Department of Cell Biology, University of Alberta, Edmonton, Alberta T6G 2H7, Canada.
Department of Medical Microbiology and Immunology, University of Alberta, Edmonton, Alberta T6G 2H7, Canada.
Mol Biol Cell. 2021 Jul 1;32(14):1273-1282. doi: 10.1091/mbc.E21-02-0074. Epub 2021 May 19.
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a novel coronavirus that has triggered global health and economic crises. Here we report the effects of SARS-CoV-2 infection on peroxisomes of human cell lines Huh-7 and SK-N-SH. Peroxisomes undergo dramatic changes in morphology in SARS-CoV-2-infected cells. Rearrangement of peroxisomal membranes is followed by redistribution of peroxisomal matrix proteins to the cytosol, resulting in a dramatic decrease in the number of mature peroxisomes. The SARS-CoV-2 ORF14 protein was shown to interact physically with human PEX14, a peroxisomal membrane protein required for matrix protein import and peroxisome biogenesis. Given the important roles of peroxisomes in innate immunity, SARS-CoV-2 may directly target peroxisomes, resulting in loss of peroxisome structural integrity, matrix protein content and ability to function in antiviral signaling.
严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)是一种新型冠状病毒,引发了全球健康和经济危机。在这里,我们报告了 SARS-CoV-2 感染对人细胞系 Huh-7 和 SK-N-SH 中的过氧化物酶体的影响。过氧化物酶体在 SARS-CoV-2 感染的细胞中形态发生剧烈变化。过氧化物酶体膜的重排伴随着过氧化物酶体基质蛋白向细胞质的重新分布,导致成熟过氧化物酶体的数量急剧减少。研究表明,SARS-CoV-2 的 ORF14 蛋白与人类 PEX14 发生物理相互作用,PEX14 是一种过氧化物酶体膜蛋白,对于基质蛋白的输入和过氧化物酶体的生物发生是必需的。鉴于过氧化物酶体在先天免疫中的重要作用,SARS-CoV-2 可能直接靶向过氧化物酶体,导致过氧化物酶体结构完整性、基质蛋白含量和抗病毒信号转导功能丧失。