| Literature DB >> 30290884 |
Alai Shalitanati1, Huan Yu1, Dongliang Liu1, Wan-Xiang Xu2, Xihong Yue3, Rong Guo3, Yijie Li1, Fei Deng4, Jianhua Yang5, Yujiang Zhang6, Surong Sun7.
Abstract
Glycoprotein (GP) is a major antigen of Crimean-Congo hemorrhagic fever virus (CCHFV), and binds to its receptor on the host cell and induces protective immunity in the host. The aim of this study is to identify all linear B cell epitopes (BCEs) on the N-terminal glycoprotein (Gn) of CCHFV using a modified overlapping peptide biosynthesis method. The eight fine BCEs (Gn-E1a, 543RTQLV547; E1b, 553EIH555; E1c, 554IHEDSY559; E1d, 557DSYG560; E2, 615CKQGFC620; E3a, 657GDILVD662; E3b, 662DCSGGQQH669, and E4, 678LGCPNVPL685) were identified using the rabbit antisera, which all were recognized by serum from IgG-positive sheep CCHFV-infected naturally in Western blotting. The multiple sequence alignment (MSA) revealed high conservation of the identified BCEs among ten CCHFV strains from different areas. These mapped epitopes of the CCHFV Gn would provide a basis for further the elucidation of CCHFV pathogenesis, and the development of CCHFV multi-epitope vaccines and detection reagents.Entities:
Keywords: Crimean-Congo hemorrhagic fever virus; Epitope motif mapping; Glycoprotein; Linear B cell epitope
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Year: 2018 PMID: 30290884 DOI: 10.1016/j.cimid.2018.09.003
Source DB: PubMed Journal: Comp Immunol Microbiol Infect Dis ISSN: 0147-9571 Impact factor: 2.268