High-Level Carbapenem Resistance in a Klebsiella pneumoniae Clinical Isolate Is Due to the Combination of blaACT-1 β-Lactamase Production, Porin OmpK35/36 Insertional Inactivation, and Down-Regulation of the Phosphate Transport Porin PhoE

• Published in: Antimicrobial Agents and Chemotherapy Vol. 50; no. 10; pp. 3396 - 3406
• Main Authors: Kaczmarek, Frank M., Dib-Hajj, Fadia, Shang, Wenchi, Gootz, Thomas D.
• Format: Journal Article
• Language: English
• Published: Washington, DC American Society for Microbiology 01-10-2006
• Subjects: Antibiotics. Antiinfectious agents. Antiparasitic agents; beta-Lactam Resistance; beta-Lactamases; Biological and medical sciences; Carbapenems; Klebsiella pneumoniae; Mechanisms of Resistance; Medical sciences; Pharmacology. Drug treatments; Porins; Human; Phosphates; Porin; Enzyme; β-Lactams; β-Lactamase; Inactivation; Resistance; Carbapenem derivatives; Regulation(control); Bacteria; Hydrolases; Antibacterial agent; Transport; Clinical isolate; Klebsiella pneumoniae; Enterobacteriaceae
• ISSN: 0066-4804; 1098-6596
• DOI: 10.1128/AAC.00285-06

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