Department of Microbiology, Harvard Medical School, Boston, MA 02115.
Program in Virology, Harvard Medical School, Boston, MA 02115.
Proc Natl Acad Sci U S A. 2022 Mar 8;119(10):e2119676119. doi: 10.1073/pnas.2119676119. Epub 2022 Mar 2.
Lymphocytic choriomeningitis virus (LCMV) is a rodent-borne zoonotic arenavirus that causes congenital abnormalities and can be fatal for transplant recipients. Using a genome-wide loss-of-function screen, we identify host factors required for LCMV entry into cells. We identify the lysosomal mucin CD164, glycosylation factors, the heparan sulfate biosynthesis machinery, and the known receptor alpha-dystroglycan (α-DG). Biochemical analysis revealed that the LCMV glycoprotein binds CD164 at acidic pH and requires a sialylated glycan at residue N104. We demonstrate that LCMV entry proceeds by the virus switching binding from heparan sulfate or α-DG at the plasma membrane to CD164 prior to membrane fusion, thus identifying additional potential targets for therapeutic intervention.
淋巴细胞性脉络丛脑膜炎病毒(Lymphocytic choriomeningitis virus,LCMV)是一种啮齿动物传播的人畜共患病正黏液病毒,可导致先天性异常,并可能对移植受者致命。使用全基因组功能丧失筛选,我们确定了宿主因子对于 LCMV 进入细胞所必需的。我们确定了溶酶体粘蛋白 CD164、糖基化因子、肝素硫酸生物合成机制以及已知的受体α- 肌营养不良蛋白(α-DG)。生化分析表明,LCMV 糖蛋白在酸性 pH 下与 CD164 结合,并且需要残基 N104 上的唾液酸化聚糖。我们证明,LCMV 进入细胞的过程是病毒在膜融合之前从细胞膜上的肝素硫酸或α-DG 切换到 CD164 进行结合,从而确定了其他潜在的治疗干预靶点。