Department of Infectious Diseases, College of Veterinary Medicine, University of Georgia, Athens, Georgia 30602, USA.
Proventus Bio, 220 Riverbend Rd, Athens, Georgia 30602, USA.
Sci Data. 2017 Mar 1;4:170023. doi: 10.1038/sdata.2017.23.
MicroRNAs (miRNAs) regulate virus replication through multiple mechanisms. Poliovirus causes a highly debilitating disease and though global efforts to eradicate polio have sharply decreased polio incidence, unfortunately three countries (Afghanistan, Nigeria and Pakistan) remain polio-endemic. We hypothesize that understanding the host factors involved in polio replication will identify novel prophylactic and therapeutic targets against polio and related viruses. In this data set, employing genome wide screens of miRNA mimics and inhibitors, we identified miRNAs which significantly suppressed polio replication. Specifically, miR-134 regulates poliovirus replication via modulation of ras-related nuclear protein (RAN), an important component of the nuclear transport system. MiR-134 also inhibited other Picornaviridae viruses including EV71, a growing concern and a high priority for vaccination in Asian countries like China. These findings demonstrate a novel mechanism for miRNA regulation of poliovirus and other Picornaviridae viruses in host cells, and thereby may provide a novel approach in combating infection and a potential approach for the development of anti-Picornaviridae strategies.
微小 RNA(miRNAs)通过多种机制调节病毒复制。脊髓灰质炎病毒会导致高度致残的疾病,尽管全球根除脊髓灰质炎的努力已大幅降低了脊髓灰质炎的发病率,但不幸的是,仍有三个国家(阿富汗、尼日利亚和巴基斯坦)为脊髓灰质炎流行区。我们假设,了解参与脊髓灰质炎复制的宿主因素将确定针对脊髓灰质炎和相关病毒的新型预防和治疗靶点。在本数据集,通过 miRNA 模拟物和抑制剂的全基因组筛选,我们鉴定了可显著抑制脊髓灰质炎复制的 miRNAs。具体而言,miR-134 通过调节 ras 相关核蛋白(RAN)来调节脊髓灰质炎病毒的复制,RAN 是核转运系统的重要组成部分。miR-134 还抑制其他小 RNA 病毒科病毒,包括在中国等亚洲国家日益受到关注且高度优先接种疫苗的 EV71。这些发现表明了 miRNA 调节宿主细胞中脊髓灰质炎病毒和其他小 RNA 病毒的新机制,从而可能为防治感染提供新方法,也可能为开发抗小 RNA 病毒策略提供一种新方法。