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DPANN

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DPANN
Parvarchaeum acidiphilum
Scientific classification Edit this classification
Domain: Archaea
Superphylum: DPANN
Rinke et al. 2013
Phyla[1]

DPANN is a superphylum of Archaea first proposed in 2013.[2] Many members show novel signs of horizontal gene transfer from other domains of life.[2] They are known as nanoarchaea or ultra-small archaea due to their smaller size (nanometric) compared to other archaea.

DPANN is an acronym formed by the initials of the first five groups discovered, Diapherotrites, Parvarchaeota, Aenigmarchaeota, Nanoarchaeota and Nanohaloarchaeota. Later Woesearchaeota and Pacearchaeota were discovered and proposed within the DPANN superphylum.[3] In 2017, another phylum Altiarchaeota was placed into this superphylum.[4] The monophyly of DPANN is not yet considered established, due to the high mutation rate of the included phyla, which can lead to the artifact of the long branch attraction (LBA) where the lineages are grouped basally or artificially at the base of the phylogenetic tree without being related.[5][6] These analyzes instead suggest that DPANN belongs to Euryarchaeota or is polyphyletic occupying various positions within Euryarchaeota.[5][6][7]

The DPANN groups together different phyla with a variety of environmental distribution and metabolism, ranging from symbiotic and thermophilic forms such as Nanoarchaeota, acidophiles like Parvarchaeota and non-extremophiles like Aenigmarchaeota and Diapherotrites. DPANN was also detected in nitrate-rich groundwater, on the water surface but not below, indicating that these taxa are still quite difficult to locate.[8]

Since the recognition of the kingdom rank by the ICNP, the proposed name for this group is kingdom Nanobdellati.[9]

Characteristics

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They are characterized by being small in size compared to other archaea (nanometric size) and in keeping with their small genome, they have limited but sufficient catabolic capacities to lead a free life, although many are thought to be episymbionts that depend on a symbiotic or parasitic association with other organisms. Many of their characteristics are similar or analogous to those of ultra-small bacteria (CPR group).[3]

Limited metabolic capacities are a product of the small genome and are reflected in the fact that many lack central biosynthetic pathways for nucleotides, aminoacids, and lipids; hence most DPANN archaea, such as ARMAN archaea, which rely on other microbes to meet their biological requirements. But those that have the potential to live freely are fermentative and aerobic heterotrophs.[3]

They are mostly anaerobic and have not been cultivated. They live in extreme environments such as thermophilic, hyperacidophilic, hyperhalophilic or metal-resistant; or also in the temperate environment of marine and lake sediments. They are rarely found on the ground or in the open ocean.[3]

Classification

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Phylogeny

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Tom A. Williams et al. 2017,[20] Castelle et al. 2015[3] and Dombrowski et al. 2020.[21] Jordan et al. 2017[7] Cavalier-Smith2020[6] and Feng et al 2021.[22]

DPANN may be the first divergent clade of archaea according to some phylogenetic analyses. Recent phylogenetic analyses have found the following phylogeny between phyla.[3][20][21]

Bacteria

Archaea

Other phylogenetic analyzes have suggested that DPANN could belong to Euryarchaeota or that it may even be polyphyletic occupying different positions within Euryarchaeota. It is also debated whether the phylum Altiarchaeota should be classified in DPANN or Euryarchaeota.[21][5] An alternative location for DPANN in the phylogenetic tree is as follows.[7][6][22] The groups marked in quotes are lineages assigned to DPANN, but phylogenetically separated from the rest.

Taxonomy

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The currently accepted taxonomy is based on the List of Prokaryotic names with Standing in Nomenclature (LPSN)[23] and National Center for Biotechnology Information (NCBI).[24]

GTDB phylogeny of "DPANN"[25][26][27]


DPANN
"Undinarchaeota"
"Undinarchaeia"

"Undinarchaeales"

DPANN

Superphylum "DPANN" Rinke et al. 2013 (= proposed kingdom Nanobdellati Rinke, Schwientek, Sczyrba, Ivanova, Anderson, Cheng, Darling, Malfatti, Swan, Gies, Dodsworth, Hedlund, Tsiamis, Sievert, Liu, Eisen, Hallam, Kyrpides, Stepanauskas, Rubin, Hugenholtz and Woyke 2024[28])

  • Phylum "Undinarchaeota" Dombrowski et al. 2020
    • Class "Undinarchaeia" Dombrowski et al. 2020
      • Order "Undinarchaeales" Dombrowski et al. 2020
  • Phylum "Huberarchaeota" Probst et al. 2019
    • Class "Huberarchaeia" corrig. Probst et al. 2019
      • Order "Huberarchaeales" Rinke et al. 2020
  • Phylum "Aenigmatarchaeota" corrig. Rinke et al. 2013 (DSEG, DUSEL2)
    • Class "Aenigmatarchaeia" corrig. Rinke et al. 2020
      • Order "Aenigmatarchaeales" corrig. Rinke et al. 2020
  • Phylum "Nanohalarchaeota" corrig. Rinke et al. 2013
    • Class "Nanohalobiia" corrig.La Cono et al. 2020
      • Order "Nanohalobiales" La Cono et al. 2020
    • Class ?"Nanohalarchaeia" corrig. Narasingarao et al. 2012
      • Order "Nanohalarchaeales"
  • Phylum Altarchaeota Probst et al. 2018 (SM1)
    • Class "Altarchaeia" corrig. Probst et al. 2014
      • Order "Altarchaeales" corrig. Probst et al. 2014
  • Phylum "Iainarchaeota" ["Diapherotrites" Rinke et al. 2013] (DUSEL-3)
    • Class "Iainarchaeia" Rinke et al. 2020
      • Order "Forterreales" Probst & Banfield 2017
      • Order "Iainarchaeales" Rinke et al. 2020
  • Phylum "Micrarchaeota" Baker & Dick 2013
    • Class "Micrarchaeia" Vazquez-Campos et al. 2021
      • Order "Anstonellales" Vazquez-Campos et al. 2021 (LFWA-IIIc)
      • Order "Burarchaeales" Vazquez-Campos et al. 2021 (LFWA-IIIb)
      • Order "Fermentimicrarchaeales" Kadnikov et al. 2020
      • Order "Gugararchaeales" Vazquez-Campos et al. 2021 (LFWA-IIIa)
      • Order "Micrarchaeales" Vazquez-Campos et al. 2021
      • Order "Norongarragalinales" Vazquez-Campos et al. 2021 (LFWA-II)
  • Phylum "Nanoarchaeota" Huber et al. 2002
  • Phylum ?"Mamarchaeota"
  • Order ?"Wiannamattarchaeales"

See also

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References

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  1. ^ Castelle CJ, Banfield JF (2018). "Major New Microbial Groups Expand Diversity and Alter our Understanding of the Tree of Life". Cell. 172 (6): 1181–1197. doi:10.1016/j.cell.2018.02.016. PMID 29522741.
  2. ^ a b Rinke C, Schwientek P, Sczyrba A, Ivanova NN, Anderson IJ, Cheng JF, Darling A, Malfatti S, Swan BK, Gies EA, Dodsworth JA, Hedlund BP, Tsiamis G, Sievert SM, Liu WT, Eisen JA, Hallam SJ, Kyrpides NC, Stepanauskas R, Rubin EM, Hugenholtz P, Woyke T (July 2013). "Insights into the phylogeny and coding potential of microbial dark matter" (PDF). Nature. 499 (7459): 431–437. Bibcode:2013Natur.499..431R. doi:10.1038/nature12352. PMID 23851394. S2CID 4394530.
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  5. ^ a b c Nina Dombrowski, Jun-Hoe Lee, Tom A Williams, Pierre Offre, Anja Spang (2019). Genomic diversity, lifestyles and evolutionary origins of DPANN archaea. Nature.
  6. ^ a b c d Cavalier-Smith, Thomas; Chao, Ema E-Yung (2020). "Multidomain ribosomal protein trees and the planctobacterial origin of neomura (Eukaryotes, archaebacteria)". Protoplasma. 257 (3): 621–753. doi:10.1007/s00709-019-01442-7. PMC 7203096. PMID 31900730.
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  10. ^ Genomes Online Database
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  14. ^ Baker BJ, Comolli LR, Dick GJ, Hauser LJ, Hyatt D, Dill BD, Land ML, Verberkmoes NC, Hettich RL, Banfield JF (May 2010). "Enigmatic, ultrasmall, uncultivated Archaea". Proceedings of the National Academy of Sciences of the United States of America. 107 (19): 8806–8811. Bibcode:2010PNAS..107.8806B. doi:10.1073/pnas.0914470107. PMC 2889320. PMID 20421484.
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  16. ^ Takai K, Moser DP, DeFlaun M, Onstott TC, Fredrickson JK (December 2001). "Archaeal diversity in waters from deep South African gold mines". Applied and Environmental Microbiology. 67 (12): 5750–5760. Bibcode:2001ApEnM..67.5750T. doi:10.1128/AEM.67.21.5750-5760.2001. PMC 93369. PMID 11722932.
  17. ^ Narasingarao P, Podell S, Ugalde JA, Brochier-Armanet C, Emerson JB, Brocks JJ, Heidelberg KB, Banfield JF, Allen EE (January 2012). "De novo metagenomic assembly reveals abundant novel major lineage of Archaea in hypersaline microbial communities". The ISME Journal. 6 (1): 81–93. Bibcode:2012ISMEJ...6...81N. doi:10.1038/ismej.2011.78. PMC 3246234. PMID 21716304.
  18. ^ Waters E, Hohn MJ, Ahel I, Graham DE, Adams MD, Barnstead M, Beeson KY, Bibbs L, Bolanos R, Keller M, Kretz K, Lin X, Mathur E, Ni J, Podar M, Richardson T, Sutton GG, Simon M, Soll D, Stetter KO, Short JM, Noordewier M (October 2003). "The genome of Nanoarchaeum equitans: insights into early archaeal evolution and derived parasitism". Proceedings of the National Academy of Sciences of the United States of America. 100 (22): 12984–12988. Bibcode:2003PNAS..10012984W. doi:10.1073/pnas.1735403100. PMC 240731. PMID 14566062.
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  21. ^ a b c Dombrowski N, Williams TA, Sun J, Woodcroft BJ, Lee JH, Minh BQ, et al. (August 2020). "Undinarchaeota illuminate DPANN phylogeny and the impact of gene transfer on archaeal evolution". Nature Communications. 11 (1): 3939. Bibcode:2020NatCo..11.3939D. doi:10.1038/s41467-020-17408-w. PMC 7414124. PMID 32770105.
  22. ^ a b Yutian Feng, Uri Neri, Sean Gosselin, Artemis S Louyakis, R Thane Papke, Uri Gophna, Johann Peter Gogarten (2021). The Evolutionary Origins of Extreme Halophilic Archaeal Lineages. Oxford Academic.
  23. ^ J.P. Euzéby. "Parvarchaeota". List of Prokaryotic names with Standing in Nomenclature (LPSN). Retrieved 2021-06-27.
  24. ^ Sayers; et al. "Parvarchaeota". National Center for Biotechnology Information (NCBI) taxonomy database. Retrieved 2021-03-20.
  25. ^ "GTDB release 08-RS214". Genome Taxonomy Database. Retrieved 6 December 2021.
  26. ^ "ar53_r214.sp_label". Genome Taxonomy Database. Retrieved 10 May 2023.
  27. ^ "Taxon History". Genome Taxonomy Database. Retrieved 6 December 2021.
  28. ^ Göker, Markus; Oren, Aharon (22 January 2024). "Valid publication of names of two domains and seven kingdoms of prokaryotes". International Journal of Systematic and Evolutionary Microbiology. 74 (1). doi:10.1099/ijsem.0.006242. ISSN 1466-5026. PMID 38252124.
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