Rodrigues Pedro Souto, Azeredo Milena de Farias, Almeida Natália de Souza, de Almeida Gisela Garcia Cabral Galaxe, Wanderley João Luiz Mendes, Seabra Sergio Henrique, DaMatta Renato Augusto
Laboratório de Biologia Celular e Tecidual, Universidade Estadual do Norte Fluminense Darcy Ribeiro, Campos dos Goytacazes 28013-602, RJ, Brazil.
Laboratório de Imunoparasitologia, Universidade Federal do Rio de Janeiro, Macaé 27930-560, RJ, Brazil.
Microorganisms. 2024 Jan 5;12(1):105. doi: 10.3390/microorganisms12010105.
Malaria is caused by apicomplexan parasites of the genus. is an excellent animal model for the study of human malaria caused by . Merozoites invade erythrocytes but are also found in other host cells including macrophages from the spleen and liver. Methodologies for obtaining merozoites usually involve treatment with protease inhibitors. However, merozoites obtained in this way may have their enzymatic profile altered and, therefore, are not ideal for cell-interaction assays. We report the obtainment of merozoites naturally egressed from a synchronous erythrocyte population infected with schizonts forms. Merozoites had their infectivity and ultrastructure analyzed. Interaction assays were performed with mice erythrocytes and classically activated mice peritoneal macrophages, a very well-established classic model. Obtained merozoites were able to kill mice and efficiently infect erythrocytes. Interestingly, a lower merozoite:erythrocyte ratio resulted in a higher percentage of infected erythrocytes. We describe a simpler method for obtaining viable and infective merozoites. Classically activated macrophages killed merozoites, suggesting that these host cells may not serve as reservoirs for these parasites. These findings have implications for our understanding of merozoite biology and may improve the comprehension of their host-parasite relationship.
疟疾由疟原虫属的顶复门寄生虫引起。是研究由引起的人类疟疾的优秀动物模型。裂殖子侵入红细胞,但也存在于其他宿主细胞中,包括脾脏和肝脏的巨噬细胞。获取裂殖子的方法通常涉及用蛋白酶抑制剂处理。然而,以这种方式获得的裂殖子可能会改变其酶谱,因此,对于细胞相互作用分析来说并不理想。我们报告了从感染裂殖体形式的同步红细胞群体中自然逸出的裂殖子的获取情况。对裂殖子的感染性和超微结构进行了分析。用小鼠红细胞和经典激活的小鼠腹腔巨噬细胞进行了相互作用分析,这是一个非常成熟的经典模型。获得的裂殖子能够杀死小鼠并有效感染红细胞。有趣的是,较低的裂殖子与红细胞比例导致被感染红细胞的百分比更高。我们描述了一种更简单的获取有活力和感染性裂殖子的方法。经典激活的巨噬细胞杀死裂殖子,表明这些宿主细胞可能不是这些寄生虫的储存库。这些发现对我们理解裂殖子生物学有影响,可能会增进对其宿主 - 寄生虫关系的理解。