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用于表征人类流感病毒抗原和基因进化的软件。

Software for Characterizing the Antigenic and Genetic Evolution of Human Influenza Viruses.

作者信息

Reimering Susanne, McHardy Alice C

机构信息

Department for Computational Biology of Infection Research, Helmholtz Centre for Infection Research, Braunschweig, Germany.

German Centre for Infection Research (DZIF), Braunschweig, Germany.

出版信息

Methods Mol Biol. 2018;1836:551-565. doi: 10.1007/978-1-4939-8678-1_26.

Abstract

Influenza viruses are rapidly evolving pathogens causing annual epidemics and occasional pandemics. The accumulation of amino acid substitutions allows the virus to adapt to changing environments like novel host species or to escape the acquired immunity of the host population. Especially substitutions in the epitope regions of the surface protein HA lead to antigenic change, facilitating the evasion of the host's immune response by the virus and making frequent updates of the vaccine composition necessary. Through the global monitoring of circulating influenza viruses, large amounts of sequence data are generated. Computational biology offers a quick and easy way to analyze these to characterize the genetic and antigenic evolution of influenza viruses. Using sequence data together with antigenic information provided by hemagglutination inhibition (HI) assays and structural information, bioinformatics methods can elucidate evolutionary relationships between isolates, infer amino acid sites or regions of the protein under positive selection, and identify amino acid changes relevant for the antigenic evolution. We here describe a selection of programs used to generate hypotheses about functionally or antigenically important amino acid changes, protein regions, or individual sites that can subsequently be tested in wet-lab experiments or have value for predicting the future evolution of seasonal influenza A viruses.

摘要

流感病毒是快速进化的病原体,可引发年度流行和偶尔的大流行。氨基酸替换的积累使病毒能够适应不断变化的环境,如新型宿主物种,或逃避宿主群体获得的免疫力。特别是表面蛋白HA抗原表位区域的替换会导致抗原变化,促使病毒逃避宿主的免疫反应,并使得疫苗成分需要频繁更新。通过对全球流行的流感病毒进行监测,可生成大量序列数据。计算生物学提供了一种快速简便的方法来分析这些数据,以表征流感病毒的遗传和抗原进化。利用序列数据以及血凝抑制(HI)试验提供的抗原信息和结构信息,生物信息学方法可以阐明分离株之间的进化关系,推断正选择下蛋白质的氨基酸位点或区域,并识别与抗原进化相关的氨基酸变化。我们在此介绍一系列程序,这些程序用于生成关于功能或抗原重要氨基酸变化、蛋白质区域或单个位点的假设,随后可在湿实验室实验中进行测试,或对预测季节性甲型流感病毒的未来进化具有价值。

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