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Genome Taxonomy Database

Australian online database

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Through Nomenclature, Prokaryote and Species

An open-source tool called GTDB-Tk is available to classify draft genomes into the GTDB hierarchy. The GTDB system, via GTDB-Tk, has been used to catalogue not-yet-named bacteria in the human gut microbiome and other metagenomic sources.

The GTDB is incorporated into the Bergey's Manual of Systematics of Archaea and Bacteria in 2019 as its phylogenomic resource.

Methodology

The genomes used to construct the phylogeny are obtained from NCBI (RefSeq and Genbank), and GTDB releases are indexed to RefSeq releases, starting with release 76. Importantly and increasingly, this dataset includes draft genomes of uncultured microorganisms obtained from metagenomes and single cells, ensuring improved genomic representation of the microbial world. All genomes are independently quality controlled using CheckM before inclusion in GTDB.

Genomes first undergo gene calling to extract genes. The taxonomy is based on trees inferred with FastTree from an aligned concatenated set of 120 single copy marker proteins for Bacteria under a WAG model, and with IQ-TREE from a concatenated set of 53 (since RS207; 122 before) marker proteins for Archaea under the PMSF model. Additional marker sets are also used to cross-validate tree topologies including concatenated ribosomal proteins and ribosomal RNA genes. The relative evolutionary divergence (RED) metric, which determines the taxonomic ranks used, is derived from the two main trees by the PhyloRank program.

Species are delimited using average nucleotide identity and alignment fraction, both calculated by skani. For species existing in a previous release, GTDB compares the quality and position of two genomes and may decide to switch to a new species representative genome.

Taxonomy comes from the following sources:

  • A previous release, if available for the neighborhood of genomic similarity.
  • National Center for Biotechnology Information (NCBI) taxonomy was initially used to decorate the genome tree via tax2tree.
  • The 16S rRNA-based Greengenes taxonomy is used to supplement the taxonomy particularly in regions of the tree with no cultured representatives.
  • List of Prokaryotic names with Standing in Nomenclature (LPSN) is used as the primary taxonomic authority for establishing naming priorities.

GTDB personnel curates the taxonomy from the aforementioned sources by checking them against the results of PhyloRank and the tree.

  • The tree node corresponding to a taxon name may have a RED inappropriate for its rank. The name may either be moved onto another node or (by changing the Latin suffix) into a different rank.
    • Splitting may happen on the level of species or genera if the divergence turns out too high. Doing so creates new taxa.
  • The taxon may turn out to be polyphyletic. The curator first restricts the taxon to the clade containing its type material. A new taxon is created for each of the other clades.

For the each new taxon, the curators try to find a proposed name in literature for it. If there is no name proposed, the taxon is given a placeholder name by adding a suffix to the original name, e.g. Lactobacillus gasseri_A. After "Z" comes "AA".

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