首页> 美国卫生研究院文献>Virology Journal >Simultaneous alteration of residues 279 and 284 of the VP2 major capsid protein of a very virulent Infectious Bursal Disease Virus (vvIBDV) strain did not lead to attenuation in chickens
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Simultaneous alteration of residues 279 and 284 of the VP2 major capsid protein of a very virulent Infectious Bursal Disease Virus (vvIBDV) strain did not lead to attenuation in chickens

机译:同时改变非常有毒的传染性法氏囊病病毒(vvIBDV)株VP2主要衣壳蛋白的279和284残基不会导致鸡的减毒

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摘要

BackgroundCell culture adaptation of very virulent infectious bursal disease virus (vvIBDV) was shown to be mainly associated with the VP2 capsid protein residues 253, 279, and 284. The single mutation A284T proved critical for cell culture tropism, but did not confer efficient virus replication, which at least required one additional mutation, Q253H or D279N. While the double mutation Q253H/A284T was unambiguously shown to confer both efficient replication in cell culture and attenuation in chickens, conflicting results have been reported regarding the replication efficiency of vvIBDV mutants bearing the D279N/A284T double mutation, and no data are hitherto available on their virulence in chickens.
机译:背景显示极强的传染性法氏囊病病毒(vvIBDV)的细胞培养适应性主要与VP2衣壳蛋白残基253、279和284相关。单突变A284T被证明对细胞培养的嗜性至关重要,但并未赋予病毒有效复制能力,至少需要一个额外的突变Q253H或D279N。虽然明确显示了双突变Q253H / A284T可以在细胞培养中有效复制并在鸡中减毒,但已报道了带有D279N / A284T双重突变的vvIBDV突变体复制效率的矛盾结果,迄今为止尚无可用数据。它们在鸡中的毒性。

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