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Characterization of Adenovirus 5 E1A Exon 1 Deletion Mutants in the Viral Replicative Cycle
Human adenovirus infection is driven by Early region 1A (E1A) proteins, which are the first proteins expressed following the delivery of the viral genome to the cellular nucleus. E1A is responsible for reprogramming the infected cell to support virus replication alongside the activation of expressio...
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/PMC7077205/ https://www.ncbi.nlm.nih.gov/pubmed/32075072 http://dx.doi.org/10.3390/v12020213 |
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author | Costa, Rita Akkerman, Nikolas Graves, Drayson Crisostomo, Leandro Bachus, Scott Pelka, Peter |
author_facet | Costa, Rita Akkerman, Nikolas Graves, Drayson Crisostomo, Leandro Bachus, Scott Pelka, Peter |
author_sort | Costa, Rita |
collection | PubMed |
description | Human adenovirus infection is driven by Early region 1A (E1A) proteins, which are the first proteins expressed following the delivery of the viral genome to the cellular nucleus. E1A is responsible for reprogramming the infected cell to support virus replication alongside the activation of expression of all viral transcriptional units during the course of the infection. Although E1A has been extensively studied, most of these studies have focused on understanding the conserved region functions outside of a full infection. Here, we investigated the effects of small deletions in E1A exon 1 on the viral replicative cycle. Almost all deletions were found to have a negative impact on viral replication with the exception of one deletion found in the mutant dl1106, which replicated better than the wild-type E1A expressing dl309. In addition to growth, we assessed the virus mutants for genome replication, induction of the cytopathic effect, gene and protein expression, sub-cellular localization of E1A mutant proteins, induction of cellular S-phase, and activation of S-phase specific cellular genes. Importantly, our study found that virus replication is likely limited by host-specific factors, rather than specific viral aspects such as the ability to replicate genomes or express late proteins, after a certain level of these has been expressed. Furthermore, we show that mutants outside of the conserved regions have significant influence on viral fitness. Overall, our study is the first comprehensive evaluation of the dl1100 series of exon 1 E1A deletion mutants in viral fitness and provides important insights into the contribution that E1A makes to viral replication in normal human cells. |
format | Online Article Text |
id | pubmed-7077205 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-70772052020-03-20 Characterization of Adenovirus 5 E1A Exon 1 Deletion Mutants in the Viral Replicative Cycle Costa, Rita Akkerman, Nikolas Graves, Drayson Crisostomo, Leandro Bachus, Scott Pelka, Peter Viruses Article Human adenovirus infection is driven by Early region 1A (E1A) proteins, which are the first proteins expressed following the delivery of the viral genome to the cellular nucleus. E1A is responsible for reprogramming the infected cell to support virus replication alongside the activation of expression of all viral transcriptional units during the course of the infection. Although E1A has been extensively studied, most of these studies have focused on understanding the conserved region functions outside of a full infection. Here, we investigated the effects of small deletions in E1A exon 1 on the viral replicative cycle. Almost all deletions were found to have a negative impact on viral replication with the exception of one deletion found in the mutant dl1106, which replicated better than the wild-type E1A expressing dl309. In addition to growth, we assessed the virus mutants for genome replication, induction of the cytopathic effect, gene and protein expression, sub-cellular localization of E1A mutant proteins, induction of cellular S-phase, and activation of S-phase specific cellular genes. Importantly, our study found that virus replication is likely limited by host-specific factors, rather than specific viral aspects such as the ability to replicate genomes or express late proteins, after a certain level of these has been expressed. Furthermore, we show that mutants outside of the conserved regions have significant influence on viral fitness. Overall, our study is the first comprehensive evaluation of the dl1100 series of exon 1 E1A deletion mutants in viral fitness and provides important insights into the contribution that E1A makes to viral replication in normal human cells. MDPI 2020-02-14 /pmc/articles/PMC7077205/ /pubmed/32075072 http://dx.doi.org/10.3390/v12020213 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 | Article Costa, Rita Akkerman, Nikolas Graves, Drayson Crisostomo, Leandro Bachus, Scott Pelka, Peter Characterization of Adenovirus 5 E1A Exon 1 Deletion Mutants in the Viral Replicative Cycle |
title | Characterization of Adenovirus 5 E1A Exon 1 Deletion Mutants in the Viral Replicative Cycle |
title_full | Characterization of Adenovirus 5 E1A Exon 1 Deletion Mutants in the Viral Replicative Cycle |
title_fullStr | Characterization of Adenovirus 5 E1A Exon 1 Deletion Mutants in the Viral Replicative Cycle |
title_full_unstemmed | Characterization of Adenovirus 5 E1A Exon 1 Deletion Mutants in the Viral Replicative Cycle |
title_short | Characterization of Adenovirus 5 E1A Exon 1 Deletion Mutants in the Viral Replicative Cycle |
title_sort | characterization of adenovirus 5 e1a exon 1 deletion mutants in the viral replicative cycle |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7077205/ https://www.ncbi.nlm.nih.gov/pubmed/32075072 http://dx.doi.org/10.3390/v12020213 |
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