Molecular analysis of Bio-makers of Chloroquine resistance in Plasmodium falciparum Isolate from Gombe Local Government Area, Gombe State, Nigeria

I. Muhammad, Pukuma Sale, M. Salisu, Tanko Muhammad, B. Abubakar, Augustine Maidala, Enock Nuwanyada
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引用次数: 9

Abstract

most cheapest and effective chemotherapeutic drugs for Plasmodium falciparum -malaria, but for a long, the drug has been officially withdrawn in almost all malaria-endemic countries including Nigeria, due to the development of resistance by the parasite. Withdrawal of the drug may make the drug regains its efficacy. Therefore, this study aimed to determine the presence of Biomarkers associated with chloroquine resistance from Gombe Local Government Area, Gombe State, Nigeria after its withdrawal in 2005. Twenty hundred blood samples were collected from consented study subjects and analysed using Microscopy, RDT and PCR. DNA was extracted using Quick-DNA™ Miniprep (No. D4069), Purity and Concentration of the DNA were determined using Nanodrop Spectrophotometer. 57 true positive samples were selected for molecular analysis. Nested PCR was used to amplify the required codon (C72S, M74I, K76T and N75E) position of PCRT the gene of P. falciparum . Both Primary and Secondary PCR was carried out. The PCR products were subjected to electrophoresis in 2% agarose and stained with ethidium bromide. The amplicons were purified and sequenced, after which the sequenced products were subjected to BLAST software. Single Nucleotide Polymorphism was recorded from C72S and K76T with a prevalence of 05(8.80%) and 46(80.70%) respectively. Confirmed biomarkers of Chloroquine resistance are still present in P. falciparum isolate from Gombe L.G.A.
尼日利亚贡贝州贡贝地方政府区恶性疟原虫分离株氯喹耐药生物标志物的分子分析
这是治疗恶性疟原虫的最便宜和最有效的化疗药物,但长期以来,由于寄生虫产生耐药性,这种药物已在包括尼日利亚在内的几乎所有疟疾流行国家被正式停用。停药可使该药恢复药效。因此,本研究旨在确定2005年从尼日利亚贡贝州贡贝地方政府区撤出后与氯喹耐药性相关的生物标志物的存在。从同意的研究对象中收集了2000份血液样本,并使用显微镜,RDT和PCR进行分析。使用Quick-DNA™Miniprep (No. 6)提取DNA。D4069),用纳米滴分光光度计测定DNA的纯度和浓度,选择57份真阳性样品进行分子分析。采用巢式PCR扩增恶性疟原虫PCRT基因所需密码子(C72S、M74I、K76T和N75E)位置。进行了一级和二级PCR。PCR产物经2%琼脂糖电泳,溴化乙啶染色。扩增子纯化并测序,测序产物经BLAST软件处理。C72S和K76T的单核苷酸多态性分别为05(8.80%)和46(80.70%)。贡贝省恶性疟原虫分离株中仍存在已证实的氯喹耐药生物标志物
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