首页> 外文期刊>Biologicals: Journal of the International Association of Biological Standardization >Sequence analysis of capsid coding region of foot-and-mouth disease virus type A vaccine strain during serial passages in BHK-21 adherent and suspension cells
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Sequence analysis of capsid coding region of foot-and-mouth disease virus type A vaccine strain during serial passages in BHK-21 adherent and suspension cells

机译:BHK-21贴壁细胞和悬浮细胞连续传代过程中口蹄疫病毒A型疫苗株衣壳编码区的序列分析

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摘要

Sequence variability within the capsid coding region of the foot-and-mouth disease virus type A vaccine strain during serial in vitro passage was investigated. Specifically, two methods of virus propagation were utilized, a monolayer and suspension culture of BHK-21 cells. At three positions (VP2131 E-K in both monolayer and suspension passages, VP385 H-R in late monolayer passages and VP3139 K-E in only suspension passages), all mapped to surface exposed loops, amino acid substitutions were apparently fixed without reversion till the end of the passage regime. Interestingly, VP2131, 121 and VP385 which form part of the heparan sulphate binding pocket, showed a tendency to acquire positively charged amino acids in either monolayer or suspension environment probably to better interact with the negatively charged cell surface glycosaminoglycans. At three identified antigenically critical positions (VP279, VP3139 and VP1154), amino acids substitutions even in the absence of immune pressure were noticed. Hence both random drift and adaptive mutations attributable to the strong selective pressure exerted by the proposed cell surface alternate receptors could play a role in modifying the capsid sequence of cell culture propagated FMDV vaccine virus, which in turn may alter the desired potency of the vaccine formulations.
机译:在连续体外传代过程中,研究了口蹄疫病毒A型疫苗株衣壳编码区内的序列变异性。具体而言,使用了两种病毒传播方法,即BHK-21细胞的单层和悬浮培养。在三个位置(在单层和悬浮通道中均使用VP2131 EK,在单层晚期通道中使用VP385 HR,仅在悬浮通道中使用VP3139 KE),所有位置都映射到表面暴露的环上,氨基酸取代显然固定,直到恢复通过为止。有趣的是,形成硫酸乙酰肝素结合袋的一部分的VP2131、121和VP385显示出在单层或悬浮环境中获得带正电荷的氨基酸的趋势,可能更好地与带负电荷的细胞表面糖胺聚糖相互作用。在三个确定的抗原关键位置(VP279,VP3139和VP1154),即使在没有免疫压力的情况下,也发现了氨基酸置换。因此,归因于拟议的细胞表面交替受体施加的强大选择性压力的随机漂移和适应性突变均可以在修饰细胞培养的FMDV疫苗病毒的衣壳序列中起作用,这反过来可能会改变所需的疫苗制剂效价。

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