4.6 Review

Reverse Genetics and Artificial Replication Systems of Borna Disease Virus 1

Journal

VIRUSES-BASEL
Volume 14, Issue 10, Pages -

Publisher

MDPI
DOI: 10.3390/v14102236

Keywords

Borna disease virus; reverse genetics; orthobornaviruses; viral replication and transcription

Categories

Funding

  1. JSPS KAKENHI [JP19J23468, JP19K22530, JP20H05682, JP21K19909]
  2. JST START Project Promotion Type [JPMJST2113]
  3. JSPS Core-to-Core Program [JPJSCCA20190008]
  4. 2021 Kaketsuken Research grant
  5. Joint Usage/Research Center Program of the Institute for Life and Medical Sciences, Kyoto University

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This review summarizes the research progress on the characteristics and pathogenic mechanisms of Borna disease virus 1, a neurotropic virus. It points out that the mechanism by which the virus causes fatal encephalitis in humans is still unclear, and effective vaccines or antiviral drugs are currently lacking. Furthermore, it explores the recent progress in rescuing the virus using reverse genetics.
Borna disease virus 1 (BoDV-1) is a neurotropic RNA virus belonging to the family Bornaviridae within the order Mononegavirales. Whereas BoDV-1 causes neurological and behavioral disorders, called Borna disease (BD), in a wide range of mammals, its virulence in humans has been debated for several decades. However, a series of case reports in recent years have established the nature of BoDV-1 as a zoonotic pathogen that causes fatal encephalitis in humans. Although many virological properties of BoDV-1 have been revealed to date, the mechanism by which it causes fatal encephalitis in humans remains unclear. In addition, there are no effective vaccines or antiviral drugs that can be used in clinical practice. A reverse genetics approach to generating replication-competent recombinant viruses from full-length cDNA clones is a powerful tool that can be used to not only understand viral properties but also to develop vaccines and antiviral drugs. The rescue of recombinant BoDV-1 (rBoDV-1) was first reported in 2005. However, due to the slow nature of the replication of this virus, the rescue of high-titer rBoDV-1 required several months, limiting the use of this system. This review summarizes the history of the reverse genetics and artificial replication systems for orthobornaviruses and explores the recent progress in efforts to rescue rBoDV-1.

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