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口蹄疫病毒变异株在细胞培养中连续传代后的抗原稳定性

Antigenic stability of foot-and-mouth disease virus variants on serial passage in cell culture.

作者信息

Gonzalez M J, Saiz J C, Laor O, Moore D M

机构信息

Plum Island Animal Disease Center, U.S. Department of Agriculture, Greenport, New York 11944-0848.

出版信息

J Virol. 1991 Jul;65(7):3949-53. doi: 10.1128/JVI.65.7.3949-3953.1991.

Abstract

Two neutralizing monoclonal antibody (MAb)-resistant variants selected from an isolate of foot-and-mouth disease virus (FMDV) type A5 were repeatedly passaged in cell culture and monitored for susceptibility to neutralization by the selecting MAb. A variant isolated with a MAb to a conformational epitope (1-OG2) lost resistance in 20 passages, while a variant isolated with a MAb to a linear epitope (1-HA6) persisted for 30 passages. In both cases, the virus population emerging after passage was antigenically and genetically indistinguishable from the original wild-type parental virus (FMDV A5 Spain-86). Coinfection assays with the wild type and each variant, and between the variants, showed rapid conversion to a homogeneous population. Wild-type virus prevailed over the variants and for coinfection between the variants, the linear epitope variant 1-HA6. While both variants arose from a single nucleotide substitution and reversion to wild type occurred for each, it appears that the variant based on the continuous epitope (1-HA6) was more stable. We discuss the implications of these results for the antigenic diversity of FMDV and its relationship to virus evolution.

摘要

从A5型口蹄疫病毒(FMDV)分离株中筛选出的两种抗中和单克隆抗体(MAb)的变异株,在细胞培养中反复传代,并监测其对筛选所用MAb中和作用的敏感性。一种针对构象表位(1-OG2)的MAb筛选出的变异株在传代20次后失去抗性,而一种针对线性表位(1-HA6)的MAb筛选出的变异株持续传代30次。在这两种情况下,传代后出现的病毒群体在抗原性和基因上与原始野生型亲本病毒(FMDV A5西班牙-86)没有区别。野生型病毒与各变异株之间以及变异株之间的共感染试验表明,病毒迅速转变为同质群体。野生型病毒在变异株中占优势,在变异株之间的共感染中,线性表位变异株1-HA6占优势。虽然两种变异株均由单个核苷酸取代产生,且每种变异株都发生了回复为野生型的情况,但基于连续表位的变异株(1-HA6)似乎更稳定。我们讨论了这些结果对口蹄疫病毒抗原多样性及其与病毒进化关系的影响。

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本文引用的文献

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A comprehensive set of sequence analysis programs for the VAX.一套适用于VAX的综合序列分析程序。
Nucleic Acids Res. 1984 Jan 11;12(1 Pt 1):387-95. doi: 10.1093/nar/12.1part1.387.

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