Complete nucleotide sequence and comparative analysis of pPR9, a 41.7-kilobase conjugative staphylococcal

Eduardo Pérez-Roth1, Stephen M Kwong, Julia Alcoba-Florez

  • 1Hospital Universitario Nuestra Señora de Candelaria, Departamento de Microbiología y Biología Celular, Universidad de La Laguna, La Laguna, Spain. eperroth@ull.es

Insights

We sequenced the pPR9 plasmid, identifying the ileS2 gene responsible for high-level mupirocin resistance. Its genetic backbone offers insights into the evolution of medically important plasmids and resistance in staphylococci.

Area of Science:

  • Microbiology
  • Genetics
  • Molecular Biology

Background:

  • High-level mupirocin resistance is a growing concern in clinical settings.
  • Conjugative plasmids play a significant role in the spread of antibiotic resistance genes.
  • The ileS2 gene has been implicated in conferring mupirocin resistance.

Purpose of the Study:

  • To sequence and characterize the conjugative plasmid pPR9.
  • To understand the genetic basis and evolution of high-level mupirocin resistance.
  • To investigate the role of insertion sequence IS257 in plasmid evolution.

Main Methods:

  • Whole-genome sequencing of the pPR9 plasmid.
  • Comparative genomic analysis with related plasmids (pSK41/pGO1 family).
  • Identification and analysis of insertion sequences.

Main Results:

  • The pPR9 plasmid carries the ileS2 gene, contributing to high-level mupirocin resistance.
  • Plasmid backbone shows conservation with pSK41/pGO1 family but with key differences.
  • Insertion sequence IS257 was identified and its role in plasmid evolution highlighted.

Conclusions:

  • The pPR9 plasmid is a key element in the dissemination of mupirocin resistance.
  • Comparative analysis provides insights into the evolution of staphylococcal plasmids.
  • IS257 is important in the evolutionary dynamics of these medically significant plasmids.

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