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Kadry, Ashraf A.
- Lacking of Efflux Mechanism in Clinical Isolate of Pseudomonas aerupinosa highly Resistant to β-Lactams and Imimnem
Authors
1 Microbiology Division. Faculty of Pharmacy. King Saud University. Riyadh, SA
Source
Scientia Pharmaceutica, Vol 71, No 2 (2003), Pagination: 89-100Abstract
In this investigation, the isolate of Pseudomonas aeruginosa from cystic fibrosis was highly resistant to β-lactarns and β-lactamase inhibitors. The resistant determinants of clinical isolate to imipenem, ceftazidime, ceftriaxone and cefepime were conjugally non-transfer. The slow or non-enzymatically mediated breakdown of imipenem and other broad spectrum β-lactams suggest the resistance of P. aeruginosa isolate to these drugs might be attributed to either permeability or efflux. Impaired penetration of imipenem and other β-lactams through the membrane was detected by a diminished expression of outer membrane (OM) proteins of approximate weight of 46 and 39 Kdal, matched to Opr D and Opr F, respectively. Efflux resistance mechanism for meropenem and β-lactams has been ruled out since the isolate failed to express outer membrane protein of about 50 Kdal, which is matched to Opr M protein channel. Thus, reduced permeability in the clinical isolate may be the main mechanism conferring resistance against β-lactarns including imipenem.Keywords
P. aeruginosac, Imipenem, β-lactams, Resistance, Permeability Barriers, Lacking Efflux, β-lactamase.References
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- Resistance of Escherichia coli and Klebsiella pneumoniae Isolated from different Sources to β-Lactam Antibiotics
Authors
1 Department of Microbiology and Immunology, Zagazig University, Zagazig, EG
2 Department of Microbiology and Biotechnology, Delta University for Science and Technology, Gamasa, Mansoura, EG
Source
Research Journal of Pharmacy and Technology, Vol 10, No 2 (2017), Pagination: 589-591Abstract
Escherichia coli and Klebsiella pneumoniae are important human pathogens that cause many infectious diseases. β-lactam antibiotics are commonly used in the treatment of these infections. However, resistance to such antibiotics complicates the treatment. Mechanisms of resistance to β-lactams include production of β-lactamases, efflux pumps, change in drug targets and outer membrane impermeability. This study was performed to investigate the resistance of Klebsiella pneumoniae and Escherichia coli to β-lactam antibiotics. The study was carried out from May 2014 to May 2015. Five hundred clinical isolates were collected from patients in Belquas Hospital and Mansoura University Hospitals. Three hundred isolates were identified as Klebsiella pneumoniae and Escherichia coli (one hundred and fifty isolates each). Klebsiella pneumoniae and Escherichia coli isolates showed high resistance to cefoperazone and ceftriaxone, intermediate resistance to cefoxitin, cefotaxime, ceftazidime and amoxicillin-clavulanic acid and low resistance to imipenem and meropenem. Klebsiella pneumoniae showed more resistance than Escherichia coli. Resistance of Klebsiella pneumoniae was higher to cefoperazone, ceftriaxone, ceftazidime, imipenem and meropenem. However, Escherichia coli was more resistant to cefotaxime and cefoxitin. The resistance to amoxicillin-clavulinic acid was more or less similar in both bacteria. In conclusion, the resistance of Klebsiella pneumoniae and Escherichia coli isolates to B-lactams was high and this needs a strict policy for antibiotic dispensing to reduce the emergence of resistance.