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Differentiation of the SH-SY5Y Human Neuroblastoma Cell Line
Published on: February 17, 2016
Viral morphogenesis and morphological changes in human neuronal cells following Tioman and Menangle virus infection
K C Yaiw1, A Hyatt, R Vandriel
1Department of Pathology, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia.
Abstract:
Tioman virus (TioPV) and Menangle virus (MenPV) are two antigenically and genetically related paramyxoviruses (genus: Rubulavirus, family: Paramyxoviridae) isolated from Peninsular Malaysia (2001) and Australia (1997), respectively. Both viruses are potential zoonotic agents. In the present study, the infectivity, growth kinetics, morphology and morphogenesis of these two paramyxoviruses in a human neuronal cell (SK-N-SH) line were investigated. Sub-confluent SK-N-SH cells were infected with TioPV and MenPV at similar multiplicity of infection. These cells were examined by conventional and immunoelectron microscopy, and virus titres in the supernatants were assayed. Syncytia were observed for both infections in SK-N-SH cells and were more pronounced during the early stages of TioPV infection. The TioPV titre increased consistently (10(1)) every 12 h after infection. In MenPV-infected cells, cellular material was frequently observed within budding virions, and microfilaments and microtubules were abundant. Viral budding was common, and extracellular MenPVs tended to be more pleomorphic compared to TioPVs, which appeared to be more spherical in appearance. The MenPV cytoplasmic viral inclusion appeared to be comparatively smaller, loose and interspersed with randomly scattered circle-like particles, whereas huge tubule-like cytoplasmic inclusions were observed in TioPV-infected cells. Both viruses also displayed different cellular pathology in the SK-N-SH cells. The intracellular ultrastructural characteristics of these two viruses in infected neuronal cells may allow them to be differentiated by electron microscopy.
Insights
Tioman virus (TioPV) and Menangle virus (MenPV) are related paramyxoviruses with zoonotic potential. Electron microscopy revealed distinct intracellular ultrastructural differences in infected human neuronal cells, aiding differentiation.
Area of Science:
- Virology
- Cell Biology
- Neuroscience
Background:
- Tioman virus (TioPV) and Menangle virus (MenPV) are antigenically and genetically related Rubulavirus paramyxoviruses.
- Both TioPV and MenPV are potential zoonotic agents, necessitating further characterization.
- Human neuronal cell lines offer a model for studying viral interactions with neural tissue.
Purpose of the Study:
- To investigate and compare the infectivity, growth kinetics, morphology, and morphogenesis of TioPV and MenPV.
- To examine the effects of TioPV and MenPV infection on a human neuronal cell (SK-N-SH) line.
- To identify potential ultrastructural markers for differentiating TioPV and MenPV in infected neuronal cells.
Main Methods:
- Infection of sub-confluent SK-N-SH cells with TioPV and MenPV at a similar multiplicity of infection.
- Analysis using conventional and immunoelectron microscopy to assess viral morphology and cellular changes.
- Assay of virus titres in cell culture supernatants to determine growth kinetics.
Main Results:
- Syncytia formation observed in both TioPV and MenPV infected SK-N-SH cells, more pronounced in early TioPV infection.
- Distinct differences in viral morphology and intracellular inclusions: TioPV showed spherical virions and large tubule-like inclusions, while MenPV exhibited pleomorphic virions with smaller, interspersed inclusions.
- Differential cellular pathology and ultrastructural characteristics observed between TioPV and MenPV infections in neuronal cells.
Conclusions:
- TioPV and MenPV exhibit distinct intracellular ultrastructural characteristics within infected human neuronal cells.
- Electron microscopy can differentiate between TioPV and MenPV based on their unique morphologies and inclusion bodies.
- These findings contribute to understanding paramyxovirus-host interactions in neuronal cells and aid in viral diagnostics.
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