尼日利亚纳萨拉瓦州纳萨拉瓦-西参议院区人群中恶性疟原虫的 Kelch 13 基因多态性

Isaac Nyiayem Igbawua, Y. Ngwai
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摘要

Kelch-13 是恶性疟原虫产生的一种基因,恶性疟原虫是疟疾寄生虫的种类之一。疟疾仍然是一项重大的公共卫生挑战,尤其是在撒哈拉以南非洲地区,它是导致死亡和发病的主要原因,尤其是对儿童和孕妇而言。世卫组织建议将青蒿素类复方疗法作为治疗无并发症疟疾的一线药物,但与 K13 基因突变相关的青蒿素抗药性的出现和传播对青蒿素类复方疗法的疗效构成了威胁。检测突变的 K13 基因可提供寄生虫对青蒿素敏感性变化的信息。本研究旨在检测尼日利亚纳萨拉瓦-西部参议院辖区人群中的 K13 基因多态性。研究人员从选定的医院共采集了 385 份血液样本,并通过显微镜(金标准)进行了疟疾筛查。使用 RDT 对恶性疟原虫进行了种属特异性筛查。从 RDT 阳性样本中提取的干燥血斑通过巢式 PCR 检测是否存在 K13 基因。测序检测出突变的 K13 基因。结果经 RDT 检测,103 份样本对恶性疟原虫呈阳性,PCR 检测确认了 48 个 K13 基因,条带大小为 848 bp。核苷酸序列比对发现了 6 个单核苷酸多态性。将核苷酸序列转换为蛋白质序列的结果显示,在测序的 20 个 Pfkelch 13 基因中,有 1 个(5.0%)发生了点突变。最后,建议在研究人群中发现突变基因后进行持续监测,以便更广泛地了解寄生虫的多样性,从而有效控制疟疾。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Kelch 13 gene polymorphisms of Plasmodium falciparum among human population in Nasarawa-West Senatorial District, Nasarawa State, Nigeria
Kelch-13 is a gene produced by Plasmodium falciparum, one of the species of Malaria parasite. Malaria remains a major public health challenge especially in Sub-Saharan Africa, a major cause of mortality and morbidity, especially in children and pregnant women. WHO recommends Artemisinin-based combination therapies as the first-line drugs for the treatment of uncomplicated malaria but the emergence and spread of Artemisinin-resistance associated with mutations in K13 gene poses a threat to ACT efficacy. Detection of mutant K13 gene may provide the information on changes in parasite susceptibility to Artemisinin. This study was aimed at detecting K13 gene polymorphisms among human population in Nasarawa-West Senatorial District, Nigeria. A total of 385 blood samples were collected from selected hospitals and screened for malaria by microscopy (the gold standard). Species specific screening of the P. falciparum was done using RDT. Dried blood spots made from RDT positive samples were investigated for the presence of K13 genes by nested PCR. Sequencing detected mutant K13 gene. Results: 103 samples were positive for Plasmodium falciparum by RDT, PCR confirmed 48 K13 genes with a band size of 848 bp. Nucleotide sequence alignment revealed six Single Nucleotides Polymorphisms. The nucleotide sequences were converted to protein sequences and results showed a point mutation in 1(5.0%) of the 20 Pfkelch 13 gene sequenced. Conclusively, the need for continuous surveillance following the detection of mutant gene in the study population is recommended in order to have a wider picture of the parasite diversity for effective malaria control.
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