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Published on: December 29, 2015
[A highly-productive attenuated variant of Japanese encephalitis virus]
Abstract:
Attenuated strain of Japanese encephalitis virus (JEV), clone 3, has been isolated from suckling mouse brain cell cultures chronically infected with JEV Nakayama strain, clone 33. Clone 3 actively replicates in 9-day chicken fibroblast cultures and possessed an uncommon for a JE agent capacity of causing cytodestruction of 1-2-day monolayer of chicken embryo cells, accumulates in these cultures in high titers (9.0 lg PFU/ml and higher), and is characterized by a high antigenic activity and a wide spectrum of antigenic relationships. New biologic properties acquired by JEV over the course of its persistence were retained after 10 and more passages through suckling mouse brain.
Insights
A new Japanese encephalitis virus (JEV) strain, clone 3, shows enhanced replication and cell-damaging abilities in chicken cells. This attenuated JEV strain maintains its novel biological properties through multiple passages, indicating potential for vaccine development.
Area of Science:
- Virology
- Immunology
Background:
- Japanese encephalitis virus (JEV) is a significant cause of viral encephalitis globally.
- Development of effective JEV vaccines and antiviral strategies remains crucial.
Purpose of the Study:
- To characterize a novel attenuated strain of Japanese encephalitis virus (JEV), clone 3, derived from chronic infection.
- To evaluate the biological properties, including replication, cytopathogenicity, and antigenic characteristics, of this JEV clone.
Main Methods:
- Isolation of JEV clone 3 from chronically infected mouse brain cell cultures.
- Assessment of viral replication and cytodestruction in chicken fibroblast and embryo cell cultures.
- Quantification of viral titers and evaluation of antigenic activity and relationships.
Main Results:
- JEV clone 3 demonstrated active replication in chicken fibroblast cultures.
- This attenuated JEV strain exhibited significant cytodestructive capacity against chicken embryo cells.
- High viral titers (≥9.0 lg PFU/ml) and strong antigenic activity with broad antigenic relationships were observed.
- Acquired biological properties were stable over multiple passages in mouse brain.
Conclusions:
- JEV clone 3 possesses unique biological properties, including enhanced replication and cytopathogenicity.
- The stability of these properties suggests potential for further investigation in JEV research and vaccine development.
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