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黑绢毛猴基因组序列为研究自然 SIV 宿主中的艾滋病抗性提供了线索。

Sooty mangabey genome sequence provides insight into AIDS resistance in a natural SIV host.

机构信息

Emory Vaccine Center and Yerkes National Primate Research Center, Emory University, Atlanta, Georgia 30329, USA.

Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia 30329, USA.

出版信息

Nature. 2018 Jan 3;553(7686):77-81. doi: 10.1038/nature25140.

DOI:10.1038/nature25140
PMID:29300007
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5843367/
Abstract

In contrast to infections with human immunodeficiency virus (HIV) in humans and simian immunodeficiency virus (SIV) in macaques, SIV infection of a natural host, sooty mangabeys (Cercocebus atys), is non-pathogenic despite high viraemia. Here we sequenced and assembled the genome of a captive sooty mangabey. We conducted genome-wide comparative analyses of transcript assemblies from C. atys and AIDS-susceptible species, such as humans and macaques, to identify candidates for host genetic factors that influence susceptibility. We identified several immune-related genes in the genome of C. atys that show substantial sequence divergence from macaques or humans. One of these sequence divergences, a C-terminal frameshift in the toll-like receptor-4 (TLR4) gene of C. atys, is associated with a blunted in vitro response to TLR-4 ligands. In addition, we found a major structural change in exons 3-4 of the immune-regulatory protein intercellular adhesion molecule 2 (ICAM-2); expression of this variant leads to reduced cell surface expression of ICAM-2. These data provide a resource for comparative genomic studies of HIV and/or SIV pathogenesis and may help to elucidate the mechanisms by which SIV-infected sooty mangabeys avoid AIDS.

摘要

与人类感染人类免疫缺陷病毒 (HIV) 和猕猴感染猴免疫缺陷病毒 (SIV) 相反,尽管 SIV 在自然宿主——黑长尾猴 (Cercocebus atys) 中引起高病毒血症,但 SIV 感染是非致病性的。在这里,我们对一只圈养黑长尾猴的基因组进行了测序和组装。我们对黑长尾猴和易感物种(如人类和猕猴)的转录组进行了全基因组比较分析,以鉴定影响易感性的宿主遗传因素候选基因。我们在黑长尾猴基因组中鉴定了几个与免疫相关的基因,这些基因与猕猴或人类的基因有很大的序列差异。其中一个序列差异是黑长尾猴 toll 样受体 4 (TLR4) 基因的 C 端移码,这与体外对 TLR-4 配体的反应迟钝有关。此外,我们还发现免疫调节蛋白细胞间黏附分子 2 (ICAM-2) 的外显子 3-4 中存在一个主要的结构变化;这种变体的表达导致 ICAM-2 的细胞表面表达减少。这些数据为 HIV 和/或 SIV 发病机制的比较基因组研究提供了资源,并可能有助于阐明 SIV 感染黑长尾猴如何避免艾滋病的机制。

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