Metamonad Explained

The metamonads are a large group of flagellate amitochondriate microscopic eukaryotes. Their composition is not entirely settled, but they include the retortamonads, diplomonads, and possibly the parabasalids and oxymonads as well. These four groups are all anaerobic (many being aerotolerant anaerobes), occurring mostly as symbiotes or parasites of animals, as is the case with Giardia lamblia which causes diarrhea in mammals.[1]

Characteristics

A number of parabasalids and oxymonads are found in termite guts, and play an important role in breaking down the cellulose found in wood. Some other metamonads are parasites.

These flagellates are unusual in lacking mitochondria. Originally they were considered among the most primitive eukaryotes, diverging from the others before mitochondria appeared. However, they are now known to have lost mitochondria secondarily, and retain both organelles and nuclear genes derived from them. Mitochondrial relics include hydrogenosomes, which produce hydrogen, and small structures called mitosomes.

It now appears the Metamonada are, together with Malawimonas, sister clades of the Podiata.[2]

All of these groups are united by having flagella or basal bodies in characteristic groups of four, which are often associated with the nucleus, forming a structure called a karyomastigont. In addition, the genera Carpediemonas and Trimastix are now known to be close relatives of the retortamonad-diplomonad line and the oxymonads, respectively. Both are free-living and amitochondriate.

Classification

The metamonads were thought to make up part of the Excavata, a paraphyletic eukaryotic supergroup including flagellates with feeding grooves and their close relatives. Their relationships are uncertain,[3] and they do not always appear together on molecular trees. It is possible that the metamonads as defined here do not form a monophyletic subgroup.

The following higher level treatment from 2013 is based on works of Cavalier-Smith[4] with amendments within Fornicata from Yubukia, Simpson & Leander.[5]

Metamonada were once again proposed to be basal eukaryotes in 2018.[6]

External links

Notes and References

  1. Al Jewari . Caesar . Baldauf . Sandra L. . 2023-04-28 . An excavate root for the eukaryote tree of life . Science Advances . 9 . 17 . eade4973 . 10.1126/sciadv.ade4973 . 2375-2548 . 10146883 . 37115919. 2023SciA....9E4973A .
  2. Cavalier-Smith. Thomas. Chao. Ema E.. Lewis. Rhodri. 2016-06-01. 187-gene phylogeny of protozoan phylum Amoebozoa reveals a new class (Cutosea) of deep-branching, ultrastructurally unique, enveloped marine Lobosa and clarifies amoeba evolution. Molecular Phylogenetics and Evolution. 99. 275–296. 10.1016/j.ympev.2016.03.023. 27001604. free.
  3. Cavalier-Smith T . The excavate protozoan phyla Metamonada Grassé emend. (Anaeromonadea, Parabasalia, Carpediemonas, Eopharyngia) and Loukozoa emend. (Jakobea, Malawimonas): their evolutionary affinities and new higher taxa . Int. J. Syst. Evol. Microbiol. . 53 . Pt 6 . 1741–58 . November 2003 . 14657102 . 10.1099/ijs.0.02548-0. free .
  4. Cavalier-Smith T . Early evolution of eukaryote feeding modes, cell structural diversity, and classification of the protozoan phyla Loukozoa, Sulcozoa, and Choanozoa . Eur. J. Protistol. . 49 . 2 . 115–178 . 2013 . 23085100 . 10.1016/j.ejop.2012.06.001 .
  5. Yubukia . Simpson . Leander . Comprehensive Ultrastructure of Kipferlia bialata Provides Evidence for Character Evolution within the Fornicata (Excavata) . Protist . 164. 3. 423–439. 2013 . 23517666. 10.1016/j.protis.2013.02.002 .
  6. Krishnan. Arunkumar. Burroughs. A. Max . Iyer . Lakshminarayan. Aravind. L.. 2018-07-04. The unexpected provenance of components in eukaryotic nucleotide-excision-repair and kinetoplast DNA-dynamics from bacterial mobile elements. bioRxiv . 361121 . 10.1101/361121 . free.
  7. Zhang . Qianqian . Táborský . Petr . Silberman . Jeffrey D. . Pánek . Tomáš . Čepička . Ivan . Simpson. Alastair G.B. . 2015 . Marine Isolates of Trimastix marina Form a Plesiomorphic Deep-branching Lineage within Preaxostyla, Separate from Other Known Trimastigids (Paratrimastix n. gen.) . Protist . 166 . 4 . 468–491 . 10.1016/j.protis.2015.07.003 . 26312987 .
  8. Radek . Renate . Platt . Katja . Öztas . Deniz . Šobotník . Jan . Sillam-Dussès . David . Hanus . Robert . Brune . Andreas . New insights into the coevolutionary history of termites and their gut flagellates: Description of Retractinympha glossotermitis gen. nov. sp. nov. (Retractinymphidae fam. nov.) . Frontiers in Ecology and Evolution . 26 January 2023 . 11 . 10.3389/fevo.2023.1111484 . free .
  9. Céza . Vít . Kotyk . Michael . Kubánková . Aneta . Yubuki . Naoji . Šťáhlavský . František . Silberman . Jeffrey D. . Čepička . Ivan . Free-living Trichomonads are Unexpectedly Diverse . Protist . August 2022 . 173 . 4 . 125883 . 10.1016/j.protis.2022.125883. 35660751 . 248586911 .
  10. Cepicka . Ivan . Hampl . Vladimír . Kulda . Jaroslav . Critical Taxonomic Revision of Parabasalids with Description of one New Genus and three New Species . Protist . July 2010 . 161 . 3 . 400–433 . 10.1016/j.protis.2009.11.005. 20093080 .