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Peroxisomes exhibit compromised structure and matrix protein content in SARS-CoV-2-infected cells.
Knoblach, Barbara; Ishida, Ray; Hobman, Tom C; Rachubinski, Richard A.
  • Knoblach B; Department of Cell Biology, University of Alberta, Edmonton, Alberta T6G 2H7, Canada.
  • Ishida R; Department of Medical Microbiology and Immunology, University of Alberta, Edmonton, Alberta T6G 2H7, Canada.
  • Hobman TC; Department of Cell Biology, University of Alberta, Edmonton, Alberta T6G 2H7, Canada.
  • Rachubinski RA; Department of Medical Microbiology and Immunology, University of Alberta, Edmonton, Alberta T6G 2H7, Canada.
Mol Biol Cell ; 32(14): 1273-1282, 2021 07 01.
Article in English | MEDLINE | ID: covidwho-1233836
ABSTRACT
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.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Peroxisomes Limits: Animals / Humans Language: English Journal: Mol Biol Cell Journal subject: Molecular Biology Year: 2021 Document Type: Article Affiliation country: Mbc.E21-02-0074

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Peroxisomes Limits: Animals / Humans Language: English Journal: Mol Biol Cell Journal subject: Molecular Biology Year: 2021 Document Type: Article Affiliation country: Mbc.E21-02-0074