Tan Mun Hua, Bangre Oscar, Rios-Teran Cecilia A, Tiedje Kathryn E, Deed Samantha L, Zhan Qi, Rasyidi Fathia, Pascual Mercedes, Ansah Patrick O, Day Karen P
Department of Microbiology and Immunology, Bio21 Institute and The Peter Doherty Institute for Infection and Immunity, The University of Melbourne, Melbourne, VIC, Australia.
Navrongo Health Research Centre, Ghana Health Service, Navrongo, Ghana.
Commun Med (Lond). 2025 Sep 10;5(1):386. doi: 10.1038/s43856-025-01088-y.
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.
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.
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.
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.
已知在疟疾流行地区,人类会出现混合物种、混合菌株的疟原虫感染。令人惊讶的是,迄今为止,在撒哈拉以南非洲的高负担国家,尤其是在维持传播的各年龄段无症状感染宿主中,这种复杂性的程度尚未得到系统研究。
在此,我们通过对加纳北部萨赫勒地区季节性高传播地区的188名无发热居民采集不同血量的样本,采用宏基因组学方法研究这些感染。我们通过对抗原和微卫星进行基因分型,估计了不同疟原虫物种的感染复数。我们进一步将“宏基因组复杂性”定义为衡量宿主内物种和菌株组合的整体复杂性的指标。
我们发现,从这些个体采集的血量越大,疟原虫物种的流行率以及种间/种内复杂性就越高。总体而言,疟疾感染表现出高水平的宏基因组复杂性,包括单物种、双物种和三物种感染,恶性疟原虫、三日疟原虫、卵形疟原虫柯蒂斯亚种和卵形疟原虫沃里克亚种的种内复杂性各不相同。我们还报告了一部分感染高度复杂的个体,其感染情况无法用年龄或地理位置来解释。通过将研究结果按地理范围扩展到加纳北部的地区和区域层面,说明了这些发现对疟疾流行病学和控制的影响。
我们的宏基因组学研究强调了更灵敏地测量感染无症状携带者体内疟原虫物种复杂性的必要性。这将优化疟疾监测和控制策略。