Article ID Journal Published Year Pages File Type
6142510 Virus Research 2014 12 Pages PDF
Abstract

•Quantitative cytopathogenic effect (Q-CPE) assay was established on fish cell model.•Genome-wide RNAi screens against tiger frog virus were performed by Q-CPE.•The RNAi results from Q-CPE were verified by quantitative RTPCR and titer assay.•The distribution of TFV proliferation-important (essential) genes was analyzed.•Conservative comparison of essential genes in Ranavirus was analyzed.

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.

Related Topics
Life Sciences Immunology and Microbiology Virology
Authors
, , , , , , , , ,