Nanobdellota (previously "Nanoarchaeota",[See the NCBI webpage on Nanoarchaeota. Data extracted from the ] The first species discovered, Nanoarchaeum equitans, was from a submarine hydrothermal vent in Iceland and described in 2002.
Discovery and taxonomy
By the end of the 1990s, three groups of Archaea were recognised: Crenarchaeota, Euryarchaeota and Korarchaeota. The groups were variously designated as kingdoms or phyla.
In 2002, Harald Huber and his colleagues at the University of Regensburg and Max Planck Institute for Medical Research discovered a new archaea from a submarine hot vent in Iceland.
The species could not be fitted into any of the known groups so that they created a new phylum "Nanoarchaeota" for the new species they named
Nanoarchaeum equitans.
In 2022, Japanese scientists led by Shingo Kato described a new species Nanobdella aerobiophila discovered from a terrestrial hot spring in Japan. For the classification, they created family Nanobdellaceae, order Nanobdellales and class Nanobdellia.
Species and diversity
Members of the Nanobdellota are associated with different host organisms and environmental conditions.
Despite small size, a reduced genome and limited respiration, they have unusual metabolic features. For example,
N. equitans has a complex and highly developed intercellular communication system.
The phylogeny of the Nanobdellota is anchored by its only cultured representative, Nanoarchaeum equitans, which clusters in a separate evolutionary group than other archaea,
The currently accepted taxonomy is based on the List of Prokaryotic names with Standing in Nomenclature (LPSN)
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Class Nanobdellia Kato et al. 2022
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Order "Tiddalikarchaeales" Vazquez-Campos et al. 2021
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Family "Tiddalikarchaeaceae" Vazquez-Campos et al. 2021
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Genus " Candidatus Tiddalikarchaeum" Vazquez-Campos et al. 2021
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" Ca. T. anstoanum" Vazquez-Campos et al. 2021
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Order "Jingweiarchaeales" Rao et al. 2023
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Family "Jingweiarchaeaceae" Rao et al. 2023
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Genus " Candidatus Jingweiarchaeum" Rao et al. 2023
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" Ca. J. tengchongense" Rao et al. 2023
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Order JAPDLS01
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Family "Haiyanarchaeaceae" Rao et al. 2023
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Genus " Candidatus Haiyanarchaeum" Rao et al. 2023
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" Ca. H. thermophilum" Rao et al. 2023
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Order "Parvarchaeales" Rinke et al. 2020
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Family "Parvarchaeaceae" Rinke et al. 2020
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Genus " Candidatus Rehaiarchaeum" Rao et al. 2023
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" Ca. R. fermentans" Rao et al. 2023
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Genus " Candidatus Acidifodinimicrobium" Luo et al. 2020
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" Ca. A. mancum" Luo et al. 2020
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Genus " Candidatus Parvarchaeum" Baker et al. 2010
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" Ca. P. acidiphilum" Baker et al. 2010
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" Ca. P. paracidiphilum" corrig. Baker et al. 2010
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" Ca. P. tengchongense" Rao et al. 2023
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Order Nanobdellales Kato et al. 2022
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Family "Nanoarchaeaceae" Huber et al. 2011
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Genus " Nanoarchaeum" Huber et al. 2002
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" N. equitans" Huber et al. 2002
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Family Nanobdellaceae Kato et al. 2022
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Genus Nanobdella Kato et al. 2022
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N. aerobiophila Kato et al. 2022
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Genus " Candidatus Nanoclepta" St. John et al. 2019
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" Ca. N. minuta" St. John et al. 2019
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Genus " Candidatus Nanopusillus" Wurch et al. 2016
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" Ca. N. acidilobi" Wurch et al. 2016
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?" Ca. N. massiliensis" Hassani et al. 2022
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?" Ca. N. phoceensis" Hassani et al. 2024
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" Ca. N. stetteri" (Castelle et al. 2015) Rinke et al. 2020
Characteristics
Cells of
N. equitans are spherical with a diameter of approximately 400
nanometre,
and have a very short and compact DNA sequence with the entire genome containing only 490,885
.
While they have the genetic code to carry out processing and repair, they cannot carry out certain biosynthetic and metabolic processes such as lipid, amino-acid, cofactor, or
nucleotide synthesis.
Due to its limited machinery, it is an obligate parasite, the only one known in the Archaea.
Because of their unusual ss rRNA sequences, they are difficult to detect using standard polymerase chain reaction methods.
Cells of
N. equitans contain a normal S-layer with sixfold symmetry with a 15 nm lattice constant.
Genome structure
Small cells between 100 and 400 nm in diameter and highly streamlined genomes of 0.491-0.606 Mbp characterize nanoarchaeotes.
The genomes of described nanoarchaeotes demonstrate different degrees of reduction, which is compatible with a host dependent lifestyle.
Certain nanaoarchaeotes still have genes for the
CRISPR-Cas systems, archaeal flagella, and the
gluconeogenesis pathway.
Habitat
Nanoarchaeotes are obligate symbionts that grow attached to an archaeal host known as
Ignicoccus.
Both terrestrial hot springs and underwater hydrothermal vents have yielded isolates in the genus
Nanoarchaeum .
However, there is evidence that nanoarcheotes reside in a variety of habitats outside of marine thermal vents.
Genetic evidence for members of the Nanoarchaeota has been discovered to be pervasive in terrestrial hot springs and mesophilic
hypersaline habitats using primers created based on the sequence of the 16S rRNA gene of
Nanoarchaeum equitans.
In addition, the discovery of ribosomal sequences in photic-zone water samples taken distant from hydrothermal vents raises the possibility that Nanoarchaeota are an ubiquitous and diversified group of Archaea that can live in habitats with a variety of temperatures and geochemical settings.
Metabolism
Although much of the metabolism of members of the Nanoarchaeota is unknown, its host is an autotroph that grows on elemental sulphur as an electron acceptor and H
2 as an
electron donor.
The majority of recognized metabolic processes, such as the creation of monomers like amino acids, nucleotides, and
coenzymes, lack recognizable genes in this organism.
See also
Further reading
