Fibrobacterota

Fibrobacterota
Scientific classification
Domain:
Superphylum:
Phylum:
Fibrobacterota

Garrity & Holt 2021[1]
Classes
Synonyms
  • "Fibrobacteraeota" Oren et al. 2015
  • "Fibrobacteres" Garrity and Holt 2001
  • "Fibrobacterota" Whitman et al. 2018
  • "Raymondbacteria" Anantharaman et al. 2016

Fibrobacterota is a small bacterial phylum which includes many of the major rumen bacteria, allowing for the degradation of plant-based cellulose in ruminant animals. Members of this phylum were categorized in other phyla. The genus Fibrobacter (the only genus of Fibrobacterota) was removed from the genus Bacteroides in 1988.[2]

Phylogeny and Comparative Genomic Studies

Although Fibrobacterota, which consists of a single genus Fibrobacter containing two species, is currently recognized as a distinct phylum, phylogenetic studies based RpoC and Gyrase B protein sequences, indicate that Fibrobacter succinogenes is closely related to the species from the phyla Bacteroidetes and Chlorobi.[3] The species from these three phyla also branch in the same position based upon conserved signature indels in a number of important proteins.[4] Lastly and most importantly, comparative genomic studies have identified two conserved signature indels (a 5-7 amino acid insert in the RpoC protein and a 13-16 amino acid insertion in serine hydroxymethyltransferase) and one signature protein (PG00081) that are uniquely shared by all of the species from these three phyla.[5] All of these results provide compelling evidence that the species from these three phyla shared a common ancestor exclusive of all other bacteria and it has been proposed that they should all recognized as part of a single “FCB”superphylum.[3][5]

Phylogeny

Phylogeny of Fibrobacterota.

16S rRNA-based LTP release 132 by The All-Species Living Tree Project[6] Annotree v1.2.0[7][8] which uses the GTDB 05-RS95 (Genome Taxonomy Database)[9][10]
Fibrobacterota

Chitinivibrio alkaliphilus

Fibrobacter

F. intestinalis

F. succinogenes

F. s. elongatus

F. s. succinogenes

"Raymondbacteria" (outgroup)

Fibrobacterota
Chitinivibrionales

Chitinispirillum alkaliphilum

Chitinivibrio alkaliphilus

Fibrobacterales

"Ca. Fibromonas termitidis"

Fibrobacter

F. intestinalis

F. succinogenes

F. s. elongatus

F. s. succinogenes

Taxonomy

The currently accepted taxonomy is based on the List of Prokaryotic names with Standing in Nomenclature (LSPN)[11] and the National Center for Biotechnology Information (NCBI).[12]

  • Class Chitinispirillia Sorokin et al. 2016
  • Class Chitinivibrionia Sorokin et al. 2014
  • Class Fibrobacteria Spain et al. 2012
    • Order Fibrobacterales Spain et al. 2012 ["Fibromonadales" Abdul Rahman et al. 2016]
      • Family Fibrobacteraceae Spain et al. 2012 [Fibromonadaceae" Abdul Rahman et al. 2016]
        • Genus "Hallerella" Wylensek et al. 2020
          • Species "H. porci" Wylensek et al. 2021
          • Species "H. succinigenes" Wylensek et al. 2020
        • Genus "Candidatus Fibromonas" Abdul Rahman et al. 2016
          • Species "Ca. F. termitidis" Abdul Rahman et al. 2016
        • Genus Fibrobacter Montgomery et al. 1988
          • Species F. intestinalis Montgomery et al. 1988
          • Species F. succinogenes (Hungate 1950) Montgomery et al. 1988
            • Subspecies F. s. elongatus Montgomery et al. 1988
            • Subspecies F. s. succinogenes (Hungate 1950) Montgomery et al. 1988
phylum Fibrobacterota and some of its phylogenetic neighbours

Distribution

The phylum Fibrobacterota is considered to be closely related to the CFB [Cytophaga-Flavibacterium-Bacteroidota].[5] The only genus in this phylum is Fibrobacter that contains strains from the guts of many mammals including cattle and pigs.[13] The two described species in this genus namely, Fibrobacter succinogenes and Fibrobacter intestinalis are important members of fibrolytic communities in mammalian guts and have received a lot of attention in recent decades due to the long-standing interest microbes capable of degrading plant fiber.

Molecular evidence based on the amplification of 16rRNA genes from various environments suggest that the phylum is much more widespread than previously thought.[14][15] Most of the clones from mammalian environments group along with the known isolates in what has been called subphylum 1.[15] Members of subphylum 2 however, have so far been found only in the gut of termites.[15][16] and in some litter-feeding cockroaches.[17] The predominance of subphylum 2 in cellulolytic fibre-associated bacterial communities in hindguts of wood-feeding Nasutitermes corniger suggests that they play an important role in the breakdown of plant material in higher termites.[18]

See also

References

  1. Oren A, Garrity GM (2021). "Valid publication of the names of forty-two phyla of prokaryotes". Int J Syst Evol Microbiol. 71 (10): 5056. doi:10.1099/ijsem.0.005056. PMID 34694987.
  2. Montgomery L, Flesher B, Stahl D (1988). "Transfer of Bacteroides succinogenes (Hungate) to Fibrobacter gen. nov. as Fibrobacter succinogenes comb. nov. and description of Fibrobacter intestinalis sp. nov". Int. J. Syst. Bacteriol. 38 (4): 430–435. doi:10.1099/00207713-38-4-430.
  3. 1 2 Gupta, R. S. (2004). "The phylogeny and signature sequences characteristics of Fibrobacteres, Chlorobi, and Bacteroidetes". Critical Reviews in Microbiology. 30 (2): 123–140. doi:10.1080/10408410490435133. PMID 15239383. S2CID 24565648.
  4. Griffiths, E; Gupta, RS (2001). "The use of signature sequences in different proteins to determine the relative branching order of bacterial divisions: evidence that Fibrobacter diverged at a similar time to Chlamydia and the Cytophaga- Flavobacterium-Bacteroides division". Microbiology. 147 (9): 2611–22. doi:10.1099/00221287-147-9-2611. PMID 11535801.
  5. 1 2 3 Gupta, R. S.; Lorenzini, E. (2007). "Phylogeny and molecular signatures (conserved proteins and indels) that are specific for the Bacteroidetes and Chlorobi species". BMC Evolutionary Biology. 7: 71. doi:10.1186/1471-2148-7-71. PMC 1887533. PMID 17488508.
  6. All-Species Living Tree Project."16S rRNA-based LTP release 132". Silva Comprehensive Ribosomal RNA Database. Retrieved 2015-08-20.
  7. "AnnoTree v1.2.0". AnnoTree.
  8. Mendler, K; Chen, H; Parks, DH; Hug, LA; Doxey, AC (2019). "AnnoTree: visualization and exploration of a functionally annotated microbial tree of life". Nucleic Acids Research. 47 (9): 4442–4448. doi:10.1093/nar/gkz246. PMC 6511854. PMID 31081040.
  9. "GTDB release 05-RS95". Genome Taxonomy Database.
  10. Parks, DH; Chuvochina, M; Chaumeil, PA; Rinke, C; Mussig, AJ; Hugenholtz, P (September 2020). "A complete domain-to-species taxonomy for Bacteria and Archaea". Nature Biotechnology. 38 (9): 1079–1086. bioRxiv 10.1101/771964. doi:10.1038/s41587-020-0501-8. PMID 32341564. S2CID 216560589.
  11. Euzéby JP. "Fibrobacteres". List of Prokaryotic names with Standing in Nomenclature (LPSN). Retrieved 2021-03-20.
  12. Sayers. "Fibrobacteres". National Center for Biotechnology Information (NCBI) taxonomy database. Retrieved 2021-03-20.
  13. Qi, M. and Nelson, K.E. and Daugherty, S.C. and Nelson, W.C. and Hance, I.R. and Morrison, M. and Forsberg, C.W. (2005). "Novel molecular features of the fibrolytic intestinal bacterium Fibrobacter intestinalis not shared with Fibrobacter succinogenes as determined by suppressive subtractive hybridization". Journal of Bacteriology. 187 (11): 3739–3751. doi:10.1128/jb.187.11.3739-3751.2005. PMC 1112041. PMID 15901698.{{cite journal}}: CS1 maint: uses authors parameter (link)
  14. McDonald, JE; Lockhart, RJ; Cox, MJ; Allison, HE; McCarthy, AJ (2008). "Detection of novel Fibrobacter populations in landfill sites and determination of their relative abundance via quantitative PCR". Environmental Microbiology. 10 (5): 1310–1319. doi:10.1111/j.1462-2920.2007.01544.x. PMID 18266756.
  15. 1 2 3 Hongoh, Y. and Deevong, P. and Hattori, S. and Inoue, T. and Noda, S. and Noparatnaraporn, N. and Kudo, T. and Ohkuma, M. (2006). "Phylogenetic diversity, localization, and cell morphologies of members of the candidate phylum TG3 and a subphylum in the phylum Fibrobacteres, recently discovered bacterial groups dominant in termite guts". Applied and Environmental Microbiology. 72 (10): 6780–6788. doi:10.1128/aem.00891-06. PMC 1610327. PMID 17021231.{{cite journal}}: CS1 maint: uses authors parameter (link)
  16. Mikaelyan, A.; Dietrich, C.; Köhler, T.; Poulsen, M.; Sillam-Dussès, D.; Brune, A. (2015). "Diet is the primary determinant of bacterial community structure in the guts of higher termites". Molecular Ecology. 24 (20): 5824–5895. doi:10.1111/mec.13376. PMID 26348261. S2CID 206182668.
  17. Mikaelyan, A.; Köhler, T.; Lampert, N.; Rohland, J.; Boga, H.; Meuser, K.; Brune, A. (2015). "Classifying the bacterial gut microbiota of termites and cockroaches: A curated phylogenetic reference database (DictDb)". Systematic and Applied Microbiology. 38 (7): 472–482. doi:10.1016/j.syapm.2015.07.004. PMID 26283320.
  18. Mikaelyan, A.; Strassert, J.; Tokuda, G.; Brune, A. (2014). "The fibre-associated cellulolytic bacterial community in the hindgut of wood-feeding higher termites (Nasutitermes spp.)". Environmental Microbiology. 16 (9): 2711–2722. doi:10.1111/1462-2920.12425.
  • Holt JG, ed. (1994). Bergey's Manual of Determinative Bacteriology (9th ed.). Williams & Wilkins. ISBN 978-0-683-00603-2.
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