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Evaluation in Swine of a Recombinant Georgia 2010 African Swine Fever Virus Lacking the I8L Gene
African swine fever virus (ASFV) is the causative agent of African swine fever, a disease currently causing significant economic losses in Europe and Asia. Specifically, the highly virulent ASFV strain Georgia 2010 (ASFV-G) is producing disease outbreaks in this large geographical region. The ASFV g...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7823879/ https://www.ncbi.nlm.nih.gov/pubmed/33383814 http://dx.doi.org/10.3390/v13010039 |
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author | Vuono, Elizabeth Ramirez-Medina, Elizabeth Pruitt, Sarah Rai, Ayushi Silva, Ediane Espinoza, Nallely Zhu, James Velazquez-Salinas, Lauro Gladue, Douglas P. Borca, Manuel V. |
author_facet | Vuono, Elizabeth Ramirez-Medina, Elizabeth Pruitt, Sarah Rai, Ayushi Silva, Ediane Espinoza, Nallely Zhu, James Velazquez-Salinas, Lauro Gladue, Douglas P. Borca, Manuel V. |
author_sort | Vuono, Elizabeth |
collection | PubMed |
description | African swine fever virus (ASFV) is the causative agent of African swine fever, a disease currently causing significant economic losses in Europe and Asia. Specifically, the highly virulent ASFV strain Georgia 2010 (ASFV-G) is producing disease outbreaks in this large geographical region. The ASFV genome encodes for over 150 genes, most of which are still not experimentally characterized. I8L is a highly conserved gene that has not been studied beyond its initial description as a virus ORF. Transcriptional analysis of swine macrophages infected with ASFV-G demonstrated that the I8L gene is transcribed early during the virus replication cycle. To assess the importance of I8L during ASFV-G replication in vitro and in vivo, as well as its role in virus virulence in domestic swine, we developed a recombinant virus lacking the I8L gene (ASFV-G-ΔI8L). Replication of ASFV-G-ΔI8L was similar to parental ASFV-G replication in primary swine macrophage cultures, suggesting that the I8L gene is not essential for ASFV-G replication in vitro. Similarly, replication of ASFV-G-ΔI8L in swine intramuscularly inoculated with 10(2) HAD(50) displayed replication kinetics similar to ASFV-G. In addition, animals inoculated with ASFV-G-ΔI8L presented with a clinical disease indistinguishable from that induced by the same dose of the virulent parental ASFV-G isolate. We conclude that deletion of the I8L gene from ASFV-G does not affect virus replication in vitro or in vivo, nor changes the disease outcome in swine. |
format | Online Article Text |
id | pubmed-7823879 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-78238792021-01-24 Evaluation in Swine of a Recombinant Georgia 2010 African Swine Fever Virus Lacking the I8L Gene Vuono, Elizabeth Ramirez-Medina, Elizabeth Pruitt, Sarah Rai, Ayushi Silva, Ediane Espinoza, Nallely Zhu, James Velazquez-Salinas, Lauro Gladue, Douglas P. Borca, Manuel V. Viruses Brief Report African swine fever virus (ASFV) is the causative agent of African swine fever, a disease currently causing significant economic losses in Europe and Asia. Specifically, the highly virulent ASFV strain Georgia 2010 (ASFV-G) is producing disease outbreaks in this large geographical region. The ASFV genome encodes for over 150 genes, most of which are still not experimentally characterized. I8L is a highly conserved gene that has not been studied beyond its initial description as a virus ORF. Transcriptional analysis of swine macrophages infected with ASFV-G demonstrated that the I8L gene is transcribed early during the virus replication cycle. To assess the importance of I8L during ASFV-G replication in vitro and in vivo, as well as its role in virus virulence in domestic swine, we developed a recombinant virus lacking the I8L gene (ASFV-G-ΔI8L). Replication of ASFV-G-ΔI8L was similar to parental ASFV-G replication in primary swine macrophage cultures, suggesting that the I8L gene is not essential for ASFV-G replication in vitro. Similarly, replication of ASFV-G-ΔI8L in swine intramuscularly inoculated with 10(2) HAD(50) displayed replication kinetics similar to ASFV-G. In addition, animals inoculated with ASFV-G-ΔI8L presented with a clinical disease indistinguishable from that induced by the same dose of the virulent parental ASFV-G isolate. We conclude that deletion of the I8L gene from ASFV-G does not affect virus replication in vitro or in vivo, nor changes the disease outcome in swine. MDPI 2020-12-29 /pmc/articles/PMC7823879/ /pubmed/33383814 http://dx.doi.org/10.3390/v13010039 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Brief Report Vuono, Elizabeth Ramirez-Medina, Elizabeth Pruitt, Sarah Rai, Ayushi Silva, Ediane Espinoza, Nallely Zhu, James Velazquez-Salinas, Lauro Gladue, Douglas P. Borca, Manuel V. Evaluation in Swine of a Recombinant Georgia 2010 African Swine Fever Virus Lacking the I8L Gene |
title | Evaluation in Swine of a Recombinant Georgia 2010 African Swine Fever Virus Lacking the I8L Gene |
title_full | Evaluation in Swine of a Recombinant Georgia 2010 African Swine Fever Virus Lacking the I8L Gene |
title_fullStr | Evaluation in Swine of a Recombinant Georgia 2010 African Swine Fever Virus Lacking the I8L Gene |
title_full_unstemmed | Evaluation in Swine of a Recombinant Georgia 2010 African Swine Fever Virus Lacking the I8L Gene |
title_short | Evaluation in Swine of a Recombinant Georgia 2010 African Swine Fever Virus Lacking the I8L Gene |
title_sort | evaluation in swine of a recombinant georgia 2010 african swine fever virus lacking the i8l gene |
topic | Brief Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7823879/ https://www.ncbi.nlm.nih.gov/pubmed/33383814 http://dx.doi.org/10.3390/v13010039 |
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