Cloned ermTR Gene Confers Low Level Erythromycin but High Level Clindamycin Resistance in Streptococcus pyogenes

Erman Oryaşın1, Hacı Halil Bıyık2, Stephen Tristram3

  • 1Recombinant DNA and Recombinant Protein Center (REDPROM), Adnan Menderes University, Aydın, Turkey.

Microbial Drug Resistance (Larchmont, N.Y.)
|January 24, 2020
PubMed

Insights

The ermTR gene in Streptococcus pyogenes confers low-level erythromycin resistance and high-level clindamycin resistance. Its distinct resistance profile suggests unique methylation mechanisms compared to other erm genes.

Area of Science:

  • Microbiology
  • Molecular Biology
  • Genetics

Background:

  • Macrolide resistance in streptococci commonly involves ermB, ermTR methylase genes, or mef efflux genes.
  • Understanding specific resistance mechanisms is crucial for effective antibiotic treatment.

Purpose of the Study:

  • To investigate the impact of the ermTR gene on macrolide and lincosamide activity in streptococci under isogenic conditions.
  • To characterize the resistance profiles conferred by ermTR with and without its regulatory region.

Main Methods:

  • Amplification and cloning of the ermTR gene (with/without regulatory region) into expression vectors.
  • Transformation of Streptococcus pyogenes with recombinant plasmids.
  • Determination of minimal inhibitory concentrations (MICs) for erythromycin and clindamycin.
  • Disk diffusion assays to assess antibiotic inhibition zones.

Main Results:

  • Transformation with ermTR (without regulatory region) resulted in increased MICs for erythromycin (8 mg/L) and clindamycin (>128 mg/L).
  • Erythromycin induction affected clindamycin MICs in strains with the ermTR regulatory region.
  • Antibiotic induction altered clindamycin inhibition zones, but not telithromycin, in transformed S. pyogenes.

Conclusions:

  • The ermTR gene confers low-level erythromycin resistance and high-level clindamycin resistance in isogenic conditions.
  • ErmTR exhibits distinct induction and resistance profiles compared to other erm genes, suggesting unique methylation processes.