Virulence of tick-borne encephalitis virus is associated with intact conformational viral RNA structures in the variable region of the 3'-UTR.

Virus Res

Laboratory of Public Health, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo, Hokkaido 060-0818, Japan. Electronic address:

Published: May 2015

AI Article Synopsis

  • Tick-borne encephalitis virus (TBEV) is a serious virus that spreads between ticks and mammals and can cause severe neurological diseases in humans.
  • Researchers found that a specific deletion in the 3'-UTR variable region of TBEV affects its ability to cause disease, particularly in the Far-Eastern subtype.
  • Experiments with modified viruses in mouse models showed that these deletions increased the virus's virulence without impacting its replication in the brain, indicating that the structure of the variable region is crucial for TBEV's pathogenicity.

Article Abstract

Tick-borne encephalitis virus (TBEV) is maintained between ticks and mammals in nature and causes severe neurological disease in human. However, the mechanism of viral pathogenicity is unknown. Previously, we showed that the deletion in the variable region of the 3'-untranslated region (UTR) is involved in the pathogenicity of the strains from the Far-Eastern subtype of TBEV. To investigate the detailed function of the variable region, we constructed recombinant TBEV with partial deletions in the region. In a mouse model, the partial deletions drastically increased the virulence of the virus, with no effect on virus multiplication in mouse brain. Furthermore, the mutations did not affect the production of subgenomic flavivirus RNA from the 3'-UTR, and the induction of interferon (IFN) and IFN-stimulated genes. These data suggested that the conformational structure of the variable region is associated with the pathogenicity of the Far-Eastern subtype of TBEV. These findings provide a foundation for further research to identify the pathogenic mechanisms of TBEV.

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http://dx.doi.org/10.1016/j.virusres.2015.03.006DOI Listing

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