant baculovirus

[0056] The recombinant shuttle plasmid pVL-NA-HA-M1-GD15 and the optimized baculovirus genomic DNA were co-transfected into Sf9 cells in logarithmic growth phase. The brief procedure is as follows:

[0057] 1) Add Sf9 cells to the six-well cell plate, 1×10 6 Place the cell plate horizontally in a 27°C incubator, incubate for 1 hour, and prepare transfection samples at the same time;

[0058] 2) Prepare the DNA transfection complex: Dilute the recombinant shuttle plasmid to a concentration of 100ng / μL for use; warm the transfection reagent to room temperature and mix gently; prepare two sterile EP tubes, add 100 μL serum-free respectively Culture medium; add 5μL (100ng) flashBAC to one tube TM For DNA, flick the EP tube to mix evenly; add 5 μL (500ng) transfer vector plasmid, flick the tube to mix evenly, then add 4 μL of transfection reagent, flick the EP tube to mix evenly, and centrifuge to precipitate; add 5 μL to anot...

Embodiment 3

[0063] Example 3: Identification of recombinant baculovirus

[0064] 1 PCR identification of exogenous genes in recombinant baculovirus genome

[0065] 1.1 Extraction of recombinant viral DNA

[0066] The extraction of recombinant baculovirus DNA was carried out according to the instructions of the whole gold virus extraction kit:

[0067] 1) Mix Poly A Carrier RNA with Binding Buffer 1:50, called MIX A;

[0068] 2) For each sample, take 200 μL supernatant, add 200 μL BB5 and 20 μL proteinase K, and vortex to mix;

[0069] 3) Incubate at 56°C for 15 minutes, add 250 μL of absolute ethanol, vortex and oscillate to mix, and then place at room temperature for 15 minutes;

[0070] 4) Install the adsorption column, transfer the mixed solution to the column, centrifuge at 12000rpm for 1min, and discard the lower liquid;

[0071] 5) Add 500 μL WB5, centrifuge at 12000 rpm for 1 min, discard the filtrate, and repeat this step once;

[0072] 6) Centrifuge at 12000rpm for 1min, dis...

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

PropertyMeasurementUnit
diameteraaaaaaaaaa
antibody titeraaaaaaaaaa
Login to View More

Abstract

The invention discloses an avian influenza virus-like particle antigen, a vaccine, a preparation method of the avian influenza virus-like particle antigen and application of the avian influenza virus-like particle antigen or the vaccine. A strain of recombinant baculovirus based on tandem expression of HA, NA and M1 genes of an H7N9 subtype avian influenza virus transfects insect cells and performs self-assembly to form the avian influenza virus-like particle antigen; and the virus-like particle antigen prepared according to the invention is used for preparing the vaccine. After a chicken group is immunized by the vaccine prepared according to the invention, HI antibodies, neutralizing antibodies and IgY antibodies with the higher titer can be generated, 100-percent clinical protection onthe H7N9 subtype highly pathogenic avian influenza virus can be provided, and virus expelling can be effectively inhibited. The rely on the chicken embryos is avoided; the production cost is low; theperiod is short; and higher protection capability can be induced only by once low-dose immunization. A foundation is laid for industrial production of VLP vaccines.

Description

technical field [0001] The invention belongs to the technical field of vaccines, and in particular relates to an avian influenza virus-like particle antigen, a vaccine and a preparation method and application thereof. Background technique [0002] Avian influenza virus (Avian Influenza Virus, AIV) belongs to type A influenza virus and is a single-stranded negative-sense RNA virus with 8 segments, which can cause disease and death of one or more birds and other animals. In 2013, the H7N9 subtype of avian influenza first appeared in the Yangtze River Delta region of my country. So far, five waves of epidemic peaks have been formed in the Chinese population, posing a major threat to public health and poultry farming. Found in the fifth wave of the epidemic, four basic amino acid residues (KRKRTAR / G or KGKRIAR / G) were inserted at the cleavage site connecting the HA1 and HA2 peptide regions, and the presence of multiple amino acids proves that H7N9 AIV has evolved from LPAI virus...

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
Patent Type & Authority Applications(China)
IPC IPC(8): C07K14/11C07K19/00C12N15/62C12N15/866A61K39/145A61P31/16
CPCC07K14/005C12N15/86A61K39/12A61P31/16C07K2319/00C12N2760/16122C12N2760/16123C12N2760/16134C12N2710/14043A61K2039/70A61K2039/5258
Inventor 胡娇刘秀梵李军李如梦胡增垒王晓泉顾敏
Owner YANGZHOU UNIV
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