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Acrasidae

From Wikipedia, the free encyclopedia
(Redirected fromAcrasis)
Family of slime moulds

Acrasid slime molds
Acrasis rosea
Scientific classificationEdit this classification
Domain:Eukaryota
Clade:Discoba
Superphylum:Discicristata
Phylum:Heterolobosea
Order:Acrasida
Family:Acrasidae
van Tieghem 1880 ex Hartog 1906
Genera
Synonyms
  • AcrasiaceaePoche 1913 em. Olive 1970
  • GuttulinaceaeZopf 1885 ex Berlese 1888 nom. rej.
  • GuttulininaeDoflein & Reichenow 1952
  • PocheinaceaeLoeblich & Tappan 1961 nom. cons.
Acrasis rosea amoebae and spores under microscope

The familyAcrasidae (ICZN, orAcrasiomycota,ICBN) is a family[1] ofslime molds which belongs to theexcavate groupHeterolobosea. The name elementacrasio- comes from the Greekakrasia, meaning "acting against one's judgement". This group consists of cellular slime molds.

The terms "Acrasiomycota" or "Acrasiomycetes" have been used when the group was classified as a fungus ("-mycota"). In some classifications,Dictyostelium was placed in Acrasiomycetes, an artificial group of cellular slime molds, which was characterized by the aggregation of individualamoebae into a multicellular fruiting body, making it an important factor that related the acrasids to the dictyostelids.[2]

Each cell keeps its individuality even when it forms a stalk and fruiting body to reproduce.[3] Slime molds were originally thought to be in a monophyletic groupMycetozoa, with little distinction betweenAcrasis andDictyostelids, however scientists uncovered that they were distinct groups, and eventually thatAcrasis was incredibly distant on the tree of life. Instead, it is found inHeterolobosia withNaegleria, away from other myxamoeba.[4]

Ecology

[edit]

Acrasis is found in terrestrial habitats on dead or decaying bark or dead tissue still attached to plants.[3] They are often cultured using yeast which makes up most of their diet, but they are known to participate in cannibalism in their solitary mobile stage of life.[5] They may also be found on living tree bark.[3]

Evolutionary history

[edit]

Historically it was thought thatAcrasis was a sister group to dictyostelids, other slime mold amoebas that belong to Amoebozoa, due to how they both aggregate in order to form a fruiting body. However, in their amoeboid form it was realized they were fundamentally different and molecular phylogenetic studies placedAcrasis inHeterolobosea alongside the infamousNaegleria[6] One particular morphological difference betweenAcrasis and dictyostelids is that the stalks of the fruiting body inAcrasis are trunk-like and do not contain a cellulose sheath.[5]

Heterolobosea belong within Discoba. Out of all discobids,Acrasis has the most compact mitochondrial genome that requires additional transport activity due to the number of genes lost. tRNA genes, which are commonly found in most mitochondria sequences, are scarce inAcrasis and require transportation in for the translation of the remaining mitochondrial genes. The reason for this gene deficiency is because of gene transfer from the mitochondria to the nucleus. This transfer of tRNA genes occurred recently in theAcrasis lineage, as sequence comparisons indicate gene transfer afterAcrasis split withNaegleria.[6]

Reproduction

[edit]

When resources such as water or food become limiting, the amoeba will releasepheromones such asacrasin to aggregateamoebal cells in preparation for movement as a large (thousands of cells)grex orpseudopod. When in the grex, the amoeboids reproduce, resulting in fruit-like structures calledspores, which develop intounicellularmolds of the samespecies.

Its reproductive cycle can be broken up to three distinct life stages where the Acrasis cell experiences morphological and intracellular changes [2].

Vegetative/solitary stage

[edit]

AfterAcrasis spores are released, they germinate into free living limax amoebae, where they use a single pseudopodium to move forward, reaching to become up to 32 micrometers long.[3] During this stage they may experience conditions of starvation or dehydration where they differentiate into a microcyst that has an extracellular cell wall.[5] This microcyst can then differentiate back into the limax amoebae form. Alternatively, if conditions are favorable, a stimulus can signal the amoebae to aggregate together.[5]

Pseudoplasmodial stage

[edit]

Upon stimulation they begin to aggregate into the “slug” that will eventually begin to form a mound with others of the same species.[3][5] Each cell keeps its individuality and only minor intracellular alterations are seen.[5] One of the alterations seen in the cells between the vegetative and pseudoplasmodial stage is the decrease in number and volume of food vacuoles.

Differentiated stage

[edit]

Within the mound one amoeba differentiates into a stalk cell that the others rest atop of, creating a structure called the sorogen. After the stalk grows from repeated cell differentiation into basal stalk cells, select cells form distal spore cells and the sporocarp structure from which they are released. This forms the fruiting body that overall has great plasticity through the ability to branch.[3] Throughout this process from the solitary stage to the formation of the fruiting body, each cell maintains its individuality. Following the formation of the fruiting body, spores are released, and the cycle begins anew.[5]

See also

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References

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  1. ^Roger AJ, Smith MW, Doolittle RF, Doolittle WF (1996)."Evidence for the Heterolobosea from phylogenetic analysis of genes encoding glyceraldehyde-3-phosphate dehydrogenase".J. Eukaryot. Microbiol.43 (6):475–85.doi:10.1111/j.1550-7408.1996.tb04507.x.PMID 8976605.
  2. ^Cavender J.C.; Spiegl F.; Swanson A. (2002). "Taxonomy, slime molds, and the questions we ask".The Mycological Society of America.94 (6):968–979.PMID 21156570.
  3. ^abcdefBrown, M. W.; Silberman; Spiegel (2010). "A Morphologically Simple Species of Acrasis (Heterolobosea, Excavata), Acrasis helenhemmesae n. sp".Journal of Eukaryotic Microbiology.57 (4):346–353.doi:10.1111/j.1550-7408.2010.00481.x.PMID 20497285.
  4. ^Brown, M. W.; Kolisko, M.; Silberman, J. D.; Roger, A. J. (2012)."Aggregative Multicellularity Evolved Independently in the Eukaryotic Supergroup Rhizaria".Current Biology.22 (12):1123–1127.Bibcode:2012CBio...22.1123B.doi:10.1016/j.cub.2012.04.021.PMID 22608512.
  5. ^abcdefgHohl, H. R.; Hamamoto, S. T. (1969). "Ultrastructure of Acrasis rosea, a Cellular Slime Mold, During Development*".The Journal of Protozoology.16 (2):333–344.doi:10.1111/j.1550-7408.1969.tb02279.x.PMID 5816073.
  6. ^abFu, C. J.; Sheikh, S.; Miao, W.; Siv, G. E.; Andersson; Baldauf, S. L. (2014)."Missing Genes, Multiple ORFs, and C-to-U Type RNA Editing in Acrasis kona (Heterolobosea, Excavata) Mitochondrial DNA".Genome Biology and Evolution.6 (9):2240–2257.doi:10.1093/gbe/evu180.PMC 4202320.PMID 25146648.

Further reading

[edit]
  • C.J. Alexopolous, Charles W. Mims, M. Blackwell et al.,Introductory Mycology, 4th ed. (John Wiley and Sons, Hoboken NJ, 2004)ISBN 0-471-52229-5
Discoba classification
Tsukubea
Jakobea
Ophirinina
Andalucina
Histionina
Petalomonadida
Ploeotiida*
Alistosa
Karavia
Anisonemia
Anisonemida
Natomonadida
Metanemina
Aphagea
Peranemida
Rapazida
Eutreptiales
Euglenales
incertae sedis
incertae sedis
Symbiontida
Diplonemea
Prokinetoplastina
Neobodonida
Parabodonida
Eubodonida
Trypanosomatida
incertae sedis
Pharyngomonada
Pharyngomonadea
Pharyngomonadida
Selenaionea
Selenaionida
Neovahlkampfiida
Naegleriida
Percolomonadida
Pseudociliatida
Creneida
Lyromonadida
Acrasidae
Acrasiomycota
Acrasida
Acrasiomycetes
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