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Mengovirus

From Wikipedia, the free encyclopedia
Species of virus
Mengovirus
Surface depiction of Mengovirus (2MEV) coloured by radial height to illuminate surface features
Virus classificationEdit this classification
(unranked):Virus
Realm:Riboviria
Kingdom:Orthornavirae
Phylum:Pisuviricota
Class:Pisoniviricetes
Order:Picornavirales
Family:Picornaviridae
Genus:Cardiovirus
Species:
Virus:
Mengovirus

Mengovirus, also known asColumbia SK virus,mouse Elberfield virus, andEncephalomyocarditis virus (EMCV), belongs to the genusCardiovirus which is a member of thePicornaviridae.[1] Its genome is a single strandedpositive-senseRNA molecule, making the Mengoviruses aclass IV virus under theBaltimore classification system. The genome is approximately 8400nt in length, and has 5’ VG protein (Virus genome protein) and a 3’ polyadenine tail. Mengovirus was isolated by George W. A. Dick in 1948, in the Mengo district of Entebbe in Uganda, from a captive rhesus monkey that had developed hind limb paralysis.[2][3]

Structure

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Mengovirus is a non-enveloped virus which has a nucleocapsid made up of 12 subunits. Thevirion is 30 nm in diameter and displays icosahedral symmetry.[citation needed]

Gene expression and genome replication

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Once inside a host cell, the Mengovirus genome acts as a piece of mRNA and is directly translated by the hostribosomes in the cytoplasm. There is a large un-translated region at the 5’ end of the RNA that has a ribosome binding site, removing the need of a cap. A single polypeptide is made and is cleaved into individual proteins by viral proteases. The genome is divided into three parts: P1, P2, and P3. P1 encodes the virus capsid proteins, P2 and P3 encode genes required for genome replication to occur. For replication to occur an intermediate double-stranded RNA molecule is made to be used as a template for the production of positive sense genomes.[citation needed]

Infection

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Mengovirus is infectious to vertebrate animals, and has been isolated from mice and other rodents. It can also cause acute fever in humans. There is no specific treatment for a Mengovirus infection; althoughdipyridamole has been shown to inhibit its replication.[4] The illness is not severe enough to require vaccination. The Mengovirus is able to suppress the host's immune response by reducing the expression ofNuclear Factor kappa B using the 5’ un-translated region.[citation needed]

References

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  1. ^Carocci, M; Bakkali-Kassimi, L (2012)."The encephalomyocarditis virus".Virulence.3 (4):351–67.doi:10.4161/viru.20573.PMC 3478238.PMID 22722247.
  2. ^Dick, G. W.; Smithburn, K. C.; Haddow, A. J. (948)."Mengo Encephalomyelitis Virus. Isolation and Immunological Properties".Br J Exp Pathol.29 (6):547–558.PMC 2073198.
  3. ^Dick, G.W.A.; Haddow, A.J.; Best, A.M.; Smithburn, K.C. (1948). "Mengo Encephalomyelitis".The Lancet.252 (6521):286–289.doi:10.1016/S0140-6736(48)90652-7.
  4. ^Fata-Hartley, Cori L.; Palmenberg, Ann C. (2005)."Dipyridamole Reversibly Inhibits Mengovirus RNA Replication".Journal of Virology.79 (17):11062–11070.doi:10.1128/jvi.79.17.11062-11070.2005.PMC 1193570.PMID 16103157.

Further reading

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Mengovirus
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