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Expression of frog virus 3 genes is impaired in mammalian cell lines

Frog virus 3 (FV3) is a large DNA virus that is the prototypic member of the family Iridoviridae. To examine levels of FV3 gene expression we generated a polyclonal antibody against the FV3 protein 75L. Following a FV3 infection in fathead minnow (FHM) cells 75L was found in vesicles throughout the...

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Autores principales: Eaton, Heather E, Metcalf, Julie, Brunetti, Craig R
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2500002/
https://www.ncbi.nlm.nih.gov/pubmed/18644137
http://dx.doi.org/10.1186/1743-422X-5-83
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author Eaton, Heather E
Metcalf, Julie
Brunetti, Craig R
author_facet Eaton, Heather E
Metcalf, Julie
Brunetti, Craig R
author_sort Eaton, Heather E
collection PubMed
description Frog virus 3 (FV3) is a large DNA virus that is the prototypic member of the family Iridoviridae. To examine levels of FV3 gene expression we generated a polyclonal antibody against the FV3 protein 75L. Following a FV3 infection in fathead minnow (FHM) cells 75L was found in vesicles throughout the cytoplasm as early as 3 hours post-infection. While 75L expressed strongly in FHM cells, our findings revealed no 75L expression in mammalian cells lines despite evidence of a FV3 infection. One explanation for the lack of gene expression in mammalian cell lines may be inefficient codon usage. As a result, 75L was codon optimized and transfection of the codon optimized construct resulted in detectable expression in mammalian cells. Therefore, although FV3 can infect and replicate in mammalian cell lines, the virus may not express its full complement of genes due to inefficient codon usage in mammalian species.
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spelling pubmed-25000022008-08-07 Expression of frog virus 3 genes is impaired in mammalian cell lines Eaton, Heather E Metcalf, Julie Brunetti, Craig R Virol J Short Report Frog virus 3 (FV3) is a large DNA virus that is the prototypic member of the family Iridoviridae. To examine levels of FV3 gene expression we generated a polyclonal antibody against the FV3 protein 75L. Following a FV3 infection in fathead minnow (FHM) cells 75L was found in vesicles throughout the cytoplasm as early as 3 hours post-infection. While 75L expressed strongly in FHM cells, our findings revealed no 75L expression in mammalian cells lines despite evidence of a FV3 infection. One explanation for the lack of gene expression in mammalian cell lines may be inefficient codon usage. As a result, 75L was codon optimized and transfection of the codon optimized construct resulted in detectable expression in mammalian cells. Therefore, although FV3 can infect and replicate in mammalian cell lines, the virus may not express its full complement of genes due to inefficient codon usage in mammalian species. BioMed Central 2008-07-21 /pmc/articles/PMC2500002/ /pubmed/18644137 http://dx.doi.org/10.1186/1743-422X-5-83 Text en Copyright © 2008 Eaton et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Report
Eaton, Heather E
Metcalf, Julie
Brunetti, Craig R
Expression of frog virus 3 genes is impaired in mammalian cell lines
title Expression of frog virus 3 genes is impaired in mammalian cell lines
title_full Expression of frog virus 3 genes is impaired in mammalian cell lines
title_fullStr Expression of frog virus 3 genes is impaired in mammalian cell lines
title_full_unstemmed Expression of frog virus 3 genes is impaired in mammalian cell lines
title_short Expression of frog virus 3 genes is impaired in mammalian cell lines
title_sort expression of frog virus 3 genes is impaired in mammalian cell lines
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2500002/
https://www.ncbi.nlm.nih.gov/pubmed/18644137
http://dx.doi.org/10.1186/1743-422X-5-83
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