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

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Publikace nespadá pod Ekonomicko-správní fakultu, ale pod Přírodovědeckou fakultu. Oficiální stránka publikace je na webu muni.cz.
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MAŠLAŇOVÁ Ivana STŘÍBNÁ Sabina DOŠKAŘ Jiří PANTŮČEK Roman

Rok publikování 2016
Druh Článek v odborném periodiku
Časopis / Zdroj FEMS Microbiology Letters
Fakulta / Pracoviště MU

Přírodovědecká fakulta

Citace
www http://femsle.oxfordjournals.org/content/363/19/fnw211
Doi http://dx.doi.org/10.1093/femsle/fnw211
Obor Genetika a molekulární biologie
Klíčová slova Staphylococcus aureus; horizontal gene tranfer; antimicrobial drug resistance; bacteriophage; plasmid transduction
Přiložené soubory
Popis 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.
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