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干扰素诱导跨膜蛋白3抑制汉坦病毒感染,其单核苷酸多态性rs12252影响肾综合征出血热的严重程度。

Interferon-Induced Transmembrane Protein 3 Inhibits Hantaan Virus Infection, and Its Single Nucleotide Polymorphism rs12252 Influences the Severity of Hemorrhagic Fever with Renal Syndrome.

作者信息

Xu-Yang Zheng, Pei-Yu Bian, Chuan-Tao Ye, Wei Ye, Hong-Wei Ma, Kang Tang, Chun-Mei Zhang, Ying-Feng Lei, Xin Wei, Ping-Zhong Wang, Chang-Xing Huang, Xue-Fan Bai, Ying Zhang, Zhan-Sheng Jia

机构信息

Department of Infectious Diseases, Tangdu Hospital, Fourth Military Medical University , Xi'an , China.

Department of Microbiology, Fourth Military Medical University , Xi'an , China.

出版信息

Front Immunol. 2017 Jan 3;7:535. doi: 10.3389/fimmu.2016.00535. eCollection 2016.

DOI:10.3389/fimmu.2016.00535
PMID:28096800
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5206578/
Abstract

Hantaan virus (HTNV) causes hemorrhagic fever with renal syndrome (HFRS). Previous studies have identified interferon-induced transmembrane proteins (IFITMs) as an interferon-stimulated gene family. However, the role of IFITMs in HTNV infection is unclear. In this study, we observed that IFITM3 single nucleotide polymorphisms (SNP) rs12252 C allele and CC genotype associated with the disease severity and HTNV load in the plasma of HFRS patients. experiments showed that the truncated protein produced by the rs12252 C allele exhibited an impaired anti-HTNV activity. We also proved that IFITM3 was able to inhibit HTNV infection in both HUVEC and A549 cells by overexpression and RNAi assays, likely a mechanism of inhibiting virus entry demonstrated by binding and entry assay. Localization of IFITM3 in late endosomes was also observed. In addition, we demonstrated that the transcription of IFITM3 is negatively regulated by an lncRNA negative regulator of interferon response (NRIR). Taken together, we conclude that IFITM3, negatively regulated by NRIR, inhibits HTNV infection, and its SNP rs12252 correlates with the plasma HTNV load and the disease severity of patients with HFRS.

摘要

汉坦病毒(HTNV)可引起肾综合征出血热(HFRS)。先前的研究已将干扰素诱导跨膜蛋白(IFITMs)鉴定为一个干扰素刺激基因家族。然而,IFITMs在HTNV感染中的作用尚不清楚。在本研究中,我们观察到IFITM3单核苷酸多态性(SNP)rs12252的C等位基因和CC基因型与HFRS患者血浆中的疾病严重程度及HTNV载量相关。实验表明,rs12252 C等位基因产生的截短蛋白表现出受损的抗HTNV活性。我们还通过过表达和RNA干扰试验证明,IFITM3能够在人脐静脉内皮细胞(HUVEC)和A549细胞中抑制HTNV感染,结合和进入试验可能证明了一种抑制病毒进入的机制。还观察到IFITM3定位于晚期内体。此外,我们证明IFITM3的转录受到干扰素反应负调控长链非编码RNA(lncRNA负调控因子,NRIR)的负调控。综上所述,我们得出结论,受NRIR负调控的IFITM3可抑制HTNV感染,其SNP rs12252与HFRS患者的血浆HTNV载量及疾病严重程度相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eea8/5206578/c7e1438a422a/fimmu-07-00535-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eea8/5206578/60b403662e72/fimmu-07-00535-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eea8/5206578/d121da22c71a/fimmu-07-00535-g003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eea8/5206578/c7e1438a422a/fimmu-07-00535-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eea8/5206578/60b403662e72/fimmu-07-00535-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eea8/5206578/d121da22c71a/fimmu-07-00535-g003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eea8/5206578/c7e1438a422a/fimmu-07-00535-g007.jpg

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