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Frequency Distribution of Antimalarial Drug Resistance Alleles among Plasmodium falciparum Isolates from Gezira State Central Sudan and Gedarif State Eastern Sudan

机译:苏丹中部吉兹拉州和苏丹东部格达里夫州的恶性疟原虫分离株中抗疟药耐药等位基因的频率分布

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摘要

In 2004, Sudan adopted artesunate + sulfadoxine/pyrimethamine (SP) combination as the first-line drug, in response to the high level of falciparum resistance to antimalarials. In 2007, a molecular study on antimalarial resistance linked genes, pfcrt, pfmdr1, pfdhfr, pfdhps, and pfATPase6, was conducted on 198 isolates from central and eastern Sudan. We observed a high frequency of point mutations at almost all loci analyzed, mainly of pfcrt 76T (72.7%), pfdhfr 51I (75.3%), and pfdhfr 108N (72.7%) alleles. The MARK III in vitro test for chloroquine sensitivity in 45 P. falciparum isolates showed that 37.8% of the isolates were low resistant and 6.7% were fully resistant. This study represents the most recent molecular investigation on antimalarial resistance in this area after the adoption of artemisinin-based combination therapy (ACT), and underlines the importance of the analysis of SP resistance evolution to monitor the efficacy of ACT therapy in endemic areas.
机译:2004年,苏丹采用青蒿琥酯+磺胺多辛/乙胺嘧啶(SP)组合作为一线药物,以应对恶性疟原虫对恶性疟疾的高度耐药性。 2007年,对苏丹中部和东部的198个分离株进行了抗疟药耐药相关基因pfcrt,pfmdr1,pfdhfr,pfdhps和pfATPase6的分子研究。我们观察到几乎所有分析的基因座都出现高频率的点突变,主要是pfcrt 76T(72.7%),pfdhfr 51I(75.3%)和pfdhfr 108N(72.7%)等位基因。 MARK III对45株恶性疟原虫分离株中氯喹敏感性的体外测试表明,其中37.8%的分离株具有低耐药性,而6.7%的分离株具有完全耐药性。这项研究代表了在采用基于青蒿素的联合疗法(ACT)之后该领域抗疟药耐药性的最新分子研究,并强调了SP耐药性演变分析对监测ACT疗法在流行地区的疗效的重要性。

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