Orjih Augustine U
Department of Medical Laboratory Sciences, Kuwait University, 90805 Sulaibikhat, Kuwait, Arabian Gulf.
Exp Biol Med (Maywood). 2008 Nov;233(11):1359-67. doi: 10.3181/0804-RM-129. Epub 2008 Sep 12.
The purpose of the present study was to confirm the effectiveness of saponin hemolysis for concentrating ring-infected erythrocytes in Plasmodium falciparum cultures and to determine the actual numbers of the enriched parasites, not just percentage parasitemia. This is important because various molecular biology and vaccine development against malaria require useable quantities of pure culture with minimal number of uninfected erythrocytes at all stages. Synchronized cultures of three P. falciparum strains were exposed to 0.015% isotonic saponin solution for 30 minutes on ice. They were centrifuged and the pellets were treated again with saponin solution for 3-7 minutes. Initially, most of the cultures contained approximately 10(10) erythrocytes and 1-7% parasitemia, but at the end of the enrichment up to 10(8) of erythrocytes containing 90-99.8% parasitemia were recovered (maximal enrichment). From microscopic examination of the cells it was calculated that the hemolysis rate of uninfected and infected erythrocytes was circa 27 to 1, which could account for the enrichment. Studies by other investigators have suggested that P. falciparum merozoite invasion decreases erythrocyte membrane lipids, and it has been reported that reduction of membrane cholesterol could make erythrocytes saponin-resistant. The possibility that merozoite invasion made erythrocytes partially resistant to saponin hemolysis was strengthened by the observation that the proportions of multiple infections increased significantly in the enriched cultures. However, mature asexual parasites could not be concentrated by this method, suggesting possible differences between the membranes of erythrocytes containing ring forms and those of trophozoites and schizonts. Ring-infected erythrocytes freshly from malaria patients could also not be concentrated by the method described here, suggesting that the ability to induce saponin resistance in erythrocytes was acquired by the parasites in vitro.
本研究的目的是证实皂素溶血法在恶性疟原虫培养中富集环状感染红细胞的有效性,并确定富集后寄生虫的实际数量,而非仅仅是疟原虫血症百分比。这一点很重要,因为针对疟疾的各种分子生物学和疫苗研发需要在各个阶段使用数量可观且未感染红细胞数量最少的纯培养物。将三株恶性疟原虫的同步培养物在冰上暴露于0.015%的等渗皂素溶液中30分钟。然后进行离心,沉淀物再用皂素溶液处理3 - 7分钟。最初,大多数培养物含有约10¹⁰个红细胞,疟原虫血症为1 - 7%,但富集结束时,回收了多达10⁸个含有90 - 99.8%疟原虫血症的红细胞(最大富集)。通过对细胞的显微镜检查计算得出,未感染和感染红细胞的溶血率约为27比1,这可以解释富集现象。其他研究者的研究表明,恶性疟原虫裂殖子入侵会降低红细胞膜脂质,并且有报道称膜胆固醇的减少可使红细胞对皂素产生抗性。在富集培养物中多重感染比例显著增加这一观察结果,强化了裂殖子入侵使红细胞对皂素溶血产生部分抗性的可能性。然而,成熟的无性寄生虫无法通过这种方法富集,这表明含有环状体的红细胞膜与滋养体和裂殖体的红细胞膜可能存在差异。刚从疟疾患者体内获取的环状感染红细胞也无法通过此处描述的方法富集,这表明寄生虫在体外获得了诱导红细胞产生皂素抗性的能力。