No retraction, correction or concern found when last checked on Oct 20, 2026.
ICTV Virus Taxonomy Profile: Iridoviridae
V. Gregory Chinchar, Paul Hick, Ikbal Agah Ince and 9 more
Journal of General Virology · 2017
Abstract
The Iridoviridae is a family of large, icosahedral viruses with double-stranded DNA genomes ranging in size from 103 to 220 kbp. Members of the subfamily Alphairidovirinae infect ectothermic vertebrates (bony fish, amphibians and reptiles), whereas members of the subfamily Betairidovirinae mainly infect insects and crustaceans. Infections can be either covert or patent, and in vertebrates they can lead to high levels of mortality among commercially and ecologically important fish and amphibians. This is a summary of the current International Committee on Taxonomy of Viruses (ICTV) Report on the taxonomy of the Iridoviridae, which is available at www.ictv.global/report/iridoviridae .
Full text
From PubMed Central, U.S. National Library of Medicine, as current on Oct 20, 2026. Paragraph numbers are ours, so an answer can point at one.
Virion
Virions display icosahedral symmetry and contain an internal lipid membrane located between the DNA–protein core and the outer capsid (Table 1, Fig. 1). Depending upon the genus, the capsid may have numerous external fibrils. Mature infectious virions may remain non-enveloped or bud from the plasma membrane and acquire an envelope.
Genome
The virus genome is a single molecule of double-stranded DNA that is circularly permuted and terminally redundant. The degree of redundancy varies from 5–50 % depending on the virus species. The genomes of all vertebrate iridoviruses, with one exception, are highly methylated due to a virus-encoded DNA cytosine methyltransferase. Twenty-six core proteins are common to all members of the family.
Replication
Replication involves both nuclear and cytoplasmic compartments. In the nucleus, host RNA polymerase II directs the synthesis of immediate–early virus mRNAs. In addition a virus-encoded DNA polymerase synthesizes genome- to twice-genome-size copies of the incoming DNA. This DNA is transported to the cytoplasm, where it undergoes a second round of replication to form large concatemers. Late gene expression is catalysed by a virus-encoded transcriptase. Virion morphogenesis occurs within assembly sites, and completed particles form paracrystalline arrays or bud from the plasma membrane (Fig. 2).
Taxonomy
Phylogenetic analyses indicate that invertebrate and vertebrate iridovirus lineages diverged early during the evolution of the family. Ascoviruses appear to have emerged recently from the former lineage and share with iridoviruses a common ancestry with marseilleviruses.
Ranavirus (Alphairidovirinae)
Ranaviruses are promiscuous pathogens capable of infecting three classes of ectothermic vertebrates (bony fish, amphibians and reptiles). Ranaviruses infect not only multiple species within a class, but some (e.g. Bohle iridovirus) are also capable of infecting hosts from different classes. Infections are systemic, involve multiple internal organs and may lead to high levels of morbidity and mortality among cultured, commercially important fish and amphibians, as well as endangered wild species.
Megalocytivirus (Alphairidovirinae)
Members infect >50 species of marine and freshwater fish; systemic disease involves multiple internal organs.
Lymphocystivirus (Alphairidovirinae)
Lymphocystiviruses infect >100 species of marine and freshwater fish, leading to the formation of wart-like growths composed of clusters of individual, infected cells (some as large as 1 mm) primarily on the skin, but sometimes on internal organs. Morbidity may be high but mortality tends to be low.
Iridovirus and Chloriridovirus (Betairidovirinae)
Members of these genera infect >100 insect and crustacean species. Patent infections involve massive levels of virus replication that result in infected larvae displaying marked iridescence, whereas covert infections may reduce the reproductive capacity of the host. The genera were previously distinguished based on virion size and the iridescent colour of infected larvae; phylogenetic analysis of complete genome sequences now gives a superior method of differentiation.
Resources
Full ICTV Online (10th) Report: www.ictv.global/report/iridoviridae.
References 7
- 1.
Yan X, Yu Z, Zhang P, Battisti AJ, Holdaway HA, et al. The capsid proteins of a large, icosahedral dsDNA virus. J Mol Biol. 2009;385:1287-1299.
Not in our library10.1016/j.jmb.2008.11.002
- 2.
Goorha R, Murti KG. The genome of frog virus 3, an animal DNA virus, is circularly permuted and terminally redundant. Proc Natl Acad Sci USA. 1982;79:248-252.
Not in our library10.1073/pnas.79.2.248
- 3.
- 4.
Jancovich JK, Qin Q, Zhang QY, Chinchar VG, Gray MJ, Chinchar VG. Ranavirus replication: molecular, cellular, and immunological events. Ranaviruses: Lethal Pathogens of Ectothermic Vertebrates. 2015;71-104.
Not in our library
- 5.
Piégu B, Asgari S, Bideshi D, Federici BA, Bigot Y. Evolutionary relationships of iridoviruses and divergence of ascoviruses from invertebrate iridoviruses in the superfamily Megavirales. Mol Phylogenet Evol. 2015;84:44-52.
Not in our library10.1016/j.ympev.2014.12.013
- 6.
Chinchar VG, Hyatt A, Miyazaki T, Williams T. Family Iridoviridae: poor viral relations no longer. Curr Top Microbiol Immunol. 2009;328:123-170.
Not in our library10.1007/978-3-540-68618-7_4
- 7.
Williams T, Bergoin M, van Oers MM. Diversity of large DNA viruses of invertebrates. J Invertebr Pathol. 2016.
Not in our library10.1016/j.jip.2016.08.001
Cited by papers we hold 1
Reads
Read by people on this page
None yet.
Checked or read by AI through naulon
None yet.
A person counts once a day per paper. We keep no cookie and no address: a reader is a hash that changes every day. Any month under five reads shows no number.
Are you an author?
Is this your paper?
Claim it to add your note and be paid when agents cite it. Free.