Domingo E, Díez J, Martínez M A, Hernández J, Holguín A, Borrego B, Mateu M G
Centro de Biología Molecular Severo Ochoa (CSIC-UAM), Universidad Autónoma de Madrid, Cantoblanco, Spain.
J Gen Virol. 1993 Oct;74 ( Pt 10):2039-45. doi: 10.1099/0022-1317-74-10-2039.
Recent results have revealed novel features in the process of antigenic diversification of FMDV. (i) Antigenic variation is not necessarily the result of immune selection. (ii) Single, critical amino acid replacements may either have a minor effect on antigenic specificity or cause a drastic antigenic change affecting many epitopes on an antigenic site. (iii) The effect of such a critical replacement may be suppressed by additional substitutions at neighbouring sites. (iv) Antigenic diversification does not necessarily involve net accumulation of amino acid substitutions over time. We review evidence that some of these features apply also to other riboviruses and retroviruses. A model is proposed to relate antigenic variation without immune selection to the quasispecies structure of RNA virus populations.
最近的研究结果揭示了口蹄疫病毒(FMDV)抗原多样化过程中的新特征。(i)抗原变异不一定是免疫选择的结果。(ii)单个关键氨基酸替换可能对抗原特异性影响较小,也可能导致影响抗原位点上多个表位的剧烈抗原变化。(iii)这种关键替换的效应可能会被邻近位点的额外替换所抑制。(iv)抗原多样化不一定涉及氨基酸替换随时间的净积累。我们综述了一些证据,表明其中一些特征也适用于其他核糖病毒和逆转录病毒。提出了一个模型,将无免疫选择的抗原变异与RNA病毒群体的准种结构联系起来。