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Multiplex PCR and Oligonucleotide Microarray for Detection of Single-Nucleotide Polymorphisms Associated with Plasmodium falciparum Drug Resistance▿ †

机译:多重PCR和寡核苷酸芯片检测与恶性疟原虫耐药相关的单核苷酸多态性

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摘要

Drug resistance in Plasmodium falciparum is a serious public health threat in the countries where this organism is endemic. Since resistance has been associated with specific single-nucleotide polymorphisms (SNPs) in parasite genes, molecular markers are becoming useful surrogates for monitoring the emergence and dispersion of drug resistance. In this study, a multiplex PCR (mPCR) and oligonucleotide microarray method was developed for the detection of these SNPs in genes encoding chloroquine resistance transporter (Pfcrt), multidrug resistance 1 (Pfmdr1), dihydrofolate reductase (Pfdhfr), dihydropteroate synthetase (Pfdhps), and ATPase 6 (PfATPase6) of P. falciparum. The results show that DNA microarray technology, combined with mPCR, is a promising and time-saving tool that supports conventional detection methods, allowing sensitive, accurate, simultaneous analysis of the SNPs associated with drug resistance in P. falciparum.
机译:在恶性疟原虫流行的国家,恶性疟原虫的耐药性是严重的公共卫生威胁。由于抗药性已与寄生虫基因中的特定单核苷酸多态性(SNP)相关联,因此分子标记已成为监测药物抗药性出现和分散的有用替代物。在这项研究中,开发了一种多重PCR(mPCR)和寡核苷酸微阵列方法,用于检测编码氯喹抗性转运蛋白(Pfcrt),多药抗性1(Pfmdr1),二氢叶酸还原酶(Pfdhfr),二氢蝶呤合成酶(Pfdhps)的基因中的这些SNP。 ,和恶性疟原虫的ATPase 6(PfATPase6)。结果表明,DNA微阵列技术与mPCR结合,是一种有前途且省时的工具,可支持常规检测方法,从而能够对恶性疟原虫的耐药性相关的SNP进行灵敏,准确,同时的分析。

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