State Key Laboratory of Biocontrol/MOE Key Laboratory of Aquatic Product Safety, School of Life Sciences, Sun Yat-sen University, Guangzhou 510275, China.
Department of Nephrology, Guangdong General Hospital, Guangdong Academy of Medical Sciences, Guangzhou 518080, China.
Virus Res. 2014 Aug 30;189:214-25. doi: 10.1016/j.virusres.2014.05.020. Epub 2014 Jun 2.
Tiger frog virus (TFV), a species of genus Ranavirus in the family Iridoviridae, is a nuclear cytoplasmic large DNA virus that infects aquatic vertebrates such as tiger frog (Rana tigrina rugulosa) and Chinese soft-shelled turtle (Trionyx sinensis). Based on the available genome sequences of TFV, the well-developed RNA interference (RNAi) technique, and the reliable cell line for infection model, we decided to analyze the functional importance of all predicted genes. Firstly, a relative quantitative cytopathogenic effect (Q-CPE) assay was established to monitor the viral proliferation in fish cells. Then, genome-wide RNAi screens of 95 small interference (si) RNAs against TFV were performed to characterize the functional importance of nearly all (95%) predicted TFV genes by Q-CPE scaling system. We identified 32 (33.7%) genes as essential, 50 (52.6%) genes as semi-essential and 13 (13.7%) genes as nonessential for TFV proliferation. Quantitative RT-PCR and titer assays of selected genes were performed to verify the screen results. Furthermore, the screened essential genes were analyzed for their genome distribution and conservative comparison within Ranavirus. Such a systematic screen for viral functional genes by cell phenotypes should provide further insights into understanding of the information in antiviral targets, and in viral replication and pathogenesis of iridovirus.
虎纹蛙病毒(TFV)是虹彩病毒科虹彩病毒属的一种核细胞质大型 DNA 病毒,感染水生脊椎动物,如虎纹蛙(Rana tigrina rugulosa)和中华鳖(Trionyx sinensis)。基于 TFV 的现有基因组序列、发达的 RNA 干扰(RNAi)技术以及可靠的感染模型细胞系,我们决定分析所有预测基因的功能重要性。首先,建立了相对定量细胞病变效应(Q-CPE)测定法,以监测鱼类细胞中的病毒增殖。然后,通过 Q-CPE 比例系统对 95 条针对 TFV 的小干扰(si)RNA 进行了全基因组 RNAi 筛选,以表征近所有(95%)预测的 TFV 基因的功能重要性。我们鉴定出 32 个(33.7%)基因是必需的,50 个(52.6%)基因是半必需的,13 个(13.7%)基因是非必需的。对选定基因进行了定量 RT-PCR 和滴度测定,以验证筛选结果。此外,对筛选出的必需基因进行了基因组分布分析,并在 Ranavirus 内进行了保守性比较。通过细胞表型对病毒功能基因进行这种系统筛选,应该可以进一步深入了解抗病毒靶标信息,以及虹彩病毒的复制和发病机制。