宿主-病毒军备竞赛的进化景观。

IF 26.9 1区 医学 Q1 IMMUNOLOGY Annual review of immunology Pub Date : 2022-04-26 DOI:10.1146/annurev-immunol-072621-084422
Jeannette L Tenthorey, Michael Emerman, Harmit S Malik
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引用次数: 17

摘要

脊椎动物的免疫系统通过先天限制因子和适应性免疫抑制病毒感染。病毒变异以逃避这些防御,驱使宿主反进化以恢复适应性。这种循环反复出现,导致了一场进化军备竞赛,其结果取决于宿主和病毒基因适应的速度和可能性。尽管病毒的进化速度比它们的脊椎动物宿主快,但它们的蛋白质受到许多影响适应可能性的功能限制。这些约束是由进化景观全局定义的,它描述了所有可能突变的适应性和适应潜力。我们回顾了深入的突变扫描实验,绘制了参与军备竞赛的宿主和病毒蛋白质的进化景观。对于限制因子和一些广泛中和的抗体,环境有利于宿主,这可能有助于平衡进化的竞争环境,以对抗快速进化的病毒。我们将讨论这些景观的生物物理基础及其治疗意义。
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Evolutionary Landscapes of Host-Virus Arms Races.

Vertebrate immune systems suppress viral infection using both innate restriction factors and adaptive immunity. Viruses mutate to escape these defenses, driving hosts to counterevolve to regain fitness. This cycle recurs repeatedly, resulting in an evolutionary arms race whose outcome depends on the pace and likelihood of adaptation by host and viral genes. Although viruses evolve faster than their vertebrate hosts, their proteins are subject to numerous functional constraints that impact the probability of adaptation. These constraints are globally defined by evolutionary landscapes, which describe the fitness and adaptive potential of all possible mutations. We review deep mutational scanning experiments mapping the evolutionary landscapes of both host and viral proteins engaged in arms races. For restriction factors and some broadly neutralizing antibodies, landscapes favor the host, which may help to level the evolutionary playing field against rapidly evolving viruses. We discuss the biophysical underpinnings of these landscapes and their therapeutic implications.

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来源期刊
Annual review of immunology
Annual review of immunology 医学-免疫学
CiteScore
57.20
自引率
0.70%
发文量
29
期刊介绍: The Annual Review of Immunology, in publication since 1983, focuses on basic immune mechanisms and molecular basis of immune diseases in humans. Topics include innate and adaptive immunity; immune cell development and differentiation; immune control of pathogens (viruses, bacteria, parasites) and cancer; and human immunodeficiency and autoimmune diseases. The current volume of this journal has been converted from gated to open access through Annual Reviews' Subscribe to Open program, with all articles published under a CC BY license.
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