Characterization of Methicillin-ResistantStaphylococcus aureus, Vancomycin-Resistant Enterococci and Extended-Spectrum Beta-Lactamase-ProducingEscherichia coliin Intensive Care Units in Canada: Results of the Canadian National Intensive Care Unit (Can-Icu) Study (2005–2006)
BACKGROUND: Methicillin-resistantStaphylococcus aureus(MRSA), extended-spectrum beta-lactamase (ESBL)-producingEscherichia coliand vancomycin-resistant enterococci (VRE) are important hospital pathogens in Canada and worldwide.OBJECTIVES: To genotypically and phenotypically characterize the isolates of MRSA, VRE and ESBL-producingE colicollected from patients in Canadian intensive care units (ICUs) in 2005 and 2006.METHODS: Between September 1, 2005, and June 30, 2006, 19 medical centres participating in the Canadian National Intensive Care Unit (CAN-ICU) study collected 4133 unique patient isolates associated with infections in ICUs. Isolates of MRSA underwentmecA polymerase chain reaction (PCR) and Panton-Valentine leukocidin analysis; they were typed using pulsed-field gel electrophoresis. All isolates ofE coliwith ceftriaxone minimum inhibitory concentrations greater than or equal to 1 μg/mL were tested for the presence of an ESBL using the Clinical Laboratory Standards Institute double-disk diffusion method. Subsequently, PCR and sequence analysis were used to identifyblaSHV,blaTEMandblaCTX-M. Isolates of VRE were tested for the presence ofvanA andvanB genes by PCR.RESULTS: Of the 4133 ICU isolates collected, MRSA accounted for 4.7% (193 of 4133) of all isolates. MRSA represented 21.9% (193 of 880) of allS aureuscollected during the study; 90.7% were health care-associated MRSA strains and 9.3% were community-associated MRSA strains. Resistance rates for the isolates of MRSA were 91.8% to levofloxacin, 89.9% to clarithromycin, 76.1% to clindamycin and 11.7% to trimethoprim-sulfamethoxazole; no isolates were resistant to vancomycin, linezolid, tigecycline or daptomycin. ESBL-producingE coliaccounted for 0.4% (18 of 4133) of all isolates and 3.7% (18 of 493) ofE coliisolates. All 18 ESBL-producingE coliwere PCR-positive for CTX-M, withblaCTX-M-15occurring in 72% (13 of 18) of isolates. All ESBL-producingE colidisplayed a multidrug-resistant phenotype (resistant to third-generation cephalosporins and one or more other classes of antimicrobials), with 77.8% of isolates resistant to ciprofloxacin, 55.6% resistant to trimethoprim-sulfamethoxazole, 27.8% resistant to gentamicin and 26.3% resistant to doxycycline; all isolates were susceptible to ertapenem, meropenem and tigecycline. VRE accounted for 0.4% (17 of 4133) of all isolates and 6.7% (17 of 255) of enterococci isolates; 88.2% of VRE had thevanA genotype. Isolated VRE that were tested were uniformly susceptible to linezolid, tigecycline and daptomycin.CONCLUSIONS: MRSA isolated in Canadian ICUs in 2005 and 2006 was predominately health care-associated (90.7%), ESBL-producingE coliwere all CTX-M producers (72%blaCTX-M-15) and VRE primarily harboured avanA genotype (88.2%). MRSA, ESBL-producingE coliand VRE were frequently multidrug resistant.