Department of Immunology and Microbiology, University of Colorado School of Medicine, Aurora, CO 80045, USA.
Laboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rocky Mountain Laboratories, Hamilton, MT 59840, USA.
Cell Rep. 2023 May 30;42(5):112418. doi: 10.1016/j.celrep.2023.112418. Epub 2023 Apr 21.
Arboviruses are public health threats that cause explosive outbreaks. Major determinants of arbovirus transmission, geographic spread, and pathogenesis are the magnitude and duration of viremia in vertebrate hosts. Previously, we determined that multiple alphaviruses are cleared efficiently from murine circulation by the scavenger receptor MARCO (Macrophage receptor with collagenous structure). Here, we define biochemical features on chikungunya (CHIKV), o'nyong 'nyong (ONNV), and Ross River (RRV) viruses required for MARCO-dependent clearance in vivo. In vitro, MARCO expression promotes binding and internalization of CHIKV, ONNV, and RRV via the scavenger receptor cysteine-rich (SRCR) domain. Furthermore, we observe species-specific effects of the MARCO SRCR domain on CHIKV internalization, where those from known amplification hosts fail to promote CHIKV internalization. Consistent with this observation, CHIKV is inefficiently cleared from the circulation of rhesus macaques in contrast with mice. These findings suggest a role for MARCO in determining whether a vertebrate serves as an amplification or dead-end host following CHIKV infection.
虫媒病毒是对公共卫生具有威胁性的病原体,可引起暴发性传染病。决定虫媒病毒传播、地理扩散和发病机制的主要因素是脊椎动物宿主中病毒血症的幅度和持续时间。此前,我们确定了多种甲病毒可被巨噬细胞清道夫受体 MARCO(具有胶原结构的巨噬细胞受体)有效从鼠类循环中清除。在此,我们确定了基孔肯雅(CHIKV)、奥尼永尼翁(ONNV)和罗斯河(RRV)病毒在体内依赖 MARCO 清除所需的生化特征。在体外,MARCO 表达通过清道夫受体富含半胱氨酸(SRCR)结构域促进 CHIKV、ONNV 和 RRV 的结合和内化。此外,我们观察到 MARCO SRCR 结构域对 CHIKV 内化的种属特异性影响,其中来自已知扩增宿主的那些不能促进 CHIKV 内化。与这一观察结果一致,与小鼠相比,恒河猴的 CHIKV 从循环中清除效率较低。这些发现表明 MARCO 在决定脊椎动物在感染基孔肯雅病毒后是作为扩增宿主还是死胡同宿主方面发挥作用。