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口蹄疫病毒在有无免疫选择情况下的不同抗原变异体库

Distinct repertoire of antigenic variants of foot-and-mouth disease virus in the presence or absence of immune selection.

作者信息

Borrego B, Novella I S, Giralt E, Andreu D, Domingo E

机构信息

Centro de Biología Molecular Severo Ochoa (Consejo Superior de Investigaciones Científicas, Universidad Autónoma de Madrid), Cantoblanco Spain.

出版信息

J Virol. 1993 Oct;67(10):6071-9. doi: 10.1128/JVI.67.10.6071-6079.1993.

Abstract

Antigenic variants of foot-and-mouth disease virus (FMDV) were generated and frequently became dominant in clonal populations of FMDV (clone C-S8c1) grown in the absence of anti-FMDV antibodies. We have now passaged eight samples of the same FMDV clone in the presence of a limited amount of neutralizing polyclonal antibodies directed to the major antigenic site A of capsid protein VP1. Complex populations of variants showing increased resistance to polyclonal sera and to site A-specific monoclonal antibodies were selected. Some populations exhibited marked decreases in viral fitness. Multiple amino acid replacements within site A--and also elsewhere in VP1--accumulated upon passage of the virus in either the absence or the presence of neutralizing antibodies. However, antigenically critical replacements at one position in site A occurred repeatedly in FMDV passaged under antibody selection, but they were never observed in many passages carried out either in the absence of antiviral antibodies or in the presence of an irrelevant antiviral serum. Thus, even though antigenic variation of FMDV can occur in the absence or presence of immune selection, critical replacements which lead to important changes in antigenic specificity were observed only as a result of selection by neutralizing antibodies.

摘要

口蹄疫病毒(FMDV)的抗原变异体产生后,在无抗FMDV抗体情况下培养的FMDV克隆群体(克隆C-S8c1)中常成为优势毒株。我们现在在存在针对衣壳蛋白VP1主要抗原位点A的有限量中和多克隆抗体的情况下,传代了同一FMDV克隆的八个样本。选择出了对多克隆血清和位点A特异性单克隆抗体显示出抗性增强的复杂变异体群体。一些群体的病毒适应性显著降低。无论在有无中和抗体的情况下传代病毒,位点A内以及VP1其他部位都积累了多个氨基酸替换。然而,在抗体选择下传代的FMDV中,位点A一个位置上具有抗原关键作用的替换反复出现,但在无抗病毒抗体或存在无关抗病毒血清的多次传代中从未观察到。因此,尽管FMDV的抗原变异在有无免疫选择的情况下都可能发生,但只有通过中和抗体选择才观察到导致抗原特异性重要变化的关键替换。

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