Complete Bypass of Restriction Systems for Major Staphylococcus aureus Lineages

mBio. 2015 May 26;6(3):e00308-15. doi: 10.1128/mBio.00308-15.

Abstract

Staphylococcus aureus is a prominent global nosocomial and community-acquired bacterial pathogen. A strong restriction barrier presents a major hurdle for the introduction of recombinant DNA into clinical isolates of S. aureus. Here, we describe the construction and characterization of the IMXXB series of Escherichia coli strains that mimic the type I adenine methylation profiles of S. aureus clonal complexes 1, 8, 30, and ST93. The IMXXB strains enable direct, high-efficiency transformation and streamlined genetic manipulation of major S. aureus lineages.

Importance: The genetic manipulation of clinical S. aureus isolates has been hampered due to the presence of restriction modification barriers that detect and subsequently degrade inappropriately methylated DNA. Current methods allow the introduction of plasmid DNA into a limited subset of S. aureus strains at high efficiency after passage of plasmid DNA through the restriction-negative, modification-proficient strain RN4220. Here, we have constructed and validated a suite of E. coli strains that mimic the adenine methylation profiles of different clonal complexes and show high-efficiency plasmid DNA transfer. The ability to bypass RN4220 will reduce the cost and time involved for plasmid transfer into S. aureus. The IMXXB series of E. coli strains should expedite the process of mutant construction in diverse genetic backgrounds and allow the application of new techniques to the genetic manipulation of S. aureus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • DNA Methylation
  • DNA Restriction-Modification Enzymes / genetics
  • DNA Restriction-Modification Enzymes / metabolism
  • DNA, Bacterial / genetics*
  • Escherichia coli / genetics
  • Genetic Vectors
  • Mutation
  • Plasmids*
  • Staphylococcus aureus / genetics*
  • Transformation, Bacterial*

Substances

  • DNA Restriction-Modification Enzymes
  • DNA, Bacterial