Peranema

Last updated

Contents

Peranema
Peranema.jpg
Peranema sp.
Scientific classification
Domain:
(unranked):
Phylum:
Class:
Order:
Family:
Genus:
Peranema

Dujardin, 1841
Species

See text

Peranema is a genus of free-living phagotrophic euglenids (Euglenida; Euglenozoa; Excavata). There are more than 20 nominal species, varying in size between 8 and 200 micrometers. [1] Peranema cells are gliding flagellates found in freshwater lakes, ponds and ditches, and are often abundant at the bottom of stagnant pools rich in decaying organic material. [2] Although they belong to the class Euglenoidea, and are morphologically similar to the green Euglena , Peranema have no chloroplasts, and do not conduct autotrophy. Instead, they capture live prey, such as yeast, bacteria and other flagellates, consuming them with the help of a rigid feeding apparatus called a "rod-organ." Unlike the green euglenids, they lack both an eyespot (stigma), and the paraflagellar body (photoreceptor) that is normally coupled with that organelle. [3] However, while Peranema lack a localized photoreceptor, they do possess the light-sensitive protein rhodopsin, and respond to changes in light with a characteristic "curling behaviour." [4]

O.F. Muller's Vibrio strictus Muller Vibrio strictus.jpg
O.F. Müller's Vibrio strictus

The earliest record of a Peranema is in O.F. Müller's Animalcula Infusoria of 1786, which describes an "elongated linear" creature, "stretched out at the front." Müller named it Vibrio strictus, placing it among the "long-necked" infusoria, along with Lacrymaria olor and Dileptus . [5] The species Peranema trichophorum was seen and described in 1838 by C.G. Ehrenberg, who, like Müller before him, took the flagellum for a necklike extension of the body, and placed it in the ciliate genus Trachelius. [6] Peranema was correctly identified as a flagellate by Félix Dujardin, who created the genus in 1842, giving it the name Pyronema, for its pyriform (pear-shaped) body. However, because that name had already been applied to a genus of fungi, he amended the genus to Peranema, formed from the Greek πέρα (a leather purse or sack) and νήμα (a thread). [7] Unfortunately, this name had also been claimed earlier, for a genus of ferns first collected in Nepal. As a result, botanists, following the International Code of Botanical Nomenclature, customarily refer to the protist Peranema as Pseudoperanema; whereas protozoologists, following the International Code of Zoological Nomenclature, have continued to call the genus by the name Dujardin gave it. [8]

Appearance and characteristics

Peranema Peranema diagram 2.jpg
Peranema

Peranema's basic anatomy is that of a typical euglenid. The cell is spindle or cigar-shaped, somewhat pointed at the anterior end. It has a pellicle with parallel finely-ridged proteinaceous strips underlain by microtubules arranged in a helical fashion around the body. With this type of pellicle, which is shared by many euglenids, the spiraling microtubular strips are able to slide past one another, giving the organism an extremely plastic and changeable body shape. This permits a type of squirming motility, sometimes referred to as "euglenoid movement" or "metaboly". [9] When it is not gliding or swimming (poorly), Peranema can move by metaboly, progressing with wavelike contractions of the body, reminiscent of peristalsis. [10] [11]

At the anterior of the cell, there is a narrow aperture, opening into a flask-shaped "reservoir", from which the organism's two flagella emerge. At the bottom of this reservoir lie the basal bodies (centrioles) from which the flagella extend. [12] One flagellum is relatively long and conspicuous, and when the Peranema is gliding it is held stiffly in front. At the tip of the flagellum, a short segment beats and flails in a rhythmic manner, possibly as a mechanism for detecting and contacting potential prey. Peranama usually glides belly-down, without rotating. [13]

The second flagellum is difficult to see with bright field microscopy, and was entirely overlooked by early observers. It emerges from the same reservoir as the larger propulsive flagellum, but turns toward the posterior. It does not sit freely, like the trailing flagella of Dinema and Entosiphon, but adheres to the outside of the cell membrane, in a groove along its ventral surface. [14]

Next to the reservoir, lies Peranema's highly developed feeding apparatus, a cytostomal sac supported on one side by a pair of rigid rods, fused together at the anterior end. The use of this "rod-organ" in feeding has attracted considerable scholarly interest. Some early researchers speculated that it might assist Peranema in tearing up and consuming its food; while others held that it was actually a tubular construction, serving as a cytopharynx. [15] In 1950, Y. T. Chen accurately identified it as a structure separate from the reservoir, which could be used by Peranama to cut and pierce its prey. [16] Brenda Nisbet questioned this, on the grounds that, when examined closely with an electron microscope, the rod-organ is blunt, and therefore an improbable instrument for either cutting or piercing. Since the rod-organ had been seen to move back and forth during feeding, Nisbet argued that its primary function is to create suction, drawing prey into the cytostome. [12]

In 1997, Richard Triemer returned to the subject, to confirm Chen's opinion that Peranema has a dual feeding technique. It can swallow prey whole, pulling large flagellates through the cytostome, in a manner similar to that proposed by Brenda Nisbet. However, it can also choose a more elaborate style of attack. Sometimes, it will press its cytostome against its prey, and then move the rod-organ up and down, using a rasping motion to chew a hole in its victim's cell membrane. After consuming some of the protoplasm, the Peranema may then insert its large flagellum into the hole, using it to churn up the contents of the cell so that they may be more easily sucked out. This continues until nothing is left of the prey but the tattered remnants of its pellicle. [17]

Phylogeny and classification

Peranema, as drawn by William Saville-Kent in 1880 Saville-kent peranema.jpg
Peranema, as drawn by William Saville-Kent in 1880

When Dujardin created the genus Peranema in 1841, he was unable to detect the second flagellum and classified it with other ostensibly uniflagellate "Eugléniens," Astasia and Euglena. In 1881 Georg Klebs drew a taxonomical distinction between colorless uniflagellates that live by phagotrophy (Peranema and Astasia) and the green uniflagellates that photosynthesize (Euglena). [18] This distinction was generally abandoned after the publication, in 1952, of a major revision of the euglenoids. [19] In 1997, a combined morphological and molecular analysis of certain euglenoids identified Peranama trichophorum, Euglena gracilis and Khawkinea quartana as a distinct monophyletic lineage, with P. trichophorum basal to the other two species. [20]

Video of Peranema sp. in phase contrast microscopy, from the YouTube channel of microuruguay.
Video of Peranema sp., showing the ingestion apparatus, from the YouTube channel of microuruguay.

Species

Further reading

Hassett, Charles (July 1944). "Photo-dynamic Action in the Flagellate Peranema Trichophorum with Special Reference to Motor Response to Light". Chicago Journals. 17 (3): 270–278. JSTOR   30151839.

Related Research Articles

<span class="mw-page-title-main">Euglenozoa</span> Phylum of protozoans

Euglenozoa are a large group of flagellate Discoba. They include a variety of common free-living species, as well as a few important parasites, some of which infect humans. Euglenozoa are represented by four major groups, i.e., Kinetoplastea, Diplonemea, Euglenida, and Symbiontida. Euglenozoa are unicellular, mostly around 15–40 μm (0.00059–0.00157 in) in size, although some euglenids get up to 500 μm (0.020 in) long.

<i>Euglena</i> Genus of unicellular flagellate eukaryotes

Euglena is a genus of single cell flagellate eukaryotes. It is the best known and most widely studied member of the class Euglenoidea, a diverse group containing some 54 genera and at least 200 species. Species of Euglena are found in fresh water and salt water. They are often abundant in quiet inland waters where they may bloom in numbers sufficient to color the surface of ponds and ditches green (E. viridis) or red (E. sanguinea).

<span class="mw-page-title-main">Euglenid</span> Class of protozoans

Euglenids are one of the best-known groups of flagellates, which are excavate eukaryotes of the phylum Euglenophyta and their cell structure is typical of that group. They are commonly found in freshwater, especially when it is rich in organic materials, with a few marine and endosymbiotic members. Many euglenids feed by phagocytosis, or strictly by diffusion. A monophyletic group consisting of the mixotrophic Rapaza viridis and the two groups Eutreptiales and Euglenales have chloroplasts and produce their own food through photosynthesis. This group is known to contain the carbohydrate paramylon.

<i>Euglena gracilis</i> Species of single-celled Eukaryote algae

Euglena gracilis is a freshwater species of single-celled alga in the genus Euglena. It has secondary chloroplasts, and is a mixotroph able to feed by photosynthesis or phagocytosis. It has a highly flexible cell surface, allowing it to change shape from a thin cell up to 100 µm long to a sphere of approximately 20 µm. Each cell has two flagella, only one of which emerges from the flagellar pocket (reservoir) in the anterior of the cell, and can move by swimming, or by so-called "euglenoid" movement across surfaces. E. gracilis has been used extensively in the laboratory as a model organism, particularly for studying cell biology and biochemistry.

<i>Trachelomonas</i> Genus of euglenoids

Trachelomonas is a genus of swimming, free-living euglenoids characterized by the presence of a shell-like covering called a lorica. Details of lorica structure determine the classification of distinct species in the genus. The lorica can exist in spherical, elliptical, cylindrical, and pyriform (pear-shaped) forms. The lorica surface can be smooth, punctuate or striate and range from hyaline, to yellow, or brown. These colors are due to the accumulation of ferric hydroxide and manganic oxide deposited with the mucilage and minerals that comprise the lorica. In Trachelomonas, the presence of a lorica obscures cytoplasmic details of the underlying cell. In each Trachelomonas cell, there is a gap at the apex of the lorica from which the flagellum protrudes. Thickening around this gap results in a rim-like or collar-like appearance. During asexual reproduction, the nucleus divides yielding two daughter cells one of which exits through the opening in the lorica. This new cell then synthesizes its own new lorica.

<span class="mw-page-title-main">Euglenales</span> Order of flagellate eukaryotes

Euglenales is an order of flagellates in the phylum Euglenozoa. The family includes the most well-known euglenoid genus, Euglena, as well as other common genera like Phacus and Lepocinclis.

<span class="mw-page-title-main">Euglenaceae</span> Family of flagellate eukaryotes

Euglenaceae is a family of flagellates in the phylum Euglenozoa. The family includes the most well-known euglenoid genus, Euglena.

<span class="mw-page-title-main">Protozoa</span> Single-celled eukaryotic organisms that feed on organic matter

Protozoa are a polyphyletic group of single-celled eukaryotes, either free-living or parasitic, that feed on organic matter such as other microorganisms or organic debris. Historically, protozoans were regarded as "one-celled animals".

<i>Colpodella</i> Genus of single-celled organisms

Colpodella is a genus of alveolates comprising 5 species, and two further possible species: They share all the synapomorphies of apicomplexans, but are free-living, rather than parasitic. Many members of this genus were previously assigned to a different genus - Spiromonas.

<i>Phacus</i> Genus of algae

Phacus is a genus of unicellular excavates, of the phylum Euglenozoa, characterized by its flat, leaf-shaped structure, and rigid cytoskeleton known as a pellicle. These eukaryotes are mostly green in colour, and have a single flagellum that extends the length of their body. They are morphologically very flat, rigid, leaf-shaped, and contain many small discoid chloroplasts.

Euglenophycin is an ichthyotoxic compound isolated from Euglena sanguinea, a protist of the genus Euglena. It exhibits anticancer and herbicidal activity in vitro.

<span class="mw-page-title-main">Diplonemidae</span> Family of protozoans

Diplonemidae is a family of biflagellated unicellular protists that may be among the more diverse and common groups of planktonic organisms in the ocean. Although this family is currently made up of three named genera; Diplonema, Rhynchopus, and Hemistasia, there likely exist thousands of still unnamed genera. Organisms are generally colourless and oblong in shape, with two flagella emerging from a subapical pocket. They possess a large mitochondrial genome composed of fragmented linear DNA. These non-coding sequences must be massively trans-spliced, making it one of the most complicated post-transcriptional editing process known to eukaryotes.

<i>Neobodo</i> Genus of protists

Neobodo are diverse protists belonging to the eukaryotic supergroup Excavata. They are Kinetoplastids in the subclass Bodonidae. They are small, free-living, heterotrophic flagellates with two flagella of unequal length used to create a propulsive current for feeding. As members of Kinetoplastids, they have an evident kinetoplast There was much confusion and debate within the class Kinetoplastid and subclass Bodonidae regarding the classification of the organism, but finally the new genera Neobodo was proposed by Keith Vickerman. Although they are one of the most common flagellates found in freshwater, they are also able to tolerate saltwater Their ability to alternate between both marine and freshwater environments in many parts of the world give them a “cosmopolitan” character. Due to their relatively microscopic size ranging between 4–12 microns, they are further distinguished as heterotrophic nanoflagellates. This small size ratio limits them as bacterivores that swim around feeding on bacteria attached to surfaces or in aggregates.

Petalomonas is a genus of phagotrophic, flagellated euglenoids. Phagotrophic euglenoids are one of the most important forms of flagellates in benthic aquatic systems, playing an important role in microbial food webs. The traits that distinguish this particular genus are highly variable, especially at higher taxa. However, general characteristics such as a rigid cell shape and single emergent flagellum can describe the species among this genus.

Heteronema is a genus of phagotrophic, flagellated euglenoids that are most widely distributed in fresh water environments. This genus consists of two very distinguishable morphogroups that are phylogenetically closely related. These morphogroups are deciphered based on shape, locomotion and other ultrastructural traits. However, this genus does impose taxonomic problems due to the varying historical descriptions of Heteronema species and its similarity to the genus Paranema. The species H. exaratum, was the first heteronemid with a skidding motion to be sequenced, which led to the discovery that it was not closely related to H. scaphrum, contrary to what was previously assumed, but instead to a sister group of primary osmotrophs. This suggests that skidding heteronemids can also be distinguished phylogenetically, being more closely related to Anisoma, Dinema and Aphageae, than to other species within Heteronema.

Cryptoglena(/ˌkɹɪptoʊˈgliːnə/) is a genus of photosynthetic euglenids that was first described in 1831 by Christian Gottfried Ehrenberg. Today, its circumscription is controversial: Bicudo and Menezes consider twenty-one species as Cryptoglena, of which, nine are uncertain. Cryptoglena species are water-based, living in both freshwater and marine environments. They are biflagellated, with one internal flagellum and one external flagellum, which allows movement through environments as demonstrated by Kim and Shin in the species C. pigra. The cells of Cryptoglena resemble a coffee bean, as they have a groove that runs the length of the cell on one side and makes them U-shaped in cross section. They are ovoid in shape and are small, with the larger cells being on average 25 x 15 μm. After being first described in 1831, little work was done on the genus until the late 1970s and early 1980s, after the scanning electron microscope completed development and was implemented into laboratories. Work then proceeded with the developments of molecular biology, which allows for classifications based on DNA sequences. For Cryptoglena the main DNA used for classification are small subunit (SSU) and large subunit (LSU) rDNA.

Postgaardia is a proposed basal clade of flagellate Euglenozoa, following Thomas Cavalier-Smith. As of April 2023, the Interim Register of Marine and Nonmarine Genera treats the group as a subphylum. A 2021 review of Euglenozoa places Cavalier-Smith's proposed members of Postgaardia in the class Symbiontida. As Euglenozoans may be basal eukaryotes, the Postgaardia may be key to studying the evolution of Eukaryotes, including the incorporation of eukaryotic traits such as the incorporation of alphaproteobacterial mitochondrial endosymbionts.

<i>Urceolus</i> Genus of flagellates

Urceolus is a genus of heterotrophic flagellates belonging to the Euglenozoa, a phylum of single-celled eukaryotes or protists. Described by Russian biologist Konstantin Mereschkowsky in 1877, its type species is Urceolus alenizini. Species of this genus are characterized by deformable flask-shaped cells that exhibit at least one flagellum that is active at the tip, arising from a neck-like structure that also hosts the feeding apparatus. They are found in a variety of water body sediments across the globe. According to evolutionary studies, Urceolus belongs to a group of Euglenozoa known as peranemids, closely related to the euglenophyte algae.

<i>Urceolus cyclostomus</i> Species of flagellate

Urceolus cyclostomus is a species of heterotrophic flagellates. It was initially described by Friedrich Stein in 1878 as Phialonema cyclostomum, from an unknown location. Due to its morphological similarities to Urceolus alenizini, the author of the latter, Konstantin Mereschkowsky, transferred it to the genus Urceolus in 1881. Like other species of the genus, its cells have a neck and a wide aperture to a canal that hosts a single flagellum and its feeding apparatus. It is distinguished from other species by a significantly more rigid cell shape, among other traits. It can be found in the bottom sediment of freshwater and brackish water bodies, as a consumer of algae.

<i>Ploeotia</i> Genus of flagellates

Ploeotia is a genus of heterotrophic flagellates belonging to the Euglenida, a diverse group of flagellated protists in the phylum Euglenozoa. Species of Ploeotia are composed of rigid cells exhibiting two flagella. The genus was described by Félix Dujardin in 1841.

References

  1. "Encyclopedia of Life".
  2. Mast, SO (Mar–Apr 1912). "The reactions of the flagellate Peranema". Journal of Animal Behavior. 2 (2): 91–97. doi:10.1037/h0072097.
  3. Brown, Virginius E. (1930). "The Cytology and Binary Fission of Peranema". Quarterly Journal of Microscopical Science. 2 (73): 6.
  4. Saranak, Jureepan; Foster, Kenneth W. (2005). "Photoreceptor for Curling Behavior in Peranema trichophorum and Evolution of Eukaryotic Rhodopsins". Eukaryotic Cell. 4 (10): 1605–1612. doi:10.1128/EC.4.10.1605-1612.2005. PMC   1265905 . PMID   16215167.
  5. Müller, OF (1786). Animalcula Infusoria: Fluvia, Tilia et Marina. Hauniae, Typis N. Mölleri. pp.  71.
  6. Saville-Kent, William (1882). A Manual of the Infusoria. Vol I. London: David Bogue.
  7. Dujardin, Felix (1841). Histoire Naturelle des Zoophytes. Infusoires. Vol. I. Paris: Roret.
  8. Patterson, David J.; Larsen, Jacob (January 1992). "A Perspective on Protistan Nomenclature". Journal of Eukaryotic Microbiology. 39 (1): 126. doi:10.1111/j.1550-7408.1992.tb01292.x.
  9. Suzaki, T; Williamson, RE (1985). "Euglenoid Movement in Euglena fusca". Protoplasma. 124 (1–2): 137–146. doi:10.1007/BF01279733. S2CID   44420415.
  10. Chang, Shih L. (January 1966). "Observations on the Organelles, Movement, and Feeding of Peranema trichophorum (Ehrb.) Stein". Transactions of the American Microscopical Society. 85 (1): 29–45. doi:10.2307/3224773. JSTOR   3224773. PMID   5907534.
  11. Chen, Y. T. (September 1950). "Investigations of the Biology of Peranema trichophorum (Euglenineae)". Quarterly Journal of Microscopical Science. 3. 91 (91): 302. PMID   24539001.
  12. 1 2 Nisbet, Brenda (February 1974). "An Ultrastructural Study of the Feeding Apparatus of Peranema trichophorum". Journal of Eukaryotic Microbiology. 21 (1): 39–48. doi:10.1111/j.1550-7408.1974.tb03614.x.
  13. Jahn, Theodore Louis (1949). How to Know the Protozoa. Dubuque, Iowa: Wm. C. Brown. p. 72. ISBN   0-697-04829-2.
  14. Patterson, D.J. (1996) [1992]. Free-Living Freshwater Protozoa: A Colour Guide. Washington: Manson. p. 51. ISBN   1-874545-40-5.
  15. Pitelka, Dorothy Riggs (May 1945). "Morphology and taxonomy of flagellates of the genus Peranema Dujardin". Journal of Morphology. 76 (3): 179–192. doi:10.1002/jmor.1050760304. S2CID   84123172.
  16. Chen, Y. T. (September 1950). "Investigations of the Biology of Peranema trichophorum (Euglenineae)". Quarterly Journal of Microscopical Science. 3. 91 (91): 279–302. PMID   24539001.
  17. Triemer, Richard E. (August 1997). "Feeding in Peranema Trichophorum Revisited (Euglenophyta)1". Journal of Phycology. 33 (4): 649–654. doi:10.1111/j.0022-3646.1997.00649.x. S2CID   84438684.
  18. Pringsheim, E.G. (1948). "Taxonomic Problems in the Euglenineae". Biological Reviews. 23 (1): 46–61. doi:10.1111/j.1469-185X.1948.tb00456.x. PMID   18901101. S2CID   33439406.
  19. Linton, Eric W.; et al. (March 1999). "A Molecular Study of Euglenoid Phylogeny using Small Subunit rDNA". Journal of Eukaryotic Microbiology. 46 (2): 217–223. doi:10.1111/j.1550-7408.1999.tb04606.x. PMID   10361741. S2CID   31420687.
  20. Montegut-Felkner, Anne E.; Triemer, Richard (June 1997). "Phylogenetic Relationships of Selected Euglenoid Genera Based on Morphological and Molecular Data1". Journal of Phycology. 33 (3): 512–519. doi:10.1111/j.0022-3646.1997.00512.x. S2CID   83579360.