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Methicillin-resistant Staphylococcus aureus clonal types in the Czech Republic
O Melter, Sanches I Santos, J Schindler, de Sousa M Aires, R Mato, V Kovarova, H Zemlickova, Lencastre H de
Jazyk angličtina Země Spojené státy americké
Typ dokumentu práce podpořená grantem
Grantová podpora
IZ3500
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Část
Zdroj
NLK
Free Medical Journals
od 1975 do Před 6 měsíci
Freely Accessible Science Journals
od 1995 do Před 6 měsíci
PubMed Central
od 1975 do Před 1 rokem
Europe PubMed Central
od 1975 do Před 6 měsíci
Open Access Digital Library
od 1975-01-01
Open Access Digital Library
od 1975-01-01
PubMed
10449455
Knihovny.cz E-zdroje
- MeSH
- bakteriální proteiny genetika MeSH
- hexosyltransferasy * MeSH
- karboxypeptidasatranspeptidasa genetika MeSH
- mikrobiální testy citlivosti MeSH
- oxacilin farmakologie MeSH
- peptidyltransferasy * MeSH
- proteiny vázající penicilin MeSH
- pulzní gelová elektroforéza MeSH
- rezistence na methicilin * MeSH
- Staphylococcus aureus * genetika klasifikace účinky léků MeSH
- transportní proteiny genetika MeSH
- transpozibilní elementy DNA MeSH
- Publikační typ
- práce podpořená grantem MeSH
Molecular surveillance studies have documented the extensive spread of methicillin-resistant Staphylococcus aureus (MRSA) clones. Studies carried out by Centro de Epidemiologia Molecular-Network for Tracking Gram-Positive Pathogenic Bacteria (CEM/NET) led to the identification of two international multidrug-resistant strains, which were designated as the Iberian and Brazilian MRSA clones and which were defined by multiple genomic typing methods; these included ClaI restriction digests hybridized with mecA- and Tn554-specific DNA probes and pulsed-field gel electrophoresis (PFGE). The genotypic characteristics of these clones are distinct: the Iberian clone is defined as mecA type I, Tn554 type E (or its variants), and PFGE pattern A (I:E:A), whereas the Brazilian clone is defined as mecA type XI (or its variants), Tn554 type B, and PFGE pattern B (XI:B:B). In this study, we characterized 59 single-patient isolates of MRSA collected during 1996 and 1997 at seven hospitals located in Prague and five other cities in the Czech Republic by using the methodologies mentioned above and by using ribotyping of EcoRI and HindIII digests hybridized with a 16S-23S DNA probe. The Brazilian MRSA clone (XI:B:B) was the major clone (80%) spread in two hospitals located in Prague and one located in Brno; the Iberian MRSA clone (I:E:A or its variant I:DD:A), although less representative (12%), was detected in two hospitals, one in Prague and the other in Plzen. Almost all the strains belonging to clone XI:B:B (45 of 47) corresponded to a unique ribotype, E1H1, whereas most strains of the I:E:A and I:DD:A clonal types (6 of 7) corresponded to ribotype E2H2.
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