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siRNA screen for genes that affect Junín virus entry uncovers voltage-gated calcium channels as a therapeutic target

机译:siRNA筛选影响胡宁病毒进入的基因发现电压门控钙通道为治疗靶标

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摘要

New world hemorrhagic fever arenaviruses infection of humans results in 15–30% mortality. We performed a high throughput siRNA screen with Junín virus glycoprotein-pseudotyped viruses to find potential host therapeutic targets. Voltage-gated calcium channels (VGCC) subunits, for which there are FDA-approved drugs, were identified in the screen. Knockdown of VGCC subunits or treatment with channel blockers diminished Junín virus-cell fusion and entry into cells and thereby decreased infection. Gabapentin, an FDA-approved drug used to treat neuropathic pain that targets the α2δ2 subunit, inhibited infection of mice by the Candid 1 vaccine strain of the virus. These findings demonstrate that VGCCs play a role in virus infection and have the potential to lead to therapeutic intervention of new world arenavirus infection.
机译:感染人类的​​新世界出血热性粒细胞病毒可导致15-30%的死亡率。我们对胡宁病毒糖蛋白假型病毒进行了高通量siRNA筛选,以发现潜在的宿主治疗靶标。在屏幕上确定了电压门控钙通道(VGCC)亚基,其中有FDA批准的药物。击倒VGCC亚基或用通道阻滞剂治疗可减少Junin病毒细胞融合和进入细胞,从而减少感染。加巴喷丁是一种FDA批准的药物,用于治疗靶向α2δ2亚基的神经性疼痛,可抑制病毒的Candid 1疫苗株对小鼠的感染。这些发现表明,VGCC在病毒感染中发挥作用,并有可能导致对新世界性鼻病毒的治疗干预。

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