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Evaluation of an ASFV RNA Helicase Gene A859L for Virus Replication and Swine Virulence

African swine fever virus (ASFV) is producing a devastating pandemic that, since 2007, has spread to a contiguous geographical area from central Europe to Asia. In July 2021, ASFV was detected in the Dominican Republic, the first report of the disease in the Americas in more than 40 years. ASFV is a...

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Autores principales: Ramirez-Medina, Elizabeth, Vuono, Elizabeth A., Pruitt, Sarah, Rai, Ayushi, Espinoza, Nallely, Velazquez-Salinas, Lauro, Gladue, Douglas P., Borca, Manuel V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8777736/
https://www.ncbi.nlm.nih.gov/pubmed/35062213
http://dx.doi.org/10.3390/v14010010
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author Ramirez-Medina, Elizabeth
Vuono, Elizabeth A.
Pruitt, Sarah
Rai, Ayushi
Espinoza, Nallely
Velazquez-Salinas, Lauro
Gladue, Douglas P.
Borca, Manuel V.
author_facet Ramirez-Medina, Elizabeth
Vuono, Elizabeth A.
Pruitt, Sarah
Rai, Ayushi
Espinoza, Nallely
Velazquez-Salinas, Lauro
Gladue, Douglas P.
Borca, Manuel V.
author_sort Ramirez-Medina, Elizabeth
collection PubMed
description African swine fever virus (ASFV) is producing a devastating pandemic that, since 2007, has spread to a contiguous geographical area from central Europe to Asia. In July 2021, ASFV was detected in the Dominican Republic, the first report of the disease in the Americas in more than 40 years. ASFV is a large, highly complex virus harboring a large dsDNA genome that encodes for more than 150 genes. The majority of these genes have not been functionally characterized. Bioinformatics analysis predicts that ASFV gene A859L encodes for an RNA helicase, although its function has not yet been experimentally assessed. Here, we evaluated the role of the A859L gene during virus replication in cell cultures and during infection in swine. For that purpose, a recombinant virus (ASFV-G-∆A859L) harboring a deletion of the A859L gene was developed using the highly virulent ASFV Georgia (ASFV-G) isolate as a template. Recombinant ASFV-G-∆A859L replicates in swine macrophage cultures as efficiently as the parental virus ASFV-G, demonstrating that the A859L gene is non-essential for ASFV replication. Experimental infection of domestic pigs demonstrated that ASFV-G-∆A859L replicates as efficiently and induces a clinical disease indistinguishable from that caused by the parental ASFV-G. These studies conclude that the predicted RNA helicase gene A859L is not involved in the processes of virus replication or disease production in swine.
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spelling pubmed-87777362022-01-22 Evaluation of an ASFV RNA Helicase Gene A859L for Virus Replication and Swine Virulence Ramirez-Medina, Elizabeth Vuono, Elizabeth A. Pruitt, Sarah Rai, Ayushi Espinoza, Nallely Velazquez-Salinas, Lauro Gladue, Douglas P. Borca, Manuel V. Viruses Brief Report African swine fever virus (ASFV) is producing a devastating pandemic that, since 2007, has spread to a contiguous geographical area from central Europe to Asia. In July 2021, ASFV was detected in the Dominican Republic, the first report of the disease in the Americas in more than 40 years. ASFV is a large, highly complex virus harboring a large dsDNA genome that encodes for more than 150 genes. The majority of these genes have not been functionally characterized. Bioinformatics analysis predicts that ASFV gene A859L encodes for an RNA helicase, although its function has not yet been experimentally assessed. Here, we evaluated the role of the A859L gene during virus replication in cell cultures and during infection in swine. For that purpose, a recombinant virus (ASFV-G-∆A859L) harboring a deletion of the A859L gene was developed using the highly virulent ASFV Georgia (ASFV-G) isolate as a template. Recombinant ASFV-G-∆A859L replicates in swine macrophage cultures as efficiently as the parental virus ASFV-G, demonstrating that the A859L gene is non-essential for ASFV replication. Experimental infection of domestic pigs demonstrated that ASFV-G-∆A859L replicates as efficiently and induces a clinical disease indistinguishable from that caused by the parental ASFV-G. These studies conclude that the predicted RNA helicase gene A859L is not involved in the processes of virus replication or disease production in swine. MDPI 2021-12-21 /pmc/articles/PMC8777736/ /pubmed/35062213 http://dx.doi.org/10.3390/v14010010 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 Brief Report
Ramirez-Medina, Elizabeth
Vuono, Elizabeth A.
Pruitt, Sarah
Rai, Ayushi
Espinoza, Nallely
Velazquez-Salinas, Lauro
Gladue, Douglas P.
Borca, Manuel V.
Evaluation of an ASFV RNA Helicase Gene A859L for Virus Replication and Swine Virulence
title Evaluation of an ASFV RNA Helicase Gene A859L for Virus Replication and Swine Virulence
title_full Evaluation of an ASFV RNA Helicase Gene A859L for Virus Replication and Swine Virulence
title_fullStr Evaluation of an ASFV RNA Helicase Gene A859L for Virus Replication and Swine Virulence
title_full_unstemmed Evaluation of an ASFV RNA Helicase Gene A859L for Virus Replication and Swine Virulence
title_short Evaluation of an ASFV RNA Helicase Gene A859L for Virus Replication and Swine Virulence
title_sort evaluation of an asfv rna helicase gene a859l for virus replication and swine virulence
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8777736/
https://www.ncbi.nlm.nih.gov/pubmed/35062213
http://dx.doi.org/10.3390/v14010010
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