| Ichthyosporea Temporal range: | |
|---|---|
 | |
| Sphaeroforma arctica | |
Scientific classification  | |
| Domain: | Eukaryota |
| Clade: | Amorphea |
| Clade: | Obazoa |
| (unranked): | Opisthokonta |
| (unranked): | Holozoa |
| Class: | Ichthyosporea Cavalier-Smith, 1998 [1] |
| Orders | |
| Synonyms | |
Mesomycetozoa Mendoza et al., 2002 | |
The Ichthyosporea (or DRIP clade, or Mesomycetozoea) are a small group of Opisthokonta in Eukaryota (formerly protists), mostly parasites of fish and other animals.
They are not particularly distinctive morphologically, appearing in host tissues as enlarged spheres or ovals containing spores, and most were originally classified in various groups as fungi, protozoa, or colorless algae. However, they form a coherent group on molecular trees, closely related to both animals and fungi and so of interest to biologists studying their origins. In a 2008 study they emerge robustly as the sibling-group of the clade Filozoa, which includes the animals. [2] [3]
Huldtgren et al., following x-ray tomography of microfossils of the Ediacaran Doushantuo Formation, has interpreted them as mesomycetozoan spore capsules. [4]
The name DRIP is an acronym for the first protozoa identified as members of the group, [5] Cavalier-Smith later treated them as the class Ichthyosporea, since they were all parasites of fish.
Since other new members have been added (e.g. the former fungal orders Eccrinales and Amoebidiales), Mendoza et al. suggested changing the name to Mesomycetozoea, which refers to their evolutionary position. On Eukaryota tree, in Opisthokont clade, Mesomycetozoea is in the middle ("Meso-") of the fungi ("-myceto-") and the animals ("-zoea"). [6] Note the name Mesomycetozoa (without a third e) is also used to refer to this group, but Mendoza et al. use it as an alternate name for basal Opisthokonts. [7]
| Ichthyosporea [8] [9] |
| ||||||||||||||||||||||||||||||||||||||||||||||||
The opisthokonts are a broad group of eukaryotes, including both the animal and fungus kingdoms. The opisthokonts, previously called the "Fungi/Metazoa group", are generally recognized as a clade. Opisthokonts together with Apusomonadida and Breviata comprise the larger clade Obazoa.
Amorphea is a taxonomic supergroup that includes the basal Amoebozoa and Obazoa. That latter contains the Opisthokonta, which includes the Fungi, Animals and the Choanomonada, or Choanoflagellates. The taxonomic affinities of the members of this clade were originally described and proposed by Thomas Cavalier-Smith in 2002.
Cristidiscoidea or Nucleariae is a proposed basal holomycota clade in which Fonticula and Nucleariida emerged, as sister of the fungi. Since it is close to the divergence between the main lineages of fungi and animals, the study of Cristidiscoidea can provide crucial information on the divergent lifestyles of these groups and the evolution of opisthokonts and slime mold multicellularity. The holomycota tree is following Tedersoo et al.
Rhinosporidium seeberi is a eukaryotic pathogen responsible for rhinosporidiosis, a disease which affects humans, horses, dogs, and to a lesser extent cattle, cats, foxes, and birds. It is most commonly found in tropical areas, especially India and Sri Lanka.
Rhinosporidiosis is an infection caused by Rhinosporidium seeberi.
Capsaspora is a monotypic genus containing the single species Capsaspora owczarzaki. C. owczarzaki is a single-celled eukaryote that occupies a key phylogenetic position in our understanding of the origin of animal multicellularity, as one of the closest unicellular relatives to animals. It is, together with Ministeria vibrans, a member of the Filasterea clade. This amoeboid protist has been pivotal to unravel the nature of the unicellular ancestor of animals, which has been proved to be much more complex than previously thought.
Corallochytrium belongs to the class of Corallochytrea within Teretosporea and is a sister group to Ichthyosporea. Corallochytrium limacisporum is the only species of Corallochytrium known so far. It was first discovered and named in the Arabian Sea’s coral lagoons by Kaghu-Kumar in 1987. It was first thought to be a member of the fungi-like thraustochytrids, however, this was later disproven due to Corallochytriums lack of cilia and sagenogenetosome. Little research has been done on the life cycle or morphology. Most research concerning this genus has been done to uncover the evolution of animals and fungi, as Corallochytrium possess both animal and fungal enzymatic trademarks.
Dermocystidium is a genus of cyst-forming, eukaryotic fish parasites, the causative agents of dermocystidiosis.
Ichthyophonida is an order of parasitic eukaryotes.
Dermocystida is an order of parasitic eukaryotes.
Filasterea is a proposed basal Filozoan clade that includes Ministeria and Capsaspora. It is a sister clade to the Choanozoa in which the Choanoflagellatea and Animals appeared. Originally proposed by Shalchian-Tabrizi et al. in 2008, based on a phylogenomic analysis with dozens of genes. Filasterea was found to be the sister-group to the clade composed of Metazoa and Choanoflagellata within the Opisthokonta, a finding that has been further corroborated with additional, more taxon-rich, phylogenetic analyses.
Holozoa is a clade of organisms that includes animals and their closest single-celled relatives, but excludes fungi and all other organisms. Together they amount to more than 1.5 million species of purely heterotrophic organisms, including around 300 unicellular species. It consists of various subgroups, namely Metazoa and the protists Choanoflagellata, Filasterea, Pluriformea and Ichthyosporea. Along with fungi and some other groups, Holozoa is part of the Opisthokonta, a supergroup of eukaryotes. Choanofila was previously used as the name for a group similar in composition to Holozoa, but its usage is discouraged now because it excludes animals and is therefore paraphyletic.
The apusomonads are a group of protozoan zooflagellates that glide on surfaces, and mostly consume prokaryotes. They are of particular evolutionary interest because they appear to be the sister group to the Opisthokonts, the clade that includes both animals and fungi. Together with the Breviatea, these form the Obazoa clade.
Amoebidiidae is a family of single-celled eukaryotes, previously thought to be zygomycete fungi belonging to the class Trichomycetes, but molecular phylogenetic analyses place the family with the opisthokont group Mesomycetozoea. The family was originally called Amoebidiaceae, and considered the sole family of the fungal order Amoebidiales that included two genera: Amoebidium and Paramoebidium. However, Amoebidiidae is now monogeneric as it was recently emended to include only Amoebidium. Species of Amoebidium are considered obligate symbionts of freshwater-dwelling arthropod hosts such as midge larvae and water fleas (Daphnia). However, because Amoebidium species attach to the exoskeleton (exterior) of the host and grow in axenic culture, at least some species may be facultative symbionts.
Choanozoa is a clade of opisthokont eukaryotes consisting of the choanoflagellates (Choanoflagellatea) and the animals. The sister-group relationship between the choanoflagellates and animals has important implications for the origin of the animals. The clade was identified in 2015 by Graham Budd and Sören Jensen, who used the name Apoikozoa. The 2018 revision of the classification first proposed by the International Society of Protistologists in 2012 recommends the use of the name Choanozoa.
Creolimax fragrantissima is a single-celled protist that occupies a key phylogenetic position to understand the origin of animals. It was isolated from the digestive tract of some marine invertebrates, mainly from the peanut worm, collected from the Northeast Pacific.
Amoebidium is a genus of unicellular, symbiotic eukaryotes in the Opisthokont group Mesomycetozoea, family Amoebidiidae. Amoebidium species attach to the exoskeleton of freshwater aquatic arthropods such as midge larvae and water fleas (Daphnia). The type species is Amoebidium parasiticum, which is also one of the only species to be cultured axenically.
Paramoebidium is a genus of unicellular, symbiotic eukaryotes that inhabit the digestive tract of immature freshwater arthropod hosts. Paramoebidium is classified in the opisthokont class Mesomycetozoea, and is the sole genus in the family Paramoebidiidae. Prior to 2005, Paramoebidium species were tentatively placed with the fungal group Trichomycetes due to their habitation of arthropod guts, host overlap between various Paramoebidium and fungal trichomycete taxa, and similar vegetative growth form.
Paramoebidiidae is a family of single-celled eukaryotes, previously thought to be zygomycete fungi belonging to the class Trichomycetes, but molecular phylogenetic analyses place the family with the opisthokont group Mesomycetozoea. The family was originally called Amoebidiaceae, and considered the sole family of the fungal order Amoebidiales that included two genera, Amoebidium and Paramoebidium. However, Paramoebidium is now the sole genus of the family Paramoebidiidae and Amoebidiidae is likewise monogeneric as it was recently emended to include only Amoebidium. Species of Paramoebidium are obligate symbionts of immature freshwater-dwelling arthropod hosts such as mayfly and stonefly nymphs and black fly larvae. Paramoebidium species attach to the digestive tract lining of their host via a secreted holdfast.
Pirum gemmata is a unicellular eukaryote that belongs to the Ichthyosporea clade, a group of protists closely related to animals. P. gemmata was isolated from the gut contents of a marine invertebrate, specifically the detritivorous peanut worm Phascolosoma agassizii.