Department of Medicine, Washington University School of Medicine, Saint Louis, MO 63110, USA.
Department of Pathology & Immunology, Washington University School of Medicine, Saint Louis, MO 63110, USA.
Cell. 2023 Oct 26;186(22):4818-4833.e25. doi: 10.1016/j.cell.2023.09.007. Epub 2023 Oct 6.
MXRA8 is a receptor for chikungunya (CHIKV) and other arthritogenic alphaviruses with mammalian hosts. However, mammalian MXRA8 does not bind to alphaviruses that infect humans and have avian reservoirs. Here, we show that avian, but not mammalian, MXRA8 can act as a receptor for Sindbis, western equine encephalitis (WEEV), and related alphaviruses with avian reservoirs. Structural analysis of duck MXRA8 complexed with WEEV reveals an inverted binding mode compared with mammalian MXRA8 bound to CHIKV. Whereas both domains of mammalian MXRA8 bind CHIKV E1 and E2, only domain 1 of avian MXRA8 engages WEEV E1, and no appreciable contacts are made with WEEV E2. Using these results, we generated a chimeric avian-mammalian MXRA8 decoy-receptor that neutralizes infection of multiple alphaviruses from distinct antigenic groups in vitro and in vivo. Thus, different alphaviruses can bind MXRA8 encoded by different vertebrate classes with distinct engagement modes, which enables development of broad-spectrum inhibitors.
MXRA8 是一种受体,可与携带哺乳动物宿主的基孔肯雅(CHIKV)和其他致关节炎的甲病毒结合。然而,感染人类且具有禽类宿主的甲病毒与哺乳动物 MXRA8 不结合。在这里,我们表明,禽类而非哺乳动物的 MXRA8 可以作为辛德毕斯、西部马脑炎(WEEV)和相关具有禽类宿主的甲病毒的受体。鸭 MXRA8 与 WEEV 复合物的结构分析显示,与哺乳动物 MXRA8 结合 CHIKV 相比,其结合模式相反。虽然哺乳动物 MXRA8 的两个结构域都与 CHIKV E1 和 E2 结合,但禽类 MXRA8 的仅结构域 1 与 WEEV E1 结合,并且与 WEEV E2 没有明显的接触。利用这些结果,我们生成了一种嵌合的禽-哺乳动物 MXRA8 诱饵受体,可在体外和体内中和多种来自不同抗原群的甲病毒的感染。因此,不同的甲病毒可以与不同的脊椎动物类别的 MXRA8 结合,具有不同的结合模式,这使得广谱抑制剂的开发成为可能。