Department of Molecular Genetics and Microbiology, Duke University School of Medicine, Durham, NC 27710, USA.
Department of Immunology, Duke University School of Medicine, Durham, NC 27710, USA.
Cell Rep. 2020 Sep 1;32(9):108103. doi: 10.1016/j.celrep.2020.108103.
Influenza viruses initiate infection in the upper respiratory tract (URT), but early viral tropism and the importance of cell-type-specific antiviral responses in this tissue remain incompletely understood. By infecting transgenic lox-stop-lox reporter mice with a Cre-recombinase-expressing influenza B virus, we identify olfactory sensory neurons (OSNs) as a major viral cell target in the URT. These cells become infected, then eliminate the virus and survive in the host post-resolution of infection. OSN responses to infection are characterized by a strong induction of interferon-stimulated genes and more rapid clearance of viral protein relative to other cells in the epithelium. We speculate that this cell-type-specific response likely serves to protect the central nervous system from infection. More broadly, these results highlight the importance of evaluating antiviral responses across different cell types, even those within the same tissue, to more fully understand the mechanisms of viral disease.
流感病毒在上呼吸道(URT)引发感染,但早期病毒嗜性和该组织中细胞类型特异性抗病毒反应的重要性仍不完全清楚。通过用表达 Cre 重组酶的流感 B 病毒感染转基因 lox-stop-lox 报告小鼠,我们确定嗅觉感觉神经元(OSN)是 URT 中的主要病毒细胞靶标。这些细胞被感染,然后在感染得到解决后消除病毒并在宿主中存活。OSN 对感染的反应特征是干扰素刺激基因的强烈诱导,并且相对于上皮细胞中的其他细胞更快地清除病毒蛋白。我们推测这种细胞类型特异性反应可能有助于保护中枢神经系统免受感染。更广泛地说,这些结果强调了评估不同细胞类型(甚至是同一组织内的细胞类型)的抗病毒反应的重要性,以更全面地了解病毒疾病的机制。