Plasmodium falciparum genetic diversity and multiplicity of infection among asymptomatic and symptomatic malaria-infected individuals in Uganda.

IF 3.6 Q1 TROPICAL MEDICINE
Alex Mwesigwa, Moses Ocan, Bryan Cummings, Benson Musinguzi, Shahid Kiyaga, Steven M Kiwuwa, Stephen Okoboi, Barbara Castelnuovo, Everd Maniple Bikaitwoha, Joan N Kalyango, Charles Karamagi, Joaniter I Nankabirwa, Samuel L Nsobya, Pauline Byakika-Kibwika
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Abstract

Background: Plasmodium falciparum (P. falciparum) remains a significant public health challenge globally, especially in sub-Saharan Africa (SSA), where it accounts for 99% of all malaria infections. The outcomes of P. falciparum infection vary, ranging from asymptomatic to severe, and are associated with factors such as host immunity, parasite genetic diversity, and multiplicity of infection (MOI). Using seven neutral microsatellite markers, the current study investigated P. falciparum genetic diversity and MOI in both asymptomatic and symptomatic malaria individuals in Uganda.

Methods: This cross-sectional study analyzed 225 P. falciparum isolates from both asymptomatic and symptomatic malaria patients, ranging in age from 6 months to ≥ 18 years. P. falciparum genetic diversity, MOI, and multi-locus linkage disequilibrium (LD) were assessed through genotyping of seven neutral microsatellite markers: Poly-α, TA1, TA109, PfPK2, 2490, C2M34-313, and C3M69-383. Genetic data analysis was performed using appropriate genetic analysis software.

Results: P. falciparum infections exhibited high genetic diversity in both asymptomatic and symptomatic individuals. The mean expected heterozygosity (He) ranged from 0.79 in symptomatic uncomplicated malaria cases to 0.81 in asymptomatic individuals. There was no significant difference (p = 0.33) in MOI between individuals with asymptomatic and symptomatic infections, with the mean MOI ranging from 1.92 in symptomatic complicated cases to 2.10 in asymptomatic individuals. Polyclonal infections were prevalent, varying from 58.5% in symptomatic complicated malaria to 63% in symptomatic uncomplicated malaria cases. A significant linkage disequilibrium (LD) was observed between asymptomatic and symptomatic uncomplicated/complicated infections (p < 0.01). Genetic differentiation was low, with FST values ranging from 0.0034 to 0.0105 among P. falciparum parasite populations in asymptomatic and symptomatic uncomplicated/complicated infections.

Conclusion: There is a high level of P. falciparum genetic diversity and MOI among both symptomatic and asymptomatic individuals in Uganda. Asymptomatic carriers harbor a diverse range of parasites, which poses challenges for malaria control and necessitates targeted interventions to develop effective strategies.

乌干达无症状和有症状疟疾感染者的恶性疟原虫遗传多样性和感染多重性。
背景:恶性疟原虫(P. falciparum)仍然是全球公共卫生面临的重大挑战,尤其是在撒哈拉以南非洲地区(SSA),该地区的疟疾感染率高达 99%。恶性疟原虫感染的结果各不相同,从无症状到病情严重不等,并与宿主免疫力、寄生虫遗传多样性和感染倍数(MOI)等因素有关。本研究使用七个中性微卫星标记,调查了乌干达无症状和有症状疟疾患者的恶性疟原虫遗传多样性和感染率:这项横断面研究分析了来自无症状和有症状疟疾患者的 225 株恶性疟原虫分离株,这些患者的年龄从 6 个月到 18 岁不等。通过对 7 个中性微卫星标记进行基因分型,评估了恶性疟原虫的遗传多样性、MOI 和多焦点连锁不平衡(LD):Poly-α、TA1、TA109、PfPK2、2490、C2M34-313 和 C3M69-383。使用适当的遗传分析软件进行遗传数据分析:结果:恶性疟原虫感染在无症状和有症状的个体中均表现出较高的遗传多样性。平均预期杂合度(He)从无症状疟疾病例的 0.79 到无症状个体的 0.81 不等。无症状感染者和有症状感染者的 MOI 没有明显差异(p = 0.33),平均 MOI 从有症状复杂病例的 1.92 到无症状感染者的 2.10 不等。多克隆感染很普遍,在有症状的复杂疟疾病例中占58.5%,在无症状的疟疾病例中占63%。在无症状感染和有症状的无并发症/并发症感染中,恶性疟原虫寄生虫种群之间存在明显的连锁不平衡(LD)(p ST 值从 0.0034 到 0.0105 不等):乌干达有症状和无症状的个体中恶性疟原虫的遗传多样性和感染率都很高。无症状带菌者携带多种寄生虫,这给疟疾控制工作带来了挑战,需要采取有针对性的干预措施来制定有效的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Tropical Medicine and Health
Tropical Medicine and Health TROPICAL MEDICINE-
CiteScore
7.00
自引率
2.20%
发文量
90
审稿时长
11 weeks
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