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PB2-E627K 突变削弱了含有 2009 年 H1N1 流感大流行聚合酶的病毒。

The PB2-E627K mutation attenuates viruses containing the 2009 H1N1 influenza pandemic polymerase.

机构信息

Viral Pathogenesis and Evolution Section, Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda,Maryland, USA.

出版信息

mBio. 2010 May 18;1(1):e00067-10. doi: 10.1128/mBio.00067-10.

Abstract

The swine-origin H1N1 influenza A virus emerged in early 2009 and caused the first influenza pandemic in 41 years. The virus has spread efficiently to both the Northern and the Southern Hemispheres and has been associated with over 16,000 deaths. Given the virus's recent zoonotic origin, there is concern that the virus could acquire signature mutations associated with the enhanced pathogenicity of previous pandemic viruses or H5N1 viruses with pandemic potential. We tested the hypothesis that mutations in the polymerase PB2 gene at residues 627 and 701 would enhance virulence but found that influenza viruses containing these mutations in the context of the pandemic virus polymerase complex are attenuated in cell culture and mice.

摘要

猪源 H1N1 甲型流感病毒于 2009 年初出现,引发了 41 年来的首次流感大流行。该病毒已在北半球和南半球高效传播,并已导致超过 16000 人死亡。鉴于该病毒最近的动物源起源,人们担心该病毒可能会获得与先前大流行病毒或具有大流行潜力的 H5N1 病毒相关的增强致病性的特征性突变。我们检验了这样一种假设,即在聚合酶 PB2 基因的 627 和 701 位的突变会增强病毒的毒力,但发现在大流行病毒聚合酶复合物背景下含有这些突变的流感病毒在细胞培养和小鼠中被削弱。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/babf/2912665/174ec046c3a1/mbo9991010080001.jpg

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