Semotivirus | |
---|---|
Virus classification | |
(unranked): | Virus |
Realm: | Riboviria |
Kingdom: | Pararnavirae |
Phylum: | Artverviricota |
Class: | Revtraviricetes |
Order: | Ortervirales |
Family: | Belpaoviridae |
Genus: | Semotivirus |
Species | |
See text |
Semotivirus is the only genus of viruses in the family Belpaoviridae (formerly included in the family Metaviridae ). [1] Species exist as retrotransposons in a eukaryotic host's genome. BEL/pao transposons are only found in animals. Semotivirus is the only genus currently recognized, the genus description corresponds to the family, Belpaoviridae description. [2]
The lone genus in the family, Semotivirus, was formerly included in the Metaviridae family but was removed due to its paraphyletic relationship to other Metaviridae genera. There is a good chance that more species and genera will be added to the family Belpaoviridae in the future, given the diversity of belpaovirids that is already recognized. The Pol domain order of the families Belpaoviridae, Metaviridae, and Retroviridae is the same within the order Ortervirales, however the integrase is either lacking in the case of the Caulimoviridae or positioned upstream of the protease domain in the case of the Pseudoviridae. [3]
The genus is made up of long terminal repeat (LTR) retrotransposons, also referred to as metazoan-infecting reverse transcriptase viruses. [4]
The genomic arrangement of members of the Belpaoviridae family is similar to that of long terminal repeat (LTR) retrotransposons of the Metaviridae family. [5] The entire genome is 4.2–10 kb, and one to three genes (pol, env, and gag) are flanked by LTRs of 0.2–1.2 kb. [6] A non-coding region that represents the initial segment of the reverse-transcribed genome is located downstream of the 5′-LTR. This is followed by an 18 nt primer-binding site that is complementary to a certain area inside the 3′-end of a host tRNAArg or a tRNAGly.
Priming the synthesis of the proviral DNA strand is a polypurine tract of approximately 10 nt located upstream of the 3′-LTR. Gag and Pol polyproteins can be encoded by one continuous gene or by two overlapping genes. [7] These genes encode the capsid and nucleocapsid domains, as well as the protease, reverse transcriptase (RT), ribonuclease H, and integrase domains.
Few information is known about the virion morphology of belpaovirids. The virion morphology of semotivirus is poorly understood. However, belpaovirids most likely replicate by forming virus-like particles (VLPs), just like retrovirids, metavirids, and pseudovirids do, since they encode a Gag polyprotein with nucleocapsid and capsid protein domains homologous to those of other members of the order Ortervirales [8] [9] . An env-like gene is present in certain belpaovirids, however its exact role is still unknown. [10]
Although the details of replication are not well known, it is thought to resemble that of members of the Metaviridae family [11] , in which RT mediates the conversion of a full transcript into a dsDNA that is incorporated into the host genome by the integrase protein. After the integrated provirus has been transcribed by the host RNA polymerase II, new virus RNAs are created, which the matching host enzymes cap and polyadenylate. Once in the host cell's cytoplasm, these fresh viral RNAs are translated into immature VLPs by Gag and Pol. VLP maturation is the end outcome of the viral protease's proteolytic processing of the polyproteins. The new viral RNAs are then reverse-transcribed by RT into dsDNA molecules, which are then sent back to the nucleus and inserted into fresh locations within the host cell genome. [12]
RT: Reverse Transcripase.
VLPS: Virus-Like Particle.
LTRs: Long Terminal Repeat.
The genus contains the following species: [13]
A retrovirus is a type of virus that inserts a DNA copy of its RNA genome into the DNA of a host cell that it invades, thus changing the genome of that cell. After invading a host cell's cytoplasm, the virus uses its own reverse transcriptase enzyme to produce DNA from its RNA genome, the reverse of the usual pattern, thus retro (backward). The new DNA is then incorporated into the host cell genome by an integrase enzyme, at which point the retroviral DNA is referred to as a provirus. The host cell then treats the viral DNA as part of its own genome, transcribing and translating the viral genes along with the cell's own genes, producing the proteins required to assemble new copies of the virus. Many retroviruses cause serious diseases in humans, other mammals, and birds.
Metaviridae is a family of viruses which exist as Ty3-gypsy LTR retrotransposons in a eukaryotic host's genome. They are closely related to retroviruses: members of the family Metaviridae share many genomic elements with retroviruses, including length, organization, and genes themselves. This includes genes that encode reverse transcriptase, integrase, and capsid proteins. The reverse transcriptase and integrase proteins are needed for the retrotransposon activity of the virus. In some cases, virus-like particles can be formed from capsid proteins.
Pseudoviridae is a family of viruses, which includes three genera.
Caulimoviridae is a family of viruses infecting plants. There are 94 species in this family, assigned to 11 genera. Viruses belonging to the family Caulimoviridae are termed double-stranded DNA (dsDNA) reverse-transcribing viruses i.e. viruses that contain a reverse transcription stage in their replication cycle. This family contains all plant viruses with a dsDNA genome that have a reverse transcribing phase in their lifecycle.
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.
Lipothrixviridae is a family of viruses in the order Ligamenvirales. Thermophilic archaea in the phylum Thermoproteota serve as natural hosts. There are 11 species in this family, assigned to 4 genera.
Guttaviridae is a family of viruses. Archaea serve as natural hosts. There are two genera in this family, containing one species each. The name is derived from the Latin gutta, meaning 'droplet'.
LTR retrotransposons are class I transposable elements (TEs) characterized by the presence of long terminal repeats (LTRs) directly flanking an internal coding region. As retrotransposons, they mobilize through reverse transcription of their mRNA and integration of the newly created cDNA into another genomic location. Their mechanism of retrotransposition is shared with retroviruses, with the difference that the rate of horizontal transfer in LTR-retrotransposons is much lower than the vertical transfer by passing active TE insertions to the progeny. LTR retrotransposons that form virus-like particles are classified under Ortervirales.
Globuloviridae is a family of hyperthermophilic archaeal viruses. Crenarchaea of the genera Pyrobaculum and Thermoproteus serve as natural hosts. There are four species in this family, assigned to a single genus, Alphaglobulovirus.
Bicaudaviridae is a family of hyperthermophilic archaeal viruses. Members of the genus Acidianus serve as natural hosts. There is only one genus, Bicaudavirus, and one species, Acidianus two-tailed virus, in this family. However, Sulfolobus tengchongensis spindle-shaped viruses 1 and 2 are regarded to belong to this family also.
Clavaviridae is a family of double-stranded viruses that infect archaea. This family was first described by the team led by D. Prangishvili in 2010. There is one genus in this family (Clavavirus). Within this genus, a single species has been described to date: Aeropyrum pernix bacilliform virus 1 (APBV1).
Yingchengvirus is a genus of double stranded DNA viruses that infect haloarchaea. The genus was previously named Betasphaerolipovirus.
Alphaguttavirus is a genus of viruses, in the family Guttaviridae. Sulfolobus newzealandicus serve as natural hosts. There is only one species in this genus: Sulfolobus newzealandicus droplet-shaped virus.
Tristromaviridae is a family of viruses. Archaea of the genera Thermoproteus and Pyrobaculum serve as natural hosts. Tristromaviridae is the sole family in the order Primavirales. There are two genera and three species in the family.
Metavirus is a genus of viruses in the family Metaviridae. They are retrotransposons that invade a eukaryotic host genome and may only replicate once the virus has infected the host. These genetic elements exist to infect and replicate in their host genome and are derived from ancestral elements unrelated from their host. Metavirus may use several different hosts for transmission, and has been found to be transmissible through ovule and pollen of some plants.
Caenorhabditis elegans Cer13 virus is a species of virus in the genus Semotivirus and the family Belpaoviridae. It exists as retrotransposons in the Caenorhabditis elegans genome.
Ortervirales is an order that contains all accepted species of single-stranded RNA viruses that replicate through a DNA intermediate and all accepted species of double-stranded DNA viruses that replicate through an RNA intermediate . The name is derived from the reverse of retro.
Riboviria is a realm of viruses that includes all viruses that use a homologous RNA-dependent polymerase for replication. It includes RNA viruses that encode an RNA-dependent RNA polymerase, as well as reverse-transcribing viruses that encode an RNA-dependent DNA polymerase. RNA-dependent RNA polymerase (RdRp), also called RNA replicase, produces RNA from RNA. RNA-dependent DNA polymerase (RdDp), also called reverse transcriptase (RT), produces DNA from RNA. These enzymes are essential for replicating the viral genome and transcribing viral genes into messenger RNA (mRNA) for translation of viral proteins.
Thaspiviridae is a family of incertae sedis spindle-shaped viruses. The family contains a single genus, Nitmarvirus, which contains a single species, Nitmarvirus NSV1.
Adnaviria is a realm of viruses that includes archaeal viruses that have a filamentous virion and a linear, double-stranded DNA genome. The genome exists in A-form (A-DNA) and encodes a dimeric major capsid protein (MCP) that contains the SIRV2 fold, a type of alpha-helix bundle containing four helices. The virion consists of the genome encased in capsid proteins to form a helical nucleoprotein complex. For some viruses, this helix is surrounded by a lipid membrane called an envelope. Some contain an additional protein layer between the nucleoprotein helix and the envelope. Complete virions are long and thin and may be flexible or a stiff like a rod.