Wellems T E, Walker-Jonah A, Panton L J
Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892.
Proc Natl Acad Sci U S A. 1991 Apr 15;88(8):3382-6. doi: 10.1073/pnas.88.8.3382.
The resurgence of malaria in recent decades has been accompanied by the worldwide spread of resistance to chloroquine, a drug once uncontested as the first-line antimalarial agent because of its efficacy and low toxicity. Chloroquine-resistant strains of Plasmodium falciparum counter the drug by expelling it rapidly via an unknown mechanism. In the absence of explicit biochemical knowledge of this efflux mechanism, reverse genetics provides a powerful approach to the molecular basis of chloroquine resistance. Here we report genetic linkage analysis in which 85 restriction fragment length polymorphism markers were used to examine inheritance of the 14 P. falciparum chromosomes in a laboratory cross between a chloroquine-resistant and a chloroquine-sensitive parasite. Inheritance data from 16 independent recombinant progeny show that the rapid efflux, chloroquine-resistant phenotype is governed by a single locus within an approximately 400-kilobase region of chromosome 7. Identification and characterization of genes within this region should lead to an understanding of the chloroquine-resistance mechanism.
近几十年来疟疾的再度流行伴随着对氯喹耐药性在全球范围内的传播。氯喹曾因其疗效显著且毒性低,毫无争议地作为一线抗疟药物。恶性疟原虫的氯喹耐药菌株通过一种未知机制迅速排出药物来对抗该药。在缺乏这种外排机制明确生化知识的情况下,反向遗传学为研究氯喹耐药性的分子基础提供了一种有力方法。在此我们报告了遗传连锁分析,其中使用85个限制性片段长度多态性标记来检测一株氯喹耐药疟原虫和一株氯喹敏感疟原虫在实验室杂交中14条恶性疟原虫染色体的遗传情况。来自16个独立重组子代的遗传数据表明,快速外排的氯喹耐药表型由7号染色体上一个约400千碱基区域内的单个基因座控制。对该区域内基因的鉴定和表征应能使我们了解氯喹耐药机制。