Department of Genetics, University of North Carolina-Chapel Hill, Chapel Hill, North Carolina, USA.
Department of Genetics, University of North Carolina-Chapel Hill, Chapel Hill, North Carolina, USA; Lineberger Comprehensive Cancer Center, University of North Carolina-Chapel Hill, Chapel Hill, North Carolina, USA.
Adv Virus Res. 2014;88:193-225. doi: 10.1016/B978-0-12-800098-4.00004-0.
While the role of viral variants has long been known to play a key role in causing variation in disease severity, it is also clear that host genetic variation plays a critical role in determining virus-induced disease responses. However, a variety of factors, including confounding environmental variables, rare genetic variants requiring extremely large cohorts, the temporal dynamics of infections, and ethical limitation on human studies, have made the identification and dissection of variant host genes and pathways difficult within human populations. This difficulty has led to the development of a variety of experimental approaches used to identify host genetic contributions to disease responses. In this chapter, we describe the history of genetic associations within the human population, the development of experimentally tractable systems, and the insights these specific approaches provide. We conclude with a discussion of recent advances that allow for the investigation of the role of complex genetic networks that underlie host responses to infection, with the goal of drawing connections to human infections. In particular, we highlight the need for robust animal models with which to directly control and assess the role of host genetics on viral infection outcomes.
虽然病毒变异体的作用早已被认为在导致疾病严重程度的变化方面起着关键作用,但宿主遗传变异在决定病毒诱导的疾病反应方面也起着至关重要的作用。然而,包括混杂的环境变量、需要极其庞大队列的罕见遗传变异、感染的时间动态以及对人体研究的伦理限制在内的各种因素,使得在人类群体中鉴定和剖析变异宿主基因和途径变得困难。这种困难导致了各种实验方法的发展,用于识别宿主遗传对疾病反应的贡献。在本章中,我们描述了人类群体中遗传关联的历史、可实验处理系统的发展以及这些特定方法提供的见解。最后,我们讨论了最近的进展,这些进展允许研究复杂的遗传网络在宿主对感染反应中的作用,目的是将其与人类感染联系起来。特别是,我们强调需要具有稳健的动物模型,以便直接控制和评估宿主遗传对病毒感染结果的作用。