Development of methods to analyse Plasmodium falciparum single nucleotide polymorphisms in PfCRT (А > C), PfMDR1 (A > T) and PfDHFR (G > A) genes that determine resistance to quinoline, diamino-pyrimidine and sulfonamide groups of antimalarial drugs

Artem R. Ariukov, Aleksey I. Solovyov, V. A. Kapatsyna, Anna A. Krutikova, Vladimir A. Romanenko, Aleksandr N. Kovalenko, Akim A. Kolesnik, Artem S. Zinin
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Abstract

BACKGROUND: The drug resistance of tropical malaria pathogens to mefloquine, chloroquine, pyrimethamine and their derivatives is associated with three single nucleotide polymorphisms: K76T (A403627C), S1034C (A960989T) and S108N (G748410A). These mutations are linked to changes in the structure of the PfCRT and PfMDR1 genes of Plasmodium falciparum. AIM: Develop methods for identifying single nucleotide polymorphisms that are suitable for early diagnosis of drug-resistant forms of tropical malaria. RESULTS: A method was developed based on restriction fragment length analysis using ApoI endonuclease to detect the K76T polymorphism (A403627C). The criterion for determining parasite resistance to chloroquine was the appearance of a single 145 bp band on the electropherogram. The genotype of the pathogens remained unchanged and their drug sensitivity was preserved, as indicated by the separation of two fragments of 98 and 47 bp. A system for detecting S108N (G748410A) was developed using the Bse1I endonuclease. The appearance of a single 507 bp band on the electropherogram indicated the mutant genotype of the pathogens, while the appearance of two fragments (323 and 184 bp) indicated an unchanged genotype and preservation of drug sensitivity of plasmodiae. To identify the A T polymorphism in the PfMDR1 gene at position 960989, polymerase chain reaction technology will be used with two allele-specific primers. One primer will detect the wild-type allele, and the other will detect the mutant genotype. The amplifiable fragment of the PfMDR1 gene contains sequences of the 1034th codon. Depending on the P. falciparum genotype, 261 bp fragments will be obtained with one of the allele-specific primers. CONCLUSION: Criteria for assessing drug resistance of P. falciparum were developed based on the analysis of obtained data. Haplotypes K76T (band 145 bp) and S1034C (band 262 bp with the direct primer S1034C-F2) serve as indicators of the relative resistance of pathogens to chloroquine, mefloquine, and their derivatives. Positive results of examination for haplotype S108N (bands 323 and 184 bp) should be considered as a sign of decreased sensitivity to pyrimethamine. The developed methods can be used in clinical practice and for epidemiological monitoring.
开发恶性疟原虫 PfCRT(А > C)、PfMDR1(A > T)和 PfDHFR(G > A)基因单核苷酸多态性分析方法,这些基因决定了对喹啉类、二氨基嘧啶类和磺胺类抗疟药物的耐药性
背景:热带疟疾病原体对甲氟喹、氯喹、乙胺嘧啶及其衍生物的耐药性与三种单核苷酸多态性有关:K76T (A403627C)、S1034C (A960989T) 和 S108N (G748410A)。这些突变与恶性疟原虫 PfCRT 和 PfMDR1 基因结构的变化有关。目的:开发适用于热带疟疾耐药性早期诊断的单核苷酸多态性鉴定方法。结果:利用 ApoI 内切酶进行限制性片段长度分析,开发出一种检测 K76T 多态性(A403627C)的方法。确定寄生虫对氯喹耐药性的标准是在电泳图上出现一条 145 bp 的条带。病原体的基因型保持不变,其对药物的敏感性也保持不变,这体现在两个分别为 98 和 47 bp 的片段上。利用 Bse1I 内切酶开发了一种检测 S108N (G748410A) 的系统。电泳图上出现一条 507 bp 的条带表示病原体的突变基因型,而出现两个片段(323 和 184 bp)则表示疟原虫的基因型未变,对药物的敏感性保持不变。为确定 PfMDR1 基因 960989 位的 A T 多态性,将使用聚合酶链反应技术和两个等位基因特异性引物。一个引物检测野生型等位基因,另一个引物检测突变基因型。PfMDR1 基因的可扩增片段包含第 1034 个密码子的序列。根据恶性疟原虫的基因型,使用其中一种等位基因特异性引物可获得 261 bp 的片段。结论:根据对所获数据的分析,制定了评估恶性疟原虫耐药性的标准。单倍型 K76T(145 bp 带)和 S1034C(直接引物 S1034C-F2 的 262 bp 带)可作为病原体对氯喹、甲氟喹及其衍生物相对耐药性的指标。单倍型 S108N 的阳性检测结果(条带 323 和 184 bp)应被视为对乙胺嘧啶敏感性降低的标志。所开发的方法可用于临床实践和流行病学监测。
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