The antimicrobial and antibiofilm activities of copper(II) complexes

被引:77
作者
Beeton, Michael L. [1 ]
Aldrich-Wright, Janice R. [2 ]
Bolhuis, Albert [1 ]
机构
[1] Univ Bath, Dept Pharm & Pharmacol, Bath BA2 7AY, Avon, England
[2] Univ Western Sydney, Sch Biomed & Hlth Sci, South Penrith, Australia
关键词
Copper(II) complexes; Antimicrobials; Meticillin-resistant Staphylococcus aureus; Biofilms; RESISTANT STAPHYLOCOCCUS-AUREUS; BIOFILM RESISTANCE; DNA CLEAVAGE; 1,10-PHENANTHROLINE; ANTIBIOTICS; PENETRATION; SURFACES; AGENTS;
D O I
10.1016/j.jinorgbio.2014.07.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Biofilm-related bacterial infections pose a significant problem, as they are generally more tolerant to antibiotics and the immune system. Development of novel compounds with antibiofilm activity is therefore paramount. In this study we have analysed metal complexes of the general structure [M(I-L)(A(L))](2+) (where I-L represents functionalised 1,10-phenanthrolines and A(L) represents 1S,2S- or 1R,2R-diaminocyclohexane) and [Cu(I-L)(3)](2+). Antimicrobial activity was tested on a number of bacterial strains, showing that copper(II) compounds were active against both Gram-positive and Gram-negative bacteria, albeit that activity was generally higher for the former. The antibiofilm activity was then determined against a clinical isolate of meticillin-resistant Staphylococcus aureus (MRSA). Strikingly, the copper complexes tested showed significant activity against biofilms, and were better in the removal of biofilms than vancomycin, an antibiotic that is currently used in the treatment of MRSA infections. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:167 / 172
页数:6
相关论文
共 35 条
[1]
Killing bacteria within biofilms by sustained release of tetracycline from triple-layered electrospun micro/nanofibre matrices of polycaprolactone and poly(ethylene-co-vinyl acetate) [J].
Alhusein, Nour ;
De Bank, Paul A. ;
Blagbrough, Ian S. ;
Bolhuis, Albert .
DRUG DELIVERY AND TRANSLATIONAL RESEARCH, 2013, 3 (06) :531-541
[2]
Role of antibiotic penetration limitation in Klebsiella pneumoniae biofilm resistance to ampicillin and ciprofloxacin [J].
Anderl, JN ;
Franklin, MJ ;
Stewart, PS .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (07) :1818-1824
[3]
Determination of minimum inhibitory concentrations [J].
Andrews, JM .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2001, 48 :5-16
[4]
Bolhuis A., 2014, BIOORG CHEM
[5]
Antimicrobial activity of ruthenium-based intercalators [J].
Bolhuis, Albert ;
Hand, Lorna ;
Marshall, Julia E. ;
Richards, Adair D. ;
Rodger, Alison ;
Aldrich-Wright, Janice .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2011, 42 (04) :313-317
[6]
Offsetting virulence and antibiotic resistance costs by MRSA [J].
Collins, James ;
Rudkin, Justine ;
Recker, Mario ;
Pozzi, Clarissa ;
O'Gara, James P. ;
Massey, Ruth C. .
ISME JOURNAL, 2010, 4 (04) :577-584
[7]
Cooney JJ, 1999, METHOD ENZYMOL, V310, P637
[8]
Bacterial biofilms: A common cause of persistent infections [J].
Costerton, JW ;
Stewart, PS ;
Greenberg, EP .
SCIENCE, 1999, 284 (5418) :1318-1322
[9]
BIOLOGICAL ACTIONS OF 1,10-PHENANTHROLINE AND 2,2'-BIPYRIDINE HYDROCHLORIDES QUATERNARY SALTS AND METAL CHELATES AND RELATED COMPOUNDS .1. BACTERIOSTATIC ACTION ON SELECTED GRAM-POSITIVE GRAM-NEGATIVE AND ACID-FAST BACTERIA [J].
DWYER, FP ;
REID, IK ;
SHULMAN, A ;
LAYCOCK, GM ;
DIXSON, S .
AUSTRALIAN JOURNAL OF EXPERIMENTAL BIOLOGY AND MEDICAL SCIENCE, 1969, 47 :203-+
[10]
BIOLOGICAL ACTIVITY OF COMPLEX IONS [J].
DWYER, FP ;
GYARFAS, EC ;
ROGERS, WP ;
KOCH, JH .
NATURE, 1952, 170 (4318) :190-191