Doyle P S, Engel J C, Gam A A, Dvorak J A
Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland 20892.
Parasitology. 1989 Dec;99 Pt 3:311-6. doi: 10.1017/s003118200005900x.
The complete intracellular cycle of the Leishmania mexicana mexicana G. S. strain was quantified in human macrophages and in the mouse IC-21 macrophage line utilizing a culture system that allows the direct observation of individual intracellular parasites. A wide range of pre-replicative lag periods exists, implying that promastigotes may be in any phase of their DNA synthetic cycle when phagocytosed by the macrophage. Amastigotes replicated 2-3 times, after which the host cell died and liberated amastigotes that were taken up by other macrophages and continued to replicate. The mean amastigote population-doubling time in human macrophages (17.5 h) was not statistically different from promastigotes growing in axenic culture (16.4 h), but was nearly 2-fold less than amastigotes growing in mouse-derived IC-21 macrophages (33.7 h). These observations are markedly different from cover-glass culture assays of Leishmania-macrophage interactions and provide an unambiguous description of the intracellular cycle of Leishmania mexicana mexicana.
利用一种能够直接观察单个细胞内寄生虫的培养系统,对墨西哥利什曼原虫墨西哥亚种G.S.株在人巨噬细胞和小鼠IC-21巨噬细胞系中的完整细胞内周期进行了定量分析。存在广泛的复制前延迟期,这意味着前鞭毛体在被巨噬细胞吞噬时可能处于其DNA合成周期的任何阶段。无鞭毛体复制2 - 3次,之后宿主细胞死亡并释放出无鞭毛体,这些无鞭毛体被其他巨噬细胞摄取并继续复制。人巨噬细胞中无鞭毛体群体倍增时间的平均值(17.5小时)与在无菌培养中生长的前鞭毛体(16.4小时)在统计学上无差异,但比在小鼠来源的IC-21巨噬细胞中生长的无鞭毛体(33.7小时)少近2倍。这些观察结果与利什曼原虫 - 巨噬细胞相互作用的盖玻片培养测定明显不同,并提供了对墨西哥利什曼原虫墨西哥亚种细胞内周期的明确描述。