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大流行(H1N1)2009 流感 A 病毒的基因组特征和突变趋势分析。

Genomic signature and mutation trend analysis of pandemic (H1N1) 2009 influenza A virus.

机构信息

Lindsley F Kimball Research Institute, New York Blood Center, New York, New York, United States of America.

出版信息

PLoS One. 2010 Mar 8;5(3):e9549. doi: 10.1371/journal.pone.0009549.

Abstract

A novel swine-origin pandemic influenza A(H1N1) virus (H1N1pdm, also referred to as S-OIV) was identified as the causative agent of the 21(st) century's first influenza pandemic, but molecular features conferring its ability of human-to-human transmission has not been identified. Here we compared the protein sequences of 2009 H1N1pdm strains with those causing other pandemics and the viruses isolated from humans, swines and avians, and then analyzed the mutation trend of the residues at the signature and non-signature positions, which are species- and non-species-associated, respectively, in the proteins of H1N1pdm during the pandemic of 2009. We confirmed that the host-specific genomic signatures of 2009 H1N1pdm, which are mainly swine-like, were highly identical to those of the 1918 H1N1pdm. During the short period of time when the pandemic alert level was raised from phase 4 to phase 6, one signature residue at the position of NP-100 mutated from valine to isoleucine. Four non-signature residues, at positions NA-91, NA-233, HA-206, and NS1-123, also changed during the epidemic in 2009. All these mutant residues, except that at NA-91, are located in the viral functional domains, suggesting that they may play roles in the human adaption and virulence of 2009 H1N1pdm.

摘要

一种新型猪源季节性流感 A(H1N1)病毒(H1N1pdm,也称为 S-OIV)被确定为 21 世纪首次流感大流行的病原体,但尚未确定其具有人际传播能力的分子特征。在这里,我们比较了 2009 年 H1N1pdm 株与引起其他大流行的病毒以及从人类、猪和禽类中分离出的病毒的蛋白质序列,并分析了大流行期间 2009 年 H1N1pdm 蛋白中特征和非特征位置残基的突变趋势,分别与物种和非物种相关。我们证实,2009 年 H1N1pdm 的宿主特异性基因组特征主要类似于 1918 年 H1N1pdm,高度相似。在大流行警戒级别从 4 级提高到 6 级的短时间内,NP-100 位置的一个特征性残基从缬氨酸突变为异亮氨酸。在 2009 年的疫情中,还有四个非特征性残基,即 NA-91、NA-233、HA-206 和 NS1-123,也发生了变化。除了 NA-91 之外,所有这些突变残基都位于病毒功能域中,表明它们可能在 2009 年 H1N1pdm 的人类适应和毒力中发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b17d/2833199/e9dfbee79050/pone.0009549.g001.jpg

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