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针对新型变异传染性法氏囊病病毒的类病毒颗粒候选疫苗的研发

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

作者信息

Wang Yulong, Jiang Nan, Fan Linjin, Gao Li, Li Kai, Gao Yulong, Niu Xinxin, Zhang Wenying, Cui Hongyu, Liu Aijing, Pan Qing, Liu Changjun, Zhang Yanping, Wang Xiaomei, Qi Xiaole

机构信息

State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, Avian Immunosuppressive Diseases Division, The Chinese Academy of Agricultural Sciences, Harbin 150069, China.

OIE Reference Laboratory for Infectious Bursal Disease, Harbin Veterinary Research Institute, The Chinese Academy of Agricultural Sciences, Harbin 150069, China.

出版信息

Vaccines (Basel). 2021 Feb 10;9(2):142. doi: 10.3390/vaccines9020142.

Abstract

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 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.

摘要

传染性法氏囊病(IBD)是幼鸡的一种免疫抑制性疾病,由传染性法氏囊病病毒(IBDV)引起。新型变异IBDV(nVarIBDV)是一种能够逃避针对超强毒力IBDV(vvIBDV)免疫保护的病毒,正成为家禽业的一大威胁。因此,非常需要针对nVarIBDV的特异性疫苗来控制nVarIBDV。在本研究中,使用表达系统成功表达了SHG19(nVarIBDV的代表性毒株)的VP2蛋白,并通过硫酸铵沉淀和尺寸排阻色谱进一步纯化。纯化后的蛋白SHG19-VP2-466能够自组装成25纳米的病毒样颗粒(VLP)。随后,通过动物实验评估了SHG19-VLP疫苗的免疫原性和保护效果,结果表明SHG19-VLP疫苗可诱导中和抗体,并对nVarIBDV提供100%的保护。此外,还评估了SHG19-VLP疫苗对vvIBDV的保护效力。尽管SHG19-VLP疫苗诱导产生的vvIBDV特异性中和抗体效价相对较低,但它对致死性vvIBDV提供了良好保护。总之,SHG19-VLP候选疫苗能够对同源nVarIBDV以及异源vvIBDV提供完全的免疫保护。本研究对近期非典型IBD疫情的综合防控具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a6e/7916800/b8f8f6f23c43/vaccines-09-00142-g001.jpg

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