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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.
Afiliação
  • Asadbeigi A; Cancer Institute, Department of Medical Genetics, Faculty of Medicine, Tehran University of Medical Sciences (TUMS), Tehran 1417613151, Iran.
  • Bakhtiarizadeh MR; Department of Animal and Poultry Science, College of Aburaihan, University of Tehran, Tehran 3391653755, Iran.
  • Saffari M; Department of Medical Genetics, Faculty of Medicine, Tehran University of Medical Sciences (TUMS), Tehran 1417613151, Iran.
  • Modarressi MH; Department of Medical Genetics, Faculty of Medicine, Tehran University of Medical Sciences (TUMS), Tehran 1417613151, Iran.
  • Sadri N; Department of Microbiology and Immunology, Faculty of Veterinary Medicine, University of Tehran, Tehran 1419963111, Iran.
  • Kafi ZZ; Department of Microbiology and Immunology, Faculty of Veterinary Medicine, University of Tehran, Tehran 1419963111, Iran.
  • Fazilaty H; Department of Molecular Life Sciences, University of Zurich, 8057 Zurich, Switzerland.
  • Ghalyanchilangeroudi A; Department of Microbiology and Immunology, Faculty of Veterinary Medicine, University of Tehran, Tehran 1419963111, Iran.
  • Esmaeili H; Department of Microbiology and Immunology, Faculty of Veterinary Medicine, University of Tehran, Tehran 1419963111, Iran.
Mol Ther Nucleic Acids ; 35(3): 102235, 2024 Sep 10.
Article em En | MEDLINE | ID: mdl-39021763
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.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article