Propidium iodide-based methods for monitoring drug action in the kinetoplastidae: Comparison with the Alamar Blue assay

被引:70
作者
Gould, Matthew K. [1 ]
Vu, Xuan Lan [2 ]
Seebeck, Thomas [2 ]
de Koning, Harry P. [1 ]
机构
[1] Univ Glasgow, Inst Biomed & Life Sci, Div Infect & Immun, Glasgow G12 8TA, Lanark, Scotland
[2] Univ Bern, Inst Cell Biol, CH-3012 Bern, Switzerland
关键词
propidium iodide; drug action; kinetoplastidae; Alamar Blue assay;
D O I
10.1016/j.ab.2008.07.036
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The urgent need for new drug development for African trypanosomiasis is widely recognized. This requires reliable and informative high-throughput assays. Currently, drug action is determined with a fluorimetric/colorimetric assay based on the metabolism of the dye Alamar Blue (resazurin) by live cells. However, this assay does not easily distinguish between cell death and growth arrest, or supply information about the rate at which test compounds affect these parameters. We report here an alternative fluorimetric assay, based on the interaction of propidium iodide with DNA, that allows either real-time monitoring of cell viability or the generation of EC(50) values at a predetermined time-point. The assay is highly sensitive and fluorescence readings easily correlate to numbers of parasites or DNA content. The EC50 values were highly similar to those obtained with the standard Alamar Blue assay. The procedure lends itself readily to applications in drug development or resistance monitoring. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:87 / 93
页数:7
相关论文
共 27 条
[1]   Purine nucleobase transport in amastigotes of Leishmania mexicana:: Involvement in allopurinol uptake [J].
Al-Salabi, MI ;
de Koning, HP .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (09) :3682-3689
[2]   The genome of the African trypanosome Trypanosoma brucei [J].
Berriman, M ;
Ghedin, E ;
Hertz-Fowler, C ;
Blandin, G ;
Renauld, H ;
Bartholomeu, DC ;
Lennard, NJ ;
Caler, E ;
Hamlin, NE ;
Haas, B ;
Böhme, W ;
Hannick, L ;
Aslett, MA ;
Shallom, J ;
Marcello, L ;
Hou, LH ;
Wickstead, B ;
Alsmark, UCM ;
Arrowsmith, C ;
Atkin, RJ ;
Barron, AJ ;
Bringaud, F ;
Brooks, K ;
Carrington, M ;
Cherevach, I ;
Chillingworth, TJ ;
Churcher, C ;
Clark, LN ;
Corton, CH ;
Cronin, A ;
Davies, RM ;
Doggett, J ;
Djikeng, A ;
Feldblyum, T ;
Field, MC ;
Fraser, A ;
Goodhead, I ;
Hance, Z ;
Harper, D ;
Harris, BR ;
Hauser, H ;
Hostetter, J ;
Ivens, A ;
Jagels, K ;
Johnson, D ;
Johnson, J ;
Jones, K ;
Kerhornou, AX ;
Koo, H ;
Larke, N .
SCIENCE, 2005, 309 (5733) :416-422
[3]   Loss of the high-affinity pentamidine transporter is responsible for high levels of cross-resistance between arsenical and diamidine drugs in African trypanosomes [J].
Bridges, Daniel J. ;
Gould, Matthew K. ;
Nerima, Barbara ;
Maeser, Pascal ;
Burchmore, Richard J. S. ;
de Koning, Harry P. .
MOLECULAR PHARMACOLOGY, 2007, 71 (04) :1098-1108
[4]   The phenomenon of treatment failures in Human African Trypanosomiasis [J].
Brun, R ;
Schumacher, R ;
Schmid, C ;
Kunz, C ;
Burri, C .
TROPICAL MEDICINE & INTERNATIONAL HEALTH, 2001, 6 (11) :906-914
[5]   Characterization of a nucleoside/proton symporter in procyclic Trypanosoma brucei brucei [J].
de Koning, HP ;
Watson, CJ ;
Jarvis, SM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (16) :9486-9494
[6]   Drugs and drug resistance in African trypanosomiasis [J].
Delespaux, Vincent ;
de Koning, Harry P. .
DRUG RESISTANCE UPDATES, 2007, 10 (1-2) :30-50
[7]  
Eichler H, 1934, FRESEN J ANAL CHEM, V99, P270
[8]   CHARACTERIZATION OF MELARSEN-RESISTANT TRYPANOSOMA-BRUCEI-BRUCEI WITH RESPECT TO CROSS-RESISTANCE TO OTHER DRUGS AND TRYPANOTHIONE METABOLISM [J].
FAIRLAMB, AH ;
CARTER, NS ;
CUNNINGHAM, M ;
SMITH, K .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1992, 53 (1-2) :213-222
[9]  
Ferlini C, 1996, CYTOMETRY, V24, P106
[10]  
FOUCHER AL, 2003, THESIS U GLASGOW UK