TRIM14通过降解病毒NS1蛋白和激活I型干扰素信号传导抑制坦布苏病毒感染。

IF 5.5 1区 医学 Q1 MICROBIOLOGY
PLoS Pathogens Pub Date : 2025-05-28 eCollection Date: 2025-05-01 DOI:10.1371/journal.ppat.1013200
Peng Zhou, Qingxiang Zhang, Yueshan Yang, Dan Liu, Wanrong Wu, Anan Jongkaewwattana, Hui Jin, Hongbo Zhou, Rui Luo
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引用次数: 0

摘要

坦布苏病毒(TMUV)是一种新出现的禽类正黄病毒,由于在家养水禽中引起蛋降综合征和致命脑炎,造成严重的经济损失。为了对抗这种威胁,宿主免疫系统在控制和消除TMUV感染方面起着至关重要的作用。因此,了解这种免疫反应的机制对于制定对抗病毒的有效策略至关重要。在这项研究中,我们研究了鸭TRIM家族蛋白(duTRIM)对TMUV的抗病毒活性,特别关注了duTRIM14作为一个有效的宿主限制因子。我们发现过表达duTRIM14显著抑制TMUV复制,而其缺失导致病毒滴度升高。我们阐明了duTRIM14与TMUV NS1蛋白相互作用的新机制,促进其K27/ k29相关的多泛素化和随后的蛋白酶体降解。NS1上的Lys141残基对这一过程至关重要,它的去除显著增强了TMUV在体外和体内的复制。此外,我们发现duTRIM14与鸭子TBK1 (duTBK1)相互作用,促进其在Lys30和Lys401上的k63连接的多泛素化,这大大增加了TMUV感染期间IFN-β的产生。综上所述,这些结果提供了一种新的双作用抗病毒机制,其中duTRIM14通过同时促进NS1蛋白酶体降解和通过调节duTBK1活性增强宿主抗病毒反应来抑制TMUV复制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
TRIM14 restricts tembusu virus infection through degrading viral NS1 protein and activating type I interferon signaling.

Tembusu virus (TMUV), an emerging avian orthoflavivirus, causes severe economic losses due to egg-drop syndrome and fatal encephalitis in domestic waterfowl. To combat this threat, the host immune system plays a crucial role in controlling and eliminating TMUV infection. Understanding the mechanisms of this immune response is thus vital for developing effective strategies against the virus. In this study, we investigated the antiviral activities of duck TRIM family proteins (duTRIM) against TMUV, focusing particularly on duTRIM14 as a potent host restriction factor. We showed that overexpression of duTRIM14 significantly inhibits TMUV replication, while its deficiency leads to increased viral titers. We elucidate a novel mechanism by which duTRIM14 interacts with the TMUV NS1 protein, facilitating its K27/K29-linked polyubiquitination and subsequent proteasomal degradation. The Lys141 residue on NS1 was identified as critical for this process, with its removal significantly enhancing TMUV replication both in vitro and in vivo. Furthermore, we showed that duTRIM14 interacts with duck TBK1 (duTBK1), promoting its K63-linked polyubiquitination on Lys30 and Lys401, which substantially augments IFN-β production during TMUV infection. Taken together, these results provide a novel dual-action antiviral mechanism in which duTRIM14 suppresses TMUV replication by simultaneously promoting proteasomal degradation of NS1 and enhancing the host antiviral response by modulating duTBK1 activity.

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来源期刊
PLoS Pathogens
PLoS Pathogens MICROBIOLOGY-PARASITOLOGY
自引率
3.00%
发文量
598
期刊介绍: Bacteria, fungi, parasites, prions and viruses cause a plethora of diseases that have important medical, agricultural, and economic consequences. Moreover, the study of microbes continues to provide novel insights into such fundamental processes as the molecular basis of cellular and organismal function.
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