采用青蒿素衍生物治疗组合十年后,野生K13螺旋桨单倍型在Côte科特迪瓦三个地方的优势

Dagnogo Oléfongo, K. Rolland, A. Bérenger, Bla Kouakou Brice, Touré Offianan André, Djaman Allico Joseph
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引用次数: 0

摘要

背景:恶性疟原虫对以青蒿素为基础的联合治疗(ACT)的耐药性的出现威胁着非洲疟疾的控制。监测与抗疟药物耐药性相关的分子标记多态性对疟疾控制和消除工作至关重要。本研究的目的是分析Côte科特迪瓦南部三个地点恶性疟原虫pfK13推进基因对青蒿素联合治疗(ACT)的多态性。方法:在征得知情同意后,采集anonkoua - kout、Port-Bouët和ayam地区无并发症恶性疟原虫患者的血液样本,患者性别不限,年龄2岁以上。利用Pfk13螺旋桨基因特异性引物提取恶性疟原虫基因组DNA并进行巢式pcr扩增。扩增产物在Eurofins Genomics使用Sanger法测序。分析了关键密码子(493、539、543、580)、分子标记和附加密码子(476、561)。结果:从三个研究地点采集的血样中提取的186个DNA被扩增并测序。在测序的93个PCR产物中,分别有84.94%(158/186)、91.39%(170/186)、95.69%(178/186)、100%(186/186)、82.79%(154/186)和94.62%(178/186)对应于密码子493、539、543、580、476、561。野生型等位基因的阳性率分别为92.40% (Tyr493)、94.11% (Arg539)、94.38% (Ile543)、91.39% (Cys580)、89.61% (Met476)和88.63% (Arg561),而突变型等位基因的阳性率分别为1.26% (His493)、3.52% (Thr539)和1.29% (Ile476)。突变等位基因Thr543、Tyr580和His561在所有三个研究地点均未观察到。分析表明,YRICMR等位基因形式占优势,代表易感单倍型(78.49%)。3个试验点野生型等位基因的阳性率差异无统计学意义(p>0.05)。结论:在采用以青蒿素为基础的联合用药管理非复杂性疟疾十多年后,这些联合用药在Côte科特迪瓦南部的anonkoua - kout、Port-Bouët和ayam仍然有效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Predominance of Wild K13 Propeller Haplotypes in three localities of Côte d'Ivoire one decade after the adoption of Therapeutic Combinations based on Artemisinin Derivatives
Background: The emergence of P. falciparum resistance to artemisinin-based combination therapy (ACT) threatens malaria control in Africa. The monitoring of polymorphisms in molecular markers associated with antimalarial drug resistance is essential for malaria control and elimination efforts. The purpose of this study is to analyze the polymorphism of the pfK13 propeller gene of P. falciparum to artemisinin-based combination therapy (ACT) in three sites in southern Côte d'Ivoire. Methods: After obtaining informed consent, blood samples were collected from patients of any sex and aged over 2 years with uncomplicated P. falciparum malaria in Anonkoua-Kouté, Port-Bouët and Ayamé. P. falciparum genomic DNA was extracted and amplified by Nested-PCR using Pfk13 propeller gene-specific primers. The amplification products were sequenced using the Sanger method at Eurofins Genomics. The key codons (493, 539, 543 and 580), molecular markers of the resistance of P. falciparum to ACTs and the additional codons (476 and 561) were analyzed. Results: A total of 186 DNA extracts from blood samples collected from the three study sites were amplified and sequenced. Of the 93 PCR products sequenced, 84.94% (158/186), 91.39% (170/186), 95.69% (178/186), 100% (186/186), 82.79% (154/186) and 94.62% (178/186) corresponding to codons 493, 539, 543, 580, 476, 561, respectively, were successfully analyzed. Thus, the prevalences of wild-type alleles were 92.40% (Tyr493), 94.11% (Arg539), 94.38% (Ile543), 91.39% (Cys580), 89.61% (Met476) and 88.63% (Arg561) against 1.26% (His493), 3.52% (Thr539) and 1.29% (Ile476) of mutant alleles. The mutant alleles Thr543, Tyr580, and His561 were not observed in all three study sites. The analysis indicated a predominance of the YRICMR allelic form representing a susceptible haplotype (78.49%). No significant difference was observed between the prevalences of the wild-type alleles determined in the three study sites (p>0.05). Conclusion: More than a decade after the adoption of ACTs for the management of uncomplicated malaria, these combinations are still effective in Anonkoua-Kouté, Port-Bouët and Ayamé in the south of Côte d'Ivoire.
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