BioFrontiers Institute, Department of Molecular, Cellular, and Developmental Biology, University of Colorado, Boulder, CO 80303, USA.
Integrated Research Facility at Fort Detrick, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Fort Detrick, Frederick, MD 21702, USA.
Cell. 2022 Oct 13;185(21):3980-3991.e18. doi: 10.1016/j.cell.2022.09.022. Epub 2022 Sep 30.
Simian arteriviruses are endemic in some African primates and can cause fatal hemorrhagic fevers when they cross into primate hosts of new species. We find that CD163 acts as an intracellular receptor for simian hemorrhagic fever virus (SHFV; a simian arterivirus), a rare mode of virus entry that is shared with other hemorrhagic fever-causing viruses (e.g., Ebola and Lassa viruses). Further, SHFV enters and replicates in human monocytes, indicating full functionality of all of the human cellular proteins required for viral replication. Thus, simian arteriviruses in nature may not require major adaptations to the human host. Given that at least three distinct simian arteriviruses have caused fatal infections in captive macaques after host-switching, and that humans are immunologically naive to this family of viruses, development of serology tests for human surveillance should be a priority.
猿猴动脉炎病毒在一些非洲灵长类动物中流行,如果它们进入新物种的灵长类动物宿主,就会引起致命的出血性发热。我们发现 CD163 作为一种细胞内受体,用于猿猴出血热病毒(SHFV;一种猿猴动脉炎病毒),这是一种罕见的病毒进入方式,与其他引起出血热的病毒(如埃博拉病毒和拉萨病毒)共享。此外,SHFV 进入并在人类单核细胞中复制,表明复制所需的所有人类细胞蛋白都具有完全的功能。因此,自然界中的猿猴动脉炎病毒可能不需要对人类宿主进行重大适应。鉴于至少有三种不同的猿猴动脉炎病毒在宿主转换后导致圈养猕猴发生致命感染,而且人类对这一家族的病毒免疫上是幼稚的,因此开发针对人类的血清学检测方法应该是当务之急。