The application of CRISPR/Cas systems for antiviral therapy
File(s)fgeed-03-745559.pdf (886.06 KB)
Published version
Author(s)
Baddeley, Helen
Isalan, Mark
Type
Journal Article
Abstract
As CRISPR/Cas systems have been refined over time, there has been an effort to apply them to real world problems, such as developing sequence-targeted antiviral therapies. Viruses pose a major threat to humans and new tools are urgently needed to combat these rapidly mutating pathogens. Importantly, a variety of CRISPR systems have the potential to directly cleave DNA and RNA viral genomes, in a targeted and easily-adaptable manner, thus preventing or treating infections. This perspective article highlights recent studies using different Cas effectors against various RNA viruses causing acute infections in humans; a latent virus (HIV-1); a chronic virus (hepatitis B); and viruses infecting livestock and animal species of industrial importance. The outlook and remaining challenges are discussed, particularly in the context of tacking newly emerging viruses, such as SARS-CoV-2.
Date Issued
2021-10-13
Date Acceptance
2021-09-23
Citation
Frontiers in Genome Editing, 2021, 3
ISSN
2673-3439
Publisher
Frontiers Media
Journal / Book Title
Frontiers in Genome Editing
Volume
3
Copyright Statement
© 2021 Baddeley and Isalan. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
License URL
Sponsor
Biotechnology and Biological Sciences Research Council (BBSRC)
VolkwagenStiftung
Grant Number
BB/P020615/1
63062
Subjects
CRISPR
Cas13
Cas9
HIV
RNA virus
SARS-CoV-2
antiviral
hepatitis B
Publication Status
Published
Article Number
ARTN 745559