Analysis of the nucleotide sequence of the guinea pig cytomegalovirus (GPCMV) genome

<p>Abstract</p> <p>In this report we describe the genomic sequence of guinea pig cytomegalovirus (GPCMV) assembled from a tissue culture-derived bacterial artificial chromosome clone, plasmid clones of viral restriction fragments, and direct PCR sequencing of viral DNA. The GPCMV g...

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Main Authors: Cui Xiaohong, Date Shailesh V, Choi K, McGregor Alistair, Schleiss Mark R, McVoy Michael A
Format: Article
Language:English
Published: BMC 2008-11-01
Series:Virology Journal
Online Access:http://www.virologyj.com/content/5/1/139
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spelling doaj-e9ac1ede981a4ba5905e034813d146902020-11-25T02:16:12ZengBMCVirology Journal1743-422X2008-11-015113910.1186/1743-422X-5-139Analysis of the nucleotide sequence of the guinea pig cytomegalovirus (GPCMV) genomeCui XiaohongDate Shailesh VChoi KMcGregor AlistairSchleiss Mark RMcVoy Michael A<p>Abstract</p> <p>In this report we describe the genomic sequence of guinea pig cytomegalovirus (GPCMV) assembled from a tissue culture-derived bacterial artificial chromosome clone, plasmid clones of viral restriction fragments, and direct PCR sequencing of viral DNA. The GPCMV genome is 232,678 bp, excluding the terminal repeats, and has a GC content of 55%. A total of 105 open reading frames (ORFs) of > 100 amino acids with sequence and/or positional homology to other CMV ORFs were annotated. Positional and sequence homologs of human cytomegalovirus open reading frames <it>UL23 </it>through <it>UL122 </it>were identified. Homology with other cytomegaloviruses was most prominent in the central ~60% of the genome, with divergence of sequence and lack of conserved homologs at the respective genomic termini. Of interest, the GPCMV genome was found in many cases to bear stronger phylogenetic similarity to primate CMVs than to rodent CMVs. The sequence of GPCMV should facilitate vaccine and pathogenesis studies in this model of congenital CMV infection.</p> http://www.virologyj.com/content/5/1/139
collection DOAJ
language English
format Article
sources DOAJ
author Cui Xiaohong
Date Shailesh V
Choi K
McGregor Alistair
Schleiss Mark R
McVoy Michael A
spellingShingle Cui Xiaohong
Date Shailesh V
Choi K
McGregor Alistair
Schleiss Mark R
McVoy Michael A
Analysis of the nucleotide sequence of the guinea pig cytomegalovirus (GPCMV) genome
Virology Journal
author_facet Cui Xiaohong
Date Shailesh V
Choi K
McGregor Alistair
Schleiss Mark R
McVoy Michael A
author_sort Cui Xiaohong
title Analysis of the nucleotide sequence of the guinea pig cytomegalovirus (GPCMV) genome
title_short Analysis of the nucleotide sequence of the guinea pig cytomegalovirus (GPCMV) genome
title_full Analysis of the nucleotide sequence of the guinea pig cytomegalovirus (GPCMV) genome
title_fullStr Analysis of the nucleotide sequence of the guinea pig cytomegalovirus (GPCMV) genome
title_full_unstemmed Analysis of the nucleotide sequence of the guinea pig cytomegalovirus (GPCMV) genome
title_sort analysis of the nucleotide sequence of the guinea pig cytomegalovirus (gpcmv) genome
publisher BMC
series Virology Journal
issn 1743-422X
publishDate 2008-11-01
description <p>Abstract</p> <p>In this report we describe the genomic sequence of guinea pig cytomegalovirus (GPCMV) assembled from a tissue culture-derived bacterial artificial chromosome clone, plasmid clones of viral restriction fragments, and direct PCR sequencing of viral DNA. The GPCMV genome is 232,678 bp, excluding the terminal repeats, and has a GC content of 55%. A total of 105 open reading frames (ORFs) of > 100 amino acids with sequence and/or positional homology to other CMV ORFs were annotated. Positional and sequence homologs of human cytomegalovirus open reading frames <it>UL23 </it>through <it>UL122 </it>were identified. Homology with other cytomegaloviruses was most prominent in the central ~60% of the genome, with divergence of sequence and lack of conserved homologs at the respective genomic termini. Of interest, the GPCMV genome was found in many cases to bear stronger phylogenetic similarity to primate CMVs than to rodent CMVs. The sequence of GPCMV should facilitate vaccine and pathogenesis studies in this model of congenital CMV infection.</p>
url http://www.virologyj.com/content/5/1/139
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AT dateshaileshv analysisofthenucleotidesequenceoftheguineapigcytomegalovirusgpcmvgenome
AT choik analysisofthenucleotidesequenceoftheguineapigcytomegalovirusgpcmvgenome
AT mcgregoralistair analysisofthenucleotidesequenceoftheguineapigcytomegalovirusgpcmvgenome
AT schleissmarkr analysisofthenucleotidesequenceoftheguineapigcytomegalovirusgpcmvgenome
AT mcvoymichaela analysisofthenucleotidesequenceoftheguineapigcytomegalovirusgpcmvgenome
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