Rapid fluorescent assay for screening drugs on Leishmania amastigotes

被引:54
作者
Shimony, Orly [1 ]
Jaffe, Charles L. [1 ]
机构
[1] Hebrew Univ Jerusalem, Hadassah Med Sch, Dept Parasitol, Kuvin Ctr Study Infect & Trop Dis, IL-91220 Jerusalem, Israel
关键词
AlamarBlue; Leishmania donovani; Leishmania tropica; Amphotericin B; Staurosporine; Protein kinase inhibitors;
D O I
10.1016/j.mimet.2008.05.026
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A rapid fluorescent viability assay employing alamarBlue was optimized for use with Leishmania axenic amastigotes, the stage of the parasite responsible for disease pathology. The activity of two protein kinase inhibitors, Staurosporine and H-89, as well as Amphotericin B, on promastigotes and amastigotes of Leishmania donovani and Leishmania tropica was compared. Both protein kinase inhibitors inhibited promastigote growth at lower concentrations than amastigotes, while the GI(50) for Amphotericin B on both stages was similar. This assay only requires a limited number of axenic amastigotes (50,000 cells/well) and can be used to rapidly screen large chemical or natural product libraries for activity against amastigotes. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:196 / 200
页数:5
相关论文
共 29 条
[1]   The use of Alamar Blue assay for quantitative analysis of viability, migration and invasion of choriocarcinoma cells [J].
Al-Nasiry, S. ;
Geusens, N. ;
Hanssens, M. ;
Luyten, C. ;
Pijnenborg, R. .
HUMAN REPRODUCTION, 2007, 22 (05) :1304-1309
[2]   On the evolution of programmed cell death:: apoptosis of the unicellular eukaryote Leishmania major involves cysteine proteinase activation and mitochondrion permeabilization [J].
Arnoult, D ;
Akarid, K ;
Grodet, A ;
Petit, PX ;
Estaquier, J ;
Ameisen, JC .
CELL DEATH AND DIFFERENTIATION, 2002, 9 (01) :65-81
[3]   Effect of protein kinase inhibitors on the growth, morphology, and infectivity of Leishmania promastigotes [J].
Becker, S ;
Jaffe, CL .
PARASITOLOGY RESEARCH, 1997, 83 (03) :273-280
[4]   Current treatment approaches to leishmaniasis [J].
Berman, J .
CURRENT OPINION IN INFECTIOUS DISEASES, 2003, 16 (05) :397-401
[5]   AN INVITRO MODEL FOR INVESTIGATION OF CHEMOTHERAPEUTIC-AGENTS IN LEISHMANIASIS [J].
BERMAN, JD ;
WYLER, DJ .
JOURNAL OF INFECTIOUS DISEASES, 1980, 142 (01) :83-86
[6]   Recent developments in leishmaniasis: Epidemiology, diagnosis, and treatment [J].
Berman J. .
Current Infectious Disease Reports, 2005, 7 (1) :33-38
[7]   Effects of protein kinase and phosphatidylinositol-3 kinase inhibitors on growth and ultrastructure of Trypanosoma cruzi [J].
Braga, MV ;
de Souza, W .
FEMS MICROBIOLOGY LETTERS, 2006, 256 (02) :209-216
[8]   Antileishmanial activity of crude extract and coumarin from Calophyllum brasiliense leaves against Leishmania amazonensis [J].
Brenzan, Mislaine Adriana ;
Nakamura, Celso Vataru ;
Dias Filho, Benedito Prado ;
Ueda-Nakamura, Tania ;
Young, Maria Claudia M. ;
Garcia Cortez, Diogenes Aparicio .
PARASITOLOGY RESEARCH, 2007, 101 (03) :715-722
[9]   An axenic amastigote system for drug screening [J].
Callahan, HL ;
Portal, AC ;
Devereaux, R ;
Grogl, M .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (04) :818-822
[10]   Leishmaniasis - current chemotherapy and recent advances in the search for novel drugs [J].
Croft, SL ;
Coombs, GH .
TRENDS IN PARASITOLOGY, 2003, 19 (11) :502-508