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Selection of Plasmodium falciparum Multidrug Resistance Gene 1 Alleles in Asexual Stages and Gametocytes by Artemether-Lumefantrine in Nigerian Children with Uncomplicated Falciparum Malaria

机译:蒿甲醚-卢美替林在无并发症恶性疟疾尼日利亚儿童中选择无性疟原虫和恶性疟原虫多药耐药基因1等位基因

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摘要

We assessed Plasmodium falciparum mdr1 (Pfmdr1) gene polymorphisms and copy numbers as well as P. falciparum Ca2+ ATPase (PfATPase6) gene polymorphisms in 90 Nigerian children presenting with uncomplicated falciparum malaria and enrolled in a study of the efficacy of artemether-lumefantrine (AL). The nested PCR-restriction fragment length polymorphism and the quantitative real-time PCR methodologies were used to determine the alleles of the Pfmdr1 and PfATPase6 genes and the Pfmdr1 copy number variation, respectively, in patients samples collected prior to treatment and at the reoccurrence of parasites during a 42-day follow-up. The Pfmdr1 haplotype 86N-184F-1246D was significantly associated (P < 0.00001) with treatment failures and was selected for among posttreatment samples obtained from patients with newly acquired or recrudescing infections (P < 0.00001; χ2 = 36.5) and in gametocytes (log rank statistic = 5; P = 0.0253) after treatment with AL. All pre- and posttreatment samples as well as gametocytes harbored a single copy of the Pfmdr1 gene and the wild-type allele (L89) at codon 89 of the PfATPase6 gene. These findings suggest that polymorphisms in the Pfmdr1 gene are under AL selection pressure. Pfmdr1 polymorphisms may result in reduction in the therapeutic efficacy of this newly adopted combination treatment for uncomplicated falciparum malaria in Saharan countries of Africa.
机译:我们评估了90名患有单纯性恶性疟疾的尼日利亚儿童的恶性疟原虫疟原虫mdr1(Pfmdr1)基因多态性和拷贝数,以及恶性疟原虫Ca 2 + ATPase(PfATPase6)基因多态性,并参加了一项研究。蒿甲醚-荧光粉(AL)的功效。巢式PCR限制性片段长度多态性和定量实时PCR方法用于分别确定治疗前和寄生虫复发患者样品中Pfmdr1和PfATPase6基因的等位基因和Pfmdr1拷贝数变异。在42天的随访中。 Pfmdr1单倍型86N-184F-1246D与治疗失败显着相关(P <0.00001),并选自新感染或复发感染患者的治疗后样品中(P <0.00001;χ 2 = 36.5)和经AL治疗后的配子细胞中(对数秩统计= 5; P = 0.0253)。所有预处理和后处理样品以及配子细胞均在PfATPase6基因的第89位密码子处包含Pfmdr1基因和野生型等位基因(L89)的单个副本。这些发现表明Pfmdr1基因的多态性处于AL选择压力下。 Pfmdr1基因的多态性可能会导致这种新近采用的联合治疗在非洲撒哈拉以南的非复杂性恶性疟疾中的治疗功效降低。

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