Zika virus inhibits cell death by inhibiting the expression of NLRP3 and A20.

IF 3.8 2区 医学 Q2 VIROLOGY Journal of Virology Pub Date : 2025-03-18 Epub Date: 2025-02-20 DOI:10.1128/jvi.01980-24
Jian Li, Changyang Zhu, Yang Meng, Linliang Zhang, Cong Liu, Yali Qin, Mingzhou Chen
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Abstract

Zika virus (ZIKV) is associated with microcephaly in neonates and neurological disorders in adults. Chronic ZIKV infection has been identified in the testes, indicating that the virus can lead to prolonged illness, yet its pathogenesis remains poorly understood. Here, we found that ZIKV infection does not induce significant cell death in mouse macrophages despite the critical role that cell death plays in the antiviral immune response. Furthermore, we discovered that ZIKV infection impairs the activation of the NLPR3-dependent inflammasome and inhibits apoptosis. Consequently, we investigated the regulatory mechanism of the NLRP3 inflammasome and apoptosis in the context of ZIKV infection. Our results revealed significant reductions in the protein expression levels of NLRP3 and A20, attributable to post-transcriptional or translational effects during ZIKV infection. These findings suggest that ZIKV infection may disrupt cell death pathways, leading to its pathogenicity.IMPORTANCEZika virus (ZIKV), first isolated from a nonhuman primate in Africa in 1947, was relatively understudied until 2016. By then, ZIKV had already been reported in more than 20 countries and territories. The infection poses a significant risk, as it is associated with microcephaly in infants and neurological disorders in adults; however, the underlying mechanisms responsible for these severe outcomes remain unclear. In this study, we demonstrate that ZIKV infection significantly reduces the expression of NLRP3 and A20 proteins through post-transcriptional or translational processes, which leads to inhibited cell death. These findings are critical because cell death plays a vital role in the host's antiviral immune response. Our findings highlight how ZIKV infection compromises essential cell death pathways, raising serious concerns about its pathogenesis. A comprehensive understanding of this disruption is vital for developing targeted interventions to mitigate the virus' impact on public health.

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寨卡病毒通过抑制NLRP3和A20的表达来抑制细胞死亡。
寨卡病毒(ZIKV)与新生儿小头畸形和成人神经系统疾病有关。在睾丸中发现了慢性寨卡病毒感染,这表明该病毒可导致长期疾病,但其发病机制仍知之甚少。在这里,我们发现,尽管细胞死亡在抗病毒免疫应答中起着关键作用,但ZIKV感染不会诱导小鼠巨噬细胞显著死亡。此外,我们发现ZIKV感染损害nlpr3依赖性炎症小体的激活并抑制细胞凋亡。因此,我们研究了在寨卡病毒感染背景下NLRP3炎性体和细胞凋亡的调控机制。我们的研究结果显示NLRP3和A20蛋白表达水平显著降低,这可归因于寨卡病毒感染期间的转录后或翻译效应。这些发现表明,寨卡病毒感染可能破坏细胞死亡途径,从而导致其致病性。寨卡病毒(ZIKV)于1947年首次从非洲的一种非人灵长类动物中分离出来,直到2016年才得到相对较少的研究。到那时,已有20多个国家和地区报告了寨卡病毒。这种感染具有重大风险,因为它与婴儿小头畸形和成人神经系统疾病有关;然而,造成这些严重后果的潜在机制尚不清楚。在本研究中,我们证明了寨卡病毒感染通过转录后或翻译过程显著降低NLRP3和A20蛋白的表达,从而抑制细胞死亡。这些发现至关重要,因为细胞死亡在宿主的抗病毒免疫反应中起着至关重要的作用。我们的发现强调了寨卡病毒感染如何破坏基本的细胞死亡途径,引起了对其发病机制的严重关注。全面了解这种破坏对于制定有针对性的干预措施以减轻该病毒对公共卫生的影响至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Virology
Journal of Virology 医学-病毒学
CiteScore
10.10
自引率
7.40%
发文量
906
审稿时长
1 months
期刊介绍: Journal of Virology (JVI) explores the nature of the viruses of animals, archaea, bacteria, fungi, plants, and protozoa. We welcome papers on virion structure and assembly, viral genome replication and regulation of gene expression, genetic diversity and evolution, virus-cell interactions, cellular responses to infection, transformation and oncogenesis, gene delivery, viral pathogenesis and immunity, and vaccines and antiviral agents.
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