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Protection of animals against devastating RNA viruses using CRISPR-Cas13s

Asadbeigi, Adnan; Bakhtiarizadeh, Mohammad Reza; Saffari, Mojtaba; Modarressi, Mohammad Hossein; Sadri, Naser; Kafi, Zahra Ziafati; Fazilaty, Hassan; Ghalyanchilangeroudi, Arash; Esmaeili, Hossein (2024). Protection of animals against devastating RNA viruses using CRISPR-Cas13s. Molecular Therapy : Nucleic Acids, 35(3):102235.

Abstract

The intrinsic nature of CRISPR-Cas in conferring immunity to bacteria and archaea has been repurposed to combat pathogenic agents in mammalian and plant cells. In this regard, CRISPR-Cas13 systems have proved their remarkable potential for single-strand RNA viruses targeting. Here, different types of Cas13 orthologs were applied to knockdown foot-and-mouth disease virus (FMDV), a highly contagious disease of a wide variety of species with genetically diverse strains and is widely geographically distributed. Using programmable CRISPR RNAs capable of targeting conserved regions of the viral genome, all Cas13s from CRISPR system type VI (subtype A/B/D) could comprehensively target and repress different serotypes of FMDV virus. This approach has the potential to destroy all strains of a virus as targets the ultra-conserved regions of genome. We experimentally compared the silencing efficiency of CRISPR and RNAi by designing the most effective short hairpin RNAs according to our developed scoring system and observed comparable results. This study showed successful usage of various Cas13 enzymes for suppression of FMDV, which provides a flexible strategy to battle with other animal infectious RNA viruses, an underdeveloped field in the biotechnology scope.

Additional indexing

Item Type:Journal Article, refereed, original work
Communities & Collections:07 Faculty of Science > Institute of Molecular Life Sciences
Dewey Decimal Classification:570 Life sciences; biology
Scopus Subject Areas:Life Sciences > Molecular Medicine
Life Sciences > Drug Discovery
Language:English
Date:10 September 2024
Deposited On:17 Jan 2025 10:04
Last Modified:31 May 2025 01:37
Publisher:Nature Publishing Group
ISSN:2162-2531
OA Status:Gold
Free access at:Publisher DOI. An embargo period may apply.
Publisher DOI:https://doi.org/10.1016/j.omtn.2024.102235
PubMed ID:39021763
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