Inclusion of Antibodies to Cell Culture Media Preserves the Integrity of Genes Encoding RL13 and the Pentameric Complex Components During Fibroblast Passage of Human Cytomegalovirus

Propagation of human cytomegalovirus (CMV) in cultured cells results in genetic adaptations that confer improved growth in vitro and significant attenuation in vivo. Mutations in RL13 arise quickly, while mutations in the UL128-131A locus emerge later during fibroblast passage and disrupt formation...

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Main Authors: Amine Ourahmane, Xiaohong Cui, Li He, Meaghan Catron, Dirk P. Dittmer, Ahmed Al Qaffasaa, Mark R. Schleiss, Laura Hertel, Michael A. McVoy
Format: Article
Language:English
Published: MDPI AG 2019-03-01
Series:Viruses
Subjects:
Online Access:http://www.mdpi.com/1999-4915/11/3/221
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spelling doaj-367d344ca2924b69829d92b63a7925af2020-11-24T22:01:57ZengMDPI AGViruses1999-49152019-03-0111322110.3390/v11030221v11030221Inclusion of Antibodies to Cell Culture Media Preserves the Integrity of Genes Encoding RL13 and the Pentameric Complex Components During Fibroblast Passage of Human CytomegalovirusAmine Ourahmane0Xiaohong Cui1Li He2Meaghan Catron3Dirk P. Dittmer4Ahmed Al Qaffasaa5Mark R. Schleiss6Laura Hertel7Michael A. McVoy8Virginia Commonwealth University, Richmond, VA 23298, USAVirginia Commonwealth University, Richmond, VA 23298, USAVirginia Commonwealth University, Richmond, VA 23298, USAVirginia Commonwealth University, Richmond, VA 23298, USADepartment of Microbiology and Immunology, Lineberger Comprehensive Cancer Center Program in Global Oncology, Center for AIDS Research (CfAR), School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USAVirginia Commonwealth University, Richmond, VA 23298, USACenter for Infectious Diseases and Microbiology Translational Research, Division of Pediatric Infectious Diseases, Minneapolis, MN 55455, USAChildren’s Hospital Oakland Research Institute, Oakland, CA 94609, USAVirginia Commonwealth University, Richmond, VA 23298, USAPropagation of human cytomegalovirus (CMV) in cultured cells results in genetic adaptations that confer improved growth in vitro and significant attenuation in vivo. Mutations in RL13 arise quickly, while mutations in the UL128-131A locus emerge later during fibroblast passage and disrupt formation of a glycoprotein complex that is important for entry into epithelial and endothelial cells. As CMV replicates in the context of host antibodies in vivo, we reasoned that antibodies might mitigate the accumulation of adaptive mutations during cell culture passage. To test this, CMV in infant urine was used to infect replicate fibroblast cultures. One lineage was passaged in the absence of CMV-hyperimmuneglobulin (HIG) while the other was passaged with HIG in the culture medium. The former lost epithelial tropism and acquired mutations disrupting RL13 and UL131A expression, whereas the latter retained epithelial tropism and both gene loci remained intact after 22 passages. Additional mutations resulting in single amino acid changes also occurred in UL100 encoding glycoprotein M, UL102 encoding a subunit of the helicase/primase complex, and UL122 encoding the Immediate Early 2 protein. An epitheliotropic RL13+/UL131A+ virus was isolated by limiting dilution in the presence of HIG and expanded to produce a working stock sufficient to conduct cell tropism experiments. Thus, production of virus stocks by culture in the presence of antibodies may facilitate in vitro experiments using viruses that are genetically more authentic than previously available.http://www.mdpi.com/1999-4915/11/3/221cytomegaloviruscell cultureantibodiesadaptation
collection DOAJ
language English
format Article
sources DOAJ
author Amine Ourahmane
Xiaohong Cui
Li He
Meaghan Catron
Dirk P. Dittmer
Ahmed Al Qaffasaa
Mark R. Schleiss
Laura Hertel
Michael A. McVoy
spellingShingle Amine Ourahmane
Xiaohong Cui
Li He
Meaghan Catron
Dirk P. Dittmer
Ahmed Al Qaffasaa
Mark R. Schleiss
Laura Hertel
Michael A. McVoy
Inclusion of Antibodies to Cell Culture Media Preserves the Integrity of Genes Encoding RL13 and the Pentameric Complex Components During Fibroblast Passage of Human Cytomegalovirus
Viruses
cytomegalovirus
cell culture
antibodies
adaptation
author_facet Amine Ourahmane
Xiaohong Cui
Li He
Meaghan Catron
Dirk P. Dittmer
Ahmed Al Qaffasaa
Mark R. Schleiss
Laura Hertel
Michael A. McVoy
author_sort Amine Ourahmane
title Inclusion of Antibodies to Cell Culture Media Preserves the Integrity of Genes Encoding RL13 and the Pentameric Complex Components During Fibroblast Passage of Human Cytomegalovirus
title_short Inclusion of Antibodies to Cell Culture Media Preserves the Integrity of Genes Encoding RL13 and the Pentameric Complex Components During Fibroblast Passage of Human Cytomegalovirus
title_full Inclusion of Antibodies to Cell Culture Media Preserves the Integrity of Genes Encoding RL13 and the Pentameric Complex Components During Fibroblast Passage of Human Cytomegalovirus
title_fullStr Inclusion of Antibodies to Cell Culture Media Preserves the Integrity of Genes Encoding RL13 and the Pentameric Complex Components During Fibroblast Passage of Human Cytomegalovirus
title_full_unstemmed Inclusion of Antibodies to Cell Culture Media Preserves the Integrity of Genes Encoding RL13 and the Pentameric Complex Components During Fibroblast Passage of Human Cytomegalovirus
title_sort inclusion of antibodies to cell culture media preserves the integrity of genes encoding rl13 and the pentameric complex components during fibroblast passage of human cytomegalovirus
publisher MDPI AG
series Viruses
issn 1999-4915
publishDate 2019-03-01
description Propagation of human cytomegalovirus (CMV) in cultured cells results in genetic adaptations that confer improved growth in vitro and significant attenuation in vivo. Mutations in RL13 arise quickly, while mutations in the UL128-131A locus emerge later during fibroblast passage and disrupt formation of a glycoprotein complex that is important for entry into epithelial and endothelial cells. As CMV replicates in the context of host antibodies in vivo, we reasoned that antibodies might mitigate the accumulation of adaptive mutations during cell culture passage. To test this, CMV in infant urine was used to infect replicate fibroblast cultures. One lineage was passaged in the absence of CMV-hyperimmuneglobulin (HIG) while the other was passaged with HIG in the culture medium. The former lost epithelial tropism and acquired mutations disrupting RL13 and UL131A expression, whereas the latter retained epithelial tropism and both gene loci remained intact after 22 passages. Additional mutations resulting in single amino acid changes also occurred in UL100 encoding glycoprotein M, UL102 encoding a subunit of the helicase/primase complex, and UL122 encoding the Immediate Early 2 protein. An epitheliotropic RL13+/UL131A+ virus was isolated by limiting dilution in the presence of HIG and expanded to produce a working stock sufficient to conduct cell tropism experiments. Thus, production of virus stocks by culture in the presence of antibodies may facilitate in vitro experiments using viruses that are genetically more authentic than previously available.
topic cytomegalovirus
cell culture
antibodies
adaptation
url http://www.mdpi.com/1999-4915/11/3/221
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