New Neutralizing Epitope Exposed on the Domain II of Tick-Borne Encephalitis Virus Envelope Glycoprotein E

被引:1
|
作者
Matveev, Andrey [1 ]
Khlusevich, Yana [1 ]
Kozlova, Irina [2 ]
Matveev, Leonid [1 ]
Emelyanova, Lyudmila [1 ]
Tikunov, Artem [1 ]
Baykov, Ivan [1 ]
Tikunova, Nina [1 ]
机构
[1] Russian Acad Sci, Inst Chem Biol & Fundamental Med, Siberian Branch, Novosibirsk 630090, Russia
[2] Russian Acad Sci, Fed State Publ Sci Inst, Siberian Branch, Sci Ctr Family Hlth & Human Reprod Problems, Irkutsk 664003, Russia
来源
VIRUSES-BASEL | 2023年 / 15卷 / 06期
基金
俄罗斯科学基金会;
关键词
tick-borne encephalitis virus; protective antibody; flavivirus; protein E; epitope mapping; STRUCTURAL BASIS; ANTIBODY; ENHANCEMENT; INFECTION; SPECIFICITY;
D O I
10.3390/v15061256
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Orthoflavivirus encephalitidis, formerly tick-borne encephalitis virus (TBEV), belongs to the Orthoflavivirus genus. TBEV is transmitted by tick bites and infection with TBEV can lead to serious disorders of the central nervous system. In this study, a new protective monoclonal mouse antibody (mAb) FVN-32, with high binding activity to glycoprotein E of TBEV, was selected and examined in post exposure prophylaxis in a mouse model of TBEV infection. BALB/c mice were injected mAb FVN-32 at doses of 200 & mu;g, 50 & mu;g, and 12.5 & mu;g per mouse one day after a TBEV challenge. mAb FVN-32 showed 37.5% protective efficacy when administered at doses of 200 & mu;g and 50 & mu;g per mouse. The epitope for protective mAb FVN-32 was localized in TBEV glycoprotein E domain I+II, using a set of truncated fragments of glycoprotein E. Additionally, the target site recognized by mAb FVN-32 was defined using combinatorial libraries of peptides. Three-dimensional modeling revealed that the site is dspatially close to the fusion loop, but does not come into contact with it, and is localized in a region between 247 and 254 amino acid residues on the envelope protein. This region is conserved among TBEV-like orthoflaviviruses.
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页数:11
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