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

Construction method for delaying attenuation and increasing expression exogenous antigen salmonella suipestifer carrier through regulation and control of gene

A technology of Salmonella and exogenous antigen is applied in the construction field where the virulence gene of wild-type Salmonella choleraesuis is gradually deleted, achieving the effect of large market applicability and significant economic benefits

Active Publication Date: 2015-04-08
YANGZHOU UNIV
View PDF0 Cites 9 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

But all of the above are studies on Salmonella typhimurium or human, studies using Salmonella choleraesuis as a carrier, especially the deletion of manA (the gene is equivalent to the pmi gene of typhoid fever) and the araC P BAD The application of activated promoter technology to construct attenuated Salmonella choleraesuis has not been reported at home and abroad

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
  • Construction method for delaying attenuation and increasing expression exogenous antigen salmonella suipestifer carrier through regulation and control of gene
  • Construction method for delaying attenuation and increasing expression exogenous antigen salmonella suipestifer carrier through regulation and control of gene
  • Construction method for delaying attenuation and increasing expression exogenous antigen salmonella suipestifer carrier through regulation and control of gene

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0039] Construction of suicide vectors lacking manA, crp, relA and asd genes

[0040] 1. Construction of a suicide vector that deletes the crp gene

[0041] Search the whole gene sequence of Salmonella choleraesuis in Genbank, find the crp gene and its upstream sequence of Salmonella choleraesuis, design homology arm sequence primers in the crp gene and upstream gene, and delete 95 nucleotides in the promoter region of the crp gene , and then insert the transcription terminator (TT) and araC P BAD The activated promoter sequence is 1335bp, and its deletion and insertion system is yhfA partial sequence upstream of the crp gene, deletion of 95 nucleotides in the promoter region of the crp gene, transcription terminator (TT) of 1335bp and araC P BAD The crp sequence after activating the promoter sequence and deleting the 95bp crp gene promoter, the full name is ΔP crp ::TT araC P BAD crp (P means promoter, TT means transcription terminator) ( figure 1 ); The specific steps a...

Embodiment 2

[0073] Construction and identification of attenuated strain x0011 of Salmonella choleraesuis

[0074] 1. C78-3(ΔP crp ::TT araC P BAD crp) mutant strain construction and identification

[0075] 1.1C78-3(ΔP crp ::TT araC P BAD crp) mutant strain construction

[0076] Add recipient bacteria C78-3 (virulent wild-type Salmonella choleraesuis) to 1 mL of LB medium and culture overnight at 37°C; , DAP), 25mg / ml of chloramphenicol (chloramphenicol, Cm) in 1mLLB culture fluid, add donor bacteria χ7213 (pYAs001) (ΔP crp ::TT araC P BAD crp suicide vector), cultivated overnight at 37°C to combine the recipient bacteria with the donor bacteria.

[0077] 1.2ΔP crp ::TT araC P BAD Screening of crp deletion strains

[0078] Streak a single colony of the combined colony on the LB solid culture plate containing chloramphenicol; take the grown single colony and culture it in 1mL of LB culture medium, and culture it with shaking at 37°C until the concentration of the bacterial sol...

Embodiment 3

[0110] Construction of Balanced-Lethal Bacteria-Vector System of Attenuated Salmonella Choleraesuis Strain χ0011

[0111] In order to avoid the use of drug-resistant or resistant gene-containing plasmid vectors and ensure the stability of the plasmid vectors in attenuated Salmonella in the host, we tested the attenuated Salmonella choleraesuis strain C78-3(ΔmanAΔP crp ::TT araC P BAD crpΔrelA::araC P BAD The asd gene was deleted on the chromosome of lacI TT), and this mutant strain was named χ0011 according to the naming sequence of our laboratory. When the asd gene-deleted strain is cultured in vitro, diaminopimelic acid (DAP) can be added to make up for the defect that the bacteria cannot grow due to the asd gene deletion. However, since there is no diaminopimelic acid in the animal body, Salmonella lacking the asd gene cannot survive in the animal body. Therefore, Dr. Curiss III's laboratory invented the addition of the asd gene of wild-type bacteria to the plasmid vect...

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 provides a construction method for delaying attenuation and increasing an expression exogenous antigen salmonella suipestifer carrier through regulation and control of gene, which is characterized in that receptor bacterium C78-3 is combined with manA, crp, relA and asd -containing deleted suicide carrier escherichia coli donor bacterium, mutants delta manA, delta Pcrp: : TT ara C PBAD crp, delta relA: : araC PBAD lacI TT and delta asd A are introduced in wild-type salmonella suipestifer C78-3, the introduced salmonella suipestifer after mutation can be called x0011; and four types of mutation enable phenotype identification. The method of the invention makes salmonella suipestifer to become safe and effective vaccine carrier of many exogenous antigens; and provides the delaying attenuation and increasing expression exogenous antigen salmonella suipestifer carrier through regulation and control of gene for various pig diseases, especially many bacteria diseases of pig, and has great market applicability.

Description

technical field [0001] The invention belongs to the field of biotechnology, in particular to a construction method for gradually deleting the virulence gene of wild-type Salmonella choleraesuis. Background technique [0002] As an invasive intracellular bacterium, Salmonella has preferential invasion ability after attenuation, grows slowly in the body, and can effectively and continuously stimulate the body to produce strong cellular immunity, humoral immunity and local mucosal immunity. In addition, the Salmonella carrier has the function of immune adjuvant, and its LPS acts as an internal adjuvant, which can stimulate the host cells to release various cytokines. Therefore, attenuated Salmonella are more effective than inactivated or subunit vaccines in inducing humoral and cellular immune responses. Salmonella typhimurium weakened by genetic engineering has been used as a gene carrier to express foreign genes widely, and it is used in the treatment of tumors, viral diseas...

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): C12N1/21C12N15/74C12R1/42
CPCC07K14/255C12N15/74
Inventor 石火英吉贞颖尚竞李玉安
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