Hongo Yuki, Tomaru Yuji
Fisheries Resources Institute, Japan Fisheries Research and Education Agency, 2-12-4 Fukuura, Kanazawa, Yokohama, Kanagawa 236-8648, Japan.
Fisheries Technology Institute, Japan Fisheries Research and Education Agency, 2-17-5 Maruishi, Hatsukaichi, Hiroshima 739-0452, Japan.
Virus Res. 2025 Jul 15;359:199605. doi: 10.1016/j.virusres.2025.199605.
The marine diatom Chaetoceros tenuissimus coexists in the coastal ocean with two distinct viruses: a circular single-stranded DNA virus and a single-stranded RNA virus. Both viruses are capable of killing the host in vitro experiments; however, the molecular mechanisms by which host genes respond and are utilized by these viruses for replication and proliferation remain unclear. In this study, RNA-seq analyses were conducted to investigate these mechanisms, and the host transcripts specific to each virus were validated by RT-qPCR. In the early phase of infection, RNA-seq analysis revealed that gene transcription related to endocytosis, vacuolar acidification, and nitrogen metabolism was commonly upregulated. In contrast, genes related to transcription and translation were downregulated in cells inoculated with the DNA virus. In the later phase of infection, cells inoculated with the DNA and RNA viruses showed upregulation of genes related to DNA replication and packing, and autophagy, respectively. These virus-specific gene transcripts were confirmed to differ significantly by RT-qPCR. Chaetoceros tenuissimus has previously inserted a fragment of the DNA viral gene (EVLF) into its genome. Intriguingly, the transcription level of EVLF was upregulated in cells inoculated with the DNA virus as time progressed. Thus, regarding specific molecular responses, the DNA virus may hijack the host replication machinery to replicate its own genome, with EVLF playing a role in viral proliferation, whereas the RNA virus may hijack the autophagosome membrane to replicate its own genome, based on the observed replication of the related RNA virus at the membrane. This fundamental information provides insight into the diatom-virus infectious mechanism.
海洋硅藻纤细角毛藻(Chaetoceros tenuissimus)在沿海水域中与两种不同的病毒共存:一种环状单链DNA病毒和一种单链RNA病毒。在体外实验中,这两种病毒都能够杀死宿主;然而,宿主基因对这些病毒作出反应并被其用于复制和增殖的分子机制仍不清楚。在本研究中,进行了RNA测序分析以探究这些机制,并通过逆转录定量聚合酶链反应(RT-qPCR)验证了每种病毒特有的宿主转录本。在感染早期,RNA测序分析表明,与内吞作用、液泡酸化和氮代谢相关的基因转录普遍上调。相比之下,在接种DNA病毒的细胞中,与转录和翻译相关的基因下调。在感染后期,接种DNA病毒和RNA病毒的细胞分别显示出与DNA复制和包装以及自噬相关的基因上调。通过RT-qPCR证实,这些病毒特异性基因转录本存在显著差异。纤细角毛藻此前已将一段DNA病毒基因(EVLF)插入其基因组。有趣的是,随着时间的推移,在接种DNA病毒的细胞中,EVLF的转录水平上调。因此,就特定的分子反应而言,DNA病毒可能劫持宿主复制机制来复制自身基因组,EVLF在病毒增殖中发挥作用,而基于观察到的相关RNA病毒在膜上的复制,RNA病毒可能劫持自噬体膜来复制自身基因组。这一基础信息为硅藻-病毒感染机制提供了见解。