Salterprovirus | |
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Diagram of virion structure | |
Transmission electron micrograph of virions, negatively stained with uranyl acetate. Scale bar = 100 nm. | |
Virus classification | |
(unranked): | Virus |
Family: | Halspiviridae |
Genus: | Salterprovirus |
Species | |
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Locality of isolation: saltern crystalliser in Avalon, Victoria, Australia | |
Synonyms | |
Salterprovirus
Salterprovirus His1
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Halspiviridae is a family of viruses that consists of a single genus, Salterprovirus, which consists of a single recognised species; Salterprovirus His1 (hereafter, 'His1'). This virus was isolated from hypersaline water in Australia and was able to be cultured on the halophilic archaeon Haloarcula hispanica . Like many other archaeoviruses, His1 has an approximately limoniform (lemon-shaped) virion. [1] [2] [3] [4]
The family name, Halspiviridae, is derived from halophilic and spindle-shaped, in reference to the habitat and virion morphology, respectively. The genus name, Salterprovirus, is derived from saltyterminal protein virus, as the linear dsDNA genome has proteins attached to the 5′ termini. [1]
The virion has a spindle-shaped morphology and is similar in shape to that of viruses infecting thermophilic archaea, the Fuselloviridae , and His1 was originally described as a probable member of that group. [1] However, it was later found that there is no genetic relationship and their replication strategies are entirely different, and so His1 was classified into a new group, genus Salterprovirus within the family Halspiviridae. [5] Halspiviridae has not been classified within any higher-ranked taxa.[ citation needed ]
Environmental DNA sequences derived from Namib salt pans indicate the presence of currently unrecognised, distant relatives of His1. [6]
Another species of virus, now named Gammapleolipovirus His2 (hereafter 'His2'), was originally considered to be related to His1, [2] [3] but later analysis of the His2 virion revealed that this species actually belongs to the family Pleolipoviridae . [7]
The virus is enveloped, with limoniform or spindle-shaped morphology. Genomes are linear, around 14.5kb in length. The genome has 35 open reading frames. [3] A negatively stained electron microscope (EM) picture of His1 virions is shown on the right of this page. There is some variation in particle length (e.g. example seen left of centre), but most display the typical limoniform capsid with a short tail. High resolution micrographs and cryoEM reconstructions have been published by Hong et al. (2015), [8] who gave average dimensions of 92 x 40 nm with a 12 nm tail.
Structure | Capsid | Genomic arrangement | Genomic segmentation |
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Limoniform | Protein | Linear | Monopartite |
Viral replication is cytoplasmic. Entry into the host cell is achieved by virus attachment to the host cell. An adsorption rate constant for His1 of 1.9 x 10−12 ml min−1 has been experimentally determined by Pietilä et al. (2013). [9] DNA-templated transcription is the method of transcription. Haloarcula hispanica may serve as a host. Transmission occurs via passive diffusion. [3]
Host details | Tissue tropism | Entry details | Release details | Replication site | Assembly site | Transmission |
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Archea: Haloarcula hispanica | None | Injection | Lytic | Cytoplasm | Cytoplasm | Passive diffusion |
NCBI genome ID | NC_007914 |
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Genome size | 14,464 nucleotides |
Year of completion | 2020 |
The linear, dsDNA genome of His1 consists of 14,464 base-pairs (bp), has imperfect inverted terminal repeat sequences of 105 bp, and is annotated to carry 35 protein coding genes, including a gene specifying a protein-primed DNA polymerase (B-family). The ends of the genome have a protein attached. [2] The protein sequence of the polymerase is 42% identical to the polymerase specified by the gammapleolipovirus His2, even though the two viruses belong to very different taxonomic groups.[ citation needed ]
Virus classification is the process of naming viruses and placing them into a taxonomic system similar to the classification systems used for cellular organisms.
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Baltimore classification is a system used to classify viruses based on their manner of messenger RNA (mRNA) synthesis. By organizing viruses based on their manner of mRNA production, it is possible to study viruses that behave similarly as a distinct group. Seven Baltimore groups are described that take into consideration whether the viral genome is made of deoxyribonucleic acid (DNA) or ribonucleic acid (RNA), whether the genome is single- or double-stranded, and whether the sense of a single-stranded RNA genome is positive or negative.
Icerudivirus is a genus of viruses in the family Rudiviridae. These viruses are non-enveloped, stiff-rod-shaped viruses with linear dsDNA genomes, that infect hyperthermophilic archaea of the species Sulfolobus islandicus. There are three species in the genus.
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Bottigliavirus is the only genus in the family Ampullaviridae and contains 3 species. Ampullaviridae infect archaea of the genus Acidianus. The name of the family and genus is derived from the Latin word for bottle, ampulla, due to the virions having the shape of a bottle. The family was first described during an investigation of the microbial flora of hot springs in Italy.
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Haloarcula hispanica pleomorphic virus 1 (HHPV1) is a double stranded DNA virus that infects the halophilic archaeon Haloarcula hispanica. It has a number of unique features unlike any previously described virus.
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Spiraviridae is a family of viruses that replicate in hyperthermophilic archaea of the genus Aeropyrum, specifically Aeropyrum pernix. The family contains one genus, Alphaspiravirus, which contains one species, Aeropyrum coil-shaped virus. The virions of Aeropyrum coil-shaped virus (ACV) are non-enveloped and in the shape of hollow cylinders that are formed by a coiling fiber that consists of two intertwining halves of the circular DNA strand inside a capsid. An appendage protrudes from each end of the cylindrical virion. The viral genome is positive-sense, single-stranded DNA ( ssDNA) and encodes for significantly more genes than other known ssDNA viruses. ACV is also unique in that it appears to lack its own enzymes to aid replication, instead likely using the host cell's replisomes. ACV has no known relation to any other archaea-infecting viruses, but it does share its coil-like morphology with some other archaeal viruses, suggesting that such viruses may be an ancient lineage that only infect archaea.
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An archaeal virus is a virus that infects and replicates in archaea, a domain of unicellular, prokaryotic organisms. Archaeal viruses, like their hosts, are found worldwide, including in extreme environments inhospitable to most life such as acidic hot springs, highly saline bodies of water, and at the bottom of the ocean. They have been also found in the human body. The first known archaeal virus was described in 1974 and since then, a large diversity of archaeal viruses have been discovered, many possessing unique characteristics not found in other viruses. Little is known about their biological processes, such as how they replicate, but they are believed to have many independent origins, some of which likely predate the last archaeal common ancestor (LACA).
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