Structural analysis and insertion study reveal the ideal sites for surface displaying foreign peptides on a betanodavirus-like particle

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• 作者：Junfeng Xie ; Kunpeng Li ; Yuanzhu Gao ; Runqing Huang ; Yuxiong Lai…
• 刊名：Veterinary Research
• 出版年：2016
• 出版时间：December 2016
• 年：2016
• 卷：47
• 期：1
• 全文大小：2,045 KB
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• 作者单位：Junfeng Xie (1)
  Kunpeng Li (1)
  Yuanzhu Gao (1)
  Runqing Huang (1)
  Yuxiong Lai (2)
  Yan Shi (1)
  Shaowei Yang (1)
  Guohua Zhu (1)
  Qinfen Zhang (1)
  Jianguo He (1) (3)
  
  1. State Key Laboratory of Biocontrol, MOE Key Laboratory of Aquatic Product Safety, Institute of Aquatic Economic Animals and Guangdong Province Key Laboratory for Aquatic Economic Animals, School of Life Sciences, Sun Yat-sen University, Guangzhou, 510275, China
  2. Department of Nephrology, Guangdong General Hospital, Guangdong Academy of Medical Sciences, Guangzhou, 518080, China
  3. School of Marine Sciences, Sun Yat-sen University, Guangzhou, 510275, China
  
• 刊物主题：Veterinary Medicine;
• 出版者：BioMed Central
• ISSN：1297-9716

文摘

Betanodavirus infection causes fatal disease of viral nervous necrosis in many cultured marine and freshwater fish worldwide and the virus-like particles (VLP) are effective vaccines against betanodavirus. But vaccine and viral vector designs of betanodavirus VLP based on their structures remain lacking. Here, the three-dimensional structure of orange-spotted grouper nervous necrosis virus (OGNNV) VLP (RBS) at 3.9 Å reveals the organization of capsid proteins (CP). Based on the structural results, seven putative important sites were selected to genetically insert a 6× histidine (His)-tag for VLP formation screen, resulting in four His-tagged VLP (HV) at positions N-terminus, Ala220, Pro292 and C-terminus. The His-tags of N-terminal HV (NHV) were concealed inside virions while those of 220HV and C-terminal HV (CHV) were displayed at the outer surface. NHV, 220HV and CHV maintained the same cell entry ability as RBS in the Asian sea bass (SB) cell line, indicating that their similar surface structures can be recognized by the cellular entry receptor(s). For application of vaccine design, chromatography-purified CHV could provoke NNV-specific antibody responses as strong as those of RBS in a sea bass immunization assay. Furthermore, in carrying capacity assays, N-terminus and Ala220 can only carry short peptides and C-terminus can even accommodate large protein such as GFP to generate fluorescent VLP (CGV). For application of a viral vector, CGV could be real-time visualized to enter SB cells in invasion study. All the results confirmed that the C-terminus of CP is a suitable site to accommodate foreign peptides for vaccine design and viral vector development. Junfeng Xie, Kunpeng Li and Yuanzhu Gao authors contributed equally.Electronic supplementary materialThe online version of this article (doi:10.​1186/​s13567-015-0294-9) contains supplementary material, which is available to authorized users.