Genetic Diversity and Allelic Distribution of Plasmodium falciparum msp1 and msp2 Genes in a High-Transmission Setting: Southern Ethiopia.

IF 1.7 Q3 PARASITOLOGY
Journal of Parasitology Research Pub Date : 2026-06-19 eCollection Date: 2026-01-01 DOI:10.1155/japr/2796576
Kefiyalew Jote, Yirgalem Gebrehiwot, Cheikh Cambel Dieng, Eugenia Lo, Lemu Golassa, Bayissa Chala
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引用次数: 0

Abstract

Background: Although both preventable and treatable, malaria remains a significant burden on health and economic stability, particularly in regions of high transmission such as Africa and parts of Asia. The parasite's genetic diversity enhances its ability to evade the host immune system and adapt, posing challenges to effective treatment strategies.

Objective: The primary objective of this study was to assess the genetic diversity of Plasmodium falciparum by analyzing polymorphisms in the merozoite surface protein genes among clinical isolates collected from public health facilities in Arba Minch town and Mirab Abaya, Southern Ethiopia.

Methods: A facility-based cross-sectional study was conducted to investigate the genetic diversity of P. falciparum. Capillary blood samples were collected from 200 participants using both microscope slides (for phenotypic analysis) and Whatman 903 filter paper (for molecular investigation using polymerase chain reaction). Parasite genomic DNA was extracted using the G-spin Total DNA Extraction Mini Kit. Nested PCR was performed to confirm the presence of P. falciparum by targeting 18S rRNA and to genotype the msp1 and msp2 gene allelic families.

Results: Of the 200 samples initially confirmed for P. falciparum infection, 138 (69%) were mono-infections. Males accounted for 55.1% of the confirmed cases, whereas 44.9% were females. More than half of the participants (58%) had parasite density of ≥ 10,000 parasites/μL. The mean hemoglobin level recorded was 13.4 g/dL (95% CI, 13.06-13.7). Genotyping revealed 131 msp1 and 164 for msp2 alleles, with MAD20 (58.8%) and FC27 (52.4%) frequently detected allelic types, respectively. msp2 infections were nearly evenly split between monoclonal (53.2%) and polyclonal. A significantly higher multiplicity of infection (MOI) was observed in Arba Minch town for msp2 (MOI = 2.19) p < 0.001.

Conclusion and recommendation: This study revealed substantial genetic diversity in P. falciparum alleles, with variations linked to geographic location, age group, and residential setting. These findings underscore the complex epidemiology of malaria in Arba Minch and the surrounding areas, emphasizing the need for geographically and demographically targeted control strategies based on local transmission patterns to guide elimination efforts. Enhancing community awareness about risk factors and vulnerable populations is critical for the success of malaria prevention programs.

埃塞俄比亚南部高传播环境中恶性疟原虫msp1和msp2基因的遗传多样性和等位基因分布
背景:虽然可以预防和治疗,但疟疾仍然是健康和经济稳定的重大负担,特别是在非洲和亚洲部分地区等高传播区域。寄生虫的遗传多样性增强了其逃避宿主免疫系统和适应的能力,对有效的治疗策略提出了挑战。目的:本研究的主要目的是通过分析从埃塞俄比亚南部Arba Minch镇和Mirab Abaya的公共卫生机构收集的临床分离株中merozoite表面蛋白基因的多态性来评估恶性疟原虫的遗传多样性。方法:采用基于设施的横断面研究方法调查恶性疟原虫的遗传多样性。使用显微镜载玻片(用于表型分析)和Whatman 903滤纸(用于聚合酶链反应的分子研究)收集200名参与者的毛细血管血样。使用G-spin总DNA提取迷你试剂盒提取寄生虫基因组DNA。采用巢式PCR方法,以18S rRNA为靶点,对msp1和msp2基因等位基因家族进行分型,证实恶性疟原虫的存在。结果:在最初确认为恶性疟原虫感染的200份样本中,138份(69%)为单一感染。男性占确诊病例的55.1%,女性占44.9%。超过一半的参与者(58%)的寄生虫密度≥10,000只/μL。记录的平均血红蛋白水平为13.4 g/dL (95% CI, 13.06-13.7)。基因分型发现msp1和msp2等位基因分别为131个和164个,其中MAD20(58.8%)和FC27(52.4%)等位基因较多。Msp2感染在单克隆和多克隆中几乎均匀分布(53.2%)。Arba Minch镇msp2感染的多重感染数(MOI)显著高于Arba Minch镇(MOI = 2.19), p < 0.001。结论和建议:本研究揭示了恶性疟原虫等位基因的大量遗传多样性,其变异与地理位置、年龄组和居住环境有关。这些发现强调了Arba Minch及周边地区疟疾流行病学的复杂性,强调需要根据当地传播模式制定有地理和人口目标的控制战略,以指导消除工作。提高社区对风险因素和弱势群体的认识对于疟疾预防规划的成功至关重要。
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来源期刊
Journal of Parasitology Research
Journal of Parasitology Research Medicine-Infectious Diseases
CiteScore
3.50
自引率
9.10%
发文量
49
审稿时长
13 weeks
期刊介绍: Journal of Parasitology Research is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies in all areas of basic and applied parasitology. Articles covering host-parasite relationships and parasitic diseases will be considered, as well as studies on disease vectors. Articles highlighting social and economic issues around the impact of parasites are also encouraged. As an international, Open Access publication, Journal of Parasitology Research aims to foster learning and collaboration between countries and communities.
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