Potent Synergy and Sustained Bactericidal Activity of a Vancomycin-Colistin Combination versus Multidrug-Resistant Strains of Acinetobacter baumannii

被引:168
作者
Gordon, N. C. [2 ]
Png, K. [3 ]
Wareham, D. W. [1 ,2 ]
机构
[1] Queen Mary Univ London, Ctr Immunol & Infect Dis, Blizard Inst Cell & Mol Sci, Barts & London Sch Med & Dent, London E1 2AT, England
[2] Barts & London NHS Trust, Div Infect, London, England
[3] Queen Mary Univ London, NanoVis Ctr, London E1 2AT, England
关键词
PREVALENT OXA CARBAPENEMASES; CRITICALLY-ILL PATIENTS; GRAM-NEGATIVE BACTERIA; PSEUDOMONAS-AERUGINOSA; OUTER-MEMBRANE; IN-VITRO; MULTIPLEX PCR; POLYMYXIN-B; TIME-KILL; IMIPENEM;
D O I
10.1128/AAC.00922-10
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Multidrug-resistant Acinetobacter baumannii (MDRAB) presents an increasing challenge to health care. Although colistin has been used as a treatment of last resort, there is concern regarding its potential for toxicity and the emergence of resistance. The mechanism of action of colistin, however, raises the possibility of synergy with compounds that are normally inactive against Gram-negative organisms by virtue of the impermeability of the bacterial outer membrane. This study evaluated the effect of colistin combined with vancomycin on 5 previously characterized epidemic strains and 34 MDRAB clinical isolates by using time-kill assay, microdilution, and Etest methods. For all the isolates, significant synergy was demonstrated by at least one method, with reductions in the MIC of vancomycin from > 256 mu g/ml to <= 48 mu g/ml for all strains after exposure to 0.5 mu g/ml colistin. This raises the possibility of the clinical use of this combination for infections due to MDRAB, with the potential for doses lower than those currently used.
引用
收藏
页码:5316 / 5322
页数:7
相关论文
共 40 条
[1]   BSAC standardized disc susceptibility testing method (version 8) [J].
Andrews, J. M. .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2009, 64 (03) :454-489
[2]   Evaluation of antibiotic synergy against Acinetobacter baumannii:: a comparison with Etest, time-kill, and checkerboard methods [J].
Bonapace, CR ;
White, RL ;
Friedrich, LV ;
Bosso, JA .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2000, 38 (01) :43-50
[3]   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
[4]   RAPID MICROPROCEDURE FOR ISOLATING DETERGENT-INSOLUBLE OUTER-MEMBRANE PROTEINS FROM HAEMOPHILUS SPECIES [J].
CARLONE, GM ;
THOMAS, ML ;
RUMSCHLAG, HS ;
SOTTNEK, FO .
JOURNAL OF CLINICAL MICROBIOLOGY, 1986, 24 (03) :330-332
[5]   Selection of colistin-resistant Acinetobacter baumannii isolates in postneurosurgical meningitis in an intensive care unit with high presence of heteroresistance to colistin [J].
Carlos Hernan, Rodriguez ;
Karina, Bombicino ;
Gabriela, Granados ;
Marcela, Nastro ;
Carlos, Vay ;
Angela, Famiglietti .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2009, 65 (02) :188-191
[6]  
Clinical and Laboratory Standards Institute, 2008, M100S18 CLSI
[7]   Occurrence of carbapenern-resistant Acinetobacter baumannii clones at multiple hospitals in London and southeast England [J].
Coelho, Juliana M. ;
Turton, Jane F. ;
Kaufmann, Mary E. ;
Glover, Judith ;
Woodford, Neil ;
Warner, Marina ;
Palepou, Marie-France ;
Pike, Rachel ;
Pitt, Tyrone L. ;
Patel, Bharat C. ;
Livermore, David M. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2006, 44 (10) :3623-3627
[8]  
Eliopolous GM., 1996, Antibiotics in laboratory medicine, P330
[9]  
European Committee on Antimicrobial Susceptibility Testing, 2010, BREAKP TABL INT MICS
[10]   The diversity of definitions of multidrug-resistant (MDR) and pandrug-resistant (PDR) Acinetobacter baumannii and Pseudomonas aeruginosa [J].
Falagas, Matthew E. ;
Koletsi, Patra K. ;
Bliziotis, Ioannis A. .
JOURNAL OF MEDICAL MICROBIOLOGY, 2006, 55 (12) :1619-1629