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We thank Professor Oren for his interest in our work and for his constructive comments.1 In our recent article in Gut, we described the discovery of a new species that rose to high abundance in the human gut after treatment with ceftriaxone.2 We made the decision to propose taxonomic Latin names for this new species and for associated taxa because we wished to create a memorable, user-friendly, sustainable and transferable nomenclature that could be readily adopted by other researchers. Our proposals included the taxonomic hierarchy: UComantemales ord. nov., UComantemaea fam. nov., UBorkfalki gen. nov, UBorkfalki ceftriaxensis sp. nov.
We adopted the superscript ‘U’ (for ‘uncultured’) prefix in line with a recent suggestion3 but accept that use of Candidatus has priority. However, in our defence, it is worth noting that recommendations for use of Candidatus cited by Professor Oren state that ‘this category should be used for describing prokaryotic entities for which more than a mere nucleic acid sequence is available’, but these recommendations remain vague on what additional information, beyond ‘mere nucleic acid sequence’ suffices.
Professor Oren criticises us for going against Recommendation 6 in the International Code of Nomenclature of Prokaryotes (ICNP) in naming a genus after ourselves. However, under General Considerations, the ICNP states that ‘Recommendations do not have the force of Rules; they are intended to be guides to desirable practice in the future. Names contrary to a Recommendation cannot be rejected for this reason’. As Oren notes, several precedents exist for scientists naming species after themselves.
We accept that we have made errors in our use of Latin. To correct these, we suggest changing the genus name to Candidatus Borkfalkia, and, following ICNP Rule 9 quoted by Oren,1 the associated family name to Candidatus Borkfalkiaceae and the order to Candidatus Borkfalkiales. For a species epithet, we suggest a change to ‘ceftriaxoniphila’, from ceftriaxonum (N. L. neuter noun for ceftriaxone) and N.L. fem. adj. phila, from Gr. fem. adj. philé; friend, loving). Thus, the Latin binomial for our species becomes Candidatus Borkfalkia ceftriaxoniphila.
We proposed a novel family Erisaceae. On reviewing a recent study, we note that the newly named family Hungateiclostridiaceae appears to have priority over our proposed Erisaceae.4 However, in that recent study, the genus Mageeibacillus was included within Hungateiclostridiaceae, whereas we have shown that Mageeibacillus forms a distinct clade outside the Hungateiclostridiaceae, supporting the need for an additional family name, for which, in line with the ICNP Rule 9, we now propose the term Mageeibacillaceae.
A more general problem is the applicability and scalability of the ICNP’s approaches in the age of high-throughput sequencing, where the number of bacterial species discovered and described by sequencing alone vastly outweighs those that can be cultured, with individual publications now often reporting hundreds of potentially novel species.5–7 Furthermore, these novel species are typically bundled into inconsistent numerical taxonomic schemes, where the same novel species will often receive multiple different numerical names. We believe that, to ensure consistency, all new species defined by sequencing deserve their own Latin binomials. We therefore welcome a recent proposal to the ICNP to accept metagenome-assembled genomes as type material for the purposes of naming new species8 and we encourage dialogue between taxonomists and microbial genome scientists on this pressing problem.
We thank Mohammad Bahram and members of the Quadram Institute for helping with early versions of this manuscript.
Contributors FH, PB and MJP wrote the letter together.
Funding The authors gratefully acknowledge the support of the Biotechnology and Biological Sciences Research Council (BBSRC); FH’s salary is funded by the BBSRC Institute Strategic Programme Gut Microbes and Health BB/R012490/1 and its constituent project BBS/E/F/000PR10355. MJP is supported by the Quadram Institute Bioscience BBSRC-funded Strategic Program: Microbes in the Food Chain (Project No. BB/R012504/1) and its constituent project BBS/E/F/000PR10351 (Theme 3, Microbial Communities in the Food Chain) and by the Medical Research Council CLIMB grant (MR/L015080/1) PB was supported by European Union’s Horizon 2020 research and innovation Programme ec/H2020/ eS/erc-adg-669830; MicrobioS.
Competing interests None declared.
Provenance and peer review Not commissioned; internally peer reviewed.
Patient consent for publication Not required.
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