Treffer: Description of three new Dryocola species: Dryocola mayonis sp. nov., Dryocola sharpae sp. nov.and Dryocola baronae sp. nov., isolated from human clinical samples.

Title:
Description of three new Dryocola species: Dryocola mayonis sp. nov., Dryocola sharpae sp. nov.and Dryocola baronae sp. nov., isolated from human clinical samples.
Authors:
Mohammed HT; Division of Clinical Microbiology, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN 55905, USA., Koscianski CA; Division of Clinical Microbiology, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN 55905, USA., Gordy GG; Division of Clinical Microbiology, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN 55905, USA., Johnson S; Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN 55905, USA., Patel R; Division of Clinical Microbiology, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN 55905, USA.; Division of Public Health, Infectious Diseases, and Occupational Medicine, Department of Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Source:
International journal of systematic and evolutionary microbiology [Int J Syst Evol Microbiol] 2025 Dec; Vol. 75 (12).
Publication Type:
Journal Article
Language:
English
Journal Info:
Publisher: Microbiology Society Country of Publication: England NLM ID: 100899600 Publication Model: Print Cited Medium: Internet ISSN: 1466-5034 (Electronic) Linking ISSN: 14665026 NLM ISO Abbreviation: Int J Syst Evol Microbiol Subsets: MEDLINE
Imprint Name(s):
Publication: 2015- : London : Microbiology Society
Original Publication: Reading, UK : Society for General Microbiology, c2000-
References:
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Contributed Indexing:
Keywords: Dryocola; novel species; whole-genome sequence
Substance Nomenclature:
0 (RNA, Ribosomal, 16S)
0 (DNA, Bacterial)
0 (Fatty Acids)
Entry Date(s):
Date Created: 20251202 Date Completed: 20251202 Latest Revision: 20251205
Update Code:
20251205
PubMed Central ID:
PMC12671600
DOI:
10.1099/ijsem.0.006986
PMID:
41329602
Database:
MEDLINE

Weitere Informationen

Three previously uncharacterized bacterial species, designated strains BD586 <sup>T</sup> , BD613 <sup>T</sup> and BD626 <sup>T</sup> , isolated from human clinical specimens, were identified at Mayo Clinic, Rochester, Minnesota, USA. Initial identification efforts using matrix-assisted laser desorption ionization-time-of-flight MS and partial 16S rRNA gene sequencing proved inconclusive. Comprehensive analysis involving phenotypic characterization, biochemical assays and whole-genome sequencing was undertaken. The isolates were Gram-negative, motile, facultatively anaerobic rods, occurring singly, in pairs and in short chains; BD613 <sup>T</sup> additionally formed small aggregates. The isolates tested positive for catalase and negative for oxidase. Their colonies appeared smooth, white, opaque and non-haemolytic. Growth was observed at 35 °C under aerobic, anaerobic and CO₂-enriched conditions, as well as in media with NaCl concentrations up to 10% and at pH 7-9. Phylogenetic relationships were inferred from core gene alignments, average nucleotide identity and digital DNA-DNA hybridization comparisons. Results confirmed the placement of BD586 <sup>T</sup> , BD613 <sup>T</sup> and BD626 <sup>T</sup> within the recently established Dryocola genus, while also indicating their novelty as distinct species. The major cellular fatty acids were C <subscript>16:0</subscript> and C <subscript>17:0</subscript> cyclo. Based on these findings, a formal description of three new species, Dryocola mayonis sp. nov. (type strain BD586 <sup>T</sup> =TSD 474 <sup>T</sup> , =NCTC 15089 <sup>T</sup> , =DSM 119465 <sup>T</sup> ), Dryocola sharpae sp. nov. (type strain BD613 <sup>T</sup> =TSD 475 <sup>T</sup> , =NCTC 15090 <sup>T</sup> , =DSM 119466 <sup>T</sup> ) and Dryocola baronae sp. nov. (type strain BD626 <sup>T</sup> =TSD 476 <sup>T</sup> , =NCTC 15091 <sup>T</sup> , =DSM 119479 <sup>T</sup> ), is proposed, and the genus description of Dryocola is emended to refine its genomic, morphological and chemotaxonomic boundaries.