TY - JOUR
T1 - Identification of CTX-M β-lactamases in Escherichia coli from hospitalized patients and residents of long-term care facilities
AU - Urban, Carl
AU - Mariano, Noriel
AU - Bradford, Patricia A.
AU - Tuckman, Margareta
AU - Segal-Maurer, Sorana
AU - Wehbeh, Wehbeh
AU - Grenner, Louise
AU - Colon-Urban, Rita
AU - Johnston, Brian
AU - Johnson, James R.
AU - Rahal, James J.
N1 - Funding Information:
The study was supported by the BMA Medical Foundation , the Beatrice Snyder Foundation , NIH grant GM008722-07 (MARC-NIGMS-RCU), and the Office of Research and Development, Medical Research Service, Department of Veterans Affairs (J.R.J.) .
PY - 2010/4
Y1 - 2010/4
N2 - Bacteria harboring CTX-M extended-spectrum β-lactamases (ESBLs) have been identified worldwide, with most reports coming from regions outside North America. We have identified CTX-M enzymes in 31% of ESBL-positive Escherichia coli isolates from our hospital and more than half (53%) of the isolates from associated long-term care facilities. Approximately 3/4 of all CTX-M-bearing isolates were from urine specimens, with a predominance of CTX-M-15. A large proportion of such isolates were nonsusceptible to levofloxacin, trimethoprim/sulfamethoxazole, and all β-lactam antimicrobials with the exception of the carbapenems, requiring carbapenem therapy for acute urinary tract infection or urinary tract-related sepsis. CTX-M β-lactamases have emerged within our location, and detection of bacteria harboring these enzymes in the clinical microbiology laboratory remains problematic because molecular methods are needed for their identification.
AB - Bacteria harboring CTX-M extended-spectrum β-lactamases (ESBLs) have been identified worldwide, with most reports coming from regions outside North America. We have identified CTX-M enzymes in 31% of ESBL-positive Escherichia coli isolates from our hospital and more than half (53%) of the isolates from associated long-term care facilities. Approximately 3/4 of all CTX-M-bearing isolates were from urine specimens, with a predominance of CTX-M-15. A large proportion of such isolates were nonsusceptible to levofloxacin, trimethoprim/sulfamethoxazole, and all β-lactam antimicrobials with the exception of the carbapenems, requiring carbapenem therapy for acute urinary tract infection or urinary tract-related sepsis. CTX-M β-lactamases have emerged within our location, and detection of bacteria harboring these enzymes in the clinical microbiology laboratory remains problematic because molecular methods are needed for their identification.
KW - Antimicrobial resistance
KW - CTX-M-15 β-lactamase
KW - Escherichia coli infections
KW - Long-term care facilities
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U2 - 10.1016/j.diagmicrobio.2009.11.012
DO - 10.1016/j.diagmicrobio.2009.11.012
M3 - Article
C2 - 20226330
AN - SCOPUS:77649303639
SN - 0732-8893
VL - 66
SP - 402
EP - 406
JO - Diagnostic Microbiology and Infectious Disease
JF - Diagnostic Microbiology and Infectious Disease
IS - 4
ER -