Biology:Alphaproteobacteria

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Alphaproteobacteria or α-proteobacteria, also called α-Purple bacteria in earlier literature, is a class of bacteria in the phylum Pseudomonadota (also called "Proteobacteria").[1] The Magnetococcales and Mariprofundales are considered basal or sister to the Alphaproteobacteria.[2][3] The Alphaproteobacteria are highly diverse and possess few commonalities, but nevertheless share a common ancestor. Like all proteobacteria, its members are gram-negative, although some of its intracellular parasitic members lack peptidoglycan and are consequently gram variable.[1][4]

Characteristics

The Alphaproteobacteria are a diverse taxon and comprise several phototrophic genera, several genera metabolising C1-compounds (e.g. Methylobacterium spp.), symbionts of plants (e.g. Rhizobium spp.), endosymbionts of arthropods (Wolbachia) and intracellular pathogens (e.g. Rickettsia). Moreover, the class is sister to the protomitochondrion, the bacterium that was engulfed by the eukaryotic ancestor and gave rise to the mitochondria, which are organelles in eukaryotic cells (see Endosymbiotic theory).[5][6] A species of technological interest is Agrobacterium tumefaciens (also called Rhizobium radiobacter): scientists often use this species to transfer foreign DNA into plant genomes.[7] Aerobic anoxygenic phototrophic bacteria, such as Pelagibacter ubique, are alphaproteobacteria that are a widely distributed and may constitute over 10% of the open ocean microbial community.

Evolution and genomics

Several points of disagreement muddy the recovery of the phylogenetic relationships among the Alphaproteobacteria clades from the genomic data. One such point centers on the placement of the Pelagibacterales stemming from the large differences in gene content (e.g. genome streamlining in Pelagibacter ubique) and GC-content between members of several orders.[5] Specifically, certain species within Pelagibacterales, Rickettsiales, and Holosporales possess AT-rich genomes, containing higher-assayed concentrations of adenine-thymine (AT) pairs than guanine-cytosine (GC) base pairs. While it could be a case of convergent evolution resulting in an artefactual clustering,[8][9][10] several studies disagree[5][11][12][13] and no consensus has been reached.

Furthermore, the GC-content of ribosomal RNA, the traditional phylogenetic marker for prokaryotes, does not correlate well with the GC-content of the genome. For example, members of the Holosporales have a much higher ribosomal GC-content than members of the Pelagibacterales and Rickettsiales, though they are more closely related to species with high genomic GC-contents than to members of the latter two orders.[5]

Alphaproteobacteria are divided into three subclasses, Magnetococcidae, Rickettsidae, and Caulobacteridae.[5] The basal group is Magnetococcidae, composed of a large diversity of magnetotactic bacteria only one of which, Magnetococcus marinus, is formally described.[14] The Rickettsidae is composed of the intracellular Rickettsiales and the free-living Pelagibacterales. The Caulobacteridae is composed of the Holosporales, Rhodospirillales, Sphingomonadales, Rhodobacterales, Caulobacterales, Kiloniellales, Kordiimonadales, Parvularculales, and Sneathiellales.

Comparative analyses of the sequenced genomes have revealed many conserved insertion-deletions (indels) in widely distributed proteins and whole proteins (i.e. signature proteins) that are distinctive characteristics of either all Alphaproteobacteria, or their different main orders (viz. Rhizobiales, Rhodobacterales, Rhodospirillales, Rickettsiales, Sphingomonadales and Caulobacterales) and families (viz. Rickettsiaceae, Anaplasmataceae, Rhodospirillaceae, Acetobacteraceae, Bradyrhiozobiaceae, Brucellaceae and Bartonellaceae).

These molecular signatures provide a means to circumscribe the taxonomic groups and to identify and assign new species accurately.[15] Phylogenetic analyses and conserved indels in large numbers of other proteins provide evidence that Alphaproteobacteria have branched off later than most other phyla and classes of Bacteria except Betaproteobacteria and Gammaproteobacteria.[16][17]

Other phylogenetic debates turn on the placement of Magnetococcidae and the protomitochondrion.[18][19] There are some debates for the inclusion of Magnetococcidae in Alphaproteobacteria. For example, an independent proteobacterial class ("Candidatus Etaproteobacteria") for Magnetococcidae has been proposed.[20][21] A recent phylogenomic study suggests the placement of the protomitochondrial clade between Magnetococcidae and all other alphaproteobacterial taxa,[2] which suggests an early divergence of the protomitochondrial lineage from the rest of alphaproteobacteria, except for Magnetococcidae. This phylogeny also suggests that the protomitochondrial lineage does not necessarily have a close relationship to Rickettsidae.

Incertae sedis

The following taxa have been assigned to the Alphaproteobacteria, but have not been assigned to one or more intervening taxonomic ranks:[22]

  • Genera not assigned to a family
    • "Candidatus Anoxipelagibacter" Ruiz-Perez et al. 2021
    • "Bilophococcus" Moench 1988
    • "Charonomicrobium" Csotonyi et al. 2011
    • "Candidatus Endolissoclinum" Kwan et al. 2012
    • "Candidatus Endowatersipora" Anderson and Haygood 2007
    • "Candidatus Halyseomicrobium" Levantesi et al. 2004
    • "Candidatus Halyseosphaera" Kragelund et al. 2006
    • "Candidatus Hodgkinia" McCutcheon et al. 2009
    • "Candidatus Lariskella" Matsuura et al. 2012
    • "Marinosulfonomonas" Holmes et al. 1997
    • "Candidatus Mesopelagibacter" Ruiz-Perez et al. 2021
    • "Methylosulfonomonas" Holmes et al. 1997
    • "Candidatus Monilibacter" Kragelund et al. 2006
    • "Nanobacterium" Ciftcioglu et al. 1997
    • "Oleomonas" Kanamori et al. 2002
    • "Candidatus Paraholospora" Eschbach et al. 2009
    • "Candidatus Phycosocius" Tanabe et al. 2015
    • "Candidatus Puniceispirillum" Oh et al. 2010
    • "Tetracoccus" Blackall et al. 1997
    • "Tuberoidobacter" Nikitin 1983[23][24][25]
  • Species not assigned to a genus

Phylogeny

The currently accepted taxonomy is based on the List of Prokaryotic names with Standing in Nomenclature (LPSN).[26] The phylogeny is based on whole-genome analysis.[3][lower-alpha 1] Subclass names are based on Ferla et al. (2013).[5]

Bacteria
Alphaproteobacteria

Magnetococcales

Mariprofundales

"Rickettsidae"

Rickettsiales (including mitochondria[5][27])

"Ca. Pelagibacterales"

Sphingomonadales

Rhodospirillales

Rhodothalassiales

Iodidimonadales

Kordiimonadales

Emcibacterales

Sneathiellales

Hyphomicrobiales

Rhodobacterales

Micropepsales

"Parvularculales"

Caulobacterales

(outgroup)

Spirochaetota

Natural genetic transformation

Although only a few studies have been reported on natural genetic transformation in the Alphaproteobacteria, this process has been described in Agrobacterium tumefaciens,[28] Methylobacterium organophilum,[29] and Bradyrhizobium japonicum.[30] Natural genetic transformation is a sexual process involving DNA transfer from one bacterial cell to another through the intervening medium, and the integration of the donor sequence into the recipient genome by homologous recombination.

Notes

  1. Holosporales and Minwuiales are omitted from this phylogenetic tree.

References

  1. 1.0 1.1 The Proteobacteria. Bergey's Manual of Systematic Bacteriology. 2C (2nd ed.). New York: Springer. July 26, 2005. p. 1388. British Library no. GBA561951. ISBN 978-0-387-24145-6. https://archive.org/details/bergeysmanualofs00boon. 
  2. 2.0 2.1 "Deep mitochondrial origin outside the sampled alphaproteobacteria". Nature 557 (7703): 101–105. May 2018. doi:10.1038/s41586-018-0059-5. PMID 29695865. Bibcode2018Natur.557..101M. 
  3. 3.0 3.1 "Analysis of 1,000+ Type-Strain Genomes Substantially Improves Taxonomic Classification of 'Alphaproteobacteria'". Frontiers in Microbiology 11: 468. 7 April 2020. doi:10.3389/fmicb.2020.00468. PMID 32373076. 
  4. Alphaproteobacteria entry in LPSN [Euzéby, J.P. (1997). "List of Bacterial Names with Standing in Nomenclature: a folder available on the Internet". Int J Syst Bacteriol (Microbiology Society) 47 (2): 590–2. doi:10.1099/00207713-47-2-590. ISSN 0020-7713. PMID 9103655. https://ijs.microbiologyresearch.org/content/journal/ijsem/10.1099/00207713-47-2-590. Retrieved 2019-02-23. ]
  5. 5.0 5.1 5.2 5.3 5.4 5.5 5.6 Cite error: Invalid <ref> tag; no text was provided for refs named Ferla2013
  6. Martijn, Joran; Vosseberg, Julian; Guy, Lionel; Offre, Pierre; Ettema, Thijs J. G. (2018-05-01). "Deep mitochondrial origin outside the sampled alphaproteobacteria" (in en). Nature 557 (7703): 101–105. doi:10.1038/s41586-018-0059-5. ISSN 1476-4687. PMID 29695865. Bibcode2018Natur.557..101M. 
  7. "Stable incorporation of plasmid DNA into higher plant cells: the molecular basis of crown gall tumorigenesis". Cell 11 (2): 263–271. June 1977. doi:10.1016/0092-8674(77)90043-5. PMID 890735. 
  8. "The SAR11 group of alpha-proteobacteria is not related to the origin of mitochondria". PLOS ONE 7 (1). 2012. doi:10.1371/journal.pone.0030520. PMID 22291975. Bibcode2012PLoSO...730520R.  open access
  9. "Independent genome reduction and phylogenetic reclassification of the oceanic SAR11 clade". Molecular Biology and Evolution 29 (2): 599–615. February 2012. doi:10.1093/molbev/msr203. PMID 21900598. 
  10. "Comparative and phylogenomic evidence that the alphaproteobacterium HIMB59 is not a member of the oceanic SAR11 clade". PLOS ONE 8 (11). 2013. doi:10.1371/journal.pone.0078858. PMID 24223857. Bibcode2013PLoSO...878858V.  open access
  11. "Phylogenomic analysis of Odyssella thessalonicensis fortifies the common origin of Rickettsiales, Pelagibacter ubique and Reclimonas americana mitochondrion". PLOS ONE 6 (9). 2011. doi:10.1371/journal.pone.0024857. PMID 21957463. Bibcode2011PLoSO...624857G.  open access
  12. "Phylogenomic evidence for a common ancestor of mitochondria and the SAR11 clade". Scientific Reports 1: 13. 2011. doi:10.1038/srep00013. PMID 22355532. Bibcode2011NatSR...1...13T. 
  13. "A robust species tree for the alphaproteobacteria". Journal of Bacteriology 189 (13): 4578–86. July 2007. doi:10.1128/JB.00269-07. PMID 17483224. 
  14. "Magnetococcus marinus gen. nov., sp. nov., a marine, magnetotactic bacterium that represents a novel lineage (Magnetococcaceae fam. nov.; Magnetococcales ord. nov.) at the base of the Alphaproteobacteria ". Int J Syst Evol Microbiol 63 (Pt 3): 801–808. 2012. doi:10.1099/ijs.0.038927-0. PMID 22581902. 
  15. "Protein signatures distinctive of alpha proteobacteria and its subgroups and a model for alpha-proteobacterial evolution". Critical Reviews in Microbiology 31 (2): 101–35. 2005. doi:10.1080/10408410590922393. PMID 15986834. 
  16. "The phylogeny of proteobacteria: relationships to other eubacterial phyla and eukaryotes". FEMS Microbiology Reviews 24 (4): 367–402. October 2000. doi:10.1111/j.1574-6976.2000.tb00547.x. PMID 10978543. 
  17. "Application of the character compatibility approach to generalized molecular sequence data: branching order of the proteobacterial subdivisions". Journal of Molecular Evolution 64 (1): 90–100. January 2007. doi:10.1007/s00239-006-0082-2. PMID 17160641. Bibcode2007JMolE..64...90G. 
  18. "Analysis of 1,000+ Type-Strain Genomes Substantially Improves Taxonomic Classification of 'Alphaproteobacteria'". Frontiers in Microbiology 11: 468. 2020-04-07. doi:10.3389/fmicb.2020.00468. PMID 32373076. 
  19. "An updated phylogeny of the Alphaproteobacteria reveals that the parasitic Rickettsiales and Holosporales have independent origins". eLife 8. February 2019. doi:10.7554/eLife.42535. PMID 30789345. 
  20. "The chimeric nature of the genomes of marine magnetotactic coccoid-ovoid bacteria defines a novel group of Proteobacteria". Environmental Microbiology 19 (3): 1103–1119. March 2017. doi:10.1111/1462-2920.13637. PMID 27902881. Bibcode2017EnvMi..19.1103J. 
  21. "Genomic expansion of magnetotactic bacteria reveals an early common origin of magnetotaxis with lineage-specific evolution". The ISME Journal 12 (6): 1508–1519. June 2018. doi:10.1038/s41396-018-0098-9. PMID 29581530. Bibcode2018ISMEJ..12.1508L. 
  22. "Alphaproteobacteria, not assigned to a family". List of Prokaryotic names with Standing in Nomenclature (LPSN). https://lpsn.dsmz.de/family/alphaproteobacteria-no-family. 
  23. Advances in Microbial Physiology. 24. Academic Press. 1983. p. 111. ISBN 0-12-027724-7. https://books.google.com/books?id=VCLiX0d-I4IC. 
  24. Tuberoidobacter, on: IniProt Taxonomy
  25. Tuberoidobacter, on: NCBI Taxonomy Browser
  26. Alphaproteobacteria entry in LPSN [Euzéby, J.P. (1997). "List of Bacterial Names with Standing in Nomenclature: a folder available on the Internet". Int J Syst Bacteriol (Microbiology Society) 47 (2): 590–2. doi:10.1099/00207713-47-2-590. ISSN 0020-7713. PMID 9103655. https://ijs.microbiologyresearch.org/content/journal/ijsem/10.1099/00207713-47-2-590. Retrieved 2019-02-23. ]
  27. "The Origin and Diversification of Mitochondria". Current Biology 27 (21): R1177–R1192. November 2017. doi:10.1016/j.cub.2017.09.015. PMID 29112874. Bibcode2017CBio...27R1177R. 
  28. "Natural transformation of Pseudomonas fluorescens and Agrobacterium tumefaciens in soil". Applied and Environmental Microbiology 67 (6): 2617–21. June 2001. doi:10.1128/AEM.67.6.2617-2621.2001. PMID 11375171. Bibcode2001ApEnM..67.2617D. 
  29. "Genetic transformation in Methylobacterium organophilum". Journal of General Microbiology 98 (1): 265–72. January 1977. doi:10.1099/00221287-98-1-265. PMID 401866. 
  30. "Deoxyribonucleate binding and transformation in Rhizobium jpaonicum". Journal of Bacteriology 111 (2): 356–60. August 1972. doi:10.1128/jb.111.2.356-360.1972. PMID 4538250. 

Wikidata ☰ Q306579 entry