4.7 Article

Development of a Viral-Like Particle Candidate Vaccine Against Novel Variant Infectious Bursal Disease Virus

期刊

VACCINES
卷 9, 期 2, 页码 -

出版社

MDPI
DOI: 10.3390/vaccines9020142

关键词

novel variant infectious bursal disease virus; vaccine; viral-like particle

资金

  1. National Natural Science Foundation of China [C180202]
  2. Heilongjiang Provincial Natural Science Foundation of China [ZD2020C006]
  3. National Key Research andDevelopment Programof China [2016YFE0203200, 2017YFD0500704]
  4. Heilongjiang Province Foundation for the National Key Research and Development Program of China [GX18B011]
  5. China Agriculture Research System [CARS-41-G15]

向作者/读者索取更多资源

The study successfully expressed the VP2 protein of nVarIBDV strain SHG19 and developed a VLP vaccine based on this protein, which provided 100% protection against nVarIBDV and good protection against vvIBDV. This research has significant implications for the comprehensive prevention and control of the recent atypical IBD epidemic.
Infectious bursal disease (IBD), an immunosuppressive disease of young chickens, is caused by infectious bursal disease virus (IBDV). Novel variant IBDV (nVarIBDV), a virus that can evade immune protection against very virulent IBDV (vvIBDV), is becoming a threat to the poultry industry. Therefore, nVarIBDV-specific vaccine is much needed for nVarIBDV control. In this study, the VP2 protein of SHG19 (a representative strain of nVarIBDV) was successfully expressed using an Escherichia coli expression system and further purified via ammonium sulfate precipitation and size-exclusion chromatography. The purified protein SHG19-VP2-466 could self-assemble into 25-nm virus-like particle (VLP). Subsequently, the immunogenicity and protective effect of the SHG19-VLP vaccine were evaluated using animal experiments, which indicated that the SHG19-VLP vaccine elicited neutralization antibodies and provided 100% protection against the nVarIBDV. Furthermore, the protective efficacy of the SHG19-VLP vaccine against the vvIBDV was evaluated. Although the SHG19-VLP vaccine induced a comparatively lower vvIBDV-specific neutralization antibody titer, it provided good protection against the lethal vvIBDV. In summary, the SHG19-VLP candidate vaccine could provide complete immune protection against the homologous nVarIBDV as well as the heterologous vvIBDV. This study is of significance to the comprehensive prevention and control of the recent atypical IBD epidemic.

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