Ferrer-Rodríguez Iván, Pérez-Rosado José, Gervais Gary W, Peters Wallace, Robinson Brian L, Serrano Adelfa E
Department of Microbiology and Medical Zoology, University of Puerto Rico, School of Medicine, P.O. Box 365067, San Juan, Puerto Rico.
J Parasitol. 2004 Feb;90(1):152-60. doi: 10.1645/GE-3225.
The molecular mechanisms by which the malarial parasite has managed to develop resistance to many antimalarial drugs remain to be completely elucidated. Mutations in the pfmdr1 gene of Plasmodium falciparum, as well as an increase in pfmdr1 copy number, have been associated with resistance to the quinoline-containing antimalarial drugs. We investigated the mechanisms of drug resistance in Plasmodium using a collection of P. yoelii lines with different drug resistance profiles. The mdr1 gene of P. yoelii (pymdr1) was identified and characterized. A 2- to 3-fold increase in the pymdr1 gene copy number was observed in the P. yoelii ART line (artemisinin resistant) when compared with the NS parental line. The pymdr1 gene was mapped to a chromosome of 2.1 Mb in all lines analyzed. Reverse transcriptase-polymerase chain reaction and Western blot experiments confirmed the expression of the gene at the RNA and protein levels.
疟原虫对多种抗疟药物产生耐药性的分子机制仍有待完全阐明。恶性疟原虫pfmdr1基因的突变以及pfmdr1拷贝数的增加与对含喹啉抗疟药物的耐药性有关。我们使用一组具有不同耐药谱的约氏疟原虫株系研究了疟原虫的耐药机制。对约氏疟原虫的mdr1基因(pymdr1)进行了鉴定和表征。与NS亲本株系相比,在约氏疟原虫ART株系(青蒿素耐药)中观察到pymdr1基因拷贝数增加了2至3倍。在所有分析的株系中,pymdr1基因被定位到一条2.1 Mb的染色体上。逆转录聚合酶链反应和蛋白质印迹实验在RNA和蛋白质水平上证实了该基因的表达。