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Neuropathogenicity of Two Saffold Virus Type 3 Isolates in Mouse Models
Osamu Kotani1,2, Asif Naeem3, Tadaki Suzuki1
1Department of Pathology, National Institute of Infectious Diseases, Tokyo, Japan.
Saffold virus type 3 (SAFV-3) shows mild neurovirulence and neurotropism in mice. Different strains infect distinct cells, impacting inflammation and demyelination, suggesting potential neuropathogenicity.
Area of Science:
- Virology
- Neuroscience
- Immunology
Background:
- Saffold virus (SAFV), a picornavirus, is linked to neurological conditions in children.
- The neuropathogenic potential of SAFV remains unclear.
Purpose of the Study:
- To evaluate the neuropathogenicity of two Saffold virus type 3 (SAFV-3) clinical isolates.
- To compare the virulence and cell tropism of aseptic meningitis (AM) and upper respiratory (UR) strains of SAFV-3.
Main Methods:
- Analysis of two SAFV-3 clinical isolates (AM and UR strains) in neonatal and young mice.
- Utilized virological, pathological, and immunological methods to assess virulence.
- Examined infectivity, neurotropism, neurovirulence, cell tropism, inflammation, demyelination, and seroconversion.
Main Results:
- Both SAFV-3 strains exhibited neurotropism and mild neurovirulence in neonatal mice.
- Strains differed in cell tropism: infecting neural progenitor and glial cells, with UR strain also infecting epithelial cells.
- UR strain caused prolonged brain/spinal cord inflammation and demyelination; AM strain showed higher cerebellar infectivity. UR strain induced seroconversion in young mice.
Conclusions:
- Both SAFV-3 isolates demonstrate neurotropism and mild neurovirulence with distinct cell tropisms.
- The mouse model effectively recapitulates potential neuropathogenicity of SAFV-3.
- Further research is warranted to understand SAFV's role in human neurological diseases.
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