In virology, realm is the highest taxonomic rank established for viruses by the International Committee on Taxonomy of Viruses (ICTV), which oversees virus taxonomy. Ten virus realms are recognized and united by specific highly conserved traits:
Adnaviria, which contains archaeal filamentous viruses with A-form double-stranded (ds) DNA genomes encoding a unique alpha-helical major capsid protein; Duplodnaviria, which contains all dsDNA viruses that encode the HK97-fold major capsid protein; Efunaviria, from the sixth Latin letter “ef” and the Latin una, meaning “one”, referring to Enterobacteria phage f1, which encodes the hallmark morphogenic module of this realm; Floreoviria, which contains all single-stranded DNA (ssDNA) viruses that encode an HUH superfamily endonuclease and their descendants; Pleomoviria, a reference to the pleomorphic morphology of viruses in this realm; Riboviria, which contains all RNA viruses that encode RNA-dependent RNA polymerase and all viruses that encode reverse transcriptase; Ribozyviria, which contains hepatitis delta virus-like viruses with circular, negative-sense ssRNA genomes; Singelaviria, which contains all DNA viruses that have two major capsid proteins (MCPs) that both have a single jelly roll (SJR) fold; Varidnaviria, which contains all dsDNA viruses that encode a vertical jelly roll major capsid protein; Volvereviria, from the Latin volvere, meaning “to roll”, referring to the rolling circle replication uniformly used by viruses in this realm. The rank of realm corresponds to the rank of domain used for cellular life, but differs in that viruses in a realm do not necessarily share a common ancestor based on common descent nor do the realms share a common ancestor. Instead, realms group viruses together based on specific traits that are highly conserved over time, which may have been obtained on a single occasion or multiple occasions. As such, each realm represents at least one instance of viruses coming into existence. While historically it was difficult to determine deep evolutionary relations between viruses, in the 21st century methods such as metagenomics and cryogenic electron microscopy have enabled such research to occur, which led to the establishment of Riboviria in 2018, three realms in 2019, and two in 2020.
Naming The names of realms consist of a descriptive first part and the suffix -viria, which is the suffix used for virus realms. The first part of Duplodnaviria means "double DNA", referring to dsDNA viruses, the first part of Monodnaviria means "single DNA", referring to ssDNA viruses, the first part of Riboviria is taken from ribonucleic acid (RNA), and the first part of Varidnaviria means "various DNA". For viroids, the suffix is designated as -viroidia, and for satellites, the suffix is -satellitia, but as of 2019 neither viroid nor satellite realms have been designated.
Realms
Duplodnaviria
Duplodnaviria contains double-stranded DNA (dsDNA) viruses that encode a major capsid protein (MCP) that has the HK97 fold. Viruses in the realm also share a number of other characteristics involving the capsid and capsid assembly, including an icosahedral capsid shape and a terminase enzyme that packages viral DNA into the capsid during assembly. Two groups of viruses are included in the realm: tailed bacteriophages, which infect prokaryotes and are assigned to the order Caudovirales, and herpesviruses, which infect animals and are assigned to the order Herpesvirales. The relation between caudoviruses and herpesviruses is not certain, as they may either share a common ancestor or herpesviruses may be a divergent clade from within Caudovirales. A common trait among duplodnaviruses is that they cause latent infections without replication while still being able to replicate in the future. Tailed bacteriophages are ubiquitous worldwide, important in marine ecology, and the subject of much research. Herpesviruses are known to cause a variety of epithelial diseases, including herpes simplex, chickenpox and shingles, and Kaposi's sarcoma.
Monodnaviria Monodnaviria contains single-stranded DNA (ssDNA) viruses that encode an endonuclease of the HUH superfamily that initiates rolling circle replication and all other viruses descended from such viruses. The prototypical members of the realm are called CRESS-DNA viruses and have circular ssDNA genomes. ssDNA viruses with linear genomes are descended from them, and in turn some dsDNA viruses with circular genomes are descended from linear ssDNA viruses. CRESS-DNA viruses include three kingdoms that infect prokaryotes: Loebvirae, Sangervirae, and Trapavirae. The kingdom Shotokuvirae contains eukaryotic CRESS-DNA viruses and the atypical members of Monodnaviria. Eukaryotic monodnaviruses are associated with many diseases, and they include papillomaviruses and polyomaviruses, which cause many cancers, and geminiviruses, which infect many economically important crops.
Riboviria Riboviria contains all RNA viruses that encode an RNA-dependent RNA polymerase (RdRp), assigned to the kingdom Orthornavirae, and all reverse transcribing viruses, i.e. all viruses that encode a reverse transcriptase (RT), assigned to the kingdom Pararnavirae. These enzymes are vital in the viral life cycle, as RdRp transcribes viral mRNA and replicates the genome, and RT likewise replicates the genome. Riboviria mostly contains eukaryotic viruses, and most eukaryotic viruses, including most human, animal, and plant viruses, belong to the realm. Most widely known viral diseases are caused by viruses in Riboviria, which includes influenza viruses, HIV, coronaviruses, ebolaviruses, and the rabies virus, as well as the first virus to be discovered, Tobacco mosaic virus. Reverse transcribing viruses are a major source of horizontal gene transfer by means of becoming endogenized in their host's genome, and a significant portion of the human genome consists of this viral DNA.
Varidnaviria
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