New -Lactamases in Gram-Negative Bacteria: Diversity and Impact on the Selection of Antimicrobial Therapy
Author(s) -
George M. Eliopoulos,
Karen Bush
Publication year - 2001
Publication title -
clinical infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.44
H-Index - 336
eISSN - 1537-6591
pISSN - 1058-4838
DOI - 10.1086/319610
Subject(s) - antimicrobial , antibiotic resistance , microbiology and biotechnology , antibiotics , efflux , plasmid , bacteria , multiple drug resistance , medicine , selection (genetic algorithm) , antibiotic therapy , beta (programming language) , gram negative bacteria , gene , biology , genetics , escherichia coli , artificial intelligence , computer science , programming language
Of the 340 discrete beta-lactamases that have been identified, the most important groups of enzymes that are continuing to proliferate include the plasmid-encoded cephalosporinases, the metallo-beta-lactamases, and the extended-spectrum beta-lactamases. Resistance to specific beta-lactam-containing antimicrobial agents frequently can be traced to a single beta-lactamase, but this task is becoming more difficult for the clinical microbiology laboratory. Other factors, such as multiple beta-lactamase production, transferable multidrug-resistance genes, alterations in outer-membrane porins, and possible antibiotic efflux, all may contribute to a resistance phenotype. Appreciation of these factors may help the physician make a more informed decision when choosing therapy to try to avoid selection of even more pathogenic strains.
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