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Distribution of aminoglycoside resistance genes in recent clinical isolates of Enterococcus faecalis, Enterococcus

N Kobayashi1, M Alam, Y Nishimoto

  • 1Department of Hygiene, Sapporo Medical University School of Medicine, Sapporo, Japan.

Insights

Aminoglycoside modifying enzyme (AME) genes vary in enterococci, impacting antibiotic resistance. Multiplex PCR revealed distinct AME profiles in Enterococcus faecalis and Enterococcus faecium, influencing resistance to gentamicin and streptomycin.

Area of Science:

  • Microbiology
  • Molecular Biology
  • Antimicrobial Resistance

Background:

  • Aminoglycoside modifying enzymes (AMEs) are key drivers of aminoglycoside resistance in bacteria.
  • Understanding the distribution of AME genes is crucial for managing antibiotic resistance in clinical settings.

Purpose of the Study:

  • To investigate the prevalence and distribution of genes encoding seven AMEs in clinical enterococcal isolates.
  • To characterize the AME gene profiles in different enterococcal species and their correlation with antibiotic resistance.

Main Methods:

  • Multiplex PCR was employed to detect genes encoding seven AMEs.
  • The study analyzed 279 recent clinical isolates of enterococci from a Japanese university hospital.

Main Results:

  • The aac(6 olyl)-aph(2 olyl) gene, linked to high-level gentamicin resistance, was more frequent in Enterococcus faecalis (42.5%) than Enterococcus faecium (4.3%).
  • Nearly half of E. faecalis and E. faecium isolates carried ant(6)-Ia and aph(3 olyl)-IIIa genes.
  • Predominant AME gene profiles differed between E. faecalis (aac(6 olyl)-aph(2 olyl) + ant(6)-Ia + aph(3 olyl)-IIIa) and E. faecium (aac(6 olyl)-Ii + ant(6)-Ia + aph(3 olyl)-IIIa).
  • The ant(4 olyl)-Ia and ant(9)-Ia genes were rarely found in enterococci, while aph(2 olyl)-Ic was absent.

Conclusions:

  • Significant variation exists in the distribution of AME genes among enterococcal species and strains.
  • These findings highlight the diverse genetic basis of aminoglycoside resistance in enterococci at the study site.
  • The identified AME profiles provide insights into the mechanisms of high-level gentamicin and streptomycin resistance in these pathogens.

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