In Vitro Activity of Ceftaroline against Gram-Positive and Gram-Negative Pathogens Isolated from Patients in Canadian Hospitals in 2009

被引:38
作者
Karlowsky, James A. [1 ,3 ]
Adam, Heather J. [1 ,3 ]
DeCorby, Melanie R. [3 ]
Lagace-Wiens, Philippe R. S. [2 ,3 ]
Hoban, Daryl J. [1 ,3 ]
Zhanel, George G. [3 ]
机构
[1] Hlth Sci Ctr, Dept Clin Microbiol, Diagnost Serv Manitoba, Winnipeg, MB R3A 1R9, Canada
[2] St Boniface Gen Hosp, Dept Clin Microbiol, Diagnost Serv Manitoba, Winnipeg, MB R2H 2A6, Canada
[3] Univ Manitoba, Fac Med, Dept Med Microbiol & Infect Dis, Winnipeg, MB, Canada
关键词
PENICILLIN-BINDING PROTEINS; STAPHYLOCOCCUS-AUREUS; ESCHERICHIA-COLI; METHICILLIN-RESISTANT; STREPTOCOCCUS-PNEUMONIAE; ANTIMICROBIAL RESISTANCE; BETA-LACTAMASES; SPECTRUM; CEPHALOSPORIN; CEFTOBIPROLE;
D O I
10.1128/AAC.01787-10
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The in vitro activities of ceftaroline and comparative agents were determined for a collection of the most frequently isolated bacterial pathogens from hospital-associated patients across Canada in 2009 as part of the ongoing CANWARD surveillance study. In total, 4,546 isolates from 15 sentinel Canadian hospital laboratories were tested using the Clinical and Laboratory Standards Institute (CLSI) broth microdilution method. Compared with other cephalosporins, including ceftobiprole, cefepime, and ceftriaxone, ceftaroline exhibited the greatest potency against methicillin-susceptible Staphylococcus aureus (MSSA), with a MIC90 of 0.25 mu g/ml. Ceftaroline also demonstrated greater potency than ceftobiprole against community-associated methicillin-resistant S. aureus (MRSA) (MIC90, 0.5 mu g/ml) and health care-associated MRSA (MIC90, 1 mu g/ml) and was at least 4-fold more active than other cephalosporins against Staphylococcus epidermidis; all isolates of MSSA and MRSA tested were susceptible to ceftaroline (MIC, <= 1 mu g/ml). Against streptococci, including Streptococcus pneumoniae, ceftaroline MICs (MIC90, <= 0.03 mu g/ml) were comparable to those of ceftobiprole; however, against penicillin-nonsusceptible, macrolide-nonsusceptible, and multidrug-nonsusceptible isolates of S. pneumoniae, ceftaroline demonstrated 2- to 4-fold and 4- to 16-fold more potent activities than those of ceftobiprole and ceftriaxone, respectively. All isolates of S. pneumoniae tested were susceptible to ceftaroline (MIC, <= 0.25 mu g/ml). Among Gram-negative isolates, ceftaroline demonstrated potent activity (MIC90, <= 0.5 mu g/ml) against Escherichia coli (92.2% of isolates were susceptible), Klebsiella pneumoniae (94.1% of isolates were susceptible), Proteus mirabilis (97.7% of isolates were susceptible), and Haemophilus influenzae (100% of isolates were susceptible). Ceftaroline demonstrated less potent activity (MIC90, >= 4 mu g/ml) against Enterobacter spp., Acinetobacter baumannii, Pseudomonas aeruginosa, Klebsiella oxytoca, Serratia marcescens, and Stenotrophomonas maltophilia. Overall, ceftaroline demonstrated potent in vitro activity against a recent collection of the most frequently encountered Gram-positive and Gram-negative isolates from patients attending hospitals across Canada in 2009.
引用
收藏
页码:2837 / 2846
页数:10
相关论文
共 30 条
[1]  
[Anonymous], PCR DED PNEUM SER
[2]   Comparison of antimicrobial resistance profiles among extended-spectrum-β-lactamase-producing and acquired AmpC β-lactamase-producing Escherichia coli isolates from Canadian intensive care units [J].
Baudry, Patricia J. ;
Nichol, Kim ;
DeCorby, Melanie ;
Mataseje, Laura ;
Mulvey, Michael R. ;
Hoban, Daryl J. ;
Zhanel, George G. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2008, 52 (05) :1846-1849
[3]   Methicillin-resistant Staphylococcus aureus resistance to non-β-lactam antimicrobials in the United States from 1996 to 2008 [J].
Bordon, Jose ;
Master, Ronald N. ;
Clark, Richard B. ;
Duvvuri, Padmaraj ;
Karlowsky, James A. ;
Ayesu, Kwabena ;
Klotchko, Alena ;
Kapoor, Rama ;
Ramirez, Julio .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2010, 67 (04) :395-398
[4]   Bad Bugs, No Drugs: No ESKAPE! An Update from the Infectious Diseases Society of America [J].
Boucher, Helen W. ;
Talbot, George H. ;
Bradley, John S. ;
Edwards, John E., Jr. ;
Gilbert, David ;
Rice, Louis B. ;
Scheld, Michael ;
Spellberg, Brad ;
Bartlett, John .
CLINICAL INFECTIOUS DISEASES, 2009, 48 (01) :1-12
[5]   Enterococcus faecium N03-0072 carries a new VanD-type vancomycin resistance determinant:: characterization of the VanD5 operon [J].
Boyd, DA ;
Kibsey, P ;
Roscoe, D ;
Mulvey, MR .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2004, 54 (03) :680-683
[6]   In Vitro Antimicrobial Activity of a New Cephalosporin, Ceftaroline, and Determination of Quality Control Ranges for MIC Testing [J].
Brown, Steven D. ;
Traczewski, Maria M. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2009, 53 (03) :1271-1274
[7]  
Caroff N, 1999, FEMS MICROBIOL LETT, V173, P459, DOI 10.1016/S0378-1097(99)00111-1
[8]   In Vitro Activity of Ceftaroline against 623 Diverse Strains of Anaerobic Bacteria [J].
Citron, D. M. ;
Tyrrell, K. L. ;
Merriam, C. V. ;
Goldstein, E. J. C. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2010, 54 (04) :1627-1632
[9]  
Clinical and Laboratory Standards Institute, 2010, M100S20
[10]  
Clinical and Laboratory Standards Institute, 2009, M07A8 CLSI