Institute for Infectious Diseases, University of Bern, 3001 Bern, Switzerland.
Graduate School for Cellular and Biomedical Sciences, University of Bern, 3012 Bern, Switzerland.
Viruses. 2023 Dec 16;15(12):2444. doi: 10.3390/v15122444.
Influenza D virus (IDV) can infect various livestock animals, such as cattle, swine, and small ruminants, and was shown to have zoonotic potential. Therefore, it is important to identify viral factors involved in the broad host tropism and identify potential antiviral compounds that can inhibit IDV infection. Recombinant reporter viruses provide powerful tools for studying viral infections and antiviral drug discovery. Here we present the generation of a fluorescent reporter IDV using our previously established reverse genetic system for IDV. The mNeonGreen (mNG) fluorescent reporter gene was incorporated into the IDV non-structural gene segment as a fusion protein with the viral NS1 or NS2 proteins, or as a separate protein flanked by two autoproteolytic cleavage sites. We demonstrate that only recombinant reporter viruses expressing mNG as an additional separate protein or as an N-terminal fusion protein with NS1 could be rescued, albeit attenuated, compared to the parental reverse genetic clone. Serial passaging experiments demonstrated that the mNG gene is stably integrated for up to three passages, after which internal deletions accumulate. We conducted a proof-of-principle antiviral screening with the established fluorescent reporter viruses and identified two compounds influencing IDV infection. These results demonstrate that the newly established recombinant IDV reporter virus can be applied for antiviral drug discovery and monitoring viral replication, adding a new molecular tool for investigating IDV.
牛传染性腹泻病毒(IDV)可感染牛、猪和小反刍动物等多种家畜,具有人畜共患的潜力。因此,确定参与广泛宿主嗜性的病毒因子,并鉴定潜在的可抑制 IDV 感染的抗病毒化合物非常重要。重组报告病毒为研究病毒感染和抗病毒药物发现提供了强大的工具。在这里,我们使用之前建立的 IDV 反向遗传系统,生成了一种荧光报告 IDV。mNeonGreen(mNG)荧光报告基因被插入 IDV 的非结构基因片段中,作为与病毒 NS1 或 NS2 蛋白融合的蛋白,或作为侧翼带有两个自切割位点的独立蛋白。我们证明,与亲本反向遗传克隆相比,只有表达 mNG 作为额外独立蛋白或与 NS1 作为 N 端融合蛋白的重组报告病毒才能被拯救,尽管是衰减的。连续传代实验表明,mNG 基因可稳定整合长达 3 代,之后会积累内部缺失。我们用建立的荧光报告病毒进行了原理验证性抗病毒筛选,鉴定出两种影响 IDV 感染的化合物。这些结果表明,新建立的重组 IDV 报告病毒可用于抗病毒药物发现和监测病毒复制,为研究 IDV 增加了一种新的分子工具。