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Why do Individuals Differ in Viral Susceptibility? A Story Told by Model Organisms

机译:为什么个体的病毒易感性不同?典范生物的故事

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摘要

Viral susceptibility and disease progression is determined by host genetic variation that underlies individual differences. Genetic polymorphisms that affect the phenotype upon infection have been well-studied for only a few viruses, such as HIV-1 and Hepatitis C virus. However, even for well-studied viruses the genetic basis of individual susceptibility differences remains elusive. Investigating the effect of causal polymorphisms in humans is complicated, because genetic methods to detect rare or small-effect polymorphisms are limited and genetic manipulation is not possible in human populations. Model organisms have proven a powerful experimental platform to identify and characterize polymorphisms that underlie natural variations in viral susceptibility using quantitative genetic tools. We summarize and compare the genetic tools available in three main model organisms, Mus musculus, Drosophila melanogaster, and Caenorhabditis elegans, and illustrate how these tools can be applied to detect polymorphisms that determine the viral susceptibility. Finally, we analyse how candidate polymorphisms from model organisms can be used to shed light on the underlying mechanism of individual variation. Insights in causal polymorphisms and mechanisms underlying individual differences in viral susceptibility in model organisms likely provide a better understanding in humans.
机译:病毒易感性和疾病进展取决于个体差异的宿主遗传变异。仅对少数几种病毒(如HIV-1和丙型肝炎病毒)进行了充分研究,研究了感染后影响表型的遗传多态性。然而,即使对于经过充分研究的病毒,个体敏感性差异的遗传基础仍然难以捉摸。调查因果多态性对人类的影响是复杂的,因为检测稀有或小效应多态性的遗传方法是有限的,并且在人类人群中不可能进行基因操纵。模式生物已证明是使用定量遗传工具鉴定和表征病毒易感性自然变异基础的多态性的强大实验平台。我们总结并比较了三种主要模型生物(小家鼠,果蝇果蝇和秀丽隐杆线虫)中可用的遗传工具,并说明了如何将这些工具应用于确定病毒易感性的多态性。最后,我们分析了如何将模型生物的候选多态性用于阐明个体变异的潜在机制。对模型生物病毒易感性的个体差异所基于的因果多态性和机制的见解可能会为人类提供更好的理解。

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