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The Application of CRISPR/Cas Systems for Antiviral Therapy

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,...

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Detalles Bibliográficos
Autores principales: Baddeley, Helen J. E., Isalan, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8549726/
https://www.ncbi.nlm.nih.gov/pubmed/34723245
http://dx.doi.org/10.3389/fgeed.2021.745559
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author Baddeley, Helen J. E.
Isalan, Mark
author_facet Baddeley, Helen J. E.
Isalan, Mark
author_sort Baddeley, Helen J. E.
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description 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.
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spelling pubmed-85497262021-10-29 The Application of CRISPR/Cas Systems for Antiviral Therapy Baddeley, Helen J. E. Isalan, Mark Front Genome Ed Genome Editing 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. Frontiers Media S.A. 2021-10-13 /pmc/articles/PMC8549726/ /pubmed/34723245 http://dx.doi.org/10.3389/fgeed.2021.745559 Text en Copyright © 2021 Baddeley and Isalan. https://creativecommons.org/licenses/by/4.0/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.
spellingShingle Genome Editing
Baddeley, Helen J. E.
Isalan, Mark
The Application of CRISPR/Cas Systems for Antiviral Therapy
title The Application of CRISPR/Cas Systems for Antiviral Therapy
title_full The Application of CRISPR/Cas Systems for Antiviral Therapy
title_fullStr The Application of CRISPR/Cas Systems for Antiviral Therapy
title_full_unstemmed The Application of CRISPR/Cas Systems for Antiviral Therapy
title_short The Application of CRISPR/Cas Systems for Antiviral Therapy
title_sort application of crispr/cas systems for antiviral therapy
topic Genome Editing
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8549726/
https://www.ncbi.nlm.nih.gov/pubmed/34723245
http://dx.doi.org/10.3389/fgeed.2021.745559
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