# Corynebacterium drakensteinense sp. nov., isolated from the nasopharynx of a healthy South African infant

**Authors:** Robbie R. Haines, Anastasia Basuki, Vanessa P. Tenaglia, Heather J. Zar, Mark P. Nicol, Ritika Kar Bahal

PMC · DOI: 10.1099/ijsem.0.007068 · International Journal of Systematic and Evolutionary Microbiology · 2026-02-05

## TL;DR

A new species of Corynebacterium, named C. drakensteinense, was discovered in the nasopharynx of a healthy South African infant and is distinct from related species.

## Contribution

The discovery and classification of a novel Corynebacterium species based on genomic and phenotypic analyses.

## Key findings

- The isolate MNWGS58T is phylogenetically close to C. propinquum and C. pseudodiphtheriticum but distinct enough to be a new species.
- Genomic analysis showed 85% ANI with C. propinquum and low digital DNA-DNA hybridization values with related species.
- The new species has a unique cell wall composition with higher C17:0 content compared to related Corynebacterium species.

## Abstract

Emerging evidence supports the role of the nasopharyngeal microbiome in respiratory health, including association with conditions such as asthma and respiratory tract infections. One dominant commensal genus is Corynebacterium, members of which are commonly present in the nasopharynx of infants. These commensal Corynebacterium spp. have been reported to correlate with respiratory health. In this paper, we present isolate MNWGS58T isolated from the nasopharynx of a South African infant. Genomic analysis of the whole-genome sequence of MNWGS58T revealed that it is phylogenetically closely related to other Corynebacterium spp. found in the nasopharynx, Corynebacterium propinquum [85% average nucleotide identity (ANI)] and Corynebacterium pseudodiphtheriticum (84% ANI). Bacterial identification using matrix-assisted laser desorption/ionization time-of-flight MS identified MNWGS58T as C. pseudodiphtheriticum. The API Coryne assay identified the novel isolate as C. propinquum, and the VITEK 2 ANC assay identified the novel isolate as Corynebacterium otitidis. Both genomic analyses and phenotypic analyses show striking similarities to C. propinquum and C. pseudodiphtheriticum. The cell wall is consistent with closely related Corynebacterium spp., albeit with a higher C17:0 content. The genome is 2.48Mbp with a G+C content of 56.9 mol%. Digital DNA–DNA hybridization values for MNWGS58T were low when compared to C. pseudodiphtheriticum MNWGS56 and C. propinquum MNWGS51 (27.4 and 28.4%, respectively). Although there are phenotypic similarities, 85% ANI with the closest Corynebacterium spp. strongly supports the classification of a novel species of Corynebacterium, for which we propose the name Corynebacterium drakensteinense sp. nov., with the type strain MNWGS58T (=TSD-445T=NCTC 15058T). It will be important to elucidate the role of this novel species of Corynebacterium in the human nasopharynx and identify additional niches for this species in future studies.

## Linked entities

- **Diseases:** asthma (MONDO:0004979)
- **Species:** Corynebacterium drakensteinense (taxon 3104612), Corynebacterium propinquum (taxon 43769), Corynebacterium pseudodiphtheriticum (taxon 37637), Corynebacterium otitidis (taxon 29321), Mus musculus (taxon 10090)

## Full-text entities

- **Diseases:** respiratory infections (MESH:D012141), respiratory syncytial virus infection (MESH:D018357), POSSIBILITY (MESH:C564217), dDDH (MESH:D004266), Infectious Diseases (MESH:D003141), asthma (MESH:D001249)
- **Chemicals:** EDTA (MESH:D004492), gentamicin (MESH:D005839), Triton X-100 (MESH:D017830), penicillin (MESH:D010406), carbon (MESH:D002244), sucrose (MESH:D013395), glycerin (MESH:D005990), agar (MESH:D000362), meropenem (MESH:D000077731), mannose (MESH:D008358), CO2 (MESH:D002245), maltose (MESH:D008320), xylose (MESH:D014994), nitrogen (MESH:D009584), arabinose (MESH:D001089), fatty acid (MESH:D005227), amino acids (MESH:D000596), ciprofloxacin (MESH:D002939), glucose (MESH:D005947), pyruvate (MESH:D019289), nitrates (MESH:D009566), erythromycin (MESH:D004917), C17:0 (-), maltotriose (MESH:C008317), Cl (MESH:D002713), vancomycin (MESH:D014640), tetracycline (MESH:D013752), iron (MESH:D007501)
- **Species:** Corynebacterium pseudodiphtheriticum (species) [taxon 37637], Corynebacterium sp. (species) [taxon 1720], Prescottella equi (species) [taxon 43767], Corynebacterium propinquum (species) [taxon 43769], Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606], Corynebacterium otitidis (species) [taxon 29321], Human immunodeficiency virus 1 (no rank) [taxon 11676], Streptococcus pneumoniae (species) [taxon 1313]
- **Cell lines:** MNWGS58T — Mus musculus (Mouse), Hybridoma (CVCL_C5M4), TSD — Rattus norvegicus (Rat), Rat malignant teratoma, Cancer cell line (CVCL_A7AM)

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12882079/full.md

## References

28 references — full list in the complete paper: https://tomesphere.com/paper/PMC12882079/full.md

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Source: https://tomesphere.com/paper/PMC12882079