Intracellular iron positively modulates the replicative cycle of mimiviruses, increasing virus production.

IF 3.8 2区 医学 Q2 VIROLOGY
Juliana Dos Santos Oliveira, Claudia F Dick, Gabriel Henrique Pereira Nunes, Victor Alejandro Essus, Jason Schrad, Sundharraman Subramanian, Jônatas Abrahão, José Roberto Meyer-Fernandes, Kristin Parent, Juliana Reis Cortines
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Abstract

Mimiviruses, members of the Nucleocytoviricota phylum, produce large, pseudo-icosahedral virions densely coated with fibrils, except at a specialized fivefold vertex known as the stargate. Stargate opening is essential for delivering the viral core into the cytoplasm of phagocytic amoebae. These professional phagocytes deploy antimicrobial mechanisms such as the modulation of transition metal concentrations within phagolysosomes to eliminate internalized pathogens. Yet, mimiviruses have evolved striking adaptations to resist such hostile environments and initiate replication within these compartments. Here, we investigated the role of metal ions-particularly iron-in the replication of three giant viruses: Acanthamoeba polyphaga mimivirus (APMV), Antarctica virus, and Tupanvirus (TPV). We show that infection by these viruses increases cellular iron uptake and that elevated intracellular iron enhances viral replication. These findings reveal a previously underappreciated facet of the mimivirus-host interaction, in which iron availability acts as a positive modulator of the viral replicative cycle.IMPORTANCEGiant viruses like Mimivirus infect amoebae, which normally destroy microbes using toxic conditions inside cellular compartments. This study shows that, instead of being harmed, these viruses benefit from one of those supposedly hostile factors: iron. Through this work, we discovered that infection by Mimivirus and related viruses increases the host cell's iron uptake-and that more iron boosts virus production by the host cell. This reveals a surprising twist in the virus-host relationship: what should be a defense mechanism is turned into an advantage by the virus. By highlighting iron as a key factor in viral success, this work opens new perspectives on how giant viruses adapt to-and even exploit-the internal environment of their hosts. It also adds an important piece to our understanding of the complex strategies viruses use to survive and thrive inside cells.

细胞内铁正向调节mimi病毒的复制周期,增加病毒产量。
mimi病毒是核细胞病毒门的成员,产生巨大的假二十面体病毒粒子,被原纤维密集地包裹着,除了一个特殊的五倍顶点,称为星门。星际之门的打开对于将病毒核心运送到吞噬性变形虫的细胞质中至关重要。这些专业的吞噬细胞部署抗菌机制,如吞噬溶酶体内过渡金属浓度的调节,以消除内化病原体。然而,mimi病毒已经进化出惊人的适应性来抵抗这种恶劣的环境,并在这些隔室中开始复制。在这里,我们研究了金属离子,特别是铁在三种巨型病毒的复制中的作用:棘阿米巴多食性mimivirus (APMV),南极洲病毒和Tupanvirus (TPV)。我们发现这些病毒的感染增加了细胞铁的摄取,细胞内铁的升高增强了病毒的复制。这些发现揭示了以前被低估的迷你病毒-宿主相互作用的一个方面,其中铁的可用性作为病毒复制周期的积极调节剂。重要意义像Mimivirus这样的巨型病毒会感染变形虫,变形虫通常会利用细胞内的有毒环境来破坏微生物。这项研究表明,这些病毒非但没有受到伤害,反而受益于其中一种被认为有害的因素:铁。通过这项工作,我们发现Mimivirus和相关病毒的感染增加了宿主细胞对铁的摄取,而更多的铁会促进宿主细胞产生病毒。这揭示了病毒-宿主关系中一个令人惊讶的转折:本应是防御机制的东西被病毒变成了优势。通过强调铁是病毒成功的关键因素,这项工作为巨型病毒如何适应甚至利用宿主的内部环境开辟了新的视角。它也为我们理解病毒在细胞内生存和繁衍的复杂策略增加了重要的一部分。
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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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