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2015-2019 年美国山区西部、欧洲和北半球流感 A pH1N1 病毒血凝素抗原位点的突变。

Mutation in Hemagglutinin Antigenic Sites in Influenza A pH1N1 Viruses from 2015-2019 in the United States Mountain West, Europe, and the Northern Hemisphere.

机构信息

Department of Microbiology and Molecular Biology, Brigham Young University, Provo, UT 84602, USA.

出版信息

Genes (Basel). 2022 May 19;13(5):909. doi: 10.3390/genes13050909.

Abstract

H1N1 influenza A virus is a respiratory pathogen that undergoes antigenic shift and antigenic drift to improve viral fitness. Tracking the evolutionary trends of H1N1 aids with the current detection and the future response to new viral strains as they emerge. Here, we characterize antigenic drift events observed in the hemagglutinin (HA) sequence of the pandemic H1N1 lineage from 2015-2019. We observed the substitutions S200P, K147N, and P154S, together with other mutations in structural, functional, and/or epitope regions in 2015-2019 HA protein sequences from the Mountain West region of the United States, the larger United States, Europe, and other Northern Hemisphere countries. We reconstructed multiple phylogenetic trees to track the relationships and spread of these mutations and tested for evidence of selection pressure on HA. We found that the prevalence of amino acid substitutions at positions 147, 154, 159, 200, and 233 significantly changed throughout the studied geographical regions between 2015 and 2019. We also found evidence of coevolution among a subset of these amino acid substitutions. The results from this study could be relevant for future epidemiological tracking and vaccine prediction efforts. Similar analyses in the future could identify additional sequence changes that could affect the pathogenicity and/or infectivity of this virus in its human host.

摘要

甲型 H1N1 流感病毒是一种呼吸道病原体,通过抗原转变和抗原漂移来提高病毒适应性。跟踪 H1N1 的进化趋势有助于当前检测和未来应对新出现的病毒株。在这里,我们描述了 2015 年至 2019 年间大流行 H1N1 谱系血凝素(HA)序列中观察到的抗原漂移事件。我们观察到 2015 年至 2019 年间,来自美国西部山区、美国大部分地区、欧洲和其他北半球国家的 HA 蛋白序列中出现了 S200P、K147N 和 P154S 等取代以及结构、功能和/或表位区域的其他突变。我们重建了多个系统发育树来追踪这些突变的关系和传播,并测试了 HA 上选择压力的证据。我们发现,在 2015 年至 2019 年期间,研究地理区域内这些位置的氨基酸取代的流行率发生了显著变化。我们还发现了这些氨基酸取代子集之间的共进化证据。这项研究的结果可能与未来的流行病学跟踪和疫苗预测工作有关。未来的类似分析可能会发现其他可能影响这种病毒在人类宿主中的致病性和/或感染力的序列变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebd1/9141826/7ebe50228fd3/genes-13-00909-g001.jpg

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