Molecular and Biological Characterization of a New Isolate of Guinea Pig Cytomegalovirus

Development of a vaccine against congenital infection with human cytomegalovirus is complicated by the issue of re-infection, with subsequent vertical transmission, in women with pre-conception immunity to the virus. The study of experimental therapeutic prevention of re-infection would ideally be u...

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Main Authors: Mark R. Schleiss, Shane McAllister, Anibal G. Armién, Nelmary Hernandez-Alvarado, Claudia Fernández-Alarcón, Jason C. Zabeli, Thiruvarangan Ramaraj, John A. Crow, Michael A. McVoy
Format: Article
Language:English
Published: MDPI AG 2014-01-01
Series:Viruses
Subjects:
Online Access:http://www.mdpi.com/1999-4915/6/2/448
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spelling doaj-257a55617d6444ce8493ca4a354c65be2020-11-25T00:26:11ZengMDPI AGViruses1999-49152014-01-016244847510.3390/v6020448v6020448Molecular and Biological Characterization of a New Isolate of Guinea Pig CytomegalovirusMark R. Schleiss0Shane McAllister1Anibal G. Armién2Nelmary Hernandez-Alvarado3Claudia Fernández-Alarcón4Jason C. Zabeli5Thiruvarangan Ramaraj6John A. Crow7Michael A. McVoy8Division of Pediatric Infectious Diseases, Department of Pediatrics, University of Minnesota Medical School, Minneapolis, MN 55455, USADivision of Pediatric Infectious Diseases, Department of Pediatrics, University of Minnesota Medical School, Minneapolis, MN 55455, USADepartment of Veterinary Population Medicine and Veterinary Diagnostic Laboratory, College of Veterinary Medicine, Saint Paul, MN 55108, USADivision of Pediatric Infectious Diseases, Department of Pediatrics, University of Minnesota Medical School, Minneapolis, MN 55455, USADivision of Pediatric Infectious Diseases, Department of Pediatrics, University of Minnesota Medical School, Minneapolis, MN 55455, USADivision of Pediatric Infectious Diseases, Department of Pediatrics, University of Minnesota Medical School, Minneapolis, MN 55455, USANational Center for Genome Resources (NCGR), Santa Fe, NM 87505, USANational Center for Genome Resources (NCGR), Santa Fe, NM 87505, USADivision of Pediatric Infectious Diseases, Department of Pediatrics, Virginia Commonwealth University School of Medicine, Richmond, VA 23298, USADevelopment of a vaccine against congenital infection with human cytomegalovirus is complicated by the issue of re-infection, with subsequent vertical transmission, in women with pre-conception immunity to the virus. The study of experimental therapeutic prevention of re-infection would ideally be undertaken in a small animal model, such as the guinea pig cytomegalovirus (GPCMV) model, prior to human clinical trials. However, the ability to model re-infection in the GPCMV model has been limited by availability of only one strain of virus, the 22122 strain, isolated in 1957. In this report, we describe the isolation of a new GPCMV strain, the CIDMTR strain. This strain demonstrated morphological characteristics of a typical Herpesvirinae by electron microscopy. Illumina and PacBio sequencing demonstrated a genome of 232,778 nt. Novel open reading frames ORFs not found in reference strain 22122 included an additional MHC Class I homolog near the right genome terminus. The CIDMTR strain was capable of dissemination in immune compromised guinea pigs, and was found to be capable of congenital transmission in GPCMV-immune dams previously infected with salivary gland‑adapted strain 22122 virus. The availability of a new GPCMV strain should facilitate study of re-infection in this small animal model.http://www.mdpi.com/1999-4915/6/2/448guinea pig cytomegaloviruscytomegalovirus strain variationCMV immune evasioncongenital cytomegalovirus infectioncongenital CMV vaccines
collection DOAJ
language English
format Article
sources DOAJ
author Mark R. Schleiss
Shane McAllister
Anibal G. Armién
Nelmary Hernandez-Alvarado
Claudia Fernández-Alarcón
Jason C. Zabeli
Thiruvarangan Ramaraj
John A. Crow
Michael A. McVoy
spellingShingle Mark R. Schleiss
Shane McAllister
Anibal G. Armién
Nelmary Hernandez-Alvarado
Claudia Fernández-Alarcón
Jason C. Zabeli
Thiruvarangan Ramaraj
John A. Crow
Michael A. McVoy
Molecular and Biological Characterization of a New Isolate of Guinea Pig Cytomegalovirus
Viruses
guinea pig cytomegalovirus
cytomegalovirus strain variation
CMV immune evasion
congenital cytomegalovirus infection
congenital CMV vaccines
author_facet Mark R. Schleiss
Shane McAllister
Anibal G. Armién
Nelmary Hernandez-Alvarado
Claudia Fernández-Alarcón
Jason C. Zabeli
Thiruvarangan Ramaraj
John A. Crow
Michael A. McVoy
author_sort Mark R. Schleiss
title Molecular and Biological Characterization of a New Isolate of Guinea Pig Cytomegalovirus
title_short Molecular and Biological Characterization of a New Isolate of Guinea Pig Cytomegalovirus
title_full Molecular and Biological Characterization of a New Isolate of Guinea Pig Cytomegalovirus
title_fullStr Molecular and Biological Characterization of a New Isolate of Guinea Pig Cytomegalovirus
title_full_unstemmed Molecular and Biological Characterization of a New Isolate of Guinea Pig Cytomegalovirus
title_sort molecular and biological characterization of a new isolate of guinea pig cytomegalovirus
publisher MDPI AG
series Viruses
issn 1999-4915
publishDate 2014-01-01
description Development of a vaccine against congenital infection with human cytomegalovirus is complicated by the issue of re-infection, with subsequent vertical transmission, in women with pre-conception immunity to the virus. The study of experimental therapeutic prevention of re-infection would ideally be undertaken in a small animal model, such as the guinea pig cytomegalovirus (GPCMV) model, prior to human clinical trials. However, the ability to model re-infection in the GPCMV model has been limited by availability of only one strain of virus, the 22122 strain, isolated in 1957. In this report, we describe the isolation of a new GPCMV strain, the CIDMTR strain. This strain demonstrated morphological characteristics of a typical Herpesvirinae by electron microscopy. Illumina and PacBio sequencing demonstrated a genome of 232,778 nt. Novel open reading frames ORFs not found in reference strain 22122 included an additional MHC Class I homolog near the right genome terminus. The CIDMTR strain was capable of dissemination in immune compromised guinea pigs, and was found to be capable of congenital transmission in GPCMV-immune dams previously infected with salivary gland‑adapted strain 22122 virus. The availability of a new GPCMV strain should facilitate study of re-infection in this small animal model.
topic guinea pig cytomegalovirus
cytomegalovirus strain variation
CMV immune evasion
congenital cytomegalovirus infection
congenital CMV vaccines
url http://www.mdpi.com/1999-4915/6/2/448
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