Baker Candice N, Duso Debra, Kothapalli Nagarama, Hart Tricia, Casey Sean, Cookenham Tres, Kummer Larry, Hvizdos Janine, Lanzer Kathleen, Vats Purva, Shanbhag Priya, Bell Isaac, Tighe Mike, Travis Kelsey, Szaba Frank, Bedard Olivia, Oberding Natalie, Ward Jerrold M, Adams Mark D, Lutz Cathleen, Bradrick Shelton S, Reiley William W, Rosenthal Nadia
The Jackson Laboratory.
Trudeau Institute.
Res Sq. 2024 Jul 29:rs.3.rs-4675061. doi: 10.21203/rs.3.rs-4675061/v1.
Mutations in SARS-CoV-2 variants of concern (VOCs) have expanded the viral host range beyond primates, and a limited range of other mammals, to mice, affording the opportunity to exploit genetically diverse mouse panels to model the broad range of responses to infection in patient populations. Here we surveyed responses to VOC infection in genetically diverse Collaborative Cross (CC) founder strains. Infection of wild-derived CC founder strains produced a broad range of viral burden, disease susceptibility and survival, whereas most other strains were resistant to disease despite measurable lung viral titers. In particular, CAST/EiJ, a wild-derived strain, developed high lung viral burdens, more severe lung pathology than seen in other CC strains, and a dysregulated cytokine profile resulting in morbidity and mortality. These inbred mouse strains may serve as a valuable platform to evaluate therapeutic countermeasures against severe COVID-19 and other coronavirus pandemics in the future.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)关注变异株(VOCs)中的突变已将病毒宿主范围从灵长类动物以及有限的其他哺乳动物扩展到小鼠,这为利用基因多样化的小鼠群体来模拟患者群体对感染的广泛反应提供了机会。在此,我们调查了基因多样化的协作杂交(CC)创始株对VOC感染的反应。野生来源的CC创始株感染后产生了广泛的病毒载量、疾病易感性和存活率,而大多数其他株尽管肺病毒滴度可测,但对疾病具有抗性。特别是野生来源的CAST/EiJ株,产生了高肺病毒载量,肺部病理学表现比其他CC株更严重,并且细胞因子谱失调导致发病和死亡。这些近交小鼠株未来可能作为评估针对重症COVID-19和其他冠状病毒大流行的治疗对策的宝贵平台。