Copper and quaternary ammonium cations exert synergistic bactericidal and antibiofilm activity against Pseudomonas aeruginosa

被引:140
作者
Harrison, Joe J. [1 ,2 ]
Turner, Raymond J. [1 ]
Joo, Daniel A. [1 ,2 ]
Stan, Michelle A. [1 ,2 ]
Chan, Catherine S. [1 ]
Allan, Nick D. [3 ]
Vrionis, Helen A. [1 ]
Olson, Merle E.
Ceri, Howard [1 ,2 ]
机构
[1] Univ Calgary, Dept Biol Sci, Calgary, AB T2N 1N4, Canada
[2] Univ Calgary, BiofIlm Res Grp, Calgary, AB T2N 1N4, Canada
[3] Innovotech Inc, Edmonton, AB TGN 1H1, Canada
关键词
D O I
10.1128/AAC.00203-08
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Biofilms are slimy aggregates of microbes that are likely responsible for many chronic infections as well as for contamination of clinical and industrial environments. Pseudomonas aeruginosa is a prevalent hospital pathogen that is well known for its ability to form biofilms that are recalcitrant to many different antimicrobial treatments. We have devised a high-throughput method for testing combinations of antimicrobials for synergistic activity against biofilms, including those formed by P. aeruginosa. This approach was used to look for changes in biofilm susceptibility to various biocides when these agents were combined with metal ions. This process identified that Cu2+ works synergistically with quaternary ammonium compounds (QACs; specifically benzalkonium chloride, cetalkonium chloride, cetylpyridinium chloride, myristalkonium chloride, and Poly-cide) to kill P. aeruginosa biofilms. In some cases, adding Cu2+ to QACs resulted in a 128-fold decrease in the biofilm minimum bactericidal concentration compared to that for single-agent treatments. In combination, these agents retained broad-spectrum antimicrobial activity that also eradicated biofilms of Escherichia coli, Staphylococcus aureus, Salmonella enterica serovar Cholerasuis, and Pseudomonas fluorescens. To investigate the mechanism of action, isothermal titration calorimetry was used to show that Cu2+ and QACs do not interact in aqueous solutions, suggesting that each agent exerts microbiological toxicity through independent biochemical routes. Additionally, Cu2+ and QACs, both alone and in combination, reduced the activity of nitrate reductases, which are enzymes that are important for normal biofilm growth. Collectively, the results of this study indicate that Cu2+ and QACs are effective combinations of antimicrobials that may be used to kill bacterial biofilms.
引用
收藏
页码:2870 / 2881
页数:12
相关论文
共 40 条
[31]   Biofilms and planktonic cells of Pseudomonas aeruginosa have similar resistance to killing by antimicrobials [J].
Spoering, AL ;
Lewis, K .
JOURNAL OF BACTERIOLOGY, 2001, 183 (23) :6746-6751
[32]   OXIDATIVE MECHANISMS IN THE TOXICITY OF METAL-IONS [J].
STOHS, SJ ;
BAGCHI, D .
FREE RADICAL BIOLOGY AND MEDICINE, 1995, 18 (02) :321-336
[33]  
TAKEO Y, 1994, MICROBIOS, V79, P19
[34]   Survival and growth in the presence of elevated copper:: Transcriptional profiling of copper-stressed Pseudomonas aeruginosa [J].
Teitzel, Gail M. ;
Geddie, Ashley ;
De Long, Susan K. ;
Kirisits, Mary Jo ;
Whiteley, Marvin ;
Parsek, Matthew R. .
JOURNAL OF BACTERIOLOGY, 2006, 188 (20) :7242-7256
[35]   Heavy metal resistance of biofilm and planktonic Pseudomonas aeruginosa [J].
Teitzel, GM ;
Parsek, MR .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2003, 69 (04) :2313-2320
[36]   Energetics of phosphate binding to ammonium and guanidinium containing metallo-receptors in water [J].
Tobey, SL ;
Anslyn, EV .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (48) :14807-14815
[37]  
Vievskii A. N., 1994, Mikrobiologichnyi Zhurnal, V56, P16
[38]  
Wood P, 1998, J APPL MICROBIOL, V84, P1092
[39]   Pseudomonas fluorescens' view of the periodic table [J].
Workentine, Matthew L. ;
Harrison, Joe J. ;
Stenroos, Pernilla U. ;
Ceri, Howard ;
Turner, Raymond J. .
ENVIRONMENTAL MICROBIOLOGY, 2008, 10 (01) :238-250
[40]   Pseudomonas aeruginosa anaerobic respiration in biofilms:: Relationships to cystic fibrosis pathogenesis [J].
Yoon, SS ;
Hennigan, RF ;
Hilliard, GM ;
Ochsner, UA ;
Parvatiyar, K ;
Kamani, MC ;
Allen, HL ;
DeKievit, TR ;
Gardner, PR ;
Schwab, U ;
Rowe, JJ ;
Iglewski, BH ;
McDermott, TR ;
Mason, RP ;
Wozniak, DJ ;
Hancock, REW ;
Parsek, MR ;
Noah, TL ;
Boucher, RC ;
Hassett, DJ .
DEVELOPMENTAL CELL, 2002, 3 (04) :593-603