SARS-CoV-2 infection and viral fusogens cause neuronal and glial fusion that compromises neuronal activity.
Ramon Martinez-MarmolRosina Giordano-SantiniEva KaulichAnn-Na ChoMagdalena PrzybylaMd Asrafuzzaman RiyadhEmilija RobinsonKeng Yih ChewRumelo AmorFrédéric A MeunierGiuseppe BalistreriKirsty R ShortYazi D KeLars M IttnerMassimo A HilliardPublished in: Science advances (2023)
Numerous viruses use specialized surface molecules called fusogens to enter host cells. Many of these viruses, including the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), can infect the brain and are associated with severe neurological symptoms through poorly understood mechanisms. We show that SARS-CoV-2 infection induces fusion between neurons and between neurons and glia in mouse and human brain organoids. We reveal that this is caused by the viral fusogen, as it is fully mimicked by the expression of the SARS-CoV-2 spike (S) protein or the unrelated fusogen p15 from the baboon orthoreovirus. We demonstrate that neuronal fusion is a progressive event, leads to the formation of multicellular syncytia, and causes the spread of large molecules and organelles. Last, using Ca 2+ imaging, we show that fusion severely compromises neuronal activity. These results provide mechanistic insights into how SARS-CoV-2 and other viruses affect the nervous system, alter its function, and cause neuropathology.
Keyphrases
- sars cov
- respiratory syndrome coronavirus
- cerebral ischemia
- spinal cord
- poor prognosis
- induced apoptosis
- subarachnoid hemorrhage
- coronavirus disease
- blood brain barrier
- high resolution
- palliative care
- binding protein
- small molecule
- gene expression
- oxidative stress
- physical activity
- brain injury
- long non coding rna
- cord blood
- cell proliferation
- genetic diversity
- depressive symptoms
- amino acid