Suppr超能文献

灵长类慢病毒受到干扰素诱导跨膜蛋白的差异性抑制。

Primate lentiviruses are differentially inhibited by interferon-induced transmembrane proteins.

作者信息

Qian Jin, Le Duff Yann, Wang Yimeng, Pan Qinghua, Ding Shilei, Zheng Yi-Min, Liu Shan-Lu, Liang Chen

机构信息

Lady Davis Institute, Jewish General Hospital, Montreal, Quebec, Canada H3T 1E2; Department of Medicine, McGill University, Montreal, Quebec, Canada H3A 2B4.

Lady Davis Institute, Jewish General Hospital, Montreal, Quebec, Canada H3T 1E2.

出版信息

Virology. 2015 Jan 1;474:10-8. doi: 10.1016/j.virol.2014.10.015. Epub 2014 Nov 7.

Abstract

Interferon-induced transmembrane (IFITM) proteins inhibit the entry of a large number of viruses. Not surprisingly, many viruses are refractory to this inhibition. In this study, we report that different strains of HIV and SIV are inhibited by human IFITM proteins to various degrees, with SIV of African green monkeys (SIV(AGM)) being mostly restricted by human IFITM2. Interestingly, SIV(AGM) is as much inhibited by human IFITM2 as by IFITM3 of its own host African green monkeys. Our data further demonstrate that the entry of SIV(AGM) is impaired by human IFITM2 and that this inhibition is overcome by the cholesterol-binding compound amphotericin B that also overcomes IFITM inhibition of influenza A viruses. These results suggest that IFITM proteins exploit similar mechanisms to inhibit the entry of both pH-independent primate lentiviruses and the pH-dependent influenza A viruses.

摘要

干扰素诱导跨膜(IFITM)蛋白可抑制多种病毒的进入。不出所料,许多病毒对这种抑制具有抗性。在本研究中,我们报告不同株的HIV和SIV受到人类IFITM蛋白的不同程度抑制,其中非洲绿猴的SIV(SIV(AGM))主要受人类IFITM2限制。有趣的是,SIV(AGM)受人类IFITM2的抑制程度与其自身宿主非洲绿猴的IFITM3相同。我们的数据进一步表明,人类IFITM2会损害SIV(AGM)的进入,而胆固醇结合化合物两性霉素B可克服这种抑制,该化合物也能克服IFITM对甲型流感病毒的抑制。这些结果表明,IFITM蛋白利用相似机制抑制非pH依赖性灵长类慢病毒和pH依赖性甲型流感病毒的进入。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a0a/7112013/07cfd11ad538/gr1_lrg.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验