No evidence of a death-like function for species B1 human adenovirus type 3 E3-9K during A549 cell line infection
<p>Abstract</p> <p>Background</p> <p>Subspecies B1 human adenoviruses (HAdV-B1) are prevalent respiratory pathogens. Compared to their species C (HAdV-C) counterparts, relatively little work has been devoted to the characterization of their unique molecular biology. The...
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doaj-32add4b6a20941a3beeb22f2bac717002020-11-25T01:44:09ZengBMCBMC Research Notes1756-05002012-08-015142910.1186/1756-0500-5-429No evidence of a death-like function for species B1 human adenovirus type 3 E3-9K during A549 cell line infectionFrietze Kathryn MCampos Samuel KKajon Adriana E<p>Abstract</p> <p>Background</p> <p>Subspecies B1 human adenoviruses (HAdV-B1) are prevalent respiratory pathogens. Compared to their species C (HAdV-C) counterparts, relatively little work has been devoted to the characterization of their unique molecular biology. The early region 3 (E3) transcription unit is an interesting target for future efforts because of its species-specific diversity in genetic content among adenoviruses. This diversity is particularly significant for the subset of E3-encoded products that are membrane glycoproteins and may account for the distinct pathobiology of the different human adenovirus species. In order to understand the role of HAdV-B-specific genes in viral pathogenesis, we initiated the characterization of unique E3 genes. As a continuation of our efforts to define the function encoded in the highly polymorphic ORF E3-10.9K and testing the hypothesis that the E3-10.9K protein orthologs with a hydrophobic domain contribute to the efficient release of viral progeny, we generated HAdV-3 mutant viruses unable to express E3-10.9K ortholog E3-9K and examined their ability to grow, disseminate, and egress in cell culture.</p> <p>Results</p> <p>No differences were observed in the kinetics of infected cell death, and virus progeny release or in the plaque size and dissemination phenotypes between cells infected with HAdV-3 E3-9K mutants or the parental virus. The ectopic expression of E3-10.9K orthologs with a hydrophobic domain did not compromise cell viability.</p> <p>Conclusions</p> <p>Our data show that despite the remarkable similarities with HAdV-C E3-11.6K, HAdV-B1 ORF E3-10.9K does not encode a product with a “death-like” biological activity.</p> http://www.biomedcentral.com/1756-0500/5/429AdenovirusE3 regionGenetic polymorphismVirus egress |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Frietze Kathryn M Campos Samuel K Kajon Adriana E |
spellingShingle |
Frietze Kathryn M Campos Samuel K Kajon Adriana E No evidence of a death-like function for species B1 human adenovirus type 3 E3-9K during A549 cell line infection BMC Research Notes Adenovirus E3 region Genetic polymorphism Virus egress |
author_facet |
Frietze Kathryn M Campos Samuel K Kajon Adriana E |
author_sort |
Frietze Kathryn M |
title |
No evidence of a death-like function for species B1 human adenovirus type 3 E3-9K during A549 cell line infection |
title_short |
No evidence of a death-like function for species B1 human adenovirus type 3 E3-9K during A549 cell line infection |
title_full |
No evidence of a death-like function for species B1 human adenovirus type 3 E3-9K during A549 cell line infection |
title_fullStr |
No evidence of a death-like function for species B1 human adenovirus type 3 E3-9K during A549 cell line infection |
title_full_unstemmed |
No evidence of a death-like function for species B1 human adenovirus type 3 E3-9K during A549 cell line infection |
title_sort |
no evidence of a death-like function for species b1 human adenovirus type 3 e3-9k during a549 cell line infection |
publisher |
BMC |
series |
BMC Research Notes |
issn |
1756-0500 |
publishDate |
2012-08-01 |
description |
<p>Abstract</p> <p>Background</p> <p>Subspecies B1 human adenoviruses (HAdV-B1) are prevalent respiratory pathogens. Compared to their species C (HAdV-C) counterparts, relatively little work has been devoted to the characterization of their unique molecular biology. The early region 3 (E3) transcription unit is an interesting target for future efforts because of its species-specific diversity in genetic content among adenoviruses. This diversity is particularly significant for the subset of E3-encoded products that are membrane glycoproteins and may account for the distinct pathobiology of the different human adenovirus species. In order to understand the role of HAdV-B-specific genes in viral pathogenesis, we initiated the characterization of unique E3 genes. As a continuation of our efforts to define the function encoded in the highly polymorphic ORF E3-10.9K and testing the hypothesis that the E3-10.9K protein orthologs with a hydrophobic domain contribute to the efficient release of viral progeny, we generated HAdV-3 mutant viruses unable to express E3-10.9K ortholog E3-9K and examined their ability to grow, disseminate, and egress in cell culture.</p> <p>Results</p> <p>No differences were observed in the kinetics of infected cell death, and virus progeny release or in the plaque size and dissemination phenotypes between cells infected with HAdV-3 E3-9K mutants or the parental virus. The ectopic expression of E3-10.9K orthologs with a hydrophobic domain did not compromise cell viability.</p> <p>Conclusions</p> <p>Our data show that despite the remarkable similarities with HAdV-C E3-11.6K, HAdV-B1 ORF E3-10.9K does not encode a product with a “death-like” biological activity.</p> |
topic |
Adenovirus E3 region Genetic polymorphism Virus egress |
url |
http://www.biomedcentral.com/1756-0500/5/429 |
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