Mapping and modeling of a strain-specific epitope in the Norwalk virus capsid inner shell

被引:10
作者
Parra, Gabriel I. [1 ]
Sosnovtsev, Stanislav V. [1 ]
Abente, Eugenio J. [1 ]
Sandoval-Jaime, Carlos [1 ]
Bok, Karin [1 ]
Dolan, Michael A. [2 ]
Green, Kim Y. [1 ]
机构
[1] NIAID, Caliciviruses Sect, Infect Dis Lab, NIH, 50 South Dr,Bldg 50,Room 6318, Bethesda, MD 20892 USA
[2] NIAID, Bioinformat & Computat Biosci Branch, NIH, 9000 Rockville Pike, Bethesda, MD 20892 USA
关键词
Noroviruses; Epitope-tagging; Caliciviruses; BLOOD GROUP ANTIGENS; PROTEIN INTERACTIONS; HOT-SPOTS; NOROVIRUS; VACCINE; GASTROENTERITIS; BINDING; INFECTION; ANTIBODY; SYSTEM;
D O I
10.1016/j.virol.2016.02.019
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Noroviruses are diverse positive-strand RNA viruses associated with acute gastroenteritis. Cross-reactive epitopes have been mapped primarily to conserved sequences in the capsid VP1 Shell (S) domain, and strain-specific epitopes to the highly variable Protruding (P) domain. In this work, we investigated a strain-specific linear epitope defined by MAb NV10 that was raised against prototype (Genogroup 1.1) strain Norwalk virus (NV). Using peptide scanning and mutagenesis, the epitope was mapped to amino acids 21-32 (LVPEVNASDPLA) of the NV S domain, and its specificity was verified by epitope transfer and reactivity with a recombinant MAb NV10 single-chain variable fragment (scFv). Comparative structural modeling of the NV10 strain-specific and the broadly cross-reactive TV20 epitopes identified two internal non-overlapping sites in the NV shell, corresponding to variable and conserved amino acid sequences among strains, respectively. The S domain, like the P domain, contains strain-specific epitopes that contribute to the antigenic diversity among the noroviruses. Published by Elsevier Inc.
引用
收藏
页码:232 / 241
页数:10
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