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中国 H7N9 流感病毒的分子进化、多样性和适应性。

Molecular Evolution, Diversity, and Adaptation of Influenza A(H7N9) Viruses in China.

出版信息

Emerg Infect Dis. 2018 Oct;24(10):1795-1805. doi: 10.3201/eid2410.171063.

Abstract

The substantial increase in prevalence and emergence of antigenically divergent or highly pathogenic influenza A(H7N9) viruses during 2016-17 raises concerns about the epizootic potential of these viruses. We investigated the evolution and adaptation of H7N9 viruses by analyzing available data and newly generated virus sequences isolated in Guangdong Province, China, during 2015-2017. Phylogenetic analyses showed that circulating H7N9 viruses belong to distinct lineages with differing spatial distributions. Hemagglutination inhibition assays performed on serum samples from patients infected with these viruses identified 3 antigenic clusters for 16 strains of different virus lineages. We used ancestral sequence reconstruction to identify parallel amino acid changes on multiple separate lineages. We inferred that mutations in hemagglutinin occur primarily at sites involved in receptor recognition or antigenicity. Our results indicate that highly pathogenic strains likely emerged from viruses circulating in eastern Guangdong Province during March 2016 and are associated with a high rate of adaptive molecular evolution.

摘要

在 2016-17 年期间,抗原差异或高致病性的甲型流感病毒(H7N9)的流行和出现显著增加,这引起了人们对这些病毒的流行潜力的关注。我们通过分析在中国广东省在 2015-2017 年期间分离的现有数据和新生成的病毒序列,研究了 H7N9 病毒的进化和适应性。系统发育分析表明,循环的 H7N9 病毒属于具有不同空间分布的不同谱系。对感染这些病毒的患者血清样本进行的血凝抑制试验确定了 16 株不同病毒谱系的 3 个抗原簇。我们使用祖先序列重建来识别多个独立谱系上的平行氨基酸变化。我们推断,血凝素中的突变主要发生在参与受体识别或抗原性的位点。我们的结果表明,高致病性株可能源自 2016 年 3 月在中国广东省东部流行的病毒,并且与高适应性分子进化率相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/373d/6154164/c83ceac2c2fa/17-1063-F1.jpg

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