Key result
Passaging SSPE virus in human neuronal cells led to viral adaptation driven by mutations in the RNA polymerase and phosphoprotein, upregulating polymerase activity and increasing cell-to-cell fusion.
Upregulation of viral RNA polymerase activity, rather than mutations in the F protein, promotes adaptation and propagation of SSPE virus in neuronal cells.
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Does not alter SSPE management; leaves open in vivo relevance of polymerase-driven neuronal adaptation.
Subacute sclerosing panencephalitis (SSPE) is a rare progressive neurodegenerative disease caused by measles virus variants (SSPE viruses) that results in eventual death. Amino acid substitution(s) in the viral fusion (F) protein are key for viral propagation in the brain in a cell-to-cell manner, a specific trait of SSPE viruses, leading to neuropathogenicity. In this study, we passaged an SSPE virus in cultured human neuronal cells and isolated an adapted virus that propagated more efficiently in neuronal cells and exhibited increased cell-to-cell fusion. Contrary to our expectation, the virus harbored mutations in the large protein, a viral RNA-dependent RNA polymerase, and in the phosphoprotein, its co-factor, rather than in the F protein. Our results imply that upregulated RNA polymerase activity, which increases F protein expression and cell-to-cell fusion, could be a viral factor that provides a growth advantage and contributes to the adaptation of SSPE viruses to neuronal cells.
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Sakamoto et al. (2022) studied Subacute sclerosing panencephalitis (SSPE). Passaging SSPE virus in cultured human neuronal cells was evaluated on Viral adaptation and mutations. Passaging SSPE virus in human neuronal cells led to viral adaptation driven by mutations in the RNA polymerase and phosphoprotein, upregulating polymerase activity and increasing cell-to-cell fusion.
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