@article{mbs:/content/journal/jgv/10.1099/jgv.0.000355, author = "Song, Yanhua and Wang, Fang and Fan, Zhiyu and Hu, Bo and Liu, Xing and Wei, Houjun and Xue, Jiabin and Xu, Weizhong and Qiu, Rulong", title = "Identification of novel rabbit hemorrhagic disease virus B-cell epitopes and their interaction with host histo-blood group antigens", journal= "Journal of General Virology", year = "2016", volume = "97", number = "2", pages = "356-365", doi = "https://doi.org/10.1099/jgv.0.000355", url = "https://www.microbiologyresearch.org/content/journal/jgv/10.1099/jgv.0.000355", publisher = "Microbiology Society", issn = "1465-2099", type = "Journal Article", abstract = "Rabbit haemorrhagic disease, caused by rabbit hemorrhagic disease virus (RHDV), results in the death of millions of adult rabbits worldwide, with a mortality rate that exceeds 90 %. The sole capsid protein, VP60, is divided into shell (S) and protruding (P) domains, and the more exposed P domain likely contains determinants for cell attachment and antigenic diversity. Nine mAbs against VP60 were screened and identified. To map antigenic epitopes, a set of partially overlapping and consecutive truncated proteins spanning VP60 were expressed. The minimal determinants of the linear B-cell epitopes of VP60 in the P domain, N326PISQV331, D338MSFV342 and K562STLVFNL569, were recognized by one (5H3), four (1B8, 3D11, 4C2 and 4G2) and four mAbs (1D4, 3F7, 5G2 and 6B2), respectively. Sequence alignment showed epitope D338MSFV342 was conserved among all RHDV isolates. Epitopes N326PISQV331 and K562STLVFNL569 were highly conserved among RHDV G1–G6 and variable in RHDV2 strains. Previous studies demonstrated that native viral particles and virus-like particles (VLPs) of RHDV specifically bound to synthetic blood group H type 2 oligosaccharides. We established an oligosaccharide-based assay to analyse the binding of VP60 and epitopes to histo-blood group antigens (HBGAs). Results showed VP60 and its epitopes (aa 326–331 and 338–342) in the P2 subdomain could significantly bind to blood group H type 2. Furthermore, mAbs 1B8 and 5H3 could block RHDV VLP binding to synthetic H type 2. Collectively, these two epitopes might play a key role in the antigenic structure of VP60 and interaction of RHDV and HBGA.", }