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Molecular characterization of a new efficiently transducing bacteriophage identified in meticillin-resistant Staphylococcus aureus
M. Varga, R. Pantůček, V. Růžičková, J. Doškař,
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Free Medical Journals
od 1967 do Před 1 rokem
Freely Accessible Science Journals
od 1967 do Před 12 měsíci
PubMed
26537974
DOI
10.1099/jgv.0.000329
Knihovny.cz E-zdroje
- MeSH
- aktivace viru MeSH
- bakteriální léková rezistence MeSH
- DNA virů chemie genetika MeSH
- fylogeneze MeSH
- genom virový MeSH
- lyzogenie MeSH
- methicilin rezistentní Staphylococcus aureus virologie MeSH
- molekulární sekvence - údaje MeSH
- otevřené čtecí rámce MeSH
- plazmidy MeSH
- pořadí genů MeSH
- přenos genů horizontální MeSH
- profágy genetika izolace a purifikace ultrastruktura MeSH
- sekvenční analýza DNA MeSH
- sekvenční homologie MeSH
- Siphoviridae genetika izolace a purifikace ultrastruktura MeSH
- syntenie MeSH
- transdukce genetická * MeSH
- transmisní elektronová mikroskopie MeSH
- výpočetní biologie MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
In Staphylococcus aureus, generalized transduction mediated by temperate bacteriophages represents a highly efficient way of transferring antibiotic resistance genes between strains. In the present study, we identified and characterized in detail a new efficiently transducing bacteriophage of the family Siphoviridae, designated ϕJB, which resides as a prophage in the meticillin-resistant S. aureus (MRSA) strain Jevons B. Whole-genome sequencing followed by detailed in silico analysis uncovered a linear dsDNA genome consisting of 43 ,12 bp and comprising 70 ORFs, of which ∼40 encoded proteins with unknown function. A global genome alignment of ϕJB and other efficiently transducing phages ϕ11, ϕ53, ϕ80, ϕ80α and ϕNM4 showed a high degree of homology with ϕNM4 and substantial differences with regard to other phages. Using a model transduction system with a well-defined donor and recipient, ϕJB transferred the tetracycline resistance plasmid pT181 and a penicillinase plasmid with outstanding frequencies, beating most of the above-mentioned phages by an order of magnitude. Moreover, ϕJB demonstrated high frequencies of transferring antibiotic resistance plasmids even upon induction from a lysogenic donor strain. Considering such transducing potential, ϕJB and related bacteriophages may serve as a suitable tool for elucidating the nature of transduction and its contribution to the spread of antibiotic resistance genes in naturally occurring MRSA populations.
Citace poskytuje Crossref.org
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