期刊
VACCINE
卷 30, 期 12, 页码 2125-2130出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.vaccine.2012.01.040
关键词
Infectious bursal disease virus; Hepatitis B virus core particle; Virus-like particle; Chimeric VLP; Mimotope vaccine
资金
- Chinese National High-Tech R&D Program (863 Program) [2011AA10A200]
- National Natural Science Foundation of China [30571371]
- Jiangsu Provincial Natural Science Foundation of China [BK2008065, BK2008352, BK2009041]
Current infectious bursal disease virus (IBDV) vaccines suffer from maternal antibody interference and mimotope vaccines might be an alternative. Previously we demonstrated an IBDV VP2 five-mimotope polypeptide, 5EPIS, elicited protective immunity in chickens. In the current study, the 5epis gene was inserted into a plasmid carrying human hepatitis B virus core protein (HBc) gene at its major immunodominant region site. The recombinant gene was efficiently expressed in Escherichia coli to produce chimeric protein HBc-5EPIS which self-assembles to virus-like particles (VLP). Two-week old specific-pathogen-free chickens were immunized intramuscularly with HBc-5EPIS VLP or 5EPIS polypeptide without adjuvant (50 mu g/injection) on day 0, 7, 14 and 21. Anti-5EPIS antibody was first detected on day 7 and day 21 in HBc-5EPIS and 5EPIS groups, respectively; on day 28, anti-5EPIS titers reached 12,800 or 1600 by ELISA, and 3200 or 800 by virus neutralization assay in HBc-5EPIS and 5EPIS groups, respectively. No anti-5EPIS antibody was detected in the buffer control group throughout the experiment. Challenge on day 28 with a virulent IBDV strain (GX8/99) resulted in 100%, 40.0% and 26.7% survival for chickens immunized with HBc-5EPIS, 5EPIS and buffer, respectively. These data suggest epitope presentation on chimeric VLP is a promising approach for improving mimotope vaccines for IBDV. (C) 2012 Elsevier Ltd. All rights reserved.
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