Modulation of Zika virus replication via glycosphingolipids.

Kouacou V Konan, Simon Alem Ogbamikael, Eric Yager, Toshiyuki Yamaji, Jennifer Cerone, Meredith Monaco-Brown, Margarida Barroso, Kentaro Hanada

Virology 2022 Jul

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The enveloped positive-sense RNA viruses including Zika virus (ZIKV) need host lipids to successfully replicate. The nature of the lipids and the replication step(s) where lipids are utilized often vary amongst viruses. In this study, we demonstrate that ZIKV particle envelope is significantly enriched in distinct sphingolipid species. To determine the role of sphingolipids in ZIKV replication, we leveraged a panel of sphingolipid-deficient cell lines. Notably, knockout of glucosylceramide and lactosylceramide synthase encoding genes (GCSKO; B4G5KO) resulted in a marked decrease in ZIKV titers. GCSKO or pharmacological inhibition of GCS also led to a significant decrease in ZIKV genome replication. Further analysis indicated that GCSKO reduced intracellular virus titers but had minimal impact on ZIKV binding. Restoration of B4G5 expression in B4G5KO cells or supplementing PDMP-treated cells with glucosylceramide led to a significant rescue of ZIKV replication. Altogether, our findings suggest that ZIKV needs glycosphingolipids to facilitate virus replication. Copyright © 2022 Elsevier Inc. All rights reserved.

Citation

Kouacou V Konan, Simon Alem Ogbamikael, Eric Yager, Toshiyuki Yamaji, Jennifer Cerone, Meredith Monaco-Brown, Margarida Barroso, Kentaro Hanada. Modulation of Zika virus replication via glycosphingolipids. Virology. 2022 Jul;572:17-27