Results 231 to 240 of about 71,036 (261)

CTX-M-33 Is a CTX-M-15 Derivative Conferring Reduced Susceptibility to Carbapenems [PDF]

open access: yesAntimicrobial Agents and Chemotherapy, 2019
CTX-M-type extended-spectrum β-lactamases (ESBLs) are widespread among Enterobacterales strains worldwide. The most common variant is CTX-M-15, which hydrolyzes ceftazidime at a high rate but spares carbapenems. Here, we identified CTX-M-33, a point mutation derivative of CTX-M-15 (Asp to Ser substitution at Ambler ...
Laurent Poirel   +2 more
exaly   +4 more sources

The CTX-M β-lactamase pandemic

Current Opinion in Microbiology, 2006
In the past decade CTX-M enzymes have become the most prevalent extended-spectrum beta-lactamases, both in nosocomial and in community settings. The insertion sequences (ISs) ISEcp1 and ISCR1 (formerly common region 1 [CR1] or orf513) appear to enable the mobilization of chromosomal beta-lactamase Kluyvera species genes, which display high homology ...
Rafael Cantón, Teresa M Coque
exaly   +3 more sources

Prevalence of O25b-ST131 clone amongEscherichia colistrains producing CTX-M-15, CTX-M-14 and CTX-M-92 β-lactamases

Infectious Diseases, 2016
Dissemination of multidrug-resistant Escherichia coli is closely associated with the worldwide spread of a single clone ST131, which is the main cause of urinary tract and bloodstream infections in patients from nursing homes and immunocompromised patients.
Giedraitienė, Agnė   +6 more
openaire   +2 more sources

Biochemical characterisation of the CTX-M-14 β-lactamase

International Journal of Antimicrobial Agents, 2007
Cefotaxime-resistant Escherichia coli TUM1121 was isolated from an abscess of an 83-year-old patient. The CTX-M-14 gene was located on a 70 kb plasmid. The enzyme was purified and its activity was analysed. CTX-M-14 was poorly active against ceftazidime and aztreonam. Aztreonam behaved as a competitive inhibitor. Among the tested suicide substrates for
Ishii, Y.   +4 more
openaire   +2 more sources

bla(CTX-M) Genes in Escherichia coli Strains from Croatian Hospitals Are Located in New (bla(CTX-M-3a)) and Widely Spread (bla(CTX-M-3a) and bla(CTX-M-15)) Genetic Structures

Antimicrobial agents and chemotherapy, 2009
CTX-M-producing Escherichia coli isolates from three Croatian hospitals were analyzed. All blaCTX-M-15 and one blaCTX-M-3a genes resided in widely-spread ISEcp1 transposition modules but other blaCTX-M-3a genes were in a new configuration with two IS26 copies, indicating a new event of gene mobilization from a Kluyvera ascorbata genome.
Bedenić, Branka   +2 more
openaire   +2 more sources

High prevalence of CTX-M-15 and first report of CTX-M-3, CTX-M-22, CTX-M-28 and plasmid-mediated AmpC beta-lactamase producing Enterobacteriaceae causing urinary tract infections in Bosnia and Herzegovina in hospital and community settings

Journal of Infection and Chemotherapy, 2015
To investigate molecular epidemiology of extended-spectrum β-lactamase/ESBL and plasmid-mediated AmpC β-lactamase/pAmpC producing Gram-negative bacteria causing urinary tract infections (UTIs) in Zenica-Doboj Canton, Bosnia and Herzegovina, in the period Decembar 2009-May 2010.Antibiotic susceptibility was determined by disc diffusion and broth ...
Amir Ibrahimagić   +3 more
openaire   +4 more sources

Biochemical characterization of CTX-M-166, a new CTX-M β-lactamase produced by a commensal Escherichia coli isolate

The Journal of Antibiotics, 2017
We thank Fundacao para a Ciencia e a Tecnologia (FCT) for project grant PEst-OE/AGR/UI0211/2011–2014, Strategic Project UI211-2011-2014. VM was supported by FCT fellowship (grant SFRH/BPD/77486/2011), financed by the European Social Funds (COMPETE-FEDER) and national funds of the Portuguese Ministry of Education and Science (POPH-QREN)
Manageiro, Vera   +5 more
openaire   +4 more sources

O204 Ceftazidime resistance evolution in ESBLs belonging to CTX-M-1 cluster (CTX-M-1, CTX-M-3, CTX-M-10) in a hypermutator background

International Journal of Antimicrobial Agents, 2007
A. Novais   +5 more
openaire   +1 more source

Interaction of carbapenems and Î2-lactamase inhibitors towards CTX-M-15 and CTX-M-15G238Cmutant

2017
Objectives The aim of this study was to evaluate the role of residue 238 in CTX-M-15 and CTX-M-15G238Cmutant with respect to carbapenems and various Î2-lactamase inhibitors. Methods A CTX-M-15G238Claboratory mutant was generated by site-directed mutagenesis from CTX-M-15 enzyme by replacing glycine 238 with cysteine.
Sabatini, Alessia   +8 more
openaire   +1 more source

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