Macrophage scavenger receptor 1 controls Chikungunya virus infection through autophagy in mice

巨噬细胞清道夫受体 1 通过小鼠自噬控制基孔肯雅病毒感染

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作者:Long Yang #, Tingting Geng #, Guang Yang #, Jinzhu Ma, Leilei Wang, Harshada Ketkar, Duomeng Yang, Tao Lin, Jesse Hwang, Shu Zhu, Yanlin Wang, Jianfeng Dai, Fuping You, Gong Cheng, Anthony T Vella, Richard A Flavell, Erol Fikrig, Penghua Wang

Abstract

Macrophage scavenger receptor 1 (MSR1) mediates the endocytosis of modified low-density lipoproteins and plays an important antiviral role. However, the molecular mechanism underlying MSR1 antiviral actions remains elusive. We report that MSR1 activates autophagy to restrict infection of Chikungunya virus (CHIKV), an arthritogenic alphavirus that causes acute and chronic crippling arthralgia. Msr1 expression was rapidly upregulated after CHIKV infection in mice. Msr1 knockout mice had elevated viral loads and increased susceptibility to CHIKV arthritis along with a normal type I IFN response. Induction of LC3 lipidation by CHIKV, a marker of autophagy, was reduced in Msr1-/- cells. Mechanistically, MSR1 interacted with ATG12 through its cytoplasmic tail and this interaction was enhanced by CHIKV nsP1 protein. MSR1 repressed CHIKV replication through ATG5-ATG12-ATG16L1 and this was dependent on the FIP200-and-WIPI2-binding domain, but not the WD40 domain of ATG16L1. Our results elucidate an antiviral role for MSR1 involving the autophagic function of ATG5-ATG12-ATG16L1.

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