Cytomegalovirus

Cytomegalovirus
Classification and external resources
ICD-10 B25
ICD-9-CM 078.5
MedlinePlus 000568
Patient UK Cytomegalovirus
MeSH D003586

Cytomegalovirus
Typical "owl eye" inclusion indicating CMV infection of a lung pneumocyte[1]
Virus classification
Group: Group I (dsDNA)
Order: Herpesvirales
Family: Herpesviridae
Subfamily: Betaherpesvirinae
Genus: Cytomegalovirus
Type species
Human cytomegalovirus

Cytomegalovirus (CMV) (from the Greek cyto-, "cell", and megalo-, "large") is a genus of viruses in the order Herpesvirales, in the family (150-200nm in diameter [hiv virus 120nm]) Herpesviridae, in the subfamily Betaherpesvirinae. Humans and monkeys serve as natural hosts. There are currently eight species in this genus including the type species, human cytomegalovirus (HCMV, human herpesvirus 5, HHV-5), which is the species that infects humans. Diseases associated with HHV-5 include glandular fever, and pneumonia.[2][3] In the medical literature, most mentions of CMV without further specification refer implicitly to human CMV. Human CMV is the most studied of all cytomegaloviruses.[4]


History

Cytomegalovirus was first observed by German pathologist Hugo Ribbert in 1881 when he noticed enlarged cells with enlarged nuclei present in the cells of an infant.[5]

Taxonomy

Within Herpesviridae, CMV belongs to the Betaherpesvirinae subfamily, which also includes the genera Muromegalovirus and Roseolovirus (HHV-6 and HHV-7).[6] It is related to other herpesviruses within the subfamilies of Alphaherpesvirinae that includes herpes simplex viruses (HSV)-1 and -2 and varicella-zoster virus (VZV), and the Gammaherpesvirinae subfamily that includes Epstein–Barr virus.[4]

Group: dsDNA

Source:[3]

Species

Classified Cytomegaloviruses
Scientific Name Host Common Name
Human herpesvirus 5 (HHV-5) Human Human CMV (HCMV)
Cercopithecine herpesvirus 5 (CeHV-5) African green monkey Simian CMV (SCCMV)
Cercopithecine herpesvirus 8 (CeHV-8) Rhesus monkey Rhesus CMV (RhCMV)
Panine herpesvirus 2 (PoHV-2) Chimpanzee Chimpanzee CMV (CCMV)
Pongine herpesvirus 4 (PoHV-4) Orangutan Chimpanzee CMV (CCMV)
Aotine herpesvirus 1 (AoHV-1) tentative classification Night monkey Herpesvirus aotus 1
Aotine herpesvirus 3 (AoHV-3) tentative classification Night monkey Herpesvirus aotus 3

Several species of Cytomegalovirus have been identified and classified for different mammals.[6] The most studied is Human cytomegalovirus (HCMV), which is also known as Human herpesvirus 5 (HHV-5). Other primate CMV species include Chimpanzee cytomegalovirus (CCMV) that infects chimpanzees and orangutans, and Simian cytomegalovirus (SCCMV) and Rhesus cytomegalovirus (RhCMV) that infect macaques; CCMV is known as both Panine herpesvirus 2 (PaHV-2) and Pongine herpesvirus-4 (PoHV-4). SCCMV is called Cercopithecine herpesvirus-5 (CeHV-5) and RhCMV, Cercopithecine herpesvirus 8 (CeHV-8). A further two viruses found in the night monkey are tentatively placed in the Cytomegalovirus genus, and are called Herpesvirus aotus 1 and Herpesvirus aotus 3. Rodents also have viruses previously called cytomegaloviruses that are now reclassified under the genus Muromegalovirus; this genus contains Mouse cytomegalovirus (MCMV) is also known as Murid herpesvirus 1 (MuHV-1) and the closely related Murid herpesvirus 2 (MuHV-2) that is found in rats. In addition, there many other viral species with the name Cytomegalovirus identified in distinct mammals that are as yet not completely classified; these were predominantly isolated from primates and rodents.

Structure

Viruses in Cytomegalovirus are enveloped, with icosahedral, Spherical to pleomorphic, and Round geometries, and T=16 symmetry. The diameter is around 150–200 nm. Genomes are linear and non-segmented, around 200kb in length.[2]

Genus Structure Symmetry Capsid Genomic arrangement Genomic segmentation
CytomegalovirusSpherical PleomorphicT=16EnvelopedLinearMonopartite

Life cycle

Viral replication is nuclear, and is lysogenic. Entry into the host cell is achieved by attachment of the viral glycoproteins to host receptors, which mediates endocytosis. Replication follows the dsDNA bidirectional replication model. DNA templated transcription, with some alternative splicing mechanism is the method of transcription. Translation takes place by leaky scanning. The virus exits the host cell by nuclear egress, and budding. Human and monkeys serve as the natural host. Transmission routes are contact, urine, and saliva.[2]

Genus Host details Tissue tropism Entry details Release details Replication site Assembly site Transmission
CytomegalovirusHumans; monkeysEpithelial mucosaGlycoproteinsBuddingNucleusNucleusUrine; saliva

All herpesviruses share a characteristic ability to remain latent within the body over long periods. Although they may be found throughout the body, CMV infections are frequently associated with the salivary glands in humans and other mammals.[6]

Genetic engineering

The CMV promoter is commonly included in vectors used in genetic engineering work conducted in mammalian cells, as it is a strong promoter and drives constitutive expression of genes under its control.[7]

References

  1. Mattes FM, McLaughlin JE, Emery VC, Clark DA, Griffiths PD (August 2000). "Histopathological detection of owl's eye inclusions is still specific for cytomegalovirus in the era of human herpesviruses 6 and 7". J. Clin. Pathol. 53 (8): 612–4. PMC 1762915Freely accessible. PMID 11002765. doi:10.1136/jcp.53.8.612.
  2. 1 2 3 "Viral Zone". ExPASy. Retrieved 15 June 2015.
  3. 1 2 ICTV. "Virus Taxonomy: 2014 Release". Retrieved 15 June 2015.
  4. 1 2 Ryan KJ, Ray CG, eds. (2004). Sherris Medical Microbiology (4th ed.). McGraw Hill. pp. 556; 566–9. ISBN 0-8385-8529-9.
  5. Reddehase, Matthias J.; Lemmermann, Niels, eds. (2006). "Preface". Cytomegaloviruses: Molecular Biology and Immunology. Horizon Scientific Press. pp. xxiv. ISBN 9781904455028.
  6. 1 2 3 Koichi Yamanishi; Arvin, Ann M; Gabriella Campadelli-Fiume; Edward Mocarski; Moore, Patrick; Roizman, Bernard; Whitley, Richard (2007). Human herpesviruses: biology, therapy, and immunoprophylaxis. Cambridge, UK: Cambridge University Press. ISBN 0-521-82714-0.
  7. Kendall Morgan for Addgene Blog. Apr 3, 2014 Plasmids 101: The Promoter Region – Let's Go!

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