Emergence of metallo- -lactamases GIM-1 and VIM in multidrug-resistant Pseudomonas aeruginosa in North Rhine-Westphalia, Germany
Author(s) -
Heime Rieber,
André Frontzek,
Heike von Baum,
Yvonne Pfeifer
Publication year - 2012
Publication title -
journal of antimicrobial chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.124
H-Index - 194
eISSN - 1460-2091
pISSN - 0305-7453
DOI - 10.1093/jac/dkr579
Subject(s) - pseudomonas aeruginosa , microbiology and biotechnology , multiple drug resistance , biology , drug resistance , bacteria , genetics
stay, Patient A received successively piperacillin/tazobactam with vancomycin, cefepime with ciprofloxacin, and imipenem with ciprofloxacin, but Patient B only received amoxicillin/clavulanate (Figure 1). It is well established that K. pneumoniae isolates are an important reservoir of b-lactamases. Thus, the dissemination of the KPC carbapenemase has been linked to the dispersion of a clonal ST258-type K. pneumoniae strain. Nevertheless, it appears that the rapid emergence of blaOXA-48 in K. pneumoniae would be explained by the horizontal transmission of an OXA-48-encoding plasmid within strains belonging to different STs. Our experience raises concern about a possible rapid rise in carbapenem resistance in enteric bacteria through the spread of blaOXA-48-positive plasmids and/or strains. Outbreaks involving different OXA-48-producing species have already been described. Early detection by sensitive screening methods is needed, with targeted surveillance and consideration given to infection control measures, to prevent this spread.
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