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鼠γ逆转录病毒与三个限制宿主因子的跨时间和空间的共进化适应模式。

Patterns of Coevolutionary Adaptations across Time and Space in Mouse Gammaretroviruses and Three Restrictive Host Factors.

机构信息

Laboratory of Molecular Microbiology, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892, USA.

Bioinformatics and Computational Biosciences Branch, Office of Cyber Infrastructure and Computational Biology, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892, USA.

出版信息

Viruses. 2021 Sep 18;13(9):1864. doi: 10.3390/v13091864.

Abstract

The classical laboratory mouse strains are genetic mosaics of three subspecies that occupy distinct regions of Eurasia. These strains and subspecies carry infectious and endogenous mouse leukemia viruses (MLVs) that can be pathogenic and mutagenic. MLVs evolved in concert with restrictive host factors with some under positive selection, including the XPR1 receptor for xenotropic/polytropic MLVs (X/P-MLVs) and the post-entry restriction factor . Since positive selection marks host-pathogen genetic conflicts, we examined MLVs for counter-adaptations at sites that interact with XPR1, , and the CAT1 receptor for ecotropic MLVs (E-MLVs). Results describe different co-adaptive evolutionary paths within the ranges occupied by these virus-infected subspecies. The interface of CAT1, and the otherwise variable E-MLV envelopes, is highly conserved; antiviral protection is afforded by the restriction factor. XPR1 and X/P-MLVs variants show coordinate geographic distributions, with receptor critical sites in envelope, under positive selection but with little variation in envelope and XPR1 in mice carrying P-ERVs. The major target in the viral capsid is under positive selection, and the distribution of alleles is subspecies-correlated. These data document adaptive, spatial and temporal, co-evolutionary trajectories at the critical interfaces of MLVs and the host factors that restrict their replication.

摘要

经典的实验小鼠品系是在欧亚大陆不同地区占据独特区域的三个亚种的遗传嵌合体。这些品系和亚种携带传染性和内源性小鼠白血病病毒(MLV),可能具有致病性和致突变性。MLV 与限制宿主因素协同进化,其中一些因素受到正选择的影响,包括对异源/多形性 MLV(X/P-MLV)具有亲嗜性的 XPR1 受体和进入后限制因子 。由于正选择标志着宿主-病原体遗传冲突,我们在与 XPR1、 和对嗜性 MLV(E-MLV)具有亲嗜性的 CAT1 受体相互作用的位点上检查了 MLV 的反向适应。结果描述了这些受病毒感染的亚种所占据的范围内不同的共同适应进化途径。CAT1 的界面和其他可变的 E-MLV 包膜高度保守;抗病毒保护由 限制因子提供。XPR1 和 X/P-MLV 变体显示出协调的地理分布,包膜中的受体关键位点受到正选择的影响,但携带 P-ERV 的小鼠中包膜和 XPR1 的变异很小。病毒衣壳中的主要 靶标受到正选择的影响, 等位基因的分布与亚种相关。这些数据记录了 MLV 和限制其复制的宿主因子的关键界面的适应性、时空协同进化轨迹。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27f5/8472935/2ef87edbce6c/viruses-13-01864-g001.jpg

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