Analysis of ESBL- and AmpC-positive Enterobacteriaceae at the Department of Neonatology, University Hospital Olomouc
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
- MeSH
- antibakteriální látky farmakologie MeSH
- bakteriální léková rezistence MeSH
- bakteriální proteiny genetika metabolismus MeSH
- beta-laktamasy genetika metabolismus MeSH
- Enterobacteriaceae klasifikace enzymologie genetika izolace a purifikace MeSH
- enterobakteriální infekce mikrobiologie MeSH
- hospitalizace MeSH
- lidé MeSH
- mikrobiální testy citlivosti MeSH
- nemoci novorozenců mikrobiologie MeSH
- nemocnice univerzitní statistika a číselné údaje MeSH
- neonatologie MeSH
- novorozenec MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- novorozenec MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Geografické názvy
- Česká republika MeSH
- Názvy látek
- antibakteriální látky MeSH
- bakteriální proteiny MeSH
- beta-laktamasy MeSH
Bacterial infections are an important issue in current clinical medicine. The severity of infectious diseases has increased dramatically in recent years, which is also due to increasing numbers of resistant bacteria, including strains producing broad-spectrum beta-lactamases. The study aimed at determining the prevalence of ESBL- and AmpC-positive Enterobacteriaceae at the Department of Neonatology, University Hospital Olomouc. Enterobacteriaceae were isolated from clinical samples from infants hospitalized at the Department of Neonatology, University Hospital Olomouc over a period of 2 years. ESBL- and AmpC-positive isolates were subjected to basic genetic analysis. In the study period, a total of 1,526 isolates of the Enterobacteriaceae family were identified, including 55 (3.6%) cases of the ESBL phenotype and 17 (1.1%) AmpC-positive isolates. Genetic analysis of ESBL-positive isolates revealed a majority of CTX-M enzymes. Among AmpC beta-lactamases, the EBC, CIT, DHA, and MOX types were detected. An Escherichia coli strain was isolated with mutations in the promoter region of the ampC chromosomal gene that are associated with overproduction of the relevant enzyme.
Zobrazit více v PubMed
Pediatr Infect Dis J. 2002 Nov;21(11):1029-33 PubMed
Antimicrob Agents Chemother. 2004 Oct;48(10):3720-8 PubMed
J Clin Microbiol. 2003 Sep;41(9):4264-9 PubMed
J Clin Microbiol. 1996 Nov;34(11):2784-90 PubMed
J Antimicrob Chemother. 1996 Apr;37(4):797-802 PubMed
Pathol Biol (Paris). 2010 Feb;58(1):78-83 PubMed
Klin Mikrobiol Infekc Lek. 2007 Oct;13(5):195-205 PubMed
J Clin Microbiol. 2002 Jun;40(6):2153-62 PubMed
J Med Microbiol. 2003 May;52(Pt 5):421-425 PubMed
J Antimicrob Chemother. 2007 Feb;59(2):165-74 PubMed
Int J Antimicrob Agents. 2007 May;29 Suppl 3:S9-S22 PubMed
FEMS Microbiol Lett. 2000 Mar 1;184(1):85-9 PubMed
Indian J Pediatr. 2010 Jan;77(1):37-9 PubMed
J Int Med Res. 2002 Jul-Aug;30(4):445-8 PubMed
Antimicrob Agents Chemother. 2006 Apr;50(4):1257-62 PubMed
Klin Mikrobiol Infekc Lek. 2005 Feb;11(1):20-4 PubMed
Indian J Med Microbiol. 2008 Oct-Dec;26(4):356-60 PubMed
J Antimicrob Chemother. 2000 Jun;45(6):783-8 PubMed
Semin Perinatol. 2007 Feb;31(1):26-32 PubMed
Turk J Pediatr. 1998 Jan-Mar;40(1):17-33 PubMed
FEMS Microbiol Lett. 1995 Dec 15;134(2-3):203-8 PubMed
Am J Infect Control. 2007 Apr;35(3):183-9 PubMed
J Clin Microbiol. 2005 Jun;43(6):2551-8 PubMed
Clin Microbiol Infect. 2003 Jun;9(6):467-74 PubMed
Infect Control Hosp Epidemiol. 2004 Sep;25(9):781-3 PubMed
Eur J Clin Microbiol Infect Dis. 2008 Oct;27(10):915-21 PubMed
Rev Infect Dis. 1988 Jul-Aug;10(4):867-78 PubMed