Development of a Nanoparticle Multiepitope DNA Vaccine against Virulent Infectious Bronchitis Virus Challenge.
Yifeng QinQingyuan TengDelan FengYu PeiYe ZhaoGuozhong ZhangPublished in: Journal of immunology (Baltimore, Md. : 1950) (2022)
To develop a safe and effective nanoparticle (NP) multiepitope DNA vaccine for controlling infectious bronchitis virus (IBV) infection, we inserted the multiepitope gene expression box SBNT into a eukaryotic expression vector pcDNA3.1(+) to construct a recombinant plasmid pcDNA/SBNT. The NP multiepitope DNA vaccine pcDNA/SBNT-NPs were prepared using chitosan to encapsulate the recombinant plasmid pcDNA/SBNT, with a high encapsulation efficiency of 94.90 ± 1.35%. These spherical pcDNA/SBNT-NPs were 140.9 ± 73.2 nm in diameter, with a mean ζ potential of +16.8 ± 4.3 mV. Our results showed that the chitosan NPs not only protected the plasmid DNA from DNase degradation but also mediated gene transfection in a slow-release manner. Immunization with pcDNA/SBNT-NPs induced a significant IBV-specific immune response and partially protected chickens against homologous IBV challenge. Therefore, the chitosan NPs could be a useful gene delivery system, and NP multiepitope DNA vaccines may be a potential alternative for use in the development of a novel, safe, and effective IBV vaccine.
Keyphrases
- cell free
- circulating tumor
- single molecule
- gene expression
- drug delivery
- escherichia coli
- immune response
- crispr cas
- nucleic acid
- genome wide
- copy number
- oxide nanoparticles
- binding protein
- poor prognosis
- disease virus
- hyaluronic acid
- high glucose
- oxidative stress
- human health
- heat stress
- endothelial cells
- stress induced
- long non coding rna