Genetic environment of 16S rRNA methylase gene rmtD

Yohei Doi1, Jennifer M Adams-Haduch, David L Paterson

  • 1Division of Infectious Diseases, University of Pittsburgh Medical Center, Falk Medical Building Suite 3A, 3601 Fifth Avenue, Pittsburgh, PA 15213, USA. doiy@dom.pitt.edu

Insights

The 16S rRNA methylase gene, rmtD, was studied in Pseudomonas aeruginosa and Klebsiella pneumoniae. It was found that IS26 likely mobilized rmtD from P. aeruginosa to K. pneumoniae.

Area of Science:

  • Microbiology
  • Genetics
  • Molecular Biology

Background:

  • The 16S rRNA methylase gene, rmtD, confers resistance to aminoglycoside antibiotics.
  • Integrons and insertion sequences are mobile genetic elements that contribute to the spread of antibiotic resistance genes.

Purpose of the Study:

  • To investigate the genetic environment of the rmtD gene in Pseudomonas aeruginosa and Klebsiella pneumoniae.
  • To elucidate the mechanism of rmtD mobilization between bacterial species.

Main Methods:

  • Plasmid DNA extraction and sequencing.
  • Bioinformatic analysis of gene sequences.
  • Comparative genomics.

Main Results:

  • The rmtD gene in the original Pseudomonas aeruginosa strain was found to be downstream of a class I integron (In163) and flanked by a novel ISCR element.
  • The rmtD gene in Klebsiella pneumoniae was associated with an IS26 insertion sequence, suggesting mobilization from P. aeruginosa.

Conclusions:

  • The ISCR element plays a role in the genetic environment of rmtD in P. aeruginosa.
  • IS26-mediated transposition is a likely mechanism for the interspecies transfer of the rmtD gene from P. aeruginosa to K. pneumoniae.
  • Understanding these mobilization mechanisms is crucial for combating the spread of antibiotic resistance.