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Metabolic reprogramming by Zika virus provokes inflammation in human placenta

Author

Listed:
  • Qian Chen

    (CNRS - Inserm - University of Toulouse)

  • Jordi Gouilly

    (CNRS - Inserm - University of Toulouse)

  • Yann J. Ferrat

    (University of Grenoble Alpes)

  • Ana Espino

    (CNRS - Inserm - University of Toulouse)

  • Quentin Glaziou

    (CNRS - Inserm - University of Toulouse)

  • Géraldine Cartron

    (Paule de Viguier Hospital)

  • Hicham El Costa

    (CNRS - Inserm - University of Toulouse)

  • Reem Al-Daccak

    (University of Paris Diderot)

  • Nabila Jabrane-Ferrat

    (CNRS - Inserm - University of Toulouse)

Abstract

The recent outbreak of Zika virus (ZIKV) was associated with birth defects and pregnancy loss when maternal infection occurs in early pregnancy, but specific mechanisms driving placental insufficiency and subsequent ZIKV-mediated pathogenesis remain unclear. Here we show, using large scale metabolomics, that ZIKV infection reprograms placental lipidome by impairing the lipogenesis pathways. ZIKV-induced metabolic alterations provide building blocks for lipid droplet biogenesis and intracellular membrane rearrangements to support viral replication. Furthermore, lipidome reprogramming by ZIKV is paralleled by the mitochondrial dysfunction and inflammatory immune imbalance, which contribute to placental damage. In addition, we demonstrate the efficacy of a commercially available inhibitor in limiting ZIKV infection, provides a proof-of-concept for blocking congenital infection by targeting metabolic pathways. Collectively, our study provides mechanistic insights on how ZIKV targets essential hubs of the lipid metabolism that may lead to placental dysfunction and loss of barrier function.

Suggested Citation

  • Qian Chen & Jordi Gouilly & Yann J. Ferrat & Ana Espino & Quentin Glaziou & Géraldine Cartron & Hicham El Costa & Reem Al-Daccak & Nabila Jabrane-Ferrat, 2020. "Metabolic reprogramming by Zika virus provokes inflammation in human placenta," Nature Communications, Nature, vol. 11(1), pages 1-16, December.
  • Handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-16754-z
    DOI: 10.1038/s41467-020-16754-z
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    Cited by:

    1. Julia Hehner & Laura Schneider & Anna Woitalla & Benjamin Ott & Kim Chi Thi Vu & Anja Schöbel & Torsten Hain & Dominik Schwudke & Eva Herker, 2024. "Glycerophospholipid remodeling is critical for orthoflavivirus infection," Nature Communications, Nature, vol. 15(1), pages 1-18, December.
    2. Emilie Branche & Ying-Ting Wang & Karla M. Viramontes & Joan M. Valls Cuevas & Jialei Xie & Fernanda Ana-Sosa-Batiz & Norazizah Shafee & Sascha H. Duttke & Rachel E. McMillan & Alex E. Clark & Michael, 2022. "SREBP2-dependent lipid gene transcription enhances the infection of human dendritic cells by Zika virus," Nature Communications, Nature, vol. 13(1), pages 1-15, December.

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