Sputnik virophage disrupts the transcriptional regulation of its host giant virus.

IF 3.8 2区 医学 Q2 VIROLOGY Journal of Virology Pub Date : 2025-04-15 Epub Date: 2025-03-12 DOI:10.1128/jvi.00192-25
Jingjie Chen, Hiroyuki Ogata, Hiroyuki Hikida
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Abstract

Sputnik virophages are small double-stranded DNA (dsDNA) viruses that replicate only inside host amoebae infected with giant dsDNA viruses, mimiviruses. Sputnik infection affects mimivirus replication, but their molecular interaction remains poorly understood. Here, we performed a time-course transcriptome analysis of Acanthamoeba castellanii cells infected with Acanthamoeba polyphaga mimivirus (APMV; hereafter referred to as Sputnik- cells) and those infected with both APMV and Sputnik 3 virophage (Sputnik+ cells). The gene expression patterns of the amoeba were similar between these two conditions, whereas the expression of APMV genes was drastically affected by Sputnik, depending on the timing of their expression. Early-expressed APMV genes showed similar expression patterns in both conditions at the early stage of infection. However, at later stages, their expression levels remained higher in Sputnik+ cells than in Sputnik- cells, suggesting a prolongation of early gene expression by Sputnik. Late-expressed APMV genes showed lower expression at earlier stages in Sputnik+ cells, but their expression levels reached or exceeded those in Sputnik- cells at later stages, indicating a delay in gene expression. Overall, our results demonstrated that Sputnik infection drastically alters the transcriptome of APMV rather than amoeba, likely by disturbing the transition from early to late stages of APMV infection.IMPORTANCEVirophages are small double-stranded DNA (dsDNA) viruses parasitizing other dsDNA viruses, such as giant viruses. Virophages inhibit the replication of giant viruses, and some protists use virophages as a defense system against giant viruses. However, molecular interactions among host cellular organisms, giant viruses, and virophages are largely unknown. Here, we performed a time-course transcriptome analysis of Acanthamoeba castellanii cells infected with Acanthamoeba polyphaga mimivirus (APMV) and those infected with both APMV and Sputnik 3 virophage. We demonstrated that the virophage has little effect on the amoeba transcriptome and primarily hijacks the transcriptional machinery of the giant virus. Furthermore, virophage infection alters giant virus gene expression, depending on their expression timing. The expression of early genes was prolonged, while that of late genes was delayed, suggesting that virophage infection disrupts the transition from the early to late stages of giant virus infection. This study provides molecular insights into the interactions within this unique tripartite system.

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Sputnik病毒噬菌体破坏了宿主巨型病毒的转录调节。
Sputnik病毒噬菌体是一种小的双链DNA (dsDNA)病毒,只能在感染了巨型dsDNA病毒(mimivirus)的宿主变形虫体内复制。Sputnik感染影响mimi病毒的复制,但它们的分子相互作用仍然知之甚少。在这里,我们对感染棘阿米巴多食性mimivirus (APMV)的棘阿米巴细胞进行了时间过程转录组分析;以下简称Sputnik-细胞)和同时感染APMV和Sputnik 3噬菌体的细胞(Sputnik+细胞)。在这两种条件下,变形虫的基因表达模式相似,而APMV基因的表达则受到Sputnik的严重影响,这取决于它们表达的时间。早期表达的APMV基因在感染早期两种情况下表现出相似的表达模式。然而,在后期,它们在Sputnik+细胞中的表达水平仍然高于Sputnik-细胞,这表明Sputnik延长了早期基因的表达。晚期表达的APMV基因在Sputnik+细胞早期表达水平较低,但在Sputnik-细胞后期表达水平达到或超过Sputnik-细胞,表明基因表达延迟。总的来说,我们的研究结果表明,Sputnik感染极大地改变了APMV的转录组,而不是变形虫,可能是通过干扰APMV感染从早期到晚期的转变。噬菌体是寄生于其他双链DNA病毒(如巨型病毒)的小双链DNA病毒。病毒噬菌体抑制巨型病毒的复制,一些原生生物利用病毒噬菌体作为防御巨型病毒的防御系统。然而,宿主细胞生物、巨型病毒和噬菌体之间的分子相互作用在很大程度上是未知的。在这里,我们对感染棘阿米巴多食mimivirus (APMV)和同时感染APMV和Sputnik 3病毒噬菌体的棘阿米巴castellanii细胞进行了时间过程转录组分析。我们证明了噬菌体对变形虫的转录组几乎没有影响,主要是劫持巨型病毒的转录机制。此外,噬菌体感染改变巨病毒基因的表达,这取决于它们的表达时间。早期基因的表达被延长,而晚期基因的表达被延迟,这表明噬菌体感染破坏了巨病毒感染从早期到晚期的过渡。这项研究为这种独特的三方系统中的相互作用提供了分子见解。
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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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