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Genome Editing Strategies to Protect Livestock from Viral Infections

The livestock industry is constantly threatened by viral disease outbreaks, including infections with zoonotic potential. While preventive vaccination is frequently applied, disease control and eradication also depend on strict biosecurity measures. Clustered regularly interspaced palindromic repeat...

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Autores principales: Söllner, Jenny-Helena, Mettenleiter, Thomas C., Petersen, Björn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8539128/
https://www.ncbi.nlm.nih.gov/pubmed/34696426
http://dx.doi.org/10.3390/v13101996
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author Söllner, Jenny-Helena
Mettenleiter, Thomas C.
Petersen, Björn
author_facet Söllner, Jenny-Helena
Mettenleiter, Thomas C.
Petersen, Björn
author_sort Söllner, Jenny-Helena
collection PubMed
description The livestock industry is constantly threatened by viral disease outbreaks, including infections with zoonotic potential. While preventive vaccination is frequently applied, disease control and eradication also depend on strict biosecurity measures. Clustered regularly interspaced palindromic repeats (CRISPR) and associated proteins (Cas) have been repurposed as genome editors to induce targeted double-strand breaks at almost any location in the genome. Thus, CRISPR/Cas genome editors can also be utilized to generate disease-resistant or resilient livestock, develop vaccines, and further understand virus–host interactions. Genes of interest in animals and viruses can be targeted to understand their functions during infection. Furthermore, transgenic animals expressing CRISPR/Cas can be generated to target the viral genome upon infection. Genetically modified livestock can thereby reduce disease outbreaks and decrease zoonotic threats.
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spelling pubmed-85391282021-10-24 Genome Editing Strategies to Protect Livestock from Viral Infections Söllner, Jenny-Helena Mettenleiter, Thomas C. Petersen, Björn Viruses Review The livestock industry is constantly threatened by viral disease outbreaks, including infections with zoonotic potential. While preventive vaccination is frequently applied, disease control and eradication also depend on strict biosecurity measures. Clustered regularly interspaced palindromic repeats (CRISPR) and associated proteins (Cas) have been repurposed as genome editors to induce targeted double-strand breaks at almost any location in the genome. Thus, CRISPR/Cas genome editors can also be utilized to generate disease-resistant or resilient livestock, develop vaccines, and further understand virus–host interactions. Genes of interest in animals and viruses can be targeted to understand their functions during infection. Furthermore, transgenic animals expressing CRISPR/Cas can be generated to target the viral genome upon infection. Genetically modified livestock can thereby reduce disease outbreaks and decrease zoonotic threats. MDPI 2021-10-04 /pmc/articles/PMC8539128/ /pubmed/34696426 http://dx.doi.org/10.3390/v13101996 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Söllner, Jenny-Helena
Mettenleiter, Thomas C.
Petersen, Björn
Genome Editing Strategies to Protect Livestock from Viral Infections
title Genome Editing Strategies to Protect Livestock from Viral Infections
title_full Genome Editing Strategies to Protect Livestock from Viral Infections
title_fullStr Genome Editing Strategies to Protect Livestock from Viral Infections
title_full_unstemmed Genome Editing Strategies to Protect Livestock from Viral Infections
title_short Genome Editing Strategies to Protect Livestock from Viral Infections
title_sort genome editing strategies to protect livestock from viral infections
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8539128/
https://www.ncbi.nlm.nih.gov/pubmed/34696426
http://dx.doi.org/10.3390/v13101996
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