尼日利亚奥贡州城乡社区恶性疟原虫分离株中 PfCRT K76T 突变高发的相关因素。

MalariaWorld journal Pub Date : 2017-08-01 eCollection Date: 2017-01-01
Olajoju T Soniran, Olufunmilayo A Idowu, Segun S Ogundapo
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摘要

背景:对抗疟药物产生抗药性的恶性疟原虫菌株一直是全球控制和消除疟疾工作的主要障碍。最近有报告称,一些国家耐氯喹恶性疟原虫的流行率有所下降,最近在马拉维和赞比亚更是完全消失,因此人们希望重新使用氯喹治疗无并发症疟疾。2005 年,尼日利亚正式宣布停止使用氯喹治疗疟疾。现有的一些报告显示,氯喹抗药性的主要生物标志物在尼日利亚西南部的流行率居高不下。然而,有关其在农村和城市地区流行情况的信息却很少。我们调查了尼日利亚西南部奥贡州氯喹抗药性生物标志物流行的可能相关因素:在城市的州立综合医院和农村的初级保健中心就诊的有疟疾症状和无症状的受试者通过指刺从干血斑中提取寄生虫 DNA。采用结构化问卷收集有关疟疾/发烧治疗史的数据。巢式聚合酶链反应(PCR)和限制性片段长度多态性(RFLP)分析用于检测恶性疟原虫氯喹抗性转运体(Pfcrt)的突变:在这项研究招募的 243 名参与者中,发现 56 人携带恶性疟原虫寄生虫,其中 62.5%(35/56)人出现疟疾症状。恶性疟原虫抗氯喹菌株(Pfcrt K76T)的流行率为 69.6%。农村地区的 Pfcrt K76T 感染率(91.7%)明显更高(PConclusions:农村地区记录到的耐药恶性疟原虫菌株与自行用药和光顾继续销售氯喹的药贩有关。这些研究结果表明,持续监测显示抗药性的生物标志物非常重要,尤其是在抗疟药物抗药性对根除疟疾构成威胁的今天。
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Factors associated with high prevalence of PfCRT K76T mutation in Plasmodium falciparum isolates in a rural and urban community of Ogun State, Nigeria.

Background: Antimalarial drug-resistant Plasmodium falciparum strains have been a major obstacle to the global efforts of controlling and eliminating malaria. The hope of reintroducing chloroquine for the treatment of uncomplicated malaria follows recent reports on decreases in the prevalence of chloroquine-resistant P. falciparum in several countries and recently, its total disappearance in Malawi and Zambia. In Nigeria, the discontinued use of chloroquine for malaria treatment was officially announced in 2005. A few available reports have shown a persistent high prevalence of the major biomarker of chloroquine resistance in southwest Nigeria. However, information on its prevalence in rural and urban areas is scanty. We investigated possible factors associated with the prevalence of a biomarker for chloroquine-resistance in Ogun State, southwest Nigeria.

Materials and methods: Parasite DNA was extracted from dried blood spots collected by finger-prick in malaria symptomatic and asymptomatic subjects attending the urban-based State General Hospital and a rural-based Primary Health Centre. A structured questionnaire was used to collect data on malaria/fever treatment history. Nested Polymerase Chain Reaction (PCR) followed by Restriction Fragment Length Polymorphisms (RFLP) analysis was used to detect mutations in the P. falciparum chloroquine resistance transporter (Pfcrt).

Results: Of the 243 participants recruited for this study, 56 were found to harbour P. falciparum parasites, of which 62.5% (35/56) showed symptoms of malaria. Prevalence of P. falciparum chloroquine-resistant strains (Pfcrt K76T) was 69.6%. The prevalence of Pfcrt K76T recorded in the rural area (91.7%) was significantly higher (P<0.05) than that in the urban area (53.1%). There was no correlation between prevalence of chloroquine-resistant strains and malaria symptoms in the rural area. However, prevalence of chloroquine-resistant strains was significantly higher in malaria-symptomatic subjects from the urban area.

Conclusions: Drug-resistant P. falciparum strains recorded in the rural area were associated with self-medication and patronage of drug vendors who continue to sell chloroquine. These findings present the importance of continuous surveillance of biomarkers indicating drug resistance especially now that antimalarial drug resistance is a threat to malaria eradication.

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