|Group:||Group I (dsDNA)|
Iridoviridae is a family of viruses with double-stranded DNA genomes. Amphibia, fish, invertebrates, lepidoptera, and orthoptera insects serve as natural hosts. There are currently 12 species in this family, divided among two subfamilies and 5 genera. The name is derived from Iris the Greek goddess of the rainbow. This name was chosen because of the "rainbow-like" iridescence observed in heavily infected insects and pelleted samples of invertebrate iridoviruses.
The term "Iridovirus" has an ambiguous meaning. It frequently appears in the literature as a description of any member of the Iridoviridae family. Yet it also is the name of a particular genus within Iridoviridae.
Other species include the shrimp haemocyte iridescent virus.
The virions are icosahedral with triangulation number (T) = 189–217, 120–350 nm in diameter and made up of three domains: an outer proteinaceous capsid, an intermediate lipid membrane, and a central core containing DNA-protein complexes. Some of the viruses also have an outer envelope. The presence or absence of an envelope depends on whether they budded from the cell membrane (enveloped viruses) or were arranged in paracrystalline arrays within the host cell cytoplasm and then were released by cell lysis (unenveloped viruses).
The linear genome varies between 150 and 303 kilobases in length. It contains terminal and redundant sequences and is circularly permuted.
Members of this family differ in their degree of genome methylation. The genera Chloriridovirus and Iridovirus lack a highly methylated genome. Members of the Lymphocystivirus, Megalocytivirus, and Ranavirus genera have genomes with about 25% of their cytosine residues methylated by a virally encoded DNA methyltransferase.
|Genus||Structure||Symmetry||Capsid||Genomic arrangement||Genomic segmentation|
|Ranavirus||Polyhedral||T=133 or 147||Linear||Monopartite|
Similar to the herpes viruses, transcription occurs in three stages: immediate-early, delayed-early, and late. Positive induction and negative feedback mechanisms exist in each stage, mediated by products of the other stages.
Virus particles enter the cell and uncoating occurs. The viral DNA is transported to the host cell nucleus, where it is transcribed by host RNA polymerase II modified by the virus. Meanwhile, host macromolecular synthesis is stopped.
Parental DNA produces a genome which is then the template for replication in the cytoplasm. Large concatemers of viral DNA are formed by recombination in the cytoplasm. Packaging of the new genomes into virions occurs in the cytoplasm and the virus is released either by budding from the cell membrane or cell lysis.
|Genus||Host details||Tissue tropism||Entry details||Release details||Replication site||Assembly site||Transmission|
|Lymphocystivirus||Fish||None||Cell receptor endocytosis||Lysis; budding||Nucleus||Cytoplasm||Unknown|
|Megalocytivirus||Fish||None||Cell receptor endocytosis||Lysis; budding||Nucleus||Cytoplasm||Unknown|
|Ranavirus||Frogs; snakes||None||Cell receptor endocytosis||Lysis; budding||Nucleus||Cytoplasm||Contact|
|Iridovirus||Insects||None||Cell receptor endocytosis||Lysis; budding||Nucleus||Cytoplasm||Contact|
|Chloriridovirus||Diptera with aquatic larval stage, mainly mosquitoes||None||Cell receptor endocytosis||Budding||Nucleus||Cytoplasm||Unknown|
Viral Bioinformatics Resource Center & Viral Bioinformatics – Canada, University of Victoria, archived from the original on August 17, 2007, retrieved 2007-03-06