Publication details

Efficient plasmid transduction to Staphylococcus aureus strains insensitive to the lytic action of transducing phage

Investor logo
Authors

MAŠLAŇOVÁ Ivana STŘÍBNÁ Sabina DOŠKAŘ Jiří PANTŮČEK Roman

Year of publication 2016
Type Article in Periodical
Magazine / Source FEMS Microbiology Letters
MU Faculty or unit

Faculty of Science

Citation
Web http://femsle.oxfordjournals.org/content/363/19/fnw211
Doi http://dx.doi.org/10.1093/femsle/fnw211
Field Genetics and molecular biology
Keywords Staphylococcus aureus; horizontal gene tranfer; antimicrobial drug resistance; bacteriophage; plasmid transduction
Attached files
Description The transduction mediated by bacteriophages is considered to be one of the primary driving forces in horizontal gene transfer in staphylococci, which is crucial to their adaptation and successful evolution. For a transduction to be effective, it is generally accepted that the recipient strain should be susceptible to the transducing phage. In this study, we demonstrate that the plasmid DNAs are effectively transduced into the recipient Staphylococcus aureus strains in spite of their insensitivity to the lytic action of the transducing phage, provided that these phages adsorb effectively to the bacterial cells. The tetracycline and penicillinase plasmids were transduced to insensitive laboratory and clinical strains by bacteriophages phi29, phi52A and phi80alpha as well as by prophage phi53 and naturally occurring prophages induced from donor lysogenic strains. Comparable frequencies of transduction were achieved in both phage-sensitive and phage-insensitive recipient strains. We have demonstrated that such mechanisms as the restriction of DNA and lysogenic immunity which are responsible for insensitivity of cells to phages may not be a barrier to the transfer, maintenance and effective spread of plasmids to a wider range of potential recipients in the staphylococcal population.
Related projects:

You are running an old browser version. We recommend updating your browser to its latest version.

More info