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Actinophryid

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The actinophryids are an order of heliozoa, a polyphyletic array of stramenopiles, having a close relationship with pedinellids and Ciliophrys. They are common in fresh water and occasionally found in marine and soil habitats. Actinophryids are unicellular and roughly spherical in shape, with many axopodia that radiate outward from the cell body. Axopodia are a type of pseudopodia that are supported by hundreds of microtubules arranged in interlocking spirals and forming a needle-like internal structure or axoneme. Small granules, extrusomes, that lie under the membrane of the body and axopodia capture flagellates, ciliates and small metazoa that make contact with the arms.[2][3]

Actinophryid
Scientific classification Edit this classification
Domain: Eukaryota
Clade: Diaphoretickes
Clade: SAR
Clade: Stramenopiles
Phylum: Gyrista
Subphylum: Ochrophytina
Class: Raphidomonadea
Subclass: Raphopoda
Order: Actinophryida
Hartmann 1913
Suborders & families[1]
Diversity
9 species

Description

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Actinophryids are largely aquatic protozoa with a spherical cell body and many needle-like axopodia. They resemble the shape of a sun due to this structure, which is the inspiration for their common name: heliozoa, or "sun-animalcules". Their bodies, without arms, range in size from a few tens of micrometers to slightly under a millimeter across.[1]

The outer region of cell body is often vacuolated. The endoplasm of actinophryids is less vacuolated than the outer layer, and a sharp boundary layer may be seen by light microscopy.[4] The organisms can be either mononucleate, with a single, well defined nucleus in the center of the cell body, or multinucleate, with 10 or more nuclei located under the outer vacuolated layer of cytoplasm. The cytoplasm of actinophryids is often granular, similar to that of Amoeba.[5]

Actinophryid cells may fuse when feeding, creating larger aggregated organisms. Fine granules that occur just under the cell membrane are used up when food vacuoles form to enclose prey.[6] Actinophryids may also form cysts when food is not readily available. A layer of siliceous plates is deposited under the cell membrane during the encystment process.[7]

Video of a contractile vacuole collapse in Actinosphaerium

Contractile vacuoles are common in these organisms, which are presumed to use them to maintain body volume by expelling fluids to compensate for the entry of water by osmosis. Contractile vacuoles are visible as clear bulges from the surface of the cell body that slowly fill then rapidly deflate, expelling their contents into the environment.

Axopodia

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Cross-section of the double spiral microtubule structure in an axopod

The most distinctive characteristic of the actinophryids is their axopodia. These axopodia consist of a central, rigid rod which is coated in a thin layer of ectoplasm. In Actinophrys the axonemes end on the surface of the central nucleus, and in the multicellular Actinosphaerium they end at or near nuclei.[5] The axonemes are composed of microtubules arranged in a double spiral pattern characteristic of the order.[8] Due to their long, parallel construction, these microtubules demonstrate strong birefringence.[9][10]

These axopodia are used for prey capture, in movement, cell fusion and perhaps division.[2][3] They are stiff but may flex especially near their tips,[4] and are highly dynamic, undergoing frequent construction and destruction. When used to collect prey items, two methods of capture have been noted, termed axopodial flow and rapid axopodial contraction.[2] Axopodial flow involves the slow movement of a prey item along the surface of the axopod as the ectoplasm itself moves, while rapid axopodial contraction involves the collapse of the axoneme's microtubule structure.[10] This behavior has been documented in many species, including Actinosphaerium nucleofilum, Actinophrys sol, and Raphidiophrys contractilis.[10][11][12] The rapid axopodial contraction occurs at high speed, often in excess of 5mm/s or tens of body lengths per second.[13]

The axopodial contractions have been shown to be highly sensitive to environmental factors such as temperature and pressure[9][14] as well as chemical signals like Ca2+ and colchicine.[11][15]

Reproduction

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Actinophrys undergoing multiple plasmotomy

Reproduction in actinophryids generally takes place via fission, where one parent cell divides into two or more daughter cells. For multinucleate heliozoa, this process is plasmotomic as the nuclei are not duplicated prior to division.[4] It has been observed that reproduction appears to be a response to food scarcity, with an increased number of divisions following the removal of food and larger organisms during times of food excess.[16]

Actinophryids also undergo autogamy during times of food scarcity. This is better described as genetic reorganization than reproduction, as the number of individuals produced is the same as the initial number. Nonetheless, it serves as a way to increase genetic diversity within an individual which may improve the likelihood of expressing favorable genetic traits.[17]

Plastogamy has also been extensively documented in actinophryids, especially in multinucleate ones. Actinosphaerium were observed to combine freely without the combination of nuclei, and this process sometimes resulted in more or less individuals than originally combined. This process is not caused merely by contact between two individuals but can be caused by damage to the cell body.[16]

Cyst function and formation

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Under unfavourable conditions, some species will form a cyst. This is often the product of autogamy, in which case the cysts produced are zygotes.[17] Cells undergoing this process withdraw their axopodia, adhere to the substrate, and take on an opaque and grayish appearance.[18] This cyst then divides until only uninucleate cells remain. The cyst wall is thickly layered 7–8 times and includes gelatinous layers, layers of silica plates, and iron.[19]

Taxonomy

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Originally placed in Heliozoa (Sarcodina), the actinophryids are now understood to be part of the stramenopiles. They are unrelated to centrohelid and desmothoracid heliozoa with which they had been previously classified.

There are several genera included within this classification.[20] Actinophrys are smaller and have a single, central nucleus.[11] Most have a cell body 40–50 micrometer in diameter with axopods around 100 μm in length, though this varies significantly. Actinosphaerium are several times larger, from 200 to 1000 μm in diameter, with many nuclei[11] and are found exclusively in fresh water.[21] A third genus, Camptonema, has a debated status. It has been observed once and was treated as a junior subjective synonym of Actinosphaerium by Mikrjukov & Patterson in 2001,[20] but as a valid genus by Cavalier-Smith & Scoble (2013).[1] Heliorapha is a further debated taxon, it being a new generic vehicle for the species azurina that was initially assigned to the genus Ciliophrys.[1]

Classification

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According to the latest review of actinophryid classifications, they are organized into two suborders, three families and three genera.[1][20]

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References

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Wikispecies has information related to Actinophryida.
  1. ^ a b c d e Cavalier-Smith, T; Scoble, JM (August 2013). "Phylogeny of Heterokonta: Incisomonas marina, a uniciliate gliding opalozoan related to Solenicola (Nanomonadea), and evidence that Actinophryida evolved from raphidophytes". European Journal of Protistology. 49 (3): 328–53. doi:10.1016/j.ejop.2012.09.002. PMID 23219323.
  2. ^ a b c Suzaki, T.; Shigenaka, Y.; Watanabe, S.; Toyohara, A. (1980). "Food capture and ingestion in the large heliozoan, Echinosphaerium nucleofilum". Journal of Cell Science. 42: 61–79. doi:10.1242/jcs.42.1.61. ISSN 0021-9533. PMID 7400244.
  3. ^ a b Ando, Motonori; Shigenaka, Yoshinobu (1989). "Structure and function of the cytoskeleton in heliozoa: I. Mechanism of rapid axopodial contraction in Echinosphaerium". Cell Motility and the Cytoskeleton. 14 (2): 288–301. doi:10.1002/cm.970140214.
  4. ^ a b c Barrett, J. (August 1958). "Some Observations on Actinosphaerium nucleofilum n. sp., a New Fresh Water Actinophryid". The Journal of Protozoology. 5 (3): 205–209. doi:10.1111/j.1550-7408.1958.tb02553.x.
  5. ^ a b Anderson, E.; Beams, H. W. (May 1960). "The Fine Structure of the Heliozoan, Actinosphaerium nucleofilum". The Journal of Protozoology. 7 (2): 190–199. doi:10.1111/j.1550-7408.1960.tb00729.x.
  6. ^ Patterson, D. J. & Hausmann, K. 1981. Feeding by Actinophrys sol (Protista, Heliozoa): I. Light microscopy. Microbios 31: 39–55.
  7. ^ Patterson, D.J. 1979. On the organization and classification of the protozoon Actinophrys sol Ehrenberg, 1830. Microbios 26: 165–208.
  8. ^ Gast, R.J. (2017). "Centrohelida and Other Heliozoan-like Protists". In Archibald, J.; Simpson, A.; Slamovits, C.; Margulis, L.; Melkonian, M.; Chapman, D.; Corliss, J. (eds.). Handbook of the Protists. Cham, Switzerland: Springer International. pp. 1–17. doi:10.1007/978-3-319-32669-6_28-1. ISBN 978-3-319-32669-6.
  9. ^ a b Tilney, L.; Porter, K. (July 1967). "Studies on the microtubules in heliozoa II. The effect of low temperature on these structures in the formation and maintenance of the axopodia". Journal of Cell Biology. 34 (1): 327–343. doi:10.1083/jcb.34.1.327. PMC 2107222. PMID 6033539.
  10. ^ a b c Suzaki, Toshinobu; Ando, Motonori; Inai, Yoko; Shigenaka, Yoshinobu (November 1994). "Structure and function of the cytoskeleton in heliozoa". European Journal of Protistology. 30 (4): 404–413. doi:10.1016/S0932-4739(11)80215-4.
  11. ^ a b c d Kinoshita, E; Shigenaka, Y; Suzaki, T (2001). "The ultrastructure of contractile tubules in the heliozoon Actinophrys sol and their possible involvement in rapid axopodial contraction". The Journal of Eukaryotic Microbiology. 48 (5): 519–26. doi:10.1111/j.1550-7408.2001.tb00187.x. PMID 11596916.
  12. ^ Kinoshita, Eiji; Suzaki, Toshinobu; Shigenaka, Yoshinobu; Sugiyama, Masanori (May 1995). "Ultrastructure and Rapid Axopodial Contraction of a Heliozoa, Raphidiophrys contractilis sp. nov". The Journal of Eukaryotic Microbiology. 42 (3): 283–288. doi:10.1111/j.1550-7408.1995.tb01581.x.
  13. ^ Shigenaka, Y.; Yano, K.; Suzaki, T. (1982). "Shigenaka, Y., Yano, K., Yogosawa, R. and Suzaki, T., 1982. Rapid contraction of the microtubule-containing axopodia in a large heliozoan Echinosphaerium". Biological functions of microtubules and related structures. Tokyo: Academic Press. pp. 105–114.
  14. ^ Tilney, Lewis G.; Byers, Breck (1 October 1969). "Studies on the Microtubules in Heliozoa V. Factors Controlling the Organization of Microtubules in the Axonemal Pattern in Echinosphaerium nucleofilum". The Journal of Cell Biology. 43 (1): 148–165. doi:10.1083/jcb.43.1.148. ISSN 0021-9525. PMC 2107851. PMID 5824062.
  15. ^ Tilney, L. (December 1968). "Studies on the microtubules in heliozoa. IV. The effect of colchicine on the formation and maintenance of the axopodia and the redevelopment of pattern in Actinosphaerium nucleofilum (Barrett)". Journal of Cell Science. 3 (4): 549–62. doi:10.1242/jcs.3.4.549. PMID 5707852.
  16. ^ a b Johnson, Herbert P. (April 1894). "The plastogamy of actinosphaerium". Journal of Morphology. 9 (2): 269–276. doi:10.1002/jmor.1050090206. hdl:2027/hvd.32044107306375.
  17. ^ a b Grell, Karl Gottlieb (2013). Protozoology. Berlin, Heidelberg: Springer Berlin Heidelberg. pp. 178–181. ISBN 9783642619588.
  18. ^ MacKinnon, D. L. (1906). "A few Observations on the Encystation of Actinosphaerium eichhorni under different conditions of Temperature" (PDF). Quarterly Journal of Microscopical Science. 52: 407–422. Archived (PDF) from the original on 2022-10-09. Retrieved 2 January 2018.
  19. ^ Patterson, D.; Thompson, D. (May 1981). "Structure and Elemental Composition of the Cyst Wall of Echinosphaerium nucleofilum Barrett (Heliozoea, Actinophryida)". The Journal of Protozoology. 28 (2): 188–192. doi:10.1111/j.1550-7408.1981.tb02831.x.
  20. ^ a b c Mikrjukov, Kirill A.; Patterson, David J. (2001). "Taxonomy and phylogeny of Heliozoa. III. Actinophryids" (PDF). Acta Protozoologica. 40: 3–25.
  21. ^ "Actinosphaerium eichhornii". Microworld. 2019-02-28. Retrieved 2020-01-29.
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