Plasmids carrying blaCTX-M-1 and qnr genes in Escherichia coli isolates from an equine clinic and a horseback riding centre
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
21393204
DOI
10.1093/jac/dkq500
PII: dkq500
Knihovny.cz E-zdroje
- MeSH
- beta-laktamasy genetika MeSH
- Diptera mikrobiologie MeSH
- DNA bakterií chemie genetika MeSH
- Escherichia coli genetika izolace a purifikace MeSH
- feces mikrobiologie MeSH
- koně mikrobiologie MeSH
- konjugace genetická MeSH
- mikrobiologie životního prostředí MeSH
- molekulární sekvence - údaje MeSH
- plazmidy * MeSH
- polymerázová řetězová reakce MeSH
- polymorfismus délky restrikčních fragmentů MeSH
- proteiny z Escherichia coli genetika MeSH
- sekvenční analýza DNA MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- beta-lactamase TEM-3 MeSH Prohlížeč
- beta-laktamasy MeSH
- DNA bakterií MeSH
- proteiny z Escherichia coli MeSH
- Qnr protein, E coli MeSH Prohlížeč
OBJECTIVES: The aim of this study was to determine the occurrence of extended-spectrum β-lactamase (ESBL)-producing Escherichia coli at an equine clinic and a horseback riding centre, and to discuss the impact of antimicrobial treatment on resistance selection. METHODS: Faeces from horses, environmental smears and flies were sampled at both the clinic and riding centre. Staff at the equine clinic were also examined. The samples were cultivated on MacConkey agar with cefotaxime (2 mg/L) to isolate ESBL-producing E. coli. The presence of bla and qnr genes was tested by PCR, and transferability was determined by conjugation. Replicon typing and restriction analysis of plasmids harbouring ESBL and qnr genes were performed. RESULTS: E. coli with the blaCTX-M-1 gene were isolated from horses, staff, environmental smears and flies at the two sites. E. coli isolates from the equine clinic harboured an IncHI1 conjugative 235-285 kb plasmid containing blaCTX-M-1, catA1, strA, sul2 and tet(B) genes. Some of these were positive for qnrS1 and/or qnrB19, and were located on 40 or 45 kb IncN or IncX1 conjugative plasmids. The gene blaCTX-M-1 in isolates from the riding centre was carried by IncN (30 kb) and IncI1 (85 kb) conjugative plasmids. Horizontal gene transfer seems to be involved in disseminating E. coli with ESBL and qnr genes at the clinic and riding centre. CONCLUSIONS: The study illustrates that ESBL-producing E. coli, as well as plasmids carrying ESBL genes of clinical interest, can be easily transferred among horses, humans and flies living in close contact.
Citace poskytuje Crossref.org
Genomic analysis of Escherichia coli strains isolated from diseased chicken in the Czech Republic
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