Zhang Ruihua, Yang Yupeng, Lan Jingjing, Lin Shaoli, Xie Zhijing, Zhang Xiansheng, Jiang Shijin
College of Life Science, Shandong Agricultural University, Taian 271018, China.
Department of Preventive Veterinary Medicine, College of Veterinary Medicine, Shandong Agricultural University, Taian 271018, China.
Vaccines (Basel). 2020 Mar 5;8(1):121. doi: 10.3390/vaccines8010121.
Duck hepatitis A virus (DHAV), the major pathogen of duck virus hepatitis (DVH), causes severe diseases that threaten the duck industry worldwide. The VP1 protein, a major structural protein of DHAV, is able to induce neutralizing antibody in ducks. The purpose of this study was to identify the antigenic mimotope of DHAV by phage display technology. A monoclonal antibody (mAb) 4E6 against DHAV-1 and DHAV-3 was prepared, and a phage library prepared with the PhD-12 Phage Display Peptide Library Kit was screened with the mAb. A novel peptide, GLTWKLPPSM was identified with high affinity to the mAb and could specifically block mAb 4E6 from binding DHAV-1 and DHAV-3. Animal tests confirmed that the immunization of ducklings with the mimotope could inhibit the virus proliferation and protect the ducklings from DVH. In summary, the neutralizing conformational mimotope GLTWKLPPSM might be a promising vaccine candidate for the prevention of DHAV infection.
鸭甲型肝炎病毒(DHAV)是鸭病毒性肝炎(DVH)的主要病原体,可引发严重疾病,威胁全球鸭业。VP1蛋白是DHAV的主要结构蛋白,能够在鸭体内诱导中和抗体。本研究旨在通过噬菌体展示技术鉴定DHAV的抗原模拟表位。制备了针对DHAV - 1和DHAV - 3的单克隆抗体(mAb)4E6,并用该mAb筛选了使用PhD - 12噬菌体展示肽库试剂盒制备的噬菌体文库。鉴定出一种与该mAb具有高亲和力的新型肽GLTWKLPPSM,它能特异性阻断mAb 4E6与DHAV - 1和DHAV - 3的结合。动物试验证实,用模拟表位免疫雏鸭可抑制病毒增殖并保护雏鸭免受DVH感染。总之,中和性构象模拟表位GLTWKLPPSM可能是预防DHAV感染的一种有前景的疫苗候选物。