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bioRxiv · 10.1101/2024.01.20.576493

A novel in vivo model of Zika virus infection unveils NS4A as a key determinant of neuropathogenesis

Abstract

Infection of pregnant women by Zika virus (ZIKV) is associated with severe neurodevelopmental defects in newborns through poorly defined mechanisms. Here, we engineered a zebrafish in vivo model of ZIKV infection to circumvent limitations of existing mammalian models. Leveraging the unique tractability of this system, we gained unprecedented access to the ZIKV-infected brain at early developmental stages. The infection of zebrafish larvae with ZIKV phenocopied the disease in mammals including a reduced head area and neural progenitor cells (NPC) infection and depletion. Moreover, transcriptomic analyses of ZIKV-infected NPCs revealed a distinct dysregulation of genes involved in survival and neuronal differentiation, including downregulation of the expression of the glutamate transporter vglut1, resulting in an altered glutamatergic network in the brain. Mechanistically, ectopic expression of ZIKV protein NS4A in the larvae recapitulated the morphological defects observed in infected animals, identifying NS4A as a key determinant of neurovirulence and a promising antiviral target for developing therapies.

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Chatel-Chaix, L., Sow, A. A., Priyanka Jamadagni, P., Scaturro, P., Patten, S. A.. 2024-01-24. A novel in vivo model of Zika virus infection unveils NS4A as a key determinant of neuropathogenesis. https://doi.org/10.1101/2024.01.20.576493

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