A CRISPR-Cas13b System Degrades SARS-CoV and SARS-CoV-2 RNA In Vitro.
CRISPR-Cas13b
SARS-CoV
SARS-CoV-2
antiviral development
Journal
Viruses
ISSN: 1999-4915
Titre abrégé: Viruses
Pays: Switzerland
ID NLM: 101509722
Informations de publication
Date de publication:
28 Sep 2024
28 Sep 2024
Historique:
received:
05
09
2024
revised:
25
09
2024
accepted:
27
09
2024
medline:
26
10
2024
pubmed:
26
10
2024
entrez:
26
10
2024
Statut:
epublish
Résumé
In a time of climate change, population growth, and globalization, the risk of viral spread has significantly increased. The 21st century has already witnessed outbreaks of Severe Acute Respiratory Syndrome virus (SARS-CoV), Severe Acute Respiratory Syndrome virus 2 (SARS-CoV-2), Ebola virus and Influenza virus, among others. Viruses rapidly adapt and evade human immune systems, complicating the development of effective antiviral countermeasures. Consequently, the need for novel antivirals resilient to viral mutations is urgent. In this study, we developed a CRISPR-Cas13b system to target SARS-CoV-2. Interestingly, this system was also efficient against SARS-CoV, demonstrating broad-spectrum potential. Our findings highlight CRISPR-Cas13b as a promising tool for antiviral therapeutics, underscoring its potential in RNA-virus-associated pandemic responses.
Identifiants
pubmed: 39459873
pii: v16101539
doi: 10.3390/v16101539
pii:
doi:
Substances chimiques
RNA, Viral
0
Antiviral Agents
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Karolinska Institutet
ID : FS-2022:0010
Organisme : Stiftelsen för Strategisk Forskning
ID : ID21-0086