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Multiepitope Subunit Peptide-Based Nanovaccine against Porcine Circovirus Type 2 (PCV2) Elicited High Antibody Titers in Vaccinated Mice
被引:2
作者:
Duong, Viet Tram
[1
]
Koirala, Prashamsa
[1
]
Chen, Sung-Po R.
[2
]
Monteiro, Michael J.
[2
]
Skwarczynski, Mariusz
[1
]
Toth, Istvan
[1
,3
]
机构:
[1] Univ Queensland, Sch Chem & Mol Biosci, St Lucia, Qld 4072, Australia
[2] Univ Queensland, Australian Inst Bioengn & Nanotechnol, St Lucia, Qld 4072, Australia
[3] Univ Queensland, Sch Pharm, Woolloongabba, Qld 4102, Australia
来源:
MOLECULES
|
2023年
/
28卷
/
05期
基金:
英国医学研究理事会;
澳大利亚研究理事会;
关键词:
peptide-based vaccine;
adjuvant;
polyleucine;
liposome;
nanoparticles;
block copolymers;
rods;
poly(methyl acrylate);
porcine circovirus;
WASTING SYNDROME PMWS;
IMMUNE-RESPONSES;
CAPSID PROTEIN;
DELIVERY;
ADJUVANTS;
SIZE;
VIRUS;
PIGS;
IMMUNOGENICITY;
PROTECTION;
D O I:
10.3390/molecules28052248
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Porcine circovirus 2 (PCV2) infection is one of the most serious threats to the swine industry. While the disease can be prevented, to some extent, by commercial PCV2a vaccines, the evolving nature of PCV2 necessitates the development of a novel vaccine that can compete with the mutations of the virus. Thus, we have developed novel multiepitope vaccines based on the PCV2b variant. Three PCV2b capsid protein epitopes, together with a universal T helper epitope, were synthesized and formulated with five delivery systems/adjuvants: complete Freund's adjuvant, poly(methyl acrylate) (PMA), poly(hydrophobic amino acid), liposomes and rod-shaped polymeric nanoparticles built from polystyrene-poly(N-isopropylacrylamide)-poly(N-dimethylacrylamide). Mice were subcutaneously immunized with the vaccine candidates three times at three-week intervals. All vaccinated mice produced high antibody titters after three immunizations as analyzed by the enzyme-linked immunosorbent assay (ELISA), while mice vaccinated with PMA-adjuvanted vaccine elicited high antibody titers even after a single immunization. Thus, the multiepitope PCV2 vaccine candidates designed and examined here show strong potential for further development.
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页数:15
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