Ictalurid herpesvirus 1

  • 文章类型: Journal Article
    疱疹病毒坚持精确的时间表达模型,其中立即早期(IE)基因在调节病毒生命周期中起关键作用。然而,目前尚缺乏对Ictaluriid疱疹病毒1型(IcHV-1)IE基因的功能研究。在这项研究中,我们通过代谢抑制试验将IcHV-1ORF24鉴定为IE基因,亚细胞分析表明其主要位于细胞核中。为了研究它的功能,我们使用含有Gal4-BD结构域的ORF24融合蛋白进行了酵母报告基因测定,发现BD-ORF24能够激活没有Gal4-AD结构域的HIS3/lacZ报告基因.我们的发现提供了具体的证据,证明ORF24确实是IE基因,在IcHV-1感染期间可能充当转录调节因子。这项工作有助于我们了解鱼类疱疹病毒IE基因表达的分子机制。
    Herpesviruses adhere to a precise temporal expression model in which immediate-early (IE) genes play a crucial role in regulating the viral life cycle. However, there is a lack of functional research on the IE genes in Ictalurid herpesvirus 1 (IcHV-1). In this study, we identified the IcHV-1 ORF24 as an IE gene via a metabolic inhibition assay, and subcellular analysis indicated its predominant localisation in the nucleus. To investigate its function, we performed yeast reporter assays using an ORF24 fusion protein containing the Gal4-BD domain and found that BD-ORF24 was able to activate HIS3/lacZ reporter genes without the Gal4-AD domain. Our findings provide concrete evidence that ORF24 is indeed an IE gene that likely functions as a transcriptional regulator during IcHV-1 infection. This work contributes to our understanding of the molecular mechanisms underlying fish herpesvirus IE gene expression.
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  • 文章类型: Journal Article
    channel鱼病毒(CCV,冰毒疱疹病毒1)由于其强大的传染性和致病性,在养鱼业中造成了持续的经济损失。因此,有必要确定病毒蛋白在CCV感染过程中的功能。本研究旨在表征CCV糖蛋白ORF59,并探讨其对宿主细胞病毒感染的影响。首先,其在细胞裂解物的膜部分中的唯一存在和亚细胞定位证实CCVORF59是在晚期感染时表达的病毒膜蛋白。使用纯化的His6标记的ORF59进行蛋白质阻断测定,使用杆状病毒表达系统在sf9昆虫细胞中表达,表明重组ORF59蛋白对病毒侵袭具有剂量依赖性的抑制作用。使用短发夹(shRNA)敲除ORF59表明,ORF59沉默降低了通道cat鱼卵巢细胞中感染性病毒颗粒的产生。这项研究的结果表明,重组ORF59蛋白可能会抑制CCV进入宿主细胞。这些发现将促进对CCV感染过程中糖蛋白ORF59关键功能的未来研究。
    The channel catfish virus (CCV, Ictalurid herpesvirus 1) has caused sustained economic losses in the fish industry because of its strong infectivity and pathogenicity. Thus, it is necessary to determine the function of viral proteins in the CCV infection process. The present study aimed to characterize CCV glycoprotein ORF59 and explore its impact on virus infection in host cells. Firstly, its exclusive presence in the membrane fraction of the cell lysate and subcellular localization verified that CCV ORF59 is a viral membrane protein expressed at late-stage infection. A protein blocking assay using purified His6 tagged ORF59, expressed in sf9 insect cells using a baculovirus expression system, indicated a dose-dependent inhibitory effect of recombinant ORF59 protein on virus invasion. Knockdown of the ORF59 using a short hairpin (shRNA) showed that ORF59 silencing decreased the production of infectious virus particles in channel catfish ovary cells. The results of this study suggest that recombinant ORF59 protein might inhibit CCV entry into the host cells. These findings will promote future studies of the key functions of glycoprotein ORF59 during CCV infection.
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  • 文章类型: Journal Article
    疱疹病毒是在脊椎动物中普遍存在的宿主特异性病原体。基因组序列数据表明,大多数鱼类和两栖动物的疱疹病毒被分组在一起(同种异体疱疹病毒科),并且与爬行动物的疱疹病毒密切相关,鸟类和哺乳动物(疱疹病毒科)。然而,Herpesvirales目成员的许多生物过程是相似的。保守的特征包括病毒体结构,复制过程,建立长期潜伏期和操纵宿主免疫反应的能力。许多类似的过程可能是由于收敛演化。对已鉴定的鱼类疱疹病毒的概述讨论了同种疱疹病毒引起的疾病,这些病毒的生物学和宿主-病原体的相互作用。我们对Alloherpesvirdae生物学的许多知识都来自两个物种的研究:Ictaluid疱疹病毒1(通道cat鱼病毒)和Cyprinid疱疹病毒3(锦草疱疹病毒)。
    Herpesviruses are host specific pathogens that are widespread among vertebrates. Genome sequence data demonstrate that most herpesviruses of fish and amphibians are grouped together (family Alloherpesviridae) and are distantly related to herpesviruses of reptiles, birds and mammals (family Herpesviridae). Yet, many of the biological processes of members of the order Herpesvirales are similar. Among the conserved characteristics are the virion structure, replication process, the ability to establish long term latency and the manipulation of the host immune response. Many of the similar processes may be due to convergent evolution. This overview of identified herpesviruses of fish discusses the diseases that alloherpesviruses cause, the biology of these viruses and the host-pathogen interactions. Much of our knowledge on the biology of Alloherpesvirdae is derived from research with two species: Ictalurid herpesvirus 1 (channel catfish virus) and Cyprinid herpesvirus 3 (koi herpesvirus).
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