Volume 16, No. 10, October 2016, Pages 2421-2427 PDF(1.27 MB)
Innovation of a New Virus-Like Nanoparticle Vaccine System for the Specific Aerosol Relative Disease
Rui-Zhe Zhang1, Shinn-Shyong Tsai2, How-Ran Chao3, Yao-Ching Shieh4, Kuo-Pin Chuang1
1 Graduate Institute of Animal Vaccine Technology, College of Veterinary Medicine, National Pingtung University of Science and Technology, Pingtung 912, Taiwan
2 Department of Veterinary Medicine, College of Veterinary Medicine, National Pingtung University of Science and Technology, Pingtung 912, Taiwan
3 Department of Environmental Science and Engineering, National Pingtung University of Science and Technology, Pingtung 912, Taiwan
4 Bureau of Animal and Plant Health Inspection and Quarantine, Council of Agriculture, Executive Yuan, Taipei 100, Taiwan
- The bacterial expressed fusion protein was self-assemble to nano VLP.
- The VLP vaccine induced a high IgG titer and neutralization activity for PRRSV.
- The VLP vaccine can induce cell-mediated immunity.
- The VLP nanoparticle is a possibly viable approach for human and animal vaccine.
Human spend a lot of time indoors and indoor air quality (IAQ) has a great effect on quality of life in humans. Traditionally, bioaerosol in IAQs is focused on bacteria and fungus. Airborne viruses, particularly for the nanoparticle-type virus, on the bioaerosol particulates are associated with the quality of human health in indoor environment. We establish the human like animal model, like pig, for testing the efficacy of the nano virus like particle (VLP) vaccine for aerosol relative disease. The porcine reproductive and respiratory syndrome virus (PRRSV), which is an airborne and a droplet infection virus coated on the small size of bioaerosol, carries a major infectious disease in the pig raising industry worldwide. There are commercial vaccines including attenuated and inactivated vaccines available, but their efficacy remains to be improved. VLP represents safe and effective vaccine platforms based on nano-technology. The fusion protein of capsid protein (Cap) from the porcine circovirus 2 (PCV2) and the glycoprotein 5 (GP5) from PRRSV were expressed by E. coli system. The fusion protein self-assembled with the GP5 to become a VLP nanoparticle. For testing, BALB/c mice were immunized with 10 µg of chimeric VLP nanoparticle once, which induced neutralization by antibody responses to PRRSV. The VLP nanoparticle vaccine induced high T cell proliferation, not evident in commercial vaccines tested on mice. Our results suggest that the cheaper VLP–based nanoparticle is a possibly viable approach model for specific airborne-relative-diseases human vaccine in the future.
Nanoparticle delivery system; Bioaerosol; Airborne virus; Virus like particle; Porcine reproductive and respiratory syndrome virus (PRRSV); Vaccine.