INSERM U944, CNRS UMR 7212, Genomes & Cell Biology of Disease Unit, Institut de Recherche Saint-Louis, Université de Paris, Hôpital Saint-Louis, Paris, France.
Institut Pasteur, Inserm U1117, Biology of Infection Unit, Paris, France.
Nature. 2019 Oct;574(7777):259-263. doi: 10.1038/s41586-019-1578-4. Epub 2019 Sep 25.
Chikungunya virus (CHIKV) is a re-emerging alphavirus that is transmitted to humans by mosquito bites and causes musculoskeletal and joint pain. Despite intensive investigations, the human cellular factors that are critical for CHIKV infection remain unknown, hampering the understanding of viral pathogenesis and the development of anti-CHIKV therapies. Here we identified the four-and-a-half LIM domain protein 1 (FHL1) as a host factor that is required for CHIKV permissiveness and pathogenesis in humans and mice. Ablation of FHL1 expression results in the inhibition of infection by several CHIKV strains and o'nyong-nyong virus, but not by other alphaviruses and flaviviruses. Conversely, expression of FHL1 promotes CHIKV infection in cells that do not normally express it. FHL1 interacts directly with the hypervariable domain of the nsP3 protein of CHIKV and is essential for the replication of viral RNA. FHL1 is highly expressed in CHIKV-target cells and is particularly abundant in muscles. Dermal fibroblasts and muscle cells derived from patients with Emery-Dreifuss muscular dystrophy that lack functional FHL1 are resistant to CHIKV infection. Furthermore, CHIKV infection is undetectable in Fhl1-knockout mice. Overall, this study shows that FHL1 is a key factor expressed by the host that enables CHIKV infection and identifies the interaction between nsP3 and FHL1 as a promising target for the development of anti-CHIKV therapies.
基孔肯雅病毒(CHIKV)是一种重新出现的甲病毒,通过蚊子叮咬传播给人类,并导致肌肉骨骼和关节疼痛。尽管进行了深入的研究,但对于人类中对 CHIKV 感染至关重要的细胞因子仍知之甚少,这阻碍了对病毒发病机制的理解和抗 CHIKV 疗法的开发。在这里,我们鉴定出四个半 LIM 结构域蛋白 1(FHL1)是一种宿主因子,它是人类和小鼠中 CHIKV 易感性和发病机制所必需的。FHL1 表达的缺失导致几种 CHIKV 株和奥尼昂-永昂病毒的感染受到抑制,但不是其他甲病毒和黄病毒。相反,FHL1 的表达促进了在通常不表达它的细胞中 CHIKV 的感染。FHL1 与 CHIKV 的 nsP3 蛋白的高变区直接相互作用,对于病毒 RNA 的复制是必需的。FHL1 在 CHIKV 靶细胞中高度表达,在肌肉中尤为丰富。缺乏功能性 FHL1 的 Emery-Dreifuss 肌营养不良症患者的真皮成纤维细胞和肌肉细胞对 CHIKV 感染具有抗性。此外,Fhl1 敲除小鼠中无法检测到 CHIKV 感染。总体而言,这项研究表明 FHL1 是宿主表达的关键因子,使 CHIKV 感染成为可能,并确定了 nsP3 和 FHL1 之间的相互作用是开发抗 CHIKV 疗法的有前途的靶点。