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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...

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Autores principales: Vuono, Elizabeth, Ramirez-Medina, Elizabeth, Pruitt, Sarah, Rai, Ayushi, Silva, Ediane, Espinoza, Nallely, Zhu, James, Velazquez-Salinas, Lauro, Gladue, Douglas P., Borca, Manuel V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
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.
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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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