Evidence map›Paper›PMID 41430566›Full record

ArticleBMC microbiology2025

Genomic and phenotypic diversity among taxonomically ambiguous clinical Corynebacterium isolates.

Holger Brüggemann, Lise Hald Schultz, Anja Poehlein, Bo Söderquist

Abstract read
In one paragraph

Article in BMC microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Holger BrüggemannDepartment of Biomedicine, Faculty of Health, Aarhus University, Aarhus, Denmark. brueggemann@biomed.au.dk.
Lise Hald SchultzDepartment of Biomedicine, Faculty of Health, Aarhus University, Aarhus, Denmark.
Anja PoehleinDepartment of Genomic and Applied Microbiology, Institute of Microbiology and Genetics, University of Göttingen, Göttingen, Germany.
Bo SöderquistSchool of Medical Sciences, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCorynebacterium is a widespread and abundant bacterial genus on human skin. Occasionally, corynebacteria are isolated from clinical specimens associated with infection. In this study, 56 bacterial isolates were examined. These isolates were obtained from 52 patients with diverse infections such as keratitis, osteitis/osteomyelitis, mastitis, (suspected) foreign body associated infections (spine, prosthetic joint), suspected meningitis, post-operative infections, among others. These isolates were identified as corynebacteria by MALDI-TOF mass spectrometry but could not be reliably assigned to a specific species. To resolve this issue, the isolates were genome-sequenced, and species identification was done with different approaches, including digital DNA-DNA hybridization, phylogenomic tree placement and Average Nucleotide Identity (ANI) calculations. A subset of 34 strains was further investigated by biochemical characterization and antimicrobial susceptibility testing (AST).

resultsThe 56 isolates belonged to 28 distinct corynebacterial species. Species identification was particularly ambiguous for 13 isolates as the ANIs were below 95% to the closest identified reference genomes. Two isolates represented potentially novel species, since no close relative could be identified (ANI < 90%). The majority of isolates belonged to the Corynebacterium marquesiae/tuberculostearicum (n = 10) and Corynebacterium kroppenstedtii/parakroppenstedtii (n = 9) complexes. Biochemical tests and AST revealed species- and strain-level variability. AST demonstrated extensive antimicrobial resistance (AMR), particularly among C. marquesiae, C. tuberculostearicum, C. lehmanniae, C. hesseae and C. resistens, with resistances observed against penicillin, clindamycin, ciprofloxacin, and rifampin. Resistance was frequently associated with acquired AMR genes, such as erm(X), tet(W) and genes encoding aminoglycoside-modifying enzymes. Among the tested antibiotics, clindamycin resistance was most common, detected in 23 of 34 tested strains (64.7%).

conclusionsThis study expands our knowledge of Corynebacterium isolates derived from clinical specimens, particularly those differing from well-characterized species. It underscores the extensive geno- and phenotypic variability within most Corynebacterium species and challenges current species boundary definitions. The extensive level of detected AMR may complicate treatment of underlying infections. However, it remains uncertain whether these isolates represent true infectious agents or contaminants derived from the skin of the patients.

Indexed as

CorynebacteriumCorynebacterium InfectionsGenetic VariationGenome, BacterialAnti-Bacterial AgentsBacterial Typing TechniquesDNA, BacterialFemaleHumansMicrobial Sensitivity TestsPhenotypePhylogenySpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationWhole Genome SequencingAnti-Bacterial AgentsDNA, BacterialAntimicrobial resistanceCorynebacterial infectionsCorynebacteriumCorynebacterium kroppenstedtii complexCorynebacterium tuberculostearicum complex

Identifiers

PMID41430566
PMCPMC12849385

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