Complete nucleotide sequence of KPC-3-encoding plasmid pKpQIL in the epidemic Klebsiella pneumoniae sequence type 258

Azita Leavitt1, Inna Chmelnitsky, Yehuda Carmeli

  • 1Division of Epidemiology, Molecular Epidemiology and Antibiotic Resistance Laboratory, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.

Insights

Researchers sequenced the bla(KPC-3) plasmid, pKpQIL, from carbapenem-resistant Klebsiella pneumoniae ST 258. This self-transmissible IncFII plasmid combines a pKPN4-like backbone with a Tn4401a transposon carrying bla(KPC-3).

Area of Science:

  • Microbiology
  • Genomics
  • Molecular Biology

Background:

  • Carbapenem resistance in Klebsiella pneumoniae poses a significant global health threat.
  • Sequence type 258 (ST 258) is a prevalent clone associated with carbapenem resistance.
  • Plasmids are key mobile genetic elements mediating the spread of antibiotic resistance genes.

Purpose of the Study:

  • To determine the complete DNA sequence of the pKpQIL plasmid.
  • To characterize the genetic elements and structure of a bla(KPC-3)-carrying plasmid in a carbapenem-resistant Klebsiella pneumoniae ST 258 isolate from Israel.

Main Methods:

  • Whole-genome sequencing of the plasmid.
  • Bioinformatic analysis to identify plasmid backbone, transposons, and resistance genes.

Main Results:

  • The complete DNA sequence of the 113,637-bp plasmid pKpQIL was determined.
  • pKpQIL was identified as a self-transmissible plasmid belonging to the IncFII incompatibility group.
  • The plasmid comprises a pKPN4-like backbone and harbors the Tn4401a transposon carrying the bla(KPC-3) gene, originating from a pNYC-like plasmid.

Conclusions:

  • The genetic architecture of pKpQIL provides insights into the evolution and dissemination of carbapenem resistance.
  • Understanding plasmid structure is crucial for developing strategies to combat antibiotic resistance spread.

Related Concept Videos