Institute of Microbiology, University Hospital Center and University of Lausanne, Rue du Bugnon 48, CH-1011, Lausanne, Switzerland; Spiez Laboratory, CH-3700, Spiez, Switzerland.
Institute of Microbiology, University Hospital Center and University of Lausanne, Rue du Bugnon 48, CH-1011, Lausanne, Switzerland.
Virology. 2020 Apr;543:54-62. doi: 10.1016/j.virol.2020.02.002. Epub 2020 Feb 9.
Hantaviruses are rodent-borne hemorrhagic fever viruses leading to serious diseases. Viral attachment and entry represent the first steps in virus transmission and are promising targets for antiviral therapeutic intervention. Here we investigated receptor use in human airway epithelium of the Old and New World hantaviruses Hantaan virus (HTNV) and Andes virus (ANDV). Using a biocontained recombinant vesicular stomatitis virus pseudotype platform, we provide first evidence for a role of the cellular phosphatidylserine (PS) receptors of the T-cell immunoglobulin and mucin (TIM) protein family in HTNV and ANDV infection. In line with previous studies, HTNV, but not ANDV, was able to use glycosaminoglycan heparan sulfate and αβ integrin as co-receptors. In sum, our studies demonstrate for the first time that hantaviruses make use of apoptotic mimicry for infection of human airway epithelium, which may explain why these viruses can easily break the species barrier.
汉坦病毒是一种啮齿动物传播的出血热病毒,可导致严重疾病。病毒附着和进入是病毒传播的第一步,也是抗病毒治疗干预的有前途的靶点。在这里,我们研究了旧世界和新世界汉坦病毒(HTNV)和安第斯病毒(ANDV)在人类气道上皮细胞中的受体利用情况。我们使用生物封闭的重组水疱性口炎病毒假型平台,首次提供了细胞磷脂酰丝氨酸(PS)受体在 HTNV 和 ANDV 感染中的作用的证据。与之前的研究一致,HTNV 而不是 ANDV 能够利用糖胺聚糖肝素硫酸和αβ整联蛋白作为辅助受体。总之,我们的研究首次证明汉坦病毒利用凋亡模拟来感染人类气道上皮细胞,这可能解释了为什么这些病毒很容易突破物种屏障。