Mimiviridae

Source: Wikipedia, the free encyclopedia.
(Redirected from
Imitervirales
)

Mimiviridae
Tupanvirus
Virus classification Edit this classification
(unranked): Virus
Realm: Varidnaviria
Kingdom: Bamfordvirae
Phylum: Nucleocytoviricota
Class: Megaviricetes
Order: Imitervirales
Family: Mimiviridae
Subfamilies and genera

Mimiviridae is a family of

giant viruses
.

Mimiviridae is the sole recognized member of order Imitervirales.

Algavirales are sister groups of Mimiviridae in many phylogenetic analyses.[5]

History

The first member of this family, Mimivirus, was discovered in 2003,[6] and the first complete genome sequence was published in 2004.[7] However, the mimivirus Cafeteria roenbergensis virus[8] was isolated and partially characterized in 1995,[9] although the host was misidentified at the time, and the virus was designated BV-PW1.[8]

Taxonomy

Group: dsDNA

Order: Imitervirales
  • Family: Mimiviridae
    • *
      Acanthamoeba polyphaga mimivirus

Family Mimiviridae is currently divided into three subfamilies.[2][3][10]

The majority of Mimiviridae appear to belong to this subfamily (Mimiviruses).[10]
It is sometimes also referred to as Mimiviridae group I.[17]

Furthermore, it has been proposed either to extend Mimiviridae by an additional tentative group III (subfamily Mesomimivirinae) or to classify this group as a sister family Mesomimiviridae instead,[19] comprising legacy OLPG (Organic Lake Phycodna Group). This extension (or sister family) may consist of the following:

This group seems to be closely related to Mimiviridae rather than to

Megaviridae although this has not been recognized by ICTV; alternatively the extended group may be referred to just as Mimiviridae.[3][23][24][25][26][17]

With recognition of new order Imitervirales by the ICTV in March 2020 there is no longer need to extend the Mimiviridae family to comprise a group of viruses of the observed high diversity. Instead, the extension (or at least its main clade) may be referred to as a sister family Mesomimiviridae.[19]

Although only a couple of members of this order have been described in detail it seems likely there are many more awaiting description and assignment[27][28] Unassigned members include Aureococcus anophagefferens virus (AaV), CpV-BQ2 and Terra2.[citation needed]

Structure

Ultrastructure of Bodo saltans virus particles and its replication

[18] Viruses in Mimiviridae have icosahedral and round geometries, with between T=972 and T=1141, or T=1200 symmetry. The diameter is around 400 nm, with a length of 125 nm. Genomes are linear and non-segmented, around 1200kb in length. The genome has 911 open reading frames.[1]

Genus Structure Symmetry Genomic arrangement Genomic segmentation
Mimivirus Icosahedral T=972-1141 or T=1200 (H=19 +/- 1, K=19 +/- 1) Linear Monopartite
Klosneuvirus Icosahedral
Cafeteriavirus Icosahedral T=499 Linear Monopartite
Tupanvirus Tailed

Life cycle

Replication follows the DNA strand displacement model. DNA-templated transcription is the method of transcription. Amoeba serve as the natural host.[1]

Genus Host details Tissue tropism Entry details Release details Replication site Assembly site Transmission
Mimivirus Amoeba None Unknown Unknown Unknown Unknown Passive diffusion
Klosneuvirus microzooplankton None Unknown Unknown Unknown Cytoplasm Passive diffusion
Cafeteriavirus microzooplankton None Unknown Unknown Unknown Cytoplasm Passive diffusion

Molecular biology

Three putative DNA base excision repair enzymes were characterized from Mimivirus.[29] The base excision repair (BER) pathway was experimentally reconstituted using the purified recombinant proteins uracil-DNA glycosylase (mvUDG), AP endonuclease (mvAPE), and DNA polymerase X protein (mvPolX).[29] When reconstituted in vitro mvUDG, mvAPE and mvPolX function cohesively to repair uracil-containing DNA predominantly by long patch base excision repair, and thus these processes likely participate in the BER pathway early in the Mimivirus life cycle.[29]

Clinical

Mimiviruses have been associated with pneumonia but their significance is currently unknown.[30] The only virus of this family isolated from a human to date is LBA 111.[31] At the Pasteur Institute of Iran (Tehran), researchers identified mimivirus DNA in bronchoalveolar lavage (BAL) and sputum samples of a child patient, utilizing real-time PCR (2018).  Analysis reported 99% homology of LBA111, lineage C of the Megavirus chilensis.[32] With only a few reported cases previous to this finding, the legitimacy of the mimivirus as an emerging infectious disease in humans remains controversial.[33][34]

Mimivirus has also been implicated in rheumatoid arthritis.[35]

See also

References

  1. ^ a b c "Viral Zone". ExPASy. Retrieved 15 June 2015.
  2. ^ a b ICTV. "Virus Taxonomy: 2014 Release". Retrieved 15 June 2015.
  3. ^
    S2CID 206655792., UCPMS ID: 1889607, PDF
  4. ^ . Fig. 4 and §Discussion: "Considering that tupanviruses comprise a sister group to amoebal mimiviruses…"
  5. .
  6. .
  7. ^ .
  8. .
  9. ^ .
  10. ^ .
  11. ^ a b c See also Abrahão & et al. 2018, fig. 4 on p. 5
  12. PMID 23071316
    .
  13. .
  14. .
  15. ^ For LBA111 and Powai lake megavirus see also Abrahão & et al. 2018, fig. 4 on p. 5
  16. ^
    PMID 26459929
    .
  17. ^ .
  18. ^
  19. ^ NCBI Complete genomes: Viruses, look for 'Yellowstone Lake'
  20. PMID 25035289
    .
  21. .
  22. PMID 25727355
    .
  23. .
  24. ^ Blog of Carolina Reyes, Kenneth Stedman: Are Phaeocystis globosa viruses (OLPG) and Organic Lake phycodnavirus a part of the Phycodnaviridae or Mimiviridae?, on ResearchGate, Jan. 8, 2016
  25. PMID 27965659
    .
  26. .
  27. .
  28. ^ a b c Lad SB, Upadhyay M, Thorat P, Nair D, Moseley GW, Srivastava S, Pradeepkumar PI, Kondabagil K. Biochemical Reconstitution of the Mimiviral Base Excision Repair Pathway. J Mol Biol. 2023 Sep 1;435(17):168188. doi: 10.1016/j.jmb.2023.168188. Epub 2023 Jun 26. PMID: 37380013
  29. PMID 23709652
    .
  30. .
  31. .
  32. .
  33. – via Oxford Academic.
  34. .

External links