Frost P, Håvarstein L S, Lygren B, Ståhl S, Endresen C, Christie K E
Intervet Norbio A/S, Bergen, Norway.
J Gen Virol. 1995 May;76 ( Pt 5):1165-72. doi: 10.1099/0022-1317-76-5-1165.
We have characterized and mapped variable and conserved neutralization epitopes of serogroup A strains of aquatic birnaviruses. Epitope mapping using monoclonal antibodies (MAbs) and Escherichia coli-expressed deletion fragments of VP2 of the N1 strain of infectious pancreatic necrosis virus (IPNV) demonstrated that two variable epitopes, H8 and B9, depend on the variable region between amino acid 204-330. A conserved neutralization epitope, F2, was shown to depend on the same region as epitopes H8 and B9 but was additionally dependent on amino acids between 153-203. The neutralization epitopes H8, B9 and F2 were also shown to overlap by a competitive binding assay. One conserved neutralization epitope, AS-1, was not exposed on any of the recombinant VP2 deletion fragments and was therefore not possible to map. However, the MAbs AS1 and F2 were partly competitive indicating that these epitopes are overlapping. All neutralization epitopes were independent of a conserved non-neutralization epitope, E4. Our results demonstrate that the central third of VP2 contains several partly overlapping neutralization epitopes, both variable and conserved among serogroup A strains of IPNV.
我们已对水生双RNA病毒A血清型毒株的可变中和表位和保守中和表位进行了鉴定和定位。使用单克隆抗体(MAb)以及传染性胰腺坏死病毒(IPNV)N1株VP2的大肠杆菌表达缺失片段进行表位定位,结果表明,两个可变表位H8和B9依赖于氨基酸204 - 330之间的可变区。一个保守中和表位F2显示出与表位H8和B9依赖于相同区域,但还依赖于153 - 203之间的氨基酸。通过竞争结合试验还表明中和表位H8、B9和F2相互重叠。一个保守中和表位AS - 1在任何重组VP2缺失片段上均未暴露,因此无法进行定位。然而,单克隆抗体AS1和F2存在部分竞争,表明这些表位相互重叠。所有中和表位均独立于一个保守的非中和表位E4。我们的结果表明,VP2的中间三分之一区域包含几个部分重叠的中和表位,在IPNV A血清型毒株中既有可变的也有保守的。