运输机
细胞生物学
生物
病毒进入
寄主因子
衣壳
小干扰RNA
RNA干扰
核糖核酸
小发夹RNA
病毒复制
病毒学
转染
受体
毒力因子
内化
病毒蛋白
信号转导
表型
RNA沉默
转运蛋白
化学
HEK 293细胞
病毒
肠道病毒71
突变
ATP结合盒运输机
肠道病毒
RNA结合蛋白
鞘脂
作者
Yu-Zhi Fu,Fang-Fang Luo,Yang Liu,Yuxia Zhang,Jing-Yang Li,Su-Yun Wang,Yong Zhang,Yan‐Yi Wang
标识
DOI:10.1073/pnas.2510020122
摘要
Human enterovirus A71 (EV-A71) is a major cause of hand, foot and mouth disease. Cellular factors critical for EV-A71 infection remain enigmatic. Here, we performed CRISPR/Cas9 screens and identified sphingolipid transporter 1 (SPNS1) as an essential factor for EV-A71. SPNS1 deficiency inhibits infection of EV-A71 and 9 of 11 examined enteroviruses. Mechanistically, the endo/lysosomal localization of SPNS1 and the acidification of the endo/lysosomes are essential for SPNS1 to support EV-A71 infection. SPNS1 deficiency inhibits EV-A71 genomic RNA replication, but barely affects replication of EV-A71 RNA directly transfected into the cytoplasm. SPNS1 interacts with the EV-A71 capsid protein VP1 and entry receptor SCARB2 in the endo/lysosomes, where it acts as a transporter to release the viral pocket factor into the cytosol, leading to uncoating. Animal experiments show that SPNS1 deficiency results in reduced viral loads, pathological effects, and lethality following EV-A71 infection. Our findings collectively identified SPNS1 as a transporter of the EV-A71 viral pocket factor.
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