加纳北部萨赫勒地区无症状携带者中疟原虫高季节性传播的宏基因组复杂性

IF 5.4 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Mun Hua Tan, Oscar Bangre, Cecilia A Rios-Teran, Kathryn E Tiedje, Samantha L Deed, Qi Zhan, Fathia Rasyidi, Mercedes Pascual, Patrick O Ansah, Karen P Day
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引用次数: 0

摘要

背景:已知在疟疾流行地区的人类中会发生混合种、混合菌株的疟原虫感染。可能令人惊讶的是,迄今为止,在撒哈拉以南非洲高负担国家,特别是在维持传播的所有年龄段无症状感染库中,尚未系统地探索这种复杂性的程度。方法:在这里,我们对这些感染采取宏基因组镜头,从生活在加纳北部萨赫勒地区高季节性传播的188名发热居民中取样不同的血容量。我们通过抗原和微卫星的基因分型估计了不同疟原虫感染的多重性。我们进一步将“宏基因组复杂性”定义为跨物种和菌株组合的整体宿主内复杂性的度量。结果:我们发现,这些个体的血容量越大,疟原虫的患病率和种间/种内复杂性就越高。总体而言,疟疾感染表现出高水平的元基因组复杂性,包括单种、双种和三种感染,以及恶性疟原虫、疟疾疟原虫、柯氏疟原虫和瓦利克氏疟原虫不同程度的种内复杂性。我们还报告了一个不能用年龄或地点解释的高度复杂感染的个体子集。这些发现对疟疾流行病学和控制的影响通过加纳北部地区和区域一级的地理缩放工作加以说明。结论:我们的宏基因组研究强调了在无症状感染携带者中更敏感地测量宿主内疟原虫复杂性的必要性。这将优化疟疾监测和控制战略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Metagenomic complexity of high, seasonal transmission of Plasmodium spp. in asymptomatic carriers in Northern Sahelian Ghana.

Background: Mixed-species, mixed-strain plasmodia infections are known to occur in humans in malaria endemic areas. It may be surprising that to date, the extent of this complexity has not been systematically explored in high-burden countries of sub-Saharan Africa, especially in the reservoir of asymptomatic infections in all ages, which sustains transmission.

Methods: Here we take a metagenomic lens to these infections by sampling variable blood volumes from 188 afebrile residents living in high, seasonal transmission in Northern Sahelian Ghana. We estimated multiplicity of infection for different Plasmodium spp. through genotyping of antigens and microsatellites. We further defined 'metagenomic complexity' as a measure of overall within-host complexity across the combination of species and strains.

Results: We show that prevalence of Plasmodium spp. and inter-/intra-species complexity is significantly higher in larger blood volumes from these individuals. Overall, malaria infections display high levels of metagenomic complexity comprising single-, double-, and triple-species infections with varying levels of intra-species complexity for P. falciparum, P. malariae, P. ovale curtisi, and P. ovale wallikeri. We also report a subset of individuals with highly-complex infections that cannot be explained by age or location. The implications of these findings to malaria epidemiology and control are illustrated by a geographic scaling exercise to district and region levels in northern Ghana.

Conclusions: Our metagenomic investigation underscores the need to more sensitively measure within-host Plasmodium spp. complexity in asymptomatic carriers of infection. This will optimise strategies for malaria surveillance and control.

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