An affinity peptide exerts antiviral activity by strongly binding nervous necrosis virus to block viral entry. Issue 86 (March 2019)

• Record Type: Journal Article
• Authors: Zhou, Qiong; Zhang, Jing; Huang, Runqing; Huang, Siyou; Wu, Yujia; Huang, Lijie; He, Jianguo; Xie, Junfeng
• Is Part Of: Fish & shellfish immunology. Issue 86(2019)
• Page Start: 465
• Page End: 473
• Publication Date: 2019-03
• Subjects: Nervous necrosis virus -- Phage display peptide library -- Affinity peptide -- Binding capacity -- Antiviral activity; Fishes -- Immunology -- Periodicals; Shellfish -- Immunology -- Periodicals; Poissons -- Immunologie -- Périodiques; Crustacés -- Immunologie -- Périodiques; 571.9617
• DOI: 10.1016/j.fsi.2018.12.003
• Languages: English
• ISSNs: 1050-4648

Abstract

Abstract: Nervous necrosis virus (NNV) causes viral nervous necrosis (VNN), a disease that leads to almost 100% mortality among larvae and juvenile fish, severely affecting the aquaculture industry. VNN vaccines based on inactivated viruses or virus-like particles (VLPs) are unsuitable for fish fry with immature adaptive immune systems. Here, we applied an anti-NNV strategy based on affinity peptides (AFPs). Three phage display peptide libraries were screened against RBS, the VLP of orange-spotted grouper nervous necrosis virus (OGNNV). From the positive clones, a dodecapeptide with the highest binding capacity (BC) to RBS was selected. This AFP agglutinated or disrupted virion particles, inhibiting RBS entry into sea bass (SB) cells. To enhance BC and solubility, we amended the AFP sequence as "LHWDFQSWVPLL" and named as 12C. One to three copies of 12C in tandem were prokaryotically expressed with a maltose binding protein (MBP) linked by a flexible peptide. Of the recombinant proteins expressed, MBP-triple-12C (MBP-T12C) exhibited the highest BC, efficiently blocked RBS entry, and strongly inhibited OGNNV infection at viral entry. Moreover, MBP-T12C bound the VLPs of all NNV serotypes, displaying broad-spectrum anti-NNV ability, and recognized only OGNNV and mud crab virus, demonstrating binding specificity. Therefore, these anti-NNV AFPs specifically bound NNV, aggregating or disrupting the viral particles, to reduce the contact probability between the virus and cell surface, subsequently inhibiting viral infection. Our results not only provided a candidate of anti-NNV AFP, but a framework for the development of antiviral AFP. Highlights: Three affinity peptides (AFP) against OGNNV VLP (RBS) were obtained by screening. A soluble 12-mer AFP agglutinated or disrupted virion particles to inhibit RBS entry. A prokaryotic fusion protein of triple tandem AFP (MBP-T12C) was generated. MBP-T12C bound all serotypes of NNV and a highly homogenous crab virus. MBP-T12C hindered RBS entry and inhibited OGNNV infection by blocking viral entry.