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Screening for Antiviral Medaka Haploid Embryonic Stem Cells by Genome Wide Mutagenesis

机译:通过基因组宽诱变筛选抗病毒Medaka单倍体胚胎干细胞

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Nervous necrosis virus (NNV), one of the most prevalent fish pathogens, has caused significant losses in both yield and economy to the aquaculture. Host factors involved in NNV infection remain to be identified due to the lack of ideal model for the study of NNV and host interaction. Haploid stem cells have proven to be ideal materials in genetic screens. Here, we generated a cell line HX1G1 (simply named G1) with the activity against red-spotted grouper nervous necrosis virus (RGNNV) by N-ethyl-N-nitrosourea (ENU)-mediated whole genome random mutagenesis from the haploid embryonic stem cell HX1a, a cell clone from haploid cell line HX1 that we previously derived from the medaka fish. G1 cells retained the characteristics of haploidy and pluripotency as indicated by the EBs differentiation ability after genetic mutagenesis. Compared with HX1a cells, no typical cytopathic effects were observed, and the expression of RNA-dependent RNA polymerase (RDRP) was significantly reduced in G1 cells post RGNNV infection, indicating the enhanced anti-RGNNV activity of G1. Furthermore, we demonstrated that RGNNV entry into G1 cells was partially inhibited, and this inhibition might be relevant to the induced mutation of heat shock cognate protein 70 (HSC70) which was decisive for NNV entry. Interestingly, G1 cells were to some extent permissive to RGNNV infection, but RGNNV was spontaneously cleared in G1 cells during serial passage. In addition, we also found that the expression levels of interferon (IFN)-related genes were higher in G1 cells than those in HX1a cells, suggesting that viral clearance might be associated with the elevated expression of IFN-related genes in G1 cells.
机译:神经坏死病毒(NNV)是最普遍的鱼类病原体之一,在水产养殖中导致产量和经济中的显着损失。由于NNV和宿主互动研究缺乏理想模型,仍然识别涉及NNV感染的宿主因子。单倍体干细胞已被证明是遗传筛中的理想材料。在这里,通过N-乙基-N-硝基脲(ENU)介导的全基因组随机诱变,我们产生了对红斑狼犬神经坏死病毒(RGNNV)的活性的细胞系HX1G1(简称为G1)。来自单倍体胚胎干细胞的全基因组随机诱变HX1A,来自单倍体细胞系HX1的细胞克隆,我们以前来自Medaka鱼。如遗传诱变后EBS分化能力所示,G1细胞保留了单倍体和多能性的特征。与HX1A细胞相比,未观察到典型的细胞病变效果,并且RNA依赖性RNA聚合酶(RDRP)的表达在RGNNV感染后的G1细胞中显着降低,表明G1的增强抗RGNNV活性。此外,我们证明RGNNV进入G1细胞被部分抑制,并且该抑制可能与热冲击同源蛋白70(HSC70)的诱导突变相关,这对于NNV进入是决定性的。有趣的是,G1细胞在某种程度上允许RGNNV感染,但在连续通过期间在G1细胞中自发地清除RGNNV。此外,我们还发现干扰素(IFN)的表达水平比HX1a细胞中的G1细胞较高,表明病毒间隙可能与G1细胞中的IFN相关基因的表达升高相关。

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