Department of Pathobiology, School of Veterinary Medicine, Shiraz University, Shiraz, Iran.
Department of Pathobiology, School of Veterinary Medicine, Razi University, Kermanshah, Iran.
Exp Parasitol. 2014 May;140:12-7. doi: 10.1016/j.exppara.2014.03.011. Epub 2014 Mar 13.
The present study investigated the ultrastructural characteristics of gamogony and oocyst wall formation of Eimeria arloingi in experimentally infected kids. The 18 newborn animals allocated to 3 equal groups. Two of groups, A, B were inoculated with a single dose of 1×10(3) and 1×10(5) sporulated oocysts of E. arloingi, respectively. At 7, 14, 21, 28, 35, and 42days postinoculation (DPI), 1 kid from each group was necropsied for ultrastructural studies. Transmission electron microscopy was used to screen for the presence of developmental stages of the parasite. All stages of microgametocyte and macrogametocyte developments and also oocyst wall formation were observed from 7 to 42DPI. Different stages of schizigony accompanied by marked proliferation of endoplasmic reticulum, mitochondria and several granular dividing nuclei were diagnosed in the affected epithelial cells. Young microgamonts were recognizable by an electron lucent parasitophorous vacuole and several dividing nuclei with prominent nucleolar and peripheral chromatin in the cytoplasm. At a later stage, the nuclei began to elongate and a single mitochondrion and two basal bodies were observed in close proximity nucleus. These bodies eventually protruded from the surface of the gametocyte and formed two flagellar structures. Up to 80-120 microgametes were produced per microgamont. Macrogamonts were recognized by the presence of wall-forming bodies of types 1 and 2. Electron lucent WFB2 appeared earlier than the electron denser WFB1 during the process of macrogametogenesis. The outer layer of the oocyst wall was formed by the release of the contents of WFB1 at the surface to form an electron dense layer. The WFB2 appeared, subsequently, to give rise to the electron lucent inner layer. WFB1 plays a major role in oocyst wall formation.
本研究调查了实验感染羔羊艾美耳球虫配子生殖和卵囊壁形成的超微结构特征。将 18 只新生动物分为 3 组,每组 6 只。A、B 两组分别接种 1×10(3)和 1×10(5)个孢子化卵囊。感染后 7、14、21、28、35 和 42 天,每组剖杀 1 只羔羊进行超微结构研究。电镜用于筛选寄生虫的发育阶段。在 7 至 42 天期间观察到了小配子体和大配子体发育以及卵囊壁形成的所有阶段。在受影响的上皮细胞中诊断出裂殖阶段和内质网、线粒体和几个颗粒状分裂核的明显增殖。在电镜下,可识别出年轻的小配子体,细胞质中存在一个电子透明的滋养体空泡和几个分裂核,核内有明显的核仁与周边染色质。在后期,核开始伸长,靠近核的位置可以观察到一个单一的线粒体和两个基体。这些体最终从配子体表面突出,并形成两个鞭毛结构。每个小配子体可产生 80-120 个小配子。大配子体通过存在 1 型和 2 型的壁形成体来识别。在大配子生殖过程中,电子透明的 WFB2 比电子致密的 WFB1 更早出现。卵囊壁的外层是通过 WFB1 在表面释放内容物形成电子致密层形成的。随后,WFB2 出现,形成电子透明的内层。WFB1 在卵囊壁形成中起主要作用。