Abstract
Understanding pathways that might impact coronavirus disease 2019 (COVID-19) manifestations and disease outcomes is necessary for better disease management and for therapeutic development. Here, we analyzed alterations in sphingolipid (SL) levels upon infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). SARS-CoV-2 infection induced elevation of SL levels in both cells and sera of infected mice. A significant increase in glycosphingolipid levels was induced early post SARS-CoV-2 infection, which was essential for viral replication. This elevation could be reversed by treatment with glucosylceramide synthase inhibitors. Levels of sphinganine, sphingosine, GA1, and GM3 were significantly increased in both cells and the murine model upon SARS-CoV-2 infection. The potential involvement of SLs in COVID-19 pathology is discussed.
© 2021 Vitner et al.
MeSH terms
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Animals
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COVID-19 / metabolism*
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COVID-19 / prevention & control
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COVID-19 / virology
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Chlorocebus aethiops
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Chromatography, Liquid / methods
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Dioxanes / pharmacology
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Disease Models, Animal*
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Gangliosides / blood
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Gangliosides / metabolism
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Glucosyltransferases / antagonists & inhibitors
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Glucosyltransferases / metabolism
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Humans
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Mass Spectrometry / methods
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Mice, Transgenic
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Pyrrolidines / pharmacology
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SARS-CoV-2 / drug effects
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SARS-CoV-2 / physiology
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Sphingolipids / blood
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Sphingolipids / metabolism*
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Sphingosine / analogs & derivatives
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Sphingosine / blood
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Sphingosine / metabolism
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Vero Cells
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Virus Replication / drug effects
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Virus Replication / physiology*
Substances
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(2-(2',3'-dihydrobenzo(1,4)dioxin-6'-yl)-2-hydroxy-1-pyrrolidin-1-ylmethylethyl)nonanoic acid amide
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Dioxanes
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Gangliosides
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Pyrrolidines
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Sphingolipids
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Glucosyltransferases
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ceramide glucosyltransferase
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Sphingosine
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safingol