Olson Mikayla C, Pierce Linley R, Orchard Robert C
Department of Immunology, University of Texas Southwestern Medical Center, Dallas, Texas, United States of America.
PLoS Pathog. 2025 May 22;21(5):e1012834. doi: 10.1371/journal.ppat.1012834. eCollection 2025 May.
Caliciviruses are significant agricultural and human pathogens that are poorly understood due to the dearth of molecular tools, including reporter systems. We report the development of a robust luciferase-based reporter system for a model calicivirus, murine norovirus (MNoV). Genetic insertion of a HiBiT tag, an 11 amino acid fragment of nanolucifersase, at the junction of the nonstructural proteins NS4 and NS5 yields infectious virus. The resultant MNoV-HiBiT produces a robust signal that is detected early in infection and occurs only in cells susceptible to MNoV infection. The MNoV-HiBiT reporter is effective at monitoring acute infection in STAT1 deficient mice. Furthermore, we used this tool to characterize two unappreciated host directed anti-MNoV compounds. The use of the MNoV-HiBiT virus enables new mechanistic studies by a rapid and quantitative means of measuring MNoV replication. The HiBiT insertion strategy we describe may be useful for the generation of other calicivirus reporters.
杯状病毒是重要的农业和人类病原体,由于缺乏包括报告系统在内的分子工具,人们对其了解甚少。我们报告了一种针对模型杯状病毒——小鼠诺如病毒(MNoV)的基于荧光素酶的强大报告系统的开发。在非结构蛋白NS4和NS5的连接处基因插入一个HiBiT标签(纳米荧光素酶的11个氨基酸片段)可产生感染性病毒。产生的MNoV-HiBiT产生强大的信号,该信号在感染早期即可检测到,且仅在易受MNoV感染的细胞中出现。MNoV-HiBiT报告基因在监测STAT1缺陷小鼠的急性感染方面有效。此外,我们使用该工具对两种未被充分认识的宿主导向抗MNoV化合物进行了表征。MNoV-HiBiT病毒的使用通过快速定量测量MNoV复制的方法实现了新的机制研究。我们描述的HiBiT插入策略可能有助于生成其他杯状病毒报告基因。