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Genomic and Resistome Analyses of Elizabethkingia anophelis Strain B2D isolated from Dental Plaque of Patient

Lookup NU author(s): Dr Chien-Yi ChangORCiD

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This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC 4.0).


Abstract

© 2024, HH Publisher. All rights reserved.In this study, strain B2D isolated from a dental plaque sample of a human patient was studied for its general characteristics, taxonomic identification, genome features, and resistome profile. The bacterium exhibited antibiotic resistance to all beta-lactam antibiotics, nitrofuran, and sulfonamides, with high minimum inhibitory concentrations. It was only sensitive to the fluoroquinolone ciprofloxacin and intermediately susceptible to aminoglycoside tobramycin. A preliminary identification through 16S rRNA gene sequences revealed that it shared the highest sequence identity with Elizabethkingia anophelis subsp. endophytica JM-87T (100%) and Elizabethkingia anophelis subsp. anophelis R26T (99.31%). The draft genome of strain B2D was approximately 3.9 Mbp with 50 contigs and 35.5% GC content. A 16S rRNA gene and core genes-based phylogenetic analyses revealed a close phylogenetic relationship between strain B2D and the other Elizabethkingia type strains. An above species level threshold average nucleotide identity value confirmed its taxonomic identity as Elizabethkingia anophelis. Furthermore, we conducted a resistome analysis of strain B2D and Elizabethkingia type strains, revealing the presence of widespread antibiotic resistance genes, including beta-lactamases and genes associated with cationic antiseptic resistance and glycopeptide resistance. Overall, the multidrug resistant profile of strain B2D as elucidated and confirmed through whole genome analysis indicated its potential as a reservoir of beta-lactamase genes. Moreover, its presence within dental plaque in the human oral cavity prompts speculation regarding its role as an opportunistic pathogen capable of causing infections, particularly in immunocompromised individuals.


Publication metadata

Author(s): Goh SY, Chua K-O, Khan SA, Kasim NHA, Liew YJM, Lau YY, Hong K-W, Yin W-F, Yong H-S, Chang C-Y, Chan K-G

Publication type: Article

Publication status: Published

Journal: Progress in Microbes and Molecular Biology

Year: 2024

Volume: 7

Issue: 1

Online publication date: 17/04/2024

Acceptance date: 12/04/2024

Date deposited: 15/05/2024

ISSN (electronic): 2637-1049

Publisher: HH Publisher

URL: https://doi.org/10.36877/pmmb.a0000440

DOI: 10.36877/pmmb.a0000440


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Funding

Funder referenceFunder name
UM-MOHE HIR Grant UM.C/625/1/HIR/MOHE/CHAN/01, No. A000001-50001)
UM-MOHE HIR Grant UM.C/625/1/HIR/MOHE/CHAN/14/1
University of Malaya (ST006-2024)

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