In Vitro Antibacterial Activity of the Ceftazidime-Avibactam (NXL104) Combination against Pseudomonas aeruginosa Clinical Isolates

被引:94
作者
Levasseur, Premavathy [1 ]
Girard, Anne-Marie [1 ]
Claudon, Monique [1 ]
Goossens, Herman [2 ]
Black, Michael T. [1 ]
Coleman, Kenneth [1 ]
Miossec, Christine [1 ]
机构
[1] Novexel SA, Romainville, France
[2] Univ Antwerp Hosp, Vaccine & Infect Dis Inst, Dept Microbiol, Edegem, Belgium
关键词
D O I
10.1128/AAC.06064-11
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The beta-lactamase inhibitor avibactam (NXL104) displays potent inhibition of both class A and C enzymes. The in vitro antibacterial activity of the combination ceftazidime-avibactam was evaluated against a clinical panel of Pseudomonas aeruginosa isolates. Avibactam offered efficient protection from hydrolysis since 94% of isolates were susceptible to ceftazidime when combined with 4 mu g/ml avibactam, compared with 65% susceptible to ceftazidime alone. Ceftazidime-avibactam also demonstrated better antipseudomonal activity than imipenem (82% susceptibility), a common reference treatment.
引用
收藏
页码:1606 / 1608
页数:3
相关论文
共 10 条
[1]   In vitro activity of AVE1330A, an innovative broad-spectrum non-β-lactam β-lactamase inhibitor [J].
Bonnefoy, A ;
Dupuis-Hamelin, C ;
Steier, V ;
Delachaume, C ;
Seys, C ;
Stachyra, T ;
Fairley, M ;
Guitton, M ;
Lampilas, M .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2004, 54 (02) :410-417
[2]  
Clinical and Laboratory Standards Institute, 2011, M100S21 CLIN LAB STA, V31, pM100
[3]   Antibacterial-Resistant Pseudomonas aeruginosa: Clinical Impact and Complex Regulation of Chromosomally Encoded Resistance Mechanisms [J].
Lister, Philip D. ;
Wolter, Daniel J. ;
Hanson, Nancy D. .
CLINICAL MICROBIOLOGY REVIEWS, 2009, 22 (04) :582-+
[4]   In vitro activity of ceftazidime+NXL104 against Pseudomonas aeruginosa and other non-fermenters [J].
Mushtaq, Shazad ;
Warner, Marina ;
Livermore, David M. .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2010, 65 (11) :2376-2381
[5]   Interplay of efflux system, ampC, and oprD expression in carbapenem resistance of Pseudomonas aeruginosa clinical isolates [J].
Quale, J ;
Bratu, S ;
Gupta, J ;
Landman, D .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2006, 50 (05) :1633-1641
[6]  
Souli M, 2008, EUROSURVEILLANCE, V13, P1
[7]   In vitro activity of the β-lactamase inhibitor NXL104 against KPC-2 carbapenemase and Enterobacteriaceae expressing KPC carbapenemases [J].
Stachyra, Therese ;
Levasseur, Premavathy ;
Pechereau, Marie-Claude ;
Girard, Anne-Marie ;
Claudon, Monique ;
Miossec, Christine ;
Black, Michael T. .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2009, 64 (02) :326-329
[8]   Impact of Multidrug-Resistant Pseudomonas aeruginosa Bacteremia on Patient Outcomes [J].
Tam, Vincent H. ;
Rogers, Cary A. ;
Chang, Kai-Tai ;
Weston, Jaye S. ;
Caeiro, Juan-Pablo ;
Garey, Kevin W. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2010, 54 (09) :3717-3722
[9]   INTERPRETING CHROMOSOMAL DNA RESTRICTION PATTERNS PRODUCED BY PULSED-FIELD GEL-ELECTROPHORESIS - CRITERIA FOR BACTERIAL STRAIN TYPING [J].
TENOVER, FC ;
ARBEIT, RD ;
GOERING, RV ;
MICKELSEN, PA ;
MURRAY, BE ;
PERSING, DH ;
SWAMINATHAN, B .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (09) :2233-2239
[10]   In Vitro Activity of Ceftazidime Combined with NXL104 versus Pseudomonas aeruginosa Isolates Obtained from Patients in Canadian Hospitals (CANWARD 2009 Study) [J].
Walkty, A. ;
DeCorby, M. ;
Lagace-Wiens, P. R. S. ;
Karlowsky, J. A. ;
Hoban, D. J. ;
Zhanel, G. G. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2011, 55 (06) :2992-2994