Aklilu Lemma Institute of Pathobiology, Addis Ababa Universitygrid.7123.7, Addis Ababa, Ethiopia.
College of Medicine and Health Sciences, Bahir Dar University, Bahir Dar, Ethiopia.
Microbiol Spectr. 2022 Oct 26;10(5):e0062822. doi: 10.1128/spectrum.00628-22. Epub 2022 Sep 6.
The membrane feeding assay is widely used to evaluate the efficacy of transmission-blocking interventions (TBIs) and identify the reservoir of malaria. This study aimed to determine the infectivity of blood meals from symptomatic Plasmodium-infected patients to an Anopheles arabiensis colony in Ethiopia. A membrane feeding assay was conducted on a total of 63 Plasmodium falciparum- and/or Plasmodium vivax-infected clinical patients in East Shoa Zone, Ethiopia. Detection of P. falciparum and P. vivax in blood samples was done using microscopy. Mosquito infection rates were determined by dissection of mosquitoes' midguts, while mosquito infectiousness was observed by dissection of their salivary glands. The proportion of infectious symptomatic patients was 68.3% (43/63). Using the chi-square or Fisher's exact test, the oocyst infection levels were higher among patients infected with P. vivax, females, and rural residents. Nearly 57% (56.7%, 17/30) of assays produced sporozoites in the salivary glands of mosquitoes. Both oocyst and sporozoite infection rates had positive correlations with parasitemia and gametocytemia. High infectiousness of symptomatic patients was observed, with a greater proportion of infectious mosquitoes per assay. Demonstrating oocyst infection in the mosquitoes might confirm estimates of the infectiousness of mosquitoes, although some of the oocyst-infected mosquitoes failed to produce sporozoites. Malaria remains one of the most devastating infectious diseases globally, and transmission-blocking activities are needed. Plasmodium transmission from human to mosquitoes is poorly studied, particularly in endemic countries, and the membrane feeding assay allows it to be determined. In this study, we demonstrated human infectious reservoirs of malaria. Moreover, the effect of Plasmodium-infected patients on the infectiousness of mosquitoes was also observed. These findings are therefore important for designing future evaluation of transmission-blocking interventions that will support the malaria elimination program.
膜喂食检测被广泛用于评估阻断传播干预措施(TBIs)的效果,并确定疟疾的储存库。本研究旨在确定来自埃塞俄比亚阿拉伯按蚊种群中症状性疟原虫感染患者血液中的感染力。在东绍阿地区,对总共 63 名感染恶性疟原虫和/或间日疟原虫的临床患者进行了膜喂食检测。使用显微镜检测血液样本中恶性疟原虫和间日疟原虫的存在。通过解剖蚊子的中肠来确定蚊子的感染率,而通过解剖它们的唾液腺来观察蚊子的感染力。感染的有症状患者比例为 68.3%(43/63)。使用卡方检验或 Fisher 精确检验,感染间日疟原虫、女性和农村居民的患者卵囊感染水平更高。近 57%(56.7%,17/30)的检测在蚊子的唾液腺中产生了子孢子。卵囊和子孢子感染率与寄生虫血症和配子体血症呈正相关。观察到有症状患者的高度传染性,每个检测中感染的蚊子比例更高。在蚊子中检测到卵囊感染可能证实了蚊子的传染性估计,尽管一些感染卵囊的蚊子未能产生子孢子。疟疾仍然是全球最具破坏性的传染病之一,需要开展阻断传播活动。人类向蚊子传播疟原虫的情况研究甚少,特别是在流行国家,而膜喂食检测可以确定这一点。在这项研究中,我们证明了人类是疟疾的感染源。此外,还观察到感染疟原虫的患者对蚊子的感染力的影响。因此,这些发现对于设计未来的阻断传播干预措施评估非常重要,这将支持疟疾消除计划。