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干扰素诱导跨膜蛋白(IFITM)被整合到HIV-1病毒粒子上,并对其感染性产生负面影响。

IFITM proteins are incorporated onto HIV-1 virion particles and negatively imprint their infectivity.

作者信息

Tartour Kevin, Appourchaux Romain, Gaillard Julien, Nguyen Xuan-Nhi, Durand Stéphanie, Turpin Jocelyn, Beaumont Elodie, Roch Emmanuelle, Berger Gregory, Mahieux Renaud, Brand Denys, Roingeard Philippe, Cimarelli Andrea

机构信息

CIRI, Centre International de Recherche en Infectiologie, Lyon, F69364, France.

INSERM, U1111, 46 Allée d'Italie, Lyon, F69364, France.

出版信息

Retrovirology. 2014 Nov 25;11:103. doi: 10.1186/s12977-014-0103-y.

Abstract

BACKGROUND

Interferon induced transmembrane proteins 1, 2 and 3 (IFITMs) belong to a family of highly related antiviral factors that have been shown to interfere with a large spectrum of viruses including Filoviruses, Coronaviruses, Influenza virus, Dengue virus and HIV-1. In all these cases, the reported mechanism of antiviral inhibition indicates that the pool of IFITM proteins present in target cells blocks incoming viral particles in endosomal vesicles where they are subsequently degraded.

RESULTS

In this study, we describe an additional mechanism through which IFITMs block HIV-1. In virus-producing cells, IFITMs coalesce with forming virions and are incorporated into viral particles. Expression of IFITMs during virion assembly leads to the production of virion particles of decreased infectivity that are mostly affected during entry in target cells. This mechanism of inhibition is exerted against different retroviruses and does not seem to be dependent on the type of Envelope present on retroviral particles.

CONCLUSIONS

The results described here identify a novel mechanism through which IFITMs affect HIV-1 infectivity during the late phases of the viral life cycle. Put in the context of data obtained by other laboratories, these results indicate that IFITMs can target HIV at two distinct moments of its life cycle, in target cells as well as in virus-producing cells. These results raise the possibility that IFITMs could similarly affect distinct steps of the life cycle of a number of other viruses.

摘要

背景

干扰素诱导跨膜蛋白1、2和3(IFITMs)属于一类高度相关的抗病毒因子家族,已被证明可干扰包括丝状病毒、冠状病毒、流感病毒、登革热病毒和HIV-1在内的多种病毒。在所有这些情况下,报道的抗病毒抑制机制表明,靶细胞中存在的IFITM蛋白池在内体小泡中阻断进入的病毒颗粒,随后这些病毒颗粒在其中被降解。

结果

在本研究中,我们描述了IFITMs阻断HIV-1的另一种机制。在病毒产生细胞中,IFITMs与正在形成的病毒粒子聚集在一起,并被整合到病毒颗粒中。在病毒粒子组装过程中IFITMs的表达导致产生感染性降低的病毒粒子,这些病毒粒子在进入靶细胞过程中受到的影响最大。这种抑制机制针对不同的逆转录病毒起作用,似乎不依赖于逆转录病毒颗粒上存在的包膜类型。

结论

此处描述的结果确定了一种新机制,通过该机制IFITMs在病毒生命周期的后期影响HIV-1的感染性。结合其他实验室获得的数据来看,这些结果表明IFITMs可在HIV生命周期的两个不同时刻靶向HIV,即在靶细胞以及病毒产生细胞中。这些结果增加了IFITMs可能同样影响许多其他病毒生命周期不同步骤的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bd3/4251951/6315baf32293/12977_2014_103_Fig1_HTML.jpg

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