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CRISPR-Cas9, a tool to efficiently increase the development of recombinant African swine fever viruses
African swine fever virus (ASFV) causes a highly contagious disease called African swine fever. This disease is often lethal for domestic pigs, causing extensive losses for the swine industry. ASFV is a large and complex double stranded DNA virus. Currently there is no commercially available treatme...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5816594/ https://www.ncbi.nlm.nih.gov/pubmed/29453406 http://dx.doi.org/10.1038/s41598-018-21575-8 |
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author | Borca, Manuel V. Holinka, Lauren G. Berggren, Keith A. Gladue, Douglas P. |
author_facet | Borca, Manuel V. Holinka, Lauren G. Berggren, Keith A. Gladue, Douglas P. |
author_sort | Borca, Manuel V. |
collection | PubMed |
description | African swine fever virus (ASFV) causes a highly contagious disease called African swine fever. This disease is often lethal for domestic pigs, causing extensive losses for the swine industry. ASFV is a large and complex double stranded DNA virus. Currently there is no commercially available treatment or vaccine to prevent this devastating disease. Development of recombinant ASFV for producing live-attenuated vaccines or studying the involvement of specific genes in virus virulence has relied on the relatively rare event of homologous recombination in primary swine macrophages, causing difficulty to purify the recombinant virus from the wild-type parental ASFV. Here we present the use of the CRISPR-Cas9 gene editing system as a more robust and efficient system to produce recombinant ASFVs. Using CRISPR-Cas9 a recombinant virus was efficiently developed by deleting the non-essential gene 8-DR from the genome of the highly virulent field strain Georgia07 using swine macrophages as cell substrate. |
format | Online Article Text |
id | pubmed-5816594 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58165942018-02-21 CRISPR-Cas9, a tool to efficiently increase the development of recombinant African swine fever viruses Borca, Manuel V. Holinka, Lauren G. Berggren, Keith A. Gladue, Douglas P. Sci Rep Article African swine fever virus (ASFV) causes a highly contagious disease called African swine fever. This disease is often lethal for domestic pigs, causing extensive losses for the swine industry. ASFV is a large and complex double stranded DNA virus. Currently there is no commercially available treatment or vaccine to prevent this devastating disease. Development of recombinant ASFV for producing live-attenuated vaccines or studying the involvement of specific genes in virus virulence has relied on the relatively rare event of homologous recombination in primary swine macrophages, causing difficulty to purify the recombinant virus from the wild-type parental ASFV. Here we present the use of the CRISPR-Cas9 gene editing system as a more robust and efficient system to produce recombinant ASFVs. Using CRISPR-Cas9 a recombinant virus was efficiently developed by deleting the non-essential gene 8-DR from the genome of the highly virulent field strain Georgia07 using swine macrophages as cell substrate. Nature Publishing Group UK 2018-02-16 /pmc/articles/PMC5816594/ /pubmed/29453406 http://dx.doi.org/10.1038/s41598-018-21575-8 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Borca, Manuel V. Holinka, Lauren G. Berggren, Keith A. Gladue, Douglas P. CRISPR-Cas9, a tool to efficiently increase the development of recombinant African swine fever viruses |
title | CRISPR-Cas9, a tool to efficiently increase the development of recombinant African swine fever viruses |
title_full | CRISPR-Cas9, a tool to efficiently increase the development of recombinant African swine fever viruses |
title_fullStr | CRISPR-Cas9, a tool to efficiently increase the development of recombinant African swine fever viruses |
title_full_unstemmed | CRISPR-Cas9, a tool to efficiently increase the development of recombinant African swine fever viruses |
title_short | CRISPR-Cas9, a tool to efficiently increase the development of recombinant African swine fever viruses |
title_sort | crispr-cas9, a tool to efficiently increase the development of recombinant african swine fever viruses |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5816594/ https://www.ncbi.nlm.nih.gov/pubmed/29453406 http://dx.doi.org/10.1038/s41598-018-21575-8 |
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