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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,
Language English Country England, Great Britain
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
Free Medical Journals
from 1967 to 1 year ago
Freely Accessible Science Journals
from 1967 to 12 months ago
PubMed
26537974
DOI
10.1099/jgv.0.000329
Knihovny.cz E-resources
- MeSH
- Virus Activation MeSH
- Drug Resistance, Bacterial MeSH
- DNA, Viral chemistry genetics MeSH
- Phylogeny MeSH
- Genome, Viral MeSH
- Lysogeny MeSH
- Methicillin-Resistant Staphylococcus aureus virology MeSH
- Molecular Sequence Data MeSH
- Open Reading Frames MeSH
- Plasmids MeSH
- Gene Order MeSH
- Gene Transfer, Horizontal MeSH
- Prophages genetics isolation & purification ultrastructure MeSH
- Sequence Analysis, DNA MeSH
- Sequence Homology MeSH
- Siphoviridae genetics isolation & purification ultrastructure MeSH
- Synteny MeSH
- Transduction, Genetic * MeSH
- Microscopy, Electron, Transmission MeSH
- Computational Biology MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't 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.
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