Abstract

Several emerging pathogens have arisen as a result of selection pressures exerted by modern health care. Klebsiella quasipneumoniae was recently defined as a new species, yet its prevalence, niche, and propensity to acquire antimicrobial resistance genes are not fully described. We have been tracking inter- and intraspecies transmission of the Klebsiella pneumoniae carbapenemase (KPC) gene, blaKPC, between bacteria isolated from a single institution. We applied a combination of Illumina and PacBio whole-genome sequencing to identify and compare K. quasipneumoniae from patients and the hospital environment over 10- and 5-year periods, respectively. There were 32 blaKPC-positive K. quasipneumoniae isolates, all of which were identified as K. pneumoniae in the clinical microbiology laboratory, from 8 patients and 11 sink drains, with evidence for seven separate blaKPC plasmid acquisitions. Analysis of a single subclade of K. quasipneumoniae subsp. quasipneumoniae (n = 23 isolates) from three patients and six rooms demonstrated seeding of a sink by a patient, subsequent persistence of the strain in the hospital environment, and then possible transmission to another patient. Longitudinal analysis of this strain demonstrated the acquisition of two unique blaKPC plasmids and then subsequent within-strain genetic rearrangement through transposition and homologous recombination. Our analysis highlights the apparent molecular propensity of K. quasipneumoniae to persist in the environment as well as acquire carbapenemase plasmids from other species and enabled an assessment of the genetic rearrangements which may facilitate horizontal transmission of carbapenemases.

Highlights

  • Several emerging pathogens have arisen as a result of selection pressures exerted by modern health care

  • From our collection of blaKPC-positive isolates from patients (2007 to 2017) and the hospital environment (2013 to 2017), there were a total of 32 blaKPC-positive K. quasipneumoniae isolates, all of which were identified as K. pneumoniae in the clinical microbiology laboratory (Table 1)

  • We describe the behavior of nosocomial blaKPC-positive K. quasipneumoniae strains within a single hospital setting, observing their propensity to take up multiple carbapenemase plasmids from other species and disseminate between patients and sink drains

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Summary

Introduction

Several emerging pathogens have arisen as a result of selection pressures exerted by modern health care. Quasipneumoniae (n ϭ 23 isolates) from three patients and six rooms demonstrated seeding of a sink by a patient, subsequent persistence of the strain in the hospital environment, and possible transmission to another patient. Longitudinal analysis of this strain demonstrated the acquisition of two unique blaKPC plasmids and subsequent within-strain genetic rearrangement through transposition and homologous recombination. Premise plumbing can be seeded by antimicrobial resistance genes in diverse bacterial strains and species and represents a difficult-totreat reservoir for ongoing gene exchange, creating successful drug-resistant bacteria that can thrive in both the environmental and human niches [7]. Understanding the mechanisms and frequency of resistance gene transfer events occurring in real world contexts can provide important insights into the wider evolutionary landscape creating modern multidrug-resistant bacteria which cannot be effectively modeled in lab experiments [12]

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