Staphylococcus epidermidis Phages Transduce Antimicrobial Resistance Plasmids and Mobilize Chromosomal Islands

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Publikace nespadá pod Filozofickou fakultu, ale pod Přírodovědeckou fakultu. Oficiální stránka publikace je na webu muni.cz.
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FIŠAROVÁ Lenka BOTKA Tibor DU Xin MAŠLAŇOVÁ Ivana BÁRDY Pavol PANTŮČEK Roman BENEŠÍK Martin ROUDNICKÝ Pavel WINSTEL Volker LARSEN Jesper ROSENSTEIN Ralf PESCHEL Andreas DOŠKAŘ Jiří

Rok publikování 2021
Druh Článek v odborném periodiku
Časopis / Zdroj mSphere
Fakulta / Pracoviště MU

Přírodovědecká fakulta

Citace
www https://journals.asm.org/doi/10.1128/mSphere.00223-21
Doi http://dx.doi.org/10.1128/mSphere.00223-21
Klíčová slova bacteriophages; Staphylococcus epidermidis; antibiotic resistance; horizontal gene transfer; pathogenicity islands; transduction
Přiložené soubory
Popis Staphylococcus epidermidis is a leading opportunistic pathogen causing nosocomial infections that is notable for its ability to form a biofilm and for its high rates of antibiotic resistance. It serves as a reservoir of multiple antimicrobial resistance genes that spread among the staphylococcal population by horizontal gene transfer such as transduction. While phage-mediated transduction is well studied in Staphylococcus aureus, S. epidermidis transducing phages have not been described in detail yet. Here, we report the characteristics of four phages, 27, 48, 456, and 459, previously used for S. epidermidis phage typing, and the newly isolated phage E72, from a clinical S. epidermidis strain. The phages, classified in the family Siphoviridae and genus Phietavirus, exhibited an S. epidermidis-specific host range, and together they infected 49% of the 35 strains tested. A whole-genome comparison revealed evolutionary relatedness to transducing S. aureus phietaviruses. In accordance with this, all the tested phages were capable of transduction with high frequencies up to 10-4 among S. epidermidis strains from different clonal complexes. Plasmids with sizes from 4 to 19?kb encoding resistance to streptomycin, tetracycline, and chloramphenicol were transferred. We provide here the first evidence of a phage-inducible chromosomal island transfer in S. epidermidis. Similarly to S. aureus pathogenicity islands, the transfer was accompanied by phage capsid remodeling; however, the interfering protein encoded by the island was distinct. Our findings underline the role of S. epidermidis temperate phages in the evolution of S. epidermidis strains by horizontal gene transfer, which can also be utilized for S. epidermidis genetic studies.
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