Biology:Rickettsiales

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Short description: Order of bacteria

Rickettsiales
"Rickettsia rickettsii" (red dots) in the cell of a deer tick
Rickettsia rickettsii (red dots) in the cell of a deer tick
Scientific classification e
Domain: Bacteria
Phylum: Pseudomonadota
Class: Alphaproteobacteria
Order: Rickettsiales
Gieszczykiewicz 1939 (Approved Lists 1980)
Families
  • "Candidatus Deianiraeaceae" Castelli et al. 2019
  • Ehrlichiaceae Moshkovski 1945 (Approved Lists 1980)
  • "Candidatus Midichloriaceae" Montagna et al. 2013
  • Rickettsiaceae Pinkerton 1936 (Approved Lists 1980)
  • "Candidatus Tenuibacteraceae" Kroer et al. 2016
  • Genera incertae sedis
    • "Candidatus Anadelfobacter veles" Vannini et al. 2010
    • "Candidatus Repentibacter" corrig. Prokopchuk et al. 2019
    • "Sinorickettsia" Li et al. 2021[1]

The Rickettsiales, informally called rickettsias, are an order of small Alphaproteobacteria. They are obligate intracellular parasites, and some are notable pathogens, including Rickettsia, which causes a variety of diseases in humans, and Ehrlichia, which causes diseases in livestock. Another genus of well-known Rickettsiales is the Wolbachia, which infect about two-thirds of all arthropods and nearly all filarial nematodes.[2] Genetic studies support the endosymbiotic theory according to which mitochondria and related organelles developed from members of this group.[3]

The Rickettsiales are difficult to culture, as they rely on living eukaryotic host cells for their survival.

Rickettsiales phylogeny

The Rickettsiales further consist of three known families, the Rickettsiaceae, the Midichloriaceae, and the Ehrlichiaceae. Most studies also support the inclusion of the Holosporaceae, but one study has challenged this view.[4] In that alternative, the Holosporaceae are the sole representatives of their own order, the Holosporales, and as such not part of the Rickettsiales (see the schematic tree below). Other lineages, not clearly part of any family, have been described, as well. Examples include Candidatus Arcanobacter lacustris [5] and Rickettsiales bacterium Ac37b.

Schematic ribosomal RNA phylogeny of Alphaproteobacteria
  Magnetococcidae  

  Magnetococcus marinus

  Caulobacteridae  

  Rhodospirillales, Sphingomonadales,
  Rhodobacteraceae, Rhizobiales, etc.

  Holosporales

  Rickettsidae  
  Pelagibacterales  
  Pelagibacteraceae  

  Pelagibacter

  Subgroups Ib, II, IIIa, IIIb, IV and V

  Rickettsiales  

  Proto-mitochondria

  Anaplasmataceae  

  Ehrlichia

  Anaplasma

  Wolbachia

  Neorickettsia

  Midichloriaceae  

  Midichloria

  Rickettsiaceae  

  Rickettsia

  Orientia

The cladogram of Rickettsidae has been inferred by Ferla et al. [6] from the comparison of 16S + 23S ribosomal RNA sequences.

Phylogenetic relationship between Rickettsiales and Pelagibacterales (SAR11)

The phylogenetic relationship between these two groups has yet to reach consensus in the scientific literature.

Early reports suggested that they represented sister clades to each other.[7][8] However, later studies suggested that this relationship is false and was due to a phylogenetic artefact, which artificially groups independent AT-rich and fast-evolving lineages (Rickettsiales and Pelagibacterales have both properties) together.[9][10] Upon correcting for this artefact, the Pelagibacterales form a sister clade to the Hyphomicrobiales, Rhodobacterales and Caulobacterales instead.

Another study [4] adheres to the sister relationship between the two clades (see schematic tree). In their classification, the relation between the two orders is retained in the subclass, the Rickettsidae, which include the Rickettsiales, the Pelagibacteriales, and the extinct protomitochondrion (mitochondria themselves are not bacteria, but organelles).[4]

Reductive evolution

Rickettsiales genomes are undergoing reductive evolution and are typically small (generally < 1,5 Mbp), AT-rich (generally < 40% GC) with a low coding density (generally < 85%) and a relatively high number of pseudogenes.[11] Reduction in genome size, % GC and coding density and genes are generally attributed to genetic drift and Muller's ratchet. Genetic drift is enhanced in Rickettsiales genomes due to low population sizes (given their endosymbiotic nature) and frequent population bottlenecks. Similarly, Muller's ratchet is activated through the lack of recombination and horizontal gene transfer (the eukaryotic host cell is a natural barrier).

References

  1. "Molecular identification of a novel intracellular proteobacteria from scallop Chlamys farreri". Aquaculture 539: 736565. 2021. doi:10.1016/j.aquaculture.2021.736565. 
  2. "Wolbachia: master manipulators of invertebrate biology". Nat. Rev. Microbiol. 6 (10): 741–51. 2008. doi:10.1038/nrmicro1969. PMID 18794912. 
  3. Thomas S. (2016). Rickettsiales:Biology, Molecular Biology, Epidemiology, and Vaccine Development. pp.529. Springer•ISBN:978-3-319-46857-0
  4. 4.0 4.1 4.2 Ferla, M. P.; Thrash, J. C.; Giovannoni, S. J.; Patrick, W. M. (2013). "New rRNA gene-based phylogenies of the Alphaproteobacteria provide perspective on major groups, mitochondrial ancestry and phylogenetic instability". PLOS ONE 8 (12): e83383. doi:10.1371/journal.pone.0083383. PMID 24349502. Bibcode2013PLoSO...883383F. 
  5. "Single-cell genomics of a rare environmental alphaproteobacterium provides unique insights into Rickettsiaceae evolution". ISME J 9 (11): 2373–85. 2015. doi:10.1038/ismej.2015.46. PMID 25848874. 
  6. "New rRNA gene-based phylogenies of the Alphaproteobacteria provide perspective on major groups, mitochondrial ancestry and phylogenetic instability". PLOS One 8 (12): e83383. 2013. doi:10.1371/journal.pone.0083383. PMID 24349502. 
  7. "A robust species tree for the alphaproteobacteria". J. Bacteriol. 189 (13): 4578–86. 2007. doi:10.1128/JB.00269-07. PMID 17483224. 
  8. "Phylogenomic evidence for a common ancestor of mitochondria and the SAR11 clade". Sci Rep 1: 13. 2011. doi:10.1038/srep00013. PMID 22355532. Bibcode2011NatSR...1E..13T. 
  9. "Independent genome reduction and phylogenetic reclassification of the oceanic SAR11 clade". Mol. Biol. Evol. 29 (2): 599–615. 2012. doi:10.1093/molbev/msr203. PMID 21900598. 
  10. "The SAR11 group of alpha-proteobacteria is not related to the origin of mitochondria". PLOS ONE 7 (1): e30520. 2012. doi:10.1371/journal.pone.0030520. PMID 22291975. Bibcode2012PLoSO...730520R. 
  11. "Intracellular pathogens go extreme: genome evolution in the Rickettsiales". Trends Genet. 23 (10): 511–20. 2007. doi:10.1016/j.tig.2007.08.002. PMID 17822801. 

Wikidata ☰ Q136644 entry