The Jackson Laboratory, Bar Harbor, ME, USA.
Trudeau Institute, Saranac Lake, NY, USA.
Sci Rep. 2024 Oct 24;14(1):25147. doi: 10.1038/s41598-024-77087-1.
Mutations in SARS-CoV-2 variants of concern (VOCs) have expanded the viral host range beyond primates, and a few other mammals, to mice, affording the opportunity to exploit genetically diverse mouse panels to model the broad spectrum 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.
SARS-CoV-2 变种(VOC)的突变扩大了病毒的宿主范围,不仅包括灵长类动物,还包括少数其他哺乳动物,使我们有机会利用遗传多样化的小鼠模型来模拟患者群体中对感染的广泛反应。在这里,我们调查了遗传多样化的合作杂交(CC)创始系对 VOC 感染的反应。野生型 CC 创始系的感染产生了广泛的病毒载量、疾病易感性和存活率,而大多数其他系尽管肺部病毒滴度可测量,但仍能抵抗疾病。特别是,CAST/EiJ,一种野生型菌株,肺部病毒载量高,肺部病理比其他 CC 菌株严重,细胞因子谱失调导致发病率和死亡率。这些近交系小鼠品系未来可能成为评估针对严重 COVID-19 和其他冠状病毒大流行的治疗对策的有价值的平台。