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甲型流感病毒核蛋白中保守氨基酸的突变分析

Mutational analysis of conserved amino acids in the influenza A virus nucleoprotein.

作者信息

Li Zejun, Watanabe Tokiko, Hatta Masato, Watanabe Shinji, Nanbo Asuka, Ozawa Makoto, Kakugawa Satoshi, Shimojima Masayuki, Yamada Shinya, Neumann Gabriele, Kawaoka Yoshihiro

机构信息

Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.

出版信息

J Virol. 2009 May;83(9):4153-62. doi: 10.1128/JVI.02642-08. Epub 2009 Feb 18.

Abstract

The nucleoprotein (NP), which has multiple functions during the virus life cycle, possesses regions that are highly conserved among influenza A, B, and C viruses. To better understand the roles of highly conserved NP amino acids in viral replication, we conducted a comprehensive mutational analysis. Using reverse genetics, we attempted to generate 74 viruses possessing mutations at conserved amino acids of NP. Of these, 48 mutant viruses were successfully rescued; 26 mutants were not viable, suggesting a critical role of the respective NP amino acids in viral replication. To identify the step(s) in the viral life cycle that is impaired by these NP mutations, we examined viral-genome replication/transcription, NP localization, and incorporation of viral-RNA segments into progeny virions. We identified 15 amino acid substitutions in NP that inhibited viral-genome replication and/or transcription, resulting in significant growth defects of viruses possessing these substitutions. We also found several NP mutations that affected the efficient incorporation of multiple viral-RNA (vRNA) segments into progeny virions even though a single vRNA segment was incorporated efficiently. The respective conserved amino acids in NP may thus be critical for the assembly and/or incorporation of sets of eight vRNA segments.

摘要

核蛋白(NP)在病毒生命周期中具有多种功能,其某些区域在甲型、乙型和丙型流感病毒中高度保守。为了更好地理解NP中高度保守氨基酸在病毒复制中的作用,我们进行了全面的突变分析。利用反向遗传学,我们试图产生74种在NP保守氨基酸处具有突变的病毒。其中,成功拯救了48种突变病毒;26种突变体无法存活,这表明相应的NP氨基酸在病毒复制中起关键作用。为了确定病毒生命周期中受这些NP突变影响的步骤,我们检查了病毒基因组复制/转录、NP定位以及病毒RNA片段掺入子代病毒粒子的情况。我们在NP中鉴定出15个氨基酸替换,这些替换抑制了病毒基因组复制和/或转录,导致具有这些替换的病毒出现显著的生长缺陷。我们还发现了几个NP突变,即使单个病毒RNA(vRNA)片段能有效掺入,但这些突变影响了多个vRNA片段有效掺入子代病毒粒子。因此,NP中各自保守的氨基酸对于八个vRNA片段的组装和/或掺入可能至关重要。

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