Acrasidae
| Acrasid slime molds | |
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| Acrasis rosea | |
Scientific classification 
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| Domain: | Eukaryota |
| Clade: | Discoba |
| Superphylum: | Discicristata |
| Phylum: | Percolozoa |
| Class: | Heterolobosea |
| Order: | Acrasida |
| Family: | Acrasidae van Tieghem 1880 ex Hartog 1906 |
| Genera | |
| Synonyms | |
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The family Acrasidae (ICZN, or Acrasiomycota, ICBN) is a family[1] of slime molds which belongs to the excavate group Percolozoa. The name element acrasio- comes from the Greek akrasia, 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 individual amoebae 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 group Mycetozoa, with little distinction between Acrasis and Dictyostelids, however scientists uncovered that they were distinct groups, and eventually that Acrasis was incredibly distant on the tree of life. Instead, it is found in Heterolobosia with Naegleria, away from other myxamoeba.[4]
Ecology
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
Historically it was thought that Acrasis was a sister group to Dictyostilids, other slime mold amoebas that belong to Amoebazoa, 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 placed Acrasis in Heterolobosea with the brain-eating amoebae Naegleria fowleri.[6] One particular morphological difference between Acrasis and Dictyostilids is that the stalks of the fruiting body in Acrasis are trunk like and do not contain a cellulose sheath.[5]
Heterolobosea belong within Discoba which belongs within Excavata. 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 in Acrasis and require transportation in for the translation of the remaining mitochondrial genes. The reason for this gene deficiency is because of lateral genetic transfer from the mitochondria to the nucleus. What is uncommon is how recently this phenomenon occurred in the Acrasis lineage, as sequence comparisons indicate lateral gene transfer after Acrasis split with Naegleria. This has rarely been found in any other living species of Eukarya including Naegleria, as most transfers between the mitochondria and nucleus happened in early endosymbiosis of mitochondrial ancestor into the ancestor of all Eukarya.[6]
Reproduction
When resources such as water or food become limiting, the amoeba will release pheromones such as acrasin to aggregate amoebal cells in preparation for movement as a large (thousands of cells) grex or pseudopod. When in the grex, the amoeboids reproduce, resulting in fruit-like structures called spores, which develop into unicellular molds of the same species.
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
After Acrasis 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
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.
Differientiated stage
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]
References
- ^ 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.
- ^ 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.
- ^ a b c d e f Brown, 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.
- ^ 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.
- ^ a b c d e f g Hohl, 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.
- ^ a b Fu, 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. PMID 25146648.
Further reading
- 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
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