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Role of RNA G-Quadruplexes in the Japanese Encephalitis Virus Genome and Their Recognition as Prospective Antiviral Targets. | LitMetric

AI Article Synopsis

  • The study highlights the emerging interest in G-quadruplexes (GQs) beyond cancer and neurodegenerative diseases, focusing on their roles in viral genomes, particularly in human pathogens like the Japanese encephalitis virus (JEV).
  • Researchers identified eight potential GQ-forming motifs in JEV that are important for the virus's replication and assembly and confirmed their stability and ability to form GQs through various assays.
  • The compound BRACO-19 was found to bind effectively to these GQs, exhibiting antiviral properties by reducing viral replication and protein expression, underscoring the potential of GQs as targets for antiviral strategies against JEV.

Article Abstract

G-quadruplexes (GQs) have been primarily studied in the context of cancer and neurodegenerative pathologies. However, recent research has shifted focus to their existence and functional roles in viral genomes, revealing GQ-regulated key pathways in various human pathogenic viruses. While GQ structures have been reported in the genomes of emerging and re-emerging viruses, RNA viruses have been understudied compared to DNA viruses, including notable examples such as human immunodeficiency virus-1, hepatitis C virus, Ebola virus, Nipah virus, Zika virus, and SARS-CoV-2. The flavivirus family, comprising the Japanese encephalitis virus (JEV), poses a significant global threat due to recurring outbreaks yet lacks approved antivirals. In this study, we identified and characterized eight putative G-quadruplex-forming motifs within essential genes involved in genome replication, assembly, and internalization in the host cell, conserved across different JEV isolates. The formation and stability of these motifs were validated through a multitude of biophysical and cell-based assays. The interaction and binding affinity of these motifs with the known GQ-binding ligand BRACO-19 were supported by biophysical assays, confirming the capability of these motifs to form GQ structures. Notably, BRACO-19 also exerted antiviral properties through reduction of viral replication and infectious virus titers as well as inhibition of viral protein expression, as evaluated by the cell-based assays. This comprehensive molecular characterization of G-quadruplex structures within the JEV genome highlights their potential as promising antiviral targets for intervention strategies against JEV infection through GQ-specific ligands.

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Source
http://dx.doi.org/10.1021/acsinfecdis.4c00507DOI Listing

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