Transposition and homologous recombination drive evolution of pUO-StVR2, a multidrug resistance derivative of pSLT, the virulence plasmid specific of Salmonella enterica serovar Typhimurium

Infect Genet Evol. 2015 Jan:29:99-102. doi: 10.1016/j.meegid.2014.11.010. Epub 2014 Nov 18.

Abstract

Five variants of a resistant derivative of pSLT (termed pUO-StVR2) were detected in clinical isolates of Salmonella enterica serovar Typhimurium recovered in Spain. The structure of these variants revealed the involvement of IS1, IS26 and Tn21-like transposition, as well as homologous recombination in the generation of deletions, inversions and insertions which, depending on the variant, affected an orf of unknown function, genes encoding a possible iron acquisition system, and/or resistance properties. These variants, which appeared at a relatively low frequency, can be used as a model to understand the co-selection mechanisms that are helping to maintain multidrug resistance in bacterial pathogens, despite the structural instability of the responsible DNA.

Keywords: Class 1 integron; Complex integron; Insertion sequence; Iron acquisition; Multidrug resistance; Transposon.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • DNA Transposable Elements
  • DNA, Bacterial / genetics*
  • Drug Resistance, Multiple, Bacterial
  • Evolution, Molecular*
  • Homologous Recombination
  • Plasmids / genetics*
  • Salmonella typhimurium / genetics*
  • Salmonella typhimurium / pathogenicity*
  • Sequence Analysis, DNA

Substances

  • DNA Transposable Elements
  • DNA, Bacterial