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Related Concept Videos

Cytomegalovirus Disease01:27

Cytomegalovirus Disease

Cytomegalovirus (CMV) disease is caused by human cytomegalovirus, a double-stranded DNA virus of the Herpesviridae family. While primary CMV infection is often asymptomatic in immunocompetent individuals, the virus can cause severe disease in neonates and immunocompromised patients. CMV is the most common cause of congenital viral infection in the United States, and a major pathogen in solid organ and hematopoietic stem cell transplant recipients.CMV is transmitted via bodily fluids, sexual...
Size and Structure of Viral Genomes01:26

Size and Structure of Viral Genomes

Viral genomes exhibit remarkable diversity in size, structure, and composition, influencing their replication strategies and interactions with host cells. These genomes consist of either DNA or RNA and may be linear or circular. Additionally, they can be single-stranded or double-stranded, with each configuration affecting how the virus propagates within a host. RNA viruses, for instance, generally have smaller genomes than DNA viruses, a factor that contributes to their high mutation rates and...
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Retroviruses

Retroviruses and retrotransposons both insert copies of their genetic elements into the genome of the host cell. Thus, the viral genes are passed on when the host genome is replicated or translated. A typical retroviral DNA sequence contains 3-4 genes that encode the different proteins required for its structural assembly and function as a molecular parasite. This DNA is transcribed into a single mRNA, which is very similar in structure to conventional mRNAs, i.e., it is capped at the 5’...
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Viruses with RNA Genomes

RNA viruses are categorized into positive-strand, negative-strand, or double-stranded groups based on their genomic structure and replication mechanisms. This classification dictates how they exploit host cellular machinery for protein synthesis and replication. Some RNA viruses also utilize reverse transcription as part of their life cycle, further diversifying their replication strategies.Positive-Strand RNA VirusesPositive-strand RNA viruses have genomes that function directly as messenger...
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The human body harbors a vast and diverse viral community known as the human virome. The virome includes bacteriophages that infect bacteria, and eukaryotic viruses that infect human cells. Transient dietary and environmental viruses also contribute to this dynamic ecosystem. Estimates suggest the human body may contain on the order of 10¹³ viral particles, though abundance varies widely by body site and detection method.Comprehensive characterization of the virome has become possible only with...
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Retrovirus Life Cycles

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Related Experiment Video

Updated: Jul 3, 2026

Use of In vivo Imaging to Monitor the Progression of Experimental Mouse Cytomegalovirus Infection in Neonates
05:53

Use of In vivo Imaging to Monitor the Progression of Experimental Mouse Cytomegalovirus Infection in Neonates

Published on: July 6, 2013

Human cytomegalovirus genome.

E Murphy1, T Shenk

  • 1Department of Molecular Biology, Princeton University, Princeton, NJ 08544-1014, USA.

Current Topics in Microbiology and Immunology
|July 22, 2008
PubMed
Summary

This study identified conserved genes in human cytomegalovirus (HCMV) clinical isolates and chimpanzee cytomegalovirus (CCMV). Researchers found 173 shared functional genes and 33 potentially unique HCMV genes.

Area of Science:

  • Virology
  • Genomics
  • Molecular Biology

Background:

  • Human cytomegalovirus (HCMV) possesses a large, complex genome with variations between clinical isolates and laboratory strains.
  • Laboratory strains of HCMV have undergone genomic rearrangements due to extensive passaging in fibroblasts.
  • Previous sequencing efforts have focused on a limited number of clinical HCMV isolates.

Purpose of the Study:

  • To re-evaluate the coding content of HCMV clinical isolates by identifying conserved open reading frames (ORFs).
  • To compare the conserved ORFs in HCMV with those found in the chimpanzee cytomegalovirus (CCMV) genome.
  • To identify potentially functional ORFs specific to HCMV.

Main Methods:

  • Sequencing of five clinical HCMV isolates.

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  • Comparative genomic analysis to identify conserved ORFs across all HCMV isolates.
  • Cross-species comparison of HCMV ORFs with the CCMV genome.
  • Main Results:

    • A total of 173 ORFs were identified as conserved across all five HCMV clinical isolates and the CCMV genome, suggesting high functional importance.
    • An additional 59 ORFs were found in all HCMV isolates but not in CCMV.
    • After excluding ORFs in non-coding regions, 33 potentially functional ORFs specific to HCMV were identified.

    Conclusions:

    • The 173 conserved ORFs are highly likely to be essential for HCMV function.
    • The 33 identified ORFs represent potential targets for further research into HCMV-specific biology and therapeutics.
    • This comparative genomic analysis refines our understanding of the core functional genome of HCMV.