Dianthovirus: Difference between revisions
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{{Short description|Genus of viruses}} |
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{{taxobox |
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| virus_group = iv |
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{{virusbox |
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| familia = ''[[Tombusviridae]]'' |
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| taxon = Dianthovirus |
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| subdivision_ranks = Type Species |
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| subdivision = |
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'''''Dianthovirus''''' is a genus of [[viruses]], in the family [[Tombusviridae]]. Dianthoviruses are [[plant viruses]]. There are |
'''''Dianthovirus''''' is a genus of [[viruses]], in the family ''[[Tombusviridae]]''. Dianthoviruses are [[plant viruses]]. There are three species in this genus. The virus probably has a worldwide distribution, and can be transmitted via [[nematodes]], by mechanical inoculation, by grafting of plants and by contact between infected hosts with previously uninfected [[Host (biology)|host]].<ref name=ViralZone>{{cite web|title=Viral Zone|url=http://viralzone.expasy.org/all_by_species/633.html|publisher=ExPASy|accessdate=15 June 2015}}</ref><ref name=ICTV>{{cite web |title=Virus Taxonomy: 2020 Release |url=https://ictv.global/taxonomy |publisher=International Committee on Taxonomy of Viruses (ICTV) |date=March 2021 |access-date=16 May 2021}}</ref> |
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==Taxonomy== |
==Taxonomy== |
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The genus contains the following species:<ref name=ICTV /> |
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<big>'''Group: ssRNA(+)'''</big> |
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{{Collapsible list|title= <big>Order: Unassigned</big> |
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|1={{Collapsible list| framestyle=border:none; padding:1.0em;|title=Family: [[Tombusviridae]] |
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|1={{hidden begin|title=<small>Genus: Dianthovirus</small>}} |
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*<small>'''''[[Carnation ringspot virus]]'''''</small> |
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{{hidden end}} |
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}} |
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}}<ref name=ICTV /> |
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==Structure== |
==Structure== |
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Viruses in Dianthovirus are non-enveloped, with icosahedral and spherical geometries, a “hexagonal” appearance, and T=3 symmetry. The diameter is around 28-34 nm. Genomes are linear and segmented, bipartite, around 11.3-1.4kb in length. The [[buoyant density]] in CsCl of virions is between 1.363 |
Viruses in ''Dianthovirus'' are non-enveloped, with icosahedral and spherical geometries, a “hexagonal” appearance, and T=3 symmetry. The diameter is around 28-34 nm. Genomes are linear and segmented, bipartite, around 11.3-1.4kb in length. The [[buoyant density]] in CsCl of virions is between 1.363 and 1.366 g cm-3. They have a sedimentation coefficient of 126-132-135 S20w. The [[pH]] of their [[isoelectric point]] is 4.5. The virions become inactive from about 80-90 °C and are inactive above those temperatures. They are viable [[in vitro]] for about 50–70 days. Treatment with [[diethyl ether|ether]] either decreases or does not alter their [[infectivity]]. No [[lipids]] have so far been reported.<ref name=ViralZone /> |
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{| class="wikitable sortable" style="text-align:center" |
{| class="wikitable sortable" style="text-align:center" |
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! Genus !! Structure || Symmetry !! Capsid !! Genomic arrangement !! Genomic segmentation |
! Genus !! Structure || Symmetry !! Capsid !! Genomic arrangement !! Genomic segmentation |
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|Dianthovirus||Icosahedral||T=3||Non-enveloped||Linear||Monopartite |
|''Dianthovirus''||Icosahedral||T=3||Non-enveloped||Linear||Monopartite |
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==Life cycle== |
==Life cycle== |
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Viral replication is cytoplasmic. Entry into the host cell is achieved by penetration into the host cell. Replication follows the positive stranded RNA virus replication model. Positive stranded |
Viral replication is cytoplasmic. Entry into the host cell is achieved by penetration into the host cell. Replication follows the positive stranded RNA virus replication model. Positive stranded RNA virus transcription, using the premature termination model of subgenomic RNA transcription is the method of transcription. Translation takes place by -1 ribosomal frameshifting. The virus exits the host cell by tubule-guided viral movement. Plants serve as the natural host. Transmission routes are mechanical, seed borne, and contact.<ref name=ViralZone /> |
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Plants serve as the natural host. Transmission routes are mechanical, seed borne, and contact.<ref name=ViralZone /> |
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{| class="wikitable sortable" style="text-align:center" |
{| class="wikitable sortable" style="text-align:center" |
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! Genus !! Host details !! Tissue tropism !! Entry details !! Release details !! Replication site !! Assembly site !! Transmission |
! Genus !! Host details !! Tissue tropism !! Entry details !! Release details !! Replication site !! Assembly site !! Transmission |
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|Dianthovirus||Plants||None||Viral movement; mechanical inoculation||Viral movement||Cytoplasm||Cytoplasm||Mechanical: contact; seed |
|''Dianthovirus''||Plants||None||Viral movement; mechanical inoculation||Viral movement||Cytoplasm||Cytoplasm||Mechanical: contact; seed |
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* [http://ictvonline.org/virusTaxonomy.asp '''ICTV'''] |
* [http://ictvonline.org/virusTaxonomy.asp '''ICTV'''] |
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{{Baltimore classification}} |
{{Baltimore classification}} |
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{{Taxonbar|from=Q5271721}} |
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[[Category:Tombusviridae]] |
[[Category:Tombusviridae]] |
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[[Category:Virus genera]] |
Latest revision as of 15:58, 13 February 2023
Dianthovirus | |
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Virus classification | |
(unranked): | Virus |
Realm: | Riboviria |
Kingdom: | Orthornavirae |
Phylum: | Kitrinoviricota |
Class: | Tolucaviricetes |
Order: | Tolivirales |
Family: | Tombusviridae |
Subfamily: | Regressovirinae |
Genus: | Dianthovirus |
Dianthovirus is a genus of viruses, in the family Tombusviridae. Dianthoviruses are plant viruses. There are three species in this genus. The virus probably has a worldwide distribution, and can be transmitted via nematodes, by mechanical inoculation, by grafting of plants and by contact between infected hosts with previously uninfected host.[1][2]
Taxonomy[edit]
The genus contains the following species:[2]
Structure[edit]
Viruses in Dianthovirus are non-enveloped, with icosahedral and spherical geometries, a “hexagonal” appearance, and T=3 symmetry. The diameter is around 28-34 nm. Genomes are linear and segmented, bipartite, around 11.3-1.4kb in length. The buoyant density in CsCl of virions is between 1.363 and 1.366 g cm-3. They have a sedimentation coefficient of 126-132-135 S20w. The pH of their isoelectric point is 4.5. The virions become inactive from about 80-90 °C and are inactive above those temperatures. They are viable in vitro for about 50–70 days. Treatment with ether either decreases or does not alter their infectivity. No lipids have so far been reported.[1]
Genus | Structure | Symmetry | Capsid | Genomic arrangement | Genomic segmentation |
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Dianthovirus | Icosahedral | T=3 | Non-enveloped | Linear | Monopartite |
Life cycle[edit]
Viral replication is cytoplasmic. Entry into the host cell is achieved by penetration into the host cell. Replication follows the positive stranded RNA virus replication model. Positive stranded RNA virus transcription, using the premature termination model of subgenomic RNA transcription is the method of transcription. Translation takes place by -1 ribosomal frameshifting. The virus exits the host cell by tubule-guided viral movement. Plants serve as the natural host. Transmission routes are mechanical, seed borne, and contact.[1]
Genus | Host details | Tissue tropism | Entry details | Release details | Replication site | Assembly site | Transmission |
---|---|---|---|---|---|---|---|
Dianthovirus | Plants | None | Viral movement; mechanical inoculation | Viral movement | Cytoplasm | Cytoplasm | Mechanical: contact; seed |
Genome[edit]
These viruses have segmented, bipartite genomes that are linear, positive-sense, single-stranded RNA (1). These genomes are about 5300 nucleotides in length (1). They have a methylated cap at the 5'-end whose sequence type is m7GpppA (1). The genome also codes for non-structural proteins as well as structural proteins (1). Three non-structural proteins have been found (1).
References[edit]
- ^ a b c "Viral Zone". ExPASy. Retrieved 15 June 2015.
- ^ a b "Virus Taxonomy: 2020 Release". International Committee on Taxonomy of Viruses (ICTV). March 2021. Retrieved 16 May 2021.