The human cytomegalovirus UL133-138 gene locus attenuates the lytic viral cycle in fibroblasts.

The genomes of HCMV clinical strains (e.g. FIX, TR, PH, etc) contain a 15 kb region that encodes 20 putative ORFs. The region, termed ULb', is lost after serial passage of virus in human foreskin fibroblast (HFF) cell culture. Compared to clinical strains, laboratory strains replicate faster an...

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Main Authors: Nirmal Dutta, Philip Lashmit, Jinxiang Yuan, Jeffery Meier, Mark F Stinski
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4370700?pdf=render
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spelling doaj-feb2276d065e423395532c298d04ba042020-11-25T02:15:27ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01103e012094610.1371/journal.pone.0120946The human cytomegalovirus UL133-138 gene locus attenuates the lytic viral cycle in fibroblasts.Nirmal DuttaPhilip LashmitJinxiang YuanJeffery MeierMark F StinskiThe genomes of HCMV clinical strains (e.g. FIX, TR, PH, etc) contain a 15 kb region that encodes 20 putative ORFs. The region, termed ULb', is lost after serial passage of virus in human foreskin fibroblast (HFF) cell culture. Compared to clinical strains, laboratory strains replicate faster and to higher titers of infectious virus. We made recombinant viruses with 22, 14, or 7 ORFs deleted from the ULb' region using FIX and TR as model clinical strains. We also introduced a stop codon into single ORFs between UL133 and UL138 to prevent protein expression. All deletions within ULb' and all stop codon mutants within the UL133 to UL138 region increased to varying degrees, viral major immediate early RNA and protein, DNA, and cell-free infectious virus compared to the wild type viruses. The wild type viral proteins slowed down the viral replication process along with cell-free infectious virus release from human fibroblast cells.http://europepmc.org/articles/PMC4370700?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Nirmal Dutta
Philip Lashmit
Jinxiang Yuan
Jeffery Meier
Mark F Stinski
spellingShingle Nirmal Dutta
Philip Lashmit
Jinxiang Yuan
Jeffery Meier
Mark F Stinski
The human cytomegalovirus UL133-138 gene locus attenuates the lytic viral cycle in fibroblasts.
PLoS ONE
author_facet Nirmal Dutta
Philip Lashmit
Jinxiang Yuan
Jeffery Meier
Mark F Stinski
author_sort Nirmal Dutta
title The human cytomegalovirus UL133-138 gene locus attenuates the lytic viral cycle in fibroblasts.
title_short The human cytomegalovirus UL133-138 gene locus attenuates the lytic viral cycle in fibroblasts.
title_full The human cytomegalovirus UL133-138 gene locus attenuates the lytic viral cycle in fibroblasts.
title_fullStr The human cytomegalovirus UL133-138 gene locus attenuates the lytic viral cycle in fibroblasts.
title_full_unstemmed The human cytomegalovirus UL133-138 gene locus attenuates the lytic viral cycle in fibroblasts.
title_sort human cytomegalovirus ul133-138 gene locus attenuates the lytic viral cycle in fibroblasts.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description The genomes of HCMV clinical strains (e.g. FIX, TR, PH, etc) contain a 15 kb region that encodes 20 putative ORFs. The region, termed ULb', is lost after serial passage of virus in human foreskin fibroblast (HFF) cell culture. Compared to clinical strains, laboratory strains replicate faster and to higher titers of infectious virus. We made recombinant viruses with 22, 14, or 7 ORFs deleted from the ULb' region using FIX and TR as model clinical strains. We also introduced a stop codon into single ORFs between UL133 and UL138 to prevent protein expression. All deletions within ULb' and all stop codon mutants within the UL133 to UL138 region increased to varying degrees, viral major immediate early RNA and protein, DNA, and cell-free infectious virus compared to the wild type viruses. The wild type viral proteins slowed down the viral replication process along with cell-free infectious virus release from human fibroblast cells.
url http://europepmc.org/articles/PMC4370700?pdf=render
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