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调节人类甲型流感病毒疾病的宿主单核苷酸多态性

Host Single Nucleotide Polymorphisms Modulating Influenza A Virus Disease in Humans.

作者信息

Nogales Aitor, L DeDiego Marta

机构信息

Center for Animal Health Research, INIA-CISA, 28130 Madrid, Spain.

Department of Molecular and Cell Biology, Centro Nacional de Biotecnología (CNB-CSIC), Campus Universidad Autónoma de Madrid, 28049 Madrid, Spain.

出版信息

Pathogens. 2019 Sep 30;8(4):168. doi: 10.3390/pathogens8040168.

Abstract

A large number of human genes associated with viral infections contain single nucleotide polymorphisms (SNPs), which represent a genetic variation caused by the change of a single nucleotide in the DNA sequence. SNPs are located in coding or non-coding genomic regions and can affect gene expression or protein function by different mechanisms. Furthermore, they have been linked to multiple human diseases, highlighting their medical relevance. Therefore, the identification and analysis of this kind of polymorphisms in the human genome has gained high importance in the research community, and an increasing number of studies have been published during the last years. As a consequence of this exhaustive exploration, an association between the presence of some specific SNPs and the susceptibility or severity of many infectious diseases in some risk population groups has been found. In this review, we discuss the relevance of SNPs that are important to understand the pathology derived from influenza A virus (IAV) infections in humans and the susceptibility of some individuals to suffer more severe symptoms. We also discuss the importance of SNPs for IAV vaccine effectiveness.

摘要

大量与病毒感染相关的人类基因包含单核苷酸多态性(SNP),单核苷酸多态性是指由DNA序列中单个核苷酸变化引起的遗传变异。SNP位于编码或非编码基因组区域,可通过不同机制影响基因表达或蛋白质功能。此外,它们与多种人类疾病有关,凸显了其医学相关性。因此,在人类基因组中识别和分析这类多态性在研究领域变得极为重要,并且在过去几年中发表的相关研究越来越多。经过这种详尽的探索,已发现某些特定SNP的存在与一些风险人群中许多传染病的易感性或严重程度之间存在关联。在本综述中,我们讨论了SNP对于理解人类甲型流感病毒(IAV)感染所致病理以及某些个体出现更严重症状的易感性的相关性。我们还讨论了SNP对IAV疫苗有效性的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/136a/6963926/389addc6035a/pathogens-08-00168-g001.jpg

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