Biology:Telonemia

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Short description: Phylum of single-celled organisms

Telonemia
Telonema rivulare (contrast micrography).jpg
Telonema rivulare by interference contrast micrography
Scientific classification e
Domain: Eukaryota
Clade: Diaphoretickes
Clade: TSAR
Phylum: Telonemia
Shalchian-Tabrizi 2006[2]
Class: Telonemea
Cavalier-Smith 1993[1]
Order: Telonemida
Cavalier-Smith 1993[1]
Family: Telonemidae
Cavalier-Smith 1993[1]
Genera
Diversity
7 species
T. rivulare by electron micrography

Telonemia is a phylum of microscopic eukaryotes. They are unicellular free-living flagellates with a unique combination of cell structures, including a highly complex cytoskeleton unseen in other eukaryotes. They present characteristics similar to their sister group, the SAR supergroup, such as cortical alveoli, tripartite mastigonemes and filopodia. Together, the two lineages compose the TSAR clade. They are classified in three genera and seven species, although numerous undescribed lineages are known. They are detected in all marine and freshwater environments, where they prey on bacteria and small phytoplankton through phagotrophy.

Morphology

Telonemia comprises microscopic unicellular eukaryotes, or protists.[3] Most of the diversity of telonemids is morphologically uncharacterized.[4] The few described species are free-living predatory phagotrophic flagellates composed of pyriform cells with two flagella. Between the flagella protrudes a short rostrum or proboscis. Their mitochondrial cristae are tubular. They present a unique multi-layered cytoskeleton of high complexity, composed of layers of microfilaments and microtubules, unseen in any other eukaryote.[4] Surprisingly, they exhibit a unique combination of cell traits only found separately in the different chromalveolate groups, such as complex tripartite mastigonemes (as in stramenopiles) and cortical alveoli-like structures (as in alveolates).[4] Despite their evolutionary proximity to chromalveolates, they lack chloroplasts.[2]

Ecology and distribution

Telonemids feed on a wide range of organisms, namely bacteria and phytoplankton ranging in size between pico- and nanoplankton.[4] Around one hundred lineages of environmental sequences from undescribed telonemids have been identified among marine and freshwater environments.[5][6] They are widely distributed and are sometimes abundant, implying they may play an important ecological role in aquatic ecosystems.[4]

Systematics

History

The first telonemid genus and species, Telonema subtile, was described by Karl Griessmann in 1913 from crude cultures of the green alga Ulva and of red algae off the coast of Roscoff and Naples.[7] Eighty years later, in 1993, American protistologist Thomas Cavalier-Smith created a family Telonemidae, order Telonemida and class Telonemea to contain this genus of protists. Initially, this group was included within the now obsolete phylum Opalozoa, along with other unrelated groups of flagellates such as apusomonads, jakobids, cercomonads, spongomonads, katablepharids, ebriids, proteomyxids and so on. In this scheme, the class Telonemea was distinguished by the presence fo two posterior cilia of equal length (isokont cilia). It contained an additional order besides Telonemida, Nephromycida, which comprised the genus Nephromyces[1] (later treated as an apicomplexan).[8] In 2005 a second species of telonemid was described, T. antarcticum, from the surface waters of the Oslofjord.[9]

Since 2006, they were treated as a new eukaryotic phylum Telonemia by protistologist Kamran Shalchian-Tabrizi and coauthors, on the basis of phylogenetic analyses that placed it near chromalveolate groups such as Haptista and Cryptista.[2] However, in 2015, Cavalier-Smith and coauthors rejected their treatment as an independent phylum and transferred Telonemea to the phylum Cryptista, under the obsolete subphylum Corbihelia. This subphylum included other protists with a pharyngeal basket or radiating axopodia[10] such as Picomonas (later classified as a separate phylum Picozoa closely related to red algae)[11] and Microheliella (now proposed as the sister group to Cryptista).[12] In addition, they transferred T. antarcticum to a new genus Lateronema, on the basis of phylogenetic distance from Telonema.[10]

Numerous phylogenetic analyses in the following years solidified the position of Telonemia as the sister clade to the SAR supergroup, both collectively composing the TSAR clade (Telonemia, Stramenopila, Alveolata and Rhizaria),[13] which lead Cavalier-Smith to finally consider Telonemia a separate phylum in 2022.[14] In the same year, five more species and a third genus, Arpakorses, were described by protistologist Denis Victorovich Tikhonenkov and coauthors.[4]

Classification

Until 2019, only two species had been formally described,[13] although DNA sequences collected from seawater suggested there were many more species not yet described.[15] In 2022, five additional species were described along with a third new genus, bringing the total number of species to seven.[4]

  • Lateronema Cavalier-Smith 2015[10]
    • Lateronema antarctica (Thomsen 2005) Cavalier-Smith 2015[10] [Telonema antarctica Thomsen 2005][9]
  • Telonema Griessmann 1913
    • Telonema papanine Zagumyonnyi & Tikhonenkov 2022[4]
    • Telonema subtile Griessmann 1913[7] [Telonema subtilis Griessmann 1913]
    • Telonema tenere Belyaev, Borodina & Tikhonenkov 2022[4]
    • Telonema rivulare Prokina & Tikhonenkov 2022[4]
  • Arpakorses Tikhonenkov & Karpov 2022[4]
    • Arpakorses versatilis Borodina, Karpov, Zagumyonnyi, Belyaev, Prokina & Tikhonenkov 2022[4]
    • Arpakorses idiomastiga Borodina, Karpov, Zagumyonnyi, Belyaev, Prokina & Tikhonenkov 2022[4]

Evolution

Telonemia on the eukaryote tree of life
 Eukaryotes 
 
Diaphoretickes  
 TSAR 
 SAR 
 
 

Stramenopila

 
 

Alveolata

 
 
 

Rhizaria

 
 
 

Telonemia

 
 
 

Haptista

 
 
 

Cryptista

 
 

Archaeplastida

 
 
 
 
 
 Amorphea 
 

Amoebozoa

 
 

Obazoa

 
 
 

CRuMs

 
 
 

Excavates

 
 

Hemimastigophora

 
 
Cladogram of eukaryotes based on revisions of the 2020 decade, showing in bold the position of Telonemia.[16][17]

Telonemia is a clade of protists that branch independently from other eukaryotic supergroups groups as their own 'micro-kingdom'.[18] Early molecular analyses of Telonemia placed them as an independent branch within the SAR supergroup, a diverse clade of eukaryotes that contain Rhizaria, Alveolata and Stramenopila.[19] Other analyses proposed a close relationship with centrohelids, katablepharids, cryptomonads and haptophytes.[20][10] At this time, they were suggested to have evolutionary significance in being a possible transitional form between ecologically important heterotrophic and photosynthetic species among chromalveolates.[2]

The present phylogenetic analyses place them as sister to the SAR supergroup in a clade commonly known as TSAR,[13][4] which is widely accepted by the scientific community.[16][17] As the sister clade to SAR, Telonemia has a pivotal position in the tree of eukaryotic life. They are morphologically complex organisms that combine characteristics of different SAR lineages. The main trait uniting each SAR lineage has been described in at least one genus of Telonemia: tripartite mastigonemes in the flagella, typical of stramenopiles and described in Lateronema; cortical alveoli underneath the plasma membrane, typical of alveolates and described in Lateronema; and fine pseudopodia (filopodia), typical of rhizarians and described in Telonema. Moreover, Arpakorses presents a kinetid structure similar to that seen in Rhizaria, and Telonema subtile presents microtubules in a formation superficially resembling the apical complex of apicomplexans.[4]

All telonemid genera possess a highly intricate multi-layered cytoskeleton, whose complexity is not found in any other eukaryote. This finding may indicate that telonemids have retained an ancestral cytoskeleton organization that has been lost in other eukaryotes.[4]

References

  1. ↑ 1.0 1.1 1.2 1.3 Cavalier-Smith, Thomas (1993). "The Protozoan Phylum Opalozoa". The Journal of Eukaryotic Microbiology 40 (5): 609–615. doi:10.1111/j.1550-7408.1993.tb06117.x. 
  2. ↑ 2.0 2.1 2.2 2.3 Shalchian-Tabrizi, K; Eikrem, W; Klaveness, D; Vaulot, D; Minge, M.A; Le Gall, F; Romari, K; Throndsen, J et al. (28 April 2006). "Telonemia, a new protist phylum with affinity to chromist lineages". Proceedings of the Royal Society B: Biological Sciences 273 (1595): 1833–1842. doi:10.1098/rspb.2006.3515. PMID 16790418. 
  3. ↑ Vogt, Yngve (February 1, 2012). "Found Unknown Group of Oceanic Life Forms". https://www.apollon.uio.no/english/articles/2006/telonemia-english.html. 
  4. ↑ 4.00 4.01 4.02 4.03 4.04 4.05 4.06 4.07 4.08 4.09 4.10 4.11 4.12 4.13 4.14 4.15 Tikhonenkov, Denis V.; Jamy, Mahwash; Borodina, Anastasia S.; Belyaev, Artem O.; Zagumyonnyi, Dmitry G.; Prokina, Kristina I.; Mylnikov, Alexander P.; Burki, Fabien et al. (2022). "On the origin of TSAR: morphology, diversity and phylogeny of Telonemia". Open Biology (The Royal Society) 12 (3). doi:10.1098/rsob.210325. ISSN 2046-2441. PMID 35291881. 
  5. ↑ Lefèvre, Emilie; Roussel, Balbine; Amblard, Christian; Sime-Ngando, Télesphore; Ibelings, Bas (11 June 2008). "The Molecular Diversity of Freshwater Picoeukaryotes Reveals High Occurrence of Putative Parasitoids in the Plankton". PLOS ONE 3 (6): e2324. doi:10.1371/journal.pone.0002324. PMID 18545660. Bibcode: 2008PLoSO...3.2324L. 
  6. ↑ Bråte, Jon; Klaveness, Dag; Rygh, Tellef; Jakobsen, Kjetill S; Shalchian-Tabrizi, Kamran (2010). "Telonemia-specific environmental 18S rDNA PCR reveals unknown diversity and multiple marine-freshwater colonizations". BMC Microbiology 10 (1): 168. doi:10.1186/1471-2180-10-168. PMID 20534135. 
  7. ↑ 7.0 7.1 Grießmann, Karl (1913). Über marine Flagellaten [About marine flagellates] (Thesis) (in Deutsch). Fischer. OCLC 638176877.
  8. ↑ Muñoz-Gómez, Sergio A.; Durnin, Keira; Eme, Laura; Paight, Christopher; Lane, Christopher E.; Saffo, Mary B.; Slamovits, Claudio H. (2019). "Nephromyces Represents a Diverse and Novel Lineage of the Apicomplexa That Has Retained Apicoplasts". Genome Biology and Evolution 11 (10): 2727–2740. doi:10.1093/gbe/evz155. 
  9. ↑ 9.0 9.1 Klaveness, Dag; Shalchian-Tabrizi, Kamran; Thomsen, Helge Abildhauge; Eikrem, Wenche; Jakobsen, Kjetill S. (2005). "Telonema antarcticum sp. nov., a common marine phagotrophic flagellate". International Journal of Systematic and Evolutionary Microbiology (The Microbiology Society) 55: 2595–2604. doi:10.1099/ijs.0.63652-0. 
  10. ↑ 10.0 10.1 10.2 10.3 10.4 Cavalier-Smith, Thomas; Chao, Ema E.; Lewis, Rhodri (December 2015). "Multiple origins of Heliozoa from flagellate ancestors: New cryptist subphylum Corbihelia, superclass Corbistoma, and monophyly of Haptista, Cryptista, Hacrobia and Chromista". Molecular Phylogenetics and Evolution 93: 331–362. doi:10.1016/j.ympev.2015.07.004. PMID 26234272. 
  11. ↑ Schön, Max E.; Zlatogursky, Vasily V.; Singh, Rohan P.; Poirier, Camille; Wilken, Susanne; Mathur, Varsha; Strassert, Jürgen F. H.; Pinhassi, Jarone et al. (2021). "Single cell genomics reveals plastid-lacking Picozoa are close relatives of red algae". Nature Communications 12: 6651. doi:10.1038/s41467-021-26918-0. 
  12. ↑ Yazaki, Euki; Yabuki, Akinori; Imaizumi, Ayaka; Kume, Keitaro; Hashimoto, Tetsuo; Inagaki, Yuji (2022). "The closest lineage of Archaeplastida is revealed by phylogenomics analyses that include Microheliella maris". Open Biol. 12: 210376. doi:10.1098/rsob.210376. 
  13. ↑ 13.0 13.1 13.2 Strassert, Jürgen F H; Jamy, Mahwash; Mylnikov, Alexander P; Tikhonenkov, Denis V; Burki, Fabien; Shapiro, Beth (April 2019). "New Phylogenomic Analysis of the Enigmatic Phylum Telonemia Further Resolves the Eukaryote Tree of Life". Molecular Biology and Evolution 36 (4): 757–765. doi:10.1093/molbev/msz012. PMID 30668767. 
  14. ↑ Cavalier-Smith, Thomas (2022). "Ciliary transition zone evolution and the root of the eukaryote tree: implications for opisthokont origin and classification of kingdoms Protozoa, Plantae, and Fungi". Protoplasma 259: 487–593. doi:10.1007/s00709-021-01665-7. 
  15. ↑ Shalchian-Tabrizi, K; Kauserud, H; Massana, R; Klaveness, D; Jakobsen, KS (18 April 2007). "Analysis of Environmental 18S Ribosomal RNA Sequences reveals Unknown Diversity of the Cosmopolitan Phylum Telonemia". Protist 158 (2): 173–180. doi:10.1016/j.protis.2006.10.003. PMID 17196879. 
  16. ↑ 16.0 16.1 Burki, Fabien; Roger, Andrew J.; Brown, Matthew W.; Simpson, Alastair G.B. (2020). "The New Tree of Eukaryotes". Trends in Ecology & Evolution 35 (1): 43–55. doi:10.1016/j.tree.2019.08.008. 
  17. ↑ 17.0 17.1 Burki, Fabien; Sandin, Miguel M.; Jamy, Mahwash (2021). "Diversity and ecology of protists revealed by metabarcoding". Current Biology 31 (19): R1267–R1280. doi:10.1016/j.cub.2021.07.066. 
  18. ↑ Pawlowski, Jan (15 April 2013). "The new micro-kingdoms of eukaryotes". BMC Biology 11: 40. doi:10.1186/1741-7007-11-40. PMID 23587248. 
  19. ↑ Reeb, Valérie C.; Peglar, Michael T.; Yoon, Hwan Su et al. (October 2009). "Interrelationships of chromalveolates within a broadly sampled tree of photosynthetic protists". Molecular Phylogenetics and Evolution 53 (1): 202–211. doi:10.1016/j.ympev.2009.04.012. PMID 19398025. 
  20. ↑ Burki, Fabien; Inagaki, Yuji; Bråte, Jon et al. (2009). "Large-Scale Phylogenomic Analyses Reveal That Two Enigmatic Protist Lineages, Telonemia and Centroheliozoa, Are Related to Photosynthetic Chromalveolates". Genome Biology and Evolution 1: 231–238. doi:10.1093/gbe/evp022. PMID 20333193. 

External links

Wikidata ☰ Q1782621 entry



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