Orjih Augustine U
Department of Medical Laboratory Sciences, Faculty of Allied Health Sciences, Kuwait University, P.O. Box 31740, Sulaibikhat, 90805, Kuwait,
Parasitol Res. 2014 Nov;113(11):4045-56. doi: 10.1007/s00436-014-4073-8. Epub 2014 Aug 15.
Erythrocytes containing two or more parasites, referred to here as multiply infected erythrocytes (MIEs), are common in the blood of humans infected by Plasmodium falciparum. It is necessary to study these cells closely because the excess numbers of parasites they contain suggest that they could be overloaded with virulence factors. Here, microscopic examinations of blood smears from patients showed that up to seven merozoites can successfully invade an erythrocyte and mature to ring stage. However, in vitro culture showed that only up to three parasites can mature to late schizont stage. These observations were made by culturing the parasites in erythrocytes containing hemoglobin AA (HbAA), HbAS, and HbSS. Biochemical analysis of saponin-concentrated culture suggests that more hemozoin is produced in a MIE than in a singly infected erythrocyte (SIE). Studies have shown that ingestion of excessive hemozoin destroys monocytes and neutrophils, which could impair the immune system. Cultured parasites were also examined by transmission electron microscopy, and it was found that the quantity of knobs was dramatically increased on the membranes of erythrocytes containing multiple schizonts, compared to those containing only one schizont. Knobs contain, among other things, P. falciparum erythrocyte membrane protein 1 (PfEMP1) complex which mediates sequestration and promotes severe malaria. These findings suggest that P. falciparum increases its virulence by producing MIEs. On sexual life cycle of the parasite, microphotographs are presented in this report showing, for the first time, that two gametocytes can develop in one erythrocyte; they are referred to here as twin gametocytes. It is not known whether they can infect mosquitoes.
含有两个或更多寄生虫的红细胞,在这里被称为多重感染红细胞(MIEs),在感染恶性疟原虫的人类血液中很常见。有必要对这些细胞进行仔细研究,因为它们所含的过量寄生虫表明它们可能携带了过多的毒力因子。在这里,对患者血涂片的显微镜检查显示,多达七个裂殖子可以成功侵入一个红细胞并发育到环状体阶段。然而,体外培养表明,只有多达三个寄生虫能够发育到晚期裂殖体阶段。这些观察结果是通过在含有血红蛋白AA(HbAA)、HbAS和HbSS的红细胞中培养寄生虫得出的。对皂素浓缩培养物的生化分析表明,与单一感染红细胞(SIE)相比,MIE产生的疟色素更多。研究表明,摄入过多的疟色素会破坏单核细胞和中性粒细胞,这可能会损害免疫系统。还通过透射电子显微镜对培养出的寄生虫进行了检查,结果发现,与只含有一个裂殖体的红细胞相比,含有多个裂殖体的红细胞膜上的凸起数量显著增加。凸起中除其他物质外,还含有恶性疟原虫红细胞膜蛋白1(PfEMP1)复合物,该复合物介导滞留并促进严重疟疾。这些发现表明,恶性疟原虫通过产生MIEs来增加其毒力。关于该寄生虫的有性生活周期,本报告展示了显微照片,首次显示两个配子体可以在一个红细胞中发育;在这里它们被称为双配子体。尚不清楚它们是否能感染蚊子。