Drug repurposing as an alternative for the treatment of recalcitrant bacterial infections

被引:133
作者
Rangel-Vega, Adrian [1 ]
Bernstein, Lawrence R. [2 ]
Ayerim Mandujano-Tinoco, Edna [3 ]
Julieta Garcia-Contreras, Silvia [4 ]
Garcia-Contreras, Rodolfo [1 ]
机构
[1] Univ Nacl Autonoma Mexico, Dept Microbiol & Parasitol, Fac Med, Ave Univ 3000, Mexico City 04510, DF, Mexico
[2] Terrametrix, Menlo Pk, CA USA
[3] Natl Inst Genom Med, Epigenet Canc Lab, Basic Res Div, Mexico City, DF, Mexico
[4] Ctr Med Coyoacan, Mexico City, DF, Mexico
关键词
gallium; 5-fluorouracil; ciclopirox; diflunisal; bacterial infections; drug repurposing; PSEUDOMONAS-AERUGINOSA; BIOFILM FORMATION; IRON-METABOLISM; IN-VITRO; ANTIBACTERIAL ACTIVITY; STAPHYLOCOCCUS-AUREUS; GALLIUM NITRATE; RESISTANCE; 5-FLUOROURACIL; ANTIBIOTICS;
D O I
10.3389/fmicb.2015.00282
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Bacterial infection remains one of the leading causes of death worldwide, and the options for treating such infections are decreasing, due the rise of antibiotic resistant bacteria. The pharmaceutical industry has produced few new types of antibiotics in more than a decade. Researchers are taking several approaches toward developing new classes of antibiotics, including (1) focusing on new targets and processes, such as bacterial cell cell communication that upregulates virulence; (2) designing inhibitors of bacterial resistance, such as blockers of multidrug efflux pumps; and (3) using alternative antimicrobials such as bacteriophages. In addition, the strategy of finding new uses for existing drugs is beginning to produce results: antibacterial properties have been discovered for existing anticancer, antifungal, anthelmintic, and anti-inflammatory drugs. In this review, we discuss the antimicrobial properties of gallium compounds, 5-fluorouracil, ciclopirox, diflunisal, and some other FDA-approved drugs and argue that their repurposing for the treatment of bacterial infections, including those that are multidrug resistant, is a feasible strategy.
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页数:8
相关论文
共 78 条
[1]  
Abedon Stephen T, 2011, Bacteriophage, V1, P46, DOI 10.4161/bact.1.1.13980
[2]   GALLIUM TOXICITY AND ADAPTATION IN PSEUDOMONAS-FLUORESCENS [J].
ALAOUKATY, A ;
APPANNA, VD ;
FALTER, H .
FEMS MICROBIOLOGY LETTERS, 1992, 92 (03) :265-272
[3]   Quorum sensing in bacterial virulence [J].
Antunes, L. Caetano M. ;
Ferreira, Rosana B. R. ;
Buckner, Michelle M. C. ;
Finlay, B. Brett .
MICROBIOLOGY-SGM, 2010, 156 :2271-2282
[4]   In Vitro and In Vivo Antimicrobial Activities of Gallium Nitrate against Multidrug-Resistant Acinetobacter baumannii [J].
Antunes, Luisa C. S. ;
Imperi, Francesco ;
Minandri, Fabrizia ;
Visca, Paolo .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2012, 56 (11) :5961-5970
[5]   Antimicrobial stewardship - can we afford to do without it? [J].
Aryee, Anna ;
Price, Nicholas .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2015, 79 (02) :173-181
[6]   5-Fluorouracil reduces biofilm formation in Escherichia coli K-12 through global regulator AriR as an antivirulence compound [J].
Attila, Can ;
Ueda, Akihiro ;
Wood, Thomas K. .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2009, 82 (03) :525-533
[7]   The overexpression of NADPH-producing enzymes counters the oxidative stress evoked by gallium, an iron mimetic [J].
Beriault, R. ;
Hamel, R. ;
Chenier, D. ;
Mailloux, Ryan J. ;
Joly, H. ;
Appanna, V. D. .
BIOMETALS, 2007, 20 (02) :165-176
[8]  
Bernstein L., 2013, Encyclopedia of metalloproteins, P823
[9]  
Bernstein LR, 2011, ANTI-CANCER AGENT ME, V11, P585
[10]  
Bernstein LR, 1998, PHARMACOL REV, V50, P665