Molecular characterization of pneumococci with efflux-mediated erythromycin resistance and identification of a novel

Ileana Cochetti1, Manuela Vecchi, Marina Mingoia

  • 1Institute of Microbiology and Biomedical Sciences, Polytechnic University of Marche Medical School, Via Ranieri, Monte d'Ago, 60131 Ancona, Italy.

Insights

This study analyzes macrolide resistance genes in clinical pneumococci, identifying mef(A) and mef(E) variants and their genetic elements. It reveals novel mef(I) gene and discusses co-resistance mechanisms with tetracycline resistance genes.

Area of Science:

  • Microbiology
  • Molecular Genetics
  • Antimicrobial Resistance

Background:

  • Macrolide resistance in Streptococcus pneumoniae is a growing public health concern.
  • Efflux-mediated resistance, specifically the M phenotype, is a common mechanism.
  • Understanding the genetic basis of macrolide resistance is crucial for effective treatment strategies.

Purpose of the Study:

  • To investigate the molecular genetics of macrolide resistance in clinical pneumococcal isolates.
  • To characterize the mef gene variants and associated mobile genetic elements.
  • To explore the genetic mechanisms of co-resistance to other antibiotics, such as tetracycline.

Main Methods:

  • Analysis of 49 clinical pneumococcal isolates with M phenotype erythromycin resistance.
  • Polymerase chain reaction (PCR)-restriction fragment length polymorphism (RFLP) for mef gene identification.
  • Pulsed-field gel electrophoresis (PFGE) and multilocus sequence typing (MLST) for genetic relatedness.
  • PCR-based analysis of mobile genetic elements (transposons and integrons).

Main Results:

  • Identified mef(A) in 30 isolates and mef(E) in 19 isolates, including Streptococcus pseudopneumoniae.
  • Mef(A) isolates were predominantly associated with the England14-9 clone and ST9.
  • A novel mef gene variant, mef(I), was identified in two mef(E) isolates.
  • Co-resistance to tetracycline was observed, mediated by tet(M) in Tn916-like transposons and tet(O).
  • Composite elements like Tn2009, formed by mega insertion into Tn916-like transposons, were identified.

Conclusions:

  • The study elucidates the genetic diversity of macrolide resistance mechanisms in pneumococci.
  • Identified distinct genetic elements and clones associated with mef(A) and mef(E) resistance.
  • The discovery of mef(I) highlights ongoing evolution of macrolide resistance genes.
  • Understanding these genetic structures is vital for tracking and controlling antimicrobial resistance spread.

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