AI Article Synopsis

  • Four isolates of Elizabethkingia anophelis were identified in a Vietnamese hospital and underwent extensive testing for antibiotic resistance and genomic analysis.
  • Three of the four isolates were found to be genetically distinct, indicating multiple strain emergence rather than a single outbreak strain.
  • The isolates showed resistance to a wide range of antibiotics and contained nine resistance genes within a predicted Integrative and Conjugative Element, suggesting a complex mechanism of resistance that warrants further research.

Article Abstract

Four isolates of the opportunistic pathogen Elizabethkingia anophelis were identified for the first time in a Vietnamese hospital and underwent antimicrobial susceptibility testing and genomic characterization by whole-genome sequencing. Complete, fully circularized genome sequences were obtained for all four isolates. Average Nucleotide Identity analysis and single nucleotide polymorphism phylogenetic analysis on the core genome showed that three of the four isolates were genetically distinct, ruling out the hypothesis of a single strain emergence. Antibiotic susceptibility testing highlighted multi-resistant phenotypes against most antimicrobial families, including beta-lactams, carbapenems, aminoglycosides, quinolones, macrolides, amphenicols, rifamycins and glycopeptides. Additionally, in silico genomic analysis was used to correlate the phenotypic susceptibility to putative resistance determinants, including resistance genes, point mutations and multidrug efflux pumps. Nine different resistance genes were located inside a single resistance pocket predicted to be a putative Integrative and Conjugative Element (ICE). This novel ICE was shared by three isolates from two different lineages and displayed similarity with ICEs previously reported in various Elizabethkingia and Chryseobacterium species. The role of such ICEs in pathogenicity, genome plasticity and antimicrobial resistance gene spread within the Flavobacteriaceae family needs to be further elucidated.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10973501PMC
http://dx.doi.org/10.1038/s41598-024-57564-3DOI Listing

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