Pharmacological targeting of bunyavirus-induced synaptic impairment prevents neuronal hyperexcitability

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Abstract
Orthobunyaviruses are linked to a broad spectrum of neurological disorders. However, the molecular determinants governing bunyavirus neuropathogenesis remain poorly understood, precluding the identification of drugs able to alleviate virus-induced neuronal dysfunctions. Here, we show that the prevalent, yet neglected, orthobunyavirus Ťahyňa virus (TAHV) disrupts neuronal integrity and proteostasis in human cerebral organoids (hCO), significantly decreasing synaptic protein expression and density. Moreover, TAHV-induced synaptic remodeling is associated with perturbed local field potential in organotypic cultures of human post-mortem adult brain explants (OPAB) and higher expression of the metabotropic Glutamate receptor 1 (mGluR1) in mice in the absence of overt neurological disease or neuroinflammation. Using proteome-based network medicine, we identified gabapentin as a therapeutic candidate that restores neurotransmitter receptor levels back to baseline in mice, and prevents TAHV-induced hyperexcitability in OPAB. Together, our data highlights the underappreciated neuropathological potential of a neglected orthobunyavirus, that interferes with neural integrity and neurotransmission, while neuromodulatory interventions may help to preserve cerebral functions.
Funding Information
  • Human Frontier Science Program (RGP012/2024-101)
  • Human Frontier Science Program (RGP012/2024-101)
  • Agence Nationale de la Recherche (ANR-20-CE15-0019-01)
  • Agence Nationale de la Recherche (ANR-22-CE15-0007-01)
  • Agence Nationale de la Recherche (ANR-22-CE15-0007-01)
  • Agence Nationale de la Recherche (ANR-20-CE15-0019-01)

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