Minute virus of mice

Minute Virus of Mice
Virus classification
Group: Group II (ssDNA)
Family: Parvoviridae
Subfamily: Parvovirinae
Genus: Protoparvovirus
Species: Minute Virus of_Mice

The Minute Virus of Mice (MVM) is the prototype virus of the Protoparvovirus genus within the Parvoviridae family of viruses.[1][2] MVM exists in two variant forms: MVMp, which is the prototype strain, infects cells of fibroblast origin, while MVMi, the immunosuppressive strain, infects T lymphocytes.[3] MVM is a common infection in laboratory mice due to its highly contagious nature.[4] The virus can be shed from infected mice via feces and urine, but also via fomites and nasal secretions.[4] Typically there are no clinical signs of infection, however, experimental infection can cause multiple organ damage during fetal development or shortly after birth.[4] While MVM infection may result in pathology of infected mice, the infection is more likely to cause problems for the ongoing study the mice are being used for as the immune system will be activated, the activity of T-lymphocytes and B-lymphocytes will be altered and tumor formation may be suppressed.[4]

Transcription profile

During replication MVM utilizes three open reading frames (ORFs) and produces three distinct mRNA transcripts which are referred to as R1, R2 and R3.[5] R1, produced from ORF 3, is translated into non-structural protein 1 (NS1).[5] mRNA transcript R2, produces non-structural protein 2 (NS2) by splicing the 5-prime end of ORF3 with ORF2, which is found within the 3-prime end of ORF.[5] The resulting NS2 protein is thus composed of spliced 5-prime and 3-prime alternative ORF sections of NS1.[5] Finally, the R3 transcript produces capsid proteins VP1 and VP2, which requires transcription from the P38 promoter, in contrast to the P4 promoter used for transcripts R1 and R2.[6]

Non-structural protein functions

NS1 functions as a required replication protein and is known to have helicase activity,[7] ATPase activity [7] and nickase activity.[2] Specifically, the nickase activity is required to resolve replication intermediate telomeres on the right-hand of the genome.[2] NS2 is known to exist in several spliced forms (isoforms) termed NS2-P, -Y and –L due to differences in the C-terminus of the isoforms as a result of alternative splicing.[8] NS2 is known to exist is both the cytoplasm and nucleus as well as in phosphorylated and non-phosphorylated forms.[8] In addition, NS2 is required for efficient infection in its natural murine host, but is dispensable in experimental infection in human cell lines.[8] Although not fully understood, in murine A9 fibroblasts NS2 interacts with nuclear export factor Crm1 resulting in efficient nuclear egress of progeny virions.[8]

DNA damage response

MVM induces a DNA damage response (DDR) during infection which is required for effective replication.[9] The ATM pathway is exclusively activated with a primarily Chk2-mediated response.[9] It is not known if viral proteins or active viral replication activate the DDR, but UV-inactivated MVM does not induce a response [9] suggesting that presence of MVM virions or MVM genome alone cannot cause the observed DDR activation.

Commercial Uses

The Minute virus of Mice is currently the smallest virus that can be easily titrated to high levels; as such it is commercially used as a "worst case" example of a very small virus.[10][11]

References

  1. ↑ http://talk.ictvonline.org/files/ictv_official_taxonomy_updates_since_the_8th_report/m/vertebrate-official/4844.aspx[]
  2. 1 2 3 Willwand, K; Deleu, L; Baldauf, A Q; Rommelaere, J; Beard, P; Costello, E; Mumtsidu, E (1997). "The minute virus of mice (MVM) nonstructural protein NS1 induces nicking of MVM DNA at a unique site of the right-end telomere in both hairpin and duplex conformations in vitro". Journal of General Virology 78 (10): 2647–55. doi:10.1099/0022-1317-78-10-2647. PMID 9349487.
  3. ↑ Brownstein, David G.; Smith, Abigail L.; Johnson, Elizabeth A.; Pintel, David J.; Naeger, Lisa Kay; Tattersall, Peter (1992). "The pathogenesis of infection with minute virus of mice depends on expression of the small nonstructural protein NS2 and on the genotype of the allotropic determinants VP1 and VP2". Journal of Virology 66 (5): 3118–24. PMC 241074. PMID 1373202.
  4. 1 2 3 4 Baker, David G. (1998). "Natural pathogens of laboratory mice, rats, and rabbits and their effects on research". Clinical Microbiology Reviews 11 (2): 231–66. PMC 106832. PMID 9564563.
  5. 1 2 3 4 Naeger, L K; Schoborg, R V; Zhao, Q; Tullis, G E; Pintel, D J (1992). "Nonsense mutations inhibit splicing of MVM RNA in cis when they interrupt the reading frame of either exon of the final spliced product". Genes & Development 6 (6): 1107–19. doi:10.1101/gad.6.6.1107. PMID 1592259.
  6. ↑ Kerr, Jonathan; Cotmore, Susan; Bloom, Marshall E, eds. (2005). Parvoviruses. CRC. ISBN 978-0-340-81198-6.
  7. 1 2 Nüesch, Jürg P. F.; Corbau, Romuald; Tattersall, Peter; Rommelaere, Jean (1998). "Biochemical activities of minute virus of mice nonstructural protein NS1 are modulated In vitro by the phosphorylation state of the polypeptide". Journal of Virology 72 (10): 8002–12. PMC 110136. PMID 9733839.
  8. 1 2 3 4 Eichwald, V.; Daeffler, L.; Klein, M.; Rommelaere, J.; Salome, N. (2002). "The NS2 Proteins of Parvovirus Minute Virus of Mice Are Required for Efficient Nuclear Egress of Progeny Virions in Mouse Cells". Journal of Virology 76 (20): 10307–19. doi:10.1128/JVI.76.20.10307-10319.2002. PMC 136550. PMID 12239307.
  9. 1 2 3 Linden, R. Michael; Adeyemi, Richard O.; Landry, Sebastien; Davis, Meredith E.; Weitzman, Matthew D.; Pintel, David J. (2010). "Parvovirus Minute Virus of Mice Induces a DNA Damage Response That Facilitates Viral Replication". PLoS Pathogens 6 (10): e1001141. doi:10.1371/journal.ppat.1001141. PMC 2951379. PMID 20949077.
  10. ↑ Weaver, Justin; Husson, Scott M.; Murphy, Louise; Wickramasinghe, S. Ranil (2013). "Anion exchange membrane adsorbers for flow-through polishing steps: Part I. clearance of minute virus of mice". Biotechnology and Bioengineering 110 (2): 491–9. doi:10.1002/bit.24720. PMID 22949170.
  11. ↑ Liu, S.; Carroll, M.; Iverson, R.; Valera, C.; Vennari, J.; Turco, K.; Piper, R.; Kiss, R.; Lutz, H. (2000). "Development and Qualification of a Novel Virus Removal Filter for Cell Culture Applications". Biotechnology Progress 16 (3): 425–34. doi:10.1021/bp000027m. PMID 10835245.
This article is issued from Wikipedia - version of the Thursday, March 31, 2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.