نتایج جستجو برای: ژن ampc

تعداد نتایج: 17449  

Journal: :The Journal of antimicrobial chemotherapy 2014
Sushmita D Lahiri Robert A Giacobbe Michele R Johnstone Richard A Alm

BACKGROUND Extended-spectrum AmpC (ESAC) β-lactamase enzymes, which are either chromosomally encoded or plasmid encoded, have minor structural changes that broaden their substrate hydrolysis profile. The derepressed AmpC enzyme found once in Enterobacter cloacae CHE was shown to contain a six residue deletion in the H-10 helix in close proximity to the active site. Avibactam is a non-β-lactam i...

Journal: :The Journal of antimicrobial chemotherapy 2007
Neil Woodford Suganya Reddy Elizabeth J Fagan Robert L R Hill Katie L Hopkins Mary E Kaufmann James Kistler Marie-France I Palepou Rachel Pike M Elaina Ward John Cheesbrough David M Livermore

OBJECTIVES To determine the distribution of acquired AmpC beta-lactamases in 173 isolates of Escherichia coli and Klebsiella spp. submitted to the UK's national reference laboratory for antibiotic resistance. METHODS MICs were determined and interpreted according to BSAC guidelines. Candidate isolates were those resistant to cefotaxime and/or ceftazidime, irrespective of addition of clavulani...

Journal: :The Journal of antimicrobial chemotherapy 2013
Mohammad Hamidian Ruth M Hall

Sir, Resistance to third-generation cephalosporins such as ceftazidime and cefotaxime in Acinetobacter baumannii is often due to increased expression of an intrinsic ampC gene. Expression increases when the ISAba1 insertion sequence (IS) is present in the appropriate orientation upstream of the ampC gene, providing an outward-facing promoter that appears to be stronger than the intrinsic promot...

2014
I. Yusuf A.H. Arzai M. Haruna A.A. Sharif M.I. Getso

Two major hospitals in Kano, North West Nigeria have recorded increasing resistance of clinical pathogens to broad spectrum β lactams, mediated by extended spectrum β-lactamase (ESβL) and non ESBLs. A study was therefore undertaken to determine the occurrence and prevalence of plasmid and chromosomal mediated AmpC βL and carbapenemase in addition to already known ESBL due to increasing resistan...

Journal: :Antimicrobial agents and chemotherapy 2011
Laura Zamorano Thomas M Reeve Carlos Juan Bartolomé Moyá Gabriel Cabot David J Vocadlo Brian L Mark Antonio Oliver

Constitutive AmpC hyperproduction is the most frequent mechanism of resistance to the weak AmpC inducers antipseudomonal penicillins and cephalosporins. Previously, we demonstrated that inhibition of the β-N-acetylglucosaminidase NagZ prevents and reverts this mechanism of resistance, which is caused by ampD and/or dacB (PBP4) mutations in Pseudomonas aeruginosa. In this work, we compared NagZ ...

Journal: :Research, Society and Development 2022

Carbapenem-resistance is a great challenge for antimicrobial therapy in Pseudomonas aeruginosa multidrug-resistant infections, as it reduces therapeutic options. This study investigated carbapenem-resistance mechanisms six strains of non-carbapenemase-producing P. aeruginosa. Minimal inhibitory concentrations imipenem and meropenem were determined by epsilometric test broth microdilution. Mutat...

2017
Ryuichi Nakano Akiyo Nakano Hisakazu Yano Ryoichi Okamoto

CFE-1 is a unique plasmid-encoded AmpC β-lactamase with the regulator gene ampR. It imparts high resistance to most cephalosporins with constitutive high-level β-lactamase activity. Here, the β-lactamase activities and expression levels of ampC with or without ampR were investigated. Results suggested that the resistance of CFE-1 to cephalosporins is caused by a substitution in AmpR, in which t...

Journal: :The Journal of antimicrobial chemotherapy 2012
Thomas Johnston Thomas Yeoman Susan Chapman Charis Marwick Dilip Nathwani

TEM/SHV+ ESBL+ E. coli. There is no immediate explanation for these results, particularly since several other TEM, SHV and CTX-M ESBL+ isolates were correctly identified as ‘exhibiting another resistance mechanism’. The ESBL activity might have been masked by the AmpC inducer (incorporated into all three discs), and hence these results highlight an important limitation of the D69C kit, i.e. it ...

Journal: :Antimicrobial agents and chemotherapy 1998
G Barnaud G Arlet C Verdet O Gaillot P H Lagrange A Philippon

DHA-1, a plasmid-mediated cephalosporinase from a single clinical Salmonella enteritidis isolate, conferred resistance to oxyimino-cephalosporins (cefotaxime and ceftazidime) and cephamycins (cefoxitin and moxalactam), and this resistance was transferable to Escherichia coli HB101. An antagonism was observed between cefoxitin and aztreonam by the diffusion method. Transformation of the transcon...

Journal: :Antimicrobial agents and chemotherapy 1998
L Bret C Chanal-Claris D Sirot E B Chaibi R Labia J Sirot

A clinical strain of Proteus mirabilis (CF09) isolated from urine specimens of a patient displayed resistance to amoxicillin (MIC >4,096 microg/ml), ticarcillin (4,096 microg/ml), cefoxitin (64 microg/ml), cefotaxime (256 microg/ml), and ceftazidime (128 microg/ml) and required an elevated MIC of aztreonam (4 microg/ml). Clavulanic acid did not act synergistically with cephalosporins. Two beta-...

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