Virology Division, Department of Infectious Diseases and Immunology, Faculty of Veterinary Medicine, Utrecht University, Utrecht, The Netherlands.
Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, California, USA.
mBio. 2019 Aug 13;10(4):e01780-19. doi: 10.1128/mBio.01780-19.
Encephalomyocarditis virus (EMCV) is an animal pathogen and an important model organism, whose receptor requirements are poorly understood. Here, we employed a genome-wide haploid genetic screen to identify novel EMCV host factors. In addition to the previously described picornavirus receptors sialic acid and glycosaminoglycans, this screen unveiled important new host factors for EMCV. These factors include components of the fibroblast growth factor (FGF) signaling pathway, such as the potential receptors FGFR1 and ADAM9, a cell-surface metalloproteinase. By employing various knockout cells, we confirmed the importance of the identified host factors for EMCV infection. The largest reduction in infection efficiency was observed in cells lacking ADAM9. Pharmacological inhibition of the metalloproteinase activity of ADAM9 did not affect virus infection. Moreover, reconstitution of inactive ADAM9 in knockout cells restored susceptibility to EMCV, pointing to a proteinase-independent role of ADAM9 in mediating EMCV infection. Using neutralization assays with ADAM9-specific antiserum and soluble receptor proteins, we provided evidence for a role of ADAM9 in EMCV entry. Finally, binding assays showed that ADAM9 facilitates attachment of EMCV to the cell surface. Together, our findings reveal a role for ADAM9 as a novel receptor or cofactor for EMCV. EMCV is an animal pathogen that causes acute viral infections, usually myocarditis or encephalitis. It is thought to circulate mainly among rodents, from which it is occasionally transmitted to other animal species, including humans. EMCV causes fatal outbreaks of myocarditis and encephalitis in pig farms and zoos, making it an important veterinary pathogen. Although EMCV has been widely used as a model to study mechanisms of viral disease in mice, little is known about its entry mechanism. Here, we employ a haploid genetic screen for EMCV host factors and identify an essential role for ADAM9 in EMCV entry.
脑心肌炎病毒(EMCV)是一种动物病原体,也是一种重要的模式生物,但人们对其受体的需求知之甚少。在这里,我们采用全基因组单倍体遗传筛选来鉴定新的 EMCV 宿主因子。除了先前描述的小核糖核酸病毒受体唾液酸和糖胺聚糖外,该筛选还揭示了 EMCV 的重要新宿主因子。这些因子包括成纤维细胞生长因子(FGF)信号通路的组成部分,如潜在的受体 FGFR1 和 ADAM9,一种细胞表面金属蛋白酶。通过使用各种敲除细胞,我们证实了鉴定的宿主因子对 EMCV 感染的重要性。在感染效率降低最大的细胞中观察到 ADAM9 的缺失。ADAM9 的金属蛋白酶活性的药理学抑制并不影响病毒感染。此外,在敲除细胞中重建无活性的 ADAM9 恢复了对 EMCV 的敏感性,表明 ADAM9 在介导 EMCV 感染中具有蛋白酶非依赖性作用。使用 ADAM9 特异性抗血清和可溶性受体蛋白进行中和测定,为 ADAM9 在 EMCV 进入中的作用提供了证据。最后,结合试验表明 ADAM9 促进 EMCV 与细胞表面的附着。总之,我们的研究结果揭示了 ADAM9 作为 EMCV 的新型受体或辅助因子的作用。EMCV 是一种引起急性病毒感染的动物病原体,通常为心肌炎或脑炎。它被认为主要在啮齿动物中传播,偶尔会传播到其他动物物种,包括人类。EMCV 在养猪场和动物园引起致命的心肌炎和脑炎爆发,使其成为一种重要的兽医病原体。尽管 EMCV 已被广泛用作研究小鼠病毒疾病机制的模型,但对其进入机制知之甚少。在这里,我们采用单倍体遗传筛选来鉴定 EMCV 的宿主因子,并确定 ADAM9 在 EMCV 进入中的重要作用。