Transfection technology and the study of drug resistance in the malaria parasite Plasmodium falciparum

被引:22
作者
Crabb, BS [1 ]
机构
[1] PO Royal Melbourne Hosp, Walter & Eliza Hall Inst Med Res, Melbourne, Vic 3050, Australia
关键词
Plasmodium falciparum; transfection; drug resistance;
D O I
10.1016/S1368-7646(02)00085-7
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Numerous approaches have been employed to identify the molecules responsible for drug resistance in the human malaria parasite Plasmodium falciparum. However, it was not until the recent development of stable transfection in this parasite that it became possible to prove the role of particular genes in drug resistance and, perhaps more importantly, to characterise the nature of the specific mutations that contribute the resistance phenotype. In this review, the contribution of various molecular genetic approaches to the dissection of drug resistance in P falciparum is described. Future possibilities in this field are also outlined in the light of recent technological advances. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:126 / 130
页数:5
相关论文
共 23 条
[1]  
Baldini A, 2000, ZEI STUD EU ECON LAW, V2, P19
[2]   A set of independent selectable markers for transfection of the human malaria parasite Plasmodium falciparum [J].
Ben Mamoun, C ;
Gluzman, IY ;
Goyard, S ;
Beverley, SM ;
Goldberg, DE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (15) :8716-8720
[3]   SELECTION FOR MEFLOQUINE RESISTANCE IN PLASMODIUM-FALCIPARUM IS LINKED TO AMPLIFICATION OF THE PFMDR1 GENE AND CROSS-RESISTANCE TO HALOFANTRINE AND QUININE [J].
COWMAN, AF ;
GALATIS, D ;
THOMPSON, JK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (03) :1143-1147
[4]   A P-GLYCOPROTEIN HOMOLOG OF PLASMODIUM-FALCIPARUM IS LOCALIZED ON THE DIGESTIVE VACUOLE [J].
COWMAN, AF ;
KARCZ, S ;
GALATIS, D ;
CULVENOR, JG .
JOURNAL OF CELL BIOLOGY, 1991, 113 (05) :1033-1042
[5]   Characterization of promoters and stable transfection by homologous and nonhomologous recombination in Plasmodium falciparum [J].
Crabb, BS ;
Cowman, AF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (14) :7289-7294
[6]   Targeted gene disruption shows that knobs enable malaria-infected red cells to cytoadhere under physiological shear stress [J].
Crabb, BS ;
Cooke, BM ;
Reeder, JC ;
Waller, RF ;
Caruana, SR ;
Davern, KM ;
Wickham, ME ;
Brown, GV ;
Coppel, RL ;
Cowman, AF .
CELL, 1997, 89 (02) :287-296
[7]   Puromycin-N-acetyltransferase as a selectable marker for use in Plasmodium falciparum [J].
de Koning-Ward, TF ;
Waters, AP ;
Crabb, BS .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 2001, 117 (02) :155-160
[8]   Gene knock-outs and allelic replacements in Toxoplasma gondii:: HXGPRT as a selectable marker for hit-and-run mutagenesis [J].
Donald, RGK ;
Roos, DS .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1998, 91 (02) :295-305
[9]   STABLE MOLECULAR-TRANSFORMATION OF TOXOPLASMA-GONDII - A SELECTABLE DIHYDROFOLATE REDUCTASE-THYMIDYLATE SYNTHASE MARKER BASED ON DRUG-RESISTANCE MUTATIONS IN MALARIA [J].
DONALD, RGK ;
ROOS, DS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (24) :11703-11707
[10]   Negative selection of Plasmodium falciparum reveals targeted gene deletion by double crossover recombination [J].
Duraisingh, MT ;
Triglia, T ;
Cowman, AF .
INTERNATIONAL JOURNAL FOR PARASITOLOGY, 2002, 32 (01) :81-89