Colponema Explained

Colponema is a genus of single-celled flagellates that feed on eukaryotes in aquatic environments and soil. The genus contains 6 known species and has not been thoroughly studied.[1] Colponema has two flagella which originate just below the anterior end of the cell. One extends forwards and the other runs through a deep groove in the surface and extends backwards.[2] Colponema is a predator that feeds on smaller flagellates using its ventral groove. Like many other alveolates, they possess trichocysts, tubular mitochondrial cristae, and alveoli. It has been recently proposed that Colponema may be the sister group to all other alveolates.[3] [4] The genus could help us understand the origin of alveolates and shed light on features that are ancestral to all eukaryotes.

Etymology

Colponema is a compound of the Greek words 'kolpos' and 'nema'. 'Kolpos' means fold or hollow and is likely referring to the pronounced groove present in Colponema. 'Nema' means thread and alludes to the organism's recurrent flagellum, which originates at the anterior end of the cell and passes through the groove. Although the initial description of Colponema does not explicitly provide an explanation of its etymology, the publication does highlight the organism's large abdominal groove and the figures show the flagellum going through it.[5]

History

Colponema was first described by Dr. Friedrich Ritter Stein in 1878 in "Der Organismus der Flagellaten", which contained a number of protist species descriptions. Colponema loxodes was described in just one line, which stated that there was a large abdominal groove and made reference to a figure depicting the organism from different angles. Following the initial conception of the genus, new species C. globosum and C. symmetricum were described.[6] [7] The ultrastructure of colponemids was not discussed in detail until 1975 with Mignot and Brugerolle's study of C. loxodes.[8] The remaining species, C. edaphicum, C. vietnamica, and C. marisrubri were introduced to the genus in recent years, and phylogenetic analyses allowed researchers to use Colponema to ask questions about alveolate evolution.

Habitat and ecology

Colponema is a single-celled predator that has been found in lakes, soil, reservoirs, marine sediment, and sewage waters. It is an obligate eukaryovore, meaning that it can only feed on other eukaryotes such as bodonids and does not tend to eat larger prey or bacteria. Their primary role in ecosystems is controlling the numbers of smaller flagellates. It is likely that larger eukaryotes and small animals are its primary predators, but the details of Colponemas ecological role have yet to be characterized because it is relatively rare and difficult to culture. The genus' scarcity further supports its position as a predator in the microbial food chain; predators are often present in smaller numbers because large amounts of prey are needed to sustain their population.

Description

Colponema is a colorless biflagellate with a pronounced ventral feeding groove. Cell size ranges from 4-14 μm in width and 8-17 μm in length and they have an oval shape that narrows at the anterior end. The cells have 1 μm long toxicysts, a type of organelle that is extruded from the cell and are used to immobilize prey. Species of Colponema vary in the presence of a contractile vacuoles, degree of dorsoventral flattening, and the length of flagella.

The flagella are heterodynamic and originate just below the anterior of the cell. One flagellum points towards the anterior end of the cell and has mastigonemes near the base. The other has a fold near the base and runs through the cell's feeding groove to point posteriorly. Prey are engulfed whole through the feeding groove and digested in large food vacuoles. 

Similar to other alveolates, the pellicle of Colponema is composed of three membranes and contains inflated cortical alveoli. They also have tubular cristae in their mitochondria. In contrast, the cells do not share important traits that characterize the other groups of alveolates, such as rhoptries, derived ciliature, or palintomy.

No resting stages or sexual reproduction has been observed in culture. Asexual reproduction occurs through longitudinal division, wherein the plane of division is parallel to the groove in the cell. They are only able to divide after engulfing many other eukaryotes.[9]

Importance

From high profile diseases like malaria to maintenance of bacterial communities in water reservoirs, alveolates can have sweeping medical and economic impacts. By looking into lineages that diverged during evolutionary transitions near the origin of alveolates, you can develop a better understanding of how the group evolved. Colponema is very useful to our understanding of alveolate evolution because they were one of the first groups to diverge and display key characters that can be used to compare them to other alveolates. We can use this information to work towards reconstructing the common ancestor to all alveolates and broadening our understanding of these extremely important and widespread organisms.

List of species

Notes and References

  1. Tikhonenkov DV, Janouškovec J, Mylnikov AP, Mikhailov KV, Simdyanov TG, Aleoshin VV, Keeling PJ . Description of Colponema vietnamica sp.n. and Acavomonas peruviana n. gen. n. sp., two new alveolate phyla (Colponemidia nom. nov. and Acavomonidia nom. nov.) and their contributions to reconstructing the ancestral state of alveolates and eukaryotes . PLOS ONE . 9 . 4 . e95467 . 2014-04-16 . 24740116 . 3989336 . 10.1371/journal.pone.0095467 . 2014PLoSO...995467T . Simonetta . Gribaldo . free .
  2. Cavalier-Smith T, Chao EE . September 2004 . Protalveolate phylogeny and systematics and the origins of Sporozoa and dinoflagellates (phylum Myzozoa nom. nov.). European Journal of Protistology. en. 40. 3. 185–212. 10.1016/j.ejop.2004.01.002.
  3. Janouškovec J, Tikhonenkov DV, Mikhailov KV, Simdyanov TG, Aleoshin VV, Mylnikov AP, Keeling PJ . Colponemids represent multiple ancient alveolate lineages . Current Biology . 23 . 24 . 2546–52 . December 2013 . 24316202 . 10.1016/j.cub.2013.10.062 . free .
  4. Tikhonenkov DV, Strassert JF, Janouskovec J, Mylnikov AP, Aleoshin VV, Burki F, Keeling PJ . Predatory colponemids are the sister group to all other alveolates. Molecular Phylogenetics and Evolution . 2020-02-07 . 149 . 106839 . 10.1016/j.ympev.2020.106839. 10.1101/2020.02.06.936658. 32325195 . 212687784 .
  5. Book: Stein, Friedrich . vanc . Der Organismus der Infusionsthiere . 1859–83 . Inter Documentation Comp . 65745719.
  6. Faria J, da Cunha AM, Pinto C . 1922. Estudos sobre Protozoarios do Mar. Memórias do Instituto Oswaldo Cruz. 15. 1. 186–208. 10.1590/s0074-02761922000200013. 0074-0276. free.
  7. Sandon H . May 1927 . The Composition and distribution of the protozoan fauna of the soil. Soil Science. 23. 5. 415. 10.1097/00010694-192705000-00009. 1927SoilS..23..415S. 0038-075X.
  8. Mignot J, Brugerolle G . 1975. E' tude ultrastructurale du flagelle phagotrophe Colponema loxodes Stein. Protistologica. 11. 429–444.
  9. Mylnikov AP, Tikhonenkov DV . 2009. The new alveolate carnivorous flagellate Colponema marisrubri sp. N. (Colponemida, Alveolata) from the Red Sea . Zool. Zhurnal . 88 . 1163–1169 .