Multi-drug resistant Pseudomonas aeruginosa nosocomial strains: Molecular epidemiology and evolution

Microb Pathog. 2018 Oct:123:233-241. doi: 10.1016/j.micpath.2018.07.020. Epub 2018 Jul 19.

Abstract

Pseudomonas aeruginosa causes a wide variety of nosocomial infections. In the study, phylogenetic, selective pressure analysis and homology modelling were applied to oprD efflux pump gene with the aim to characterize multi-drug resistant strains circulating in the nosocomial setting, their transmission dynamics and ongoing evolution. One hundred ninety-three consecutive inpatients with Pseudomonas aeruginosa infection were enrolled at the University Campus Bio-Medico of Rome, between January 2015 and December 2016. oprD gene was sequenced in 20 nosocomial multi-drug resistant P. aeruginosa strains. Phylogeographic, selective pressure, residue conservation analysis and homology modelling were performed. Clinical epidemiological data were extracted from patient medical records. Multi-drug resistant strains accounted for the 36% of total strains and were responsible of 20 cases of nosocomial infections. P. aeruginosa infections occurred prevalently in the West area, especially at the location IIIW and in the Geriatric ward. The time of the most recent common ancestor indicated that strains could have been introduced in the hospital since the end of the year 2009 with the most probable location in general surgery ward. By selective pressure analysis, 29 positions under diversifying selection have been identified and mapped onto the OprD model. Most of the observed residue substitutions are predicted to be destabilizing and some of them occurred in the Loops 2 and 3 that are involved in solute selection and carbapenem susceptibility. The molecular and evolutionary analysis of Multi-drug resistant strains circulating in the nosocomial setting may provide useful insights into the epidemiology and the mechanisms leading to resistance, contributing to infection control improvement.

Keywords: MDR P. aeruginosa; Nosocomial infection; Phylogenetic analysis.

MeSH terms

  • Base Sequence
  • Carbapenems / pharmacology
  • Cross Infection / epidemiology*
  • Drug Resistance, Multiple, Bacterial* / drug effects
  • Hospitals
  • Humans
  • Microbial Sensitivity Tests
  • Models, Molecular
  • Molecular Epidemiology*
  • Phylogeny*
  • Porins / chemistry
  • Porins / classification
  • Porins / genetics*
  • Pseudomonas Infections
  • Pseudomonas aeruginosa / drug effects
  • Pseudomonas aeruginosa / pathogenicity*
  • Rome / epidemiology
  • Sequence Alignment

Substances

  • Carbapenems
  • Porins
  • OprD protein, Pseudomonas aeruginosa