Role of bacteriophages in genomic variability of related coagulase-negative staphylococci

FEMS Microbiol Lett. 1993 May 15;109(2-3):273-7. doi: 10.1016/0378-1097(93)90032-w.

Abstract

DNA analysis using pulsed-field gel electrophoresis (PFGE) has emerged as one of the most sensitive epidemiological tools for the characterization of coagulase-negative staphylococci (CNST). The significance of some minor differences observed between the DNA restriction pulsed patterns of two CNST strains are difficult to interpret since they can theoretically be due to minor chromosomal rearrangements or to phage DNA integration. The latter possibility was investigated by comparing DNA restriction patterns of Staphylococcus epidermidis strains with those of their lysogenized derivatives. In vitro lysogenisation was obtained by exposing the strains to phage 118II. The pulsed patterns of the lysogenized strains were compared to those of their parental strains, revealing a shift in size of approximately 50 kb in a single band which was shown by Southern blotting to contain prophage. One strain was lysogenized ten times, revealing a potential preferred attachment site for phage 118II. These results confirm that chromosomal integration of a phage can be responsible for minor stable variations in DNA restriction patterns.

MeSH terms

  • Blotting, Southern
  • Coagulase / metabolism
  • Electrophoresis, Gel, Pulsed-Field
  • Genetic Variation*
  • Staphylococcus Phages / genetics*
  • Staphylococcus epidermidis / enzymology
  • Staphylococcus epidermidis / genetics*

Substances

  • Coagulase