Manzoni Giulia, Marinach Carine, Topçu Selma, Briquet Sylvie, Grand Morgane, Tolle Matthieu, Gransagne Marion, Lescar Julien, Andolina Chiara, Franetich Jean-François, Zeisel Mirjam B, Huby Thierry, Rubinstein Eric, Snounou Georges, Mazier Dominique, Nosten François, Baumert Thomas F, Silvie Olivier
Sorbonne Universités, UPMC Univ Paris 06, INSERM, CNRS, Centre d'Immunologie et des Maladies Infectieuses, U1135, ERL8255, Paris, France.
Shoklo Malaria Research Unit, Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Mae Sot, Thailand.
Elife. 2017 May 16;6:e25903. doi: 10.7554/eLife.25903.
sporozoites, the mosquito-transmitted forms of the malaria parasite, first infect the liver for an initial round of replication before the emergence of pathogenic blood stages. Sporozoites represent attractive targets for antimalarial preventive strategies, yet the mechanisms of parasite entry into hepatocytes remain poorly understood. Here we show that the two main species causing malaria in humans, and , rely on two distinct host cell surface proteins, CD81 and the Scavenger Receptor BI (SR-BI), respectively, to infect hepatocytes. By contrast, CD81 and SR-BI fulfil redundant functions during infection by the rodent parasite . Genetic analysis of sporozoite factors reveals the 6-cysteine domain protein P36 as a major parasite determinant of host cell receptor usage. Our data provide molecular insights into the invasion pathways used by different malaria parasites to infect hepatocytes, and establish a functional link between a sporozoite putative ligand and host cell receptors.
疟原虫的子孢子是通过蚊子传播的形式,在致病性血液阶段出现之前,首先感染肝脏进行第一轮复制。子孢子是抗疟预防策略的有吸引力的靶点,但寄生虫进入肝细胞的机制仍知之甚少。在这里,我们表明,导致人类疟疾的两种主要疟原虫,分别依赖两种不同的宿主细胞表面蛋白,即CD81和清道夫受体BI(SR-BI)来感染肝细胞。相比之下,在啮齿动物疟原虫感染期间,CD81和SR-BI发挥冗余功能。对子孢子因子的遗传分析揭示了6-半胱氨酸结构域蛋白P36是宿主细胞受体使用的主要寄生虫决定因素。我们的数据提供了对不同疟原虫感染肝细胞所使用的入侵途径的分子见解,并在子孢子推定配体和宿主细胞受体之间建立了功能联系。