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Generating Recombinant Avian Herpesvirus Vectors with CRISPR/Cas9 Gene Editing
Published on: January 7, 2019
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CRISPR/Cas9, a powerful tool to target human herpesviruses
Ferdy R van Diemen1,2, Robert Jan Lebbink1
1Department of Medical Microbiology, University Medical Center Utrecht, Utrecht, The Netherlands.
Cellular Microbiology
|November 19, 2016
Summary
Genome editing with CRISPR/Cas9 shows promise for treating lifelong herpesvirus infections. This technology targets latent viruses, offering potential cures where traditional drugs fail.
Area of Science:
- Virology
- Molecular Biology
- Gene Editing
Background:
- Herpesviruses infect over 90% of adults, establishing lifelong latent infections.
- Latent herpesviruses cause diseases like cold sores, shingles, and cancers.
- Current treatments are ineffective against latent herpesviruses, failing to clear infections.
Purpose of the Study:
- To review CRISPR/Cas9 applications in herpesvirus research.
- To discuss the therapeutic potential of CRISPR/Cas9 for herpesvirus infections.
Main Methods:
- Review of recent literature on CRISPR/Cas9 system applications.
- Analysis of CRISPR/Cas9's potential for targeting productive and latent herpesviruses.
Main Results:
- CRISPR/Cas9 facilitates herpesvirus research.
- CRISPR/Cas9 demonstrates potential for treating herpesvirus infections.
Conclusions:
- CRISPR/Cas9 offers a novel approach to combatting herpesviruses.
- Genome engineering may provide a cure for previously incurable herpesvirus infections.
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